Jump To Section:

Identification Taxonomy Ontology Physical properties Spectra Biological properties Concentrations Links References XML

Record Information

Version

5.0

Status

Detected but not Quantified

Creation Date

2021-09-11 01:39:23 UTC

Update Date

2021-09-26 22:58:35 UTC

HMDB ID

HMDB0248355

Secondary Accession Numbers

None

Metabolite Identification

Common Name

Phosphoaminophosphonic acid-adenylate ester

Description

Phosphoaminophosphonic acid-adenylate ester belongs to the class of organic compounds known as purine ribonucleoside monophosphates. These are nucleotides consisting of a purine base linked to a ribose to which one monophosphate group is attached. Based on a literature review very few articles have been published on Phosphoaminophosphonic acid-adenylate ester. This compound has been identified in human blood as reported by (PMID: 31557052 ). Phosphoaminophosphonic acid-adenylate ester is not a naturally occurring metabolite and is only found in those individuals exposed to this compound or its derivatives. Technically Phosphoaminophosphonic acid-adenylate ester is part of the human exposome. The exposome can be defined as the collection of all the exposures of an individual in a lifetime and how those exposures relate to health. An individual's exposure begins before birth and includes insults from environmental and occupational sources.

Structure

MOL 3D MOL SDF 3D SDF PDB 3D PDB SMILES InChI

  Mrv1652309112103392D          

 31 33  0  0  0  0            999 V2000
    2.0701    1.1104    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.3556    0.6979    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    0.6411    1.1104    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.6411    1.9354    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.3556    2.3479    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0701    1.9354    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    1.3556    3.1729    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1435    2.1904    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6284    1.5229    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1435    0.8555    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3984    0.0709    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0865   -0.5966    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3984   -1.2640    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1831   -1.0091    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1831   -0.1841    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8505   -1.4940    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6042   -1.1584    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2716   -1.6433    0.0000 P   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7565   -0.9759    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7867   -2.3108    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9391   -2.1283    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.6927   -1.7927    0.0000 P   0  0  0  0  0  0  0  0  0  0  0  0
   -4.3572   -1.0390    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -5.4464   -1.4572    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
   -6.1138   -1.9421    0.0000 P   0  0  0  0  0  0  0  0  0  0  0  0
   -6.7813   -2.4270    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -6.5988   -1.2746    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -5.6289   -2.6095    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -5.0283   -2.5464    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1435   -2.0486    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.9115   -0.5966    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  2  0  0  0  0
  2  3  1  0  0  0  0
  3  4  2  0  0  0  0
  4  5  1  0  0  0  0
  5  6  2  0  0  0  0
  1  6  1  0  0  0  0
  5  7  1  0  0  0  0
  4  8  1  0  0  0  0
  8  9  2  0  0  0  0
  9 10  1  0  0  0  0
  3 10  1  0  0  0  0
 10 11  1  0  0  0  0
 11 12  1  0  0  0  0
 12 13  1  0  0  0  0
 13 14  1  0  0  0  0
 14 15  1  0  0  0  0
 11 15  1  0  0  0  0
 14 16  1  0  0  0  0
 16 17  1  0  0  0  0
 17 18  1  0  0  0  0
 18 19  2  0  0  0  0
 18 20  1  0  0  0  0
 18 21  1  0  0  0  0
 21 22  1  0  0  0  0
 22 23  2  0  0  0  0
 22 24  1  0  0  0  0
 24 25  1  0  0  0  0
 25 26  2  0  0  0  0
 25 27  1  0  0  0  0
 25 28  1  0  0  0  0
 22 29  1  0  0  0  0
 13 30  1  0  0  0  0
 12 31  1  0  0  0  0
M  END

HMDB0248355
     RDKit          3D
Phosphoaminophosphonic acid-adenylate ester
 48 50  0  0  0  0  0  0  0  0999 V2000
   -6.0048    4.1918    0.8190 N   0  0  0  0  0  0  0  0  0  0  0  0
   -5.8177    2.8202    0.5052 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.7944    2.0302    0.0188 N   0  0  0  0  0  0  0  0  0  0  0  0
   -6.5974    0.7322   -0.2726 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.3989    0.1537   -0.0894 N   0  0  0  0  0  0  0  0  0  0  0  0
   -4.3800    0.8752    0.3906 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.5830    2.2119    0.6906 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3896    2.6377    1.1408 N   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5057    1.6243    1.1191 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1101    0.5187    0.6532 N   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4935   -0.7993    0.4747 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1365   -0.6686    0.5798 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5501   -0.9659   -0.6203 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.8209   -1.5506   -0.3463 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5486   -0.5833    0.3446 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.1083   -1.1284    0.7075 P   0  0  0  0  0  5  0  0  0  0  0  0
    3.0358   -2.6294    0.9131 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.7014   -0.4040    2.1111 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.1171   -0.7562   -0.6019 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.7186   -1.1423   -0.2647 P   0  0  0  0  0  5  0  0  0  0  0  0
    6.4285   -1.5249   -1.5577 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.8462   -2.4157    0.8376 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.5980    0.2284    0.3910 N   0  0  0  0  0  0  0  0  0  0  0  0
    6.4970    1.5677   -0.7414 P   0  0  0  0  0  5  0  0  0  0  0  0
    7.4370    2.6713   -0.3336 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.9080    2.1296   -0.7948 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.9627    1.0374   -2.2872 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4667   -1.9869   -1.2619 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3480   -3.2013   -0.5879 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8263   -1.4052   -0.8500 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8003   -2.3755   -0.8049 O   0  0  0  0  0  0  0  0  0  0  0  0
   -6.5854    4.7731    0.1810 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.5995    4.6667    1.6508 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.3921    0.1343   -0.6564 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4628    1.7072    1.4352 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8335   -1.5033    1.2639 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4197   -0.0922   -1.2938 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.3581   -1.8452   -1.2503 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.7266   -2.4185    0.3532 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.9524   -0.1460    2.6944 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.4941   -2.1295    1.7105 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.1046    0.4928    1.2766 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.8930    3.0084   -1.2374 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.7874    0.4828   -2.2080 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3570   -2.0645   -2.3405 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5958   -3.0479    0.3580 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1194   -0.6306   -1.6102 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4759   -3.2803   -0.6090 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  2  3  2  0
  3  4  1  0
  4  5  2  0
  5  6  1  0
  6  7  2  0
  7  8  1  0
  8  9  2  0
  9 10  1  0
 10 11  1  0
 11 12  1  0
 12 13  1  0
 13 14  1  0
 14 15  1  0
 15 16  1  0
 16 17  2  0
 16 18  1  0
 16 19  1  0
 19 20  1  0
 20 21  2  0
 20 22  1  0
 20 23  1  0
 23 24  1  0
 24 25  2  0
 24 26  1  0
 24 27  1  0
 13 28  1  0
 28 29  1  0
 28 30  1  0
 30 31  1  0
  7  2  1  0
 30 11  1  0
 10  6  1  0
  1 32  1  0
  1 33  1  0
  4 34  1  0
  9 35  1  0
 11 36  1  0
 13 37  1  0
 14 38  1  0
 14 39  1  0
 18 40  1  0
 22 41  1  0
 23 42  1  0
 26 43  1  0
 27 44  1  0
 28 45  1  0
 29 46  1  0
 30 47  1  0
 31 48  1  0
M  END

  Mrv1652309112103392D          

 31 33  0  0  0  0            999 V2000
    2.0701    1.1104    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.3556    0.6979    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    0.6411    1.1104    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.6411    1.9354    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.3556    2.3479    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0701    1.9354    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    1.3556    3.1729    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1435    2.1904    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6284    1.5229    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1435    0.8555    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3984    0.0709    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0865   -0.5966    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3984   -1.2640    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1831   -1.0091    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1831   -0.1841    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8505   -1.4940    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6042   -1.1584    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2716   -1.6433    0.0000 P   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7565   -0.9759    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7867   -2.3108    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9391   -2.1283    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.6927   -1.7927    0.0000 P   0  0  0  0  0  0  0  0  0  0  0  0
   -4.3572   -1.0390    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -5.4464   -1.4572    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
   -6.1138   -1.9421    0.0000 P   0  0  0  0  0  0  0  0  0  0  0  0
   -6.7813   -2.4270    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -6.5988   -1.2746    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -5.6289   -2.6095    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -5.0283   -2.5464    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1435   -2.0486    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.9115   -0.5966    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  2  0  0  0  0
  2  3  1  0  0  0  0
  3  4  2  0  0  0  0
  4  5  1  0  0  0  0
  5  6  2  0  0  0  0
  1  6  1  0  0  0  0
  5  7  1  0  0  0  0
  4  8  1  0  0  0  0
  8  9  2  0  0  0  0
  9 10  1  0  0  0  0
  3 10  1  0  0  0  0
 10 11  1  0  0  0  0
 11 12  1  0  0  0  0
 12 13  1  0  0  0  0
 13 14  1  0  0  0  0
 14 15  1  0  0  0  0
 11 15  1  0  0  0  0
 14 16  1  0  0  0  0
 16 17  1  0  0  0  0
 17 18  1  0  0  0  0
 18 19  2  0  0  0  0
 18 20  1  0  0  0  0
 18 21  1  0  0  0  0
 21 22  1  0  0  0  0
 22 23  2  0  0  0  0
 22 24  1  0  0  0  0
 24 25  1  0  0  0  0
 25 26  2  0  0  0  0
 25 27  1  0  0  0  0
 25 28  1  0  0  0  0
 22 29  1  0  0  0  0
 13 30  1  0  0  0  0
 12 31  1  0  0  0  0
M  END
> <DATABASE_ID>
HMDB0248355

> <DATABASE_NAME>
hmdb

> <SMILES>
NC1=NC=NC2=C1N=CN2C1OC(COP(O)(=O)OP(O)(=O)NP(O)(O)=O)C(O)C1O

> <INCHI_IDENTIFIER>
InChI=1S/C10H17N6O12P3/c11-8-5-9(13-2-12-8)16(3-14-5)10-7(18)6(17)4(27-10)1-26-31(24,25)28-30(22,23)15-29(19,20)21/h2-4,6-7,10,17-18H,1H2,(H,24,25)(H2,11,12,13)(H4,15,19,20,21,22,23)

> <INCHI_KEY>
PVKSNHVPLWYQGJ-UHFFFAOYSA-N

> <FORMULA>
C10H17N6O12P3

> <MOLECULAR_WEIGHT>
506.197

> <EXACT_MASS>
506.011731005

> <JCHEM_ACCEPTOR_COUNT>
14

> <JCHEM_ATOM_COUNT>
48

> <JCHEM_AVERAGE_POLARIZABILITY>
39.895095343920815

> <JCHEM_BIOAVAILABILITY>
0

> <JCHEM_DONOR_COUNT>
8

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
({[({[5-(6-amino-9H-purin-9-yl)-3,4-dihydroxyoxolan-2-yl]methoxy}(hydroxy)phosphoryl)oxy](hydroxy)phosphoryl}amino)phosphonic acid

> <ALOGPS_LOGP>
-0.99

> <JCHEM_LOGP>
-6.466746638698051

> <ALOGPS_LOGS>
-2.08

> <JCHEM_MDDR_LIKE_RULE>
1

> <JCHEM_NUMBER_OF_RINGS>
3

> <JCHEM_PHYSIOLOGICAL_CHARGE>
-3

> <JCHEM_PKA>
1.4527592406109249

> <JCHEM_PKA_STRONGEST_ACIDIC>
-9.481362254237268

> <JCHEM_PKA_STRONGEST_BASIC>
3.430379359973872

> <JCHEM_POLAR_SURFACE_AREA>
281.93

> <JCHEM_REFRACTIVITY>
97.76409999999998

> <JCHEM_ROTATABLE_BOND_COUNT>
8

> <JCHEM_RULE_OF_FIVE>
0

> <ALOGPS_SOLUBILITY>
4.17e+00 g/l

> <JCHEM_TRADITIONAL_IUPAC>
({[5-(6-aminopurin-9-yl)-3,4-dihydroxyoxolan-2-yl]methoxy(hydroxy)phosphoryl}oxy(hydroxy)phosphoryl)aminophosphonic acid

> <JCHEM_VEBER_RULE>
0

$$$$

HMDB0248355
     RDKit          3D
Phosphoaminophosphonic acid-adenylate ester
 48 50  0  0  0  0  0  0  0  0999 V2000
   -6.0048    4.1918    0.8190 N   0  0  0  0  0  0  0  0  0  0  0  0
   -5.8177    2.8202    0.5052 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.7944    2.0302    0.0188 N   0  0  0  0  0  0  0  0  0  0  0  0
   -6.5974    0.7322   -0.2726 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.3989    0.1537   -0.0894 N   0  0  0  0  0  0  0  0  0  0  0  0
   -4.3800    0.8752    0.3906 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.5830    2.2119    0.6906 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3896    2.6377    1.1408 N   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5057    1.6243    1.1191 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1101    0.5187    0.6532 N   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4935   -0.7993    0.4747 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1365   -0.6686    0.5798 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5501   -0.9659   -0.6203 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.8209   -1.5506   -0.3463 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5486   -0.5833    0.3446 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.1083   -1.1284    0.7075 P   0  0  0  0  0  5  0  0  0  0  0  0
    3.0358   -2.6294    0.9131 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.7014   -0.4040    2.1111 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.1171   -0.7562   -0.6019 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.7186   -1.1423   -0.2647 P   0  0  0  0  0  5  0  0  0  0  0  0
    6.4285   -1.5249   -1.5577 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.8462   -2.4157    0.8376 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.5980    0.2284    0.3910 N   0  0  0  0  0  0  0  0  0  0  0  0
    6.4970    1.5677   -0.7414 P   0  0  0  0  0  5  0  0  0  0  0  0
    7.4370    2.6713   -0.3336 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.9080    2.1296   -0.7948 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.9627    1.0374   -2.2872 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4667   -1.9869   -1.2619 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3480   -3.2013   -0.5879 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8263   -1.4052   -0.8500 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8003   -2.3755   -0.8049 O   0  0  0  0  0  0  0  0  0  0  0  0
   -6.5854    4.7731    0.1810 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.5995    4.6667    1.6508 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.3921    0.1343   -0.6564 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4628    1.7072    1.4352 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8335   -1.5033    1.2639 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4197   -0.0922   -1.2938 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.3581   -1.8452   -1.2503 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.7266   -2.4185    0.3532 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.9524   -0.1460    2.6944 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.4941   -2.1295    1.7105 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.1046    0.4928    1.2766 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.8930    3.0084   -1.2374 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.7874    0.4828   -2.2080 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3570   -2.0645   -2.3405 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5958   -3.0479    0.3580 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1194   -0.6306   -1.6102 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4759   -3.2803   -0.6090 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  2  3  2  0
  3  4  1  0
  4  5  2  0
  5  6  1  0
  6  7  2  0
  7  8  1  0
  8  9  2  0
  9 10  1  0
 10 11  1  0
 11 12  1  0
 12 13  1  0
 13 14  1  0
 14 15  1  0
 15 16  1  0
 16 17  2  0
 16 18  1  0
 16 19  1  0
 19 20  1  0
 20 21  2  0
 20 22  1  0
 20 23  1  0
 23 24  1  0
 24 25  2  0
 24 26  1  0
 24 27  1  0
 13 28  1  0
 28 29  1  0
 28 30  1  0
 30 31  1  0
  7  2  1  0
 30 11  1  0
 10  6  1  0
  1 32  1  0
  1 33  1  0
  4 34  1  0
  9 35  1  0
 11 36  1  0
 13 37  1  0
 14 38  1  0
 14 39  1  0
 18 40  1  0
 22 41  1  0
 23 42  1  0
 26 43  1  0
 27 44  1  0
 28 45  1  0
 29 46  1  0
 30 47  1  0
 31 48  1  0
M  END

HEADER    PROTEIN                                 11-SEP-21   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   11-SEP-21         0                                  
HETATM    1  C   UNK     0       3.864   2.073   0.000  0.00  0.00           C+0
HETATM    2  N   UNK     0       2.530   1.303   0.000  0.00  0.00           N+0
HETATM    3  C   UNK     0       1.197   2.073   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0       1.197   3.613   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0       2.530   4.383   0.000  0.00  0.00           C+0
HETATM    6  N   UNK     0       3.864   3.613   0.000  0.00  0.00           N+0
HETATM    7  N   UNK     0       2.530   5.923   0.000  0.00  0.00           N+0
HETATM    8  N   UNK     0      -0.268   4.089   0.000  0.00  0.00           N+0
HETATM    9  C   UNK     0      -1.173   2.843   0.000  0.00  0.00           C+0
HETATM   10  N   UNK     0      -0.268   1.597   0.000  0.00  0.00           N+0
HETATM   11  C   UNK     0      -0.744   0.132   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0       0.161  -1.114   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0      -0.744  -2.359   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0      -2.208  -1.884   0.000  0.00  0.00           C+0
HETATM   15  O   UNK     0      -2.208  -0.344   0.000  0.00  0.00           O+0
HETATM   16  C   UNK     0      -3.454  -2.789   0.000  0.00  0.00           C+0
HETATM   17  O   UNK     0      -4.861  -2.162   0.000  0.00  0.00           O+0
HETATM   18  P   UNK     0      -6.107  -3.068   0.000  0.00  0.00           P+0
HETATM   19  O   UNK     0      -7.012  -1.822   0.000  0.00  0.00           O+0
HETATM   20  O   UNK     0      -5.202  -4.313   0.000  0.00  0.00           O+0
HETATM   21  O   UNK     0      -7.353  -3.973   0.000  0.00  0.00           O+0
HETATM   22  P   UNK     0      -8.760  -3.346   0.000  0.00  0.00           P+0
HETATM   23  O   UNK     0      -8.133  -1.940   0.000  0.00  0.00           O+0
HETATM   24  N   UNK     0     -10.167  -2.720   0.000  0.00  0.00           N+0
HETATM   25  P   UNK     0     -11.413  -3.625   0.000  0.00  0.00           P+0
HETATM   26  O   UNK     0     -12.658  -4.530   0.000  0.00  0.00           O+0
HETATM   27  O   UNK     0     -12.318  -2.379   0.000  0.00  0.00           O+0
HETATM   28  O   UNK     0     -10.507  -4.871   0.000  0.00  0.00           O+0
HETATM   29  O   UNK     0      -9.386  -4.753   0.000  0.00  0.00           O+0
HETATM   30  O   UNK     0      -0.268  -3.824   0.000  0.00  0.00           O+0
HETATM   31  O   UNK     0       1.701  -1.114   0.000  0.00  0.00           O+0
CONECT    1    2    6                                                       
CONECT    2    1    3                                                       
CONECT    3    2    4   10                                                  
CONECT    4    3    5    8                                                  
CONECT    5    4    6    7                                                  
CONECT    6    5    1                                                       
CONECT    7    5                                                            
CONECT    8    4    9                                                       
CONECT    9    8   10                                                       
CONECT   10    9    3   11                                                  
CONECT   11   10   12   15                                                  
CONECT   12   11   13   31                                                  
CONECT   13   12   14   30                                                  
CONECT   14   13   15   16                                                  
CONECT   15   14   11                                                       
CONECT   16   14   17                                                       
CONECT   17   16   18                                                       
CONECT   18   17   19   20   21                                             
CONECT   19   18                                                            
CONECT   20   18                                                            
CONECT   21   18   22                                                       
CONECT   22   21   23   24   29                                             
CONECT   23   22                                                            
CONECT   24   22   25                                                       
CONECT   25   24   26   27   28                                             
CONECT   26   25                                                            
CONECT   27   25                                                            
CONECT   28   25                                                            
CONECT   29   22                                                            
CONECT   30   13                                                            
CONECT   31   12                                                            
MASTER        0    0    0    0    0    0    0    0   31    0   66    0
END

COMPND    HMDB0248355
HETATM    1  N1  UNL     1      -6.005   4.192   0.819  1.00  0.00           N  
HETATM    2  C1  UNL     1      -5.818   2.820   0.505  1.00  0.00           C  
HETATM    3  N2  UNL     1      -6.794   2.030   0.019  1.00  0.00           N  
HETATM    4  C2  UNL     1      -6.597   0.732  -0.273  1.00  0.00           C  
HETATM    5  N3  UNL     1      -5.399   0.154  -0.089  1.00  0.00           N  
HETATM    6  C3  UNL     1      -4.380   0.875   0.391  1.00  0.00           C  
HETATM    7  C4  UNL     1      -4.583   2.212   0.691  1.00  0.00           C  
HETATM    8  N4  UNL     1      -3.390   2.638   1.141  1.00  0.00           N  
HETATM    9  C5  UNL     1      -2.506   1.624   1.119  1.00  0.00           C  
HETATM   10  N5  UNL     1      -3.110   0.519   0.653  1.00  0.00           N  
HETATM   11  C6  UNL     1      -2.493  -0.799   0.475  1.00  0.00           C  
HETATM   12  O1  UNL     1      -1.137  -0.669   0.580  1.00  0.00           O  
HETATM   13  C7  UNL     1      -0.550  -0.966  -0.620  1.00  0.00           C  
HETATM   14  C8  UNL     1       0.821  -1.551  -0.346  1.00  0.00           C  
HETATM   15  O2  UNL     1       1.549  -0.583   0.345  1.00  0.00           O  
HETATM   16  P1  UNL     1       3.108  -1.128   0.707  1.00  0.00           P  
HETATM   17  O3  UNL     1       3.036  -2.629   0.913  1.00  0.00           O  
HETATM   18  O4  UNL     1       3.701  -0.404   2.111  1.00  0.00           O  
HETATM   19  O5  UNL     1       4.117  -0.756  -0.602  1.00  0.00           O  
HETATM   20  P2  UNL     1       5.719  -1.142  -0.265  1.00  0.00           P  
HETATM   21  O6  UNL     1       6.429  -1.525  -1.558  1.00  0.00           O  
HETATM   22  O7  UNL     1       5.846  -2.416   0.838  1.00  0.00           O  
HETATM   23  N6  UNL     1       6.598   0.228   0.391  1.00  0.00           N  
HETATM   24  P3  UNL     1       6.497   1.568  -0.741  1.00  0.00           P  
HETATM   25  O8  UNL     1       7.437   2.671  -0.334  1.00  0.00           O  
HETATM   26  O9  UNL     1       4.908   2.130  -0.795  1.00  0.00           O  
HETATM   27  O10 UNL     1       6.963   1.037  -2.287  1.00  0.00           O  
HETATM   28  C9  UNL     1      -1.467  -1.987  -1.262  1.00  0.00           C  
HETATM   29  O11 UNL     1      -1.348  -3.201  -0.588  1.00  0.00           O  
HETATM   30  C10 UNL     1      -2.826  -1.405  -0.850  1.00  0.00           C  
HETATM   31  O12 UNL     1      -3.800  -2.375  -0.805  1.00  0.00           O  
HETATM   32  H1  UNL     1      -6.585   4.773   0.181  1.00  0.00           H  
HETATM   33  H2  UNL     1      -5.599   4.667   1.651  1.00  0.00           H  
HETATM   34  H3  UNL     1      -7.392   0.134  -0.656  1.00  0.00           H  
HETATM   35  H4  UNL     1      -1.463   1.707   1.435  1.00  0.00           H  
HETATM   36  H5  UNL     1      -2.834  -1.503   1.264  1.00  0.00           H  
HETATM   37  H6  UNL     1      -0.420  -0.092  -1.294  1.00  0.00           H  
HETATM   38  H7  UNL     1       1.358  -1.845  -1.250  1.00  0.00           H  
HETATM   39  H8  UNL     1       0.727  -2.419   0.353  1.00  0.00           H  
HETATM   40  H9  UNL     1       2.952  -0.146   2.694  1.00  0.00           H  
HETATM   41  H10 UNL     1       5.494  -2.129   1.710  1.00  0.00           H  
HETATM   42  H11 UNL     1       6.105   0.493   1.277  1.00  0.00           H  
HETATM   43  H12 UNL     1       4.893   3.008  -1.237  1.00  0.00           H  
HETATM   44  H13 UNL     1       7.787   0.483  -2.208  1.00  0.00           H  
HETATM   45  H14 UNL     1      -1.357  -2.065  -2.340  1.00  0.00           H  
HETATM   46  H15 UNL     1      -1.596  -3.048   0.358  1.00  0.00           H  
HETATM   47  H16 UNL     1      -3.119  -0.631  -1.610  1.00  0.00           H  
HETATM   48  H17 UNL     1      -3.476  -3.280  -0.609  1.00  0.00           H  
CONECT    1    2   32   33
CONECT    2    3    3    7
CONECT    3    4
CONECT    4    5    5   34
CONECT    5    6
CONECT    6    7    7   10
CONECT    7    8
CONECT    8    9    9
CONECT    9   10   35
CONECT   10   11
CONECT   11   12   30   36
CONECT   12   13
CONECT   13   14   28   37
CONECT   14   15   38   39
CONECT   15   16
CONECT   16   17   17   18   19
CONECT   18   40
CONECT   19   20
CONECT   20   21   21   22   23
CONECT   22   41
CONECT   23   24   42
CONECT   24   25   25   26   27
CONECT   26   43
CONECT   27   44
CONECT   28   29   30   45
CONECT   29   46
CONECT   30   31   47
CONECT   31   48
END

HMDB0248355
     RDKit          3D
Phosphoaminophosphonic acid-adenylate ester
 48 50  0  0  0  0  0  0  0  0999 V2000
   -6.0048    4.1918    0.8190 N   0  0  0  0  0  0  0  0  0  0  0  0
   -5.8177    2.8202    0.5052 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.7944    2.0302    0.0188 N   0  0  0  0  0  0  0  0  0  0  0  0
   -6.5974    0.7322   -0.2726 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.3989    0.1537   -0.0894 N   0  0  0  0  0  0  0  0  0  0  0  0
   -4.3800    0.8752    0.3906 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.5830    2.2119    0.6906 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3896    2.6377    1.1408 N   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5057    1.6243    1.1191 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1101    0.5187    0.6532 N   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4935   -0.7993    0.4747 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1365   -0.6686    0.5798 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5501   -0.9659   -0.6203 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.8209   -1.5506   -0.3463 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5486   -0.5833    0.3446 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.1083   -1.1284    0.7075 P   0  0  0  0  0  5  0  0  0  0  0  0
    3.0358   -2.6294    0.9131 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.7014   -0.4040    2.1111 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.1171   -0.7562   -0.6019 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.7186   -1.1423   -0.2647 P   0  0  0  0  0  5  0  0  0  0  0  0
    6.4285   -1.5249   -1.5577 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.8462   -2.4157    0.8376 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.5980    0.2284    0.3910 N   0  0  0  0  0  0  0  0  0  0  0  0
    6.4970    1.5677   -0.7414 P   0  0  0  0  0  5  0  0  0  0  0  0
    7.4370    2.6713   -0.3336 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.9080    2.1296   -0.7948 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.9627    1.0374   -2.2872 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4667   -1.9869   -1.2619 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3480   -3.2013   -0.5879 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8263   -1.4052   -0.8500 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8003   -2.3755   -0.8049 O   0  0  0  0  0  0  0  0  0  0  0  0
   -6.5854    4.7731    0.1810 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.5995    4.6667    1.6508 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.3921    0.1343   -0.6564 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4628    1.7072    1.4352 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8335   -1.5033    1.2639 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4197   -0.0922   -1.2938 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.3581   -1.8452   -1.2503 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.7266   -2.4185    0.3532 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.9524   -0.1460    2.6944 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.4941   -2.1295    1.7105 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.1046    0.4928    1.2766 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.8930    3.0084   -1.2374 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.7874    0.4828   -2.2080 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3570   -2.0645   -2.3405 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5958   -3.0479    0.3580 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1194   -0.6306   -1.6102 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4759   -3.2803   -0.6090 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  2  3  2  0
  3  4  1  0
  4  5  2  0
  5  6  1  0
  6  7  2  0
  7  8  1  0
  8  9  2  0
  9 10  1  0
 10 11  1  0
 11 12  1  0
 12 13  1  0
 13 14  1  0
 14 15  1  0
 15 16  1  0
 16 17  2  0
 16 18  1  0
 16 19  1  0
 19 20  1  0
 20 21  2  0
 20 22  1  0
 20 23  1  0
 23 24  1  0
 24 25  2  0
 24 26  1  0
 24 27  1  0
 13 28  1  0
 28 29  1  0
 28 30  1  0
 30 31  1  0
  7  2  1  0
 30 11  1  0
 10  6  1  0
  1 32  1  0
  1 33  1  0
  4 34  1  0
  9 35  1  0
 11 36  1  0
 13 37  1  0
 14 38  1  0
 14 39  1  0
 18 40  1  0
 22 41  1  0
 23 42  1  0
 26 43  1  0
 27 44  1  0
 28 45  1  0
 29 46  1  0
 30 47  1  0
 31 48  1  0
M  END

View in JSmol View NMR Assignments View Stereo Labels

Synonyms

Value	Source
Phosphoaminophosphonate-adenylate ester	Generator
Phosphoaminophosphonic acid-adenylic acid ester	Generator

Chemical Formula

C₁₀H₁₇N₆O₁₂P₃

Average Molecular Weight

506.197

Monoisotopic Molecular Weight

506.011731005

IUPAC Name

({[({[5-(6-amino-9H-purin-9-yl)-3,4-dihydroxyoxolan-2-yl]methoxy}(hydroxy)phosphoryl)oxy](hydroxy)phosphoryl}amino)phosphonic acid

Traditional Name

({[5-(6-aminopurin-9-yl)-3,4-dihydroxyoxolan-2-yl]methoxy(hydroxy)phosphoryl}oxy(hydroxy)phosphoryl)aminophosphonic acid

CAS Registry Number

Not Available

SMILES

NC1=NC=NC2=C1N=CN2C1OC(COP(O)(=O)OP(O)(=O)NP(O)(O)=O)C(O)C1O

InChI Identifier

InChI=1S/C10H17N6O12P3/c11-8-5-9(13-2-12-8)16(3-14-5)10-7(18)6(17)4(27-10)1-26-31(24,25)28-30(22,23)15-29(19,20)21/h2-4,6-7,10,17-18H,1H2,(H,24,25)(H2,11,12,13)(H4,15,19,20,21,22,23)

InChI Key

PVKSNHVPLWYQGJ-UHFFFAOYSA-N

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as purine ribonucleoside monophosphates. These are nucleotides consisting of a purine base linked to a ribose to which one monophosphate group is attached.

Kingdom

Organic compounds

Super Class

Nucleosides, nucleotides, and analogues

Class

Purine nucleotides

Sub Class

Purine ribonucleotides

Direct Parent

Purine ribonucleoside monophosphates

Alternative Parents

Substituents

Purine ribonucleoside monophosphate
Pentose phosphate
Pentose-5-phosphate
Glycosyl compound
N-glycosyl compound
6-aminopurine
Monosaccharide phosphate
Pentose monosaccharide
Imidazopyrimidine
Purine
Aminopyrimidine
Monoalkyl phosphate
Alkyl phosphate
Monosaccharide
Pyrimidine
Imidolactam
N-substituted imidazole
Organic phosphoric acid derivative
Phosphoric acid ester
Tetrahydrofuran
Azole
Imidazole
Heteroaromatic compound
Secondary alcohol
1,2-diol
Organoheterocyclic compound
Oxacycle
Azacycle
Organonitrogen compound
Primary amine
Hydrocarbon derivative
Organic oxide
Alcohol
Organopnictogen compound
Organic oxygen compound
Organic nitrogen compound
Organooxygen compound
Amine
Aromatic heteropolycyclic compound

Molecular Framework

Aromatic heteropolycyclic compounds

External Descriptors

Not Available

Ontology

Physiological effect

Not Available

Disposition

Biological location

Non-excretory biofluid

Biofluid or Excreta

Blood (PMID: 31557052)

Source

Exogenous

Exogenous (PMID: 31557052)

Process

Not Available

Role

Not Available

Physical Properties

State

Not Available

Experimental Molecular Properties

Property	Value	Reference
Melting Point	Not Available	Not Available
Boiling Point	Not Available	Not Available
Water Solubility	Not Available	Not Available
LogP	Not Available	Not Available

Experimental Chromatographic Properties

Not Available

Predicted Molecular Properties

Property	Value	Source
logP	-0.99	ALOGPS
logP	-6.5	ChemAxon
logS	-2.1	ALOGPS
pKa (Strongest Acidic)	-9.5	ChemAxon
pKa (Strongest Basic)	3.43	ChemAxon
Physiological Charge	-3	ChemAxon
Hydrogen Acceptor Count	14	ChemAxon
Hydrogen Donor Count	8	ChemAxon
Polar Surface Area	281.93 Å²	ChemAxon
Rotatable Bond Count	8	ChemAxon
Refractivity	97.76 m³·mol⁻¹	ChemAxon
Polarizability	39.9 Å³	ChemAxon
Number of Rings	3	ChemAxon
Bioavailability	No	ChemAxon
Rule of Five	No	ChemAxon
Ghose Filter	No	ChemAxon
Veber's Rule	No	ChemAxon
MDDR-like Rule	Yes	ChemAxon

Predicted Chromatographic Properties

Predicted Collision Cross Sections

Predictor	Adduct Type	CCS Value (Å²)	Reference
DeepCCS	[M+H]+	187.022	30932474
DeepCCS	[M-H]-	184.184	30932474
DeepCCS	[M-2H]-	220.11	30932474
DeepCCS	[M+Na]+	195.5	30932474
AllCCS	[M+H]+	200.0	32859911
AllCCS	[M+H-H2O]+	198.2	32859911
AllCCS	[M+NH4]+	201.7	32859911
AllCCS	[M+Na]+	202.1	32859911
AllCCS	[M-H]-	190.6	32859911
AllCCS	[M+Na-2H]-	190.8	32859911
AllCCS	[M+HCOO]-	191.1	32859911

Predicted Kovats Retention Indices

Underivatized

Metabolite	SMILES	Kovats RI Value	Column Type	Reference
Phosphoaminophosphonic acid-adenylate ester	NC1=NC=NC2=C1N=CN2C1OC(COP(O)(=O)OP(O)(=O)NP(O)(O)=O)C(O)C1O	4837.8	Standard polar	33892256
Phosphoaminophosphonic acid-adenylate ester	NC1=NC=NC2=C1N=CN2C1OC(COP(O)(=O)OP(O)(=O)NP(O)(O)=O)C(O)C1O	2922.4	Standard non polar	33892256
Phosphoaminophosphonic acid-adenylate ester	NC1=NC=NC2=C1N=CN2C1OC(COP(O)(=O)OP(O)(=O)NP(O)(O)=O)C(O)C1O	4488.4	Semi standard non polar	33892256

