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Record Information

Version

5.0

Status

Detected but not Quantified

Creation Date

2017-02-24 01:29:32 UTC

Update Date

2022-03-07 03:17:49 UTC

HMDB ID

HMDB0062186

Secondary Accession Numbers

HMDB62186

Metabolite Identification

Common Name

1-Deoxy-1-(N6-lysino)-D-fructose

Description

(2S)-2-amino-6-({[(2R,3S,4S,5R)-2,3,4-trihydroxy-5-(hydroxymethyl)oxolan-2-yl]methyl}amino)hexanoic acid belongs to the class of organic compounds known as c-glycosyl compounds. These are glycoside in which a sugar group is bonded through one carbon to another group via a C-glycosidic bond (2S)-2-amino-6-({[(2R,3S,4S,5R)-2,3,4-trihydroxy-5-(hydroxymethyl)oxolan-2-yl]methyl}amino)hexanoic acid is a very strong basic compound (based on its pKa).

Structure

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

HMDB0062186
     RDKit          3D
1-Deoxy-1-(N6-lysino)-D-fructose
 45 45  0  0  0  0  0  0  0  0999 V2000
    5.5405    1.3253    1.2207 N   0  0  0  0  0  0  0  0  0  0  0  0
    5.2510    0.1159    0.4754 C   0  0  1  0  0  0  0  0  0  0  0  0
    3.8058   -0.3025    0.6265 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8672    0.7776    0.1106 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4312    0.3568    0.2714 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1321   -0.9271   -0.4821 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2502   -1.2900   -0.2985 N   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1760   -0.3906   -0.9486 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5763   -0.8965   -0.6375 C   0  0  1  0  0  0  0  0  0  0  0  0
   -2.6866   -2.2007   -1.1339 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7689   -0.8276    0.7358 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7040    0.1804    0.9571 C   0  0  2  0  0  0  0  0  0  0  0  0
   -4.3929    0.0935    2.2739 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3887    0.1770    3.2653 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.6638    0.0545   -0.2350 C   0  0  1  0  0  0  0  0  0  0  0  0
   -5.4529    1.1846   -0.3710 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6288   -0.0682   -1.3270 C   0  0  2  0  0  0  0  0  0  0  0  0
   -4.1433   -0.6763   -2.4654 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.5836    0.3181   -0.9754 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.4163   -0.6072   -1.8260 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.0849    1.5114   -1.4651 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.0054    2.1003    0.7703 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.2728    1.2501    2.2037 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.8803   -0.7012    0.8573 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.6899   -1.2070   -0.0257 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.6152   -0.5727    1.6626 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.0109    1.6947    0.7197 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.0956    0.9632   -0.9521 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.2166    0.2082    1.3521 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.8132    1.2067   -0.1075 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.7302   -1.7370   -0.0005 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.3927   -0.7822   -1.5317 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3952   -2.2545   -0.6363 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0009   -0.2864   -2.0228 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0889    0.5941   -0.4282 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1150   -2.8250   -0.5010 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1940    1.1428    0.8796 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.9962    1.0143    2.4134 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.9770   -0.8260    2.4184 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8774    1.0211    3.1698 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.2666   -0.8855   -0.1280 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.3573    0.9545   -0.7598 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2807    0.9684   -1.5292 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4415   -0.8495   -3.1273 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.9877    1.9001   -1.1526 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  2  3  1  0
  3  4  1  0
  4  5  1  0
  5  6  1  0
  6  7  1  0
  7  8  1  0
  8  9  1  0
  9 10  1  6
  9 11  1  0
 11 12  1  0
 12 13  1  0
 13 14  1  0
 12 15  1  0
 15 16  1  0
 15 17  1  0
 17 18  1  0
  2 19  1  0
 19 20  2  0
 19 21  1  0
 17  9  1  0
  1 22  1  0
  1 23  1  0
  2 24  1  1
  3 25  1  0
  3 26  1  0
  4 27  1  0
  4 28  1  0
  5 29  1  0
  5 30  1  0
  6 31  1  0
  6 32  1  0
  7 33  1  0
  8 34  1  0
  8 35  1  0
 10 36  1  0
 12 37  1  6
 13 38  1  0
 13 39  1  0
 14 40  1  0
 15 41  1  1
 16 42  1  0
 17 43  1  6
 18 44  1  0
 21 45  1  0
M  END


  Mrv1652305261919172D          

 21 21  0  0  0  0            999 V2000
 9998.871110000.5174    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
 9999.585710000.1051    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
10000.299410000.5174    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
10001.014810000.1051    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
10001.730210000.5174    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
10002.443510000.1051    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
10003.161010000.5174    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
10003.876410000.1051    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
10004.589710000.5174    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
10003.8764 9999.2802    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
10003.161010001.3421    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
 9998.7892 9999.5750    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
 9998.3633 9998.6578    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
 9996.5738 9998.6659    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
 9996.104810000.5174    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
 9995.390210000.1051    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
 9997.485710000.5993    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
 9996.818310000.1143    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
 9997.0732 9999.3297    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
 9997.8982 9999.3297    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
 9998.153110000.1143    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
  1  2  1  0  0  0  0
  2  3  1  0  0  0  0
  3  4  1  0  0  0  0
  4  5  1  0  0  0  0
  5  6  1  0  0  0  0
  6  7  1  0  0  0  0
  7  8  1  0  0  0  0
  7 11  1  6  0  0  0
  8  9  1  0  0  0  0
  8 10  2  0  0  0  0
 15 16  1  0  0  0  0
 18 19  1  0  0  0  0
 19 20  1  0  0  0  0
 20 21  1  0  0  0  0
 17 18  1  0  0  0  0
 17 21  1  0  0  0  0
  1 21  1  0  0  0  0
 21 12  1  1  0  0  0
 18 15  1  1  0  0  0
 19 14  1  6  0  0  0
 20 13  1  1  0  0  0
M  END
> <DATABASE_ID>
HMDB0062186

> <DATABASE_NAME>
hmdb

> <SMILES>
N[C@@H](CCCCNC[C@@]1(O)O[C@H](CO)[C@@H](O)[C@@H]1O)C(O)=O

> <INCHI_IDENTIFIER>
InChI=1S/C12H24N2O7/c13-7(11(18)19)3-1-2-4-14-6-12(20)10(17)9(16)8(5-15)21-12/h7-10,14-17,20H,1-6,13H2,(H,18,19)/t7-,8+,9+,10-,12+/m0/s1

> <INCHI_KEY>
ZAWLGBRDVQURAK-TYCYOEEFSA-N

> <FORMULA>
C12H24N2O7

> <MOLECULAR_WEIGHT>
308.331

> <EXACT_MASS>
308.158351121

> <JCHEM_ACCEPTOR_COUNT>
9

> <JCHEM_ATOM_COUNT>
45

> <JCHEM_AVERAGE_POLARIZABILITY>
31.03595568592265

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
7

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
(2S)-2-amino-6-({[(2R,3S,4S,5R)-2,3,4-trihydroxy-5-(hydroxymethyl)oxolan-2-yl]methyl}amino)hexanoic acid

> <ALOGPS_LOGP>
-2.93

> <JCHEM_LOGP>
-5.082369331258076

> <ALOGPS_LOGS>
-0.76

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
1

> <JCHEM_PHYSIOLOGICAL_CHARGE>
1

> <JCHEM_PKA>
10.770256375344529

> <JCHEM_PKA_STRONGEST_ACIDIC>
2.051548887531848

> <JCHEM_PKA_STRONGEST_BASIC>
9.551282992016104

> <JCHEM_POLAR_SURFACE_AREA>
165.49999999999997

> <JCHEM_REFRACTIVITY>
70.68359999999998

> <JCHEM_ROTATABLE_BOND_COUNT>
9

> <JCHEM_RULE_OF_FIVE>
0

> <ALOGPS_SOLUBILITY>
5.30e+01 g/l

> <JCHEM_TRADITIONAL_IUPAC>
(2S)-2-amino-6-({[(2R,3S,4S,5R)-2,3,4-trihydroxy-5-(hydroxymethyl)oxolan-2-yl]methyl}amino)hexanoic acid

> <JCHEM_VEBER_RULE>
0

$$$$

HMDB0062186
     RDKit          3D
1-Deoxy-1-(N6-lysino)-D-fructose
 45 45  0  0  0  0  0  0  0  0999 V2000
    5.5405    1.3253    1.2207 N   0  0  0  0  0  0  0  0  0  0  0  0
    5.2510    0.1159    0.4754 C   0  0  1  0  0  0  0  0  0  0  0  0
    3.8058   -0.3025    0.6265 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8672    0.7776    0.1106 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4312    0.3568    0.2714 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1321   -0.9271   -0.4821 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2502   -1.2900   -0.2985 N   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1760   -0.3906   -0.9486 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5763   -0.8965   -0.6375 C   0  0  1  0  0  0  0  0  0  0  0  0
   -2.6866   -2.2007   -1.1339 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7689   -0.8276    0.7358 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7040    0.1804    0.9571 C   0  0  2  0  0  0  0  0  0  0  0  0
   -4.3929    0.0935    2.2739 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3887    0.1770    3.2653 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.6638    0.0545   -0.2350 C   0  0  1  0  0  0  0  0  0  0  0  0
   -5.4529    1.1846   -0.3710 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6288   -0.0682   -1.3270 C   0  0  2  0  0  0  0  0  0  0  0  0
   -4.1433   -0.6763   -2.4654 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.5836    0.3181   -0.9754 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.4163   -0.6072   -1.8260 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.0849    1.5114   -1.4651 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.0054    2.1003    0.7703 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.2728    1.2501    2.2037 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.8803   -0.7012    0.8573 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.6899   -1.2070   -0.0257 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.6152   -0.5727    1.6626 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.0109    1.6947    0.7197 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.0956    0.9632   -0.9521 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.2166    0.2082    1.3521 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.8132    1.2067   -0.1075 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.7302   -1.7370   -0.0005 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.3927   -0.7822   -1.5317 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3952   -2.2545   -0.6363 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0009   -0.2864   -2.0228 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0889    0.5941   -0.4282 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1150   -2.8250   -0.5010 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1940    1.1428    0.8796 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.9962    1.0143    2.4134 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.9770   -0.8260    2.4184 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8774    1.0211    3.1698 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.2666   -0.8855   -0.1280 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.3573    0.9545   -0.7598 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2807    0.9684   -1.5292 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4415   -0.8495   -3.1273 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.9877    1.9001   -1.1526 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  2  3  1  0
  3  4  1  0
  4  5  1  0
  5  6  1  0
  6  7  1  0
  7  8  1  0
  8  9  1  0
  9 10  1  6
  9 11  1  0
 11 12  1  0
 12 13  1  0
 13 14  1  0
 12 15  1  0
 15 16  1  0
 15 17  1  0
 17 18  1  0
  2 19  1  0
 19 20  2  0
 19 21  1  0
 17  9  1  0
  1 22  1  0
  1 23  1  0
  2 24  1  1
  3 25  1  0
  3 26  1  0
  4 27  1  0
  4 28  1  0
  5 29  1  0
  5 30  1  0
  6 31  1  0
  6 32  1  0
  7 33  1  0
  8 34  1  0
  8 35  1  0
 10 36  1  0
 12 37  1  6
 13 38  1  0
 13 39  1  0
 14 40  1  0
 15 41  1  1
 16 42  1  0
 17 43  1  6
 18 44  1  0
 21 45  1  0
M  END

HEADER    PROTEIN                                 26-MAY-19   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   26-MAY-19         0                                  
HETATM    1  C   UNK     0    8664.5598667.632   0.000  0.00  0.00           C+0
HETATM    2  N   UNK     0    8665.8938666.863   0.000  0.00  0.00           N+0
HETATM    3  C   UNK     0    8667.2268667.632   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0    8668.5618666.863   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0    8669.8968667.632   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0    8671.2288666.863   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0    8672.5678667.632   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0    8673.9038666.863   0.000  0.00  0.00           C+0
HETATM    9  O   UNK     0    8675.2348667.632   0.000  0.00  0.00           O+0
HETATM   10  O   UNK     0    8673.9038665.323   0.000  0.00  0.00           O+0
HETATM   11  N   UNK     0    8672.5678669.172   0.000  0.00  0.00           N+0
HETATM   12  O   UNK     0    8664.4078665.873   0.000  0.00  0.00           O+0
HETATM   13  O   UNK     0    8663.6118664.161   0.000  0.00  0.00           O+0
HETATM   14  O   UNK     0    8660.2718664.176   0.000  0.00  0.00           O+0
HETATM   15  C   UNK     0    8659.3968667.632   0.000  0.00  0.00           C+0
HETATM   16  O   UNK     0    8658.0628666.863   0.000  0.00  0.00           O+0
HETATM   17  O   UNK     0    8661.9738667.785   0.000  0.00  0.00           O+0
HETATM   18  C   UNK     0    8660.7278666.880   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0    8661.2038665.415   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0    8662.7438665.415   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0    8663.2198666.880   0.000  0.00  0.00           C+0
CONECT    1    2   21                                                       
CONECT    2    1    3                                                       
CONECT    3    2    4                                                       
CONECT    4    3    5                                                       
CONECT    5    4    6                                                       
CONECT    6    5    7                                                       
CONECT    7    6    8   11                                                  
CONECT    8    7    9   10                                                  
CONECT    9    8                                                            
CONECT   10    8                                                            
CONECT   11    7                                                            
CONECT   12   21                                                            
CONECT   13   20                                                            
CONECT   14   19                                                            
CONECT   15   16   18                                                       
CONECT   16   15                                                            
CONECT   17   18   21                                                       
CONECT   18   19   17   15                                                  
CONECT   19   18   20   14                                                  
CONECT   20   19   21   13                                                  
CONECT   21   20   17    1   12                                             
MASTER        0    0    0    0    0    0    0    0   21    0   42    0
END

COMPND    HMDB0062186
HETATM    1  N1  UNL     1       5.541   1.325   1.221  1.00  0.00           N  
HETATM    2  C1  UNL     1       5.251   0.116   0.475  1.00  0.00           C  
HETATM    3  C2  UNL     1       3.806  -0.303   0.626  1.00  0.00           C  
HETATM    4  C3  UNL     1       2.867   0.778   0.111  1.00  0.00           C  
HETATM    5  C4  UNL     1       1.431   0.357   0.271  1.00  0.00           C  
HETATM    6  C5  UNL     1       1.132  -0.927  -0.482  1.00  0.00           C  
HETATM    7  N2  UNL     1      -0.250  -1.290  -0.299  1.00  0.00           N  
HETATM    8  C6  UNL     1      -1.176  -0.391  -0.949  1.00  0.00           C  
HETATM    9  C7  UNL     1      -2.576  -0.896  -0.637  1.00  0.00           C  
HETATM   10  O1  UNL     1      -2.687  -2.201  -1.134  1.00  0.00           O  
HETATM   11  O2  UNL     1      -2.769  -0.828   0.736  1.00  0.00           O  
HETATM   12  C8  UNL     1      -3.704   0.180   0.957  1.00  0.00           C  
HETATM   13  C9  UNL     1      -4.393   0.094   2.274  1.00  0.00           C  
HETATM   14  O3  UNL     1      -3.389   0.177   3.265  1.00  0.00           O  
HETATM   15  C10 UNL     1      -4.664   0.054  -0.235  1.00  0.00           C  
HETATM   16  O4  UNL     1      -5.453   1.185  -0.371  1.00  0.00           O  
HETATM   17  C11 UNL     1      -3.629  -0.068  -1.327  1.00  0.00           C  
HETATM   18  O5  UNL     1      -4.143  -0.676  -2.465  1.00  0.00           O  
HETATM   19  C12 UNL     1       5.584   0.318  -0.975  1.00  0.00           C  
HETATM   20  O6  UNL     1       5.416  -0.607  -1.826  1.00  0.00           O  
HETATM   21  O7  UNL     1       6.085   1.511  -1.465  1.00  0.00           O  
HETATM   22  H1  UNL     1       5.005   2.100   0.770  1.00  0.00           H  
HETATM   23  H2  UNL     1       5.273   1.250   2.204  1.00  0.00           H  
HETATM   24  H3  UNL     1       5.880  -0.701   0.857  1.00  0.00           H  
HETATM   25  H4  UNL     1       3.690  -1.207  -0.026  1.00  0.00           H  
HETATM   26  H5  UNL     1       3.615  -0.573   1.663  1.00  0.00           H  
HETATM   27  H6  UNL     1       3.011   1.695   0.720  1.00  0.00           H  
HETATM   28  H7  UNL     1       3.096   0.963  -0.952  1.00  0.00           H  
HETATM   29  H8  UNL     1       1.217   0.208   1.352  1.00  0.00           H  
HETATM   30  H9  UNL     1       0.813   1.207  -0.108  1.00  0.00           H  
HETATM   31  H10 UNL     1       1.730  -1.737  -0.000  1.00  0.00           H  
HETATM   32  H11 UNL     1       1.393  -0.782  -1.532  1.00  0.00           H  
HETATM   33  H12 UNL     1      -0.395  -2.254  -0.636  1.00  0.00           H  
HETATM   34  H13 UNL     1      -1.001  -0.286  -2.023  1.00  0.00           H  
HETATM   35  H14 UNL     1      -1.089   0.594  -0.428  1.00  0.00           H  
HETATM   36  H15 UNL     1      -3.115  -2.825  -0.501  1.00  0.00           H  
HETATM   37  H16 UNL     1      -3.194   1.143   0.880  1.00  0.00           H  
HETATM   38  H17 UNL     1      -4.996   1.014   2.413  1.00  0.00           H  
HETATM   39  H18 UNL     1      -4.977  -0.826   2.418  1.00  0.00           H  
HETATM   40  H19 UNL     1      -2.877   1.021   3.170  1.00  0.00           H  
HETATM   41  H20 UNL     1      -5.267  -0.886  -0.128  1.00  0.00           H  
HETATM   42  H21 UNL     1      -6.357   0.954  -0.760  1.00  0.00           H  
HETATM   43  H22 UNL     1      -3.281   0.968  -1.529  1.00  0.00           H  
HETATM   44  H23 UNL     1      -3.441  -0.849  -3.127  1.00  0.00           H  
HETATM   45  H24 UNL     1       6.988   1.900  -1.153  1.00  0.00           H  
CONECT    1    2   22   23
CONECT    2    3   19   24
CONECT    3    4   25   26
CONECT    4    5   27   28
CONECT    5    6   29   30
CONECT    6    7   31   32
CONECT    7    8   33
CONECT    8    9   34   35
CONECT    9   10   11   17
CONECT   10   36
CONECT   11   12
CONECT   12   13   15   37
CONECT   13   14   38   39
CONECT   14   40
CONECT   15   16   17   41
CONECT   16   42
CONECT   17   18   43
CONECT   18   44
CONECT   19   20   20   21
CONECT   21   45
END

HMDB0062186
     RDKit          3D
1-Deoxy-1-(N6-lysino)-D-fructose
 45 45  0  0  0  0  0  0  0  0999 V2000
    5.5405    1.3253    1.2207 N   0  0  0  0  0  0  0  0  0  0  0  0
    5.2510    0.1159    0.4754 C   0  0  1  0  0  0  0  0  0  0  0  0
    3.8058   -0.3025    0.6265 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8672    0.7776    0.1106 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4312    0.3568    0.2714 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1321   -0.9271   -0.4821 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2502   -1.2900   -0.2985 N   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1760   -0.3906   -0.9486 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5763   -0.8965   -0.6375 C   0  0  1  0  0  0  0  0  0  0  0  0
   -2.6866   -2.2007   -1.1339 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7689   -0.8276    0.7358 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7040    0.1804    0.9571 C   0  0  2  0  0  0  0  0  0  0  0  0
   -4.3929    0.0935    2.2739 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3887    0.1770    3.2653 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.6638    0.0545   -0.2350 C   0  0  1  0  0  0  0  0  0  0  0  0
   -5.4529    1.1846   -0.3710 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6288   -0.0682   -1.3270 C   0  0  2  0  0  0  0  0  0  0  0  0
   -4.1433   -0.6763   -2.4654 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.5836    0.3181   -0.9754 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.4163   -0.6072   -1.8260 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.0849    1.5114   -1.4651 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.0054    2.1003    0.7703 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.2728    1.2501    2.2037 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.8803   -0.7012    0.8573 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.6899   -1.2070   -0.0257 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.6152   -0.5727    1.6626 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.0109    1.6947    0.7197 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.0956    0.9632   -0.9521 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.2166    0.2082    1.3521 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.8132    1.2067   -0.1075 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.7302   -1.7370   -0.0005 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.3927   -0.7822   -1.5317 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3952   -2.2545   -0.6363 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0009   -0.2864   -2.0228 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0889    0.5941   -0.4282 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1150   -2.8250   -0.5010 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1940    1.1428    0.8796 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.9962    1.0143    2.4134 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.9770   -0.8260    2.4184 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8774    1.0211    3.1698 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.2666   -0.8855   -0.1280 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.3573    0.9545   -0.7598 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2807    0.9684   -1.5292 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4415   -0.8495   -3.1273 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.9877    1.9001   -1.1526 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  2  3  1  0
  3  4  1  0
  4  5  1  0
  5  6  1  0
  6  7  1  0
  7  8  1  0
  8  9  1  0
  9 10  1  6
  9 11  1  0
 11 12  1  0
 12 13  1  0
 13 14  1  0
 12 15  1  0
 15 16  1  0
 15 17  1  0
 17 18  1  0
  2 19  1  0
 19 20  2  0
 19 21  1  0
 17  9  1  0
  1 22  1  0
  1 23  1  0
  2 24  1  1
  3 25  1  0
  3 26  1  0
  4 27  1  0
  4 28  1  0
  5 29  1  0
  5 30  1  0
  6 31  1  0
  6 32  1  0
  7 33  1  0
  8 34  1  0
  8 35  1  0
 10 36  1  0
 12 37  1  6
 13 38  1  0
 13 39  1  0
 14 40  1  0
 15 41  1  1
 16 42  1  0
 17 43  1  6
 18 44  1  0
 21 45  1  0
M  END

View in JSmol View NMR Assignments View Stereo Labels

Synonyms

Value	Source
(2S)-2-Amino-6-({[(2R,3S,4S,5R)-2,3,4-trihydroxy-5-(hydroxymethyl)oxolan-2-yl]methyl}amino)hexanoate	Generator
1-Deoxy-1-(N6-lysino)-D-fructose	HMDB
N6-(1-Deoxy-beta-D-fructopyranos-1-yl)-L-lysine	HMDB
N6-(1-Deoxy-β-D-fructopyranos-1-yl)-L-lysine	HMDB
Nepsilon-Fructosyllysine	HMDB
Nε-Fructosyllysine	HMDB

Chemical Formula

C₁₂H₂₄N₂O₇

Average Molecular Weight

308.331

Monoisotopic Molecular Weight

308.158351121

IUPAC Name

(2S)-2-amino-6-({[(2R,3S,4S,5R)-2,3,4-trihydroxy-5-(hydroxymethyl)oxolan-2-yl]methyl}amino)hexanoic acid

Traditional Name

(2S)-2-amino-6-({[(2R,3S,4S,5R)-2,3,4-trihydroxy-5-(hydroxymethyl)oxolan-2-yl]methyl}amino)hexanoic acid

CAS Registry Number

78525-25-4

SMILES

N[C@@H](CCCCNC[C@@]1(O)O[C@H](CO)[C@@H](O)[C@@H]1O)C(O)=O

InChI Identifier

InChI=1S/C12H24N2O7/c13-7(11(18)19)3-1-2-4-14-6-12(20)10(17)9(16)8(5-15)21-12/h7-10,14-17,20H,1-6,13H2,(H,18,19)/t7-,8+,9+,10-,12+/m0/s1

InChI Key

ZAWLGBRDVQURAK-TYCYOEEFSA-N

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as c-glycosyl compounds. These are glycoside in which a sugar group is bonded through one carbon to another group via a C-glycosidic bond.