Derivatized

Derivative Name / Structure	SMILES	Kovats RI Value	Column Type	Reference
Phosphoaminophosphonic acid-adenylate ester,3TMS,isomer #1	C[Si](C)(C)OC1C(COP(=O)(O[Si](C)(C)C)OP(=O)(O)NP(=O)(O)O)OC(N2C=NC3=C(N)N=CN=C32)C1O[Si](C)(C)C	4108.6	Semi standard non polar	33892256
Phosphoaminophosphonic acid-adenylate ester,3TMS,isomer #1	C[Si](C)(C)OC1C(COP(=O)(O[Si](C)(C)C)OP(=O)(O)NP(=O)(O)O)OC(N2C=NC3=C(N)N=CN=C32)C1O[Si](C)(C)C	3797.4	Standard non polar	33892256
Phosphoaminophosphonic acid-adenylate ester,3TMS,isomer #1	C[Si](C)(C)OC1C(COP(=O)(O[Si](C)(C)C)OP(=O)(O)NP(=O)(O)O)OC(N2C=NC3=C(N)N=CN=C32)C1O[Si](C)(C)C	6752.9	Standard polar	33892256
Phosphoaminophosphonic acid-adenylate ester,3TMS,isomer #10	C[Si](C)(C)OC1C(COP(=O)(O)OP(=O)(NP(=O)(O)O[Si](C)(C)C)O[Si](C)(C)C)OC(N2C=NC3=C(N)N=CN=C32)C1O	4069.5	Semi standard non polar	33892256
Phosphoaminophosphonic acid-adenylate ester,3TMS,isomer #10	C[Si](C)(C)OC1C(COP(=O)(O)OP(=O)(NP(=O)(O)O[Si](C)(C)C)O[Si](C)(C)C)OC(N2C=NC3=C(N)N=CN=C32)C1O	3874.3	Standard non polar	33892256
Phosphoaminophosphonic acid-adenylate ester,3TMS,isomer #10	C[Si](C)(C)OC1C(COP(=O)(O)OP(=O)(NP(=O)(O)O[Si](C)(C)C)O[Si](C)(C)C)OC(N2C=NC3=C(N)N=CN=C32)C1O	6682.9	Standard polar	33892256
Phosphoaminophosphonic acid-adenylate ester,3TMS,isomer #11	C[Si](C)(C)NC1=NC=NC2=C1N=CN2C1OC(COP(=O)(O)OP(=O)(NP(=O)(O)O)O[Si](C)(C)C)C(O[Si](C)(C)C)C1O	4158.5	Semi standard non polar	33892256
Phosphoaminophosphonic acid-adenylate ester,3TMS,isomer #11	C[Si](C)(C)NC1=NC=NC2=C1N=CN2C1OC(COP(=O)(O)OP(=O)(NP(=O)(O)O)O[Si](C)(C)C)C(O[Si](C)(C)C)C1O	3905.9	Standard non polar	33892256
Phosphoaminophosphonic acid-adenylate ester,3TMS,isomer #11	C[Si](C)(C)NC1=NC=NC2=C1N=CN2C1OC(COP(=O)(O)OP(=O)(NP(=O)(O)O)O[Si](C)(C)C)C(O[Si](C)(C)C)C1O	6666.9	Standard polar	33892256
Phosphoaminophosphonic acid-adenylate ester,3TMS,isomer #12	C[Si](C)(C)OC1C(COP(=O)(O)OP(=O)(O[Si](C)(C)C)N([Si](C)(C)C)P(=O)(O)O)OC(N2C=NC3=C(N)N=CN=C32)C1O	4161.1	Semi standard non polar	33892256
Phosphoaminophosphonic acid-adenylate ester,3TMS,isomer #12	C[Si](C)(C)OC1C(COP(=O)(O)OP(=O)(O[Si](C)(C)C)N([Si](C)(C)C)P(=O)(O)O)OC(N2C=NC3=C(N)N=CN=C32)C1O	4056.2	Standard non polar	33892256
Phosphoaminophosphonic acid-adenylate ester,3TMS,isomer #12	C[Si](C)(C)OC1C(COP(=O)(O)OP(=O)(O[Si](C)(C)C)N([Si](C)(C)C)P(=O)(O)O)OC(N2C=NC3=C(N)N=CN=C32)C1O	6636.1	Standard polar	33892256
Phosphoaminophosphonic acid-adenylate ester,3TMS,isomer #13	C[Si](C)(C)OC1C(COP(=O)(O)OP(=O)(O)NP(=O)(O[Si](C)(C)C)O[Si](C)(C)C)OC(N2C=NC3=C(N)N=CN=C32)C1O	4081.9	Semi standard non polar	33892256
Phosphoaminophosphonic acid-adenylate ester,3TMS,isomer #13	C[Si](C)(C)OC1C(COP(=O)(O)OP(=O)(O)NP(=O)(O[Si](C)(C)C)O[Si](C)(C)C)OC(N2C=NC3=C(N)N=CN=C32)C1O	3846.9	Standard non polar	33892256
Phosphoaminophosphonic acid-adenylate ester,3TMS,isomer #13	C[Si](C)(C)OC1C(COP(=O)(O)OP(=O)(O)NP(=O)(O[Si](C)(C)C)O[Si](C)(C)C)OC(N2C=NC3=C(N)N=CN=C32)C1O	6666.2	Standard polar	33892256
Phosphoaminophosphonic acid-adenylate ester,3TMS,isomer #14	C[Si](C)(C)NC1=NC=NC2=C1N=CN2C1OC(COP(=O)(O)OP(=O)(O)NP(=O)(O)O[Si](C)(C)C)C(O[Si](C)(C)C)C1O	4129.3	Semi standard non polar	33892256
Phosphoaminophosphonic acid-adenylate ester,3TMS,isomer #14	C[Si](C)(C)NC1=NC=NC2=C1N=CN2C1OC(COP(=O)(O)OP(=O)(O)NP(=O)(O)O[Si](C)(C)C)C(O[Si](C)(C)C)C1O	3901.0	Standard non polar	33892256
Phosphoaminophosphonic acid-adenylate ester,3TMS,isomer #14	C[Si](C)(C)NC1=NC=NC2=C1N=CN2C1OC(COP(=O)(O)OP(=O)(O)NP(=O)(O)O[Si](C)(C)C)C(O[Si](C)(C)C)C1O	6680.2	Standard polar	33892256
Phosphoaminophosphonic acid-adenylate ester,3TMS,isomer #15	C[Si](C)(C)OC1C(COP(=O)(O)OP(=O)(O)N([Si](C)(C)C)P(=O)(O)O[Si](C)(C)C)OC(N2C=NC3=C(N)N=CN=C32)C1O	4120.3	Semi standard non polar	33892256
Phosphoaminophosphonic acid-adenylate ester,3TMS,isomer #15	C[Si](C)(C)OC1C(COP(=O)(O)OP(=O)(O)N([Si](C)(C)C)P(=O)(O)O[Si](C)(C)C)OC(N2C=NC3=C(N)N=CN=C32)C1O	4020.3	Standard non polar	33892256
Phosphoaminophosphonic acid-adenylate ester,3TMS,isomer #15	C[Si](C)(C)OC1C(COP(=O)(O)OP(=O)(O)N([Si](C)(C)C)P(=O)(O)O[Si](C)(C)C)OC(N2C=NC3=C(N)N=CN=C32)C1O	6621.5	Standard polar	33892256
Phosphoaminophosphonic acid-adenylate ester,3TMS,isomer #16	C[Si](C)(C)OC1C(COP(=O)(O)OP(=O)(O)NP(=O)(O)O)OC(N2C=NC3=C(N([Si](C)(C)C)[Si](C)(C)C)N=CN=C32)C1O	4161.3	Semi standard non polar	33892256
Phosphoaminophosphonic acid-adenylate ester,3TMS,isomer #16	C[Si](C)(C)OC1C(COP(=O)(O)OP(=O)(O)NP(=O)(O)O)OC(N2C=NC3=C(N([Si](C)(C)C)[Si](C)(C)C)N=CN=C32)C1O	3950.6	Standard non polar	33892256
Phosphoaminophosphonic acid-adenylate ester,3TMS,isomer #16	C[Si](C)(C)OC1C(COP(=O)(O)OP(=O)(O)NP(=O)(O)O)OC(N2C=NC3=C(N([Si](C)(C)C)[Si](C)(C)C)N=CN=C32)C1O	6792.0	Standard polar	33892256
Phosphoaminophosphonic acid-adenylate ester,3TMS,isomer #17	C[Si](C)(C)NC1=NC=NC2=C1N=CN2C1OC(COP(=O)(O)OP(=O)(O)N([Si](C)(C)C)P(=O)(O)O)C(O[Si](C)(C)C)C1O	4178.1	Semi standard non polar	33892256
Phosphoaminophosphonic acid-adenylate ester,3TMS,isomer #17	C[Si](C)(C)NC1=NC=NC2=C1N=CN2C1OC(COP(=O)(O)OP(=O)(O)N([Si](C)(C)C)P(=O)(O)O)C(O[Si](C)(C)C)C1O	4068.3	Standard non polar	33892256
Phosphoaminophosphonic acid-adenylate ester,3TMS,isomer #17	C[Si](C)(C)NC1=NC=NC2=C1N=CN2C1OC(COP(=O)(O)OP(=O)(O)N([Si](C)(C)C)P(=O)(O)O)C(O[Si](C)(C)C)C1O	6622.4	Standard polar	33892256
Phosphoaminophosphonic acid-adenylate ester,3TMS,isomer #18	C[Si](C)(C)OC1C(O)C(COP(=O)(O[Si](C)(C)C)OP(=O)(NP(=O)(O)O)O[Si](C)(C)C)OC1N1C=NC2=C(N)N=CN=C21	4116.0	Semi standard non polar	33892256
Phosphoaminophosphonic acid-adenylate ester,3TMS,isomer #18	C[Si](C)(C)OC1C(O)C(COP(=O)(O[Si](C)(C)C)OP(=O)(NP(=O)(O)O)O[Si](C)(C)C)OC1N1C=NC2=C(N)N=CN=C21	3893.8	Standard non polar	33892256
Phosphoaminophosphonic acid-adenylate ester,3TMS,isomer #18	C[Si](C)(C)OC1C(O)C(COP(=O)(O[Si](C)(C)C)OP(=O)(NP(=O)(O)O)O[Si](C)(C)C)OC1N1C=NC2=C(N)N=CN=C21	6652.8	Standard polar	33892256
Phosphoaminophosphonic acid-adenylate ester,3TMS,isomer #19	C[Si](C)(C)OC1C(O)C(COP(=O)(O[Si](C)(C)C)OP(=O)(O)NP(=O)(O)O[Si](C)(C)C)OC1N1C=NC2=C(N)N=CN=C21	4089.7	Semi standard non polar	33892256
Phosphoaminophosphonic acid-adenylate ester,3TMS,isomer #19	C[Si](C)(C)OC1C(O)C(COP(=O)(O[Si](C)(C)C)OP(=O)(O)NP(=O)(O)O[Si](C)(C)C)OC1N1C=NC2=C(N)N=CN=C21	3890.6	Standard non polar	33892256
Phosphoaminophosphonic acid-adenylate ester,3TMS,isomer #19	C[Si](C)(C)OC1C(O)C(COP(=O)(O[Si](C)(C)C)OP(=O)(O)NP(=O)(O)O[Si](C)(C)C)OC1N1C=NC2=C(N)N=CN=C21	6636.1	Standard polar	33892256
Phosphoaminophosphonic acid-adenylate ester,3TMS,isomer #2	C[Si](C)(C)OC1C(COP(=O)(O)OP(=O)(NP(=O)(O)O)O[Si](C)(C)C)OC(N2C=NC3=C(N)N=CN=C32)C1O[Si](C)(C)C	4082.9	Semi standard non polar	33892256
Phosphoaminophosphonic acid-adenylate ester,3TMS,isomer #2	C[Si](C)(C)OC1C(COP(=O)(O)OP(=O)(NP(=O)(O)O)O[Si](C)(C)C)OC(N2C=NC3=C(N)N=CN=C32)C1O[Si](C)(C)C	3787.0	Standard non polar	33892256
Phosphoaminophosphonic acid-adenylate ester,3TMS,isomer #2	C[Si](C)(C)OC1C(COP(=O)(O)OP(=O)(NP(=O)(O)O)O[Si](C)(C)C)OC(N2C=NC3=C(N)N=CN=C32)C1O[Si](C)(C)C	6830.6	Standard polar	33892256
Phosphoaminophosphonic acid-adenylate ester,3TMS,isomer #20	C[Si](C)(C)NC1=NC=NC2=C1N=CN2C1OC(COP(=O)(O[Si](C)(C)C)OP(=O)(O)NP(=O)(O)O)C(O)C1O[Si](C)(C)C	4172.9	Semi standard non polar	33892256
Phosphoaminophosphonic acid-adenylate ester,3TMS,isomer #20	C[Si](C)(C)NC1=NC=NC2=C1N=CN2C1OC(COP(=O)(O[Si](C)(C)C)OP(=O)(O)NP(=O)(O)O)C(O)C1O[Si](C)(C)C	3910.9	Standard non polar	33892256
Phosphoaminophosphonic acid-adenylate ester,3TMS,isomer #20	C[Si](C)(C)NC1=NC=NC2=C1N=CN2C1OC(COP(=O)(O[Si](C)(C)C)OP(=O)(O)NP(=O)(O)O)C(O)C1O[Si](C)(C)C	6643.3	Standard polar	33892256
Phosphoaminophosphonic acid-adenylate ester,3TMS,isomer #21	C[Si](C)(C)OC1C(O)C(COP(=O)(O[Si](C)(C)C)OP(=O)(O)N([Si](C)(C)C)P(=O)(O)O)OC1N1C=NC2=C(N)N=CN=C21	4151.5	Semi standard non polar	33892256
Phosphoaminophosphonic acid-adenylate ester,3TMS,isomer #21	C[Si](C)(C)OC1C(O)C(COP(=O)(O[Si](C)(C)C)OP(=O)(O)N([Si](C)(C)C)P(=O)(O)O)OC1N1C=NC2=C(N)N=CN=C21	4057.3	Standard non polar	33892256
Phosphoaminophosphonic acid-adenylate ester,3TMS,isomer #21	C[Si](C)(C)OC1C(O)C(COP(=O)(O[Si](C)(C)C)OP(=O)(O)N([Si](C)(C)C)P(=O)(O)O)OC1N1C=NC2=C(N)N=CN=C21	6593.0	Standard polar	33892256
Phosphoaminophosphonic acid-adenylate ester,3TMS,isomer #22	C[Si](C)(C)OC1C(O)C(COP(=O)(O)OP(=O)(NP(=O)(O)O[Si](C)(C)C)O[Si](C)(C)C)OC1N1C=NC2=C(N)N=CN=C21	4063.2	Semi standard non polar	33892256
Phosphoaminophosphonic acid-adenylate ester,3TMS,isomer #22	C[Si](C)(C)OC1C(O)C(COP(=O)(O)OP(=O)(NP(=O)(O)O[Si](C)(C)C)O[Si](C)(C)C)OC1N1C=NC2=C(N)N=CN=C21	3876.8	Standard non polar	33892256
Phosphoaminophosphonic acid-adenylate ester,3TMS,isomer #22	C[Si](C)(C)OC1C(O)C(COP(=O)(O)OP(=O)(NP(=O)(O)O[Si](C)(C)C)O[Si](C)(C)C)OC1N1C=NC2=C(N)N=CN=C21	6692.5	Standard polar	33892256
Phosphoaminophosphonic acid-adenylate ester,3TMS,isomer #23	C[Si](C)(C)NC1=NC=NC2=C1N=CN2C1OC(COP(=O)(O)OP(=O)(NP(=O)(O)O)O[Si](C)(C)C)C(O)C1O[Si](C)(C)C	4155.7	Semi standard non polar	33892256
Phosphoaminophosphonic acid-adenylate ester,3TMS,isomer #23	C[Si](C)(C)NC1=NC=NC2=C1N=CN2C1OC(COP(=O)(O)OP(=O)(NP(=O)(O)O)O[Si](C)(C)C)C(O)C1O[Si](C)(C)C	3907.6	Standard non polar	33892256
Phosphoaminophosphonic acid-adenylate ester,3TMS,isomer #23	C[Si](C)(C)NC1=NC=NC2=C1N=CN2C1OC(COP(=O)(O)OP(=O)(NP(=O)(O)O)O[Si](C)(C)C)C(O)C1O[Si](C)(C)C	6678.2	Standard polar	33892256
Phosphoaminophosphonic acid-adenylate ester,3TMS,isomer #24	C[Si](C)(C)OC1C(O)C(COP(=O)(O)OP(=O)(O[Si](C)(C)C)N([Si](C)(C)C)P(=O)(O)O)OC1N1C=NC2=C(N)N=CN=C21	4151.2	Semi standard non polar	33892256
Phosphoaminophosphonic acid-adenylate ester,3TMS,isomer #24	C[Si](C)(C)OC1C(O)C(COP(=O)(O)OP(=O)(O[Si](C)(C)C)N([Si](C)(C)C)P(=O)(O)O)OC1N1C=NC2=C(N)N=CN=C21	4053.2	Standard non polar	33892256
Phosphoaminophosphonic acid-adenylate ester,3TMS,isomer #24	C[Si](C)(C)OC1C(O)C(COP(=O)(O)OP(=O)(O[Si](C)(C)C)N([Si](C)(C)C)P(=O)(O)O)OC1N1C=NC2=C(N)N=CN=C21	6646.0	Standard polar	33892256
Phosphoaminophosphonic acid-adenylate ester,3TMS,isomer #25	C[Si](C)(C)OC1C(O)C(COP(=O)(O)OP(=O)(O)NP(=O)(O[Si](C)(C)C)O[Si](C)(C)C)OC1N1C=NC2=C(N)N=CN=C21	4075.0	Semi standard non polar	33892256
Phosphoaminophosphonic acid-adenylate ester,3TMS,isomer #25	C[Si](C)(C)OC1C(O)C(COP(=O)(O)OP(=O)(O)NP(=O)(O[Si](C)(C)C)O[Si](C)(C)C)OC1N1C=NC2=C(N)N=CN=C21	3850.6	Standard non polar	33892256
Phosphoaminophosphonic acid-adenylate ester,3TMS,isomer #25	C[Si](C)(C)OC1C(O)C(COP(=O)(O)OP(=O)(O)NP(=O)(O[Si](C)(C)C)O[Si](C)(C)C)OC1N1C=NC2=C(N)N=CN=C21	6676.0	Standard polar	33892256
Phosphoaminophosphonic acid-adenylate ester,3TMS,isomer #26	C[Si](C)(C)NC1=NC=NC2=C1N=CN2C1OC(COP(=O)(O)OP(=O)(O)NP(=O)(O)O[Si](C)(C)C)C(O)C1O[Si](C)(C)C	4127.0	Semi standard non polar	33892256
Phosphoaminophosphonic acid-adenylate ester,3TMS,isomer #26	C[Si](C)(C)NC1=NC=NC2=C1N=CN2C1OC(COP(=O)(O)OP(=O)(O)NP(=O)(O)O[Si](C)(C)C)C(O)C1O[Si](C)(C)C	3902.0	Standard non polar	33892256
Phosphoaminophosphonic acid-adenylate ester,3TMS,isomer #26	C[Si](C)(C)NC1=NC=NC2=C1N=CN2C1OC(COP(=O)(O)OP(=O)(O)NP(=O)(O)O[Si](C)(C)C)C(O)C1O[Si](C)(C)C	6691.5	Standard polar	33892256
Phosphoaminophosphonic acid-adenylate ester,3TMS,isomer #27	C[Si](C)(C)OC1C(O)C(COP(=O)(O)OP(=O)(O)N([Si](C)(C)C)P(=O)(O)O[Si](C)(C)C)OC1N1C=NC2=C(N)N=CN=C21	4108.6	Semi standard non polar	33892256
Phosphoaminophosphonic acid-adenylate ester,3TMS,isomer #27	C[Si](C)(C)OC1C(O)C(COP(=O)(O)OP(=O)(O)N([Si](C)(C)C)P(=O)(O)O[Si](C)(C)C)OC1N1C=NC2=C(N)N=CN=C21	4018.9	Standard non polar	33892256
Phosphoaminophosphonic acid-adenylate ester,3TMS,isomer #27	C[Si](C)(C)OC1C(O)C(COP(=O)(O)OP(=O)(O)N([Si](C)(C)C)P(=O)(O)O[Si](C)(C)C)OC1N1C=NC2=C(N)N=CN=C21	6631.4	Standard polar	33892256
Phosphoaminophosphonic acid-adenylate ester,3TMS,isomer #28	C[Si](C)(C)OC1C(O)C(COP(=O)(O)OP(=O)(O)NP(=O)(O)O)OC1N1C=NC2=C(N([Si](C)(C)C)[Si](C)(C)C)N=CN=C21	4155.5	Semi standard non polar	33892256
Phosphoaminophosphonic acid-adenylate ester,3TMS,isomer #28	C[Si](C)(C)OC1C(O)C(COP(=O)(O)OP(=O)(O)NP(=O)(O)O)OC1N1C=NC2=C(N([Si](C)(C)C)[Si](C)(C)C)N=CN=C21	3955.8	Standard non polar	33892256
Phosphoaminophosphonic acid-adenylate ester,3TMS,isomer #28	C[Si](C)(C)OC1C(O)C(COP(=O)(O)OP(=O)(O)NP(=O)(O)O)OC1N1C=NC2=C(N([Si](C)(C)C)[Si](C)(C)C)N=CN=C21	6803.6	Standard polar	33892256
Phosphoaminophosphonic acid-adenylate ester,3TMS,isomer #29	C[Si](C)(C)NC1=NC=NC2=C1N=CN2C1OC(COP(=O)(O)OP(=O)(O)N([Si](C)(C)C)P(=O)(O)O)C(O)C1O[Si](C)(C)C	4168.0	Semi standard non polar	33892256
Phosphoaminophosphonic acid-adenylate ester,3TMS,isomer #29	C[Si](C)(C)NC1=NC=NC2=C1N=CN2C1OC(COP(=O)(O)OP(=O)(O)N([Si](C)(C)C)P(=O)(O)O)C(O)C1O[Si](C)(C)C	4065.1	Standard non polar	33892256
Phosphoaminophosphonic acid-adenylate ester,3TMS,isomer #29	C[Si](C)(C)NC1=NC=NC2=C1N=CN2C1OC(COP(=O)(O)OP(=O)(O)N([Si](C)(C)C)P(=O)(O)O)C(O)C1O[Si](C)(C)C	6633.8	Standard polar	33892256
Phosphoaminophosphonic acid-adenylate ester,3TMS,isomer #3	C[Si](C)(C)OC1C(COP(=O)(O)OP(=O)(O)NP(=O)(O)O[Si](C)(C)C)OC(N2C=NC3=C(N)N=CN=C32)C1O[Si](C)(C)C	4057.5	Semi standard non polar	33892256
Phosphoaminophosphonic acid-adenylate ester,3TMS,isomer #3	C[Si](C)(C)OC1C(COP(=O)(O)OP(=O)(O)NP(=O)(O)O[Si](C)(C)C)OC(N2C=NC3=C(N)N=CN=C32)C1O[Si](C)(C)C	3786.3	Standard non polar	33892256
Phosphoaminophosphonic acid-adenylate ester,3TMS,isomer #3	C[Si](C)(C)OC1C(COP(=O)(O)OP(=O)(O)NP(=O)(O)O[Si](C)(C)C)OC(N2C=NC3=C(N)N=CN=C32)C1O[Si](C)(C)C	6781.8	Standard polar	33892256
Phosphoaminophosphonic acid-adenylate ester,3TMS,isomer #30	C[Si](C)(C)OP(=O)(O)NP(=O)(O[Si](C)(C)C)OP(=O)(OCC1OC(N2C=NC3=C(N)N=CN=C32)C(O)C1O)O[Si](C)(C)C	4109.5	Semi standard non polar	33892256
Phosphoaminophosphonic acid-adenylate ester,3TMS,isomer #30	C[Si](C)(C)OP(=O)(O)NP(=O)(O[Si](C)(C)C)OP(=O)(OCC1OC(N2C=NC3=C(N)N=CN=C32)C(O)C1O)O[Si](C)(C)C	4001.0	Standard non polar	33892256
Phosphoaminophosphonic acid-adenylate ester,3TMS,isomer #30	C[Si](C)(C)OP(=O)(O)NP(=O)(O[Si](C)(C)C)OP(=O)(OCC1OC(N2C=NC3=C(N)N=CN=C32)C(O)C1O)O[Si](C)(C)C	6525.5	Standard polar	33892256
Phosphoaminophosphonic acid-adenylate ester,3TMS,isomer #31	C[Si](C)(C)NC1=NC=NC2=C1N=CN2C1OC(COP(=O)(O[Si](C)(C)C)OP(=O)(NP(=O)(O)O)O[Si](C)(C)C)C(O)C1O	4205.4	Semi standard non polar	33892256
Phosphoaminophosphonic acid-adenylate ester,3TMS,isomer #31	C[Si](C)(C)NC1=NC=NC2=C1N=CN2C1OC(COP(=O)(O[Si](C)(C)C)OP(=O)(NP(=O)(O)O)O[Si](C)(C)C)C(O)C1O	4063.6	Standard non polar	33892256
Phosphoaminophosphonic acid-adenylate ester,3TMS,isomer #31	C[Si](C)(C)NC1=NC=NC2=C1N=CN2C1OC(COP(=O)(O[Si](C)(C)C)OP(=O)(NP(=O)(O)O)O[Si](C)(C)C)C(O)C1O	6457.0	Standard polar	33892256
Phosphoaminophosphonic acid-adenylate ester,3TMS,isomer #32	C[Si](C)(C)OP(=O)(OCC1OC(N2C=NC3=C(N)N=CN=C32)C(O)C1O)OP(=O)(O[Si](C)(C)C)N([Si](C)(C)C)P(=O)(O)O	4204.3	Semi standard non polar	33892256
Phosphoaminophosphonic acid-adenylate ester,3TMS,isomer #32	C[Si](C)(C)OP(=O)(OCC1OC(N2C=NC3=C(N)N=CN=C32)C(O)C1O)OP(=O)(O[Si](C)(C)C)N([Si](C)(C)C)P(=O)(O)O	4188.1	Standard non polar	33892256
Phosphoaminophosphonic acid-adenylate ester,3TMS,isomer #32	C[Si](C)(C)OP(=O)(OCC1OC(N2C=NC3=C(N)N=CN=C32)C(O)C1O)OP(=O)(O[Si](C)(C)C)N([Si](C)(C)C)P(=O)(O)O	6501.9	Standard polar	33892256
Phosphoaminophosphonic acid-adenylate ester,3TMS,isomer #33	C[Si](C)(C)OP(=O)(NP(=O)(O)OP(=O)(OCC1OC(N2C=NC3=C(N)N=CN=C32)C(O)C1O)O[Si](C)(C)C)O[Si](C)(C)C	4127.7	Semi standard non polar	33892256
Phosphoaminophosphonic acid-adenylate ester,3TMS,isomer #33	C[Si](C)(C)OP(=O)(NP(=O)(O)OP(=O)(OCC1OC(N2C=NC3=C(N)N=CN=C32)C(O)C1O)O[Si](C)(C)C)O[Si](C)(C)C	3973.5	Standard non polar	33892256
Phosphoaminophosphonic acid-adenylate ester,3TMS,isomer #33	C[Si](C)(C)OP(=O)(NP(=O)(O)OP(=O)(OCC1OC(N2C=NC3=C(N)N=CN=C32)C(O)C1O)O[Si](C)(C)C)O[Si](C)(C)C	6545.3	Standard polar	33892256
Phosphoaminophosphonic acid-adenylate ester,3TMS,isomer #34	C[Si](C)(C)NC1=NC=NC2=C1N=CN2C1OC(COP(=O)(O[Si](C)(C)C)OP(=O)(O)NP(=O)(O)O[Si](C)(C)C)C(O)C1O	4177.9	Semi standard non polar	33892256
Phosphoaminophosphonic acid-adenylate ester,3TMS,isomer #34	C[Si](C)(C)NC1=NC=NC2=C1N=CN2C1OC(COP(=O)(O[Si](C)(C)C)OP(=O)(O)NP(=O)(O)O[Si](C)(C)C)C(O)C1O	4059.2	Standard non polar	33892256
Phosphoaminophosphonic acid-adenylate ester,3TMS,isomer #34	C[Si](C)(C)NC1=NC=NC2=C1N=CN2C1OC(COP(=O)(O[Si](C)(C)C)OP(=O)(O)NP(=O)(O)O[Si](C)(C)C)C(O)C1O	6493.5	Standard polar	33892256
Phosphoaminophosphonic acid-adenylate ester,3TMS,isomer #35	C[Si](C)(C)OP(=O)(OCC1OC(N2C=NC3=C(N)N=CN=C32)C(O)C1O)OP(=O)(O)N([Si](C)(C)C)P(=O)(O)O[Si](C)(C)C	4169.2	Semi standard non polar	33892256
Phosphoaminophosphonic acid-adenylate ester,3TMS,isomer #35	C[Si](C)(C)OP(=O)(OCC1OC(N2C=NC3=C(N)N=CN=C32)C(O)C1O)OP(=O)(O)N([Si](C)(C)C)P(=O)(O)O[Si](C)(C)C	4161.5	Standard non polar	33892256
Phosphoaminophosphonic acid-adenylate ester,3TMS,isomer #35	C[Si](C)(C)OP(=O)(OCC1OC(N2C=NC3=C(N)N=CN=C32)C(O)C1O)OP(=O)(O)N([Si](C)(C)C)P(=O)(O)O[Si](C)(C)C	6507.9	Standard polar	33892256
Phosphoaminophosphonic acid-adenylate ester,3TMS,isomer #36	C[Si](C)(C)OP(=O)(OCC1OC(N2C=NC3=C(N([Si](C)(C)C)[Si](C)(C)C)N=CN=C32)C(O)C1O)OP(=O)(O)NP(=O)(O)O	4212.2	Semi standard non polar	33892256
Phosphoaminophosphonic acid-adenylate ester,3TMS,isomer #36	C[Si](C)(C)OP(=O)(OCC1OC(N2C=NC3=C(N([Si](C)(C)C)[Si](C)(C)C)N=CN=C32)C(O)C1O)OP(=O)(O)NP(=O)(O)O	4115.8	Standard non polar	33892256
Phosphoaminophosphonic acid-adenylate ester,3TMS,isomer #36	C[Si](C)(C)OP(=O)(OCC1OC(N2C=NC3=C(N([Si](C)(C)C)[Si](C)(C)C)N=CN=C32)C(O)C1O)OP(=O)(O)NP(=O)(O)O	6580.9	Standard polar	33892256
Phosphoaminophosphonic acid-adenylate ester,3TMS,isomer #37	C[Si](C)(C)NC1=NC=NC2=C1N=CN2C1OC(COP(=O)(O[Si](C)(C)C)OP(=O)(O)N([Si](C)(C)C)P(=O)(O)O)C(O)C1O	4241.0	Semi standard non polar	33892256
Phosphoaminophosphonic acid-adenylate ester,3TMS,isomer #37	C[Si](C)(C)NC1=NC=NC2=C1N=CN2C1OC(COP(=O)(O[Si](C)(C)C)OP(=O)(O)N([Si](C)(C)C)P(=O)(O)O)C(O)C1O	4224.4	Standard non polar	33892256
Phosphoaminophosphonic acid-adenylate ester,3TMS,isomer #37	C[Si](C)(C)NC1=NC=NC2=C1N=CN2C1OC(COP(=O)(O[Si](C)(C)C)OP(=O)(O)N([Si](C)(C)C)P(=O)(O)O)C(O)C1O	6453.8	Standard polar	33892256
Phosphoaminophosphonic acid-adenylate ester,3TMS,isomer #38	C[Si](C)(C)OP(=O)(NP(=O)(O[Si](C)(C)C)OP(=O)(O)OCC1OC(N2C=NC3=C(N)N=CN=C32)C(O)C1O)O[Si](C)(C)C	4105.9	Semi standard non polar	33892256
Phosphoaminophosphonic acid-adenylate ester,3TMS,isomer #38	C[Si](C)(C)OP(=O)(NP(=O)(O[Si](C)(C)C)OP(=O)(O)OCC1OC(N2C=NC3=C(N)N=CN=C32)C(O)C1O)O[Si](C)(C)C	3949.2	Standard non polar	33892256
Phosphoaminophosphonic acid-adenylate ester,3TMS,isomer #38	C[Si](C)(C)OP(=O)(NP(=O)(O[Si](C)(C)C)OP(=O)(O)OCC1OC(N2C=NC3=C(N)N=CN=C32)C(O)C1O)O[Si](C)(C)C	6579.8	Standard polar	33892256
Phosphoaminophosphonic acid-adenylate ester,3TMS,isomer #39	C[Si](C)(C)NC1=NC=NC2=C1N=CN2C1OC(COP(=O)(O)OP(=O)(NP(=O)(O)O[Si](C)(C)C)O[Si](C)(C)C)C(O)C1O	4162.9	Semi standard non polar	33892256
Phosphoaminophosphonic acid-adenylate ester,3TMS,isomer #39	C[Si](C)(C)NC1=NC=NC2=C1N=CN2C1OC(COP(=O)(O)OP(=O)(NP(=O)(O)O[Si](C)(C)C)O[Si](C)(C)C)C(O)C1O	4045.9	Standard non polar	33892256
Phosphoaminophosphonic acid-adenylate ester,3TMS,isomer #39	C[Si](C)(C)NC1=NC=NC2=C1N=CN2C1OC(COP(=O)(O)OP(=O)(NP(=O)(O)O[Si](C)(C)C)O[Si](C)(C)C)C(O)C1O	6515.7	Standard polar	33892256
Phosphoaminophosphonic acid-adenylate ester,3TMS,isomer #4	C[Si](C)(C)NC1=NC=NC2=C1N=CN2C1OC(COP(=O)(O)OP(=O)(O)NP(=O)(O)O)C(O[Si](C)(C)C)C1O[Si](C)(C)C	4131.5	Semi standard non polar	33892256
Phosphoaminophosphonic acid-adenylate ester,3TMS,isomer #4	C[Si](C)(C)NC1=NC=NC2=C1N=CN2C1OC(COP(=O)(O)OP(=O)(O)NP(=O)(O)O)C(O[Si](C)(C)C)C1O[Si](C)(C)C	3789.2	Standard non polar	33892256
Phosphoaminophosphonic acid-adenylate ester,3TMS,isomer #4	C[Si](C)(C)NC1=NC=NC2=C1N=CN2C1OC(COP(=O)(O)OP(=O)(O)NP(=O)(O)O)C(O[Si](C)(C)C)C1O[Si](C)(C)C	6833.9	Standard polar	33892256
Phosphoaminophosphonic acid-adenylate ester,3TMS,isomer #40	C[Si](C)(C)OP(=O)(O)N([Si](C)(C)C)P(=O)(O[Si](C)(C)C)OP(=O)(O)OCC1OC(N2C=NC3=C(N)N=CN=C32)C(O)C1O	4167.8	Semi standard non polar	33892256
Phosphoaminophosphonic acid-adenylate ester,3TMS,isomer #40	C[Si](C)(C)OP(=O)(O)N([Si](C)(C)C)P(=O)(O[Si](C)(C)C)OP(=O)(O)OCC1OC(N2C=NC3=C(N)N=CN=C32)C(O)C1O	4139.6	Standard non polar	33892256
Phosphoaminophosphonic acid-adenylate ester,3TMS,isomer #40	C[Si](C)(C)OP(=O)(O)N([Si](C)(C)C)P(=O)(O[Si](C)(C)C)OP(=O)(O)OCC1OC(N2C=NC3=C(N)N=CN=C32)C(O)C1O	6540.8	Standard polar	33892256
Phosphoaminophosphonic acid-adenylate ester,3TMS,isomer #41	C[Si](C)(C)OP(=O)(NP(=O)(O)O)OP(=O)(O)OCC1OC(N2C=NC3=C(N([Si](C)(C)C)[Si](C)(C)C)N=CN=C32)C(O)C1O	4203.1	Semi standard non polar	33892256
Phosphoaminophosphonic acid-adenylate ester,3TMS,isomer #41	C[Si](C)(C)OP(=O)(NP(=O)(O)O)OP(=O)(O)OCC1OC(N2C=NC3=C(N([Si](C)(C)C)[Si](C)(C)C)N=CN=C32)C(O)C1O	4109.4	Standard non polar	33892256
Phosphoaminophosphonic acid-adenylate ester,3TMS,isomer #41	C[Si](C)(C)OP(=O)(NP(=O)(O)O)OP(=O)(O)OCC1OC(N2C=NC3=C(N([Si](C)(C)C)[Si](C)(C)C)N=CN=C32)C(O)C1O	6608.9	Standard polar	33892256
Phosphoaminophosphonic acid-adenylate ester,3TMS,isomer #42	C[Si](C)(C)NC1=NC=NC2=C1N=CN2C1OC(COP(=O)(O)OP(=O)(O[Si](C)(C)C)N([Si](C)(C)C)P(=O)(O)O)C(O)C1O	4240.1	Semi standard non polar	33892256
Phosphoaminophosphonic acid-adenylate ester,3TMS,isomer #42	C[Si](C)(C)NC1=NC=NC2=C1N=CN2C1OC(COP(=O)(O)OP(=O)(O[Si](C)(C)C)N([Si](C)(C)C)P(=O)(O)O)C(O)C1O	4220.0	Standard non polar	33892256
Phosphoaminophosphonic acid-adenylate ester,3TMS,isomer #42	C[Si](C)(C)NC1=NC=NC2=C1N=CN2C1OC(COP(=O)(O)OP(=O)(O[Si](C)(C)C)N([Si](C)(C)C)P(=O)(O)O)C(O)C1O	6480.3	Standard polar	33892256
Phosphoaminophosphonic acid-adenylate ester,3TMS,isomer #43	C[Si](C)(C)NC1=NC=NC2=C1N=CN2C1OC(COP(=O)(O)OP(=O)(O)NP(=O)(O[Si](C)(C)C)O[Si](C)(C)C)C(O)C1O	4171.3	Semi standard non polar	33892256
Phosphoaminophosphonic acid-adenylate ester,3TMS,isomer #43	C[Si](C)(C)NC1=NC=NC2=C1N=CN2C1OC(COP(=O)(O)OP(=O)(O)NP(=O)(O[Si](C)(C)C)O[Si](C)(C)C)C(O)C1O	4018.1	Standard non polar	33892256
Phosphoaminophosphonic acid-adenylate ester,3TMS,isomer #43	C[Si](C)(C)NC1=NC=NC2=C1N=CN2C1OC(COP(=O)(O)OP(=O)(O)NP(=O)(O[Si](C)(C)C)O[Si](C)(C)C)C(O)C1O	6528.3	Standard polar	33892256
Phosphoaminophosphonic acid-adenylate ester,3TMS,isomer #44	C[Si](C)(C)OP(=O)(O[Si](C)(C)C)N([Si](C)(C)C)P(=O)(O)OP(=O)(O)OCC1OC(N2C=NC3=C(N)N=CN=C32)C(O)C1O	4157.8	Semi standard non polar	33892256
Phosphoaminophosphonic acid-adenylate ester,3TMS,isomer #44	C[Si](C)(C)OP(=O)(O[Si](C)(C)C)N([Si](C)(C)C)P(=O)(O)OP(=O)(O)OCC1OC(N2C=NC3=C(N)N=CN=C32)C(O)C1O	4130.6	Standard non polar	33892256
Phosphoaminophosphonic acid-adenylate ester,3TMS,isomer #44	C[Si](C)(C)OP(=O)(O[Si](C)(C)C)N([Si](C)(C)C)P(=O)(O)OP(=O)(O)OCC1OC(N2C=NC3=C(N)N=CN=C32)C(O)C1O	6537.4	Standard polar	33892256
Phosphoaminophosphonic acid-adenylate ester,3TMS,isomer #45	C[Si](C)(C)OP(=O)(O)NP(=O)(O)OP(=O)(O)OCC1OC(N2C=NC3=C(N([Si](C)(C)C)[Si](C)(C)C)N=CN=C32)C(O)C1O	4194.6	Semi standard non polar	33892256
Phosphoaminophosphonic acid-adenylate ester,3TMS,isomer #45	C[Si](C)(C)OP(=O)(O)NP(=O)(O)OP(=O)(O)OCC1OC(N2C=NC3=C(N([Si](C)(C)C)[Si](C)(C)C)N=CN=C32)C(O)C1O	4104.7	Standard non polar	33892256
Phosphoaminophosphonic acid-adenylate ester,3TMS,isomer #45	C[Si](C)(C)OP(=O)(O)NP(=O)(O)OP(=O)(O)OCC1OC(N2C=NC3=C(N([Si](C)(C)C)[Si](C)(C)C)N=CN=C32)C(O)C1O	6634.3	Standard polar	33892256
Phosphoaminophosphonic acid-adenylate ester,3TMS,isomer #46	C[Si](C)(C)NC1=NC=NC2=C1N=CN2C1OC(COP(=O)(O)OP(=O)(O)N([Si](C)(C)C)P(=O)(O)O[Si](C)(C)C)C(O)C1O	4203.9	Semi standard non polar	33892256
Phosphoaminophosphonic acid-adenylate ester,3TMS,isomer #46	C[Si](C)(C)NC1=NC=NC2=C1N=CN2C1OC(COP(=O)(O)OP(=O)(O)N([Si](C)(C)C)P(=O)(O)O[Si](C)(C)C)C(O)C1O	4188.8	Standard non polar	33892256
Phosphoaminophosphonic acid-adenylate ester,3TMS,isomer #46	C[Si](C)(C)NC1=NC=NC2=C1N=CN2C1OC(COP(=O)(O)OP(=O)(O)N([Si](C)(C)C)P(=O)(O)O[Si](C)(C)C)C(O)C1O	6507.4	Standard polar	33892256
Phosphoaminophosphonic acid-adenylate ester,3TMS,isomer #47	C[Si](C)(C)N(C1=NC=NC2=C1N=CN2C1OC(COP(=O)(O)OP(=O)(O)N([Si](C)(C)C)P(=O)(O)O)C(O)C1O)[Si](C)(C)C	4251.4	Semi standard non polar	33892256
Phosphoaminophosphonic acid-adenylate ester,3TMS,isomer #47	C[Si](C)(C)N(C1=NC=NC2=C1N=CN2C1OC(COP(=O)(O)OP(=O)(O)N([Si](C)(C)C)P(=O)(O)O)C(O)C1O)[Si](C)(C)C	4275.6	Standard non polar	33892256
Phosphoaminophosphonic acid-adenylate ester,3TMS,isomer #47	C[Si](C)(C)N(C1=NC=NC2=C1N=CN2C1OC(COP(=O)(O)OP(=O)(O)N([Si](C)(C)C)P(=O)(O)O)C(O)C1O)[Si](C)(C)C	6578.3	Standard polar	33892256
Phosphoaminophosphonic acid-adenylate ester,3TMS,isomer #5	C[Si](C)(C)OC1C(COP(=O)(O)OP(=O)(O)N([Si](C)(C)C)P(=O)(O)O)OC(N2C=NC3=C(N)N=CN=C32)C1O[Si](C)(C)C	4111.0	Semi standard non polar	33892256
Phosphoaminophosphonic acid-adenylate ester,3TMS,isomer #5	C[Si](C)(C)OC1C(COP(=O)(O)OP(=O)(O)N([Si](C)(C)C)P(=O)(O)O)OC(N2C=NC3=C(N)N=CN=C32)C1O[Si](C)(C)C	3952.6	Standard non polar	33892256
Phosphoaminophosphonic acid-adenylate ester,3TMS,isomer #5	C[Si](C)(C)OC1C(COP(=O)(O)OP(=O)(O)N([Si](C)(C)C)P(=O)(O)O)OC(N2C=NC3=C(N)N=CN=C32)C1O[Si](C)(C)C	6726.1	Standard polar	33892256
Phosphoaminophosphonic acid-adenylate ester,3TMS,isomer #6	C[Si](C)(C)OC1C(COP(=O)(O[Si](C)(C)C)OP(=O)(NP(=O)(O)O)O[Si](C)(C)C)OC(N2C=NC3=C(N)N=CN=C32)C1O	4122.9	Semi standard non polar	33892256
Phosphoaminophosphonic acid-adenylate ester,3TMS,isomer #6	C[Si](C)(C)OC1C(COP(=O)(O[Si](C)(C)C)OP(=O)(NP(=O)(O)O)O[Si](C)(C)C)OC(N2C=NC3=C(N)N=CN=C32)C1O	3889.6	Standard non polar	33892256
Phosphoaminophosphonic acid-adenylate ester,3TMS,isomer #6	C[Si](C)(C)OC1C(COP(=O)(O[Si](C)(C)C)OP(=O)(NP(=O)(O)O)O[Si](C)(C)C)OC(N2C=NC3=C(N)N=CN=C32)C1O	6641.5	Standard polar	33892256
Phosphoaminophosphonic acid-adenylate ester,3TMS,isomer #7	C[Si](C)(C)OC1C(COP(=O)(O[Si](C)(C)C)OP(=O)(O)NP(=O)(O)O[Si](C)(C)C)OC(N2C=NC3=C(N)N=CN=C32)C1O	4095.7	Semi standard non polar	33892256
Phosphoaminophosphonic acid-adenylate ester,3TMS,isomer #7	C[Si](C)(C)OC1C(COP(=O)(O[Si](C)(C)C)OP(=O)(O)NP(=O)(O)O[Si](C)(C)C)OC(N2C=NC3=C(N)N=CN=C32)C1O	3887.0	Standard non polar	33892256
Phosphoaminophosphonic acid-adenylate ester,3TMS,isomer #7	C[Si](C)(C)OC1C(COP(=O)(O[Si](C)(C)C)OP(=O)(O)NP(=O)(O)O[Si](C)(C)C)OC(N2C=NC3=C(N)N=CN=C32)C1O	6624.8	Standard polar	33892256
Phosphoaminophosphonic acid-adenylate ester,3TMS,isomer #8	C[Si](C)(C)NC1=NC=NC2=C1N=CN2C1OC(COP(=O)(O[Si](C)(C)C)OP(=O)(O)NP(=O)(O)O)C(O[Si](C)(C)C)C1O	4177.1	Semi standard non polar	33892256
Phosphoaminophosphonic acid-adenylate ester,3TMS,isomer #8	C[Si](C)(C)NC1=NC=NC2=C1N=CN2C1OC(COP(=O)(O[Si](C)(C)C)OP(=O)(O)NP(=O)(O)O)C(O[Si](C)(C)C)C1O	3910.2	Standard non polar	33892256
Phosphoaminophosphonic acid-adenylate ester,3TMS,isomer #8	C[Si](C)(C)NC1=NC=NC2=C1N=CN2C1OC(COP(=O)(O[Si](C)(C)C)OP(=O)(O)NP(=O)(O)O)C(O[Si](C)(C)C)C1O	6627.2	Standard polar	33892256
Phosphoaminophosphonic acid-adenylate ester,3TMS,isomer #9	C[Si](C)(C)OC1C(COP(=O)(O[Si](C)(C)C)OP(=O)(O)N([Si](C)(C)C)P(=O)(O)O)OC(N2C=NC3=C(N)N=CN=C32)C1O	4164.8	Semi standard non polar	33892256
Phosphoaminophosphonic acid-adenylate ester,3TMS,isomer #9	C[Si](C)(C)OC1C(COP(=O)(O[Si](C)(C)C)OP(=O)(O)N([Si](C)(C)C)P(=O)(O)O)OC(N2C=NC3=C(N)N=CN=C32)C1O	4056.9	Standard non polar	33892256
Phosphoaminophosphonic acid-adenylate ester,3TMS,isomer #9	C[Si](C)(C)OC1C(COP(=O)(O[Si](C)(C)C)OP(=O)(O)N([Si](C)(C)C)P(=O)(O)O)OC(N2C=NC3=C(N)N=CN=C32)C1O	6581.9	Standard polar	33892256
Phosphoaminophosphonic acid-adenylate ester,4TMS,isomer #1	C[Si](C)(C)OC1C(COP(=O)(O[Si](C)(C)C)OP(=O)(NP(=O)(O)O)O[Si](C)(C)C)OC(N2C=NC3=C(N)N=CN=C32)C1O[Si](C)(C)C	4031.5	Semi standard non polar	33892256
Phosphoaminophosphonic acid-adenylate ester,4TMS,isomer #1	C[Si](C)(C)OC1C(COP(=O)(O[Si](C)(C)C)OP(=O)(NP(=O)(O)O)O[Si](C)(C)C)OC(N2C=NC3=C(N)N=CN=C32)C1O[Si](C)(C)C	3811.8	Standard non polar	33892256
Phosphoaminophosphonic acid-adenylate ester,4TMS,isomer #1	C[Si](C)(C)OC1C(COP(=O)(O[Si](C)(C)C)OP(=O)(NP(=O)(O)O)O[Si](C)(C)C)OC(N2C=NC3=C(N)N=CN=C32)C1O[Si](C)(C)C	6405.4	Standard polar	33892256
Phosphoaminophosphonic acid-adenylate ester,4TMS,isomer #10	C[Si](C)(C)OC1C(COP(=O)(O)OP(=O)(O)N([Si](C)(C)C)P(=O)(O)O[Si](C)(C)C)OC(N2C=NC3=C(N)N=CN=C32)C1O[Si](C)(C)C	4033.5	Semi standard non polar	33892256
Phosphoaminophosphonic acid-adenylate ester,4TMS,isomer #10	C[Si](C)(C)OC1C(COP(=O)(O)OP(=O)(O)N([Si](C)(C)C)P(=O)(O)O[Si](C)(C)C)OC(N2C=NC3=C(N)N=CN=C32)C1O[Si](C)(C)C	3961.1	Standard non polar	33892256
Phosphoaminophosphonic acid-adenylate ester,4TMS,isomer #10	C[Si](C)(C)OC1C(COP(=O)(O)OP(=O)(O)N([Si](C)(C)C)P(=O)(O)O[Si](C)(C)C)OC(N2C=NC3=C(N)N=CN=C32)C1O[Si](C)(C)C	6403.4	Standard polar	33892256
Phosphoaminophosphonic acid-adenylate ester,4TMS,isomer #11	C[Si](C)(C)OC1C(COP(=O)(O)OP(=O)(O)NP(=O)(O)O)OC(N2C=NC3=C(N([Si](C)(C)C)[Si](C)(C)C)N=CN=C32)C1O[Si](C)(C)C	4074.7	Semi standard non polar	33892256
Phosphoaminophosphonic acid-adenylate ester,4TMS,isomer #11	C[Si](C)(C)OC1C(COP(=O)(O)OP(=O)(O)NP(=O)(O)O)OC(N2C=NC3=C(N([Si](C)(C)C)[Si](C)(C)C)N=CN=C32)C1O[Si](C)(C)C	3873.8	Standard non polar	33892256
Phosphoaminophosphonic acid-adenylate ester,4TMS,isomer #11	C[Si](C)(C)OC1C(COP(=O)(O)OP(=O)(O)NP(=O)(O)O)OC(N2C=NC3=C(N([Si](C)(C)C)[Si](C)(C)C)N=CN=C32)C1O[Si](C)(C)C	6426.6	Standard polar	33892256
Phosphoaminophosphonic acid-adenylate ester,4TMS,isomer #12	C[Si](C)(C)NC1=NC=NC2=C1N=CN2C1OC(COP(=O)(O)OP(=O)(O)N([Si](C)(C)C)P(=O)(O)O)C(O[Si](C)(C)C)C1O[Si](C)(C)C	4100.3	Semi standard non polar	33892256
Phosphoaminophosphonic acid-adenylate ester,4TMS,isomer #12	C[Si](C)(C)NC1=NC=NC2=C1N=CN2C1OC(COP(=O)(O)OP(=O)(O)N([Si](C)(C)C)P(=O)(O)O)C(O[Si](C)(C)C)C1O[Si](C)(C)C	4018.2	Standard non polar	33892256
Phosphoaminophosphonic acid-adenylate ester,4TMS,isomer #12	C[Si](C)(C)NC1=NC=NC2=C1N=CN2C1OC(COP(=O)(O)OP(=O)(O)N([Si](C)(C)C)P(=O)(O)O)C(O[Si](C)(C)C)C1O[Si](C)(C)C	6338.0	Standard polar	33892256
Phosphoaminophosphonic acid-adenylate ester,4TMS,isomer #13	C[Si](C)(C)OC1C(COP(=O)(O[Si](C)(C)C)OP(=O)(NP(=O)(O)O[Si](C)(C)C)O[Si](C)(C)C)OC(N2C=NC3=C(N)N=CN=C32)C1O	4019.8	Semi standard non polar	33892256
Phosphoaminophosphonic acid-adenylate ester,4TMS,isomer #13	C[Si](C)(C)OC1C(COP(=O)(O[Si](C)(C)C)OP(=O)(NP(=O)(O)O[Si](C)(C)C)O[Si](C)(C)C)OC(N2C=NC3=C(N)N=CN=C32)C1O	3899.3	Standard non polar	33892256
Phosphoaminophosphonic acid-adenylate ester,4TMS,isomer #13	C[Si](C)(C)OC1C(COP(=O)(O[Si](C)(C)C)OP(=O)(NP(=O)(O)O[Si](C)(C)C)O[Si](C)(C)C)OC(N2C=NC3=C(N)N=CN=C32)C1O	6281.0	Standard polar	33892256
Phosphoaminophosphonic acid-adenylate ester,4TMS,isomer #14	C[Si](C)(C)NC1=NC=NC2=C1N=CN2C1OC(COP(=O)(O[Si](C)(C)C)OP(=O)(NP(=O)(O)O)O[Si](C)(C)C)C(O[Si](C)(C)C)C1O	4098.0	Semi standard non polar	33892256
Phosphoaminophosphonic acid-adenylate ester,4TMS,isomer #14	C[Si](C)(C)NC1=NC=NC2=C1N=CN2C1OC(COP(=O)(O[Si](C)(C)C)OP(=O)(NP(=O)(O)O)O[Si](C)(C)C)C(O[Si](C)(C)C)C1O	3948.9	Standard non polar	33892256
Phosphoaminophosphonic acid-adenylate ester,4TMS,isomer #14	C[Si](C)(C)NC1=NC=NC2=C1N=CN2C1OC(COP(=O)(O[Si](C)(C)C)OP(=O)(NP(=O)(O)O)O[Si](C)(C)C)C(O[Si](C)(C)C)C1O	6164.0	Standard polar	33892256
Phosphoaminophosphonic acid-adenylate ester,4TMS,isomer #15	C[Si](C)(C)OC1C(COP(=O)(O[Si](C)(C)C)OP(=O)(O[Si](C)(C)C)N([Si](C)(C)C)P(=O)(O)O)OC(N2C=NC3=C(N)N=CN=C32)C1O	4106.4	Semi standard non polar	33892256
Phosphoaminophosphonic acid-adenylate ester,4TMS,isomer #15	C[Si](C)(C)OC1C(COP(=O)(O[Si](C)(C)C)OP(=O)(O[Si](C)(C)C)N([Si](C)(C)C)P(=O)(O)O)OC(N2C=NC3=C(N)N=CN=C32)C1O	4078.2	Standard non polar	33892256
Phosphoaminophosphonic acid-adenylate ester,4TMS,isomer #15	C[Si](C)(C)OC1C(COP(=O)(O[Si](C)(C)C)OP(=O)(O[Si](C)(C)C)N([Si](C)(C)C)P(=O)(O)O)OC(N2C=NC3=C(N)N=CN=C32)C1O	6257.7	Standard polar	33892256
Phosphoaminophosphonic acid-adenylate ester,4TMS,isomer #16	C[Si](C)(C)OC1C(COP(=O)(O[Si](C)(C)C)OP(=O)(O)NP(=O)(O[Si](C)(C)C)O[Si](C)(C)C)OC(N2C=NC3=C(N)N=CN=C32)C1O	4034.8	Semi standard non polar	33892256
Phosphoaminophosphonic acid-adenylate ester,4TMS,isomer #16	C[Si](C)(C)OC1C(COP(=O)(O[Si](C)(C)C)OP(=O)(O)NP(=O)(O[Si](C)(C)C)O[Si](C)(C)C)OC(N2C=NC3=C(N)N=CN=C32)C1O	3868.8	Standard non polar	33892256
Phosphoaminophosphonic acid-adenylate ester,4TMS,isomer #16	C[Si](C)(C)OC1C(COP(=O)(O[Si](C)(C)C)OP(=O)(O)NP(=O)(O[Si](C)(C)C)O[Si](C)(C)C)OC(N2C=NC3=C(N)N=CN=C32)C1O	6308.3	Standard polar	33892256
Phosphoaminophosphonic acid-adenylate ester,4TMS,isomer #17	C[Si](C)(C)NC1=NC=NC2=C1N=CN2C1OC(COP(=O)(O[Si](C)(C)C)OP(=O)(O)NP(=O)(O)O[Si](C)(C)C)C(O[Si](C)(C)C)C1O	4081.3	Semi standard non polar	33892256
Phosphoaminophosphonic acid-adenylate ester,4TMS,isomer #17	C[Si](C)(C)NC1=NC=NC2=C1N=CN2C1OC(COP(=O)(O[Si](C)(C)C)OP(=O)(O)NP(=O)(O)O[Si](C)(C)C)C(O[Si](C)(C)C)C1O	3942.4	Standard non polar	33892256
Phosphoaminophosphonic acid-adenylate ester,4TMS,isomer #17	C[Si](C)(C)NC1=NC=NC2=C1N=CN2C1OC(COP(=O)(O[Si](C)(C)C)OP(=O)(O)NP(=O)(O)O[Si](C)(C)C)C(O[Si](C)(C)C)C1O	6219.1	Standard polar	33892256
Phosphoaminophosphonic acid-adenylate ester,4TMS,isomer #18	C[Si](C)(C)OC1C(COP(=O)(O[Si](C)(C)C)OP(=O)(O)N([Si](C)(C)C)P(=O)(O)O[Si](C)(C)C)OC(N2C=NC3=C(N)N=CN=C32)C1O	4072.5	Semi standard non polar	33892256
Phosphoaminophosphonic acid-adenylate ester,4TMS,isomer #18	C[Si](C)(C)OC1C(COP(=O)(O[Si](C)(C)C)OP(=O)(O)N([Si](C)(C)C)P(=O)(O)O[Si](C)(C)C)OC(N2C=NC3=C(N)N=CN=C32)C1O	4048.5	Standard non polar	33892256
Phosphoaminophosphonic acid-adenylate ester,4TMS,isomer #18	C[Si](C)(C)OC1C(COP(=O)(O[Si](C)(C)C)OP(=O)(O)N([Si](C)(C)C)P(=O)(O)O[Si](C)(C)C)OC(N2C=NC3=C(N)N=CN=C32)C1O	6281.3	Standard polar	33892256
Phosphoaminophosphonic acid-adenylate ester,4TMS,isomer #19	C[Si](C)(C)OC1C(COP(=O)(O[Si](C)(C)C)OP(=O)(O)NP(=O)(O)O)OC(N2C=NC3=C(N([Si](C)(C)C)[Si](C)(C)C)N=CN=C32)C1O	4120.4	Semi standard non polar	33892256
Phosphoaminophosphonic acid-adenylate ester,4TMS,isomer #19	C[Si](C)(C)OC1C(COP(=O)(O[Si](C)(C)C)OP(=O)(O)NP(=O)(O)O)OC(N2C=NC3=C(N([Si](C)(C)C)[Si](C)(C)C)N=CN=C32)C1O	3983.1	Standard non polar	33892256
Phosphoaminophosphonic acid-adenylate ester,4TMS,isomer #19	C[Si](C)(C)OC1C(COP(=O)(O[Si](C)(C)C)OP(=O)(O)NP(=O)(O)O)OC(N2C=NC3=C(N([Si](C)(C)C)[Si](C)(C)C)N=CN=C32)C1O	6244.5	Standard polar	33892256
Phosphoaminophosphonic acid-adenylate ester,4TMS,isomer #2	C[Si](C)(C)OC1C(COP(=O)(O[Si](C)(C)C)OP(=O)(O)NP(=O)(O)O[Si](C)(C)C)OC(N2C=NC3=C(N)N=CN=C32)C1O[Si](C)(C)C	4018.0	Semi standard non polar	33892256
Phosphoaminophosphonic acid-adenylate ester,4TMS,isomer #2	C[Si](C)(C)OC1C(COP(=O)(O[Si](C)(C)C)OP(=O)(O)NP(=O)(O)O[Si](C)(C)C)OC(N2C=NC3=C(N)N=CN=C32)C1O[Si](C)(C)C	3815.0	Standard non polar	33892256
Phosphoaminophosphonic acid-adenylate ester,4TMS,isomer #2	C[Si](C)(C)OC1C(COP(=O)(O[Si](C)(C)C)OP(=O)(O)NP(=O)(O)O[Si](C)(C)C)OC(N2C=NC3=C(N)N=CN=C32)C1O[Si](C)(C)C	6408.9	Standard polar	33892256
Phosphoaminophosphonic acid-adenylate ester,4TMS,isomer #20	C[Si](C)(C)NC1=NC=NC2=C1N=CN2C1OC(COP(=O)(O[Si](C)(C)C)OP(=O)(O)N([Si](C)(C)C)P(=O)(O)O)C(O[Si](C)(C)C)C1O	4134.6	Semi standard non polar	33892256
Phosphoaminophosphonic acid-adenylate ester,4TMS,isomer #20	C[Si](C)(C)NC1=NC=NC2=C1N=CN2C1OC(COP(=O)(O[Si](C)(C)C)OP(=O)(O)N([Si](C)(C)C)P(=O)(O)O)C(O[Si](C)(C)C)C1O	4116.7	Standard non polar	33892256
Phosphoaminophosphonic acid-adenylate ester,4TMS,isomer #20	C[Si](C)(C)NC1=NC=NC2=C1N=CN2C1OC(COP(=O)(O[Si](C)(C)C)OP(=O)(O)N([Si](C)(C)C)P(=O)(O)O)C(O[Si](C)(C)C)C1O	6192.0	Standard polar	33892256
Phosphoaminophosphonic acid-adenylate ester,4TMS,isomer #21	C[Si](C)(C)OC1C(COP(=O)(O)OP(=O)(NP(=O)(O[Si](C)(C)C)O[Si](C)(C)C)O[Si](C)(C)C)OC(N2C=NC3=C(N)N=CN=C32)C1O	4011.7	Semi standard non polar	33892256
Phosphoaminophosphonic acid-adenylate ester,4TMS,isomer #21	C[Si](C)(C)OC1C(COP(=O)(O)OP(=O)(NP(=O)(O[Si](C)(C)C)O[Si](C)(C)C)O[Si](C)(C)C)OC(N2C=NC3=C(N)N=CN=C32)C1O	3852.5	Standard non polar	33892256
Phosphoaminophosphonic acid-adenylate ester,4TMS,isomer #21	C[Si](C)(C)OC1C(COP(=O)(O)OP(=O)(NP(=O)(O[Si](C)(C)C)O[Si](C)(C)C)O[Si](C)(C)C)OC(N2C=NC3=C(N)N=CN=C32)C1O	6333.7	Standard polar	33892256
Phosphoaminophosphonic acid-adenylate ester,4TMS,isomer #22	C[Si](C)(C)NC1=NC=NC2=C1N=CN2C1OC(COP(=O)(O)OP(=O)(NP(=O)(O)O[Si](C)(C)C)O[Si](C)(C)C)C(O[Si](C)(C)C)C1O	4062.3	Semi standard non polar	33892256
Phosphoaminophosphonic acid-adenylate ester,4TMS,isomer #22	C[Si](C)(C)NC1=NC=NC2=C1N=CN2C1OC(COP(=O)(O)OP(=O)(NP(=O)(O)O[Si](C)(C)C)O[Si](C)(C)C)C(O[Si](C)(C)C)C1O	3936.1	Standard non polar	33892256
Phosphoaminophosphonic acid-adenylate ester,4TMS,isomer #22	C[Si](C)(C)NC1=NC=NC2=C1N=CN2C1OC(COP(=O)(O)OP(=O)(NP(=O)(O)O[Si](C)(C)C)O[Si](C)(C)C)C(O[Si](C)(C)C)C1O	6224.8	Standard polar	33892256
Phosphoaminophosphonic acid-adenylate ester,4TMS,isomer #23	C[Si](C)(C)OC1C(COP(=O)(O)OP(=O)(O[Si](C)(C)C)N([Si](C)(C)C)P(=O)(O)O[Si](C)(C)C)OC(N2C=NC3=C(N)N=CN=C32)C1O	4069.0	Semi standard non polar	33892256
Phosphoaminophosphonic acid-adenylate ester,4TMS,isomer #23	C[Si](C)(C)OC1C(COP(=O)(O)OP(=O)(O[Si](C)(C)C)N([Si](C)(C)C)P(=O)(O)O[Si](C)(C)C)OC(N2C=NC3=C(N)N=CN=C32)C1O	4032.0	Standard non polar	33892256
Phosphoaminophosphonic acid-adenylate ester,4TMS,isomer #23	C[Si](C)(C)OC1C(COP(=O)(O)OP(=O)(O[Si](C)(C)C)N([Si](C)(C)C)P(=O)(O)O[Si](C)(C)C)OC(N2C=NC3=C(N)N=CN=C32)C1O	6292.0	Standard polar	33892256
Phosphoaminophosphonic acid-adenylate ester,4TMS,isomer #24	C[Si](C)(C)OC1C(COP(=O)(O)OP(=O)(NP(=O)(O)O)O[Si](C)(C)C)OC(N2C=NC3=C(N([Si](C)(C)C)[Si](C)(C)C)N=CN=C32)C1O	4090.2	Semi standard non polar	33892256
Phosphoaminophosphonic acid-adenylate ester,4TMS,isomer #24	C[Si](C)(C)OC1C(COP(=O)(O)OP(=O)(NP(=O)(O)O)O[Si](C)(C)C)OC(N2C=NC3=C(N([Si](C)(C)C)[Si](C)(C)C)N=CN=C32)C1O	3980.5	Standard non polar	33892256
Phosphoaminophosphonic acid-adenylate ester,4TMS,isomer #24	C[Si](C)(C)OC1C(COP(=O)(O)OP(=O)(NP(=O)(O)O)O[Si](C)(C)C)OC(N2C=NC3=C(N([Si](C)(C)C)[Si](C)(C)C)N=CN=C32)C1O	6235.8	Standard polar	33892256
Phosphoaminophosphonic acid-adenylate ester,4TMS,isomer #25	C[Si](C)(C)NC1=NC=NC2=C1N=CN2C1OC(COP(=O)(O)OP(=O)(O[Si](C)(C)C)N([Si](C)(C)C)P(=O)(O)O)C(O[Si](C)(C)C)C1O	4129.5	Semi standard non polar	33892256
Phosphoaminophosphonic acid-adenylate ester,4TMS,isomer #25	C[Si](C)(C)NC1=NC=NC2=C1N=CN2C1OC(COP(=O)(O)OP(=O)(O[Si](C)(C)C)N([Si](C)(C)C)P(=O)(O)O)C(O[Si](C)(C)C)C1O	4118.7	Standard non polar	33892256
Phosphoaminophosphonic acid-adenylate ester,4TMS,isomer #25	C[Si](C)(C)NC1=NC=NC2=C1N=CN2C1OC(COP(=O)(O)OP(=O)(O[Si](C)(C)C)N([Si](C)(C)C)P(=O)(O)O)C(O[Si](C)(C)C)C1O	6191.6	Standard polar	33892256
Phosphoaminophosphonic acid-adenylate ester,4TMS,isomer #26	C[Si](C)(C)NC1=NC=NC2=C1N=CN2C1OC(COP(=O)(O)OP(=O)(O)NP(=O)(O[Si](C)(C)C)O[Si](C)(C)C)C(O[Si](C)(C)C)C1O	4074.7	Semi standard non polar	33892256
Phosphoaminophosphonic acid-adenylate ester,4TMS,isomer #26	C[Si](C)(C)NC1=NC=NC2=C1N=CN2C1OC(COP(=O)(O)OP(=O)(O)NP(=O)(O[Si](C)(C)C)O[Si](C)(C)C)C(O[Si](C)(C)C)C1O	3905.3	Standard non polar	33892256
Phosphoaminophosphonic acid-adenylate ester,4TMS,isomer #26	C[Si](C)(C)NC1=NC=NC2=C1N=CN2C1OC(COP(=O)(O)OP(=O)(O)NP(=O)(O[Si](C)(C)C)O[Si](C)(C)C)C(O[Si](C)(C)C)C1O	6250.6	Standard polar	33892256
Phosphoaminophosphonic acid-adenylate ester,4TMS,isomer #27	C[Si](C)(C)OC1C(COP(=O)(O)OP(=O)(O)N([Si](C)(C)C)P(=O)(O[Si](C)(C)C)O[Si](C)(C)C)OC(N2C=NC3=C(N)N=CN=C32)C1O	4068.0	Semi standard non polar	33892256
Phosphoaminophosphonic acid-adenylate ester,4TMS,isomer #27	C[Si](C)(C)OC1C(COP(=O)(O)OP(=O)(O)N([Si](C)(C)C)P(=O)(O[Si](C)(C)C)O[Si](C)(C)C)OC(N2C=NC3=C(N)N=CN=C32)C1O	4023.2	Standard non polar	33892256
Phosphoaminophosphonic acid-adenylate ester,4TMS,isomer #27	C[Si](C)(C)OC1C(COP(=O)(O)OP(=O)(O)N([Si](C)(C)C)P(=O)(O[Si](C)(C)C)O[Si](C)(C)C)OC(N2C=NC3=C(N)N=CN=C32)C1O	6299.0	Standard polar	33892256
Phosphoaminophosphonic acid-adenylate ester,4TMS,isomer #28	C[Si](C)(C)OC1C(COP(=O)(O)OP(=O)(O)NP(=O)(O)O[Si](C)(C)C)OC(N2C=NC3=C(N([Si](C)(C)C)[Si](C)(C)C)N=CN=C32)C1O	4085.4	Semi standard non polar	33892256
Phosphoaminophosphonic acid-adenylate ester,4TMS,isomer #28	C[Si](C)(C)OC1C(COP(=O)(O)OP(=O)(O)NP(=O)(O)O[Si](C)(C)C)OC(N2C=NC3=C(N([Si](C)(C)C)[Si](C)(C)C)N=CN=C32)C1O	3975.3	Standard non polar	33892256
Phosphoaminophosphonic acid-adenylate ester,4TMS,isomer #28	C[Si](C)(C)OC1C(COP(=O)(O)OP(=O)(O)NP(=O)(O)O[Si](C)(C)C)OC(N2C=NC3=C(N([Si](C)(C)C)[Si](C)(C)C)N=CN=C32)C1O	6305.2	Standard polar	33892256
Phosphoaminophosphonic acid-adenylate ester,4TMS,isomer #29	C[Si](C)(C)NC1=NC=NC2=C1N=CN2C1OC(COP(=O)(O)OP(=O)(O)N([Si](C)(C)C)P(=O)(O)O[Si](C)(C)C)C(O[Si](C)(C)C)C1O	4093.6	Semi standard non polar	33892256
Phosphoaminophosphonic acid-adenylate ester,4TMS,isomer #29	C[Si](C)(C)NC1=NC=NC2=C1N=CN2C1OC(COP(=O)(O)OP(=O)(O)N([Si](C)(C)C)P(=O)(O)O[Si](C)(C)C)C(O[Si](C)(C)C)C1O	4081.9	Standard non polar	33892256
Phosphoaminophosphonic acid-adenylate ester,4TMS,isomer #29	C[Si](C)(C)NC1=NC=NC2=C1N=CN2C1OC(COP(=O)(O)OP(=O)(O)N([Si](C)(C)C)P(=O)(O)O[Si](C)(C)C)C(O[Si](C)(C)C)C1O	6242.0	Standard polar	33892256
Phosphoaminophosphonic acid-adenylate ester,4TMS,isomer #3	C[Si](C)(C)NC1=NC=NC2=C1N=CN2C1OC(COP(=O)(O[Si](C)(C)C)OP(=O)(O)NP(=O)(O)O)C(O[Si](C)(C)C)C1O[Si](C)(C)C	4089.5	Semi standard non polar	33892256
Phosphoaminophosphonic acid-adenylate ester,4TMS,isomer #3	C[Si](C)(C)NC1=NC=NC2=C1N=CN2C1OC(COP(=O)(O[Si](C)(C)C)OP(=O)(O)NP(=O)(O)O)C(O[Si](C)(C)C)C1O[Si](C)(C)C	3849.5	Standard non polar	33892256
Phosphoaminophosphonic acid-adenylate ester,4TMS,isomer #3	C[Si](C)(C)NC1=NC=NC2=C1N=CN2C1OC(COP(=O)(O[Si](C)(C)C)OP(=O)(O)NP(=O)(O)O)C(O[Si](C)(C)C)C1O[Si](C)(C)C	6329.0	Standard polar	33892256
Phosphoaminophosphonic acid-adenylate ester,4TMS,isomer #30	C[Si](C)(C)OC1C(COP(=O)(O)OP(=O)(O)N([Si](C)(C)C)P(=O)(O)O)OC(N2C=NC3=C(N([Si](C)(C)C)[Si](C)(C)C)N=CN=C32)C1O	4127.6	Semi standard non polar	33892256
Phosphoaminophosphonic acid-adenylate ester,4TMS,isomer #30	C[Si](C)(C)OC1C(COP(=O)(O)OP(=O)(O)N([Si](C)(C)C)P(=O)(O)O)OC(N2C=NC3=C(N([Si](C)(C)C)[Si](C)(C)C)N=CN=C32)C1O	4164.9	Standard non polar	33892256
Phosphoaminophosphonic acid-adenylate ester,4TMS,isomer #30	C[Si](C)(C)OC1C(COP(=O)(O)OP(=O)(O)N([Si](C)(C)C)P(=O)(O)O)OC(N2C=NC3=C(N([Si](C)(C)C)[Si](C)(C)C)N=CN=C32)C1O	6260.3	Standard polar	33892256
Phosphoaminophosphonic acid-adenylate ester,4TMS,isomer #31	C[Si](C)(C)OC1C(O)C(COP(=O)(O[Si](C)(C)C)OP(=O)(NP(=O)(O)O[Si](C)(C)C)O[Si](C)(C)C)OC1N1C=NC2=C(N)N=CN=C21	4009.8	Semi standard non polar	33892256
Phosphoaminophosphonic acid-adenylate ester,4TMS,isomer #31	C[Si](C)(C)OC1C(O)C(COP(=O)(O[Si](C)(C)C)OP(=O)(NP(=O)(O)O[Si](C)(C)C)O[Si](C)(C)C)OC1N1C=NC2=C(N)N=CN=C21	3909.8	Standard non polar	33892256
Phosphoaminophosphonic acid-adenylate ester,4TMS,isomer #31	C[Si](C)(C)OC1C(O)C(COP(=O)(O[Si](C)(C)C)OP(=O)(NP(=O)(O)O[Si](C)(C)C)O[Si](C)(C)C)OC1N1C=NC2=C(N)N=CN=C21	6292.0	Standard polar	33892256
Phosphoaminophosphonic acid-adenylate ester,4TMS,isomer #32	C[Si](C)(C)NC1=NC=NC2=C1N=CN2C1OC(COP(=O)(O[Si](C)(C)C)OP(=O)(NP(=O)(O)O)O[Si](C)(C)C)C(O)C1O[Si](C)(C)C	4092.1	Semi standard non polar	33892256
Phosphoaminophosphonic acid-adenylate ester,4TMS,isomer #32	C[Si](C)(C)NC1=NC=NC2=C1N=CN2C1OC(COP(=O)(O[Si](C)(C)C)OP(=O)(NP(=O)(O)O)O[Si](C)(C)C)C(O)C1O[Si](C)(C)C	3957.7	Standard non polar	33892256
Phosphoaminophosphonic acid-adenylate ester,4TMS,isomer #32	C[Si](C)(C)NC1=NC=NC2=C1N=CN2C1OC(COP(=O)(O[Si](C)(C)C)OP(=O)(NP(=O)(O)O)O[Si](C)(C)C)C(O)C1O[Si](C)(C)C	6180.6	Standard polar	33892256
Phosphoaminophosphonic acid-adenylate ester,4TMS,isomer #33	C[Si](C)(C)OC1C(O)C(COP(=O)(O[Si](C)(C)C)OP(=O)(O[Si](C)(C)C)N([Si](C)(C)C)P(=O)(O)O)OC1N1C=NC2=C(N)N=CN=C21	4090.8	Semi standard non polar	33892256
Phosphoaminophosphonic acid-adenylate ester,4TMS,isomer #33	C[Si](C)(C)OC1C(O)C(COP(=O)(O[Si](C)(C)C)OP(=O)(O[Si](C)(C)C)N([Si](C)(C)C)P(=O)(O)O)OC1N1C=NC2=C(N)N=CN=C21	4084.4	Standard non polar	33892256
Phosphoaminophosphonic acid-adenylate ester,4TMS,isomer #33	C[Si](C)(C)OC1C(O)C(COP(=O)(O[Si](C)(C)C)OP(=O)(O[Si](C)(C)C)N([Si](C)(C)C)P(=O)(O)O)OC1N1C=NC2=C(N)N=CN=C21	6268.6	Standard polar	33892256
Phosphoaminophosphonic acid-adenylate ester,4TMS,isomer #34	C[Si](C)(C)OC1C(O)C(COP(=O)(O[Si](C)(C)C)OP(=O)(O)NP(=O)(O[Si](C)(C)C)O[Si](C)(C)C)OC1N1C=NC2=C(N)N=CN=C21	4024.0	Semi standard non polar	33892256
Phosphoaminophosphonic acid-adenylate ester,4TMS,isomer #34	C[Si](C)(C)OC1C(O)C(COP(=O)(O[Si](C)(C)C)OP(=O)(O)NP(=O)(O[Si](C)(C)C)O[Si](C)(C)C)OC1N1C=NC2=C(N)N=CN=C21	3879.4	Standard non polar	33892256
Phosphoaminophosphonic acid-adenylate ester,4TMS,isomer #34	C[Si](C)(C)OC1C(O)C(COP(=O)(O[Si](C)(C)C)OP(=O)(O)NP(=O)(O[Si](C)(C)C)O[Si](C)(C)C)OC1N1C=NC2=C(N)N=CN=C21	6319.2	Standard polar	33892256
Phosphoaminophosphonic acid-adenylate ester,4TMS,isomer #35	C[Si](C)(C)NC1=NC=NC2=C1N=CN2C1OC(COP(=O)(O[Si](C)(C)C)OP(=O)(O)NP(=O)(O)O[Si](C)(C)C)C(O)C1O[Si](C)(C)C	4078.6	Semi standard non polar	33892256
Phosphoaminophosphonic acid-adenylate ester,4TMS,isomer #35	C[Si](C)(C)NC1=NC=NC2=C1N=CN2C1OC(COP(=O)(O[Si](C)(C)C)OP(=O)(O)NP(=O)(O)O[Si](C)(C)C)C(O)C1O[Si](C)(C)C	3951.4	Standard non polar	33892256
Phosphoaminophosphonic acid-adenylate ester,4TMS,isomer #35	C[Si](C)(C)NC1=NC=NC2=C1N=CN2C1OC(COP(=O)(O[Si](C)(C)C)OP(=O)(O)NP(=O)(O)O[Si](C)(C)C)C(O)C1O[Si](C)(C)C	6235.0	Standard polar	33892256
Phosphoaminophosphonic acid-adenylate ester,4TMS,isomer #36	C[Si](C)(C)OC1C(O)C(COP(=O)(O[Si](C)(C)C)OP(=O)(O)N([Si](C)(C)C)P(=O)(O)O[Si](C)(C)C)OC1N1C=NC2=C(N)N=CN=C21	4058.7	Semi standard non polar	33892256
Phosphoaminophosphonic acid-adenylate ester,4TMS,isomer #36	C[Si](C)(C)OC1C(O)C(COP(=O)(O[Si](C)(C)C)OP(=O)(O)N([Si](C)(C)C)P(=O)(O)O[Si](C)(C)C)OC1N1C=NC2=C(N)N=CN=C21	4055.0	Standard non polar	33892256
Phosphoaminophosphonic acid-adenylate ester,4TMS,isomer #36	C[Si](C)(C)OC1C(O)C(COP(=O)(O[Si](C)(C)C)OP(=O)(O)N([Si](C)(C)C)P(=O)(O)O[Si](C)(C)C)OC1N1C=NC2=C(N)N=CN=C21	6292.4	Standard polar	33892256
Phosphoaminophosphonic acid-adenylate ester,4TMS,isomer #37	C[Si](C)(C)OC1C(O)C(COP(=O)(O[Si](C)(C)C)OP(=O)(O)NP(=O)(O)O)OC1N1C=NC2=C(N([Si](C)(C)C)[Si](C)(C)C)N=CN=C21	4113.3	Semi standard non polar	33892256
Phosphoaminophosphonic acid-adenylate ester,4TMS,isomer #37	C[Si](C)(C)OC1C(O)C(COP(=O)(O[Si](C)(C)C)OP(=O)(O)NP(=O)(O)O)OC1N1C=NC2=C(N([Si](C)(C)C)[Si](C)(C)C)N=CN=C21	3994.4	Standard non polar	33892256
Phosphoaminophosphonic acid-adenylate ester,4TMS,isomer #37	C[Si](C)(C)OC1C(O)C(COP(=O)(O[Si](C)(C)C)OP(=O)(O)NP(=O)(O)O)OC1N1C=NC2=C(N([Si](C)(C)C)[Si](C)(C)C)N=CN=C21	6262.3	Standard polar	33892256
Phosphoaminophosphonic acid-adenylate ester,4TMS,isomer #38	C[Si](C)(C)NC1=NC=NC2=C1N=CN2C1OC(COP(=O)(O[Si](C)(C)C)OP(=O)(O)N([Si](C)(C)C)P(=O)(O)O)C(O)C1O[Si](C)(C)C	4124.5	Semi standard non polar	33892256
Phosphoaminophosphonic acid-adenylate ester,4TMS,isomer #38	C[Si](C)(C)NC1=NC=NC2=C1N=CN2C1OC(COP(=O)(O[Si](C)(C)C)OP(=O)(O)N([Si](C)(C)C)P(=O)(O)O)C(O)C1O[Si](C)(C)C	4118.7	Standard non polar	33892256
Phosphoaminophosphonic acid-adenylate ester,4TMS,isomer #38	C[Si](C)(C)NC1=NC=NC2=C1N=CN2C1OC(COP(=O)(O[Si](C)(C)C)OP(=O)(O)N([Si](C)(C)C)P(=O)(O)O)C(O)C1O[Si](C)(C)C	6207.7	Standard polar	33892256
Phosphoaminophosphonic acid-adenylate ester,4TMS,isomer #39	C[Si](C)(C)OC1C(O)C(COP(=O)(O)OP(=O)(NP(=O)(O[Si](C)(C)C)O[Si](C)(C)C)O[Si](C)(C)C)OC1N1C=NC2=C(N)N=CN=C21	4003.9	Semi standard non polar	33892256