Kingdom

Organic compounds

Super Class

Organic oxygen compounds

Class

Organooxygen compounds

Sub Class

Carbohydrates and carbohydrate conjugates

Direct Parent

C-glycosyl compounds

Alternative Parents

Substituents

C-glycosyl compound
L-alpha-amino acid
Pentose monosaccharide
Alpha-amino acid or derivatives
Alpha-amino acid
Medium-chain fatty acid
Hydroxy fatty acid
Heterocyclic fatty acid
Amino fatty acid
Fatty acyl
Fatty acid
Monosaccharide
Tetrahydrofuran
Amino acid
Secondary alcohol
Hemiacetal
Amino acid or derivatives
Oxacycle
Organoheterocyclic compound
Secondary amine
Polyol
Monocarboxylic acid or derivatives
Secondary aliphatic amine
Carboxylic acid
Carboxylic acid derivative
Organic nitrogen compound
Organopnictogen compound
Organic oxide
Hydrocarbon derivative
Primary amine
Primary alcohol
Organonitrogen compound
Primary aliphatic amine
Carbonyl group
Amine
Alcohol
Aliphatic heteromonocyclic compound

Molecular Framework

Aliphatic heteromonocyclic compounds

External Descriptors

Not Available

Ontology

Not Available

Sweat (PMID: 26755145)

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	142 g/l	ALOGPS
LogP	-3.52	ALOGPS

Experimental Chromatographic Properties

Not Available

Predicted Molecular Properties

Property	Value	Source
logP	-2.9	ALOGPS
logP	-5.1	ChemAxon
logS	-0.76	ALOGPS
pKa (Strongest Acidic)	2.05	ChemAxon
pKa (Strongest Basic)	9.55	ChemAxon
Physiological Charge	1	ChemAxon
Hydrogen Acceptor Count	9	ChemAxon
Hydrogen Donor Count	7	ChemAxon
Polar Surface Area	165.5 Å²	ChemAxon
Rotatable Bond Count	9	ChemAxon
Refractivity	70.68 m³·mol⁻¹	ChemAxon
Polarizability	31.04 Å³	ChemAxon
Number of Rings	1	ChemAxon
Bioavailability	Yes	ChemAxon
Rule of Five	No	ChemAxon
Ghose Filter	No	ChemAxon
Veber's Rule	No	ChemAxon
MDDR-like Rule	No	ChemAxon

Predicted Chromatographic Properties

Predicted Collision Cross Sections

Predictor	Adduct Type	CCS Value (Å²)	Reference
DeepCCS	[M+H]+	174.582	30932474
DeepCCS	[M-H]-	172.218	30932474
DeepCCS	[M-2H]-	206.535	30932474
DeepCCS	[M+Na]+	182.701	30932474

Predicted Kovats Retention Indices

Underivatized

Metabolite	SMILES	Kovats RI Value	Column Type	Reference
1-Deoxy-1-(N6-lysino)-D-fructose	N[C@@H](CCCCNC[C@@]1(O)O[C@H](CO)[C@@H](O)[C@@H]1O)C(O)=O	3678.4	Standard polar	33892256
1-Deoxy-1-(N6-lysino)-D-fructose	N[C@@H](CCCCNC[C@@]1(O)O[C@H](CO)[C@@H](O)[C@@H]1O)C(O)=O	2878.0	Standard non polar	33892256
1-Deoxy-1-(N6-lysino)-D-fructose	N[C@@H](CCCCNC[C@@]1(O)O[C@H](CO)[C@@H](O)[C@@H]1O)C(O)=O	2678.3	Semi standard non polar	33892256