Phosphoaminophosphonic acid-adenylate ester,4TMS,isomer #39	C[Si](C)(C)OC1C(O)C(COP(=O)(O)OP(=O)(NP(=O)(O[Si](C)(C)C)O[Si](C)(C)C)O[Si](C)(C)C)OC1N1C=NC2=C(N)N=CN=C21	3860.5	Standard non polar	33892256
Phosphoaminophosphonic acid-adenylate ester,4TMS,isomer #39	C[Si](C)(C)OC1C(O)C(COP(=O)(O)OP(=O)(NP(=O)(O[Si](C)(C)C)O[Si](C)(C)C)O[Si](C)(C)C)OC1N1C=NC2=C(N)N=CN=C21	6342.4	Standard polar	33892256
Phosphoaminophosphonic acid-adenylate ester,4TMS,isomer #4	C[Si](C)(C)OC1C(COP(=O)(O[Si](C)(C)C)OP(=O)(O)N([Si](C)(C)C)P(=O)(O)O)OC(N2C=NC3=C(N)N=CN=C32)C1O[Si](C)(C)C	4072.8	Semi standard non polar	33892256
Phosphoaminophosphonic acid-adenylate ester,4TMS,isomer #4	C[Si](C)(C)OC1C(COP(=O)(O[Si](C)(C)C)OP(=O)(O)N([Si](C)(C)C)P(=O)(O)O)OC(N2C=NC3=C(N)N=CN=C32)C1O[Si](C)(C)C	3991.2	Standard non polar	33892256
Phosphoaminophosphonic acid-adenylate ester,4TMS,isomer #4	C[Si](C)(C)OC1C(COP(=O)(O[Si](C)(C)C)OP(=O)(O)N([Si](C)(C)C)P(=O)(O)O)OC(N2C=NC3=C(N)N=CN=C32)C1O[Si](C)(C)C	6376.8	Standard polar	33892256
Phosphoaminophosphonic acid-adenylate ester,4TMS,isomer #40	C[Si](C)(C)NC1=NC=NC2=C1N=CN2C1OC(COP(=O)(O)OP(=O)(NP(=O)(O)O[Si](C)(C)C)O[Si](C)(C)C)C(O)C1O[Si](C)(C)C	4060.9	Semi standard non polar	33892256
Phosphoaminophosphonic acid-adenylate ester,4TMS,isomer #40	C[Si](C)(C)NC1=NC=NC2=C1N=CN2C1OC(COP(=O)(O)OP(=O)(NP(=O)(O)O[Si](C)(C)C)O[Si](C)(C)C)C(O)C1O[Si](C)(C)C	3943.3	Standard non polar	33892256
Phosphoaminophosphonic acid-adenylate ester,4TMS,isomer #40	C[Si](C)(C)NC1=NC=NC2=C1N=CN2C1OC(COP(=O)(O)OP(=O)(NP(=O)(O)O[Si](C)(C)C)O[Si](C)(C)C)C(O)C1O[Si](C)(C)C	6235.6	Standard polar	33892256
Phosphoaminophosphonic acid-adenylate ester,4TMS,isomer #41	C[Si](C)(C)OC1C(O)C(COP(=O)(O)OP(=O)(O[Si](C)(C)C)N([Si](C)(C)C)P(=O)(O)O[Si](C)(C)C)OC1N1C=NC2=C(N)N=CN=C21	4057.5	Semi standard non polar	33892256
Phosphoaminophosphonic acid-adenylate ester,4TMS,isomer #41	C[Si](C)(C)OC1C(O)C(COP(=O)(O)OP(=O)(O[Si](C)(C)C)N([Si](C)(C)C)P(=O)(O)O[Si](C)(C)C)OC1N1C=NC2=C(N)N=CN=C21	4035.7	Standard non polar	33892256
Phosphoaminophosphonic acid-adenylate ester,4TMS,isomer #41	C[Si](C)(C)OC1C(O)C(COP(=O)(O)OP(=O)(O[Si](C)(C)C)N([Si](C)(C)C)P(=O)(O)O[Si](C)(C)C)OC1N1C=NC2=C(N)N=CN=C21	6300.7	Standard polar	33892256
Phosphoaminophosphonic acid-adenylate ester,4TMS,isomer #42	C[Si](C)(C)OC1C(O)C(COP(=O)(O)OP(=O)(NP(=O)(O)O)O[Si](C)(C)C)OC1N1C=NC2=C(N([Si](C)(C)C)[Si](C)(C)C)N=CN=C21	4085.4	Semi standard non polar	33892256
Phosphoaminophosphonic acid-adenylate ester,4TMS,isomer #42	C[Si](C)(C)OC1C(O)C(COP(=O)(O)OP(=O)(NP(=O)(O)O)O[Si](C)(C)C)OC1N1C=NC2=C(N([Si](C)(C)C)[Si](C)(C)C)N=CN=C21	3989.5	Standard non polar	33892256
Phosphoaminophosphonic acid-adenylate ester,4TMS,isomer #42	C[Si](C)(C)OC1C(O)C(COP(=O)(O)OP(=O)(NP(=O)(O)O)O[Si](C)(C)C)OC1N1C=NC2=C(N([Si](C)(C)C)[Si](C)(C)C)N=CN=C21	6247.9	Standard polar	33892256
Phosphoaminophosphonic acid-adenylate ester,4TMS,isomer #43	C[Si](C)(C)NC1=NC=NC2=C1N=CN2C1OC(COP(=O)(O)OP(=O)(O[Si](C)(C)C)N([Si](C)(C)C)P(=O)(O)O)C(O)C1O[Si](C)(C)C	4122.0	Semi standard non polar	33892256
Phosphoaminophosphonic acid-adenylate ester,4TMS,isomer #43	C[Si](C)(C)NC1=NC=NC2=C1N=CN2C1OC(COP(=O)(O)OP(=O)(O[Si](C)(C)C)N([Si](C)(C)C)P(=O)(O)O)C(O)C1O[Si](C)(C)C	4118.1	Standard non polar	33892256
Phosphoaminophosphonic acid-adenylate ester,4TMS,isomer #43	C[Si](C)(C)NC1=NC=NC2=C1N=CN2C1OC(COP(=O)(O)OP(=O)(O[Si](C)(C)C)N([Si](C)(C)C)P(=O)(O)O)C(O)C1O[Si](C)(C)C	6202.5	Standard polar	33892256
Phosphoaminophosphonic acid-adenylate ester,4TMS,isomer #44	C[Si](C)(C)NC1=NC=NC2=C1N=CN2C1OC(COP(=O)(O)OP(=O)(O)NP(=O)(O[Si](C)(C)C)O[Si](C)(C)C)C(O)C1O[Si](C)(C)C	4071.7	Semi standard non polar	33892256
Phosphoaminophosphonic acid-adenylate ester,4TMS,isomer #44	C[Si](C)(C)NC1=NC=NC2=C1N=CN2C1OC(COP(=O)(O)OP(=O)(O)NP(=O)(O[Si](C)(C)C)O[Si](C)(C)C)C(O)C1O[Si](C)(C)C	3913.1	Standard non polar	33892256
Phosphoaminophosphonic acid-adenylate ester,4TMS,isomer #44	C[Si](C)(C)NC1=NC=NC2=C1N=CN2C1OC(COP(=O)(O)OP(=O)(O)NP(=O)(O[Si](C)(C)C)O[Si](C)(C)C)C(O)C1O[Si](C)(C)C	6261.3	Standard polar	33892256
Phosphoaminophosphonic acid-adenylate ester,4TMS,isomer #45	C[Si](C)(C)OC1C(O)C(COP(=O)(O)OP(=O)(O)N([Si](C)(C)C)P(=O)(O[Si](C)(C)C)O[Si](C)(C)C)OC1N1C=NC2=C(N)N=CN=C21	4055.7	Semi standard non polar	33892256
Phosphoaminophosphonic acid-adenylate ester,4TMS,isomer #45	C[Si](C)(C)OC1C(O)C(COP(=O)(O)OP(=O)(O)N([Si](C)(C)C)P(=O)(O[Si](C)(C)C)O[Si](C)(C)C)OC1N1C=NC2=C(N)N=CN=C21	4028.3	Standard non polar	33892256
Phosphoaminophosphonic acid-adenylate ester,4TMS,isomer #45	C[Si](C)(C)OC1C(O)C(COP(=O)(O)OP(=O)(O)N([Si](C)(C)C)P(=O)(O[Si](C)(C)C)O[Si](C)(C)C)OC1N1C=NC2=C(N)N=CN=C21	6308.2	Standard polar	33892256
Phosphoaminophosphonic acid-adenylate ester,4TMS,isomer #46	C[Si](C)(C)OC1C(O)C(COP(=O)(O)OP(=O)(O)NP(=O)(O)O[Si](C)(C)C)OC1N1C=NC2=C(N([Si](C)(C)C)[Si](C)(C)C)N=CN=C21	4082.1	Semi standard non polar	33892256
Phosphoaminophosphonic acid-adenylate ester,4TMS,isomer #46	C[Si](C)(C)OC1C(O)C(COP(=O)(O)OP(=O)(O)NP(=O)(O)O[Si](C)(C)C)OC1N1C=NC2=C(N([Si](C)(C)C)[Si](C)(C)C)N=CN=C21	3984.6	Standard non polar	33892256
Phosphoaminophosphonic acid-adenylate ester,4TMS,isomer #46	C[Si](C)(C)OC1C(O)C(COP(=O)(O)OP(=O)(O)NP(=O)(O)O[Si](C)(C)C)OC1N1C=NC2=C(N([Si](C)(C)C)[Si](C)(C)C)N=CN=C21	6316.9	Standard polar	33892256
Phosphoaminophosphonic acid-adenylate ester,4TMS,isomer #47	C[Si](C)(C)NC1=NC=NC2=C1N=CN2C1OC(COP(=O)(O)OP(=O)(O)N([Si](C)(C)C)P(=O)(O)O[Si](C)(C)C)C(O)C1O[Si](C)(C)C	4089.3	Semi standard non polar	33892256
Phosphoaminophosphonic acid-adenylate ester,4TMS,isomer #47	C[Si](C)(C)NC1=NC=NC2=C1N=CN2C1OC(COP(=O)(O)OP(=O)(O)N([Si](C)(C)C)P(=O)(O)O[Si](C)(C)C)C(O)C1O[Si](C)(C)C	4083.0	Standard non polar	33892256
Phosphoaminophosphonic acid-adenylate ester,4TMS,isomer #47	C[Si](C)(C)NC1=NC=NC2=C1N=CN2C1OC(COP(=O)(O)OP(=O)(O)N([Si](C)(C)C)P(=O)(O)O[Si](C)(C)C)C(O)C1O[Si](C)(C)C	6252.8	Standard polar	33892256
Phosphoaminophosphonic acid-adenylate ester,4TMS,isomer #48	C[Si](C)(C)OC1C(O)C(COP(=O)(O)OP(=O)(O)N([Si](C)(C)C)P(=O)(O)O)OC1N1C=NC2=C(N([Si](C)(C)C)[Si](C)(C)C)N=CN=C21	4119.7	Semi standard non polar	33892256
Phosphoaminophosphonic acid-adenylate ester,4TMS,isomer #48	C[Si](C)(C)OC1C(O)C(COP(=O)(O)OP(=O)(O)N([Si](C)(C)C)P(=O)(O)O)OC1N1C=NC2=C(N([Si](C)(C)C)[Si](C)(C)C)N=CN=C21	4172.7	Standard non polar	33892256
Phosphoaminophosphonic acid-adenylate ester,4TMS,isomer #48	C[Si](C)(C)OC1C(O)C(COP(=O)(O)OP(=O)(O)N([Si](C)(C)C)P(=O)(O)O)OC1N1C=NC2=C(N([Si](C)(C)C)[Si](C)(C)C)N=CN=C21	6271.7	Standard polar	33892256
Phosphoaminophosphonic acid-adenylate ester,4TMS,isomer #49	C[Si](C)(C)OP(=O)(NP(=O)(O[Si](C)(C)C)OP(=O)(OCC1OC(N2C=NC3=C(N)N=CN=C32)C(O)C1O)O[Si](C)(C)C)O[Si](C)(C)C	4054.8	Semi standard non polar	33892256
Phosphoaminophosphonic acid-adenylate ester,4TMS,isomer #49	C[Si](C)(C)OP(=O)(NP(=O)(O[Si](C)(C)C)OP(=O)(OCC1OC(N2C=NC3=C(N)N=CN=C32)C(O)C1O)O[Si](C)(C)C)O[Si](C)(C)C	3950.2	Standard non polar	33892256
Phosphoaminophosphonic acid-adenylate ester,4TMS,isomer #49	C[Si](C)(C)OP(=O)(NP(=O)(O[Si](C)(C)C)OP(=O)(OCC1OC(N2C=NC3=C(N)N=CN=C32)C(O)C1O)O[Si](C)(C)C)O[Si](C)(C)C	6187.0	Standard polar	33892256
Phosphoaminophosphonic acid-adenylate ester,4TMS,isomer #5	C[Si](C)(C)OC1C(COP(=O)(O)OP(=O)(NP(=O)(O)O[Si](C)(C)C)O[Si](C)(C)C)OC(N2C=NC3=C(N)N=CN=C32)C1O[Si](C)(C)C	3992.8	Semi standard non polar	33892256
Phosphoaminophosphonic acid-adenylate ester,4TMS,isomer #5	C[Si](C)(C)OC1C(COP(=O)(O)OP(=O)(NP(=O)(O)O[Si](C)(C)C)O[Si](C)(C)C)OC(N2C=NC3=C(N)N=CN=C32)C1O[Si](C)(C)C	3804.3	Standard non polar	33892256
Phosphoaminophosphonic acid-adenylate ester,4TMS,isomer #5	C[Si](C)(C)OC1C(COP(=O)(O)OP(=O)(NP(=O)(O)O[Si](C)(C)C)O[Si](C)(C)C)OC(N2C=NC3=C(N)N=CN=C32)C1O[Si](C)(C)C	6446.4	Standard polar	33892256
Phosphoaminophosphonic acid-adenylate ester,4TMS,isomer #50	C[Si](C)(C)NC1=NC=NC2=C1N=CN2C1OC(COP(=O)(O[Si](C)(C)C)OP(=O)(NP(=O)(O)O[Si](C)(C)C)O[Si](C)(C)C)C(O)C1O	4099.2	Semi standard non polar	33892256
Phosphoaminophosphonic acid-adenylate ester,4TMS,isomer #50	C[Si](C)(C)NC1=NC=NC2=C1N=CN2C1OC(COP(=O)(O[Si](C)(C)C)OP(=O)(NP(=O)(O)O[Si](C)(C)C)O[Si](C)(C)C)C(O)C1O	4058.1	Standard non polar	33892256
Phosphoaminophosphonic acid-adenylate ester,4TMS,isomer #50	C[Si](C)(C)NC1=NC=NC2=C1N=CN2C1OC(COP(=O)(O[Si](C)(C)C)OP(=O)(NP(=O)(O)O[Si](C)(C)C)O[Si](C)(C)C)C(O)C1O	6048.8	Standard polar	33892256
Phosphoaminophosphonic acid-adenylate ester,4TMS,isomer #51	C[Si](C)(C)OP(=O)(OCC1OC(N2C=NC3=C(N)N=CN=C32)C(O)C1O)OP(=O)(O[Si](C)(C)C)N([Si](C)(C)C)P(=O)(O)O[Si](C)(C)C	4106.8	Semi standard non polar	33892256
Phosphoaminophosphonic acid-adenylate ester,4TMS,isomer #51	C[Si](C)(C)OP(=O)(OCC1OC(N2C=NC3=C(N)N=CN=C32)C(O)C1O)OP(=O)(O[Si](C)(C)C)N([Si](C)(C)C)P(=O)(O)O[Si](C)(C)C	4130.6	Standard non polar	33892256
Phosphoaminophosphonic acid-adenylate ester,4TMS,isomer #51	C[Si](C)(C)OP(=O)(OCC1OC(N2C=NC3=C(N)N=CN=C32)C(O)C1O)OP(=O)(O[Si](C)(C)C)N([Si](C)(C)C)P(=O)(O)O[Si](C)(C)C	6178.8	Standard polar	33892256
Phosphoaminophosphonic acid-adenylate ester,4TMS,isomer #52	C[Si](C)(C)OP(=O)(NP(=O)(O)O)OP(=O)(OCC1OC(N2C=NC3=C(N([Si](C)(C)C)[Si](C)(C)C)N=CN=C32)C(O)C1O)O[Si](C)(C)C	4164.7	Semi standard non polar	33892256
Phosphoaminophosphonic acid-adenylate ester,4TMS,isomer #52	C[Si](C)(C)OP(=O)(NP(=O)(O)O)OP(=O)(OCC1OC(N2C=NC3=C(N([Si](C)(C)C)[Si](C)(C)C)N=CN=C32)C(O)C1O)O[Si](C)(C)C	4118.5	Standard non polar	33892256
Phosphoaminophosphonic acid-adenylate ester,4TMS,isomer #52	C[Si](C)(C)OP(=O)(NP(=O)(O)O)OP(=O)(OCC1OC(N2C=NC3=C(N([Si](C)(C)C)[Si](C)(C)C)N=CN=C32)C(O)C1O)O[Si](C)(C)C	6056.4	Standard polar	33892256
Phosphoaminophosphonic acid-adenylate ester,4TMS,isomer #53	C[Si](C)(C)NC1=NC=NC2=C1N=CN2C1OC(COP(=O)(O[Si](C)(C)C)OP(=O)(O[Si](C)(C)C)N([Si](C)(C)C)P(=O)(O)O)C(O)C1O	4176.5	Semi standard non polar	33892256
Phosphoaminophosphonic acid-adenylate ester,4TMS,isomer #53	C[Si](C)(C)NC1=NC=NC2=C1N=CN2C1OC(COP(=O)(O[Si](C)(C)C)OP(=O)(O[Si](C)(C)C)N([Si](C)(C)C)P(=O)(O)O)C(O)C1O	4240.9	Standard non polar	33892256
Phosphoaminophosphonic acid-adenylate ester,4TMS,isomer #53	C[Si](C)(C)NC1=NC=NC2=C1N=CN2C1OC(COP(=O)(O[Si](C)(C)C)OP(=O)(O[Si](C)(C)C)N([Si](C)(C)C)P(=O)(O)O)C(O)C1O	6037.7	Standard polar	33892256
Phosphoaminophosphonic acid-adenylate ester,4TMS,isomer #54	C[Si](C)(C)NC1=NC=NC2=C1N=CN2C1OC(COP(=O)(O[Si](C)(C)C)OP(=O)(O)NP(=O)(O[Si](C)(C)C)O[Si](C)(C)C)C(O)C1O	4119.6	Semi standard non polar	33892256
Phosphoaminophosphonic acid-adenylate ester,4TMS,isomer #54	C[Si](C)(C)NC1=NC=NC2=C1N=CN2C1OC(COP(=O)(O[Si](C)(C)C)OP(=O)(O)NP(=O)(O[Si](C)(C)C)O[Si](C)(C)C)C(O)C1O	4028.6	Standard non polar	33892256
Phosphoaminophosphonic acid-adenylate ester,4TMS,isomer #54	C[Si](C)(C)NC1=NC=NC2=C1N=CN2C1OC(COP(=O)(O[Si](C)(C)C)OP(=O)(O)NP(=O)(O[Si](C)(C)C)O[Si](C)(C)C)C(O)C1O	6073.4	Standard polar	33892256
Phosphoaminophosphonic acid-adenylate ester,4TMS,isomer #55	C[Si](C)(C)OP(=O)(OCC1OC(N2C=NC3=C(N)N=CN=C32)C(O)C1O)OP(=O)(O)N([Si](C)(C)C)P(=O)(O[Si](C)(C)C)O[Si](C)(C)C	4107.8	Semi standard non polar	33892256
Phosphoaminophosphonic acid-adenylate ester,4TMS,isomer #55	C[Si](C)(C)OP(=O)(OCC1OC(N2C=NC3=C(N)N=CN=C32)C(O)C1O)OP(=O)(O)N([Si](C)(C)C)P(=O)(O[Si](C)(C)C)O[Si](C)(C)C	4126.7	Standard non polar	33892256
Phosphoaminophosphonic acid-adenylate ester,4TMS,isomer #55	C[Si](C)(C)OP(=O)(OCC1OC(N2C=NC3=C(N)N=CN=C32)C(O)C1O)OP(=O)(O)N([Si](C)(C)C)P(=O)(O[Si](C)(C)C)O[Si](C)(C)C	6199.8	Standard polar	33892256
Phosphoaminophosphonic acid-adenylate ester,4TMS,isomer #56	C[Si](C)(C)OP(=O)(O)NP(=O)(O)OP(=O)(OCC1OC(N2C=NC3=C(N([Si](C)(C)C)[Si](C)(C)C)N=CN=C32)C(O)C1O)O[Si](C)(C)C	4145.5	Semi standard non polar	33892256
Phosphoaminophosphonic acid-adenylate ester,4TMS,isomer #56	C[Si](C)(C)OP(=O)(O)NP(=O)(O)OP(=O)(OCC1OC(N2C=NC3=C(N([Si](C)(C)C)[Si](C)(C)C)N=CN=C32)C(O)C1O)O[Si](C)(C)C	4116.0	Standard non polar	33892256
Phosphoaminophosphonic acid-adenylate ester,4TMS,isomer #56	C[Si](C)(C)OP(=O)(O)NP(=O)(O)OP(=O)(OCC1OC(N2C=NC3=C(N([Si](C)(C)C)[Si](C)(C)C)N=CN=C32)C(O)C1O)O[Si](C)(C)C	6127.8	Standard polar	33892256
Phosphoaminophosphonic acid-adenylate ester,4TMS,isomer #57	C[Si](C)(C)NC1=NC=NC2=C1N=CN2C1OC(COP(=O)(O[Si](C)(C)C)OP(=O)(O)N([Si](C)(C)C)P(=O)(O)O[Si](C)(C)C)C(O)C1O	4143.9	Semi standard non polar	33892256
Phosphoaminophosphonic acid-adenylate ester,4TMS,isomer #57	C[Si](C)(C)NC1=NC=NC2=C1N=CN2C1OC(COP(=O)(O[Si](C)(C)C)OP(=O)(O)N([Si](C)(C)C)P(=O)(O)O[Si](C)(C)C)C(O)C1O	4211.4	Standard non polar	33892256
Phosphoaminophosphonic acid-adenylate ester,4TMS,isomer #57	C[Si](C)(C)NC1=NC=NC2=C1N=CN2C1OC(COP(=O)(O[Si](C)(C)C)OP(=O)(O)N([Si](C)(C)C)P(=O)(O)O[Si](C)(C)C)C(O)C1O	6097.9	Standard polar	33892256
Phosphoaminophosphonic acid-adenylate ester,4TMS,isomer #58	C[Si](C)(C)OP(=O)(OCC1OC(N2C=NC3=C(N([Si](C)(C)C)[Si](C)(C)C)N=CN=C32)C(O)C1O)OP(=O)(O)N([Si](C)(C)C)P(=O)(O)O	4200.6	Semi standard non polar	33892256
Phosphoaminophosphonic acid-adenylate ester,4TMS,isomer #58	C[Si](C)(C)OP(=O)(OCC1OC(N2C=NC3=C(N([Si](C)(C)C)[Si](C)(C)C)N=CN=C32)C(O)C1O)OP(=O)(O)N([Si](C)(C)C)P(=O)(O)O	4304.4	Standard non polar	33892256
Phosphoaminophosphonic acid-adenylate ester,4TMS,isomer #58	C[Si](C)(C)OP(=O)(OCC1OC(N2C=NC3=C(N([Si](C)(C)C)[Si](C)(C)C)N=CN=C32)C(O)C1O)OP(=O)(O)N([Si](C)(C)C)P(=O)(O)O	6115.3	Standard polar	33892256
Phosphoaminophosphonic acid-adenylate ester,4TMS,isomer #59	C[Si](C)(C)NC1=NC=NC2=C1N=CN2C1OC(COP(=O)(O)OP(=O)(NP(=O)(O[Si](C)(C)C)O[Si](C)(C)C)O[Si](C)(C)C)C(O)C1O	4102.1	Semi standard non polar	33892256
Phosphoaminophosphonic acid-adenylate ester,4TMS,isomer #59	C[Si](C)(C)NC1=NC=NC2=C1N=CN2C1OC(COP(=O)(O)OP(=O)(NP(=O)(O[Si](C)(C)C)O[Si](C)(C)C)O[Si](C)(C)C)C(O)C1O	4012.9	Standard non polar	33892256
Phosphoaminophosphonic acid-adenylate ester,4TMS,isomer #59	C[Si](C)(C)NC1=NC=NC2=C1N=CN2C1OC(COP(=O)(O)OP(=O)(NP(=O)(O[Si](C)(C)C)O[Si](C)(C)C)O[Si](C)(C)C)C(O)C1O	6081.9	Standard polar	33892256
Phosphoaminophosphonic acid-adenylate ester,4TMS,isomer #6	C[Si](C)(C)NC1=NC=NC2=C1N=CN2C1OC(COP(=O)(O)OP(=O)(NP(=O)(O)O)O[Si](C)(C)C)C(O[Si](C)(C)C)C1O[Si](C)(C)C	4068.9	Semi standard non polar	33892256
Phosphoaminophosphonic acid-adenylate ester,4TMS,isomer #6	C[Si](C)(C)NC1=NC=NC2=C1N=CN2C1OC(COP(=O)(O)OP(=O)(NP(=O)(O)O)O[Si](C)(C)C)C(O[Si](C)(C)C)C1O[Si](C)(C)C	3844.0	Standard non polar	33892256
Phosphoaminophosphonic acid-adenylate ester,4TMS,isomer #6	C[Si](C)(C)NC1=NC=NC2=C1N=CN2C1OC(COP(=O)(O)OP(=O)(NP(=O)(O)O)O[Si](C)(C)C)C(O[Si](C)(C)C)C1O[Si](C)(C)C	6340.5	Standard polar	33892256
Phosphoaminophosphonic acid-adenylate ester,4TMS,isomer #60	C[Si](C)(C)OP(=O)(O[Si](C)(C)C)N([Si](C)(C)C)P(=O)(O[Si](C)(C)C)OP(=O)(O)OCC1OC(N2C=NC3=C(N)N=CN=C32)C(O)C1O	4107.4	Semi standard non polar	33892256
Phosphoaminophosphonic acid-adenylate ester,4TMS,isomer #60	C[Si](C)(C)OP(=O)(O[Si](C)(C)C)N([Si](C)(C)C)P(=O)(O[Si](C)(C)C)OP(=O)(O)OCC1OC(N2C=NC3=C(N)N=CN=C32)C(O)C1O	4106.9	Standard non polar	33892256
Phosphoaminophosphonic acid-adenylate ester,4TMS,isomer #60	C[Si](C)(C)OP(=O)(O[Si](C)(C)C)N([Si](C)(C)C)P(=O)(O[Si](C)(C)C)OP(=O)(O)OCC1OC(N2C=NC3=C(N)N=CN=C32)C(O)C1O	6214.1	Standard polar	33892256
Phosphoaminophosphonic acid-adenylate ester,4TMS,isomer #61	C[Si](C)(C)OP(=O)(O)NP(=O)(O[Si](C)(C)C)OP(=O)(O)OCC1OC(N2C=NC3=C(N([Si](C)(C)C)[Si](C)(C)C)N=CN=C32)C(O)C1O	4123.5	Semi standard non polar	33892256
Phosphoaminophosphonic acid-adenylate ester,4TMS,isomer #61	C[Si](C)(C)OP(=O)(O)NP(=O)(O[Si](C)(C)C)OP(=O)(O)OCC1OC(N2C=NC3=C(N([Si](C)(C)C)[Si](C)(C)C)N=CN=C32)C(O)C1O	4104.7	Standard non polar	33892256
Phosphoaminophosphonic acid-adenylate ester,4TMS,isomer #61	C[Si](C)(C)OP(=O)(O)NP(=O)(O[Si](C)(C)C)OP(=O)(O)OCC1OC(N2C=NC3=C(N([Si](C)(C)C)[Si](C)(C)C)N=CN=C32)C(O)C1O	6115.4	Standard polar	33892256
Phosphoaminophosphonic acid-adenylate ester,4TMS,isomer #62	C[Si](C)(C)NC1=NC=NC2=C1N=CN2C1OC(COP(=O)(O)OP(=O)(O[Si](C)(C)C)N([Si](C)(C)C)P(=O)(O)O[Si](C)(C)C)C(O)C1O	4144.4	Semi standard non polar	33892256
Phosphoaminophosphonic acid-adenylate ester,4TMS,isomer #62	C[Si](C)(C)NC1=NC=NC2=C1N=CN2C1OC(COP(=O)(O)OP(=O)(O[Si](C)(C)C)N([Si](C)(C)C)P(=O)(O)O[Si](C)(C)C)C(O)C1O	4192.7	Standard non polar	33892256
Phosphoaminophosphonic acid-adenylate ester,4TMS,isomer #62	C[Si](C)(C)NC1=NC=NC2=C1N=CN2C1OC(COP(=O)(O)OP(=O)(O[Si](C)(C)C)N([Si](C)(C)C)P(=O)(O)O[Si](C)(C)C)C(O)C1O	6072.1	Standard polar	33892256
Phosphoaminophosphonic acid-adenylate ester,4TMS,isomer #63	C[Si](C)(C)OP(=O)(OP(=O)(O)OCC1OC(N2C=NC3=C(N([Si](C)(C)C)[Si](C)(C)C)N=CN=C32)C(O)C1O)N([Si](C)(C)C)P(=O)(O)O	4193.9	Semi standard non polar	33892256
Phosphoaminophosphonic acid-adenylate ester,4TMS,isomer #63	C[Si](C)(C)OP(=O)(OP(=O)(O)OCC1OC(N2C=NC3=C(N([Si](C)(C)C)[Si](C)(C)C)N=CN=C32)C(O)C1O)N([Si](C)(C)C)P(=O)(O)O	4315.6	Standard non polar	33892256
Phosphoaminophosphonic acid-adenylate ester,4TMS,isomer #63	C[Si](C)(C)OP(=O)(OP(=O)(O)OCC1OC(N2C=NC3=C(N([Si](C)(C)C)[Si](C)(C)C)N=CN=C32)C(O)C1O)N([Si](C)(C)C)P(=O)(O)O	6093.6	Standard polar	33892256
Phosphoaminophosphonic acid-adenylate ester,4TMS,isomer #64	C[Si](C)(C)OP(=O)(NP(=O)(O)OP(=O)(O)OCC1OC(N2C=NC3=C(N([Si](C)(C)C)[Si](C)(C)C)N=CN=C32)C(O)C1O)O[Si](C)(C)C	4138.2	Semi standard non polar	33892256
Phosphoaminophosphonic acid-adenylate ester,4TMS,isomer #64	C[Si](C)(C)OP(=O)(NP(=O)(O)OP(=O)(O)OCC1OC(N2C=NC3=C(N([Si](C)(C)C)[Si](C)(C)C)N=CN=C32)C(O)C1O)O[Si](C)(C)C	4071.5	Standard non polar	33892256
Phosphoaminophosphonic acid-adenylate ester,4TMS,isomer #64	C[Si](C)(C)OP(=O)(NP(=O)(O)OP(=O)(O)OCC1OC(N2C=NC3=C(N([Si](C)(C)C)[Si](C)(C)C)N=CN=C32)C(O)C1O)O[Si](C)(C)C	6153.2	Standard polar	33892256
Phosphoaminophosphonic acid-adenylate ester,4TMS,isomer #65	C[Si](C)(C)NC1=NC=NC2=C1N=CN2C1OC(COP(=O)(O)OP(=O)(O)N([Si](C)(C)C)P(=O)(O[Si](C)(C)C)O[Si](C)(C)C)C(O)C1O	4146.4	Semi standard non polar	33892256
Phosphoaminophosphonic acid-adenylate ester,4TMS,isomer #65	C[Si](C)(C)NC1=NC=NC2=C1N=CN2C1OC(COP(=O)(O)OP(=O)(O)N([Si](C)(C)C)P(=O)(O[Si](C)(C)C)O[Si](C)(C)C)C(O)C1O	4186.8	Standard non polar	33892256
Phosphoaminophosphonic acid-adenylate ester,4TMS,isomer #65	C[Si](C)(C)NC1=NC=NC2=C1N=CN2C1OC(COP(=O)(O)OP(=O)(O)N([Si](C)(C)C)P(=O)(O[Si](C)(C)C)O[Si](C)(C)C)C(O)C1O	6108.7	Standard polar	33892256
Phosphoaminophosphonic acid-adenylate ester,4TMS,isomer #66	C[Si](C)(C)OP(=O)(O)N([Si](C)(C)C)P(=O)(O)OP(=O)(O)OCC1OC(N2C=NC3=C(N([Si](C)(C)C)[Si](C)(C)C)N=CN=C32)C(O)C1O	4168.0	Semi standard non polar	33892256
Phosphoaminophosphonic acid-adenylate ester,4TMS,isomer #66	C[Si](C)(C)OP(=O)(O)N([Si](C)(C)C)P(=O)(O)OP(=O)(O)OCC1OC(N2C=NC3=C(N([Si](C)(C)C)[Si](C)(C)C)N=CN=C32)C(O)C1O	4273.9	Standard non polar	33892256
Phosphoaminophosphonic acid-adenylate ester,4TMS,isomer #66	C[Si](C)(C)OP(=O)(O)N([Si](C)(C)C)P(=O)(O)OP(=O)(O)OCC1OC(N2C=NC3=C(N([Si](C)(C)C)[Si](C)(C)C)N=CN=C32)C(O)C1O	6162.1	Standard polar	33892256
Phosphoaminophosphonic acid-adenylate ester,4TMS,isomer #7	C[Si](C)(C)OC1C(COP(=O)(O)OP(=O)(O[Si](C)(C)C)N([Si](C)(C)C)P(=O)(O)O)OC(N2C=NC3=C(N)N=CN=C32)C1O[Si](C)(C)C	4064.4	Semi standard non polar	33892256
Phosphoaminophosphonic acid-adenylate ester,4TMS,isomer #7	C[Si](C)(C)OC1C(COP(=O)(O)OP(=O)(O[Si](C)(C)C)N([Si](C)(C)C)P(=O)(O)O)OC(N2C=NC3=C(N)N=CN=C32)C1O[Si](C)(C)C	3992.2	Standard non polar	33892256
Phosphoaminophosphonic acid-adenylate ester,4TMS,isomer #7	C[Si](C)(C)OC1C(COP(=O)(O)OP(=O)(O[Si](C)(C)C)N([Si](C)(C)C)P(=O)(O)O)OC(N2C=NC3=C(N)N=CN=C32)C1O[Si](C)(C)C	6396.3	Standard polar	33892256
Phosphoaminophosphonic acid-adenylate ester,4TMS,isomer #8	C[Si](C)(C)OC1C(COP(=O)(O)OP(=O)(O)NP(=O)(O[Si](C)(C)C)O[Si](C)(C)C)OC(N2C=NC3=C(N)N=CN=C32)C1O[Si](C)(C)C	4009.1	Semi standard non polar	33892256
Phosphoaminophosphonic acid-adenylate ester,4TMS,isomer #8	C[Si](C)(C)OC1C(COP(=O)(O)OP(=O)(O)NP(=O)(O[Si](C)(C)C)O[Si](C)(C)C)OC(N2C=NC3=C(N)N=CN=C32)C1O[Si](C)(C)C	3772.3	Standard non polar	33892256
Phosphoaminophosphonic acid-adenylate ester,4TMS,isomer #8	C[Si](C)(C)OC1C(COP(=O)(O)OP(=O)(O)NP(=O)(O[Si](C)(C)C)O[Si](C)(C)C)OC(N2C=NC3=C(N)N=CN=C32)C1O[Si](C)(C)C	6444.8	Standard polar	33892256
Phosphoaminophosphonic acid-adenylate ester,4TMS,isomer #9	C[Si](C)(C)NC1=NC=NC2=C1N=CN2C1OC(COP(=O)(O)OP(=O)(O)NP(=O)(O)O[Si](C)(C)C)C(O[Si](C)(C)C)C1O[Si](C)(C)C	4052.7	Semi standard non polar	33892256
Phosphoaminophosphonic acid-adenylate ester,4TMS,isomer #9	C[Si](C)(C)NC1=NC=NC2=C1N=CN2C1OC(COP(=O)(O)OP(=O)(O)NP(=O)(O)O[Si](C)(C)C)C(O[Si](C)(C)C)C1O[Si](C)(C)C	3842.5	Standard non polar	33892256
Phosphoaminophosphonic acid-adenylate ester,4TMS,isomer #9	C[Si](C)(C)NC1=NC=NC2=C1N=CN2C1OC(COP(=O)(O)OP(=O)(O)NP(=O)(O)O[Si](C)(C)C)C(O[Si](C)(C)C)C1O[Si](C)(C)C	6383.4	Standard polar	33892256
Phosphoaminophosphonic acid-adenylate ester,5TMS,isomer #1	C[Si](C)(C)OC1C(COP(=O)(O[Si](C)(C)C)OP(=O)(NP(=O)(O)O[Si](C)(C)C)O[Si](C)(C)C)OC(N2C=NC3=C(N)N=CN=C32)C1O[Si](C)(C)C	3965.5	Semi standard non polar	33892256
Phosphoaminophosphonic acid-adenylate ester,5TMS,isomer #1	C[Si](C)(C)OC1C(COP(=O)(O[Si](C)(C)C)OP(=O)(NP(=O)(O)O[Si](C)(C)C)O[Si](C)(C)C)OC(N2C=NC3=C(N)N=CN=C32)C1O[Si](C)(C)C	3797.8	Standard non polar	33892256
Phosphoaminophosphonic acid-adenylate ester,5TMS,isomer #1	C[Si](C)(C)OC1C(COP(=O)(O[Si](C)(C)C)OP(=O)(NP(=O)(O)O[Si](C)(C)C)O[Si](C)(C)C)OC(N2C=NC3=C(N)N=CN=C32)C1O[Si](C)(C)C	6081.3	Standard polar	33892256
Phosphoaminophosphonic acid-adenylate ester,5TMS,isomer #10	C[Si](C)(C)NC1=NC=NC2=C1N=CN2C1OC(COP(=O)(O)OP(=O)(NP(=O)(O)O[Si](C)(C)C)O[Si](C)(C)C)C(O[Si](C)(C)C)C1O[Si](C)(C)C	4017.0	Semi standard non polar	33892256
Phosphoaminophosphonic acid-adenylate ester,5TMS,isomer #10	C[Si](C)(C)NC1=NC=NC2=C1N=CN2C1OC(COP(=O)(O)OP(=O)(NP(=O)(O)O[Si](C)(C)C)O[Si](C)(C)C)C(O[Si](C)(C)C)C1O[Si](C)(C)C	3856.1	Standard non polar	33892256
Phosphoaminophosphonic acid-adenylate ester,5TMS,isomer #10	C[Si](C)(C)NC1=NC=NC2=C1N=CN2C1OC(COP(=O)(O)OP(=O)(NP(=O)(O)O[Si](C)(C)C)O[Si](C)(C)C)C(O[Si](C)(C)C)C1O[Si](C)(C)C	5944.3	Standard polar	33892256
Phosphoaminophosphonic acid-adenylate ester,5TMS,isomer #11	C[Si](C)(C)OC1C(COP(=O)(O)OP(=O)(O[Si](C)(C)C)N([Si](C)(C)C)P(=O)(O)O[Si](C)(C)C)OC(N2C=NC3=C(N)N=CN=C32)C1O[Si](C)(C)C	4000.2	Semi standard non polar	33892256
Phosphoaminophosphonic acid-adenylate ester,5TMS,isomer #11	C[Si](C)(C)OC1C(COP(=O)(O)OP(=O)(O[Si](C)(C)C)N([Si](C)(C)C)P(=O)(O)O[Si](C)(C)C)OC(N2C=NC3=C(N)N=CN=C32)C1O[Si](C)(C)C	3940.6	Standard non polar	33892256
Phosphoaminophosphonic acid-adenylate ester,5TMS,isomer #11	C[Si](C)(C)OC1C(COP(=O)(O)OP(=O)(O[Si](C)(C)C)N([Si](C)(C)C)P(=O)(O)O[Si](C)(C)C)OC(N2C=NC3=C(N)N=CN=C32)C1O[Si](C)(C)C	6106.2	Standard polar	33892256
Phosphoaminophosphonic acid-adenylate ester,5TMS,isomer #12	C[Si](C)(C)OC1C(COP(=O)(O)OP(=O)(NP(=O)(O)O)O[Si](C)(C)C)OC(N2C=NC3=C(N([Si](C)(C)C)[Si](C)(C)C)N=CN=C32)C1O[Si](C)(C)C	4040.7	Semi standard non polar	33892256
Phosphoaminophosphonic acid-adenylate ester,5TMS,isomer #12	C[Si](C)(C)OC1C(COP(=O)(O)OP(=O)(NP(=O)(O)O)O[Si](C)(C)C)OC(N2C=NC3=C(N([Si](C)(C)C)[Si](C)(C)C)N=CN=C32)C1O[Si](C)(C)C	3877.2	Standard non polar	33892256
Phosphoaminophosphonic acid-adenylate ester,5TMS,isomer #12	C[Si](C)(C)OC1C(COP(=O)(O)OP(=O)(NP(=O)(O)O)O[Si](C)(C)C)OC(N2C=NC3=C(N([Si](C)(C)C)[Si](C)(C)C)N=CN=C32)C1O[Si](C)(C)C	5892.3	Standard polar	33892256
Phosphoaminophosphonic acid-adenylate ester,5TMS,isomer #13	C[Si](C)(C)NC1=NC=NC2=C1N=CN2C1OC(COP(=O)(O)OP(=O)(O[Si](C)(C)C)N([Si](C)(C)C)P(=O)(O)O)C(O[Si](C)(C)C)C1O[Si](C)(C)C	4078.8	Semi standard non polar	33892256