Derivatized

Derivative Name / Structure	SMILES	Kovats RI Value	Column Type	Reference
1-Deoxy-1-(N6-lysino)-D-fructose,1TMS,isomer #1	C[Si](C)(C)O[C@]1(CNCCCC[C@H](N)C(=O)O)O[C@H](CO)[C@@H](O)[C@@H]1O	2713.9	Semi standard non polar	33892256
1-Deoxy-1-(N6-lysino)-D-fructose,1TMS,isomer #2	C[Si](C)(C)OC[C@H]1O[C@](O)(CNCCCC[C@H](N)C(=O)O)[C@@H](O)[C@@H]1O	2704.7	Semi standard non polar	33892256
1-Deoxy-1-(N6-lysino)-D-fructose,1TMS,isomer #3	C[Si](C)(C)O[C@H]1[C@H](O)[C@@](O)(CNCCCC[C@H](N)C(=O)O)O[C@@H]1CO	2710.6	Semi standard non polar	33892256
1-Deoxy-1-(N6-lysino)-D-fructose,1TMS,isomer #4	C[Si](C)(C)O[C@H]1[C@H](O)[C@@H](CO)O[C@]1(O)CNCCCC[C@H](N)C(=O)O	2715.7	Semi standard non polar	33892256
1-Deoxy-1-(N6-lysino)-D-fructose,1TMS,isomer #5	C[Si](C)(C)OC(=O)[C@@H](N)CCCCNC[C@@]1(O)O[C@H](CO)[C@@H](O)[C@@H]1O	2619.9	Semi standard non polar	33892256
1-Deoxy-1-(N6-lysino)-D-fructose,1TMS,isomer #6	C[Si](C)(C)N[C@@H](CCCCNC[C@@]1(O)O[C@H](CO)[C@@H](O)[C@@H]1O)C(=O)O	2746.1	Semi standard non polar	33892256
1-Deoxy-1-(N6-lysino)-D-fructose,1TMS,isomer #7	C[Si](C)(C)N(CCCC[C@H](N)C(=O)O)C[C@@]1(O)O[C@H](CO)[C@@H](O)[C@@H]1O	2767.7	Semi standard non polar	33892256
1-Deoxy-1-(N6-lysino)-D-fructose,2TMS,isomer #1	C[Si](C)(C)OC(=O)[C@@H](N)CCCCNC[C@@]1(O[Si](C)(C)C)O[C@H](CO)[C@@H](O)[C@@H]1O	2612.7	Semi standard non polar	33892256
1-Deoxy-1-(N6-lysino)-D-fructose,2TMS,isomer #10	C[Si](C)(C)N[C@@H](CCCCNC[C@@]1(O)O[C@H](CO[Si](C)(C)C)[C@@H](O)[C@@H]1O)C(=O)O	2717.9	Semi standard non polar	33892256
1-Deoxy-1-(N6-lysino)-D-fructose,2TMS,isomer #11	C[Si](C)(C)OC[C@H]1O[C@](O)(CN(CCCC[C@H](N)C(=O)O)[Si](C)(C)C)[C@@H](O)[C@@H]1O	2759.7	Semi standard non polar	33892256
1-Deoxy-1-(N6-lysino)-D-fructose,2TMS,isomer #12	C[Si](C)(C)O[C@H]1[C@H](O[Si](C)(C)C)[C@@H](CO)O[C@]1(O)CNCCCC[C@H](N)C(=O)O	2679.1	Semi standard non polar	33892256
1-Deoxy-1-(N6-lysino)-D-fructose,2TMS,isomer #13	C[Si](C)(C)OC(=O)[C@@H](N)CCCCNC[C@@]1(O)O[C@H](CO)[C@@H](O[Si](C)(C)C)[C@@H]1O	2614.0	Semi standard non polar	33892256
1-Deoxy-1-(N6-lysino)-D-fructose,2TMS,isomer #14	C[Si](C)(C)N[C@@H](CCCCNC[C@@]1(O)O[C@H](CO)[C@@H](O[Si](C)(C)C)[C@@H]1O)C(=O)O	2723.1	Semi standard non polar	33892256
1-Deoxy-1-(N6-lysino)-D-fructose,2TMS,isomer #15	C[Si](C)(C)O[C@H]1[C@H](O)[C@@](O)(CN(CCCC[C@H](N)C(=O)O)[Si](C)(C)C)O[C@@H]1CO	2747.6	Semi standard non polar	33892256
1-Deoxy-1-(N6-lysino)-D-fructose,2TMS,isomer #16	C[Si](C)(C)OC(=O)[C@@H](N)CCCCNC[C@@]1(O)O[C@H](CO)[C@@H](O)[C@@H]1O[Si](C)(C)C	2628.1	Semi standard non polar	33892256
1-Deoxy-1-(N6-lysino)-D-fructose,2TMS,isomer #17	C[Si](C)(C)N[C@@H](CCCCNC[C@@]1(O)O[C@H](CO)[C@@H](O)[C@@H]1O[Si](C)(C)C)C(=O)O	2729.3	Semi standard non polar	33892256
1-Deoxy-1-(N6-lysino)-D-fructose,2TMS,isomer #18	C[Si](C)(C)O[C@H]1[C@H](O)[C@@H](CO)O[C@]1(O)CN(CCCC[C@H](N)C(=O)O)[Si](C)(C)C	2764.5	Semi standard non polar	33892256
1-Deoxy-1-(N6-lysino)-D-fructose,2TMS,isomer #19	C[Si](C)(C)N[C@@H](CCCCNC[C@@]1(O)O[C@H](CO)[C@@H](O)[C@@H]1O)C(=O)O[Si](C)(C)C	2660.4	Semi standard non polar	33892256
1-Deoxy-1-(N6-lysino)-D-fructose,2TMS,isomer #2	C[Si](C)(C)OC[C@H]1O[C@@](CNCCCC[C@H](N)C(=O)O)(O[Si](C)(C)C)[C@@H](O)[C@@H]1O	2685.3	Semi standard non polar	33892256
1-Deoxy-1-(N6-lysino)-D-fructose,2TMS,isomer #20	C[Si](C)(C)OC(=O)[C@@H](N)CCCCN(C[C@@]1(O)O[C@H](CO)[C@@H](O)[C@@H]1O)[Si](C)(C)C	2694.3	Semi standard non polar	33892256
1-Deoxy-1-(N6-lysino)-D-fructose,2TMS,isomer #21	C[Si](C)(C)N([C@@H](CCCCNC[C@@]1(O)O[C@H](CO)[C@@H](O)[C@@H]1O)C(=O)O)[Si](C)(C)C	2834.1	Semi standard non polar	33892256
1-Deoxy-1-(N6-lysino)-D-fructose,2TMS,isomer #22	C[Si](C)(C)N[C@@H](CCCCN(C[C@@]1(O)O[C@H](CO)[C@@H](O)[C@@H]1O)[Si](C)(C)C)C(=O)O	2809.0	Semi standard non polar	33892256
1-Deoxy-1-(N6-lysino)-D-fructose,2TMS,isomer #3	C[Si](C)(C)O[C@H]1[C@H](O)[C@](CNCCCC[C@H](N)C(=O)O)(O[Si](C)(C)C)O[C@@H]1CO	2677.7	Semi standard non polar	33892256
1-Deoxy-1-(N6-lysino)-D-fructose,2TMS,isomer #4	C[Si](C)(C)O[C@H]1[C@H](O)[C@@H](CO)O[C@@]1(CNCCCC[C@H](N)C(=O)O)O[Si](C)(C)C	2693.9	Semi standard non polar	33892256
1-Deoxy-1-(N6-lysino)-D-fructose,2TMS,isomer #5	C[Si](C)(C)N[C@@H](CCCCNC[C@@]1(O[Si](C)(C)C)O[C@H](CO)[C@@H](O)[C@@H]1O)C(=O)O	2742.2	Semi standard non polar	33892256
1-Deoxy-1-(N6-lysino)-D-fructose,2TMS,isomer #6	C[Si](C)(C)O[C@]1(CN(CCCC[C@H](N)C(=O)O)[Si](C)(C)C)O[C@H](CO)[C@@H](O)[C@@H]1O	2774.5	Semi standard non polar	33892256
1-Deoxy-1-(N6-lysino)-D-fructose,2TMS,isomer #7	C[Si](C)(C)OC[C@H]1O[C@](O)(CNCCCC[C@H](N)C(=O)O[Si](C)(C)C)[C@@H](O)[C@@H]1O	2605.2	Semi standard non polar	33892256
1-Deoxy-1-(N6-lysino)-D-fructose,2TMS,isomer #8	C[Si](C)(C)OC[C@H]1O[C@](O)(CNCCCC[C@H](N)C(=O)O)[C@@H](O[Si](C)(C)C)[C@@H]1O	2684.9	Semi standard non polar	33892256
1-Deoxy-1-(N6-lysino)-D-fructose,2TMS,isomer #9	C[Si](C)(C)OC[C@H]1O[C@](O)(CNCCCC[C@H](N)C(=O)O)[C@@H](O)[C@@H]1O[Si](C)(C)C	2660.9	Semi standard non polar	33892256
1-Deoxy-1-(N6-lysino)-D-fructose,3TMS,isomer #1	C[Si](C)(C)OC[C@H]1O[C@@](CNCCCC[C@H](N)C(=O)O[Si](C)(C)C)(O[Si](C)(C)C)[C@@H](O)[C@@H]1O	2592.5	Semi standard non polar	33892256
1-Deoxy-1-(N6-lysino)-D-fructose,3TMS,isomer #10	C[Si](C)(C)O[C@H]1[C@H](O[Si](C)(C)C)[C@@H](CO)O[C@@]1(CNCCCC[C@H](N)C(=O)O)O[Si](C)(C)C	2646.2	Semi standard non polar	33892256
1-Deoxy-1-(N6-lysino)-D-fructose,3TMS,isomer #11	C[Si](C)(C)N[C@@H](CCCCNC[C@@]1(O[Si](C)(C)C)O[C@H](CO)[C@@H](O[Si](C)(C)C)[C@@H]1O)C(=O)O	2718.3	Semi standard non polar	33892256
1-Deoxy-1-(N6-lysino)-D-fructose,3TMS,isomer #12	C[Si](C)(C)O[C@H]1[C@H](O)[C@](CN(CCCC[C@H](N)C(=O)O)[Si](C)(C)C)(O[Si](C)(C)C)O[C@@H]1CO	2737.2	Semi standard non polar	33892256
1-Deoxy-1-(N6-lysino)-D-fructose,3TMS,isomer #13	C[Si](C)(C)N[C@@H](CCCCNC[C@@]1(O[Si](C)(C)C)O[C@H](CO)[C@@H](O)[C@@H]1O[Si](C)(C)C)C(=O)O	2718.3	Semi standard non polar	33892256
1-Deoxy-1-(N6-lysino)-D-fructose,3TMS,isomer #14	C[Si](C)(C)O[C@H]1[C@H](O)[C@@H](CO)O[C@@]1(CN(CCCC[C@H](N)C(=O)O)[Si](C)(C)C)O[Si](C)(C)C	2755.7	Semi standard non polar	33892256
1-Deoxy-1-(N6-lysino)-D-fructose,3TMS,isomer #15	C[Si](C)(C)O[C@]1(CNCCCC[C@@H](C(=O)O)N([Si](C)(C)C)[Si](C)(C)C)O[C@H](CO)[C@@H](O)[C@@H]1O	2816.1	Semi standard non polar	33892256
1-Deoxy-1-(N6-lysino)-D-fructose,3TMS,isomer #16	C[Si](C)(C)N[C@@H](CCCCN(C[C@@]1(O[Si](C)(C)C)O[C@H](CO)[C@@H](O)[C@@H]1O)[Si](C)(C)C)C(=O)O	2800.1	Semi standard non polar	33892256
1-Deoxy-1-(N6-lysino)-D-fructose,3TMS,isomer #17	C[Si](C)(C)OC[C@H]1O[C@](O)(CNCCCC[C@H](N)C(=O)O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@@H]1O	2620.2	Semi standard non polar	33892256
1-Deoxy-1-(N6-lysino)-D-fructose,3TMS,isomer #18	C[Si](C)(C)OC[C@H]1O[C@](O)(CNCCCC[C@H](N)C(=O)O[Si](C)(C)C)[C@@H](O)[C@@H]1O[Si](C)(C)C	2583.4	Semi standard non polar	33892256
1-Deoxy-1-(N6-lysino)-D-fructose,3TMS,isomer #19	C[Si](C)(C)N[C@@H](CCCCNC[C@@]1(O)O[C@H](CO[Si](C)(C)C)[C@@H](O)[C@@H]1O)C(=O)O[Si](C)(C)C	2630.2	Semi standard non polar	33892256
1-Deoxy-1-(N6-lysino)-D-fructose,3TMS,isomer #2	C[Si](C)(C)OC(=O)[C@@H](N)CCCCNC[C@@]1(O[Si](C)(C)C)O[C@H](CO)[C@@H](O[Si](C)(C)C)[C@@H]1O	2600.9	Semi standard non polar	33892256
1-Deoxy-1-(N6-lysino)-D-fructose,3TMS,isomer #20	C[Si](C)(C)OC[C@H]1O[C@](O)(CN(CCCC[C@H](N)C(=O)O[Si](C)(C)C)[Si](C)(C)C)[C@@H](O)[C@@H]1O	2687.1	Semi standard non polar	33892256
1-Deoxy-1-(N6-lysino)-D-fructose,3TMS,isomer #21	C[Si](C)(C)OC[C@H]1O[C@](O)(CNCCCC[C@H](N)C(=O)O)[C@@H](O[Si](C)(C)C)[C@@H]1O[Si](C)(C)C	2636.2	Semi standard non polar	33892256
1-Deoxy-1-(N6-lysino)-D-fructose,3TMS,isomer #22	C[Si](C)(C)N[C@@H](CCCCNC[C@@]1(O)O[C@H](CO[Si](C)(C)C)[C@@H](O)[C@@H]1O[Si](C)(C)C)C(=O)O	2718.9	Semi standard non polar	33892256
1-Deoxy-1-(N6-lysino)-D-fructose,3TMS,isomer #23	C[Si](C)(C)OC[C@H]1O[C@](O)(CN(CCCC[C@H](N)C(=O)O)[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@@H]1O	2741.9	Semi standard non polar	33892256
1-Deoxy-1-(N6-lysino)-D-fructose,3TMS,isomer #24	C[Si](C)(C)N[C@@H](CCCCNC[C@@]1(O)O[C@H](CO[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@@H]1O)C(=O)O	2701.7	Semi standard non polar	33892256
1-Deoxy-1-(N6-lysino)-D-fructose,3TMS,isomer #25	C[Si](C)(C)OC[C@H]1O[C@](O)(CN(CCCC[C@H](N)C(=O)O)[Si](C)(C)C)[C@@H](O)[C@@H]1O[Si](C)(C)C	2713.5	Semi standard non polar	33892256
1-Deoxy-1-(N6-lysino)-D-fructose,3TMS,isomer #26	C[Si](C)(C)OC[C@H]1O[C@](O)(CNCCCC[C@@H](C(=O)O)N([Si](C)(C)C)[Si](C)(C)C)[C@@H](O)[C@@H]1O	2816.7	Semi standard non polar	33892256
1-Deoxy-1-(N6-lysino)-D-fructose,3TMS,isomer #27	C[Si](C)(C)N[C@@H](CCCCN(C[C@@]1(O)O[C@H](CO[Si](C)(C)C)[C@@H](O)[C@@H]1O)[Si](C)(C)C)C(=O)O	2780.0	Semi standard non polar	33892256
1-Deoxy-1-(N6-lysino)-D-fructose,3TMS,isomer #28	C[Si](C)(C)OC(=O)[C@@H](N)CCCCNC[C@@]1(O)O[C@H](CO)[C@@H](O[Si](C)(C)C)[C@@H]1O[Si](C)(C)C	2613.6	Semi standard non polar	33892256
1-Deoxy-1-(N6-lysino)-D-fructose,3TMS,isomer #29	C[Si](C)(C)N[C@@H](CCCCNC[C@@]1(O)O[C@H](CO)[C@@H](O[Si](C)(C)C)[C@@H]1O[Si](C)(C)C)C(=O)O	2703.0	Semi standard non polar	33892256
1-Deoxy-1-(N6-lysino)-D-fructose,3TMS,isomer #3	C[Si](C)(C)OC(=O)[C@@H](N)CCCCNC[C@@]1(O[Si](C)(C)C)O[C@H](CO)[C@@H](O)[C@@H]1O[Si](C)(C)C	2618.9	Semi standard non polar	33892256
1-Deoxy-1-(N6-lysino)-D-fructose,3TMS,isomer #30	C[Si](C)(C)O[C@H]1[C@H](O[Si](C)(C)C)[C@@H](CO)O[C@]1(O)CN(CCCC[C@H](N)C(=O)O)[Si](C)(C)C	2708.8	Semi standard non polar	33892256
1-Deoxy-1-(N6-lysino)-D-fructose,3TMS,isomer #31	C[Si](C)(C)N[C@@H](CCCCNC[C@@]1(O)O[C@H](CO)[C@@H](O[Si](C)(C)C)[C@@H]1O)C(=O)O[Si](C)(C)C	2641.8	Semi standard non polar	33892256
1-Deoxy-1-(N6-lysino)-D-fructose,3TMS,isomer #32	C[Si](C)(C)OC(=O)[C@@H](N)CCCCN(C[C@@]1(O)O[C@H](CO)[C@@H](O[Si](C)(C)C)[C@@H]1O)[Si](C)(C)C	2679.1	Semi standard non polar	33892256
1-Deoxy-1-(N6-lysino)-D-fructose,3TMS,isomer #33	C[Si](C)(C)O[C@H]1[C@H](O)[C@@](O)(CNCCCC[C@@H](C(=O)O)N([Si](C)(C)C)[Si](C)(C)C)O[C@@H]1CO	2784.8	Semi standard non polar	33892256
1-Deoxy-1-(N6-lysino)-D-fructose,3TMS,isomer #34	C[Si](C)(C)N[C@@H](CCCCN(C[C@@]1(O)O[C@H](CO)[C@@H](O[Si](C)(C)C)[C@@H]1O)[Si](C)(C)C)C(=O)O	2771.5	Semi standard non polar	33892256
1-Deoxy-1-(N6-lysino)-D-fructose,3TMS,isomer #35	C[Si](C)(C)N[C@@H](CCCCNC[C@@]1(O)O[C@H](CO)[C@@H](O)[C@@H]1O[Si](C)(C)C)C(=O)O[Si](C)(C)C	2656.0	Semi standard non polar	33892256
1-Deoxy-1-(N6-lysino)-D-fructose,3TMS,isomer #36	C[Si](C)(C)OC(=O)[C@@H](N)CCCCN(C[C@@]1(O)O[C@H](CO)[C@@H](O)[C@@H]1O[Si](C)(C)C)[Si](C)(C)C	2694.0	Semi standard non polar	33892256
1-Deoxy-1-(N6-lysino)-D-fructose,3TMS,isomer #37	C[Si](C)(C)O[C@H]1[C@H](O)[C@@H](CO)O[C@]1(O)CNCCCC[C@@H](C(=O)O)N([Si](C)(C)C)[Si](C)(C)C	2807.6	Semi standard non polar	33892256
1-Deoxy-1-(N6-lysino)-D-fructose,3TMS,isomer #38	C[Si](C)(C)N[C@@H](CCCCN(C[C@@]1(O)O[C@H](CO)[C@@H](O)[C@@H]1O[Si](C)(C)C)[Si](C)(C)C)C(=O)O	2782.8	Semi standard non polar	33892256
1-Deoxy-1-(N6-lysino)-D-fructose,3TMS,isomer #39	C[Si](C)(C)OC(=O)[C@H](CCCCNC[C@@]1(O)O[C@H](CO)[C@@H](O)[C@@H]1O)N([Si](C)(C)C)[Si](C)(C)C	2798.0	Semi standard non polar	33892256
1-Deoxy-1-(N6-lysino)-D-fructose,3TMS,isomer #4	C[Si](C)(C)N[C@@H](CCCCNC[C@@]1(O[Si](C)(C)C)O[C@H](CO)[C@@H](O)[C@@H]1O)C(=O)O[Si](C)(C)C	2645.1	Semi standard non polar	33892256
1-Deoxy-1-(N6-lysino)-D-fructose,3TMS,isomer #40	C[Si](C)(C)N[C@@H](CCCCN(C[C@@]1(O)O[C@H](CO)[C@@H](O)[C@@H]1O)[Si](C)(C)C)C(=O)O[Si](C)(C)C	2730.3	Semi standard non polar	33892256
1-Deoxy-1-(N6-lysino)-D-fructose,3TMS,isomer #41	C[Si](C)(C)N(CCCC[C@@H](C(=O)O)N([Si](C)(C)C)[Si](C)(C)C)C[C@@]1(O)O[C@H](CO)[C@@H](O)[C@@H]1O	2864.6	Semi standard non polar	33892256
1-Deoxy-1-(N6-lysino)-D-fructose,3TMS,isomer #5	C[Si](C)(C)OC(=O)[C@@H](N)CCCCN(C[C@@]1(O[Si](C)(C)C)O[C@H](CO)[C@@H](O)[C@@H]1O)[Si](C)(C)C	2706.8	Semi standard non polar	33892256
1-Deoxy-1-(N6-lysino)-D-fructose,3TMS,isomer #6	C[Si](C)(C)OC[C@H]1O[C@@](CNCCCC[C@H](N)C(=O)O)(O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@@H]1O	2654.1	Semi standard non polar	33892256
1-Deoxy-1-(N6-lysino)-D-fructose,3TMS,isomer #7	C[Si](C)(C)OC[C@H]1O[C@@](CNCCCC[C@H](N)C(=O)O)(O[Si](C)(C)C)[C@@H](O)[C@@H]1O[Si](C)(C)C	2642.5	Semi standard non polar	33892256
1-Deoxy-1-(N6-lysino)-D-fructose,3TMS,isomer #8	C[Si](C)(C)N[C@@H](CCCCNC[C@@]1(O[Si](C)(C)C)O[C@H](CO[Si](C)(C)C)[C@@H](O)[C@@H]1O)C(=O)O	2725.6	Semi standard non polar	33892256
1-Deoxy-1-(N6-lysino)-D-fructose,3TMS,isomer #9	C[Si](C)(C)OC[C@H]1O[C@@](CN(CCCC[C@H](N)C(=O)O)[Si](C)(C)C)(O[Si](C)(C)C)[C@@H](O)[C@@H]1O	2756.1	Semi standard non polar	33892256
1-Deoxy-1-(N6-lysino)-D-fructose,4TMS,isomer #1	C[Si](C)(C)OC[C@H]1O[C@@](CNCCCC[C@H](N)C(=O)O[Si](C)(C)C)(O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@@H]1O	2597.1	Semi standard non polar	33892256
1-Deoxy-1-(N6-lysino)-D-fructose,4TMS,isomer #10	C[Si](C)(C)OC(=O)[C@H](CCCCNC[C@@]1(O[Si](C)(C)C)O[C@H](CO)[C@@H](O)[C@@H]1O)N([Si](C)(C)C)[Si](C)(C)C	2790.6	Semi standard non polar	33892256
1-Deoxy-1-(N6-lysino)-D-fructose,4TMS,isomer #11	C[Si](C)(C)N[C@@H](CCCCN(C[C@@]1(O[Si](C)(C)C)O[C@H](CO)[C@@H](O)[C@@H]1O)[Si](C)(C)C)C(=O)O[Si](C)(C)C	2743.1	Semi standard non polar	33892256
1-Deoxy-1-(N6-lysino)-D-fructose,4TMS,isomer #12	C[Si](C)(C)OC[C@H]1O[C@@](CNCCCC[C@H](N)C(=O)O)(O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@@H]1O[Si](C)(C)C	2578.3	Semi standard non polar	33892256
1-Deoxy-1-(N6-lysino)-D-fructose,4TMS,isomer #13	C[Si](C)(C)N[C@@H](CCCCNC[C@@]1(O[Si](C)(C)C)O[C@H](CO[Si](C)(C)C)[C@@H](O)[C@@H]1O[Si](C)(C)C)C(=O)O	2711.7	Semi standard non polar	33892256
1-Deoxy-1-(N6-lysino)-D-fructose,4TMS,isomer #14	C[Si](C)(C)OC[C@H]1O[C@@](CN(CCCC[C@H](N)C(=O)O)[Si](C)(C)C)(O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@@H]1O	2730.7	Semi standard non polar	33892256
1-Deoxy-1-(N6-lysino)-D-fructose,4TMS,isomer #15	C[Si](C)(C)N[C@@H](CCCCNC[C@@]1(O[Si](C)(C)C)O[C@H](CO[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@@H]1O)C(=O)O	2707.2	Semi standard non polar	33892256
1-Deoxy-1-(N6-lysino)-D-fructose,4TMS,isomer #16	C[Si](C)(C)OC[C@H]1O[C@@](CN(CCCC[C@H](N)C(=O)O)[Si](C)(C)C)(O[Si](C)(C)C)[C@@H](O)[C@@H]1O[Si](C)(C)C	2707.6	Semi standard non polar	33892256
1-Deoxy-1-(N6-lysino)-D-fructose,4TMS,isomer #17	C[Si](C)(C)OC[C@H]1O[C@@](CNCCCC[C@@H](C(=O)O)N([Si](C)(C)C)[Si](C)(C)C)(O[Si](C)(C)C)[C@@H](O)[C@@H]1O	2812.0	Semi standard non polar	33892256
1-Deoxy-1-(N6-lysino)-D-fructose,4TMS,isomer #18	C[Si](C)(C)N[C@@H](CCCCN(C[C@@]1(O[Si](C)(C)C)O[C@H](CO[Si](C)(C)C)[C@@H](O)[C@@H]1O)[Si](C)(C)C)C(=O)O	2795.7	Semi standard non polar	33892256
1-Deoxy-1-(N6-lysino)-D-fructose,4TMS,isomer #19	C[Si](C)(C)N[C@@H](CCCCNC[C@@]1(O[Si](C)(C)C)O[C@H](CO)[C@@H](O[Si](C)(C)C)[C@@H]1O[Si](C)(C)C)C(=O)O	2676.0	Semi standard non polar	33892256
1-Deoxy-1-(N6-lysino)-D-fructose,4TMS,isomer #2	C[Si](C)(C)OC[C@H]1O[C@@](CNCCCC[C@H](N)C(=O)O[Si](C)(C)C)(O[Si](C)(C)C)[C@@H](O)[C@@H]1O[Si](C)(C)C	2578.7	Semi standard non polar	33892256
1-Deoxy-1-(N6-lysino)-D-fructose,4TMS,isomer #20	C[Si](C)(C)O[C@H]1[C@H](O[Si](C)(C)C)[C@@H](CO)O[C@@]1(CN(CCCC[C@H](N)C(=O)O)[Si](C)(C)C)O[Si](C)(C)C	2722.8	Semi standard non polar	33892256
1-Deoxy-1-(N6-lysino)-D-fructose,4TMS,isomer #21	C[Si](C)(C)O[C@H]1[C@H](O)[C@](CNCCCC[C@@H](C(=O)O)N([Si](C)(C)C)[Si](C)(C)C)(O[Si](C)(C)C)O[C@@H]1CO	2797.0	Semi standard non polar	33892256
1-Deoxy-1-(N6-lysino)-D-fructose,4TMS,isomer #22	C[Si](C)(C)N[C@@H](CCCCN(C[C@@]1(O[Si](C)(C)C)O[C@H](CO)[C@@H](O[Si](C)(C)C)[C@@H]1O)[Si](C)(C)C)C(=O)O	2772.9	Semi standard non polar	33892256
1-Deoxy-1-(N6-lysino)-D-fructose,4TMS,isomer #23	C[Si](C)(C)O[C@H]1[C@H](O)[C@@H](CO)O[C@@]1(CNCCCC[C@@H](C(=O)O)N([Si](C)(C)C)[Si](C)(C)C)O[Si](C)(C)C	2800.7	Semi standard non polar	33892256
1-Deoxy-1-(N6-lysino)-D-fructose,4TMS,isomer #24	C[Si](C)(C)N[C@@H](CCCCN(C[C@@]1(O[Si](C)(C)C)O[C@H](CO)[C@@H](O)[C@@H]1O[Si](C)(C)C)[Si](C)(C)C)C(=O)O	2783.0	Semi standard non polar	33892256
1-Deoxy-1-(N6-lysino)-D-fructose,4TMS,isomer #25	C[Si](C)(C)O[C@]1(CN(CCCC[C@@H](C(=O)O)N([Si](C)(C)C)[Si](C)(C)C)[Si](C)(C)C)O[C@H](CO)[C@@H](O)[C@@H]1O	2868.0	Semi standard non polar	33892256
1-Deoxy-1-(N6-lysino)-D-fructose,4TMS,isomer #26	C[Si](C)(C)OC[C@H]1O[C@](O)(CNCCCC[C@H](N)C(=O)O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@@H]1O[Si](C)(C)C	2574.5	Semi standard non polar	33892256
1-Deoxy-1-(N6-lysino)-D-fructose,4TMS,isomer #27	C[Si](C)(C)N[C@@H](CCCCNC[C@@]1(O)O[C@H](CO[Si](C)(C)C)[C@@H](O)[C@@H]1O[Si](C)(C)C)C(=O)O[Si](C)(C)C	2665.5	Semi standard non polar	33892256
1-Deoxy-1-(N6-lysino)-D-fructose,4TMS,isomer #28	C[Si](C)(C)OC[C@H]1O[C@](O)(CN(CCCC[C@H](N)C(=O)O[Si](C)(C)C)[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@@H]1O	2692.1	Semi standard non polar	33892256
1-Deoxy-1-(N6-lysino)-D-fructose,4TMS,isomer #29	C[Si](C)(C)N[C@@H](CCCCNC[C@@]1(O)O[C@H](CO[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@@H]1O)C(=O)O[Si](C)(C)C	2634.7	Semi standard non polar	33892256
1-Deoxy-1-(N6-lysino)-D-fructose,4TMS,isomer #3	C[Si](C)(C)N[C@@H](CCCCNC[C@@]1(O[Si](C)(C)C)O[C@H](CO[Si](C)(C)C)[C@@H](O)[C@@H]1O)C(=O)O[Si](C)(C)C	2651.7	Semi standard non polar	33892256
1-Deoxy-1-(N6-lysino)-D-fructose,4TMS,isomer #30	C[Si](C)(C)OC[C@H]1O[C@](O)(CN(CCCC[C@H](N)C(=O)O[Si](C)(C)C)[Si](C)(C)C)[C@@H](O)[C@@H]1O[Si](C)(C)C	2659.9	Semi standard non polar	33892256
1-Deoxy-1-(N6-lysino)-D-fructose,4TMS,isomer #31	C[Si](C)(C)OC[C@H]1O[C@](O)(CNCCCC[C@@H](C(=O)O[Si](C)(C)C)N([Si](C)(C)C)[Si](C)(C)C)[C@@H](O)[C@@H]1O	2767.7	Semi standard non polar	33892256
1-Deoxy-1-(N6-lysino)-D-fructose,4TMS,isomer #32	C[Si](C)(C)N[C@@H](CCCCN(C[C@@]1(O)O[C@H](CO[Si](C)(C)C)[C@@H](O)[C@@H]1O)[Si](C)(C)C)C(=O)O[Si](C)(C)C	2716.7	Semi standard non polar	33892256
1-Deoxy-1-(N6-lysino)-D-fructose,4TMS,isomer #33	C[Si](C)(C)N[C@@H](CCCCNC[C@@]1(O)O[C@H](CO[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@@H]1O[Si](C)(C)C)C(=O)O	2687.8	Semi standard non polar	33892256
1-Deoxy-1-(N6-lysino)-D-fructose,4TMS,isomer #34	C[Si](C)(C)OC[C@H]1O[C@](O)(CN(CCCC[C@H](N)C(=O)O)[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@@H]1O[Si](C)(C)C	2670.5	Semi standard non polar	33892256
1-Deoxy-1-(N6-lysino)-D-fructose,4TMS,isomer #35	C[Si](C)(C)OC[C@H]1O[C@](O)(CNCCCC[C@@H](C(=O)O)N([Si](C)(C)C)[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@@H]1O	2801.5	Semi standard non polar	33892256
1-Deoxy-1-(N6-lysino)-D-fructose,4TMS,isomer #36	C[Si](C)(C)N[C@@H](CCCCN(C[C@@]1(O)O[C@H](CO[Si](C)(C)C)[C@@H](O)[C@@H]1O[Si](C)(C)C)[Si](C)(C)C)C(=O)O	2770.9	Semi standard non polar	33892256
1-Deoxy-1-(N6-lysino)-D-fructose,4TMS,isomer #37	C[Si](C)(C)OC[C@H]1O[C@](O)(CNCCCC[C@@H](C(=O)O)N([Si](C)(C)C)[Si](C)(C)C)[C@@H](O)[C@@H]1O[Si](C)(C)C	2782.5	Semi standard non polar	33892256
1-Deoxy-1-(N6-lysino)-D-fructose,4TMS,isomer #38	C[Si](C)(C)N[C@@H](CCCCN(C[C@@]1(O)O[C@H](CO[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@@H]1O)[Si](C)(C)C)C(=O)O	2748.0	Semi standard non polar	33892256
1-Deoxy-1-(N6-lysino)-D-fructose,4TMS,isomer #39	C[Si](C)(C)OC[C@H]1O[C@](O)(CN(CCCC[C@@H](C(=O)O)N([Si](C)(C)C)[Si](C)(C)C)[Si](C)(C)C)[C@@H](O)[C@@H]1O	2845.0	Semi standard non polar	33892256
1-Deoxy-1-(N6-lysino)-D-fructose,4TMS,isomer #4	C[Si](C)(C)OC[C@H]1O[C@@](CN(CCCC[C@H](N)C(=O)O[Si](C)(C)C)[Si](C)(C)C)(O[Si](C)(C)C)[C@@H](O)[C@@H]1O	2697.1	Semi standard non polar	33892256
1-Deoxy-1-(N6-lysino)-D-fructose,4TMS,isomer #40	C[Si](C)(C)N[C@@H](CCCCNC[C@@]1(O)O[C@H](CO)[C@@H](O[Si](C)(C)C)[C@@H]1O[Si](C)(C)C)C(=O)O[Si](C)(C)C	2638.6	Semi standard non polar	33892256
1-Deoxy-1-(N6-lysino)-D-fructose,4TMS,isomer #41	C[Si](C)(C)OC(=O)[C@@H](N)CCCCN(C[C@@]1(O)O[C@H](CO)[C@@H](O[Si](C)(C)C)[C@@H]1O[Si](C)(C)C)[Si](C)(C)C	2669.4	Semi standard non polar	33892256
1-Deoxy-1-(N6-lysino)-D-fructose,4TMS,isomer #42	C[Si](C)(C)O[C@H]1[C@H](O[Si](C)(C)C)[C@@H](CO)O[C@]1(O)CNCCCC[C@@H](C(=O)O)N([Si](C)(C)C)[Si](C)(C)C	2768.4	Semi standard non polar	33892256
1-Deoxy-1-(N6-lysino)-D-fructose,4TMS,isomer #43	C[Si](C)(C)N[C@@H](CCCCN(C[C@@]1(O)O[C@H](CO)[C@@H](O[Si](C)(C)C)[C@@H]1O[Si](C)(C)C)[Si](C)(C)C)C(=O)O	2728.5	Semi standard non polar	33892256
1-Deoxy-1-(N6-lysino)-D-fructose,4TMS,isomer #44	C[Si](C)(C)OC(=O)[C@H](CCCCNC[C@@]1(O)O[C@H](CO)[C@@H](O[Si](C)(C)C)[C@@H]1O)N([Si](C)(C)C)[Si](C)(C)C	2772.6	Semi standard non polar	33892256
1-Deoxy-1-(N6-lysino)-D-fructose,4TMS,isomer #45	C[Si](C)(C)N[C@@H](CCCCN(C[C@@]1(O)O[C@H](CO)[C@@H](O[Si](C)(C)C)[C@@H]1O)[Si](C)(C)C)C(=O)O[Si](C)(C)C	2713.8	Semi standard non polar	33892256
1-Deoxy-1-(N6-lysino)-D-fructose,4TMS,isomer #46	C[Si](C)(C)O[C@H]1[C@H](O)[C@@](O)(CN(CCCC[C@@H](C(=O)O)N([Si](C)(C)C)[Si](C)(C)C)[Si](C)(C)C)O[C@@H]1CO	2840.8	Semi standard non polar	33892256
1-Deoxy-1-(N6-lysino)-D-fructose,4TMS,isomer #47	C[Si](C)(C)OC(=O)[C@H](CCCCNC[C@@]1(O)O[C@H](CO)[C@@H](O)[C@@H]1O[Si](C)(C)C)N([Si](C)(C)C)[Si](C)(C)C	2798.3	Semi standard non polar	33892256
1-Deoxy-1-(N6-lysino)-D-fructose,4TMS,isomer #48	C[Si](C)(C)N[C@@H](CCCCN(C[C@@]1(O)O[C@H](CO)[C@@H](O)[C@@H]1O[Si](C)(C)C)[Si](C)(C)C)C(=O)O[Si](C)(C)C	2729.2	Semi standard non polar	33892256
1-Deoxy-1-(N6-lysino)-D-fructose,4TMS,isomer #49	C[Si](C)(C)O[C@H]1[C@H](O)[C@@H](CO)O[C@]1(O)CN(CCCC[C@@H](C(=O)O)N([Si](C)(C)C)[Si](C)(C)C)[Si](C)(C)C	2862.9	Semi standard non polar	33892256
1-Deoxy-1-(N6-lysino)-D-fructose,4TMS,isomer #5	C[Si](C)(C)OC(=O)[C@@H](N)CCCCNC[C@@]1(O[Si](C)(C)C)O[C@H](CO)[C@@H](O[Si](C)(C)C)[C@@H]1O[Si](C)(C)C	2585.0	Semi standard non polar	33892256
1-Deoxy-1-(N6-lysino)-D-fructose,4TMS,isomer #50	C[Si](C)(C)OC(=O)[C@H](CCCCN(C[C@@]1(O)O[C@H](CO)[C@@H](O)[C@@H]1O)[Si](C)(C)C)N([Si](C)(C)C)[Si](C)(C)C	2847.9	Semi standard non polar	33892256
1-Deoxy-1-(N6-lysino)-D-fructose,4TMS,isomer #6	C[Si](C)(C)N[C@@H](CCCCNC[C@@]1(O[Si](C)(C)C)O[C@H](CO)[C@@H](O[Si](C)(C)C)[C@@H]1O)C(=O)O[Si](C)(C)C	2652.4	Semi standard non polar	33892256
1-Deoxy-1-(N6-lysino)-D-fructose,4TMS,isomer #7	C[Si](C)(C)OC(=O)[C@@H](N)CCCCN(C[C@@]1(O[Si](C)(C)C)O[C@H](CO)[C@@H](O[Si](C)(C)C)[C@@H]1O)[Si](C)(C)C	2696.0	Semi standard non polar	33892256
1-Deoxy-1-(N6-lysino)-D-fructose,4TMS,isomer #8	C[Si](C)(C)N[C@@H](CCCCNC[C@@]1(O[Si](C)(C)C)O[C@H](CO)[C@@H](O)[C@@H]1O[Si](C)(C)C)C(=O)O[Si](C)(C)C	2651.4	Semi standard non polar	33892256
1-Deoxy-1-(N6-lysino)-D-fructose,4TMS,isomer #9	C[Si](C)(C)OC(=O)[C@@H](N)CCCCN(C[C@@]1(O[Si](C)(C)C)O[C@H](CO)[C@@H](O)[C@@H]1O[Si](C)(C)C)[Si](C)(C)C	2715.9	Semi standard non polar	33892256
1-Deoxy-1-(N6-lysino)-D-fructose,5TMS,isomer #1	C[Si](C)(C)OC[C@H]1O[C@@](CNCCCC[C@H](N)C(=O)O[Si](C)(C)C)(O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@@H]1O[Si](C)(C)C	2535.8	Semi standard non polar	33892256
1-Deoxy-1-(N6-lysino)-D-fructose,5TMS,isomer #10	C[Si](C)(C)OC(=O)[C@H](CCCCNC[C@@]1(O[Si](C)(C)C)O[C@H](CO)[C@@H](O[Si](C)(C)C)[C@@H]1O)N([Si](C)(C)C)[Si](C)(C)C	2795.4	Semi standard non polar	33892256
1-Deoxy-1-(N6-lysino)-D-fructose,5TMS,isomer #11	C[Si](C)(C)N[C@@H](CCCCN(C[C@@]1(O[Si](C)(C)C)O[C@H](CO)[C@@H](O[Si](C)(C)C)[C@@H]1O)[Si](C)(C)C)C(=O)O[Si](C)(C)C	2733.8	Semi standard non polar	33892256
1-Deoxy-1-(N6-lysino)-D-fructose,5TMS,isomer #12	C[Si](C)(C)OC(=O)[C@H](CCCCNC[C@@]1(O[Si](C)(C)C)O[C@H](CO)[C@@H](O)[C@@H]1O[Si](C)(C)C)N([Si](C)(C)C)[Si](C)(C)C	2806.9	Semi standard non polar	33892256
1-Deoxy-1-(N6-lysino)-D-fructose,5TMS,isomer #13	C[Si](C)(C)N[C@@H](CCCCN(C[C@@]1(O[Si](C)(C)C)O[C@H](CO)[C@@H](O)[C@@H]1O[Si](C)(C)C)[Si](C)(C)C)C(=O)O[Si](C)(C)C	2749.1	Semi standard non polar	33892256
1-Deoxy-1-(N6-lysino)-D-fructose,5TMS,isomer #14	C[Si](C)(C)OC(=O)[C@H](CCCCN(C[C@@]1(O[Si](C)(C)C)O[C@H](CO)[C@@H](O)[C@@H]1O)[Si](C)(C)C)N([Si](C)(C)C)[Si](C)(C)C	2889.8	Semi standard non polar	33892256
1-Deoxy-1-(N6-lysino)-D-fructose,5TMS,isomer #15	C[Si](C)(C)N[C@@H](CCCCNC[C@@]1(O[Si](C)(C)C)O[C@H](CO[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@@H]1O[Si](C)(C)C)C(=O)O	2660.5	Semi standard non polar	33892256
1-Deoxy-1-(N6-lysino)-D-fructose,5TMS,isomer #16	C[Si](C)(C)OC[C@H]1O[C@@](CN(CCCC[C@H](N)C(=O)O)[Si](C)(C)C)(O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@@H]1O[Si](C)(C)C	2704.4	Semi standard non polar	33892256
1-Deoxy-1-(N6-lysino)-D-fructose,5TMS,isomer #17	C[Si](C)(C)OC[C@H]1O[C@@](CNCCCC[C@@H](C(=O)O)N([Si](C)(C)C)[Si](C)(C)C)(O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@@H]1O	2799.0	Semi standard non polar	33892256
1-Deoxy-1-(N6-lysino)-D-fructose,5TMS,isomer #18	C[Si](C)(C)N[C@@H](CCCCN(C[C@@]1(O[Si](C)(C)C)O[C@H](CO[Si](C)(C)C)[C@@H](O)[C@@H]1O[Si](C)(C)C)[Si](C)(C)C)C(=O)O	2774.1	Semi standard non polar	33892256
1-Deoxy-1-(N6-lysino)-D-fructose,5TMS,isomer #19	C[Si](C)(C)OC[C@H]1O[C@@](CNCCCC[C@@H](C(=O)O)N([Si](C)(C)C)[Si](C)(C)C)(O[Si](C)(C)C)[C@@H](O)[C@@H]1O[Si](C)(C)C	2796.4	Semi standard non polar	33892256
1-Deoxy-1-(N6-lysino)-D-fructose,5TMS,isomer #2	C[Si](C)(C)N[C@@H](CCCCNC[C@@]1(O[Si](C)(C)C)O[C@H](CO[Si](C)(C)C)[C@@H](O)[C@@H]1O[Si](C)(C)C)C(=O)O[Si](C)(C)C	2651.9	Semi standard non polar	33892256
1-Deoxy-1-(N6-lysino)-D-fructose,5TMS,isomer #20	C[Si](C)(C)N[C@@H](CCCCN(C[C@@]1(O[Si](C)(C)C)O[C@H](CO[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@@H]1O)[Si](C)(C)C)C(=O)O	2756.6	Semi standard non polar	33892256
1-Deoxy-1-(N6-lysino)-D-fructose,5TMS,isomer #21	C[Si](C)(C)OC[C@H]1O[C@@](CN(CCCC[C@@H](C(=O)O)N([Si](C)(C)C)[Si](C)(C)C)[Si](C)(C)C)(O[Si](C)(C)C)[C@@H](O)[C@@H]1O	2893.2	Semi standard non polar	33892256
1-Deoxy-1-(N6-lysino)-D-fructose,5TMS,isomer #22	C[Si](C)(C)O[C@H]1[C@H](O[Si](C)(C)C)[C@@H](CO)O[C@@]1(CNCCCC[C@@H](C(=O)O)N([Si](C)(C)C)[Si](C)(C)C)O[Si](C)(C)C	2779.0	Semi standard non polar	33892256
1-Deoxy-1-(N6-lysino)-D-fructose,5TMS,isomer #23	C[Si](C)(C)N[C@@H](CCCCN(C[C@@]1(O[Si](C)(C)C)O[C@H](CO)[C@@H](O[Si](C)(C)C)[C@@H]1O[Si](C)(C)C)[Si](C)(C)C)C(=O)O	2754.4	Semi standard non polar	33892256
1-Deoxy-1-(N6-lysino)-D-fructose,5TMS,isomer #24	C[Si](C)(C)O[C@H]1[C@H](O)[C@](CN(CCCC[C@@H](C(=O)O)N([Si](C)(C)C)[Si](C)(C)C)[Si](C)(C)C)(O[Si](C)(C)C)O[C@@H]1CO	2875.6	Semi standard non polar	33892256
1-Deoxy-1-(N6-lysino)-D-fructose,5TMS,isomer #25	C[Si](C)(C)O[C@H]1[C@H](O)[C@@H](CO)O[C@@]1(CN(CCCC[C@@H](C(=O)O)N([Si](C)(C)C)[Si](C)(C)C)[Si](C)(C)C)O[Si](C)(C)C	2891.2	Semi standard non polar	33892256
1-Deoxy-1-(N6-lysino)-D-fructose,5TMS,isomer #26	C[Si](C)(C)N[C@@H](CCCCNC[C@@]1(O)O[C@H](CO[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@@H]1O[Si](C)(C)C)C(=O)O[Si](C)(C)C	2637.8	Semi standard non polar	33892256
1-Deoxy-1-(N6-lysino)-D-fructose,5TMS,isomer #27	C[Si](C)(C)OC[C@H]1O[C@](O)(CN(CCCC[C@H](N)C(=O)O[Si](C)(C)C)[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@@H]1O[Si](C)(C)C	2648.2	Semi standard non polar	33892256
1-Deoxy-1-(N6-lysino)-D-fructose,5TMS,isomer #28	C[Si](C)(C)OC[C@H]1O[C@](O)(CNCCCC[C@@H](C(=O)O[Si](C)(C)C)N([Si](C)(C)C)[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@@H]1O	2812.1	Semi standard non polar	33892256
1-Deoxy-1-(N6-lysino)-D-fructose,5TMS,isomer #29	C[Si](C)(C)N[C@@H](CCCCN(C[C@@]1(O)O[C@H](CO[Si](C)(C)C)[C@@H](O)[C@@H]1O[Si](C)(C)C)[Si](C)(C)C)C(=O)O[Si](C)(C)C	2733.2	Semi standard non polar	33892256
1-Deoxy-1-(N6-lysino)-D-fructose,5TMS,isomer #3	C[Si](C)(C)OC[C@H]1O[C@@](CN(CCCC[C@H](N)C(=O)O[Si](C)(C)C)[Si](C)(C)C)(O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@@H]1O	2704.4	Semi standard non polar	33892256
1-Deoxy-1-(N6-lysino)-D-fructose,5TMS,isomer #30	C[Si](C)(C)OC[C@H]1O[C@](O)(CNCCCC[C@@H](C(=O)O[Si](C)(C)C)N([Si](C)(C)C)[Si](C)(C)C)[C@@H](O)[C@@H]1O[Si](C)(C)C	2777.7	Semi standard non polar	33892256