Phosphoaminophosphonic acid-adenylate ester,5TMS,isomer #13	C[Si](C)(C)NC1=NC=NC2=C1N=CN2C1OC(COP(=O)(O)OP(=O)(O[Si](C)(C)C)N([Si](C)(C)C)P(=O)(O)O)C(O[Si](C)(C)C)C1O[Si](C)(C)C	4043.8	Standard non polar	33892256
Phosphoaminophosphonic acid-adenylate ester,5TMS,isomer #13	C[Si](C)(C)NC1=NC=NC2=C1N=CN2C1OC(COP(=O)(O)OP(=O)(O[Si](C)(C)C)N([Si](C)(C)C)P(=O)(O)O)C(O[Si](C)(C)C)C1O[Si](C)(C)C	5931.1	Standard polar	33892256
Phosphoaminophosphonic acid-adenylate ester,5TMS,isomer #14	C[Si](C)(C)NC1=NC=NC2=C1N=CN2C1OC(COP(=O)(O)OP(=O)(O)NP(=O)(O[Si](C)(C)C)O[Si](C)(C)C)C(O[Si](C)(C)C)C1O[Si](C)(C)C	4022.3	Semi standard non polar	33892256
Phosphoaminophosphonic acid-adenylate ester,5TMS,isomer #14	C[Si](C)(C)NC1=NC=NC2=C1N=CN2C1OC(COP(=O)(O)OP(=O)(O)NP(=O)(O[Si](C)(C)C)O[Si](C)(C)C)C(O[Si](C)(C)C)C1O[Si](C)(C)C	3825.8	Standard non polar	33892256
Phosphoaminophosphonic acid-adenylate ester,5TMS,isomer #14	C[Si](C)(C)NC1=NC=NC2=C1N=CN2C1OC(COP(=O)(O)OP(=O)(O)NP(=O)(O[Si](C)(C)C)O[Si](C)(C)C)C(O[Si](C)(C)C)C1O[Si](C)(C)C	5998.1	Standard polar	33892256
Phosphoaminophosphonic acid-adenylate ester,5TMS,isomer #15	C[Si](C)(C)OC1C(COP(=O)(O)OP(=O)(O)N([Si](C)(C)C)P(=O)(O[Si](C)(C)C)O[Si](C)(C)C)OC(N2C=NC3=C(N)N=CN=C32)C1O[Si](C)(C)C	3996.6	Semi standard non polar	33892256
Phosphoaminophosphonic acid-adenylate ester,5TMS,isomer #15	C[Si](C)(C)OC1C(COP(=O)(O)OP(=O)(O)N([Si](C)(C)C)P(=O)(O[Si](C)(C)C)O[Si](C)(C)C)OC(N2C=NC3=C(N)N=CN=C32)C1O[Si](C)(C)C	3933.6	Standard non polar	33892256
Phosphoaminophosphonic acid-adenylate ester,5TMS,isomer #15	C[Si](C)(C)OC1C(COP(=O)(O)OP(=O)(O)N([Si](C)(C)C)P(=O)(O[Si](C)(C)C)O[Si](C)(C)C)OC(N2C=NC3=C(N)N=CN=C32)C1O[Si](C)(C)C	6133.3	Standard polar	33892256
Phosphoaminophosphonic acid-adenylate ester,5TMS,isomer #16	C[Si](C)(C)OC1C(COP(=O)(O)OP(=O)(O)NP(=O)(O)O[Si](C)(C)C)OC(N2C=NC3=C(N([Si](C)(C)C)[Si](C)(C)C)N=CN=C32)C1O[Si](C)(C)C	4040.1	Semi standard non polar	33892256
Phosphoaminophosphonic acid-adenylate ester,5TMS,isomer #16	C[Si](C)(C)OC1C(COP(=O)(O)OP(=O)(O)NP(=O)(O)O[Si](C)(C)C)OC(N2C=NC3=C(N([Si](C)(C)C)[Si](C)(C)C)N=CN=C32)C1O[Si](C)(C)C	3877.1	Standard non polar	33892256
Phosphoaminophosphonic acid-adenylate ester,5TMS,isomer #16	C[Si](C)(C)OC1C(COP(=O)(O)OP(=O)(O)NP(=O)(O)O[Si](C)(C)C)OC(N2C=NC3=C(N([Si](C)(C)C)[Si](C)(C)C)N=CN=C32)C1O[Si](C)(C)C	5982.1	Standard polar	33892256
Phosphoaminophosphonic acid-adenylate ester,5TMS,isomer #17	C[Si](C)(C)NC1=NC=NC2=C1N=CN2C1OC(COP(=O)(O)OP(=O)(O)N([Si](C)(C)C)P(=O)(O)O[Si](C)(C)C)C(O[Si](C)(C)C)C1O[Si](C)(C)C	4036.6	Semi standard non polar	33892256
Phosphoaminophosphonic acid-adenylate ester,5TMS,isomer #17	C[Si](C)(C)NC1=NC=NC2=C1N=CN2C1OC(COP(=O)(O)OP(=O)(O)N([Si](C)(C)C)P(=O)(O)O[Si](C)(C)C)C(O[Si](C)(C)C)C1O[Si](C)(C)C	4010.4	Standard non polar	33892256
Phosphoaminophosphonic acid-adenylate ester,5TMS,isomer #17	C[Si](C)(C)NC1=NC=NC2=C1N=CN2C1OC(COP(=O)(O)OP(=O)(O)N([Si](C)(C)C)P(=O)(O)O[Si](C)(C)C)C(O[Si](C)(C)C)C1O[Si](C)(C)C	6012.2	Standard polar	33892256
Phosphoaminophosphonic acid-adenylate ester,5TMS,isomer #18	C[Si](C)(C)OC1C(COP(=O)(O)OP(=O)(O)N([Si](C)(C)C)P(=O)(O)O)OC(N2C=NC3=C(N([Si](C)(C)C)[Si](C)(C)C)N=CN=C32)C1O[Si](C)(C)C	4052.2	Semi standard non polar	33892256
Phosphoaminophosphonic acid-adenylate ester,5TMS,isomer #18	C[Si](C)(C)OC1C(COP(=O)(O)OP(=O)(O)N([Si](C)(C)C)P(=O)(O)O)OC(N2C=NC3=C(N([Si](C)(C)C)[Si](C)(C)C)N=CN=C32)C1O[Si](C)(C)C	4073.2	Standard non polar	33892256
Phosphoaminophosphonic acid-adenylate ester,5TMS,isomer #18	C[Si](C)(C)OC1C(COP(=O)(O)OP(=O)(O)N([Si](C)(C)C)P(=O)(O)O)OC(N2C=NC3=C(N([Si](C)(C)C)[Si](C)(C)C)N=CN=C32)C1O[Si](C)(C)C	5973.7	Standard polar	33892256
Phosphoaminophosphonic acid-adenylate ester,5TMS,isomer #19	C[Si](C)(C)OC1C(COP(=O)(O[Si](C)(C)C)OP(=O)(NP(=O)(O[Si](C)(C)C)O[Si](C)(C)C)O[Si](C)(C)C)OC(N2C=NC3=C(N)N=CN=C32)C1O	3979.2	Semi standard non polar	33892256
Phosphoaminophosphonic acid-adenylate ester,5TMS,isomer #19	C[Si](C)(C)OC1C(COP(=O)(O[Si](C)(C)C)OP(=O)(NP(=O)(O[Si](C)(C)C)O[Si](C)(C)C)O[Si](C)(C)C)OC(N2C=NC3=C(N)N=CN=C32)C1O	3851.4	Standard non polar	33892256
Phosphoaminophosphonic acid-adenylate ester,5TMS,isomer #19	C[Si](C)(C)OC1C(COP(=O)(O[Si](C)(C)C)OP(=O)(NP(=O)(O[Si](C)(C)C)O[Si](C)(C)C)O[Si](C)(C)C)OC(N2C=NC3=C(N)N=CN=C32)C1O	5961.4	Standard polar	33892256
Phosphoaminophosphonic acid-adenylate ester,5TMS,isomer #2	C[Si](C)(C)NC1=NC=NC2=C1N=CN2C1OC(COP(=O)(O[Si](C)(C)C)OP(=O)(NP(=O)(O)O)O[Si](C)(C)C)C(O[Si](C)(C)C)C1O[Si](C)(C)C	4052.1	Semi standard non polar	33892256
Phosphoaminophosphonic acid-adenylate ester,5TMS,isomer #2	C[Si](C)(C)NC1=NC=NC2=C1N=CN2C1OC(COP(=O)(O[Si](C)(C)C)OP(=O)(NP(=O)(O)O)O[Si](C)(C)C)C(O[Si](C)(C)C)C1O[Si](C)(C)C	3861.5	Standard non polar	33892256
Phosphoaminophosphonic acid-adenylate ester,5TMS,isomer #2	C[Si](C)(C)NC1=NC=NC2=C1N=CN2C1OC(COP(=O)(O[Si](C)(C)C)OP(=O)(NP(=O)(O)O)O[Si](C)(C)C)C(O[Si](C)(C)C)C1O[Si](C)(C)C	5888.1	Standard polar	33892256
Phosphoaminophosphonic acid-adenylate ester,5TMS,isomer #20	C[Si](C)(C)NC1=NC=NC2=C1N=CN2C1OC(COP(=O)(O[Si](C)(C)C)OP(=O)(NP(=O)(O)O[Si](C)(C)C)O[Si](C)(C)C)C(O[Si](C)(C)C)C1O	4037.5	Semi standard non polar	33892256
Phosphoaminophosphonic acid-adenylate ester,5TMS,isomer #20	C[Si](C)(C)NC1=NC=NC2=C1N=CN2C1OC(COP(=O)(O[Si](C)(C)C)OP(=O)(NP(=O)(O)O[Si](C)(C)C)O[Si](C)(C)C)C(O[Si](C)(C)C)C1O	3954.6	Standard non polar	33892256
Phosphoaminophosphonic acid-adenylate ester,5TMS,isomer #20	C[Si](C)(C)NC1=NC=NC2=C1N=CN2C1OC(COP(=O)(O[Si](C)(C)C)OP(=O)(NP(=O)(O)O[Si](C)(C)C)O[Si](C)(C)C)C(O[Si](C)(C)C)C1O	5793.0	Standard polar	33892256
Phosphoaminophosphonic acid-adenylate ester,5TMS,isomer #21	C[Si](C)(C)OC1C(COP(=O)(O[Si](C)(C)C)OP(=O)(O[Si](C)(C)C)N([Si](C)(C)C)P(=O)(O)O[Si](C)(C)C)OC(N2C=NC3=C(N)N=CN=C32)C1O	4025.1	Semi standard non polar	33892256
Phosphoaminophosphonic acid-adenylate ester,5TMS,isomer #21	C[Si](C)(C)OC1C(COP(=O)(O[Si](C)(C)C)OP(=O)(O[Si](C)(C)C)N([Si](C)(C)C)P(=O)(O)O[Si](C)(C)C)OC(N2C=NC3=C(N)N=CN=C32)C1O	4028.1	Standard non polar	33892256
Phosphoaminophosphonic acid-adenylate ester,5TMS,isomer #21	C[Si](C)(C)OC1C(COP(=O)(O[Si](C)(C)C)OP(=O)(O[Si](C)(C)C)N([Si](C)(C)C)P(=O)(O)O[Si](C)(C)C)OC(N2C=NC3=C(N)N=CN=C32)C1O	5983.5	Standard polar	33892256
Phosphoaminophosphonic acid-adenylate ester,5TMS,isomer #22	C[Si](C)(C)OC1C(COP(=O)(O[Si](C)(C)C)OP(=O)(NP(=O)(O)O)O[Si](C)(C)C)OC(N2C=NC3=C(N([Si](C)(C)C)[Si](C)(C)C)N=CN=C32)C1O	4071.2	Semi standard non polar	33892256
Phosphoaminophosphonic acid-adenylate ester,5TMS,isomer #22	C[Si](C)(C)OC1C(COP(=O)(O[Si](C)(C)C)OP(=O)(NP(=O)(O)O)O[Si](C)(C)C)OC(N2C=NC3=C(N([Si](C)(C)C)[Si](C)(C)C)N=CN=C32)C1O	3980.6	Standard non polar	33892256
Phosphoaminophosphonic acid-adenylate ester,5TMS,isomer #22	C[Si](C)(C)OC1C(COP(=O)(O[Si](C)(C)C)OP(=O)(NP(=O)(O)O)O[Si](C)(C)C)OC(N2C=NC3=C(N([Si](C)(C)C)[Si](C)(C)C)N=CN=C32)C1O	5749.5	Standard polar	33892256
Phosphoaminophosphonic acid-adenylate ester,5TMS,isomer #23	C[Si](C)(C)NC1=NC=NC2=C1N=CN2C1OC(COP(=O)(O[Si](C)(C)C)OP(=O)(O[Si](C)(C)C)N([Si](C)(C)C)P(=O)(O)O)C(O[Si](C)(C)C)C1O	4111.4	Semi standard non polar	33892256
Phosphoaminophosphonic acid-adenylate ester,5TMS,isomer #23	C[Si](C)(C)NC1=NC=NC2=C1N=CN2C1OC(COP(=O)(O[Si](C)(C)C)OP(=O)(O[Si](C)(C)C)N([Si](C)(C)C)P(=O)(O)O)C(O[Si](C)(C)C)C1O	4135.4	Standard non polar	33892256
Phosphoaminophosphonic acid-adenylate ester,5TMS,isomer #23	C[Si](C)(C)NC1=NC=NC2=C1N=CN2C1OC(COP(=O)(O[Si](C)(C)C)OP(=O)(O[Si](C)(C)C)N([Si](C)(C)C)P(=O)(O)O)C(O[Si](C)(C)C)C1O	5809.8	Standard polar	33892256
Phosphoaminophosphonic acid-adenylate ester,5TMS,isomer #24	C[Si](C)(C)NC1=NC=NC2=C1N=CN2C1OC(COP(=O)(O[Si](C)(C)C)OP(=O)(O)NP(=O)(O[Si](C)(C)C)O[Si](C)(C)C)C(O[Si](C)(C)C)C1O	4045.2	Semi standard non polar	33892256
Phosphoaminophosphonic acid-adenylate ester,5TMS,isomer #24	C[Si](C)(C)NC1=NC=NC2=C1N=CN2C1OC(COP(=O)(O[Si](C)(C)C)OP(=O)(O)NP(=O)(O[Si](C)(C)C)O[Si](C)(C)C)C(O[Si](C)(C)C)C1O	3923.0	Standard non polar	33892256
Phosphoaminophosphonic acid-adenylate ester,5TMS,isomer #24	C[Si](C)(C)NC1=NC=NC2=C1N=CN2C1OC(COP(=O)(O[Si](C)(C)C)OP(=O)(O)NP(=O)(O[Si](C)(C)C)O[Si](C)(C)C)C(O[Si](C)(C)C)C1O	5843.1	Standard polar	33892256
Phosphoaminophosphonic acid-adenylate ester,5TMS,isomer #25	C[Si](C)(C)OC1C(COP(=O)(O[Si](C)(C)C)OP(=O)(O)N([Si](C)(C)C)P(=O)(O[Si](C)(C)C)O[Si](C)(C)C)OC(N2C=NC3=C(N)N=CN=C32)C1O	4023.8	Semi standard non polar	33892256
Phosphoaminophosphonic acid-adenylate ester,5TMS,isomer #25	C[Si](C)(C)OC1C(COP(=O)(O[Si](C)(C)C)OP(=O)(O)N([Si](C)(C)C)P(=O)(O[Si](C)(C)C)O[Si](C)(C)C)OC(N2C=NC3=C(N)N=CN=C32)C1O	4021.0	Standard non polar	33892256
Phosphoaminophosphonic acid-adenylate ester,5TMS,isomer #25	C[Si](C)(C)OC1C(COP(=O)(O[Si](C)(C)C)OP(=O)(O)N([Si](C)(C)C)P(=O)(O[Si](C)(C)C)O[Si](C)(C)C)OC(N2C=NC3=C(N)N=CN=C32)C1O	6018.9	Standard polar	33892256
Phosphoaminophosphonic acid-adenylate ester,5TMS,isomer #26	C[Si](C)(C)OC1C(COP(=O)(O[Si](C)(C)C)OP(=O)(O)NP(=O)(O)O[Si](C)(C)C)OC(N2C=NC3=C(N([Si](C)(C)C)[Si](C)(C)C)N=CN=C32)C1O	4065.3	Semi standard non polar	33892256
Phosphoaminophosphonic acid-adenylate ester,5TMS,isomer #26	C[Si](C)(C)OC1C(COP(=O)(O[Si](C)(C)C)OP(=O)(O)NP(=O)(O)O[Si](C)(C)C)OC(N2C=NC3=C(N([Si](C)(C)C)[Si](C)(C)C)N=CN=C32)C1O	3976.4	Standard non polar	33892256
Phosphoaminophosphonic acid-adenylate ester,5TMS,isomer #26	C[Si](C)(C)OC1C(COP(=O)(O[Si](C)(C)C)OP(=O)(O)NP(=O)(O)O[Si](C)(C)C)OC(N2C=NC3=C(N([Si](C)(C)C)[Si](C)(C)C)N=CN=C32)C1O	5839.2	Standard polar	33892256
Phosphoaminophosphonic acid-adenylate ester,5TMS,isomer #27	C[Si](C)(C)NC1=NC=NC2=C1N=CN2C1OC(COP(=O)(O[Si](C)(C)C)OP(=O)(O)N([Si](C)(C)C)P(=O)(O)O[Si](C)(C)C)C(O[Si](C)(C)C)C1O	4069.8	Semi standard non polar	33892256
Phosphoaminophosphonic acid-adenylate ester,5TMS,isomer #27	C[Si](C)(C)NC1=NC=NC2=C1N=CN2C1OC(COP(=O)(O[Si](C)(C)C)OP(=O)(O)N([Si](C)(C)C)P(=O)(O)O[Si](C)(C)C)C(O[Si](C)(C)C)C1O	4102.3	Standard non polar	33892256
Phosphoaminophosphonic acid-adenylate ester,5TMS,isomer #27	C[Si](C)(C)NC1=NC=NC2=C1N=CN2C1OC(COP(=O)(O[Si](C)(C)C)OP(=O)(O)N([Si](C)(C)C)P(=O)(O)O[Si](C)(C)C)C(O[Si](C)(C)C)C1O	5894.7	Standard polar	33892256
Phosphoaminophosphonic acid-adenylate ester,5TMS,isomer #28	C[Si](C)(C)OC1C(COP(=O)(O[Si](C)(C)C)OP(=O)(O)N([Si](C)(C)C)P(=O)(O)O)OC(N2C=NC3=C(N([Si](C)(C)C)[Si](C)(C)C)N=CN=C32)C1O	4094.7	Semi standard non polar	33892256
Phosphoaminophosphonic acid-adenylate ester,5TMS,isomer #28	C[Si](C)(C)OC1C(COP(=O)(O[Si](C)(C)C)OP(=O)(O)N([Si](C)(C)C)P(=O)(O)O)OC(N2C=NC3=C(N([Si](C)(C)C)[Si](C)(C)C)N=CN=C32)C1O	4162.8	Standard non polar	33892256
Phosphoaminophosphonic acid-adenylate ester,5TMS,isomer #28	C[Si](C)(C)OC1C(COP(=O)(O[Si](C)(C)C)OP(=O)(O)N([Si](C)(C)C)P(=O)(O)O)OC(N2C=NC3=C(N([Si](C)(C)C)[Si](C)(C)C)N=CN=C32)C1O	5850.4	Standard polar	33892256
Phosphoaminophosphonic acid-adenylate ester,5TMS,isomer #29	C[Si](C)(C)NC1=NC=NC2=C1N=CN2C1OC(COP(=O)(O)OP(=O)(NP(=O)(O[Si](C)(C)C)O[Si](C)(C)C)O[Si](C)(C)C)C(O[Si](C)(C)C)C1O	4031.7	Semi standard non polar	33892256
Phosphoaminophosphonic acid-adenylate ester,5TMS,isomer #29	C[Si](C)(C)NC1=NC=NC2=C1N=CN2C1OC(COP(=O)(O)OP(=O)(NP(=O)(O[Si](C)(C)C)O[Si](C)(C)C)O[Si](C)(C)C)C(O[Si](C)(C)C)C1O	3911.6	Standard non polar	33892256
Phosphoaminophosphonic acid-adenylate ester,5TMS,isomer #29	C[Si](C)(C)NC1=NC=NC2=C1N=CN2C1OC(COP(=O)(O)OP(=O)(NP(=O)(O[Si](C)(C)C)O[Si](C)(C)C)O[Si](C)(C)C)C(O[Si](C)(C)C)C1O	5834.1	Standard polar	33892256
Phosphoaminophosphonic acid-adenylate ester,5TMS,isomer #3	C[Si](C)(C)OC1C(COP(=O)(O[Si](C)(C)C)OP(=O)(O[Si](C)(C)C)N([Si](C)(C)C)P(=O)(O)O)OC(N2C=NC3=C(N)N=CN=C32)C1O[Si](C)(C)C	4039.1	Semi standard non polar	33892256
Phosphoaminophosphonic acid-adenylate ester,5TMS,isomer #3	C[Si](C)(C)OC1C(COP(=O)(O[Si](C)(C)C)OP(=O)(O[Si](C)(C)C)N([Si](C)(C)C)P(=O)(O)O)OC(N2C=NC3=C(N)N=CN=C32)C1O[Si](C)(C)C	3983.2	Standard non polar	33892256
Phosphoaminophosphonic acid-adenylate ester,5TMS,isomer #3	C[Si](C)(C)OC1C(COP(=O)(O[Si](C)(C)C)OP(=O)(O[Si](C)(C)C)N([Si](C)(C)C)P(=O)(O)O)OC(N2C=NC3=C(N)N=CN=C32)C1O[Si](C)(C)C	6074.0	Standard polar	33892256
Phosphoaminophosphonic acid-adenylate ester,5TMS,isomer #30	C[Si](C)(C)OC1C(COP(=O)(O)OP(=O)(O[Si](C)(C)C)N([Si](C)(C)C)P(=O)(O[Si](C)(C)C)O[Si](C)(C)C)OC(N2C=NC3=C(N)N=CN=C32)C1O	4028.3	Semi standard non polar	33892256
Phosphoaminophosphonic acid-adenylate ester,5TMS,isomer #30	C[Si](C)(C)OC1C(COP(=O)(O)OP(=O)(O[Si](C)(C)C)N([Si](C)(C)C)P(=O)(O[Si](C)(C)C)O[Si](C)(C)C)OC(N2C=NC3=C(N)N=CN=C32)C1O	4002.8	Standard non polar	33892256
Phosphoaminophosphonic acid-adenylate ester,5TMS,isomer #30	C[Si](C)(C)OC1C(COP(=O)(O)OP(=O)(O[Si](C)(C)C)N([Si](C)(C)C)P(=O)(O[Si](C)(C)C)O[Si](C)(C)C)OC(N2C=NC3=C(N)N=CN=C32)C1O	6012.0	Standard polar	33892256
Phosphoaminophosphonic acid-adenylate ester,5TMS,isomer #31	C[Si](C)(C)OC1C(COP(=O)(O)OP(=O)(NP(=O)(O)O[Si](C)(C)C)O[Si](C)(C)C)OC(N2C=NC3=C(N([Si](C)(C)C)[Si](C)(C)C)N=CN=C32)C1O	4046.9	Semi standard non polar	33892256
Phosphoaminophosphonic acid-adenylate ester,5TMS,isomer #31	C[Si](C)(C)OC1C(COP(=O)(O)OP(=O)(NP(=O)(O)O[Si](C)(C)C)O[Si](C)(C)C)OC(N2C=NC3=C(N([Si](C)(C)C)[Si](C)(C)C)N=CN=C32)C1O	3974.5	Standard non polar	33892256
Phosphoaminophosphonic acid-adenylate ester,5TMS,isomer #31	C[Si](C)(C)OC1C(COP(=O)(O)OP(=O)(NP(=O)(O)O[Si](C)(C)C)O[Si](C)(C)C)OC(N2C=NC3=C(N([Si](C)(C)C)[Si](C)(C)C)N=CN=C32)C1O	5810.8	Standard polar	33892256
Phosphoaminophosphonic acid-adenylate ester,5TMS,isomer #32	C[Si](C)(C)NC1=NC=NC2=C1N=CN2C1OC(COP(=O)(O)OP(=O)(O[Si](C)(C)C)N([Si](C)(C)C)P(=O)(O)O[Si](C)(C)C)C(O[Si](C)(C)C)C1O	4069.2	Semi standard non polar	33892256
Phosphoaminophosphonic acid-adenylate ester,5TMS,isomer #32	C[Si](C)(C)NC1=NC=NC2=C1N=CN2C1OC(COP(=O)(O)OP(=O)(O[Si](C)(C)C)N([Si](C)(C)C)P(=O)(O)O[Si](C)(C)C)C(O[Si](C)(C)C)C1O	4091.0	Standard non polar	33892256
Phosphoaminophosphonic acid-adenylate ester,5TMS,isomer #32	C[Si](C)(C)NC1=NC=NC2=C1N=CN2C1OC(COP(=O)(O)OP(=O)(O[Si](C)(C)C)N([Si](C)(C)C)P(=O)(O)O[Si](C)(C)C)C(O[Si](C)(C)C)C1O	5843.2	Standard polar	33892256
Phosphoaminophosphonic acid-adenylate ester,5TMS,isomer #33	C[Si](C)(C)OC1C(COP(=O)(O)OP(=O)(O[Si](C)(C)C)N([Si](C)(C)C)P(=O)(O)O)OC(N2C=NC3=C(N([Si](C)(C)C)[Si](C)(C)C)N=CN=C32)C1O	4089.5	Semi standard non polar	33892256
Phosphoaminophosphonic acid-adenylate ester,5TMS,isomer #33	C[Si](C)(C)OC1C(COP(=O)(O)OP(=O)(O[Si](C)(C)C)N([Si](C)(C)C)P(=O)(O)O)OC(N2C=NC3=C(N([Si](C)(C)C)[Si](C)(C)C)N=CN=C32)C1O	4176.0	Standard non polar	33892256
Phosphoaminophosphonic acid-adenylate ester,5TMS,isomer #33	C[Si](C)(C)OC1C(COP(=O)(O)OP(=O)(O[Si](C)(C)C)N([Si](C)(C)C)P(=O)(O)O)OC(N2C=NC3=C(N([Si](C)(C)C)[Si](C)(C)C)N=CN=C32)C1O	5804.4	Standard polar	33892256
Phosphoaminophosphonic acid-adenylate ester,5TMS,isomer #34	C[Si](C)(C)OC1C(COP(=O)(O)OP(=O)(O)NP(=O)(O[Si](C)(C)C)O[Si](C)(C)C)OC(N2C=NC3=C(N([Si](C)(C)C)[Si](C)(C)C)N=CN=C32)C1O	4057.3	Semi standard non polar	33892256
Phosphoaminophosphonic acid-adenylate ester,5TMS,isomer #34	C[Si](C)(C)OC1C(COP(=O)(O)OP(=O)(O)NP(=O)(O[Si](C)(C)C)O[Si](C)(C)C)OC(N2C=NC3=C(N([Si](C)(C)C)[Si](C)(C)C)N=CN=C32)C1O	3938.6	Standard non polar	33892256
Phosphoaminophosphonic acid-adenylate ester,5TMS,isomer #34	C[Si](C)(C)OC1C(COP(=O)(O)OP(=O)(O)NP(=O)(O[Si](C)(C)C)O[Si](C)(C)C)OC(N2C=NC3=C(N([Si](C)(C)C)[Si](C)(C)C)N=CN=C32)C1O	5869.1	Standard polar	33892256
Phosphoaminophosphonic acid-adenylate ester,5TMS,isomer #35	C[Si](C)(C)NC1=NC=NC2=C1N=CN2C1OC(COP(=O)(O)OP(=O)(O)N([Si](C)(C)C)P(=O)(O[Si](C)(C)C)O[Si](C)(C)C)C(O[Si](C)(C)C)C1O	4071.7	Semi standard non polar	33892256
Phosphoaminophosphonic acid-adenylate ester,5TMS,isomer #35	C[Si](C)(C)NC1=NC=NC2=C1N=CN2C1OC(COP(=O)(O)OP(=O)(O)N([Si](C)(C)C)P(=O)(O[Si](C)(C)C)O[Si](C)(C)C)C(O[Si](C)(C)C)C1O	4086.8	Standard non polar	33892256
Phosphoaminophosphonic acid-adenylate ester,5TMS,isomer #35	C[Si](C)(C)NC1=NC=NC2=C1N=CN2C1OC(COP(=O)(O)OP(=O)(O)N([Si](C)(C)C)P(=O)(O[Si](C)(C)C)O[Si](C)(C)C)C(O[Si](C)(C)C)C1O	5900.0	Standard polar	33892256
Phosphoaminophosphonic acid-adenylate ester,5TMS,isomer #36	C[Si](C)(C)OC1C(COP(=O)(O)OP(=O)(O)N([Si](C)(C)C)P(=O)(O)O[Si](C)(C)C)OC(N2C=NC3=C(N([Si](C)(C)C)[Si](C)(C)C)N=CN=C32)C1O	4060.7	Semi standard non polar	33892256
Phosphoaminophosphonic acid-adenylate ester,5TMS,isomer #36	C[Si](C)(C)OC1C(COP(=O)(O)OP(=O)(O)N([Si](C)(C)C)P(=O)(O)O[Si](C)(C)C)OC(N2C=NC3=C(N([Si](C)(C)C)[Si](C)(C)C)N=CN=C32)C1O	4139.4	Standard non polar	33892256
Phosphoaminophosphonic acid-adenylate ester,5TMS,isomer #36	C[Si](C)(C)OC1C(COP(=O)(O)OP(=O)(O)N([Si](C)(C)C)P(=O)(O)O[Si](C)(C)C)OC(N2C=NC3=C(N([Si](C)(C)C)[Si](C)(C)C)N=CN=C32)C1O	5897.2	Standard polar	33892256
Phosphoaminophosphonic acid-adenylate ester,5TMS,isomer #37	C[Si](C)(C)OC1C(O)C(COP(=O)(O[Si](C)(C)C)OP(=O)(NP(=O)(O[Si](C)(C)C)O[Si](C)(C)C)O[Si](C)(C)C)OC1N1C=NC2=C(N)N=CN=C21	3969.6	Semi standard non polar	33892256
Phosphoaminophosphonic acid-adenylate ester,5TMS,isomer #37	C[Si](C)(C)OC1C(O)C(COP(=O)(O[Si](C)(C)C)OP(=O)(NP(=O)(O[Si](C)(C)C)O[Si](C)(C)C)O[Si](C)(C)C)OC1N1C=NC2=C(N)N=CN=C21	3864.0	Standard non polar	33892256
Phosphoaminophosphonic acid-adenylate ester,5TMS,isomer #37	C[Si](C)(C)OC1C(O)C(COP(=O)(O[Si](C)(C)C)OP(=O)(NP(=O)(O[Si](C)(C)C)O[Si](C)(C)C)O[Si](C)(C)C)OC1N1C=NC2=C(N)N=CN=C21	5974.3	Standard polar	33892256
Phosphoaminophosphonic acid-adenylate ester,5TMS,isomer #38	C[Si](C)(C)NC1=NC=NC2=C1N=CN2C1OC(COP(=O)(O[Si](C)(C)C)OP(=O)(NP(=O)(O)O[Si](C)(C)C)O[Si](C)(C)C)C(O)C1O[Si](C)(C)C	4036.1	Semi standard non polar	33892256
Phosphoaminophosphonic acid-adenylate ester,5TMS,isomer #38	C[Si](C)(C)NC1=NC=NC2=C1N=CN2C1OC(COP(=O)(O[Si](C)(C)C)OP(=O)(NP(=O)(O)O[Si](C)(C)C)O[Si](C)(C)C)C(O)C1O[Si](C)(C)C	3966.4	Standard non polar	33892256
Phosphoaminophosphonic acid-adenylate ester,5TMS,isomer #38	C[Si](C)(C)NC1=NC=NC2=C1N=CN2C1OC(COP(=O)(O[Si](C)(C)C)OP(=O)(NP(=O)(O)O[Si](C)(C)C)O[Si](C)(C)C)C(O)C1O[Si](C)(C)C	5810.7	Standard polar	33892256
Phosphoaminophosphonic acid-adenylate ester,5TMS,isomer #39	C[Si](C)(C)OC1C(O)C(COP(=O)(O[Si](C)(C)C)OP(=O)(O[Si](C)(C)C)N([Si](C)(C)C)P(=O)(O)O[Si](C)(C)C)OC1N1C=NC2=C(N)N=CN=C21	4013.7	Semi standard non polar	33892256
Phosphoaminophosphonic acid-adenylate ester,5TMS,isomer #39	C[Si](C)(C)OC1C(O)C(COP(=O)(O[Si](C)(C)C)OP(=O)(O[Si](C)(C)C)N([Si](C)(C)C)P(=O)(O)O[Si](C)(C)C)OC1N1C=NC2=C(N)N=CN=C21	4038.5	Standard non polar	33892256
Phosphoaminophosphonic acid-adenylate ester,5TMS,isomer #39	C[Si](C)(C)OC1C(O)C(COP(=O)(O[Si](C)(C)C)OP(=O)(O[Si](C)(C)C)N([Si](C)(C)C)P(=O)(O)O[Si](C)(C)C)OC1N1C=NC2=C(N)N=CN=C21	5995.2	Standard polar	33892256
Phosphoaminophosphonic acid-adenylate ester,5TMS,isomer #4	C[Si](C)(C)OC1C(COP(=O)(O[Si](C)(C)C)OP(=O)(O)NP(=O)(O[Si](C)(C)C)O[Si](C)(C)C)OC(N2C=NC3=C(N)N=CN=C32)C1O[Si](C)(C)C	3976.4	Semi standard non polar	33892256
Phosphoaminophosphonic acid-adenylate ester,5TMS,isomer #4	C[Si](C)(C)OC1C(COP(=O)(O[Si](C)(C)C)OP(=O)(O)NP(=O)(O[Si](C)(C)C)O[Si](C)(C)C)OC(N2C=NC3=C(N)N=CN=C32)C1O[Si](C)(C)C	3762.7	Standard non polar	33892256
Phosphoaminophosphonic acid-adenylate ester,5TMS,isomer #4	C[Si](C)(C)OC1C(COP(=O)(O[Si](C)(C)C)OP(=O)(O)NP(=O)(O[Si](C)(C)C)O[Si](C)(C)C)OC(N2C=NC3=C(N)N=CN=C32)C1O[Si](C)(C)C	6127.6	Standard polar	33892256
Phosphoaminophosphonic acid-adenylate ester,5TMS,isomer #40	C[Si](C)(C)OC1C(O)C(COP(=O)(O[Si](C)(C)C)OP(=O)(NP(=O)(O)O)O[Si](C)(C)C)OC1N1C=NC2=C(N([Si](C)(C)C)[Si](C)(C)C)N=CN=C21	4063.3	Semi standard non polar	33892256
Phosphoaminophosphonic acid-adenylate ester,5TMS,isomer #40	C[Si](C)(C)OC1C(O)C(COP(=O)(O[Si](C)(C)C)OP(=O)(NP(=O)(O)O)O[Si](C)(C)C)OC1N1C=NC2=C(N([Si](C)(C)C)[Si](C)(C)C)N=CN=C21	3995.5	Standard non polar	33892256
Phosphoaminophosphonic acid-adenylate ester,5TMS,isomer #40	C[Si](C)(C)OC1C(O)C(COP(=O)(O[Si](C)(C)C)OP(=O)(NP(=O)(O)O)O[Si](C)(C)C)OC1N1C=NC2=C(N([Si](C)(C)C)[Si](C)(C)C)N=CN=C21	5767.7	Standard polar	33892256
Phosphoaminophosphonic acid-adenylate ester,5TMS,isomer #41	C[Si](C)(C)NC1=NC=NC2=C1N=CN2C1OC(COP(=O)(O[Si](C)(C)C)OP(=O)(O[Si](C)(C)C)N([Si](C)(C)C)P(=O)(O)O)C(O)C1O[Si](C)(C)C	4104.4	Semi standard non polar	33892256
Phosphoaminophosphonic acid-adenylate ester,5TMS,isomer #41	C[Si](C)(C)NC1=NC=NC2=C1N=CN2C1OC(COP(=O)(O[Si](C)(C)C)OP(=O)(O[Si](C)(C)C)N([Si](C)(C)C)P(=O)(O)O)C(O)C1O[Si](C)(C)C	4145.6	Standard non polar	33892256
Phosphoaminophosphonic acid-adenylate ester,5TMS,isomer #41	C[Si](C)(C)NC1=NC=NC2=C1N=CN2C1OC(COP(=O)(O[Si](C)(C)C)OP(=O)(O[Si](C)(C)C)N([Si](C)(C)C)P(=O)(O)O)C(O)C1O[Si](C)(C)C	5826.3	Standard polar	33892256
Phosphoaminophosphonic acid-adenylate ester,5TMS,isomer #42	C[Si](C)(C)NC1=NC=NC2=C1N=CN2C1OC(COP(=O)(O[Si](C)(C)C)OP(=O)(O)NP(=O)(O[Si](C)(C)C)O[Si](C)(C)C)C(O)C1O[Si](C)(C)C	4042.6	Semi standard non polar	33892256
Phosphoaminophosphonic acid-adenylate ester,5TMS,isomer #42	C[Si](C)(C)NC1=NC=NC2=C1N=CN2C1OC(COP(=O)(O[Si](C)(C)C)OP(=O)(O)NP(=O)(O[Si](C)(C)C)O[Si](C)(C)C)C(O)C1O[Si](C)(C)C	3935.0	Standard non polar	33892256
Phosphoaminophosphonic acid-adenylate ester,5TMS,isomer #42	C[Si](C)(C)NC1=NC=NC2=C1N=CN2C1OC(COP(=O)(O[Si](C)(C)C)OP(=O)(O)NP(=O)(O[Si](C)(C)C)O[Si](C)(C)C)C(O)C1O[Si](C)(C)C	5860.2	Standard polar	33892256
Phosphoaminophosphonic acid-adenylate ester,5TMS,isomer #43	C[Si](C)(C)OC1C(O)C(COP(=O)(O[Si](C)(C)C)OP(=O)(O)N([Si](C)(C)C)P(=O)(O[Si](C)(C)C)O[Si](C)(C)C)OC1N1C=NC2=C(N)N=CN=C21	4012.7	Semi standard non polar	33892256
Phosphoaminophosphonic acid-adenylate ester,5TMS,isomer #43	C[Si](C)(C)OC1C(O)C(COP(=O)(O[Si](C)(C)C)OP(=O)(O)N([Si](C)(C)C)P(=O)(O[Si](C)(C)C)O[Si](C)(C)C)OC1N1C=NC2=C(N)N=CN=C21	4032.1	Standard non polar	33892256
Phosphoaminophosphonic acid-adenylate ester,5TMS,isomer #43	C[Si](C)(C)OC1C(O)C(COP(=O)(O[Si](C)(C)C)OP(=O)(O)N([Si](C)(C)C)P(=O)(O[Si](C)(C)C)O[Si](C)(C)C)OC1N1C=NC2=C(N)N=CN=C21	6030.5	Standard polar	33892256
Phosphoaminophosphonic acid-adenylate ester,5TMS,isomer #44	C[Si](C)(C)OC1C(O)C(COP(=O)(O[Si](C)(C)C)OP(=O)(O)NP(=O)(O)O[Si](C)(C)C)OC1N1C=NC2=C(N([Si](C)(C)C)[Si](C)(C)C)N=CN=C21	4060.1	Semi standard non polar	33892256
Phosphoaminophosphonic acid-adenylate ester,5TMS,isomer #44	C[Si](C)(C)OC1C(O)C(COP(=O)(O[Si](C)(C)C)OP(=O)(O)NP(=O)(O)O[Si](C)(C)C)OC1N1C=NC2=C(N([Si](C)(C)C)[Si](C)(C)C)N=CN=C21	3990.1	Standard non polar	33892256
Phosphoaminophosphonic acid-adenylate ester,5TMS,isomer #44	C[Si](C)(C)OC1C(O)C(COP(=O)(O[Si](C)(C)C)OP(=O)(O)NP(=O)(O)O[Si](C)(C)C)OC1N1C=NC2=C(N([Si](C)(C)C)[Si](C)(C)C)N=CN=C21	5856.5	Standard polar	33892256
Phosphoaminophosphonic acid-adenylate ester,5TMS,isomer #45	C[Si](C)(C)NC1=NC=NC2=C1N=CN2C1OC(COP(=O)(O[Si](C)(C)C)OP(=O)(O)N([Si](C)(C)C)P(=O)(O)O[Si](C)(C)C)C(O)C1O[Si](C)(C)C	4065.7	Semi standard non polar	33892256
Phosphoaminophosphonic acid-adenylate ester,5TMS,isomer #45	C[Si](C)(C)NC1=NC=NC2=C1N=CN2C1OC(COP(=O)(O[Si](C)(C)C)OP(=O)(O)N([Si](C)(C)C)P(=O)(O)O[Si](C)(C)C)C(O)C1O[Si](C)(C)C	4112.7	Standard non polar	33892256
Phosphoaminophosphonic acid-adenylate ester,5TMS,isomer #45	C[Si](C)(C)NC1=NC=NC2=C1N=CN2C1OC(COP(=O)(O[Si](C)(C)C)OP(=O)(O)N([Si](C)(C)C)P(=O)(O)O[Si](C)(C)C)C(O)C1O[Si](C)(C)C	5910.5	Standard polar	33892256
Phosphoaminophosphonic acid-adenylate ester,5TMS,isomer #46	C[Si](C)(C)OC1C(O)C(COP(=O)(O[Si](C)(C)C)OP(=O)(O)N([Si](C)(C)C)P(=O)(O)O)OC1N1C=NC2=C(N([Si](C)(C)C)[Si](C)(C)C)N=CN=C21	4087.4	Semi standard non polar	33892256
Phosphoaminophosphonic acid-adenylate ester,5TMS,isomer #46	C[Si](C)(C)OC1C(O)C(COP(=O)(O[Si](C)(C)C)OP(=O)(O)N([Si](C)(C)C)P(=O)(O)O)OC1N1C=NC2=C(N([Si](C)(C)C)[Si](C)(C)C)N=CN=C21	4175.1	Standard non polar	33892256