1-Deoxy-1-(N6-lysino)-D-fructose,5TMS,isomer #31	C[Si](C)(C)N[C@@H](CCCCN(C[C@@]1(O)O[C@H](CO[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@@H]1O)[Si](C)(C)C)C(=O)O[Si](C)(C)C	2704.5	Semi standard non polar	33892256
1-Deoxy-1-(N6-lysino)-D-fructose,5TMS,isomer #32	C[Si](C)(C)OC[C@H]1O[C@](O)(CN(CCCC[C@@H](C(=O)O[Si](C)(C)C)N([Si](C)(C)C)[Si](C)(C)C)[Si](C)(C)C)[C@@H](O)[C@@H]1O	2857.0	Semi standard non polar	33892256
1-Deoxy-1-(N6-lysino)-D-fructose,5TMS,isomer #33	C[Si](C)(C)OC[C@H]1O[C@](O)(CNCCCC[C@@H](C(=O)O)N([Si](C)(C)C)[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@@H]1O[Si](C)(C)C	2770.7	Semi standard non polar	33892256
1-Deoxy-1-(N6-lysino)-D-fructose,5TMS,isomer #34	C[Si](C)(C)N[C@@H](CCCCN(C[C@@]1(O)O[C@H](CO[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@@H]1O[Si](C)(C)C)[Si](C)(C)C)C(=O)O	2722.7	Semi standard non polar	33892256
1-Deoxy-1-(N6-lysino)-D-fructose,5TMS,isomer #35	C[Si](C)(C)OC[C@H]1O[C@](O)(CN(CCCC[C@@H](C(=O)O)N([Si](C)(C)C)[Si](C)(C)C)[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@@H]1O	2872.5	Semi standard non polar	33892256
1-Deoxy-1-(N6-lysino)-D-fructose,5TMS,isomer #36	C[Si](C)(C)OC[C@H]1O[C@](O)(CN(CCCC[C@@H](C(=O)O)N([Si](C)(C)C)[Si](C)(C)C)[Si](C)(C)C)[C@@H](O)[C@@H]1O[Si](C)(C)C	2849.0	Semi standard non polar	33892256
1-Deoxy-1-(N6-lysino)-D-fructose,5TMS,isomer #37	C[Si](C)(C)OC(=O)[C@H](CCCCNC[C@@]1(O)O[C@H](CO)[C@@H](O[Si](C)(C)C)[C@@H]1O[Si](C)(C)C)N([Si](C)(C)C)[Si](C)(C)C	2791.8	Semi standard non polar	33892256
1-Deoxy-1-(N6-lysino)-D-fructose,5TMS,isomer #38	C[Si](C)(C)N[C@@H](CCCCN(C[C@@]1(O)O[C@H](CO)[C@@H](O[Si](C)(C)C)[C@@H]1O[Si](C)(C)C)[Si](C)(C)C)C(=O)O[Si](C)(C)C	2700.9	Semi standard non polar	33892256
1-Deoxy-1-(N6-lysino)-D-fructose,5TMS,isomer #39	C[Si](C)(C)O[C@H]1[C@H](O[Si](C)(C)C)[C@@H](CO)O[C@]1(O)CN(CCCC[C@@H](C(=O)O)N([Si](C)(C)C)[Si](C)(C)C)[Si](C)(C)C	2843.0	Semi standard non polar	33892256
1-Deoxy-1-(N6-lysino)-D-fructose,5TMS,isomer #4	C[Si](C)(C)N[C@@H](CCCCNC[C@@]1(O[Si](C)(C)C)O[C@H](CO[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@@H]1O)C(=O)O[Si](C)(C)C	2637.4	Semi standard non polar	33892256
1-Deoxy-1-(N6-lysino)-D-fructose,5TMS,isomer #40	C[Si](C)(C)OC(=O)[C@H](CCCCN(C[C@@]1(O)O[C@H](CO)[C@@H](O[Si](C)(C)C)[C@@H]1O)[Si](C)(C)C)N([Si](C)(C)C)[Si](C)(C)C	2864.8	Semi standard non polar	33892256
1-Deoxy-1-(N6-lysino)-D-fructose,5TMS,isomer #41	C[Si](C)(C)OC(=O)[C@H](CCCCN(C[C@@]1(O)O[C@H](CO)[C@@H](O)[C@@H]1O[Si](C)(C)C)[Si](C)(C)C)N([Si](C)(C)C)[Si](C)(C)C	2885.7	Semi standard non polar	33892256
1-Deoxy-1-(N6-lysino)-D-fructose,5TMS,isomer #5	C[Si](C)(C)OC[C@H]1O[C@@](CN(CCCC[C@H](N)C(=O)O[Si](C)(C)C)[Si](C)(C)C)(O[Si](C)(C)C)[C@@H](O)[C@@H]1O[Si](C)(C)C	2679.0	Semi standard non polar	33892256
1-Deoxy-1-(N6-lysino)-D-fructose,5TMS,isomer #6	C[Si](C)(C)OC[C@H]1O[C@@](CNCCCC[C@@H](C(=O)O[Si](C)(C)C)N([Si](C)(C)C)[Si](C)(C)C)(O[Si](C)(C)C)[C@@H](O)[C@@H]1O	2783.5	Semi standard non polar	33892256
1-Deoxy-1-(N6-lysino)-D-fructose,5TMS,isomer #7	C[Si](C)(C)N[C@@H](CCCCN(C[C@@]1(O[Si](C)(C)C)O[C@H](CO[Si](C)(C)C)[C@@H](O)[C@@H]1O)[Si](C)(C)C)C(=O)O[Si](C)(C)C	2747.2	Semi standard non polar	33892256
1-Deoxy-1-(N6-lysino)-D-fructose,5TMS,isomer #8	C[Si](C)(C)N[C@@H](CCCCNC[C@@]1(O[Si](C)(C)C)O[C@H](CO)[C@@H](O[Si](C)(C)C)[C@@H]1O[Si](C)(C)C)C(=O)O[Si](C)(C)C	2631.0	Semi standard non polar	33892256
1-Deoxy-1-(N6-lysino)-D-fructose,5TMS,isomer #9	C[Si](C)(C)OC(=O)[C@@H](N)CCCCN(C[C@@]1(O[Si](C)(C)C)O[C@H](CO)[C@@H](O[Si](C)(C)C)[C@@H]1O[Si](C)(C)C)[Si](C)(C)C	2697.2	Semi standard non polar	33892256
1-Deoxy-1-(N6-lysino)-D-fructose,6TMS,isomer #1	C[Si](C)(C)N[C@@H](CCCCNC[C@@]1(O[Si](C)(C)C)O[C@H](CO[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@@H]1O[Si](C)(C)C)C(=O)O[Si](C)(C)C	2618.2	Semi standard non polar	33892256
1-Deoxy-1-(N6-lysino)-D-fructose,6TMS,isomer #1	C[Si](C)(C)N[C@@H](CCCCNC[C@@]1(O[Si](C)(C)C)O[C@H](CO[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@@H]1O[Si](C)(C)C)C(=O)O[Si](C)(C)C	2735.6	Standard non polar	33892256
1-Deoxy-1-(N6-lysino)-D-fructose,6TMS,isomer #1	C[Si](C)(C)N[C@@H](CCCCNC[C@@]1(O[Si](C)(C)C)O[C@H](CO[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@@H]1O[Si](C)(C)C)C(=O)O[Si](C)(C)C	2870.1	Standard polar	33892256
1-Deoxy-1-(N6-lysino)-D-fructose,6TMS,isomer #10	C[Si](C)(C)OC(=O)[C@H](CCCCN(C[C@@]1(O[Si](C)(C)C)O[C@H](CO)[C@@H](O[Si](C)(C)C)[C@@H]1O)[Si](C)(C)C)N([Si](C)(C)C)[Si](C)(C)C	2914.3	Semi standard non polar	33892256
1-Deoxy-1-(N6-lysino)-D-fructose,6TMS,isomer #10	C[Si](C)(C)OC(=O)[C@H](CCCCN(C[C@@]1(O[Si](C)(C)C)O[C@H](CO)[C@@H](O[Si](C)(C)C)[C@@H]1O)[Si](C)(C)C)N([Si](C)(C)C)[Si](C)(C)C	2800.0	Standard non polar	33892256
1-Deoxy-1-(N6-lysino)-D-fructose,6TMS,isomer #10	C[Si](C)(C)OC(=O)[C@H](CCCCN(C[C@@]1(O[Si](C)(C)C)O[C@H](CO)[C@@H](O[Si](C)(C)C)[C@@H]1O)[Si](C)(C)C)N([Si](C)(C)C)[Si](C)(C)C	3088.4	Standard polar	33892256
1-Deoxy-1-(N6-lysino)-D-fructose,6TMS,isomer #11	C[Si](C)(C)OC(=O)[C@H](CCCCN(C[C@@]1(O[Si](C)(C)C)O[C@H](CO)[C@@H](O)[C@@H]1O[Si](C)(C)C)[Si](C)(C)C)N([Si](C)(C)C)[Si](C)(C)C	2930.3	Semi standard non polar	33892256
1-Deoxy-1-(N6-lysino)-D-fructose,6TMS,isomer #11	C[Si](C)(C)OC(=O)[C@H](CCCCN(C[C@@]1(O[Si](C)(C)C)O[C@H](CO)[C@@H](O)[C@@H]1O[Si](C)(C)C)[Si](C)(C)C)N([Si](C)(C)C)[Si](C)(C)C	2835.9	Standard non polar	33892256
1-Deoxy-1-(N6-lysino)-D-fructose,6TMS,isomer #11	C[Si](C)(C)OC(=O)[C@H](CCCCN(C[C@@]1(O[Si](C)(C)C)O[C@H](CO)[C@@H](O)[C@@H]1O[Si](C)(C)C)[Si](C)(C)C)N([Si](C)(C)C)[Si](C)(C)C	3095.2	Standard polar	33892256
1-Deoxy-1-(N6-lysino)-D-fructose,6TMS,isomer #12	C[Si](C)(C)OC[C@H]1O[C@@](CNCCCC[C@@H](C(=O)O)N([Si](C)(C)C)[Si](C)(C)C)(O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@@H]1O[Si](C)(C)C	2794.4	Semi standard non polar	33892256
1-Deoxy-1-(N6-lysino)-D-fructose,6TMS,isomer #12	C[Si](C)(C)OC[C@H]1O[C@@](CNCCCC[C@@H](C(=O)O)N([Si](C)(C)C)[Si](C)(C)C)(O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@@H]1O[Si](C)(C)C	2791.0	Standard non polar	33892256
1-Deoxy-1-(N6-lysino)-D-fructose,6TMS,isomer #12	C[Si](C)(C)OC[C@H]1O[C@@](CNCCCC[C@@H](C(=O)O)N([Si](C)(C)C)[Si](C)(C)C)(O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@@H]1O[Si](C)(C)C	2997.6	Standard polar	33892256
1-Deoxy-1-(N6-lysino)-D-fructose,6TMS,isomer #13	C[Si](C)(C)N[C@@H](CCCCN(C[C@@]1(O[Si](C)(C)C)O[C@H](CO[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@@H]1O[Si](C)(C)C)[Si](C)(C)C)C(=O)O	2772.7	Semi standard non polar	33892256
1-Deoxy-1-(N6-lysino)-D-fructose,6TMS,isomer #13	C[Si](C)(C)N[C@@H](CCCCN(C[C@@]1(O[Si](C)(C)C)O[C@H](CO[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@@H]1O[Si](C)(C)C)[Si](C)(C)C)C(=O)O	2704.0	Standard non polar	33892256
1-Deoxy-1-(N6-lysino)-D-fructose,6TMS,isomer #13	C[Si](C)(C)N[C@@H](CCCCN(C[C@@]1(O[Si](C)(C)C)O[C@H](CO[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@@H]1O[Si](C)(C)C)[Si](C)(C)C)C(=O)O	3065.1	Standard polar	33892256
1-Deoxy-1-(N6-lysino)-D-fructose,6TMS,isomer #14	C[Si](C)(C)OC[C@H]1O[C@@](CN(CCCC[C@@H](C(=O)O)N([Si](C)(C)C)[Si](C)(C)C)[Si](C)(C)C)(O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@@H]1O	2923.4	Semi standard non polar	33892256
1-Deoxy-1-(N6-lysino)-D-fructose,6TMS,isomer #14	C[Si](C)(C)OC[C@H]1O[C@@](CN(CCCC[C@@H](C(=O)O)N([Si](C)(C)C)[Si](C)(C)C)[Si](C)(C)C)(O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@@H]1O	2818.6	Standard non polar	33892256
1-Deoxy-1-(N6-lysino)-D-fructose,6TMS,isomer #14	C[Si](C)(C)OC[C@H]1O[C@@](CN(CCCC[C@@H](C(=O)O)N([Si](C)(C)C)[Si](C)(C)C)[Si](C)(C)C)(O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@@H]1O	3170.2	Standard polar	33892256
1-Deoxy-1-(N6-lysino)-D-fructose,6TMS,isomer #15	C[Si](C)(C)OC[C@H]1O[C@@](CN(CCCC[C@@H](C(=O)O)N([Si](C)(C)C)[Si](C)(C)C)[Si](C)(C)C)(O[Si](C)(C)C)[C@@H](O)[C@@H]1O[Si](C)(C)C	2907.6	Semi standard non polar	33892256
1-Deoxy-1-(N6-lysino)-D-fructose,6TMS,isomer #15	C[Si](C)(C)OC[C@H]1O[C@@](CN(CCCC[C@@H](C(=O)O)N([Si](C)(C)C)[Si](C)(C)C)[Si](C)(C)C)(O[Si](C)(C)C)[C@@H](O)[C@@H]1O[Si](C)(C)C	2789.8	Standard non polar	33892256
1-Deoxy-1-(N6-lysino)-D-fructose,6TMS,isomer #15	C[Si](C)(C)OC[C@H]1O[C@@](CN(CCCC[C@@H](C(=O)O)N([Si](C)(C)C)[Si](C)(C)C)[Si](C)(C)C)(O[Si](C)(C)C)[C@@H](O)[C@@H]1O[Si](C)(C)C	3165.3	Standard polar	33892256
1-Deoxy-1-(N6-lysino)-D-fructose,6TMS,isomer #16	C[Si](C)(C)O[C@H]1[C@H](O[Si](C)(C)C)[C@@H](CO)O[C@@]1(CN(CCCC[C@@H](C(=O)O)N([Si](C)(C)C)[Si](C)(C)C)[Si](C)(C)C)O[Si](C)(C)C	2912.6	Semi standard non polar	33892256
1-Deoxy-1-(N6-lysino)-D-fructose,6TMS,isomer #16	C[Si](C)(C)O[C@H]1[C@H](O[Si](C)(C)C)[C@@H](CO)O[C@@]1(CN(CCCC[C@@H](C(=O)O)N([Si](C)(C)C)[Si](C)(C)C)[Si](C)(C)C)O[Si](C)(C)C	2797.3	Standard non polar	33892256
1-Deoxy-1-(N6-lysino)-D-fructose,6TMS,isomer #16	C[Si](C)(C)O[C@H]1[C@H](O[Si](C)(C)C)[C@@H](CO)O[C@@]1(CN(CCCC[C@@H](C(=O)O)N([Si](C)(C)C)[Si](C)(C)C)[Si](C)(C)C)O[Si](C)(C)C	3095.3	Standard polar	33892256
1-Deoxy-1-(N6-lysino)-D-fructose,6TMS,isomer #17	C[Si](C)(C)OC[C@H]1O[C@](O)(CNCCCC[C@@H](C(=O)O[Si](C)(C)C)N([Si](C)(C)C)[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@@H]1O[Si](C)(C)C	2802.7	Semi standard non polar	33892256
1-Deoxy-1-(N6-lysino)-D-fructose,6TMS,isomer #17	C[Si](C)(C)OC[C@H]1O[C@](O)(CNCCCC[C@@H](C(=O)O[Si](C)(C)C)N([Si](C)(C)C)[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@@H]1O[Si](C)(C)C	2763.3	Standard non polar	33892256
1-Deoxy-1-(N6-lysino)-D-fructose,6TMS,isomer #17	C[Si](C)(C)OC[C@H]1O[C@](O)(CNCCCC[C@@H](C(=O)O[Si](C)(C)C)N([Si](C)(C)C)[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@@H]1O[Si](C)(C)C	2950.8	Standard polar	33892256
1-Deoxy-1-(N6-lysino)-D-fructose,6TMS,isomer #18	C[Si](C)(C)N[C@@H](CCCCN(C[C@@]1(O)O[C@H](CO[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@@H]1O[Si](C)(C)C)[Si](C)(C)C)C(=O)O[Si](C)(C)C	2713.6	Semi standard non polar	33892256
1-Deoxy-1-(N6-lysino)-D-fructose,6TMS,isomer #18	C[Si](C)(C)N[C@@H](CCCCN(C[C@@]1(O)O[C@H](CO[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@@H]1O[Si](C)(C)C)[Si](C)(C)C)C(=O)O[Si](C)(C)C	2707.7	Standard non polar	33892256
1-Deoxy-1-(N6-lysino)-D-fructose,6TMS,isomer #18	C[Si](C)(C)N[C@@H](CCCCN(C[C@@]1(O)O[C@H](CO[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@@H]1O[Si](C)(C)C)[Si](C)(C)C)C(=O)O[Si](C)(C)C	2979.4	Standard polar	33892256
1-Deoxy-1-(N6-lysino)-D-fructose,6TMS,isomer #19	C[Si](C)(C)OC[C@H]1O[C@](O)(CN(CCCC[C@@H](C(=O)O[Si](C)(C)C)N([Si](C)(C)C)[Si](C)(C)C)[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@@H]1O	2906.6	Semi standard non polar	33892256
1-Deoxy-1-(N6-lysino)-D-fructose,6TMS,isomer #19	C[Si](C)(C)OC[C@H]1O[C@](O)(CN(CCCC[C@@H](C(=O)O[Si](C)(C)C)N([Si](C)(C)C)[Si](C)(C)C)[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@@H]1O	2808.2	Standard non polar	33892256
1-Deoxy-1-(N6-lysino)-D-fructose,6TMS,isomer #19	C[Si](C)(C)OC[C@H]1O[C@](O)(CN(CCCC[C@@H](C(=O)O[Si](C)(C)C)N([Si](C)(C)C)[Si](C)(C)C)[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@@H]1O	3115.6	Standard polar	33892256
1-Deoxy-1-(N6-lysino)-D-fructose,6TMS,isomer #2	C[Si](C)(C)OC[C@H]1O[C@@](CN(CCCC[C@H](N)C(=O)O[Si](C)(C)C)[Si](C)(C)C)(O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@@H]1O[Si](C)(C)C	2704.5	Semi standard non polar	33892256
1-Deoxy-1-(N6-lysino)-D-fructose,6TMS,isomer #2	C[Si](C)(C)OC[C@H]1O[C@@](CN(CCCC[C@H](N)C(=O)O[Si](C)(C)C)[Si](C)(C)C)(O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@@H]1O[Si](C)(C)C	2655.9	Standard non polar	33892256
1-Deoxy-1-(N6-lysino)-D-fructose,6TMS,isomer #2	C[Si](C)(C)OC[C@H]1O[C@@](CN(CCCC[C@H](N)C(=O)O[Si](C)(C)C)[Si](C)(C)C)(O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@@H]1O[Si](C)(C)C	3437.7	Standard polar	33892256
1-Deoxy-1-(N6-lysino)-D-fructose,6TMS,isomer #20	C[Si](C)(C)OC[C@H]1O[C@](O)(CN(CCCC[C@@H](C(=O)O[Si](C)(C)C)N([Si](C)(C)C)[Si](C)(C)C)[Si](C)(C)C)[C@@H](O)[C@@H]1O[Si](C)(C)C	2877.0	Semi standard non polar	33892256
1-Deoxy-1-(N6-lysino)-D-fructose,6TMS,isomer #20	C[Si](C)(C)OC[C@H]1O[C@](O)(CN(CCCC[C@@H](C(=O)O[Si](C)(C)C)N([Si](C)(C)C)[Si](C)(C)C)[Si](C)(C)C)[C@@H](O)[C@@H]1O[Si](C)(C)C	2781.8	Standard non polar	33892256
1-Deoxy-1-(N6-lysino)-D-fructose,6TMS,isomer #20	C[Si](C)(C)OC[C@H]1O[C@](O)(CN(CCCC[C@@H](C(=O)O[Si](C)(C)C)N([Si](C)(C)C)[Si](C)(C)C)[Si](C)(C)C)[C@@H](O)[C@@H]1O[Si](C)(C)C	3150.0	Standard polar	33892256
1-Deoxy-1-(N6-lysino)-D-fructose,6TMS,isomer #21	C[Si](C)(C)OC[C@H]1O[C@](O)(CN(CCCC[C@@H](C(=O)O)N([Si](C)(C)C)[Si](C)(C)C)[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@@H]1O[Si](C)(C)C	2871.8	Semi standard non polar	33892256
1-Deoxy-1-(N6-lysino)-D-fructose,6TMS,isomer #21	C[Si](C)(C)OC[C@H]1O[C@](O)(CN(CCCC[C@@H](C(=O)O)N([Si](C)(C)C)[Si](C)(C)C)[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@@H]1O[Si](C)(C)C	2777.5	Standard non polar	33892256
1-Deoxy-1-(N6-lysino)-D-fructose,6TMS,isomer #21	C[Si](C)(C)OC[C@H]1O[C@](O)(CN(CCCC[C@@H](C(=O)O)N([Si](C)(C)C)[Si](C)(C)C)[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@@H]1O[Si](C)(C)C	3115.6	Standard polar	33892256
1-Deoxy-1-(N6-lysino)-D-fructose,6TMS,isomer #22	C[Si](C)(C)OC(=O)[C@H](CCCCN(C[C@@]1(O)O[C@H](CO)[C@@H](O[Si](C)(C)C)[C@@H]1O[Si](C)(C)C)[Si](C)(C)C)N([Si](C)(C)C)[Si](C)(C)C	2888.0	Semi standard non polar	33892256
1-Deoxy-1-(N6-lysino)-D-fructose,6TMS,isomer #22	C[Si](C)(C)OC(=O)[C@H](CCCCN(C[C@@]1(O)O[C@H](CO)[C@@H](O[Si](C)(C)C)[C@@H]1O[Si](C)(C)C)[Si](C)(C)C)N([Si](C)(C)C)[Si](C)(C)C	2786.0	Standard non polar	33892256
1-Deoxy-1-(N6-lysino)-D-fructose,6TMS,isomer #22	C[Si](C)(C)OC(=O)[C@H](CCCCN(C[C@@]1(O)O[C@H](CO)[C@@H](O[Si](C)(C)C)[C@@H]1O[Si](C)(C)C)[Si](C)(C)C)N([Si](C)(C)C)[Si](C)(C)C	3038.2	Standard polar	33892256
1-Deoxy-1-(N6-lysino)-D-fructose,6TMS,isomer #3	C[Si](C)(C)OC[C@H]1O[C@@](CNCCCC[C@@H](C(=O)O[Si](C)(C)C)N([Si](C)(C)C)[Si](C)(C)C)(O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@@H]1O	2805.7	Semi standard non polar	33892256
1-Deoxy-1-(N6-lysino)-D-fructose,6TMS,isomer #3	C[Si](C)(C)OC[C@H]1O[C@@](CNCCCC[C@@H](C(=O)O[Si](C)(C)C)N([Si](C)(C)C)[Si](C)(C)C)(O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@@H]1O	2838.5	Standard non polar	33892256
1-Deoxy-1-(N6-lysino)-D-fructose,6TMS,isomer #3	C[Si](C)(C)OC[C@H]1O[C@@](CNCCCC[C@@H](C(=O)O[Si](C)(C)C)N([Si](C)(C)C)[Si](C)(C)C)(O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@@H]1O	2980.3	Standard polar	33892256
1-Deoxy-1-(N6-lysino)-D-fructose,6TMS,isomer #4	C[Si](C)(C)N[C@@H](CCCCN(C[C@@]1(O[Si](C)(C)C)O[C@H](CO[Si](C)(C)C)[C@@H](O)[C@@H]1O[Si](C)(C)C)[Si](C)(C)C)C(=O)O[Si](C)(C)C	2754.8	Semi standard non polar	33892256
1-Deoxy-1-(N6-lysino)-D-fructose,6TMS,isomer #4	C[Si](C)(C)N[C@@H](CCCCN(C[C@@]1(O[Si](C)(C)C)O[C@H](CO[Si](C)(C)C)[C@@H](O)[C@@H]1O[Si](C)(C)C)[Si](C)(C)C)C(=O)O[Si](C)(C)C	2743.8	Standard non polar	33892256
1-Deoxy-1-(N6-lysino)-D-fructose,6TMS,isomer #4	C[Si](C)(C)N[C@@H](CCCCN(C[C@@]1(O[Si](C)(C)C)O[C@H](CO[Si](C)(C)C)[C@@H](O)[C@@H]1O[Si](C)(C)C)[Si](C)(C)C)C(=O)O[Si](C)(C)C	3034.6	Standard polar	33892256
1-Deoxy-1-(N6-lysino)-D-fructose,6TMS,isomer #5	C[Si](C)(C)OC[C@H]1O[C@@](CNCCCC[C@@H](C(=O)O[Si](C)(C)C)N([Si](C)(C)C)[Si](C)(C)C)(O[Si](C)(C)C)[C@@H](O)[C@@H]1O[Si](C)(C)C	2797.5	Semi standard non polar	33892256
1-Deoxy-1-(N6-lysino)-D-fructose,6TMS,isomer #5	C[Si](C)(C)OC[C@H]1O[C@@](CNCCCC[C@@H](C(=O)O[Si](C)(C)C)N([Si](C)(C)C)[Si](C)(C)C)(O[Si](C)(C)C)[C@@H](O)[C@@H]1O[Si](C)(C)C	2806.4	Standard non polar	33892256
1-Deoxy-1-(N6-lysino)-D-fructose,6TMS,isomer #5	C[Si](C)(C)OC[C@H]1O[C@@](CNCCCC[C@@H](C(=O)O[Si](C)(C)C)N([Si](C)(C)C)[Si](C)(C)C)(O[Si](C)(C)C)[C@@H](O)[C@@H]1O[Si](C)(C)C	2985.2	Standard polar	33892256
1-Deoxy-1-(N6-lysino)-D-fructose,6TMS,isomer #6	C[Si](C)(C)N[C@@H](CCCCN(C[C@@]1(O[Si](C)(C)C)O[C@H](CO[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@@H]1O)[Si](C)(C)C)C(=O)O[Si](C)(C)C	2739.4	Semi standard non polar	33892256
1-Deoxy-1-(N6-lysino)-D-fructose,6TMS,isomer #6	C[Si](C)(C)N[C@@H](CCCCN(C[C@@]1(O[Si](C)(C)C)O[C@H](CO[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@@H]1O)[Si](C)(C)C)C(=O)O[Si](C)(C)C	2721.3	Standard non polar	33892256
1-Deoxy-1-(N6-lysino)-D-fructose,6TMS,isomer #6	C[Si](C)(C)N[C@@H](CCCCN(C[C@@]1(O[Si](C)(C)C)O[C@H](CO[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@@H]1O)[Si](C)(C)C)C(=O)O[Si](C)(C)C	3031.4	Standard polar	33892256
1-Deoxy-1-(N6-lysino)-D-fructose,6TMS,isomer #7	C[Si](C)(C)OC[C@H]1O[C@@](CN(CCCC[C@@H](C(=O)O[Si](C)(C)C)N([Si](C)(C)C)[Si](C)(C)C)[Si](C)(C)C)(O[Si](C)(C)C)[C@@H](O)[C@@H]1O	2919.5	Semi standard non polar	33892256
1-Deoxy-1-(N6-lysino)-D-fructose,6TMS,isomer #7	C[Si](C)(C)OC[C@H]1O[C@@](CN(CCCC[C@@H](C(=O)O[Si](C)(C)C)N([Si](C)(C)C)[Si](C)(C)C)[Si](C)(C)C)(O[Si](C)(C)C)[C@@H](O)[C@@H]1O	2822.5	Standard non polar	33892256
1-Deoxy-1-(N6-lysino)-D-fructose,6TMS,isomer #7	C[Si](C)(C)OC[C@H]1O[C@@](CN(CCCC[C@@H](C(=O)O[Si](C)(C)C)N([Si](C)(C)C)[Si](C)(C)C)[Si](C)(C)C)(O[Si](C)(C)C)[C@@H](O)[C@@H]1O	3188.4	Standard polar	33892256
1-Deoxy-1-(N6-lysino)-D-fructose,6TMS,isomer #8	C[Si](C)(C)OC(=O)[C@H](CCCCNC[C@@]1(O[Si](C)(C)C)O[C@H](CO)[C@@H](O[Si](C)(C)C)[C@@H]1O[Si](C)(C)C)N([Si](C)(C)C)[Si](C)(C)C	2800.0	Semi standard non polar	33892256
1-Deoxy-1-(N6-lysino)-D-fructose,6TMS,isomer #8	C[Si](C)(C)OC(=O)[C@H](CCCCNC[C@@]1(O[Si](C)(C)C)O[C@H](CO)[C@@H](O[Si](C)(C)C)[C@@H]1O[Si](C)(C)C)N([Si](C)(C)C)[Si](C)(C)C	2805.6	Standard non polar	33892256
1-Deoxy-1-(N6-lysino)-D-fructose,6TMS,isomer #8	C[Si](C)(C)OC(=O)[C@H](CCCCNC[C@@]1(O[Si](C)(C)C)O[C@H](CO)[C@@H](O[Si](C)(C)C)[C@@H]1O[Si](C)(C)C)N([Si](C)(C)C)[Si](C)(C)C	2903.0	Standard polar	33892256
1-Deoxy-1-(N6-lysino)-D-fructose,6TMS,isomer #9	C[Si](C)(C)N[C@@H](CCCCN(C[C@@]1(O[Si](C)(C)C)O[C@H](CO)[C@@H](O[Si](C)(C)C)[C@@H]1O[Si](C)(C)C)[Si](C)(C)C)C(=O)O[Si](C)(C)C	2749.5	Semi standard non polar	33892256
1-Deoxy-1-(N6-lysino)-D-fructose,6TMS,isomer #9	C[Si](C)(C)N[C@@H](CCCCN(C[C@@]1(O[Si](C)(C)C)O[C@H](CO)[C@@H](O[Si](C)(C)C)[C@@H]1O[Si](C)(C)C)[Si](C)(C)C)C(=O)O[Si](C)(C)C	2727.6	Standard non polar	33892256
1-Deoxy-1-(N6-lysino)-D-fructose,6TMS,isomer #9	C[Si](C)(C)N[C@@H](CCCCN(C[C@@]1(O[Si](C)(C)C)O[C@H](CO)[C@@H](O[Si](C)(C)C)[C@@H]1O[Si](C)(C)C)[Si](C)(C)C)C(=O)O[Si](C)(C)C	2957.8	Standard polar	33892256
1-Deoxy-1-(N6-lysino)-D-fructose,7TMS,isomer #1	C[Si](C)(C)OC[C@H]1O[C@@](CNCCCC[C@@H](C(=O)O[Si](C)(C)C)N([Si](C)(C)C)[Si](C)(C)C)(O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@@H]1O[Si](C)(C)C	2812.0	Semi standard non polar	33892256
1-Deoxy-1-(N6-lysino)-D-fructose,7TMS,isomer #1	C[Si](C)(C)OC[C@H]1O[C@@](CNCCCC[C@@H](C(=O)O[Si](C)(C)C)N([Si](C)(C)C)[Si](C)(C)C)(O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@@H]1O[Si](C)(C)C	2818.3	Standard non polar	33892256
1-Deoxy-1-(N6-lysino)-D-fructose,7TMS,isomer #1	C[Si](C)(C)OC[C@H]1O[C@@](CNCCCC[C@@H](C(=O)O[Si](C)(C)C)N([Si](C)(C)C)[Si](C)(C)C)(O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@@H]1O[Si](C)(C)C	2851.9	Standard polar	33892256
1-Deoxy-1-(N6-lysino)-D-fructose,7TMS,isomer #2	C[Si](C)(C)N[C@@H](CCCCN(C[C@@]1(O[Si](C)(C)C)O[C@H](CO[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@@H]1O[Si](C)(C)C)[Si](C)(C)C)C(=O)O[Si](C)(C)C	2754.0	Semi standard non polar	33892256
1-Deoxy-1-(N6-lysino)-D-fructose,7TMS,isomer #2	C[Si](C)(C)N[C@@H](CCCCN(C[C@@]1(O[Si](C)(C)C)O[C@H](CO[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@@H]1O[Si](C)(C)C)[Si](C)(C)C)C(=O)O[Si](C)(C)C	2756.2	Standard non polar	33892256
1-Deoxy-1-(N6-lysino)-D-fructose,7TMS,isomer #2	C[Si](C)(C)N[C@@H](CCCCN(C[C@@]1(O[Si](C)(C)C)O[C@H](CO[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@@H]1O[Si](C)(C)C)[Si](C)(C)C)C(=O)O[Si](C)(C)C	2879.2	Standard polar	33892256
1-Deoxy-1-(N6-lysino)-D-fructose,7TMS,isomer #3	C[Si](C)(C)OC[C@H]1O[C@@](CN(CCCC[C@@H](C(=O)O[Si](C)(C)C)N([Si](C)(C)C)[Si](C)(C)C)[Si](C)(C)C)(O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@@H]1O	2960.0	Semi standard non polar	33892256
1-Deoxy-1-(N6-lysino)-D-fructose,7TMS,isomer #3	C[Si](C)(C)OC[C@H]1O[C@@](CN(CCCC[C@@H](C(=O)O[Si](C)(C)C)N([Si](C)(C)C)[Si](C)(C)C)[Si](C)(C)C)(O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@@H]1O	2842.8	Standard non polar	33892256
1-Deoxy-1-(N6-lysino)-D-fructose,7TMS,isomer #3	C[Si](C)(C)OC[C@H]1O[C@@](CN(CCCC[C@@H](C(=O)O[Si](C)(C)C)N([Si](C)(C)C)[Si](C)(C)C)[Si](C)(C)C)(O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@@H]1O	2978.6	Standard polar	33892256
1-Deoxy-1-(N6-lysino)-D-fructose,7TMS,isomer #4	C[Si](C)(C)OC[C@H]1O[C@@](CN(CCCC[C@@H](C(=O)O[Si](C)(C)C)N([Si](C)(C)C)[Si](C)(C)C)[Si](C)(C)C)(O[Si](C)(C)C)[C@@H](O)[C@@H]1O[Si](C)(C)C	2948.1	Semi standard non polar	33892256
1-Deoxy-1-(N6-lysino)-D-fructose,7TMS,isomer #4	C[Si](C)(C)OC[C@H]1O[C@@](CN(CCCC[C@@H](C(=O)O[Si](C)(C)C)N([Si](C)(C)C)[Si](C)(C)C)[Si](C)(C)C)(O[Si](C)(C)C)[C@@H](O)[C@@H]1O[Si](C)(C)C	2814.9	Standard non polar	33892256
1-Deoxy-1-(N6-lysino)-D-fructose,7TMS,isomer #4	C[Si](C)(C)OC[C@H]1O[C@@](CN(CCCC[C@@H](C(=O)O[Si](C)(C)C)N([Si](C)(C)C)[Si](C)(C)C)[Si](C)(C)C)(O[Si](C)(C)C)[C@@H](O)[C@@H]1O[Si](C)(C)C	2977.0	Standard polar	33892256
1-Deoxy-1-(N6-lysino)-D-fructose,7TMS,isomer #5	C[Si](C)(C)OC(=O)[C@H](CCCCN(C[C@@]1(O[Si](C)(C)C)O[C@H](CO)[C@@H](O[Si](C)(C)C)[C@@H]1O[Si](C)(C)C)[Si](C)(C)C)N([Si](C)(C)C)[Si](C)(C)C	2948.1	Semi standard non polar	33892256
1-Deoxy-1-(N6-lysino)-D-fructose,7TMS,isomer #5	C[Si](C)(C)OC(=O)[C@H](CCCCN(C[C@@]1(O[Si](C)(C)C)O[C@H](CO)[C@@H](O[Si](C)(C)C)[C@@H]1O[Si](C)(C)C)[Si](C)(C)C)N([Si](C)(C)C)[Si](C)(C)C	2823.3	Standard non polar	33892256
1-Deoxy-1-(N6-lysino)-D-fructose,7TMS,isomer #5	C[Si](C)(C)OC(=O)[C@H](CCCCN(C[C@@]1(O[Si](C)(C)C)O[C@H](CO)[C@@H](O[Si](C)(C)C)[C@@H]1O[Si](C)(C)C)[Si](C)(C)C)N([Si](C)(C)C)[Si](C)(C)C	2914.5	Standard polar	33892256
1-Deoxy-1-(N6-lysino)-D-fructose,7TMS,isomer #6	C[Si](C)(C)OC[C@H]1O[C@@](CN(CCCC[C@@H](C(=O)O)N([Si](C)(C)C)[Si](C)(C)C)[Si](C)(C)C)(O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@@H]1O[Si](C)(C)C	2960.3	Semi standard non polar	33892256
1-Deoxy-1-(N6-lysino)-D-fructose,7TMS,isomer #6	C[Si](C)(C)OC[C@H]1O[C@@](CN(CCCC[C@@H](C(=O)O)N([Si](C)(C)C)[Si](C)(C)C)[Si](C)(C)C)(O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@@H]1O[Si](C)(C)C	2809.9	Standard non polar	33892256
1-Deoxy-1-(N6-lysino)-D-fructose,7TMS,isomer #6	C[Si](C)(C)OC[C@H]1O[C@@](CN(CCCC[C@@H](C(=O)O)N([Si](C)(C)C)[Si](C)(C)C)[Si](C)(C)C)(O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@@H]1O[Si](C)(C)C	2982.6	Standard polar	33892256
1-Deoxy-1-(N6-lysino)-D-fructose,7TMS,isomer #7	C[Si](C)(C)OC[C@H]1O[C@](O)(CN(CCCC[C@@H](C(=O)O[Si](C)(C)C)N([Si](C)(C)C)[Si](C)(C)C)[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@@H]1O[Si](C)(C)C	2909.9	Semi standard non polar	33892256
1-Deoxy-1-(N6-lysino)-D-fructose,7TMS,isomer #7	C[Si](C)(C)OC[C@H]1O[C@](O)(CN(CCCC[C@@H](C(=O)O[Si](C)(C)C)N([Si](C)(C)C)[Si](C)(C)C)[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@@H]1O[Si](C)(C)C	2801.2	Standard non polar	33892256
1-Deoxy-1-(N6-lysino)-D-fructose,7TMS,isomer #7	C[Si](C)(C)OC[C@H]1O[C@](O)(CN(CCCC[C@@H](C(=O)O[Si](C)(C)C)N([Si](C)(C)C)[Si](C)(C)C)[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@@H]1O[Si](C)(C)C	2936.9	Standard polar	33892256
1-Deoxy-1-(N6-lysino)-D-fructose,8TMS,isomer #1	C[Si](C)(C)OC[C@H]1O[C@@](CN(CCCC[C@@H](C(=O)O[Si](C)(C)C)N([Si](C)(C)C)[Si](C)(C)C)[Si](C)(C)C)(O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@@H]1O[Si](C)(C)C	2986.9	Semi standard non polar	33892256
1-Deoxy-1-(N6-lysino)-D-fructose,8TMS,isomer #1	C[Si](C)(C)OC[C@H]1O[C@@](CN(CCCC[C@@H](C(=O)O[Si](C)(C)C)N([Si](C)(C)C)[Si](C)(C)C)[Si](C)(C)C)(O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@@H]1O[Si](C)(C)C	2860.2	Standard non polar	33892256
1-Deoxy-1-(N6-lysino)-D-fructose,8TMS,isomer #1	C[Si](C)(C)OC[C@H]1O[C@@](CN(CCCC[C@@H](C(=O)O[Si](C)(C)C)N([Si](C)(C)C)[Si](C)(C)C)[Si](C)(C)C)(O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@@H]1O[Si](C)(C)C	2900.8	Standard polar	33892256
1-Deoxy-1-(N6-lysino)-D-fructose,1TBDMS,isomer #1	CC(C)(C)[Si](C)(C)O[C@]1(CNCCCC[C@H](N)C(=O)O)O[C@H](CO)[C@@H](O)[C@@H]1O	2969.6	Semi standard non polar	33892256
1-Deoxy-1-(N6-lysino)-D-fructose,1TBDMS,isomer #2	CC(C)(C)[Si](C)(C)OC[C@H]1O[C@](O)(CNCCCC[C@H](N)C(=O)O)[C@@H](O)[C@@H]1O	2957.7	Semi standard non polar	33892256
1-Deoxy-1-(N6-lysino)-D-fructose,1TBDMS,isomer #3	CC(C)(C)[Si](C)(C)O[C@H]1[C@H](O)[C@@](O)(CNCCCC[C@H](N)C(=O)O)O[C@@H]1CO	2967.5	Semi standard non polar	33892256
1-Deoxy-1-(N6-lysino)-D-fructose,1TBDMS,isomer #4	CC(C)(C)[Si](C)(C)O[C@H]1[C@H](O)[C@@H](CO)O[C@]1(O)CNCCCC[C@H](N)C(=O)O	2973.5	Semi standard non polar	33892256
1-Deoxy-1-(N6-lysino)-D-fructose,1TBDMS,isomer #5	CC(C)(C)[Si](C)(C)OC(=O)[C@@H](N)CCCCNC[C@@]1(O)O[C@H](CO)[C@@H](O)[C@@H]1O	2873.0	Semi standard non polar	33892256
1-Deoxy-1-(N6-lysino)-D-fructose,1TBDMS,isomer #6	CC(C)(C)[Si](C)(C)N[C@@H](CCCCNC[C@@]1(O)O[C@H](CO)[C@@H](O)[C@@H]1O)C(=O)O	3014.6	Semi standard non polar	33892256
1-Deoxy-1-(N6-lysino)-D-fructose,1TBDMS,isomer #7	CC(C)(C)[Si](C)(C)N(CCCC[C@H](N)C(=O)O)C[C@@]1(O)O[C@H](CO)[C@@H](O)[C@@H]1O	3019.4	Semi standard non polar	33892256
1-Deoxy-1-(N6-lysino)-D-fructose,2TBDMS,isomer #1	CC(C)(C)[Si](C)(C)OC(=O)[C@@H](N)CCCCNC[C@@]1(O[Si](C)(C)C(C)(C)C)O[C@H](CO)[C@@H](O)[C@@H]1O	3111.9	Semi standard non polar	33892256
1-Deoxy-1-(N6-lysino)-D-fructose,2TBDMS,isomer #10	CC(C)(C)[Si](C)(C)N[C@@H](CCCCNC[C@@]1(O)O[C@H](CO[Si](C)(C)C(C)(C)C)[C@@H](O)[C@@H]1O)C(=O)O	3192.2	Semi standard non polar	33892256
1-Deoxy-1-(N6-lysino)-D-fructose,2TBDMS,isomer #11	CC(C)(C)[Si](C)(C)OC[C@H]1O[C@](O)(CN(CCCC[C@H](N)C(=O)O)[Si](C)(C)C(C)(C)C)[C@@H](O)[C@@H]1O	3229.6	Semi standard non polar	33892256
1-Deoxy-1-(N6-lysino)-D-fructose,2TBDMS,isomer #12	CC(C)(C)[Si](C)(C)O[C@H]1[C@H](O[Si](C)(C)C(C)(C)C)[C@@H](CO)O[C@]1(O)CNCCCC[C@H](N)C(=O)O	3151.1	Semi standard non polar	33892256
1-Deoxy-1-(N6-lysino)-D-fructose,2TBDMS,isomer #13	CC(C)(C)[Si](C)(C)OC(=O)[C@@H](N)CCCCNC[C@@]1(O)O[C@H](CO)[C@@H](O[Si](C)(C)C(C)(C)C)[C@@H]1O	3115.3	Semi standard non polar	33892256
1-Deoxy-1-(N6-lysino)-D-fructose,2TBDMS,isomer #14	CC(C)(C)[Si](C)(C)N[C@@H](CCCCNC[C@@]1(O)O[C@H](CO)[C@@H](O[Si](C)(C)C(C)(C)C)[C@@H]1O)C(=O)O	3215.4	Semi standard non polar	33892256
1-Deoxy-1-(N6-lysino)-D-fructose,2TBDMS,isomer #15	CC(C)(C)[Si](C)(C)O[C@H]1[C@H](O)[C@@](O)(CN(CCCC[C@H](N)C(=O)O)[Si](C)(C)C(C)(C)C)O[C@@H]1CO	3234.5	Semi standard non polar	33892256
1-Deoxy-1-(N6-lysino)-D-fructose,2TBDMS,isomer #16	CC(C)(C)[Si](C)(C)OC(=O)[C@@H](N)CCCCNC[C@@]1(O)O[C@H](CO)[C@@H](O)[C@@H]1O[Si](C)(C)C(C)(C)C	3120.9	Semi standard non polar	33892256
1-Deoxy-1-(N6-lysino)-D-fructose,2TBDMS,isomer #17	CC(C)(C)[Si](C)(C)N[C@@H](CCCCNC[C@@]1(O)O[C@H](CO)[C@@H](O)[C@@H]1O[Si](C)(C)C(C)(C)C)C(=O)O	3219.9	Semi standard non polar	33892256
1-Deoxy-1-(N6-lysino)-D-fructose,2TBDMS,isomer #18	CC(C)(C)[Si](C)(C)O[C@H]1[C@H](O)[C@@H](CO)O[C@]1(O)CN(CCCC[C@H](N)C(=O)O)[Si](C)(C)C(C)(C)C	3237.9	Semi standard non polar	33892256
1-Deoxy-1-(N6-lysino)-D-fructose,2TBDMS,isomer #19	CC(C)(C)[Si](C)(C)N[C@@H](CCCCNC[C@@]1(O)O[C@H](CO)[C@@H](O)[C@@H]1O)C(=O)O[Si](C)(C)C(C)(C)C	3152.3	Semi standard non polar	33892256
1-Deoxy-1-(N6-lysino)-D-fructose,2TBDMS,isomer #2	CC(C)(C)[Si](C)(C)OC[C@H]1O[C@@](CNCCCC[C@H](N)C(=O)O)(O[Si](C)(C)C(C)(C)C)[C@@H](O)[C@@H]1O	3159.6	Semi standard non polar	33892256