Phosphoaminophosphonic acid-adenylate ester,5TMS,isomer #46	C[Si](C)(C)OC1C(O)C(COP(=O)(O[Si](C)(C)C)OP(=O)(O)N([Si](C)(C)C)P(=O)(O)O)OC1N1C=NC2=C(N([Si](C)(C)C)[Si](C)(C)C)N=CN=C21	5867.3	Standard polar	33892256
Phosphoaminophosphonic acid-adenylate ester,5TMS,isomer #47	C[Si](C)(C)NC1=NC=NC2=C1N=CN2C1OC(COP(=O)(O)OP(=O)(NP(=O)(O[Si](C)(C)C)O[Si](C)(C)C)O[Si](C)(C)C)C(O)C1O[Si](C)(C)C	4031.2	Semi standard non polar	33892256
Phosphoaminophosphonic acid-adenylate ester,5TMS,isomer #47	C[Si](C)(C)NC1=NC=NC2=C1N=CN2C1OC(COP(=O)(O)OP(=O)(NP(=O)(O[Si](C)(C)C)O[Si](C)(C)C)O[Si](C)(C)C)C(O)C1O[Si](C)(C)C	3921.2	Standard non polar	33892256
Phosphoaminophosphonic acid-adenylate ester,5TMS,isomer #47	C[Si](C)(C)NC1=NC=NC2=C1N=CN2C1OC(COP(=O)(O)OP(=O)(NP(=O)(O[Si](C)(C)C)O[Si](C)(C)C)O[Si](C)(C)C)C(O)C1O[Si](C)(C)C	5845.2	Standard polar	33892256
Phosphoaminophosphonic acid-adenylate ester,5TMS,isomer #48	C[Si](C)(C)OC1C(O)C(COP(=O)(O)OP(=O)(O[Si](C)(C)C)N([Si](C)(C)C)P(=O)(O[Si](C)(C)C)O[Si](C)(C)C)OC1N1C=NC2=C(N)N=CN=C21	4021.5	Semi standard non polar	33892256
Phosphoaminophosphonic acid-adenylate ester,5TMS,isomer #48	C[Si](C)(C)OC1C(O)C(COP(=O)(O)OP(=O)(O[Si](C)(C)C)N([Si](C)(C)C)P(=O)(O[Si](C)(C)C)O[Si](C)(C)C)OC1N1C=NC2=C(N)N=CN=C21	4008.3	Standard non polar	33892256
Phosphoaminophosphonic acid-adenylate ester,5TMS,isomer #48	C[Si](C)(C)OC1C(O)C(COP(=O)(O)OP(=O)(O[Si](C)(C)C)N([Si](C)(C)C)P(=O)(O[Si](C)(C)C)O[Si](C)(C)C)OC1N1C=NC2=C(N)N=CN=C21	6020.8	Standard polar	33892256
Phosphoaminophosphonic acid-adenylate ester,5TMS,isomer #49	C[Si](C)(C)OC1C(O)C(COP(=O)(O)OP(=O)(NP(=O)(O)O[Si](C)(C)C)O[Si](C)(C)C)OC1N1C=NC2=C(N([Si](C)(C)C)[Si](C)(C)C)N=CN=C21	4043.9	Semi standard non polar	33892256
Phosphoaminophosphonic acid-adenylate ester,5TMS,isomer #49	C[Si](C)(C)OC1C(O)C(COP(=O)(O)OP(=O)(NP(=O)(O)O[Si](C)(C)C)O[Si](C)(C)C)OC1N1C=NC2=C(N([Si](C)(C)C)[Si](C)(C)C)N=CN=C21	3984.5	Standard non polar	33892256
Phosphoaminophosphonic acid-adenylate ester,5TMS,isomer #49	C[Si](C)(C)OC1C(O)C(COP(=O)(O)OP(=O)(NP(=O)(O)O[Si](C)(C)C)O[Si](C)(C)C)OC1N1C=NC2=C(N([Si](C)(C)C)[Si](C)(C)C)N=CN=C21	5821.7	Standard polar	33892256
Phosphoaminophosphonic acid-adenylate ester,5TMS,isomer #5	C[Si](C)(C)NC1=NC=NC2=C1N=CN2C1OC(COP(=O)(O[Si](C)(C)C)OP(=O)(O)NP(=O)(O)O[Si](C)(C)C)C(O[Si](C)(C)C)C1O[Si](C)(C)C	4033.9	Semi standard non polar	33892256
Phosphoaminophosphonic acid-adenylate ester,5TMS,isomer #5	C[Si](C)(C)NC1=NC=NC2=C1N=CN2C1OC(COP(=O)(O[Si](C)(C)C)OP(=O)(O)NP(=O)(O)O[Si](C)(C)C)C(O[Si](C)(C)C)C1O[Si](C)(C)C	3862.1	Standard non polar	33892256
Phosphoaminophosphonic acid-adenylate ester,5TMS,isomer #5	C[Si](C)(C)NC1=NC=NC2=C1N=CN2C1OC(COP(=O)(O[Si](C)(C)C)OP(=O)(O)NP(=O)(O)O[Si](C)(C)C)C(O[Si](C)(C)C)C1O[Si](C)(C)C	5967.8	Standard polar	33892256
Phosphoaminophosphonic acid-adenylate ester,5TMS,isomer #50	C[Si](C)(C)NC1=NC=NC2=C1N=CN2C1OC(COP(=O)(O)OP(=O)(O[Si](C)(C)C)N([Si](C)(C)C)P(=O)(O)O[Si](C)(C)C)C(O)C1O[Si](C)(C)C	4066.3	Semi standard non polar	33892256
Phosphoaminophosphonic acid-adenylate ester,5TMS,isomer #50	C[Si](C)(C)NC1=NC=NC2=C1N=CN2C1OC(COP(=O)(O)OP(=O)(O[Si](C)(C)C)N([Si](C)(C)C)P(=O)(O)O[Si](C)(C)C)C(O)C1O[Si](C)(C)C	4095.5	Standard non polar	33892256
Phosphoaminophosphonic acid-adenylate ester,5TMS,isomer #50	C[Si](C)(C)NC1=NC=NC2=C1N=CN2C1OC(COP(=O)(O)OP(=O)(O[Si](C)(C)C)N([Si](C)(C)C)P(=O)(O)O[Si](C)(C)C)C(O)C1O[Si](C)(C)C	5853.5	Standard polar	33892256
Phosphoaminophosphonic acid-adenylate ester,5TMS,isomer #51	C[Si](C)(C)OC1C(O)C(COP(=O)(O)OP(=O)(O[Si](C)(C)C)N([Si](C)(C)C)P(=O)(O)O)OC1N1C=NC2=C(N([Si](C)(C)C)[Si](C)(C)C)N=CN=C21	4084.7	Semi standard non polar	33892256
Phosphoaminophosphonic acid-adenylate ester,5TMS,isomer #51	C[Si](C)(C)OC1C(O)C(COP(=O)(O)OP(=O)(O[Si](C)(C)C)N([Si](C)(C)C)P(=O)(O)O)OC1N1C=NC2=C(N([Si](C)(C)C)[Si](C)(C)C)N=CN=C21	4182.3	Standard non polar	33892256
Phosphoaminophosphonic acid-adenylate ester,5TMS,isomer #51	C[Si](C)(C)OC1C(O)C(COP(=O)(O)OP(=O)(O[Si](C)(C)C)N([Si](C)(C)C)P(=O)(O)O)OC1N1C=NC2=C(N([Si](C)(C)C)[Si](C)(C)C)N=CN=C21	5815.4	Standard polar	33892256
Phosphoaminophosphonic acid-adenylate ester,5TMS,isomer #52	C[Si](C)(C)OC1C(O)C(COP(=O)(O)OP(=O)(O)NP(=O)(O[Si](C)(C)C)O[Si](C)(C)C)OC1N1C=NC2=C(N([Si](C)(C)C)[Si](C)(C)C)N=CN=C21	4053.7	Semi standard non polar	33892256
Phosphoaminophosphonic acid-adenylate ester,5TMS,isomer #52	C[Si](C)(C)OC1C(O)C(COP(=O)(O)OP(=O)(O)NP(=O)(O[Si](C)(C)C)O[Si](C)(C)C)OC1N1C=NC2=C(N([Si](C)(C)C)[Si](C)(C)C)N=CN=C21	3949.7	Standard non polar	33892256
Phosphoaminophosphonic acid-adenylate ester,5TMS,isomer #52	C[Si](C)(C)OC1C(O)C(COP(=O)(O)OP(=O)(O)NP(=O)(O[Si](C)(C)C)O[Si](C)(C)C)OC1N1C=NC2=C(N([Si](C)(C)C)[Si](C)(C)C)N=CN=C21	5880.1	Standard polar	33892256
Phosphoaminophosphonic acid-adenylate ester,5TMS,isomer #53	C[Si](C)(C)NC1=NC=NC2=C1N=CN2C1OC(COP(=O)(O)OP(=O)(O)N([Si](C)(C)C)P(=O)(O[Si](C)(C)C)O[Si](C)(C)C)C(O)C1O[Si](C)(C)C	4069.0	Semi standard non polar	33892256
Phosphoaminophosphonic acid-adenylate ester,5TMS,isomer #53	C[Si](C)(C)NC1=NC=NC2=C1N=CN2C1OC(COP(=O)(O)OP(=O)(O)N([Si](C)(C)C)P(=O)(O[Si](C)(C)C)O[Si](C)(C)C)C(O)C1O[Si](C)(C)C	4093.7	Standard non polar	33892256
Phosphoaminophosphonic acid-adenylate ester,5TMS,isomer #53	C[Si](C)(C)NC1=NC=NC2=C1N=CN2C1OC(COP(=O)(O)OP(=O)(O)N([Si](C)(C)C)P(=O)(O[Si](C)(C)C)O[Si](C)(C)C)C(O)C1O[Si](C)(C)C	5910.2	Standard polar	33892256
Phosphoaminophosphonic acid-adenylate ester,5TMS,isomer #54	C[Si](C)(C)OC1C(O)C(COP(=O)(O)OP(=O)(O)N([Si](C)(C)C)P(=O)(O)O[Si](C)(C)C)OC1N1C=NC2=C(N([Si](C)(C)C)[Si](C)(C)C)N=CN=C21	4058.9	Semi standard non polar	33892256
Phosphoaminophosphonic acid-adenylate ester,5TMS,isomer #54	C[Si](C)(C)OC1C(O)C(COP(=O)(O)OP(=O)(O)N([Si](C)(C)C)P(=O)(O)O[Si](C)(C)C)OC1N1C=NC2=C(N([Si](C)(C)C)[Si](C)(C)C)N=CN=C21	4149.0	Standard non polar	33892256
Phosphoaminophosphonic acid-adenylate ester,5TMS,isomer #54	C[Si](C)(C)OC1C(O)C(COP(=O)(O)OP(=O)(O)N([Si](C)(C)C)P(=O)(O)O[Si](C)(C)C)OC1N1C=NC2=C(N([Si](C)(C)C)[Si](C)(C)C)N=CN=C21	5908.0	Standard polar	33892256
Phosphoaminophosphonic acid-adenylate ester,5TMS,isomer #55	C[Si](C)(C)NC1=NC=NC2=C1N=CN2C1OC(COP(=O)(O[Si](C)(C)C)OP(=O)(NP(=O)(O[Si](C)(C)C)O[Si](C)(C)C)O[Si](C)(C)C)C(O)C1O	4076.4	Semi standard non polar	33892256
Phosphoaminophosphonic acid-adenylate ester,5TMS,isomer #55	C[Si](C)(C)NC1=NC=NC2=C1N=CN2C1OC(COP(=O)(O[Si](C)(C)C)OP(=O)(NP(=O)(O[Si](C)(C)C)O[Si](C)(C)C)O[Si](C)(C)C)C(O)C1O	4010.1	Standard non polar	33892256
Phosphoaminophosphonic acid-adenylate ester,5TMS,isomer #55	C[Si](C)(C)NC1=NC=NC2=C1N=CN2C1OC(COP(=O)(O[Si](C)(C)C)OP(=O)(NP(=O)(O[Si](C)(C)C)O[Si](C)(C)C)O[Si](C)(C)C)C(O)C1O	5640.2	Standard polar	33892256
Phosphoaminophosphonic acid-adenylate ester,5TMS,isomer #56	C[Si](C)(C)OP(=O)(OCC1OC(N2C=NC3=C(N)N=CN=C32)C(O)C1O)OP(=O)(O[Si](C)(C)C)N([Si](C)(C)C)P(=O)(O[Si](C)(C)C)O[Si](C)(C)C	4063.7	Semi standard non polar	33892256
Phosphoaminophosphonic acid-adenylate ester,5TMS,isomer #56	C[Si](C)(C)OP(=O)(OCC1OC(N2C=NC3=C(N)N=CN=C32)C(O)C1O)OP(=O)(O[Si](C)(C)C)N([Si](C)(C)C)P(=O)(O[Si](C)(C)C)O[Si](C)(C)C	4085.2	Standard non polar	33892256
Phosphoaminophosphonic acid-adenylate ester,5TMS,isomer #56	C[Si](C)(C)OP(=O)(OCC1OC(N2C=NC3=C(N)N=CN=C32)C(O)C1O)OP(=O)(O[Si](C)(C)C)N([Si](C)(C)C)P(=O)(O[Si](C)(C)C)O[Si](C)(C)C	5902.3	Standard polar	33892256
Phosphoaminophosphonic acid-adenylate ester,5TMS,isomer #57	C[Si](C)(C)OP(=O)(O)NP(=O)(O[Si](C)(C)C)OP(=O)(OCC1OC(N2C=NC3=C(N([Si](C)(C)C)[Si](C)(C)C)N=CN=C32)C(O)C1O)O[Si](C)(C)C	4094.5	Semi standard non polar	33892256
Phosphoaminophosphonic acid-adenylate ester,5TMS,isomer #57	C[Si](C)(C)OP(=O)(O)NP(=O)(O[Si](C)(C)C)OP(=O)(OCC1OC(N2C=NC3=C(N([Si](C)(C)C)[Si](C)(C)C)N=CN=C32)C(O)C1O)O[Si](C)(C)C	4083.0	Standard non polar	33892256
Phosphoaminophosphonic acid-adenylate ester,5TMS,isomer #57	C[Si](C)(C)OP(=O)(O)NP(=O)(O[Si](C)(C)C)OP(=O)(OCC1OC(N2C=NC3=C(N([Si](C)(C)C)[Si](C)(C)C)N=CN=C32)C(O)C1O)O[Si](C)(C)C	5656.7	Standard polar	33892256
Phosphoaminophosphonic acid-adenylate ester,5TMS,isomer #58	C[Si](C)(C)NC1=NC=NC2=C1N=CN2C1OC(COP(=O)(O[Si](C)(C)C)OP(=O)(O[Si](C)(C)C)N([Si](C)(C)C)P(=O)(O)O[Si](C)(C)C)C(O)C1O	4111.8	Semi standard non polar	33892256
Phosphoaminophosphonic acid-adenylate ester,5TMS,isomer #58	C[Si](C)(C)NC1=NC=NC2=C1N=CN2C1OC(COP(=O)(O[Si](C)(C)C)OP(=O)(O[Si](C)(C)C)N([Si](C)(C)C)P(=O)(O)O[Si](C)(C)C)C(O)C1O	4189.1	Standard non polar	33892256
Phosphoaminophosphonic acid-adenylate ester,5TMS,isomer #58	C[Si](C)(C)NC1=NC=NC2=C1N=CN2C1OC(COP(=O)(O[Si](C)(C)C)OP(=O)(O[Si](C)(C)C)N([Si](C)(C)C)P(=O)(O)O[Si](C)(C)C)C(O)C1O	5713.0	Standard polar	33892256
Phosphoaminophosphonic acid-adenylate ester,5TMS,isomer #59	C[Si](C)(C)OP(=O)(OCC1OC(N2C=NC3=C(N([Si](C)(C)C)[Si](C)(C)C)N=CN=C32)C(O)C1O)OP(=O)(O[Si](C)(C)C)N([Si](C)(C)C)P(=O)(O)O	4149.7	Semi standard non polar	33892256
Phosphoaminophosphonic acid-adenylate ester,5TMS,isomer #59	C[Si](C)(C)OP(=O)(OCC1OC(N2C=NC3=C(N([Si](C)(C)C)[Si](C)(C)C)N=CN=C32)C(O)C1O)OP(=O)(O[Si](C)(C)C)N([Si](C)(C)C)P(=O)(O)O	4284.6	Standard non polar	33892256
Phosphoaminophosphonic acid-adenylate ester,5TMS,isomer #59	C[Si](C)(C)OP(=O)(OCC1OC(N2C=NC3=C(N([Si](C)(C)C)[Si](C)(C)C)N=CN=C32)C(O)C1O)OP(=O)(O[Si](C)(C)C)N([Si](C)(C)C)P(=O)(O)O	5680.4	Standard polar	33892256
Phosphoaminophosphonic acid-adenylate ester,5TMS,isomer #6	C[Si](C)(C)OC1C(COP(=O)(O[Si](C)(C)C)OP(=O)(O)N([Si](C)(C)C)P(=O)(O)O[Si](C)(C)C)OC(N2C=NC3=C(N)N=CN=C32)C1O[Si](C)(C)C	3997.6	Semi standard non polar	33892256
Phosphoaminophosphonic acid-adenylate ester,5TMS,isomer #6	C[Si](C)(C)OC1C(COP(=O)(O[Si](C)(C)C)OP(=O)(O)N([Si](C)(C)C)P(=O)(O)O[Si](C)(C)C)OC(N2C=NC3=C(N)N=CN=C32)C1O[Si](C)(C)C	3956.3	Standard non polar	33892256
Phosphoaminophosphonic acid-adenylate ester,5TMS,isomer #6	C[Si](C)(C)OC1C(COP(=O)(O[Si](C)(C)C)OP(=O)(O)N([Si](C)(C)C)P(=O)(O)O[Si](C)(C)C)OC(N2C=NC3=C(N)N=CN=C32)C1O[Si](C)(C)C	6119.4	Standard polar	33892256
Phosphoaminophosphonic acid-adenylate ester,5TMS,isomer #60	C[Si](C)(C)OP(=O)(NP(=O)(O)OP(=O)(OCC1OC(N2C=NC3=C(N([Si](C)(C)C)[Si](C)(C)C)N=CN=C32)C(O)C1O)O[Si](C)(C)C)O[Si](C)(C)C	4107.5	Semi standard non polar	33892256
Phosphoaminophosphonic acid-adenylate ester,5TMS,isomer #60	C[Si](C)(C)OP(=O)(NP(=O)(O)OP(=O)(OCC1OC(N2C=NC3=C(N([Si](C)(C)C)[Si](C)(C)C)N=CN=C32)C(O)C1O)O[Si](C)(C)C)O[Si](C)(C)C	4052.4	Standard non polar	33892256
Phosphoaminophosphonic acid-adenylate ester,5TMS,isomer #60	C[Si](C)(C)OP(=O)(NP(=O)(O)OP(=O)(OCC1OC(N2C=NC3=C(N([Si](C)(C)C)[Si](C)(C)C)N=CN=C32)C(O)C1O)O[Si](C)(C)C)O[Si](C)(C)C	5701.6	Standard polar	33892256
Phosphoaminophosphonic acid-adenylate ester,5TMS,isomer #61	C[Si](C)(C)NC1=NC=NC2=C1N=CN2C1OC(COP(=O)(O[Si](C)(C)C)OP(=O)(O)N([Si](C)(C)C)P(=O)(O[Si](C)(C)C)O[Si](C)(C)C)C(O)C1O	4122.1	Semi standard non polar	33892256
Phosphoaminophosphonic acid-adenylate ester,5TMS,isomer #61	C[Si](C)(C)NC1=NC=NC2=C1N=CN2C1OC(COP(=O)(O[Si](C)(C)C)OP(=O)(O)N([Si](C)(C)C)P(=O)(O[Si](C)(C)C)O[Si](C)(C)C)C(O)C1O	4187.3	Standard non polar	33892256
Phosphoaminophosphonic acid-adenylate ester,5TMS,isomer #61	C[Si](C)(C)NC1=NC=NC2=C1N=CN2C1OC(COP(=O)(O[Si](C)(C)C)OP(=O)(O)N([Si](C)(C)C)P(=O)(O[Si](C)(C)C)O[Si](C)(C)C)C(O)C1O	5763.9	Standard polar	33892256
Phosphoaminophosphonic acid-adenylate ester,5TMS,isomer #62	C[Si](C)(C)OP(=O)(OCC1OC(N2C=NC3=C(N([Si](C)(C)C)[Si](C)(C)C)N=CN=C32)C(O)C1O)OP(=O)(O)N([Si](C)(C)C)P(=O)(O)O[Si](C)(C)C	4120.6	Semi standard non polar	33892256
Phosphoaminophosphonic acid-adenylate ester,5TMS,isomer #62	C[Si](C)(C)OP(=O)(OCC1OC(N2C=NC3=C(N([Si](C)(C)C)[Si](C)(C)C)N=CN=C32)C(O)C1O)OP(=O)(O)N([Si](C)(C)C)P(=O)(O)O[Si](C)(C)C	4251.7	Standard non polar	33892256
Phosphoaminophosphonic acid-adenylate ester,5TMS,isomer #62	C[Si](C)(C)OP(=O)(OCC1OC(N2C=NC3=C(N([Si](C)(C)C)[Si](C)(C)C)N=CN=C32)C(O)C1O)OP(=O)(O)N([Si](C)(C)C)P(=O)(O)O[Si](C)(C)C	5777.0	Standard polar	33892256
Phosphoaminophosphonic acid-adenylate ester,5TMS,isomer #63	C[Si](C)(C)OP(=O)(NP(=O)(O[Si](C)(C)C)OP(=O)(O)OCC1OC(N2C=NC3=C(N([Si](C)(C)C)[Si](C)(C)C)N=CN=C32)C(O)C1O)O[Si](C)(C)C	4087.6	Semi standard non polar	33892256
Phosphoaminophosphonic acid-adenylate ester,5TMS,isomer #63	C[Si](C)(C)OP(=O)(NP(=O)(O[Si](C)(C)C)OP(=O)(O)OCC1OC(N2C=NC3=C(N([Si](C)(C)C)[Si](C)(C)C)N=CN=C32)C(O)C1O)O[Si](C)(C)C	4037.6	Standard non polar	33892256
Phosphoaminophosphonic acid-adenylate ester,5TMS,isomer #63	C[Si](C)(C)OP(=O)(NP(=O)(O[Si](C)(C)C)OP(=O)(O)OCC1OC(N2C=NC3=C(N([Si](C)(C)C)[Si](C)(C)C)N=CN=C32)C(O)C1O)O[Si](C)(C)C	5687.2	Standard polar	33892256
Phosphoaminophosphonic acid-adenylate ester,5TMS,isomer #64	C[Si](C)(C)NC1=NC=NC2=C1N=CN2C1OC(COP(=O)(O)OP(=O)(O[Si](C)(C)C)N([Si](C)(C)C)P(=O)(O[Si](C)(C)C)O[Si](C)(C)C)C(O)C1O	4119.8	Semi standard non polar	33892256
Phosphoaminophosphonic acid-adenylate ester,5TMS,isomer #64	C[Si](C)(C)NC1=NC=NC2=C1N=CN2C1OC(COP(=O)(O)OP(=O)(O[Si](C)(C)C)N([Si](C)(C)C)P(=O)(O[Si](C)(C)C)O[Si](C)(C)C)C(O)C1O	4170.1	Standard non polar	33892256
Phosphoaminophosphonic acid-adenylate ester,5TMS,isomer #64	C[Si](C)(C)NC1=NC=NC2=C1N=CN2C1OC(COP(=O)(O)OP(=O)(O[Si](C)(C)C)N([Si](C)(C)C)P(=O)(O[Si](C)(C)C)O[Si](C)(C)C)C(O)C1O	5728.3	Standard polar	33892256
Phosphoaminophosphonic acid-adenylate ester,5TMS,isomer #65	C[Si](C)(C)OP(=O)(O)N([Si](C)(C)C)P(=O)(O[Si](C)(C)C)OP(=O)(O)OCC1OC(N2C=NC3=C(N([Si](C)(C)C)[Si](C)(C)C)N=CN=C32)C(O)C1O	4121.7	Semi standard non polar	33892256
Phosphoaminophosphonic acid-adenylate ester,5TMS,isomer #65	C[Si](C)(C)OP(=O)(O)N([Si](C)(C)C)P(=O)(O[Si](C)(C)C)OP(=O)(O)OCC1OC(N2C=NC3=C(N([Si](C)(C)C)[Si](C)(C)C)N=CN=C32)C(O)C1O	4246.3	Standard non polar	33892256
Phosphoaminophosphonic acid-adenylate ester,5TMS,isomer #65	C[Si](C)(C)OP(=O)(O)N([Si](C)(C)C)P(=O)(O[Si](C)(C)C)OP(=O)(O)OCC1OC(N2C=NC3=C(N([Si](C)(C)C)[Si](C)(C)C)N=CN=C32)C(O)C1O	5711.5	Standard polar	33892256
Phosphoaminophosphonic acid-adenylate ester,5TMS,isomer #66	C[Si](C)(C)OP(=O)(O[Si](C)(C)C)N([Si](C)(C)C)P(=O)(O)OP(=O)(O)OCC1OC(N2C=NC3=C(N([Si](C)(C)C)[Si](C)(C)C)N=CN=C32)C(O)C1O	4126.8	Semi standard non polar	33892256
Phosphoaminophosphonic acid-adenylate ester,5TMS,isomer #66	C[Si](C)(C)OP(=O)(O[Si](C)(C)C)N([Si](C)(C)C)P(=O)(O)OP(=O)(O)OCC1OC(N2C=NC3=C(N([Si](C)(C)C)[Si](C)(C)C)N=CN=C32)C(O)C1O	4239.4	Standard non polar	33892256
Phosphoaminophosphonic acid-adenylate ester,5TMS,isomer #66	C[Si](C)(C)OP(=O)(O[Si](C)(C)C)N([Si](C)(C)C)P(=O)(O)OP(=O)(O)OCC1OC(N2C=NC3=C(N([Si](C)(C)C)[Si](C)(C)C)N=CN=C32)C(O)C1O	5775.3	Standard polar	33892256
Phosphoaminophosphonic acid-adenylate ester,5TMS,isomer #7	C[Si](C)(C)OC1C(COP(=O)(O[Si](C)(C)C)OP(=O)(O)NP(=O)(O)O)OC(N2C=NC3=C(N([Si](C)(C)C)[Si](C)(C)C)N=CN=C32)C1O[Si](C)(C)C	4064.6	Semi standard non polar	33892256
Phosphoaminophosphonic acid-adenylate ester,5TMS,isomer #7	C[Si](C)(C)OC1C(COP(=O)(O[Si](C)(C)C)OP(=O)(O)NP(=O)(O)O)OC(N2C=NC3=C(N([Si](C)(C)C)[Si](C)(C)C)N=CN=C32)C1O[Si](C)(C)C	3880.2	Standard non polar	33892256
Phosphoaminophosphonic acid-adenylate ester,5TMS,isomer #7	C[Si](C)(C)OC1C(COP(=O)(O[Si](C)(C)C)OP(=O)(O)NP(=O)(O)O)OC(N2C=NC3=C(N([Si](C)(C)C)[Si](C)(C)C)N=CN=C32)C1O[Si](C)(C)C	5925.0	Standard polar	33892256
Phosphoaminophosphonic acid-adenylate ester,5TMS,isomer #8	C[Si](C)(C)NC1=NC=NC2=C1N=CN2C1OC(COP(=O)(O[Si](C)(C)C)OP(=O)(O)N([Si](C)(C)C)P(=O)(O)O)C(O[Si](C)(C)C)C1O[Si](C)(C)C	4086.1	Semi standard non polar	33892256
Phosphoaminophosphonic acid-adenylate ester,5TMS,isomer #8	C[Si](C)(C)NC1=NC=NC2=C1N=CN2C1OC(COP(=O)(O[Si](C)(C)C)OP(=O)(O)N([Si](C)(C)C)P(=O)(O)O)C(O[Si](C)(C)C)C1O[Si](C)(C)C	4038.5	Standard non polar	33892256
Phosphoaminophosphonic acid-adenylate ester,5TMS,isomer #8	C[Si](C)(C)NC1=NC=NC2=C1N=CN2C1OC(COP(=O)(O[Si](C)(C)C)OP(=O)(O)N([Si](C)(C)C)P(=O)(O)O)C(O[Si](C)(C)C)C1O[Si](C)(C)C	5967.0	Standard polar	33892256
Phosphoaminophosphonic acid-adenylate ester,5TMS,isomer #9	C[Si](C)(C)OC1C(COP(=O)(O)OP(=O)(NP(=O)(O[Si](C)(C)C)O[Si](C)(C)C)O[Si](C)(C)C)OC(N2C=NC3=C(N)N=CN=C32)C1O[Si](C)(C)C	3959.1	Semi standard non polar	33892256
Phosphoaminophosphonic acid-adenylate ester,5TMS,isomer #9	C[Si](C)(C)OC1C(COP(=O)(O)OP(=O)(NP(=O)(O[Si](C)(C)C)O[Si](C)(C)C)O[Si](C)(C)C)OC(N2C=NC3=C(N)N=CN=C32)C1O[Si](C)(C)C	3753.6	Standard non polar	33892256
Phosphoaminophosphonic acid-adenylate ester,5TMS,isomer #9	C[Si](C)(C)OC1C(COP(=O)(O)OP(=O)(NP(=O)(O[Si](C)(C)C)O[Si](C)(C)C)O[Si](C)(C)C)OC(N2C=NC3=C(N)N=CN=C32)C1O[Si](C)(C)C	6131.8	Standard polar	33892256
Phosphoaminophosphonic acid-adenylate ester,3TBDMS,isomer #1	CC(C)(C)[Si](C)(C)OC1C(COP(=O)(O[Si](C)(C)C(C)(C)C)OP(=O)(O)NP(=O)(O)O)OC(N2C=NC3=C(N)N=CN=C32)C1O[Si](C)(C)C(C)(C)C	4743.6	Semi standard non polar	33892256
Phosphoaminophosphonic acid-adenylate ester,3TBDMS,isomer #1	CC(C)(C)[Si](C)(C)OC1C(COP(=O)(O[Si](C)(C)C(C)(C)C)OP(=O)(O)NP(=O)(O)O)OC(N2C=NC3=C(N)N=CN=C32)C1O[Si](C)(C)C(C)(C)C	4254.4	Standard non polar	33892256
Phosphoaminophosphonic acid-adenylate ester,3TBDMS,isomer #1	CC(C)(C)[Si](C)(C)OC1C(COP(=O)(O[Si](C)(C)C(C)(C)C)OP(=O)(O)NP(=O)(O)O)OC(N2C=NC3=C(N)N=CN=C32)C1O[Si](C)(C)C(C)(C)C	6840.0	Standard polar	33892256
Phosphoaminophosphonic acid-adenylate ester,3TBDMS,isomer #10	CC(C)(C)[Si](C)(C)OC1C(COP(=O)(O)OP(=O)(NP(=O)(O)O[Si](C)(C)C(C)(C)C)O[Si](C)(C)C(C)(C)C)OC(N2C=NC3=C(N)N=CN=C32)C1O	4677.5	Semi standard non polar	33892256
Phosphoaminophosphonic acid-adenylate ester,3TBDMS,isomer #10	CC(C)(C)[Si](C)(C)OC1C(COP(=O)(O)OP(=O)(NP(=O)(O)O[Si](C)(C)C(C)(C)C)O[Si](C)(C)C(C)(C)C)OC(N2C=NC3=C(N)N=CN=C32)C1O	4341.3	Standard non polar	33892256
Phosphoaminophosphonic acid-adenylate ester,3TBDMS,isomer #10	CC(C)(C)[Si](C)(C)OC1C(COP(=O)(O)OP(=O)(NP(=O)(O)O[Si](C)(C)C(C)(C)C)O[Si](C)(C)C(C)(C)C)OC(N2C=NC3=C(N)N=CN=C32)C1O	6753.6	Standard polar	33892256
Phosphoaminophosphonic acid-adenylate ester,3TBDMS,isomer #11	CC(C)(C)[Si](C)(C)NC1=NC=NC2=C1N=CN2C1OC(COP(=O)(O)OP(=O)(NP(=O)(O)O)O[Si](C)(C)C(C)(C)C)C(O[Si](C)(C)C(C)(C)C)C1O	4723.9	Semi standard non polar	33892256
Phosphoaminophosphonic acid-adenylate ester,3TBDMS,isomer #11	CC(C)(C)[Si](C)(C)NC1=NC=NC2=C1N=CN2C1OC(COP(=O)(O)OP(=O)(NP(=O)(O)O)O[Si](C)(C)C(C)(C)C)C(O[Si](C)(C)C(C)(C)C)C1O	4397.6	Standard non polar	33892256
Phosphoaminophosphonic acid-adenylate ester,3TBDMS,isomer #11	CC(C)(C)[Si](C)(C)NC1=NC=NC2=C1N=CN2C1OC(COP(=O)(O)OP(=O)(NP(=O)(O)O)O[Si](C)(C)C(C)(C)C)C(O[Si](C)(C)C(C)(C)C)C1O	6700.0	Standard polar	33892256
Phosphoaminophosphonic acid-adenylate ester,3TBDMS,isomer #12	CC(C)(C)[Si](C)(C)OC1C(COP(=O)(O)OP(=O)(O[Si](C)(C)C(C)(C)C)N([Si](C)(C)C(C)(C)C)P(=O)(O)O)OC(N2C=NC3=C(N)N=CN=C32)C1O	4765.0	Semi standard non polar	33892256
Phosphoaminophosphonic acid-adenylate ester,3TBDMS,isomer #12	CC(C)(C)[Si](C)(C)OC1C(COP(=O)(O)OP(=O)(O[Si](C)(C)C(C)(C)C)N([Si](C)(C)C(C)(C)C)P(=O)(O)O)OC(N2C=NC3=C(N)N=CN=C32)C1O	4485.0	Standard non polar	33892256
Phosphoaminophosphonic acid-adenylate ester,3TBDMS,isomer #12	CC(C)(C)[Si](C)(C)OC1C(COP(=O)(O)OP(=O)(O[Si](C)(C)C(C)(C)C)N([Si](C)(C)C(C)(C)C)P(=O)(O)O)OC(N2C=NC3=C(N)N=CN=C32)C1O	6724.1	Standard polar	33892256
Phosphoaminophosphonic acid-adenylate ester,3TBDMS,isomer #13	CC(C)(C)[Si](C)(C)OC1C(COP(=O)(O)OP(=O)(O)NP(=O)(O[Si](C)(C)C(C)(C)C)O[Si](C)(C)C(C)(C)C)OC(N2C=NC3=C(N)N=CN=C32)C1O	4683.7	Semi standard non polar	33892256
Phosphoaminophosphonic acid-adenylate ester,3TBDMS,isomer #13	CC(C)(C)[Si](C)(C)OC1C(COP(=O)(O)OP(=O)(O)NP(=O)(O[Si](C)(C)C(C)(C)C)O[Si](C)(C)C(C)(C)C)OC(N2C=NC3=C(N)N=CN=C32)C1O	4308.3	Standard non polar	33892256
Phosphoaminophosphonic acid-adenylate ester,3TBDMS,isomer #13	CC(C)(C)[Si](C)(C)OC1C(COP(=O)(O)OP(=O)(O)NP(=O)(O[Si](C)(C)C(C)(C)C)O[Si](C)(C)C(C)(C)C)OC(N2C=NC3=C(N)N=CN=C32)C1O	6775.5	Standard polar	33892256
Phosphoaminophosphonic acid-adenylate ester,3TBDMS,isomer #14	CC(C)(C)[Si](C)(C)NC1=NC=NC2=C1N=CN2C1OC(COP(=O)(O)OP(=O)(O)NP(=O)(O)O[Si](C)(C)C(C)(C)C)C(O[Si](C)(C)C(C)(C)C)C1O	4723.4	Semi standard non polar	33892256
Phosphoaminophosphonic acid-adenylate ester,3TBDMS,isomer #14	CC(C)(C)[Si](C)(C)NC1=NC=NC2=C1N=CN2C1OC(COP(=O)(O)OP(=O)(O)NP(=O)(O)O[Si](C)(C)C(C)(C)C)C(O[Si](C)(C)C(C)(C)C)C1O	4400.5	Standard non polar	33892256
Phosphoaminophosphonic acid-adenylate ester,3TBDMS,isomer #14	CC(C)(C)[Si](C)(C)NC1=NC=NC2=C1N=CN2C1OC(COP(=O)(O)OP(=O)(O)NP(=O)(O)O[Si](C)(C)C(C)(C)C)C(O[Si](C)(C)C(C)(C)C)C1O	6728.7	Standard polar	33892256
Phosphoaminophosphonic acid-adenylate ester,3TBDMS,isomer #15	CC(C)(C)[Si](C)(C)OC1C(COP(=O)(O)OP(=O)(O)N([Si](C)(C)C(C)(C)C)P(=O)(O)O[Si](C)(C)C(C)(C)C)OC(N2C=NC3=C(N)N=CN=C32)C1O	4735.0	Semi standard non polar	33892256
Phosphoaminophosphonic acid-adenylate ester,3TBDMS,isomer #15	CC(C)(C)[Si](C)(C)OC1C(COP(=O)(O)OP(=O)(O)N([Si](C)(C)C(C)(C)C)P(=O)(O)O[Si](C)(C)C(C)(C)C)OC(N2C=NC3=C(N)N=CN=C32)C1O	4450.5	Standard non polar	33892256
Phosphoaminophosphonic acid-adenylate ester,3TBDMS,isomer #15	CC(C)(C)[Si](C)(C)OC1C(COP(=O)(O)OP(=O)(O)N([Si](C)(C)C(C)(C)C)P(=O)(O)O[Si](C)(C)C(C)(C)C)OC(N2C=NC3=C(N)N=CN=C32)C1O	6733.5	Standard polar	33892256
Phosphoaminophosphonic acid-adenylate ester,3TBDMS,isomer #16	CC(C)(C)[Si](C)(C)OC1C(COP(=O)(O)OP(=O)(O)NP(=O)(O)O)OC(N2C=NC3=C(N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)N=CN=C32)C1O	4738.8	Semi standard non polar	33892256
Phosphoaminophosphonic acid-adenylate ester,3TBDMS,isomer #16	CC(C)(C)[Si](C)(C)OC1C(COP(=O)(O)OP(=O)(O)NP(=O)(O)O)OC(N2C=NC3=C(N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)N=CN=C32)C1O	4440.4	Standard non polar	33892256
Phosphoaminophosphonic acid-adenylate ester,3TBDMS,isomer #16	CC(C)(C)[Si](C)(C)OC1C(COP(=O)(O)OP(=O)(O)NP(=O)(O)O)OC(N2C=NC3=C(N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)N=CN=C32)C1O	6714.0	Standard polar	33892256
Phosphoaminophosphonic acid-adenylate ester,3TBDMS,isomer #17	CC(C)(C)[Si](C)(C)NC1=NC=NC2=C1N=CN2C1OC(COP(=O)(O)OP(=O)(O)N([Si](C)(C)C(C)(C)C)P(=O)(O)O)C(O[Si](C)(C)C(C)(C)C)C1O	4762.9	Semi standard non polar	33892256
Phosphoaminophosphonic acid-adenylate ester,3TBDMS,isomer #17	CC(C)(C)[Si](C)(C)NC1=NC=NC2=C1N=CN2C1OC(COP(=O)(O)OP(=O)(O)N([Si](C)(C)C(C)(C)C)P(=O)(O)O)C(O[Si](C)(C)C(C)(C)C)C1O	4562.7	Standard non polar	33892256
Phosphoaminophosphonic acid-adenylate ester,3TBDMS,isomer #17	CC(C)(C)[Si](C)(C)NC1=NC=NC2=C1N=CN2C1OC(COP(=O)(O)OP(=O)(O)N([Si](C)(C)C(C)(C)C)P(=O)(O)O)C(O[Si](C)(C)C(C)(C)C)C1O	6691.1	Standard polar	33892256
Phosphoaminophosphonic acid-adenylate ester,3TBDMS,isomer #18	CC(C)(C)[Si](C)(C)OC1C(O)C(COP(=O)(O[Si](C)(C)C(C)(C)C)OP(=O)(NP(=O)(O)O)O[Si](C)(C)C(C)(C)C)OC1N1C=NC2=C(N)N=CN=C21	4723.4	Semi standard non polar	33892256
Phosphoaminophosphonic acid-adenylate ester,3TBDMS,isomer #18	CC(C)(C)[Si](C)(C)OC1C(O)C(COP(=O)(O[Si](C)(C)C(C)(C)C)OP(=O)(NP(=O)(O)O)O[Si](C)(C)C(C)(C)C)OC1N1C=NC2=C(N)N=CN=C21	4348.1	Standard non polar	33892256
Phosphoaminophosphonic acid-adenylate ester,3TBDMS,isomer #18	CC(C)(C)[Si](C)(C)OC1C(O)C(COP(=O)(O[Si](C)(C)C(C)(C)C)OP(=O)(NP(=O)(O)O)O[Si](C)(C)C(C)(C)C)OC1N1C=NC2=C(N)N=CN=C21	6737.9	Standard polar	33892256
Phosphoaminophosphonic acid-adenylate ester,3TBDMS,isomer #19	CC(C)(C)[Si](C)(C)OC1C(O)C(COP(=O)(O[Si](C)(C)C(C)(C)C)OP(=O)(O)NP(=O)(O)O[Si](C)(C)C(C)(C)C)OC1N1C=NC2=C(N)N=CN=C21	4718.6	Semi standard non polar	33892256
Phosphoaminophosphonic acid-adenylate ester,3TBDMS,isomer #19	CC(C)(C)[Si](C)(C)OC1C(O)C(COP(=O)(O[Si](C)(C)C(C)(C)C)OP(=O)(O)NP(=O)(O)O[Si](C)(C)C(C)(C)C)OC1N1C=NC2=C(N)N=CN=C21	4348.6	Standard non polar	33892256
Phosphoaminophosphonic acid-adenylate ester,3TBDMS,isomer #19	CC(C)(C)[Si](C)(C)OC1C(O)C(COP(=O)(O[Si](C)(C)C(C)(C)C)OP(=O)(O)NP(=O)(O)O[Si](C)(C)C(C)(C)C)OC1N1C=NC2=C(N)N=CN=C21	6738.6	Standard polar	33892256