1-Deoxy-1-(N6-lysino)-D-fructose,2TBDMS,isomer #20	CC(C)(C)[Si](C)(C)OC(=O)[C@@H](N)CCCCN(C[C@@]1(O)O[C@H](CO)[C@@H](O)[C@@H]1O)[Si](C)(C)C(C)(C)C	3166.5	Semi standard non polar	33892256
1-Deoxy-1-(N6-lysino)-D-fructose,2TBDMS,isomer #21	CC(C)(C)[Si](C)(C)N([C@@H](CCCCNC[C@@]1(O)O[C@H](CO)[C@@H](O)[C@@H]1O)C(=O)O)[Si](C)(C)C(C)(C)C	3276.9	Semi standard non polar	33892256
1-Deoxy-1-(N6-lysino)-D-fructose,2TBDMS,isomer #22	CC(C)(C)[Si](C)(C)N[C@@H](CCCCN(C[C@@]1(O)O[C@H](CO)[C@@H](O)[C@@H]1O)[Si](C)(C)C(C)(C)C)C(=O)O	3285.0	Semi standard non polar	33892256
1-Deoxy-1-(N6-lysino)-D-fructose,2TBDMS,isomer #3	CC(C)(C)[Si](C)(C)O[C@H]1[C@H](O)[C@](CNCCCC[C@H](N)C(=O)O)(O[Si](C)(C)C(C)(C)C)O[C@@H]1CO	3161.9	Semi standard non polar	33892256
1-Deoxy-1-(N6-lysino)-D-fructose,2TBDMS,isomer #4	CC(C)(C)[Si](C)(C)O[C@H]1[C@H](O)[C@@H](CO)O[C@@]1(CNCCCC[C@H](N)C(=O)O)O[Si](C)(C)C(C)(C)C	3170.9	Semi standard non polar	33892256
1-Deoxy-1-(N6-lysino)-D-fructose,2TBDMS,isomer #5	CC(C)(C)[Si](C)(C)N[C@@H](CCCCNC[C@@]1(O[Si](C)(C)C(C)(C)C)O[C@H](CO)[C@@H](O)[C@@H]1O)C(=O)O	3227.4	Semi standard non polar	33892256
1-Deoxy-1-(N6-lysino)-D-fructose,2TBDMS,isomer #6	CC(C)(C)[Si](C)(C)O[C@]1(CN(CCCC[C@H](N)C(=O)O)[Si](C)(C)C(C)(C)C)O[C@H](CO)[C@@H](O)[C@@H]1O	3247.2	Semi standard non polar	33892256
1-Deoxy-1-(N6-lysino)-D-fructose,2TBDMS,isomer #7	CC(C)(C)[Si](C)(C)OC[C@H]1O[C@](O)(CNCCCC[C@H](N)C(=O)O[Si](C)(C)C(C)(C)C)[C@@H](O)[C@@H]1O	3094.2	Semi standard non polar	33892256
1-Deoxy-1-(N6-lysino)-D-fructose,2TBDMS,isomer #8	CC(C)(C)[Si](C)(C)OC[C@H]1O[C@](O)(CNCCCC[C@H](N)C(=O)O)[C@@H](O[Si](C)(C)C(C)(C)C)[C@@H]1O	3160.3	Semi standard non polar	33892256
1-Deoxy-1-(N6-lysino)-D-fructose,2TBDMS,isomer #9	CC(C)(C)[Si](C)(C)OC[C@H]1O[C@](O)(CNCCCC[C@H](N)C(=O)O)[C@@H](O)[C@@H]1O[Si](C)(C)C(C)(C)C	3122.1	Semi standard non polar	33892256
1-Deoxy-1-(N6-lysino)-D-fructose,3TBDMS,isomer #1	CC(C)(C)[Si](C)(C)OC[C@H]1O[C@@](CNCCCC[C@H](N)C(=O)O[Si](C)(C)C(C)(C)C)(O[Si](C)(C)C(C)(C)C)[C@@H](O)[C@@H]1O	3316.1	Semi standard non polar	33892256
1-Deoxy-1-(N6-lysino)-D-fructose,3TBDMS,isomer #10	CC(C)(C)[Si](C)(C)O[C@H]1[C@H](O[Si](C)(C)C(C)(C)C)[C@@H](CO)O[C@@]1(CNCCCC[C@H](N)C(=O)O)O[Si](C)(C)C(C)(C)C	3334.1	Semi standard non polar	33892256
1-Deoxy-1-(N6-lysino)-D-fructose,3TBDMS,isomer #11	CC(C)(C)[Si](C)(C)N[C@@H](CCCCNC[C@@]1(O[Si](C)(C)C(C)(C)C)O[C@H](CO)[C@@H](O[Si](C)(C)C(C)(C)C)[C@@H]1O)C(=O)O	3417.2	Semi standard non polar	33892256
1-Deoxy-1-(N6-lysino)-D-fructose,3TBDMS,isomer #12	CC(C)(C)[Si](C)(C)O[C@H]1[C@H](O)[C@](CN(CCCC[C@H](N)C(=O)O)[Si](C)(C)C(C)(C)C)(O[Si](C)(C)C(C)(C)C)O[C@@H]1CO	3444.2	Semi standard non polar	33892256
1-Deoxy-1-(N6-lysino)-D-fructose,3TBDMS,isomer #13	CC(C)(C)[Si](C)(C)N[C@@H](CCCCNC[C@@]1(O[Si](C)(C)C(C)(C)C)O[C@H](CO)[C@@H](O)[C@@H]1O[Si](C)(C)C(C)(C)C)C(=O)O	3420.5	Semi standard non polar	33892256
1-Deoxy-1-(N6-lysino)-D-fructose,3TBDMS,isomer #14	CC(C)(C)[Si](C)(C)O[C@H]1[C@H](O)[C@@H](CO)O[C@@]1(CN(CCCC[C@H](N)C(=O)O)[Si](C)(C)C(C)(C)C)O[Si](C)(C)C(C)(C)C	3453.3	Semi standard non polar	33892256
1-Deoxy-1-(N6-lysino)-D-fructose,3TBDMS,isomer #15	CC(C)(C)[Si](C)(C)O[C@]1(CNCCCC[C@@H](C(=O)O)N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)O[C@H](CO)[C@@H](O)[C@@H]1O	3535.4	Semi standard non polar	33892256
1-Deoxy-1-(N6-lysino)-D-fructose,3TBDMS,isomer #16	CC(C)(C)[Si](C)(C)N[C@@H](CCCCN(C[C@@]1(O[Si](C)(C)C(C)(C)C)O[C@H](CO)[C@@H](O)[C@@H]1O)[Si](C)(C)C(C)(C)C)C(=O)O	3499.8	Semi standard non polar	33892256
1-Deoxy-1-(N6-lysino)-D-fructose,3TBDMS,isomer #17	CC(C)(C)[Si](C)(C)OC[C@H]1O[C@](O)(CNCCCC[C@H](N)C(=O)O[Si](C)(C)C(C)(C)C)[C@@H](O[Si](C)(C)C(C)(C)C)[C@@H]1O	3318.2	Semi standard non polar	33892256
1-Deoxy-1-(N6-lysino)-D-fructose,3TBDMS,isomer #18	CC(C)(C)[Si](C)(C)OC[C@H]1O[C@](O)(CNCCCC[C@H](N)C(=O)O[Si](C)(C)C(C)(C)C)[C@@H](O)[C@@H]1O[Si](C)(C)C(C)(C)C	3297.4	Semi standard non polar	33892256
1-Deoxy-1-(N6-lysino)-D-fructose,3TBDMS,isomer #19	CC(C)(C)[Si](C)(C)N[C@@H](CCCCNC[C@@]1(O)O[C@H](CO[Si](C)(C)C(C)(C)C)[C@@H](O)[C@@H]1O)C(=O)O[Si](C)(C)C(C)(C)C	3337.8	Semi standard non polar	33892256
1-Deoxy-1-(N6-lysino)-D-fructose,3TBDMS,isomer #2	CC(C)(C)[Si](C)(C)OC(=O)[C@@H](N)CCCCNC[C@@]1(O[Si](C)(C)C(C)(C)C)O[C@H](CO)[C@@H](O[Si](C)(C)C(C)(C)C)[C@@H]1O	3316.4	Semi standard non polar	33892256
1-Deoxy-1-(N6-lysino)-D-fructose,3TBDMS,isomer #20	CC(C)(C)[Si](C)(C)OC[C@H]1O[C@](O)(CN(CCCC[C@H](N)C(=O)O[Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)[C@@H](O)[C@@H]1O	3372.6	Semi standard non polar	33892256
1-Deoxy-1-(N6-lysino)-D-fructose,3TBDMS,isomer #21	CC(C)(C)[Si](C)(C)OC[C@H]1O[C@](O)(CNCCCC[C@H](N)C(=O)O)[C@@H](O[Si](C)(C)C(C)(C)C)[C@@H]1O[Si](C)(C)C(C)(C)C	3327.8	Semi standard non polar	33892256
1-Deoxy-1-(N6-lysino)-D-fructose,3TBDMS,isomer #22	CC(C)(C)[Si](C)(C)N[C@@H](CCCCNC[C@@]1(O)O[C@H](CO[Si](C)(C)C(C)(C)C)[C@@H](O)[C@@H]1O[Si](C)(C)C(C)(C)C)C(=O)O	3405.7	Semi standard non polar	33892256
1-Deoxy-1-(N6-lysino)-D-fructose,3TBDMS,isomer #23	CC(C)(C)[Si](C)(C)OC[C@H]1O[C@](O)(CN(CCCC[C@H](N)C(=O)O)[Si](C)(C)C(C)(C)C)[C@@H](O[Si](C)(C)C(C)(C)C)[C@@H]1O	3441.7	Semi standard non polar	33892256
1-Deoxy-1-(N6-lysino)-D-fructose,3TBDMS,isomer #24	CC(C)(C)[Si](C)(C)N[C@@H](CCCCNC[C@@]1(O)O[C@H](CO[Si](C)(C)C(C)(C)C)[C@@H](O[Si](C)(C)C(C)(C)C)[C@@H]1O)C(=O)O	3375.3	Semi standard non polar	33892256
1-Deoxy-1-(N6-lysino)-D-fructose,3TBDMS,isomer #25	CC(C)(C)[Si](C)(C)OC[C@H]1O[C@](O)(CN(CCCC[C@H](N)C(=O)O)[Si](C)(C)C(C)(C)C)[C@@H](O)[C@@H]1O[Si](C)(C)C(C)(C)C	3411.2	Semi standard non polar	33892256
1-Deoxy-1-(N6-lysino)-D-fructose,3TBDMS,isomer #26	CC(C)(C)[Si](C)(C)OC[C@H]1O[C@](O)(CNCCCC[C@@H](C(=O)O)N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)[C@@H](O)[C@@H]1O	3516.7	Semi standard non polar	33892256
1-Deoxy-1-(N6-lysino)-D-fructose,3TBDMS,isomer #27	CC(C)(C)[Si](C)(C)N[C@@H](CCCCN(C[C@@]1(O)O[C@H](CO[Si](C)(C)C(C)(C)C)[C@@H](O)[C@@H]1O)[Si](C)(C)C(C)(C)C)C(=O)O	3464.9	Semi standard non polar	33892256
1-Deoxy-1-(N6-lysino)-D-fructose,3TBDMS,isomer #28	CC(C)(C)[Si](C)(C)OC(=O)[C@@H](N)CCCCNC[C@@]1(O)O[C@H](CO)[C@@H](O[Si](C)(C)C(C)(C)C)[C@@H]1O[Si](C)(C)C(C)(C)C	3311.7	Semi standard non polar	33892256
1-Deoxy-1-(N6-lysino)-D-fructose,3TBDMS,isomer #29	CC(C)(C)[Si](C)(C)N[C@@H](CCCCNC[C@@]1(O)O[C@H](CO)[C@@H](O[Si](C)(C)C(C)(C)C)[C@@H]1O[Si](C)(C)C(C)(C)C)C(=O)O	3401.1	Semi standard non polar	33892256
1-Deoxy-1-(N6-lysino)-D-fructose,3TBDMS,isomer #3	CC(C)(C)[Si](C)(C)OC(=O)[C@@H](N)CCCCNC[C@@]1(O[Si](C)(C)C(C)(C)C)O[C@H](CO)[C@@H](O)[C@@H]1O[Si](C)(C)C(C)(C)C	3317.6	Semi standard non polar	33892256
1-Deoxy-1-(N6-lysino)-D-fructose,3TBDMS,isomer #30	CC(C)(C)[Si](C)(C)O[C@H]1[C@H](O[Si](C)(C)C(C)(C)C)[C@@H](CO)O[C@]1(O)CN(CCCC[C@H](N)C(=O)O)[Si](C)(C)C(C)(C)C	3426.5	Semi standard non polar	33892256
1-Deoxy-1-(N6-lysino)-D-fructose,3TBDMS,isomer #31	CC(C)(C)[Si](C)(C)N[C@@H](CCCCNC[C@@]1(O)O[C@H](CO)[C@@H](O[Si](C)(C)C(C)(C)C)[C@@H]1O)C(=O)O[Si](C)(C)C(C)(C)C	3364.9	Semi standard non polar	33892256
1-Deoxy-1-(N6-lysino)-D-fructose,3TBDMS,isomer #32	CC(C)(C)[Si](C)(C)OC(=O)[C@@H](N)CCCCN(C[C@@]1(O)O[C@H](CO)[C@@H](O[Si](C)(C)C(C)(C)C)[C@@H]1O)[Si](C)(C)C(C)(C)C	3386.9	Semi standard non polar	33892256
1-Deoxy-1-(N6-lysino)-D-fructose,3TBDMS,isomer #33	CC(C)(C)[Si](C)(C)O[C@H]1[C@H](O)[C@@](O)(CNCCCC[C@@H](C(=O)O)N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)O[C@@H]1CO	3528.7	Semi standard non polar	33892256
1-Deoxy-1-(N6-lysino)-D-fructose,3TBDMS,isomer #34	CC(C)(C)[Si](C)(C)N[C@@H](CCCCN(C[C@@]1(O)O[C@H](CO)[C@@H](O[Si](C)(C)C(C)(C)C)[C@@H]1O)[Si](C)(C)C(C)(C)C)C(=O)O	3486.6	Semi standard non polar	33892256
1-Deoxy-1-(N6-lysino)-D-fructose,3TBDMS,isomer #35	CC(C)(C)[Si](C)(C)N[C@@H](CCCCNC[C@@]1(O)O[C@H](CO)[C@@H](O)[C@@H]1O[Si](C)(C)C(C)(C)C)C(=O)O[Si](C)(C)C(C)(C)C	3365.8	Semi standard non polar	33892256
1-Deoxy-1-(N6-lysino)-D-fructose,3TBDMS,isomer #36	CC(C)(C)[Si](C)(C)OC(=O)[C@@H](N)CCCCN(C[C@@]1(O)O[C@H](CO)[C@@H](O)[C@@H]1O[Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C	3388.4	Semi standard non polar	33892256
1-Deoxy-1-(N6-lysino)-D-fructose,3TBDMS,isomer #37	CC(C)(C)[Si](C)(C)O[C@H]1[C@H](O)[C@@H](CO)O[C@]1(O)CNCCCC[C@@H](C(=O)O)N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C	3525.2	Semi standard non polar	33892256
1-Deoxy-1-(N6-lysino)-D-fructose,3TBDMS,isomer #38	CC(C)(C)[Si](C)(C)N[C@@H](CCCCN(C[C@@]1(O)O[C@H](CO)[C@@H](O)[C@@H]1O[Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)C(=O)O	3497.1	Semi standard non polar	33892256
1-Deoxy-1-(N6-lysino)-D-fructose,3TBDMS,isomer #39	CC(C)(C)[Si](C)(C)OC(=O)[C@H](CCCCNC[C@@]1(O)O[C@H](CO)[C@@H](O)[C@@H]1O)N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C	3470.8	Semi standard non polar	33892256
1-Deoxy-1-(N6-lysino)-D-fructose,3TBDMS,isomer #4	CC(C)(C)[Si](C)(C)N[C@@H](CCCCNC[C@@]1(O[Si](C)(C)C(C)(C)C)O[C@H](CO)[C@@H](O)[C@@H]1O)C(=O)O[Si](C)(C)C(C)(C)C	3368.1	Semi standard non polar	33892256
1-Deoxy-1-(N6-lysino)-D-fructose,3TBDMS,isomer #40	CC(C)(C)[Si](C)(C)N[C@@H](CCCCN(C[C@@]1(O)O[C@H](CO)[C@@H](O)[C@@H]1O)[Si](C)(C)C(C)(C)C)C(=O)O[Si](C)(C)C(C)(C)C	3434.6	Semi standard non polar	33892256
1-Deoxy-1-(N6-lysino)-D-fructose,3TBDMS,isomer #41	CC(C)(C)[Si](C)(C)N(CCCC[C@@H](C(=O)O)N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)C[C@@]1(O)O[C@H](CO)[C@@H](O)[C@@H]1O	3552.2	Semi standard non polar	33892256
1-Deoxy-1-(N6-lysino)-D-fructose,3TBDMS,isomer #5	CC(C)(C)[Si](C)(C)OC(=O)[C@@H](N)CCCCN(C[C@@]1(O[Si](C)(C)C(C)(C)C)O[C@H](CO)[C@@H](O)[C@@H]1O)[Si](C)(C)C(C)(C)C	3404.3	Semi standard non polar	33892256
1-Deoxy-1-(N6-lysino)-D-fructose,3TBDMS,isomer #6	CC(C)(C)[Si](C)(C)OC[C@H]1O[C@@](CNCCCC[C@H](N)C(=O)O)(O[Si](C)(C)C(C)(C)C)[C@@H](O[Si](C)(C)C(C)(C)C)[C@@H]1O	3347.5	Semi standard non polar	33892256
1-Deoxy-1-(N6-lysino)-D-fructose,3TBDMS,isomer #7	CC(C)(C)[Si](C)(C)OC[C@H]1O[C@@](CNCCCC[C@H](N)C(=O)O)(O[Si](C)(C)C(C)(C)C)[C@@H](O)[C@@H]1O[Si](C)(C)C(C)(C)C	3334.4	Semi standard non polar	33892256
1-Deoxy-1-(N6-lysino)-D-fructose,3TBDMS,isomer #8	CC(C)(C)[Si](C)(C)N[C@@H](CCCCNC[C@@]1(O[Si](C)(C)C(C)(C)C)O[C@H](CO[Si](C)(C)C(C)(C)C)[C@@H](O)[C@@H]1O)C(=O)O	3417.5	Semi standard non polar	33892256
1-Deoxy-1-(N6-lysino)-D-fructose,3TBDMS,isomer #9	CC(C)(C)[Si](C)(C)OC[C@H]1O[C@@](CN(CCCC[C@H](N)C(=O)O)[Si](C)(C)C(C)(C)C)(O[Si](C)(C)C(C)(C)C)[C@@H](O)[C@@H]1O	3451.4	Semi standard non polar	33892256
1-Deoxy-1-(N6-lysino)-D-fructose,4TBDMS,isomer #1	CC(C)(C)[Si](C)(C)OC[C@H]1O[C@@](CNCCCC[C@H](N)C(=O)O[Si](C)(C)C(C)(C)C)(O[Si](C)(C)C(C)(C)C)[C@@H](O[Si](C)(C)C(C)(C)C)[C@@H]1O	3487.1	Semi standard non polar	33892256
1-Deoxy-1-(N6-lysino)-D-fructose,4TBDMS,isomer #10	CC(C)(C)[Si](C)(C)OC(=O)[C@H](CCCCNC[C@@]1(O[Si](C)(C)C(C)(C)C)O[C@H](CO)[C@@H](O)[C@@H]1O)N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C	3689.9	Semi standard non polar	33892256
1-Deoxy-1-(N6-lysino)-D-fructose,4TBDMS,isomer #11	CC(C)(C)[Si](C)(C)N[C@@H](CCCCN(C[C@@]1(O[Si](C)(C)C(C)(C)C)O[C@H](CO)[C@@H](O)[C@@H]1O)[Si](C)(C)C(C)(C)C)C(=O)O[Si](C)(C)C(C)(C)C	3640.5	Semi standard non polar	33892256
1-Deoxy-1-(N6-lysino)-D-fructose,4TBDMS,isomer #12	CC(C)(C)[Si](C)(C)OC[C@H]1O[C@@](CNCCCC[C@H](N)C(=O)O)(O[Si](C)(C)C(C)(C)C)[C@@H](O[Si](C)(C)C(C)(C)C)[C@@H]1O[Si](C)(C)C(C)(C)C	3503.4	Semi standard non polar	33892256
1-Deoxy-1-(N6-lysino)-D-fructose,4TBDMS,isomer #13	CC(C)(C)[Si](C)(C)N[C@@H](CCCCNC[C@@]1(O[Si](C)(C)C(C)(C)C)O[C@H](CO[Si](C)(C)C(C)(C)C)[C@@H](O)[C@@H]1O[Si](C)(C)C(C)(C)C)C(=O)O	3580.5	Semi standard non polar	33892256
1-Deoxy-1-(N6-lysino)-D-fructose,4TBDMS,isomer #14	CC(C)(C)[Si](C)(C)OC[C@H]1O[C@@](CN(CCCC[C@H](N)C(=O)O)[Si](C)(C)C(C)(C)C)(O[Si](C)(C)C(C)(C)C)[C@@H](O[Si](C)(C)C(C)(C)C)[C@@H]1O	3643.7	Semi standard non polar	33892256
1-Deoxy-1-(N6-lysino)-D-fructose,4TBDMS,isomer #15	CC(C)(C)[Si](C)(C)N[C@@H](CCCCNC[C@@]1(O[Si](C)(C)C(C)(C)C)O[C@H](CO[Si](C)(C)C(C)(C)C)[C@@H](O[Si](C)(C)C(C)(C)C)[C@@H]1O)C(=O)O	3562.6	Semi standard non polar	33892256
1-Deoxy-1-(N6-lysino)-D-fructose,4TBDMS,isomer #16	CC(C)(C)[Si](C)(C)OC[C@H]1O[C@@](CN(CCCC[C@H](N)C(=O)O)[Si](C)(C)C(C)(C)C)(O[Si](C)(C)C(C)(C)C)[C@@H](O)[C@@H]1O[Si](C)(C)C(C)(C)C	3627.5	Semi standard non polar	33892256
1-Deoxy-1-(N6-lysino)-D-fructose,4TBDMS,isomer #17	CC(C)(C)[Si](C)(C)OC[C@H]1O[C@@](CNCCCC[C@@H](C(=O)O)N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)(O[Si](C)(C)C(C)(C)C)[C@@H](O)[C@@H]1O	3755.4	Semi standard non polar	33892256
1-Deoxy-1-(N6-lysino)-D-fructose,4TBDMS,isomer #18	CC(C)(C)[Si](C)(C)N[C@@H](CCCCN(C[C@@]1(O[Si](C)(C)C(C)(C)C)O[C@H](CO[Si](C)(C)C(C)(C)C)[C@@H](O)[C@@H]1O)[Si](C)(C)C(C)(C)C)C(=O)O	3687.9	Semi standard non polar	33892256
1-Deoxy-1-(N6-lysino)-D-fructose,4TBDMS,isomer #19	CC(C)(C)[Si](C)(C)N[C@@H](CCCCNC[C@@]1(O[Si](C)(C)C(C)(C)C)O[C@H](CO)[C@@H](O[Si](C)(C)C(C)(C)C)[C@@H]1O[Si](C)(C)C(C)(C)C)C(=O)O	3555.2	Semi standard non polar	33892256
1-Deoxy-1-(N6-lysino)-D-fructose,4TBDMS,isomer #2	CC(C)(C)[Si](C)(C)OC[C@H]1O[C@@](CNCCCC[C@H](N)C(=O)O[Si](C)(C)C(C)(C)C)(O[Si](C)(C)C(C)(C)C)[C@@H](O)[C@@H]1O[Si](C)(C)C(C)(C)C	3473.6	Semi standard non polar	33892256
1-Deoxy-1-(N6-lysino)-D-fructose,4TBDMS,isomer #20	CC(C)(C)[Si](C)(C)O[C@H]1[C@H](O[Si](C)(C)C(C)(C)C)[C@@H](CO)O[C@@]1(CN(CCCC[C@H](N)C(=O)O)[Si](C)(C)C(C)(C)C)O[Si](C)(C)C(C)(C)C	3617.2	Semi standard non polar	33892256
1-Deoxy-1-(N6-lysino)-D-fructose,4TBDMS,isomer #21	CC(C)(C)[Si](C)(C)O[C@H]1[C@H](O)[C@](CNCCCC[C@@H](C(=O)O)N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)(O[Si](C)(C)C(C)(C)C)O[C@@H]1CO	3730.9	Semi standard non polar	33892256