Phosphoaminophosphonic acid-adenylate ester,3TBDMS,isomer #2	CC(C)(C)[Si](C)(C)OC1C(COP(=O)(O)OP(=O)(NP(=O)(O)O)O[Si](C)(C)C(C)(C)C)OC(N2C=NC3=C(N)N=CN=C32)C1O[Si](C)(C)C(C)(C)C	4693.5	Semi standard non polar	33892256
Phosphoaminophosphonic acid-adenylate ester,3TBDMS,isomer #2	CC(C)(C)[Si](C)(C)OC1C(COP(=O)(O)OP(=O)(NP(=O)(O)O)O[Si](C)(C)C(C)(C)C)OC(N2C=NC3=C(N)N=CN=C32)C1O[Si](C)(C)C(C)(C)C	4253.5	Standard non polar	33892256
Phosphoaminophosphonic acid-adenylate ester,3TBDMS,isomer #2	CC(C)(C)[Si](C)(C)OC1C(COP(=O)(O)OP(=O)(NP(=O)(O)O)O[Si](C)(C)C(C)(C)C)OC(N2C=NC3=C(N)N=CN=C32)C1O[Si](C)(C)C(C)(C)C	6884.4	Standard polar	33892256
Phosphoaminophosphonic acid-adenylate ester,3TBDMS,isomer #20	CC(C)(C)[Si](C)(C)NC1=NC=NC2=C1N=CN2C1OC(COP(=O)(O[Si](C)(C)C(C)(C)C)OP(=O)(O)NP(=O)(O)O)C(O)C1O[Si](C)(C)C(C)(C)C	4777.4	Semi standard non polar	33892256
Phosphoaminophosphonic acid-adenylate ester,3TBDMS,isomer #20	CC(C)(C)[Si](C)(C)NC1=NC=NC2=C1N=CN2C1OC(COP(=O)(O[Si](C)(C)C(C)(C)C)OP(=O)(O)NP(=O)(O)O)C(O)C1O[Si](C)(C)C(C)(C)C	4402.9	Standard non polar	33892256
Phosphoaminophosphonic acid-adenylate ester,3TBDMS,isomer #20	CC(C)(C)[Si](C)(C)NC1=NC=NC2=C1N=CN2C1OC(COP(=O)(O[Si](C)(C)C(C)(C)C)OP(=O)(O)NP(=O)(O)O)C(O)C1O[Si](C)(C)C(C)(C)C	6704.5	Standard polar	33892256
Phosphoaminophosphonic acid-adenylate ester,3TBDMS,isomer #21	CC(C)(C)[Si](C)(C)OC1C(O)C(COP(=O)(O[Si](C)(C)C(C)(C)C)OP(=O)(O)N([Si](C)(C)C(C)(C)C)P(=O)(O)O)OC1N1C=NC2=C(N)N=CN=C21	4760.8	Semi standard non polar	33892256
Phosphoaminophosphonic acid-adenylate ester,3TBDMS,isomer #21	CC(C)(C)[Si](C)(C)OC1C(O)C(COP(=O)(O[Si](C)(C)C(C)(C)C)OP(=O)(O)N([Si](C)(C)C(C)(C)C)P(=O)(O)O)OC1N1C=NC2=C(N)N=CN=C21	4503.9	Standard non polar	33892256
Phosphoaminophosphonic acid-adenylate ester,3TBDMS,isomer #21	CC(C)(C)[Si](C)(C)OC1C(O)C(COP(=O)(O[Si](C)(C)C(C)(C)C)OP(=O)(O)N([Si](C)(C)C(C)(C)C)P(=O)(O)O)OC1N1C=NC2=C(N)N=CN=C21	6718.7	Standard polar	33892256
Phosphoaminophosphonic acid-adenylate ester,3TBDMS,isomer #22	CC(C)(C)[Si](C)(C)OC1C(O)C(COP(=O)(O)OP(=O)(NP(=O)(O)O[Si](C)(C)C(C)(C)C)O[Si](C)(C)C(C)(C)C)OC1N1C=NC2=C(N)N=CN=C21	4673.2	Semi standard non polar	33892256
Phosphoaminophosphonic acid-adenylate ester,3TBDMS,isomer #22	CC(C)(C)[Si](C)(C)OC1C(O)C(COP(=O)(O)OP(=O)(NP(=O)(O)O[Si](C)(C)C(C)(C)C)O[Si](C)(C)C(C)(C)C)OC1N1C=NC2=C(N)N=CN=C21	4351.5	Standard non polar	33892256
Phosphoaminophosphonic acid-adenylate ester,3TBDMS,isomer #22	CC(C)(C)[Si](C)(C)OC1C(O)C(COP(=O)(O)OP(=O)(NP(=O)(O)O[Si](C)(C)C(C)(C)C)O[Si](C)(C)C(C)(C)C)OC1N1C=NC2=C(N)N=CN=C21	6763.0	Standard polar	33892256
Phosphoaminophosphonic acid-adenylate ester,3TBDMS,isomer #23	CC(C)(C)[Si](C)(C)NC1=NC=NC2=C1N=CN2C1OC(COP(=O)(O)OP(=O)(NP(=O)(O)O)O[Si](C)(C)C(C)(C)C)C(O)C1O[Si](C)(C)C(C)(C)C	4721.5	Semi standard non polar	33892256
Phosphoaminophosphonic acid-adenylate ester,3TBDMS,isomer #23	CC(C)(C)[Si](C)(C)NC1=NC=NC2=C1N=CN2C1OC(COP(=O)(O)OP(=O)(NP(=O)(O)O)O[Si](C)(C)C(C)(C)C)C(O)C1O[Si](C)(C)C(C)(C)C	4404.3	Standard non polar	33892256
Phosphoaminophosphonic acid-adenylate ester,3TBDMS,isomer #23	CC(C)(C)[Si](C)(C)NC1=NC=NC2=C1N=CN2C1OC(COP(=O)(O)OP(=O)(NP(=O)(O)O)O[Si](C)(C)C(C)(C)C)C(O)C1O[Si](C)(C)C(C)(C)C	6711.0	Standard polar	33892256
Phosphoaminophosphonic acid-adenylate ester,3TBDMS,isomer #24	CC(C)(C)[Si](C)(C)OC1C(O)C(COP(=O)(O)OP(=O)(O[Si](C)(C)C(C)(C)C)N([Si](C)(C)C(C)(C)C)P(=O)(O)O)OC1N1C=NC2=C(N)N=CN=C21	4758.7	Semi standard non polar	33892256
Phosphoaminophosphonic acid-adenylate ester,3TBDMS,isomer #24	CC(C)(C)[Si](C)(C)OC1C(O)C(COP(=O)(O)OP(=O)(O[Si](C)(C)C(C)(C)C)N([Si](C)(C)C(C)(C)C)P(=O)(O)O)OC1N1C=NC2=C(N)N=CN=C21	4487.5	Standard non polar	33892256
Phosphoaminophosphonic acid-adenylate ester,3TBDMS,isomer #24	CC(C)(C)[Si](C)(C)OC1C(O)C(COP(=O)(O)OP(=O)(O[Si](C)(C)C(C)(C)C)N([Si](C)(C)C(C)(C)C)P(=O)(O)O)OC1N1C=NC2=C(N)N=CN=C21	6733.3	Standard polar	33892256
Phosphoaminophosphonic acid-adenylate ester,3TBDMS,isomer #25	CC(C)(C)[Si](C)(C)OC1C(O)C(COP(=O)(O)OP(=O)(O)NP(=O)(O[Si](C)(C)C(C)(C)C)O[Si](C)(C)C(C)(C)C)OC1N1C=NC2=C(N)N=CN=C21	4678.5	Semi standard non polar	33892256
Phosphoaminophosphonic acid-adenylate ester,3TBDMS,isomer #25	CC(C)(C)[Si](C)(C)OC1C(O)C(COP(=O)(O)OP(=O)(O)NP(=O)(O[Si](C)(C)C(C)(C)C)O[Si](C)(C)C(C)(C)C)OC1N1C=NC2=C(N)N=CN=C21	4319.0	Standard non polar	33892256
Phosphoaminophosphonic acid-adenylate ester,3TBDMS,isomer #25	CC(C)(C)[Si](C)(C)OC1C(O)C(COP(=O)(O)OP(=O)(O)NP(=O)(O[Si](C)(C)C(C)(C)C)O[Si](C)(C)C(C)(C)C)OC1N1C=NC2=C(N)N=CN=C21	6785.1	Standard polar	33892256
Phosphoaminophosphonic acid-adenylate ester,3TBDMS,isomer #26	CC(C)(C)[Si](C)(C)NC1=NC=NC2=C1N=CN2C1OC(COP(=O)(O)OP(=O)(O)NP(=O)(O)O[Si](C)(C)C(C)(C)C)C(O)C1O[Si](C)(C)C(C)(C)C	4723.3	Semi standard non polar	33892256
Phosphoaminophosphonic acid-adenylate ester,3TBDMS,isomer #26	CC(C)(C)[Si](C)(C)NC1=NC=NC2=C1N=CN2C1OC(COP(=O)(O)OP(=O)(O)NP(=O)(O)O[Si](C)(C)C(C)(C)C)C(O)C1O[Si](C)(C)C(C)(C)C	4408.4	Standard non polar	33892256
Phosphoaminophosphonic acid-adenylate ester,3TBDMS,isomer #26	CC(C)(C)[Si](C)(C)NC1=NC=NC2=C1N=CN2C1OC(COP(=O)(O)OP(=O)(O)NP(=O)(O)O[Si](C)(C)C(C)(C)C)C(O)C1O[Si](C)(C)C(C)(C)C	6739.7	Standard polar	33892256
Phosphoaminophosphonic acid-adenylate ester,3TBDMS,isomer #27	CC(C)(C)[Si](C)(C)OC1C(O)C(COP(=O)(O)OP(=O)(O)N([Si](C)(C)C(C)(C)C)P(=O)(O)O[Si](C)(C)C(C)(C)C)OC1N1C=NC2=C(N)N=CN=C21	4729.4	Semi standard non polar	33892256
Phosphoaminophosphonic acid-adenylate ester,3TBDMS,isomer #27	CC(C)(C)[Si](C)(C)OC1C(O)C(COP(=O)(O)OP(=O)(O)N([Si](C)(C)C(C)(C)C)P(=O)(O)O[Si](C)(C)C(C)(C)C)OC1N1C=NC2=C(N)N=CN=C21	4456.3	Standard non polar	33892256
Phosphoaminophosphonic acid-adenylate ester,3TBDMS,isomer #27	CC(C)(C)[Si](C)(C)OC1C(O)C(COP(=O)(O)OP(=O)(O)N([Si](C)(C)C(C)(C)C)P(=O)(O)O[Si](C)(C)C(C)(C)C)OC1N1C=NC2=C(N)N=CN=C21	6743.1	Standard polar	33892256
Phosphoaminophosphonic acid-adenylate ester,3TBDMS,isomer #28	CC(C)(C)[Si](C)(C)OC1C(O)C(COP(=O)(O)OP(=O)(O)NP(=O)(O)O)OC1N1C=NC2=C(N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)N=CN=C21	4735.9	Semi standard non polar	33892256
Phosphoaminophosphonic acid-adenylate ester,3TBDMS,isomer #28	CC(C)(C)[Si](C)(C)OC1C(O)C(COP(=O)(O)OP(=O)(O)NP(=O)(O)O)OC1N1C=NC2=C(N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)N=CN=C21	4445.1	Standard non polar	33892256
Phosphoaminophosphonic acid-adenylate ester,3TBDMS,isomer #28	CC(C)(C)[Si](C)(C)OC1C(O)C(COP(=O)(O)OP(=O)(O)NP(=O)(O)O)OC1N1C=NC2=C(N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)N=CN=C21	6725.1	Standard polar	33892256
Phosphoaminophosphonic acid-adenylate ester,3TBDMS,isomer #29	CC(C)(C)[Si](C)(C)NC1=NC=NC2=C1N=CN2C1OC(COP(=O)(O)OP(=O)(O)N([Si](C)(C)C(C)(C)C)P(=O)(O)O)C(O)C1O[Si](C)(C)C(C)(C)C	4759.3	Semi standard non polar	33892256
Phosphoaminophosphonic acid-adenylate ester,3TBDMS,isomer #29	CC(C)(C)[Si](C)(C)NC1=NC=NC2=C1N=CN2C1OC(COP(=O)(O)OP(=O)(O)N([Si](C)(C)C(C)(C)C)P(=O)(O)O)C(O)C1O[Si](C)(C)C(C)(C)C	4564.9	Standard non polar	33892256
Phosphoaminophosphonic acid-adenylate ester,3TBDMS,isomer #29	CC(C)(C)[Si](C)(C)NC1=NC=NC2=C1N=CN2C1OC(COP(=O)(O)OP(=O)(O)N([Si](C)(C)C(C)(C)C)P(=O)(O)O)C(O)C1O[Si](C)(C)C(C)(C)C	6701.9	Standard polar	33892256
Phosphoaminophosphonic acid-adenylate ester,3TBDMS,isomer #3	CC(C)(C)[Si](C)(C)OC1C(COP(=O)(O)OP(=O)(O)NP(=O)(O)O[Si](C)(C)C(C)(C)C)OC(N2C=NC3=C(N)N=CN=C32)C1O[Si](C)(C)C(C)(C)C	4690.3	Semi standard non polar	33892256
Phosphoaminophosphonic acid-adenylate ester,3TBDMS,isomer #3	CC(C)(C)[Si](C)(C)OC1C(COP(=O)(O)OP(=O)(O)NP(=O)(O)O[Si](C)(C)C(C)(C)C)OC(N2C=NC3=C(N)N=CN=C32)C1O[Si](C)(C)C(C)(C)C	4259.6	Standard non polar	33892256
Phosphoaminophosphonic acid-adenylate ester,3TBDMS,isomer #3	CC(C)(C)[Si](C)(C)OC1C(COP(=O)(O)OP(=O)(O)NP(=O)(O)O[Si](C)(C)C(C)(C)C)OC(N2C=NC3=C(N)N=CN=C32)C1O[Si](C)(C)C(C)(C)C	6857.2	Standard polar	33892256
Phosphoaminophosphonic acid-adenylate ester,3TBDMS,isomer #30	CC(C)(C)[Si](C)(C)OP(=O)(O)NP(=O)(O[Si](C)(C)C(C)(C)C)OP(=O)(OCC1OC(N2C=NC3=C(N)N=CN=C32)C(O)C1O)O[Si](C)(C)C(C)(C)C	4703.7	Semi standard non polar	33892256
Phosphoaminophosphonic acid-adenylate ester,3TBDMS,isomer #30	CC(C)(C)[Si](C)(C)OP(=O)(O)NP(=O)(O[Si](C)(C)C(C)(C)C)OP(=O)(OCC1OC(N2C=NC3=C(N)N=CN=C32)C(O)C1O)O[Si](C)(C)C(C)(C)C	4426.4	Standard non polar	33892256
Phosphoaminophosphonic acid-adenylate ester,3TBDMS,isomer #30	CC(C)(C)[Si](C)(C)OP(=O)(O)NP(=O)(O[Si](C)(C)C(C)(C)C)OP(=O)(OCC1OC(N2C=NC3=C(N)N=CN=C32)C(O)C1O)O[Si](C)(C)C(C)(C)C	6609.8	Standard polar	33892256
Phosphoaminophosphonic acid-adenylate ester,3TBDMS,isomer #31	CC(C)(C)[Si](C)(C)NC1=NC=NC2=C1N=CN2C1OC(COP(=O)(O[Si](C)(C)C(C)(C)C)OP(=O)(NP(=O)(O)O)O[Si](C)(C)C(C)(C)C)C(O)C1O	4776.3	Semi standard non polar	33892256
Phosphoaminophosphonic acid-adenylate ester,3TBDMS,isomer #31	CC(C)(C)[Si](C)(C)NC1=NC=NC2=C1N=CN2C1OC(COP(=O)(O[Si](C)(C)C(C)(C)C)OP(=O)(NP(=O)(O)O)O[Si](C)(C)C(C)(C)C)C(O)C1O	4503.4	Standard non polar	33892256
Phosphoaminophosphonic acid-adenylate ester,3TBDMS,isomer #31	CC(C)(C)[Si](C)(C)NC1=NC=NC2=C1N=CN2C1OC(COP(=O)(O[Si](C)(C)C(C)(C)C)OP(=O)(NP(=O)(O)O)O[Si](C)(C)C(C)(C)C)C(O)C1O	6555.8	Standard polar	33892256
Phosphoaminophosphonic acid-adenylate ester,3TBDMS,isomer #32	CC(C)(C)[Si](C)(C)OP(=O)(OCC1OC(N2C=NC3=C(N)N=CN=C32)C(O)C1O)OP(=O)(O[Si](C)(C)C(C)(C)C)N([Si](C)(C)C(C)(C)C)P(=O)(O)O	4786.1	Semi standard non polar	33892256
Phosphoaminophosphonic acid-adenylate ester,3TBDMS,isomer #32	CC(C)(C)[Si](C)(C)OP(=O)(OCC1OC(N2C=NC3=C(N)N=CN=C32)C(O)C1O)OP(=O)(O[Si](C)(C)C(C)(C)C)N([Si](C)(C)C(C)(C)C)P(=O)(O)O	4576.3	Standard non polar	33892256
Phosphoaminophosphonic acid-adenylate ester,3TBDMS,isomer #32	CC(C)(C)[Si](C)(C)OP(=O)(OCC1OC(N2C=NC3=C(N)N=CN=C32)C(O)C1O)OP(=O)(O[Si](C)(C)C(C)(C)C)N([Si](C)(C)C(C)(C)C)P(=O)(O)O	6619.1	Standard polar	33892256
Phosphoaminophosphonic acid-adenylate ester,3TBDMS,isomer #33	CC(C)(C)[Si](C)(C)OP(=O)(NP(=O)(O)OP(=O)(OCC1OC(N2C=NC3=C(N)N=CN=C32)C(O)C1O)O[Si](C)(C)C(C)(C)C)O[Si](C)(C)C(C)(C)C	4719.8	Semi standard non polar	33892256
Phosphoaminophosphonic acid-adenylate ester,3TBDMS,isomer #33	CC(C)(C)[Si](C)(C)OP(=O)(NP(=O)(O)OP(=O)(OCC1OC(N2C=NC3=C(N)N=CN=C32)C(O)C1O)O[Si](C)(C)C(C)(C)C)O[Si](C)(C)C(C)(C)C	4392.5	Standard non polar	33892256
Phosphoaminophosphonic acid-adenylate ester,3TBDMS,isomer #33	CC(C)(C)[Si](C)(C)OP(=O)(NP(=O)(O)OP(=O)(OCC1OC(N2C=NC3=C(N)N=CN=C32)C(O)C1O)O[Si](C)(C)C(C)(C)C)O[Si](C)(C)C(C)(C)C	6663.0	Standard polar	33892256
Phosphoaminophosphonic acid-adenylate ester,3TBDMS,isomer #34	CC(C)(C)[Si](C)(C)NC1=NC=NC2=C1N=CN2C1OC(COP(=O)(O[Si](C)(C)C(C)(C)C)OP(=O)(O)NP(=O)(O)O[Si](C)(C)C(C)(C)C)C(O)C1O	4772.1	Semi standard non polar	33892256
Phosphoaminophosphonic acid-adenylate ester,3TBDMS,isomer #34	CC(C)(C)[Si](C)(C)NC1=NC=NC2=C1N=CN2C1OC(COP(=O)(O[Si](C)(C)C(C)(C)C)OP(=O)(O)NP(=O)(O)O[Si](C)(C)C(C)(C)C)C(O)C1O	4503.5	Standard non polar	33892256
Phosphoaminophosphonic acid-adenylate ester,3TBDMS,isomer #34	CC(C)(C)[Si](C)(C)NC1=NC=NC2=C1N=CN2C1OC(COP(=O)(O[Si](C)(C)C(C)(C)C)OP(=O)(O)NP(=O)(O)O[Si](C)(C)C(C)(C)C)C(O)C1O	6601.5	Standard polar	33892256
Phosphoaminophosphonic acid-adenylate ester,3TBDMS,isomer #35	CC(C)(C)[Si](C)(C)OP(=O)(OCC1OC(N2C=NC3=C(N)N=CN=C32)C(O)C1O)OP(=O)(O)N([Si](C)(C)C(C)(C)C)P(=O)(O)O[Si](C)(C)C(C)(C)C	4760.8	Semi standard non polar	33892256
Phosphoaminophosphonic acid-adenylate ester,3TBDMS,isomer #35	CC(C)(C)[Si](C)(C)OP(=O)(OCC1OC(N2C=NC3=C(N)N=CN=C32)C(O)C1O)OP(=O)(O)N([Si](C)(C)C(C)(C)C)P(=O)(O)O[Si](C)(C)C(C)(C)C	4548.4	Standard non polar	33892256
Phosphoaminophosphonic acid-adenylate ester,3TBDMS,isomer #35	CC(C)(C)[Si](C)(C)OP(=O)(OCC1OC(N2C=NC3=C(N)N=CN=C32)C(O)C1O)OP(=O)(O)N([Si](C)(C)C(C)(C)C)P(=O)(O)O[Si](C)(C)C(C)(C)C	6646.3	Standard polar	33892256
Phosphoaminophosphonic acid-adenylate ester,3TBDMS,isomer #36	CC(C)(C)[Si](C)(C)OP(=O)(OCC1OC(N2C=NC3=C(N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)N=CN=C32)C(O)C1O)OP(=O)(O)NP(=O)(O)O	4798.4	Semi standard non polar	33892256
Phosphoaminophosphonic acid-adenylate ester,3TBDMS,isomer #36	CC(C)(C)[Si](C)(C)OP(=O)(OCC1OC(N2C=NC3=C(N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)N=CN=C32)C(O)C1O)OP(=O)(O)NP(=O)(O)O	4553.2	Standard non polar	33892256
Phosphoaminophosphonic acid-adenylate ester,3TBDMS,isomer #36	CC(C)(C)[Si](C)(C)OP(=O)(OCC1OC(N2C=NC3=C(N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)N=CN=C32)C(O)C1O)OP(=O)(O)NP(=O)(O)O	6593.3	Standard polar	33892256
Phosphoaminophosphonic acid-adenylate ester,3TBDMS,isomer #37	CC(C)(C)[Si](C)(C)NC1=NC=NC2=C1N=CN2C1OC(COP(=O)(O[Si](C)(C)C(C)(C)C)OP(=O)(O)N([Si](C)(C)C(C)(C)C)P(=O)(O)O)C(O)C1O	4804.4	Semi standard non polar	33892256
Phosphoaminophosphonic acid-adenylate ester,3TBDMS,isomer #37	CC(C)(C)[Si](C)(C)NC1=NC=NC2=C1N=CN2C1OC(COP(=O)(O[Si](C)(C)C(C)(C)C)OP(=O)(O)N([Si](C)(C)C(C)(C)C)P(=O)(O)O)C(O)C1O	4671.6	Standard non polar	33892256
Phosphoaminophosphonic acid-adenylate ester,3TBDMS,isomer #37	CC(C)(C)[Si](C)(C)NC1=NC=NC2=C1N=CN2C1OC(COP(=O)(O[Si](C)(C)C(C)(C)C)OP(=O)(O)N([Si](C)(C)C(C)(C)C)P(=O)(O)O)C(O)C1O	6592.2	Standard polar	33892256
Phosphoaminophosphonic acid-adenylate ester,3TBDMS,isomer #38	CC(C)(C)[Si](C)(C)OP(=O)(NP(=O)(O[Si](C)(C)C(C)(C)C)OP(=O)(O)OCC1OC(N2C=NC3=C(N)N=CN=C32)C(O)C1O)O[Si](C)(C)C(C)(C)C	4675.8	Semi standard non polar	33892256
Phosphoaminophosphonic acid-adenylate ester,3TBDMS,isomer #38	CC(C)(C)[Si](C)(C)OP(=O)(NP(=O)(O[Si](C)(C)C(C)(C)C)OP(=O)(O)OCC1OC(N2C=NC3=C(N)N=CN=C32)C(O)C1O)O[Si](C)(C)C(C)(C)C	4387.4	Standard non polar	33892256
Phosphoaminophosphonic acid-adenylate ester,3TBDMS,isomer #38	CC(C)(C)[Si](C)(C)OP(=O)(NP(=O)(O[Si](C)(C)C(C)(C)C)OP(=O)(O)OCC1OC(N2C=NC3=C(N)N=CN=C32)C(O)C1O)O[Si](C)(C)C(C)(C)C	6669.9	Standard polar	33892256
Phosphoaminophosphonic acid-adenylate ester,3TBDMS,isomer #39	CC(C)(C)[Si](C)(C)NC1=NC=NC2=C1N=CN2C1OC(COP(=O)(O)OP(=O)(NP(=O)(O)O[Si](C)(C)C(C)(C)C)O[Si](C)(C)C(C)(C)C)C(O)C1O	4720.8	Semi standard non polar	33892256
Phosphoaminophosphonic acid-adenylate ester,3TBDMS,isomer #39	CC(C)(C)[Si](C)(C)NC1=NC=NC2=C1N=CN2C1OC(COP(=O)(O)OP(=O)(NP(=O)(O)O[Si](C)(C)C(C)(C)C)O[Si](C)(C)C(C)(C)C)C(O)C1O	4511.7	Standard non polar	33892256
Phosphoaminophosphonic acid-adenylate ester,3TBDMS,isomer #39	CC(C)(C)[Si](C)(C)NC1=NC=NC2=C1N=CN2C1OC(COP(=O)(O)OP(=O)(NP(=O)(O)O[Si](C)(C)C(C)(C)C)O[Si](C)(C)C(C)(C)C)C(O)C1O	6600.0	Standard polar	33892256
Phosphoaminophosphonic acid-adenylate ester,3TBDMS,isomer #4	CC(C)(C)[Si](C)(C)NC1=NC=NC2=C1N=CN2C1OC(COP(=O)(O)OP(=O)(O)NP(=O)(O)O)C(O[Si](C)(C)C(C)(C)C)C1O[Si](C)(C)C(C)(C)C	4729.9	Semi standard non polar	33892256
Phosphoaminophosphonic acid-adenylate ester,3TBDMS,isomer #4	CC(C)(C)[Si](C)(C)NC1=NC=NC2=C1N=CN2C1OC(COP(=O)(O)OP(=O)(O)NP(=O)(O)O)C(O[Si](C)(C)C(C)(C)C)C1O[Si](C)(C)C(C)(C)C	4299.5	Standard non polar	33892256
Phosphoaminophosphonic acid-adenylate ester,3TBDMS,isomer #4	CC(C)(C)[Si](C)(C)NC1=NC=NC2=C1N=CN2C1OC(COP(=O)(O)OP(=O)(O)NP(=O)(O)O)C(O[Si](C)(C)C(C)(C)C)C1O[Si](C)(C)C(C)(C)C	6816.4	Standard polar	33892256
Phosphoaminophosphonic acid-adenylate ester,3TBDMS,isomer #40	CC(C)(C)[Si](C)(C)OP(=O)(O)N([Si](C)(C)C(C)(C)C)P(=O)(O[Si](C)(C)C(C)(C)C)OP(=O)(O)OCC1OC(N2C=NC3=C(N)N=CN=C32)C(O)C1O	4752.5	Semi standard non polar	33892256
Phosphoaminophosphonic acid-adenylate ester,3TBDMS,isomer #40	CC(C)(C)[Si](C)(C)OP(=O)(O)N([Si](C)(C)C(C)(C)C)P(=O)(O[Si](C)(C)C(C)(C)C)OP(=O)(O)OCC1OC(N2C=NC3=C(N)N=CN=C32)C(O)C1O	4521.5	Standard non polar	33892256
Phosphoaminophosphonic acid-adenylate ester,3TBDMS,isomer #40	CC(C)(C)[Si](C)(C)OP(=O)(O)N([Si](C)(C)C(C)(C)C)P(=O)(O[Si](C)(C)C(C)(C)C)OP(=O)(O)OCC1OC(N2C=NC3=C(N)N=CN=C32)C(O)C1O	6655.1	Standard polar	33892256
Phosphoaminophosphonic acid-adenylate ester,3TBDMS,isomer #41	CC(C)(C)[Si](C)(C)OP(=O)(NP(=O)(O)O)OP(=O)(O)OCC1OC(N2C=NC3=C(N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)N=CN=C32)C(O)C1O	4753.3	Semi standard non polar	33892256
Phosphoaminophosphonic acid-adenylate ester,3TBDMS,isomer #41	CC(C)(C)[Si](C)(C)OP(=O)(NP(=O)(O)O)OP(=O)(O)OCC1OC(N2C=NC3=C(N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)N=CN=C32)C(O)C1O	4555.6	Standard non polar	33892256
Phosphoaminophosphonic acid-adenylate ester,3TBDMS,isomer #41	CC(C)(C)[Si](C)(C)OP(=O)(NP(=O)(O)O)OP(=O)(O)OCC1OC(N2C=NC3=C(N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)N=CN=C32)C(O)C1O	6586.8	Standard polar	33892256
Phosphoaminophosphonic acid-adenylate ester,3TBDMS,isomer #42	CC(C)(C)[Si](C)(C)NC1=NC=NC2=C1N=CN2C1OC(COP(=O)(O)OP(=O)(O[Si](C)(C)C(C)(C)C)N([Si](C)(C)C(C)(C)C)P(=O)(O)O)C(O)C1O	4804.6	Semi standard non polar	33892256
Phosphoaminophosphonic acid-adenylate ester,3TBDMS,isomer #42	CC(C)(C)[Si](C)(C)NC1=NC=NC2=C1N=CN2C1OC(COP(=O)(O)OP(=O)(O[Si](C)(C)C(C)(C)C)N([Si](C)(C)C(C)(C)C)P(=O)(O)O)C(O)C1O	4659.4	Standard non polar	33892256
Phosphoaminophosphonic acid-adenylate ester,3TBDMS,isomer #42	CC(C)(C)[Si](C)(C)NC1=NC=NC2=C1N=CN2C1OC(COP(=O)(O)OP(=O)(O[Si](C)(C)C(C)(C)C)N([Si](C)(C)C(C)(C)C)P(=O)(O)O)C(O)C1O	6579.9	Standard polar	33892256
Phosphoaminophosphonic acid-adenylate ester,3TBDMS,isomer #43	CC(C)(C)[Si](C)(C)NC1=NC=NC2=C1N=CN2C1OC(COP(=O)(O)OP(=O)(O)NP(=O)(O[Si](C)(C)C(C)(C)C)O[Si](C)(C)C(C)(C)C)C(O)C1O	4733.8	Semi standard non polar	33892256
Phosphoaminophosphonic acid-adenylate ester,3TBDMS,isomer #43	CC(C)(C)[Si](C)(C)NC1=NC=NC2=C1N=CN2C1OC(COP(=O)(O)OP(=O)(O)NP(=O)(O[Si](C)(C)C(C)(C)C)O[Si](C)(C)C(C)(C)C)C(O)C1O	4476.6	Standard non polar	33892256
Phosphoaminophosphonic acid-adenylate ester,3TBDMS,isomer #43	CC(C)(C)[Si](C)(C)NC1=NC=NC2=C1N=CN2C1OC(COP(=O)(O)OP(=O)(O)NP(=O)(O[Si](C)(C)C(C)(C)C)O[Si](C)(C)C(C)(C)C)C(O)C1O	6643.7	Standard polar	33892256
Phosphoaminophosphonic acid-adenylate ester,3TBDMS,isomer #44	CC(C)(C)[Si](C)(C)OP(=O)(O[Si](C)(C)C(C)(C)C)N([Si](C)(C)C(C)(C)C)P(=O)(O)OP(=O)(O)OCC1OC(N2C=NC3=C(N)N=CN=C32)C(O)C1O	4753.8	Semi standard non polar	33892256
Phosphoaminophosphonic acid-adenylate ester,3TBDMS,isomer #44	CC(C)(C)[Si](C)(C)OP(=O)(O[Si](C)(C)C(C)(C)C)N([Si](C)(C)C(C)(C)C)P(=O)(O)OP(=O)(O)OCC1OC(N2C=NC3=C(N)N=CN=C32)C(O)C1O	4510.2	Standard non polar	33892256
Phosphoaminophosphonic acid-adenylate ester,3TBDMS,isomer #44	CC(C)(C)[Si](C)(C)OP(=O)(O[Si](C)(C)C(C)(C)C)N([Si](C)(C)C(C)(C)C)P(=O)(O)OP(=O)(O)OCC1OC(N2C=NC3=C(N)N=CN=C32)C(O)C1O	6674.3	Standard polar	33892256
Phosphoaminophosphonic acid-adenylate ester,3TBDMS,isomer #45	CC(C)(C)[Si](C)(C)OP(=O)(O)NP(=O)(O)OP(=O)(O)OCC1OC(N2C=NC3=C(N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)N=CN=C32)C(O)C1O	4735.5	Semi standard non polar	33892256
Phosphoaminophosphonic acid-adenylate ester,3TBDMS,isomer #45	CC(C)(C)[Si](C)(C)OP(=O)(O)NP(=O)(O)OP(=O)(O)OCC1OC(N2C=NC3=C(N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)N=CN=C32)C(O)C1O	4559.8	Standard non polar	33892256
Phosphoaminophosphonic acid-adenylate ester,3TBDMS,isomer #45	CC(C)(C)[Si](C)(C)OP(=O)(O)NP(=O)(O)OP(=O)(O)OCC1OC(N2C=NC3=C(N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)N=CN=C32)C(O)C1O	6630.2	Standard polar	33892256
Phosphoaminophosphonic acid-adenylate ester,3TBDMS,isomer #46	CC(C)(C)[Si](C)(C)NC1=NC=NC2=C1N=CN2C1OC(COP(=O)(O)OP(=O)(O)N([Si](C)(C)C(C)(C)C)P(=O)(O)O[Si](C)(C)C(C)(C)C)C(O)C1O	4768.0	Semi standard non polar	33892256
Phosphoaminophosphonic acid-adenylate ester,3TBDMS,isomer #46	CC(C)(C)[Si](C)(C)NC1=NC=NC2=C1N=CN2C1OC(COP(=O)(O)OP(=O)(O)N([Si](C)(C)C(C)(C)C)P(=O)(O)O[Si](C)(C)C(C)(C)C)C(O)C1O	4627.4	Standard non polar	33892256
Phosphoaminophosphonic acid-adenylate ester,3TBDMS,isomer #46	CC(C)(C)[Si](C)(C)NC1=NC=NC2=C1N=CN2C1OC(COP(=O)(O)OP(=O)(O)N([Si](C)(C)C(C)(C)C)P(=O)(O)O[Si](C)(C)C(C)(C)C)C(O)C1O	6630.8	Standard polar	33892256
Phosphoaminophosphonic acid-adenylate ester,3TBDMS,isomer #47	CC(C)(C)[Si](C)(C)N(C1=NC=NC2=C1N=CN2C1OC(COP(=O)(O)OP(=O)(O)N([Si](C)(C)C(C)(C)C)P(=O)(O)O)C(O)C1O)[Si](C)(C)C(C)(C)C	4790.4	Semi standard non polar	33892256
Phosphoaminophosphonic acid-adenylate ester,3TBDMS,isomer #47	CC(C)(C)[Si](C)(C)N(C1=NC=NC2=C1N=CN2C1OC(COP(=O)(O)OP(=O)(O)N([Si](C)(C)C(C)(C)C)P(=O)(O)O)C(O)C1O)[Si](C)(C)C(C)(C)C	4725.6	Standard non polar	33892256
Phosphoaminophosphonic acid-adenylate ester,3TBDMS,isomer #47	CC(C)(C)[Si](C)(C)N(C1=NC=NC2=C1N=CN2C1OC(COP(=O)(O)OP(=O)(O)N([Si](C)(C)C(C)(C)C)P(=O)(O)O)C(O)C1O)[Si](C)(C)C(C)(C)C	6600.2	Standard polar	33892256
Phosphoaminophosphonic acid-adenylate ester,3TBDMS,isomer #5	CC(C)(C)[Si](C)(C)OC1C(COP(=O)(O)OP(=O)(O)N([Si](C)(C)C(C)(C)C)P(=O)(O)O)OC(N2C=NC3=C(N)N=CN=C32)C1O[Si](C)(C)C(C)(C)C	4738.2	Semi standard non polar	33892256
Phosphoaminophosphonic acid-adenylate ester,3TBDMS,isomer #5	CC(C)(C)[Si](C)(C)OC1C(COP(=O)(O)OP(=O)(O)N([Si](C)(C)C(C)(C)C)P(=O)(O)O)OC(N2C=NC3=C(N)N=CN=C32)C1O[Si](C)(C)C(C)(C)C	4411.2	Standard non polar	33892256
Phosphoaminophosphonic acid-adenylate ester,3TBDMS,isomer #5	CC(C)(C)[Si](C)(C)OC1C(COP(=O)(O)OP(=O)(O)N([Si](C)(C)C(C)(C)C)P(=O)(O)O)OC(N2C=NC3=C(N)N=CN=C32)C1O[Si](C)(C)C(C)(C)C	6813.6	Standard polar	33892256
Phosphoaminophosphonic acid-adenylate ester,3TBDMS,isomer #6	CC(C)(C)[Si](C)(C)OC1C(COP(=O)(O[Si](C)(C)C(C)(C)C)OP(=O)(NP(=O)(O)O)O[Si](C)(C)C(C)(C)C)OC(N2C=NC3=C(N)N=CN=C32)C1O	4731.0	Semi standard non polar	33892256
Phosphoaminophosphonic acid-adenylate ester,3TBDMS,isomer #6	CC(C)(C)[Si](C)(C)OC1C(COP(=O)(O[Si](C)(C)C(C)(C)C)OP(=O)(NP(=O)(O)O)O[Si](C)(C)C(C)(C)C)OC(N2C=NC3=C(N)N=CN=C32)C1O	4337.3	Standard non polar	33892256
Phosphoaminophosphonic acid-adenylate ester,3TBDMS,isomer #6	CC(C)(C)[Si](C)(C)OC1C(COP(=O)(O[Si](C)(C)C(C)(C)C)OP(=O)(NP(=O)(O)O)O[Si](C)(C)C(C)(C)C)OC(N2C=NC3=C(N)N=CN=C32)C1O	6725.9	Standard polar	33892256
Phosphoaminophosphonic acid-adenylate ester,3TBDMS,isomer #7	CC(C)(C)[Si](C)(C)OC1C(COP(=O)(O[Si](C)(C)C(C)(C)C)OP(=O)(O)NP(=O)(O)O[Si](C)(C)C(C)(C)C)OC(N2C=NC3=C(N)N=CN=C32)C1O	4725.8	Semi standard non polar	33892256
Phosphoaminophosphonic acid-adenylate ester,3TBDMS,isomer #7	CC(C)(C)[Si](C)(C)OC1C(COP(=O)(O[Si](C)(C)C(C)(C)C)OP(=O)(O)NP(=O)(O)O[Si](C)(C)C(C)(C)C)OC(N2C=NC3=C(N)N=CN=C32)C1O	4337.7	Standard non polar	33892256
Phosphoaminophosphonic acid-adenylate ester,3TBDMS,isomer #7	CC(C)(C)[Si](C)(C)OC1C(COP(=O)(O[Si](C)(C)C(C)(C)C)OP(=O)(O)NP(=O)(O)O[Si](C)(C)C(C)(C)C)OC(N2C=NC3=C(N)N=CN=C32)C1O	6726.5	Standard polar	33892256
Phosphoaminophosphonic acid-adenylate ester,3TBDMS,isomer #8	CC(C)(C)[Si](C)(C)NC1=NC=NC2=C1N=CN2C1OC(COP(=O)(O[Si](C)(C)C(C)(C)C)OP(=O)(O)NP(=O)(O)O)C(O[Si](C)(C)C(C)(C)C)C1O	4779.4	Semi standard non polar	33892256
Phosphoaminophosphonic acid-adenylate ester,3TBDMS,isomer #8	CC(C)(C)[Si](C)(C)NC1=NC=NC2=C1N=CN2C1OC(COP(=O)(O[Si](C)(C)C(C)(C)C)OP(=O)(O)NP(=O)(O)O)C(O[Si](C)(C)C(C)(C)C)C1O	4394.7	Standard non polar	33892256
Phosphoaminophosphonic acid-adenylate ester,3TBDMS,isomer #8	CC(C)(C)[Si](C)(C)NC1=NC=NC2=C1N=CN2C1OC(COP(=O)(O[Si](C)(C)C(C)(C)C)OP(=O)(O)NP(=O)(O)O)C(O[Si](C)(C)C(C)(C)C)C1O	6688.6	Standard polar	33892256
Phosphoaminophosphonic acid-adenylate ester,3TBDMS,isomer #9	CC(C)(C)[Si](C)(C)OC1C(COP(=O)(O[Si](C)(C)C(C)(C)C)OP(=O)(O)N([Si](C)(C)C(C)(C)C)P(=O)(O)O)OC(N2C=NC3=C(N)N=CN=C32)C1O	4769.3	Semi standard non polar	33892256
Phosphoaminophosphonic acid-adenylate ester,3TBDMS,isomer #9	CC(C)(C)[Si](C)(C)OC1C(COP(=O)(O[Si](C)(C)C(C)(C)C)OP(=O)(O)N([Si](C)(C)C(C)(C)C)P(=O)(O)O)OC(N2C=NC3=C(N)N=CN=C32)C1O	4496.5	Standard non polar	33892256
Phosphoaminophosphonic acid-adenylate ester,3TBDMS,isomer #9	CC(C)(C)[Si](C)(C)OC1C(COP(=O)(O[Si](C)(C)C(C)(C)C)OP(=O)(O)N([Si](C)(C)C(C)(C)C)P(=O)(O)O)OC(N2C=NC3=C(N)N=CN=C32)C1O	6707.3	Standard polar	33892256

Spectra

GC-MS Spectra

Spectrum Type	Description	Splash Key	Deposition Date	Source	View
Predicted GC-MS	Predicted GC-MS Spectrum - Phosphoaminophosphonic acid-adenylate ester GC-MS (TMS_1_1) - 70eV, Positive	Not Available	2021-11-03	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - Phosphoaminophosphonic acid-adenylate ester GC-MS (TMS_1_2) - 70eV, Positive	Not Available	2021-11-03	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - Phosphoaminophosphonic acid-adenylate ester GC-MS (TMS_1_3) - 70eV, Positive	Not Available	2021-11-03	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - Phosphoaminophosphonic acid-adenylate ester GC-MS (TMS_1_4) - 70eV, Positive	Not Available	2021-11-03	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - Phosphoaminophosphonic acid-adenylate ester GC-MS (TMS_1_5) - 70eV, Positive	Not Available	2021-11-03	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - Phosphoaminophosphonic acid-adenylate ester GC-MS (TMS_1_6) - 70eV, Positive	Not Available	2021-11-03	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - Phosphoaminophosphonic acid-adenylate ester GC-MS (TMS_1_7) - 70eV, Positive	Not Available	2021-11-03	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - Phosphoaminophosphonic acid-adenylate ester GC-MS (TMS_2_1) - 70eV, Positive	Not Available	2021-11-03	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - Phosphoaminophosphonic acid-adenylate ester GC-MS (TMS_2_2) - 70eV, Positive	Not Available	2021-11-03	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - Phosphoaminophosphonic acid-adenylate ester GC-MS (TMS_2_3) - 70eV, Positive	Not Available	2021-11-03	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - Phosphoaminophosphonic acid-adenylate ester GC-MS (TMS_2_4) - 70eV, Positive	Not Available	2021-11-03	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - Phosphoaminophosphonic acid-adenylate ester GC-MS (TMS_2_5) - 70eV, Positive	Not Available	2021-11-03	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - Phosphoaminophosphonic acid-adenylate ester GC-MS (TMS_2_6) - 70eV, Positive	Not Available	2021-11-03	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - Phosphoaminophosphonic acid-adenylate ester GC-MS (TMS_2_7) - 70eV, Positive	Not Available	2021-11-03	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - Phosphoaminophosphonic acid-adenylate ester GC-MS (TMS_2_8) - 70eV, Positive	Not Available	2021-11-03	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - Phosphoaminophosphonic acid-adenylate ester GC-MS (TMS_2_9) - 70eV, Positive	Not Available	2021-11-03	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - Phosphoaminophosphonic acid-adenylate ester GC-MS (TMS_2_10) - 70eV, Positive	Not Available	2021-11-03	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - Phosphoaminophosphonic acid-adenylate ester GC-MS (TMS_2_11) - 70eV, Positive	Not Available	2021-11-03	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - Phosphoaminophosphonic acid-adenylate ester GC-MS (TMS_2_12) - 70eV, Positive	Not Available	2021-11-03	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - Phosphoaminophosphonic acid-adenylate ester GC-MS (TMS_2_13) - 70eV, Positive	Not Available	2021-11-03	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - Phosphoaminophosphonic acid-adenylate ester GC-MS (TMS_2_14) - 70eV, Positive	Not Available	2021-11-03	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - Phosphoaminophosphonic acid-adenylate ester GC-MS (TMS_2_15) - 70eV, Positive	Not Available	2021-11-03	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - Phosphoaminophosphonic acid-adenylate ester GC-MS (TMS_2_16) - 70eV, Positive	Not Available	2021-11-03	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - Phosphoaminophosphonic acid-adenylate ester GC-MS (TMS_2_17) - 70eV, Positive	Not Available	2021-11-03	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - Phosphoaminophosphonic acid-adenylate ester GC-MS (TMS_2_18) - 70eV, Positive	Not Available	2021-11-03	Wishart Lab	View Spectrum

MS/MS Spectra

Spectrum Type	Description	Splash Key	Deposition Date	Source	View
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - Phosphoaminophosphonic acid-adenylate ester 10V, Positive-QTOF	splash10-0bt9-0200890000-46b8521e0e897fcc950b	2021-10-12	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - Phosphoaminophosphonic acid-adenylate ester 20V, Positive-QTOF	splash10-0a70-1921710000-783b7ff119a02e148b5c	2021-10-12	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - Phosphoaminophosphonic acid-adenylate ester 40V, Positive-QTOF	splash10-000i-1920000000-191edf94cc2f75b6f802	2021-10-12	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - Phosphoaminophosphonic acid-adenylate ester 10V, Negative-QTOF	splash10-0a4i-0000090000-18878df96523802852ba	2021-10-12	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - Phosphoaminophosphonic acid-adenylate ester 20V, Negative-QTOF	splash10-0a6r-2212940000-eb922401d91f5e1f2c33	2021-10-12	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - Phosphoaminophosphonic acid-adenylate ester 40V, Negative-QTOF	splash10-0a6s-6922800000-ede0d1c3025536d86a69	2021-10-12	Wishart Lab	View Spectrum

NMR Spectra

Spectrum Type	Description	Deposition Date	Source	View
Predicted 1D NMR	¹H NMR Spectrum (1D, 100 MHz, D₂O, predicted)	2021-10-13	Wishart Lab	View Spectrum
Predicted 1D NMR	¹³C NMR Spectrum (1D, 100 MHz, D₂O, predicted)	2021-10-13	Wishart Lab	View Spectrum
Predicted 1D NMR	¹H NMR Spectrum (1D, 1000 MHz, D₂O, predicted)	2021-10-13	Wishart Lab	View Spectrum
Predicted 1D NMR	¹³C NMR Spectrum (1D, 1000 MHz, D₂O, predicted)	2021-10-13	Wishart Lab	View Spectrum
Predicted 1D NMR	¹³C NMR Spectrum (1D, 200 MHz, D₂O, predicted)	2021-10-13	Wishart Lab	View Spectrum
Predicted 1D NMR	¹H NMR Spectrum (1D, 200 MHz, D₂O, predicted)	2021-10-13	Wishart Lab	View Spectrum
Predicted 1D NMR	¹H NMR Spectrum (1D, 300 MHz, D₂O, predicted)	2021-10-13	Wishart Lab	View Spectrum
Predicted 1D NMR	¹³C NMR Spectrum (1D, 300 MHz, D₂O, predicted)	2021-10-13	Wishart Lab	View Spectrum
Predicted 1D NMR	¹³C NMR Spectrum (1D, 400 MHz, D₂O, predicted)	2021-10-13	Wishart Lab	View Spectrum
Predicted 1D NMR	¹H NMR Spectrum (1D, 400 MHz, D₂O, predicted)	2021-10-13	Wishart Lab	View Spectrum
Predicted 1D NMR	¹H NMR Spectrum (1D, 500 MHz, D₂O, predicted)	2021-10-13	Wishart Lab	View Spectrum
Predicted 1D NMR	¹³C NMR Spectrum (1D, 500 MHz, D₂O, predicted)	2021-10-13	Wishart Lab	View Spectrum
Predicted 1D NMR	¹H NMR Spectrum (1D, 600 MHz, D₂O, predicted)	2021-10-13	Wishart Lab	View Spectrum
Predicted 1D NMR	¹³C NMR Spectrum (1D, 600 MHz, D₂O, predicted)	2021-10-13	Wishart Lab	View Spectrum
Predicted 1D NMR	¹H NMR Spectrum (1D, 700 MHz, D₂O, predicted)	2021-10-13	Wishart Lab	View Spectrum
Predicted 1D NMR	¹³C NMR Spectrum (1D, 700 MHz, D₂O, predicted)	2021-10-13	Wishart Lab	View Spectrum
Predicted 1D NMR	¹³C NMR Spectrum (1D, 800 MHz, D₂O, predicted)	2021-10-13	Wishart Lab	View Spectrum
Predicted 1D NMR	¹H NMR Spectrum (1D, 800 MHz, D₂O, predicted)	2021-10-13	Wishart Lab	View Spectrum
Predicted 1D NMR	¹³C NMR Spectrum (1D, 900 MHz, D₂O, predicted)	2021-10-13	Wishart Lab	View Spectrum
Predicted 1D NMR	¹H NMR Spectrum (1D, 900 MHz, D₂O, predicted)	2021-10-13	Wishart Lab	View Spectrum

Biological Properties

Cellular Locations

Not Available

Biospecimen Locations

Blood

Tissue Locations

Not Available

Pathways

Not Available

Name	SMPDB/PathBank	KEGG

Normal Concentrations

Biospecimen	Status	Value	Age	Sex	Condition	Reference	Details
Blood	Detected but not Quantified	Not Quantified	Not Specified	Not Specified	Normal	31557052	details

Abnormal Concentrations

Not Available

Associated Disorders and Diseases

Disease References

None

Associated OMIM IDs

None

External Links

DrugBank ID

Not Available

Phenol Explorer Compound ID

Not Available

FooDB ID

Not Available

KNApSAcK ID

Not Available

Chemspider ID

4631

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

4795

PDB ID

Not Available

ChEBI ID

Not Available

Food Biomarker Ontology

Not Available

VMH ID

Not Available

MarkerDB ID

Not Available

Good Scents ID

Not Available

References

Synthesis Reference

Not Available

Material Safety Data Sheet (MSDS)

Not Available

General References

Barupal DK, Fiehn O: Generating the Blood Exposome Database Using a Comprehensive Text Mining and Database Fusion Approach. Environ Health Perspect. 2019 Sep;127(9):97008. doi: 10.1289/EHP4713. Epub 2019 Sep 26. [PubMed:31557052 ]

Showing metabocard for Phosphoaminophosphonic acid-adenylate ester (HMDB0248355)

MOL for HMDB0248355 (Phosphoaminophosphonic acid-adenylate ester)

3D MOL for HMDB0248355 (Phosphoaminophosphonic acid-adenylate ester)

3D SDF for HMDB0248355 (Phosphoaminophosphonic acid-adenylate ester)

3D-SDF for HMDB0248355 (Phosphoaminophosphonic acid-adenylate ester)

PDB for HMDB0248355 (Phosphoaminophosphonic acid-adenylate ester)

3D PDB for HMDB0248355 (Phosphoaminophosphonic acid-adenylate ester)

SMILES for HMDB0248355 (Phosphoaminophosphonic acid-adenylate ester)

INCHI for HMDB0248355 (Phosphoaminophosphonic acid-adenylate ester)

Structure for HMDB0248355 (Phosphoaminophosphonic acid-adenylate ester)

3D Structure for HMDB0248355 (Phosphoaminophosphonic acid-adenylate ester)

Predicted Collision Cross Sections

Predicted Kovats Retention Indices

Underivatized

Derivatized

GC-MS Spectra

MS/MS Spectra

NMR Spectra