1-Deoxy-1-(N6-lysino)-D-fructose,4TBDMS,isomer #22	CC(C)(C)[Si](C)(C)N[C@@H](CCCCN(C[C@@]1(O[Si](C)(C)C(C)(C)C)O[C@H](CO)[C@@H](O[Si](C)(C)C(C)(C)C)[C@@H]1O)[Si](C)(C)C(C)(C)C)C(=O)O	3672.3	Semi standard non polar	33892256
1-Deoxy-1-(N6-lysino)-D-fructose,4TBDMS,isomer #23	CC(C)(C)[Si](C)(C)O[C@H]1[C@H](O)[C@@H](CO)O[C@@]1(CNCCCC[C@@H](C(=O)O)N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)O[Si](C)(C)C(C)(C)C	3738.7	Semi standard non polar	33892256
1-Deoxy-1-(N6-lysino)-D-fructose,4TBDMS,isomer #24	CC(C)(C)[Si](C)(C)N[C@@H](CCCCN(C[C@@]1(O[Si](C)(C)C(C)(C)C)O[C@H](CO)[C@@H](O)[C@@H]1O[Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)C(=O)O	3681.6	Semi standard non polar	33892256
1-Deoxy-1-(N6-lysino)-D-fructose,4TBDMS,isomer #25	CC(C)(C)[Si](C)(C)O[C@]1(CN(CCCC[C@@H](C(=O)O)N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)O[C@H](CO)[C@@H](O)[C@@H]1O	3795.6	Semi standard non polar	33892256
1-Deoxy-1-(N6-lysino)-D-fructose,4TBDMS,isomer #26	CC(C)(C)[Si](C)(C)OC[C@H]1O[C@](O)(CNCCCC[C@H](N)C(=O)O[Si](C)(C)C(C)(C)C)[C@@H](O[Si](C)(C)C(C)(C)C)[C@@H]1O[Si](C)(C)C(C)(C)C	3488.0	Semi standard non polar	33892256
1-Deoxy-1-(N6-lysino)-D-fructose,4TBDMS,isomer #27	CC(C)(C)[Si](C)(C)N[C@@H](CCCCNC[C@@]1(O)O[C@H](CO[Si](C)(C)C(C)(C)C)[C@@H](O)[C@@H]1O[Si](C)(C)C(C)(C)C)C(=O)O[Si](C)(C)C(C)(C)C	3547.3	Semi standard non polar	33892256
1-Deoxy-1-(N6-lysino)-D-fructose,4TBDMS,isomer #28	CC(C)(C)[Si](C)(C)OC[C@H]1O[C@](O)(CN(CCCC[C@H](N)C(=O)O[Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)[C@@H](O[Si](C)(C)C(C)(C)C)[C@@H]1O	3576.1	Semi standard non polar	33892256
1-Deoxy-1-(N6-lysino)-D-fructose,4TBDMS,isomer #29	CC(C)(C)[Si](C)(C)N[C@@H](CCCCNC[C@@]1(O)O[C@H](CO[Si](C)(C)C(C)(C)C)[C@@H](O[Si](C)(C)C(C)(C)C)[C@@H]1O)C(=O)O[Si](C)(C)C(C)(C)C	3515.0	Semi standard non polar	33892256
1-Deoxy-1-(N6-lysino)-D-fructose,4TBDMS,isomer #3	CC(C)(C)[Si](C)(C)N[C@@H](CCCCNC[C@@]1(O[Si](C)(C)C(C)(C)C)O[C@H](CO[Si](C)(C)C(C)(C)C)[C@@H](O)[C@@H]1O)C(=O)O[Si](C)(C)C(C)(C)C	3529.5	Semi standard non polar	33892256
1-Deoxy-1-(N6-lysino)-D-fructose,4TBDMS,isomer #30	CC(C)(C)[Si](C)(C)OC[C@H]1O[C@](O)(CN(CCCC[C@H](N)C(=O)O[Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)[C@@H](O)[C@@H]1O[Si](C)(C)C(C)(C)C	3556.2	Semi standard non polar	33892256
1-Deoxy-1-(N6-lysino)-D-fructose,4TBDMS,isomer #31	CC(C)(C)[Si](C)(C)OC[C@H]1O[C@](O)(CNCCCC[C@@H](C(=O)O[Si](C)(C)C(C)(C)C)N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)[C@@H](O)[C@@H]1O	3682.2	Semi standard non polar	33892256
1-Deoxy-1-(N6-lysino)-D-fructose,4TBDMS,isomer #32	CC(C)(C)[Si](C)(C)N[C@@H](CCCCN(C[C@@]1(O)O[C@H](CO[Si](C)(C)C(C)(C)C)[C@@H](O)[C@@H]1O)[Si](C)(C)C(C)(C)C)C(=O)O[Si](C)(C)C(C)(C)C	3606.9	Semi standard non polar	33892256
1-Deoxy-1-(N6-lysino)-D-fructose,4TBDMS,isomer #33	CC(C)(C)[Si](C)(C)N[C@@H](CCCCNC[C@@]1(O)O[C@H](CO[Si](C)(C)C(C)(C)C)[C@@H](O[Si](C)(C)C(C)(C)C)[C@@H]1O[Si](C)(C)C(C)(C)C)C(=O)O	3563.0	Semi standard non polar	33892256
1-Deoxy-1-(N6-lysino)-D-fructose,4TBDMS,isomer #34	CC(C)(C)[Si](C)(C)OC[C@H]1O[C@](O)(CN(CCCC[C@H](N)C(=O)O)[Si](C)(C)C(C)(C)C)[C@@H](O[Si](C)(C)C(C)(C)C)[C@@H]1O[Si](C)(C)C(C)(C)C	3597.1	Semi standard non polar	33892256
1-Deoxy-1-(N6-lysino)-D-fructose,4TBDMS,isomer #35	CC(C)(C)[Si](C)(C)OC[C@H]1O[C@](O)(CNCCCC[C@@H](C(=O)O)N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)[C@@H](O[Si](C)(C)C(C)(C)C)[C@@H]1O	3733.7	Semi standard non polar	33892256
1-Deoxy-1-(N6-lysino)-D-fructose,4TBDMS,isomer #36	CC(C)(C)[Si](C)(C)N[C@@H](CCCCN(C[C@@]1(O)O[C@H](CO[Si](C)(C)C(C)(C)C)[C@@H](O)[C@@H]1O[Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)C(=O)O	3669.4	Semi standard non polar	33892256
1-Deoxy-1-(N6-lysino)-D-fructose,4TBDMS,isomer #37	CC(C)(C)[Si](C)(C)OC[C@H]1O[C@](O)(CNCCCC[C@@H](C(=O)O)N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)[C@@H](O)[C@@H]1O[Si](C)(C)C(C)(C)C	3721.9	Semi standard non polar	33892256
1-Deoxy-1-(N6-lysino)-D-fructose,4TBDMS,isomer #38	CC(C)(C)[Si](C)(C)N[C@@H](CCCCN(C[C@@]1(O)O[C@H](CO[Si](C)(C)C(C)(C)C)[C@@H](O[Si](C)(C)C(C)(C)C)[C@@H]1O)[Si](C)(C)C(C)(C)C)C(=O)O	3640.4	Semi standard non polar	33892256
1-Deoxy-1-(N6-lysino)-D-fructose,4TBDMS,isomer #39	CC(C)(C)[Si](C)(C)OC[C@H]1O[C@](O)(CN(CCCC[C@@H](C(=O)O)N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)[C@@H](O)[C@@H]1O	3774.2	Semi standard non polar	33892256
1-Deoxy-1-(N6-lysino)-D-fructose,4TBDMS,isomer #4	CC(C)(C)[Si](C)(C)OC[C@H]1O[C@@](CN(CCCC[C@H](N)C(=O)O[Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)(O[Si](C)(C)C(C)(C)C)[C@@H](O)[C@@H]1O	3598.4	Semi standard non polar	33892256
1-Deoxy-1-(N6-lysino)-D-fructose,4TBDMS,isomer #40	CC(C)(C)[Si](C)(C)N[C@@H](CCCCNC[C@@]1(O)O[C@H](CO)[C@@H](O[Si](C)(C)C(C)(C)C)[C@@H]1O[Si](C)(C)C(C)(C)C)C(=O)O[Si](C)(C)C(C)(C)C	3533.3	Semi standard non polar	33892256
1-Deoxy-1-(N6-lysino)-D-fructose,4TBDMS,isomer #41	CC(C)(C)[Si](C)(C)OC(=O)[C@@H](N)CCCCN(C[C@@]1(O)O[C@H](CO)[C@@H](O[Si](C)(C)C(C)(C)C)[C@@H]1O[Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C	3563.2	Semi standard non polar	33892256
1-Deoxy-1-(N6-lysino)-D-fructose,4TBDMS,isomer #42	CC(C)(C)[Si](C)(C)O[C@H]1[C@H](O[Si](C)(C)C(C)(C)C)[C@@H](CO)O[C@]1(O)CNCCCC[C@@H](C(=O)O)N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C	3722.2	Semi standard non polar	33892256
1-Deoxy-1-(N6-lysino)-D-fructose,4TBDMS,isomer #43	CC(C)(C)[Si](C)(C)N[C@@H](CCCCN(C[C@@]1(O)O[C@H](CO)[C@@H](O[Si](C)(C)C(C)(C)C)[C@@H]1O[Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)C(=O)O	3654.1	Semi standard non polar	33892256
1-Deoxy-1-(N6-lysino)-D-fructose,4TBDMS,isomer #44	CC(C)(C)[Si](C)(C)OC(=O)[C@H](CCCCNC[C@@]1(O)O[C@H](CO)[C@@H](O[Si](C)(C)C(C)(C)C)[C@@H]1O)N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C	3694.5	Semi standard non polar	33892256
1-Deoxy-1-(N6-lysino)-D-fructose,4TBDMS,isomer #45	CC(C)(C)[Si](C)(C)N[C@@H](CCCCN(C[C@@]1(O)O[C@H](CO)[C@@H](O[Si](C)(C)C(C)(C)C)[C@@H]1O)[Si](C)(C)C(C)(C)C)C(=O)O[Si](C)(C)C(C)(C)C	3619.7	Semi standard non polar	33892256
1-Deoxy-1-(N6-lysino)-D-fructose,4TBDMS,isomer #46	CC(C)(C)[Si](C)(C)O[C@H]1[C@H](O)[C@@](O)(CN(CCCC[C@@H](C(=O)O)N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)O[C@@H]1CO	3777.2	Semi standard non polar	33892256
1-Deoxy-1-(N6-lysino)-D-fructose,4TBDMS,isomer #47	CC(C)(C)[Si](C)(C)OC(=O)[C@H](CCCCNC[C@@]1(O)O[C@H](CO)[C@@H](O)[C@@H]1O[Si](C)(C)C(C)(C)C)N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C	3688.1	Semi standard non polar	33892256
1-Deoxy-1-(N6-lysino)-D-fructose,4TBDMS,isomer #48	CC(C)(C)[Si](C)(C)N[C@@H](CCCCN(C[C@@]1(O)O[C@H](CO)[C@@H](O)[C@@H]1O[Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)C(=O)O[Si](C)(C)C(C)(C)C	3629.8	Semi standard non polar	33892256
1-Deoxy-1-(N6-lysino)-D-fructose,4TBDMS,isomer #49	CC(C)(C)[Si](C)(C)O[C@H]1[C@H](O)[C@@H](CO)O[C@]1(O)CN(CCCC[C@@H](C(=O)O)N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C	3786.6	Semi standard non polar	33892256
1-Deoxy-1-(N6-lysino)-D-fructose,4TBDMS,isomer #5	CC(C)(C)[Si](C)(C)OC(=O)[C@@H](N)CCCCNC[C@@]1(O[Si](C)(C)C(C)(C)C)O[C@H](CO)[C@@H](O[Si](C)(C)C(C)(C)C)[C@@H]1O[Si](C)(C)C(C)(C)C	3459.2	Semi standard non polar	33892256
1-Deoxy-1-(N6-lysino)-D-fructose,4TBDMS,isomer #50	CC(C)(C)[Si](C)(C)OC(=O)[C@H](CCCCN(C[C@@]1(O)O[C@H](CO)[C@@H](O)[C@@H]1O)[Si](C)(C)C(C)(C)C)N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C	3733.7	Semi standard non polar	33892256
1-Deoxy-1-(N6-lysino)-D-fructose,4TBDMS,isomer #6	CC(C)(C)[Si](C)(C)N[C@@H](CCCCNC[C@@]1(O[Si](C)(C)C(C)(C)C)O[C@H](CO)[C@@H](O[Si](C)(C)C(C)(C)C)[C@@H]1O)C(=O)O[Si](C)(C)C(C)(C)C	3527.2	Semi standard non polar	33892256
1-Deoxy-1-(N6-lysino)-D-fructose,4TBDMS,isomer #7	CC(C)(C)[Si](C)(C)OC(=O)[C@@H](N)CCCCN(C[C@@]1(O[Si](C)(C)C(C)(C)C)O[C@H](CO)[C@@H](O[Si](C)(C)C(C)(C)C)[C@@H]1O)[Si](C)(C)C(C)(C)C	3584.5	Semi standard non polar	33892256
1-Deoxy-1-(N6-lysino)-D-fructose,4TBDMS,isomer #8	CC(C)(C)[Si](C)(C)N[C@@H](CCCCNC[C@@]1(O[Si](C)(C)C(C)(C)C)O[C@H](CO)[C@@H](O)[C@@H]1O[Si](C)(C)C(C)(C)C)C(=O)O[Si](C)(C)C(C)(C)C	3532.7	Semi standard non polar	33892256
1-Deoxy-1-(N6-lysino)-D-fructose,4TBDMS,isomer #9	CC(C)(C)[Si](C)(C)OC(=O)[C@@H](N)CCCCN(C[C@@]1(O[Si](C)(C)C(C)(C)C)O[C@H](CO)[C@@H](O)[C@@H]1O[Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C	3586.6	Semi standard non polar	33892256
1-Deoxy-1-(N6-lysino)-D-fructose,5TBDMS,isomer #1	CC(C)(C)[Si](C)(C)OC[C@H]1O[C@@](CNCCCC[C@H](N)C(=O)O[Si](C)(C)C(C)(C)C)(O[Si](C)(C)C(C)(C)C)[C@@H](O[Si](C)(C)C(C)(C)C)[C@@H]1O[Si](C)(C)C(C)(C)C	3671.2	Semi standard non polar	33892256
1-Deoxy-1-(N6-lysino)-D-fructose,5TBDMS,isomer #10	CC(C)(C)[Si](C)(C)OC(=O)[C@H](CCCCNC[C@@]1(O[Si](C)(C)C(C)(C)C)O[C@H](CO)[C@@H](O[Si](C)(C)C(C)(C)C)[C@@H]1O)N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C	3872.8	Semi standard non polar	33892256
1-Deoxy-1-(N6-lysino)-D-fructose,5TBDMS,isomer #11	CC(C)(C)[Si](C)(C)N[C@@H](CCCCN(C[C@@]1(O[Si](C)(C)C(C)(C)C)O[C@H](CO)[C@@H](O[Si](C)(C)C(C)(C)C)[C@@H]1O)[Si](C)(C)C(C)(C)C)C(=O)O[Si](C)(C)C(C)(C)C	3793.1	Semi standard non polar	33892256
1-Deoxy-1-(N6-lysino)-D-fructose,5TBDMS,isomer #12	CC(C)(C)[Si](C)(C)OC(=O)[C@H](CCCCNC[C@@]1(O[Si](C)(C)C(C)(C)C)O[C@H](CO)[C@@H](O)[C@@H]1O[Si](C)(C)C(C)(C)C)N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C	3872.5	Semi standard non polar	33892256
1-Deoxy-1-(N6-lysino)-D-fructose,5TBDMS,isomer #13	CC(C)(C)[Si](C)(C)N[C@@H](CCCCN(C[C@@]1(O[Si](C)(C)C(C)(C)C)O[C@H](CO)[C@@H](O)[C@@H]1O[Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)C(=O)O[Si](C)(C)C(C)(C)C	3796.9	Semi standard non polar	33892256
1-Deoxy-1-(N6-lysino)-D-fructose,5TBDMS,isomer #14	CC(C)(C)[Si](C)(C)OC(=O)[C@H](CCCCN(C[C@@]1(O[Si](C)(C)C(C)(C)C)O[C@H](CO)[C@@H](O)[C@@H]1O)[Si](C)(C)C(C)(C)C)N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C	3958.9	Semi standard non polar	33892256
1-Deoxy-1-(N6-lysino)-D-fructose,5TBDMS,isomer #15	CC(C)(C)[Si](C)(C)N[C@@H](CCCCNC[C@@]1(O[Si](C)(C)C(C)(C)C)O[C@H](CO[Si](C)(C)C(C)(C)C)[C@@H](O[Si](C)(C)C(C)(C)C)[C@@H]1O[Si](C)(C)C(C)(C)C)C(=O)O	3736.5	Semi standard non polar	33892256
1-Deoxy-1-(N6-lysino)-D-fructose,5TBDMS,isomer #16	CC(C)(C)[Si](C)(C)OC[C@H]1O[C@@](CN(CCCC[C@H](N)C(=O)O)[Si](C)(C)C(C)(C)C)(O[Si](C)(C)C(C)(C)C)[C@@H](O[Si](C)(C)C(C)(C)C)[C@@H]1O[Si](C)(C)C(C)(C)C	3822.0	Semi standard non polar	33892256
1-Deoxy-1-(N6-lysino)-D-fructose,5TBDMS,isomer #17	CC(C)(C)[Si](C)(C)OC[C@H]1O[C@@](CNCCCC[C@@H](C(=O)O)N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)(O[Si](C)(C)C(C)(C)C)[C@@H](O[Si](C)(C)C(C)(C)C)[C@@H]1O	3933.6	Semi standard non polar	33892256
1-Deoxy-1-(N6-lysino)-D-fructose,5TBDMS,isomer #18	CC(C)(C)[Si](C)(C)N[C@@H](CCCCN(C[C@@]1(O[Si](C)(C)C(C)(C)C)O[C@H](CO[Si](C)(C)C(C)(C)C)[C@@H](O)[C@@H]1O[Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)C(=O)O	3865.7	Semi standard non polar	33892256
1-Deoxy-1-(N6-lysino)-D-fructose,5TBDMS,isomer #19	CC(C)(C)[Si](C)(C)OC[C@H]1O[C@@](CNCCCC[C@@H](C(=O)O)N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)(O[Si](C)(C)C(C)(C)C)[C@@H](O)[C@@H]1O[Si](C)(C)C(C)(C)C	3924.9	Semi standard non polar	33892256
1-Deoxy-1-(N6-lysino)-D-fructose,5TBDMS,isomer #2	CC(C)(C)[Si](C)(C)N[C@@H](CCCCNC[C@@]1(O[Si](C)(C)C(C)(C)C)O[C@H](CO[Si](C)(C)C(C)(C)C)[C@@H](O)[C@@H]1O[Si](C)(C)C(C)(C)C)C(=O)O[Si](C)(C)C(C)(C)C	3683.0	Semi standard non polar	33892256
1-Deoxy-1-(N6-lysino)-D-fructose,5TBDMS,isomer #20	CC(C)(C)[Si](C)(C)N[C@@H](CCCCN(C[C@@]1(O[Si](C)(C)C(C)(C)C)O[C@H](CO[Si](C)(C)C(C)(C)C)[C@@H](O[Si](C)(C)C(C)(C)C)[C@@H]1O)[Si](C)(C)C(C)(C)C)C(=O)O	3857.8	Semi standard non polar	33892256
1-Deoxy-1-(N6-lysino)-D-fructose,5TBDMS,isomer #21	CC(C)(C)[Si](C)(C)OC[C@H]1O[C@@](CN(CCCC[C@@H](C(=O)O)N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)(O[Si](C)(C)C(C)(C)C)[C@@H](O)[C@@H]1O	4018.8	Semi standard non polar	33892256
1-Deoxy-1-(N6-lysino)-D-fructose,5TBDMS,isomer #22	CC(C)(C)[Si](C)(C)O[C@H]1[C@H](O[Si](C)(C)C(C)(C)C)[C@@H](CO)O[C@@]1(CNCCCC[C@@H](C(=O)O)N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)O[Si](C)(C)C(C)(C)C	3901.0	Semi standard non polar	33892256
1-Deoxy-1-(N6-lysino)-D-fructose,5TBDMS,isomer #23	CC(C)(C)[Si](C)(C)N[C@@H](CCCCN(C[C@@]1(O[Si](C)(C)C(C)(C)C)O[C@H](CO)[C@@H](O[Si](C)(C)C(C)(C)C)[C@@H]1O[Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)C(=O)O	3836.8	Semi standard non polar	33892256
1-Deoxy-1-(N6-lysino)-D-fructose,5TBDMS,isomer #24	CC(C)(C)[Si](C)(C)O[C@H]1[C@H](O)[C@](CN(CCCC[C@@H](C(=O)O)N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)(O[Si](C)(C)C(C)(C)C)O[C@@H]1CO	3990.2	Semi standard non polar	33892256
1-Deoxy-1-(N6-lysino)-D-fructose,5TBDMS,isomer #25	CC(C)(C)[Si](C)(C)O[C@H]1[C@H](O)[C@@H](CO)O[C@@]1(CN(CCCC[C@@H](C(=O)O)N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)O[Si](C)(C)C(C)(C)C	3996.2	Semi standard non polar	33892256
1-Deoxy-1-(N6-lysino)-D-fructose,5TBDMS,isomer #26	CC(C)(C)[Si](C)(C)N[C@@H](CCCCNC[C@@]1(O)O[C@H](CO[Si](C)(C)C(C)(C)C)[C@@H](O[Si](C)(C)C(C)(C)C)[C@@H]1O[Si](C)(C)C(C)(C)C)C(=O)O[Si](C)(C)C(C)(C)C	3694.0	Semi standard non polar	33892256
1-Deoxy-1-(N6-lysino)-D-fructose,5TBDMS,isomer #27	CC(C)(C)[Si](C)(C)OC[C@H]1O[C@](O)(CN(CCCC[C@H](N)C(=O)O[Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)[C@@H](O[Si](C)(C)C(C)(C)C)[C@@H]1O[Si](C)(C)C(C)(C)C	3742.2	Semi standard non polar	33892256
1-Deoxy-1-(N6-lysino)-D-fructose,5TBDMS,isomer #28	CC(C)(C)[Si](C)(C)OC[C@H]1O[C@](O)(CNCCCC[C@@H](C(=O)O[Si](C)(C)C(C)(C)C)N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)[C@@H](O[Si](C)(C)C(C)(C)C)[C@@H]1O	3898.0	Semi standard non polar	33892256
1-Deoxy-1-(N6-lysino)-D-fructose,5TBDMS,isomer #29	CC(C)(C)[Si](C)(C)N[C@@H](CCCCN(C[C@@]1(O)O[C@H](CO[Si](C)(C)C(C)(C)C)[C@@H](O)[C@@H]1O[Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)C(=O)O[Si](C)(C)C(C)(C)C	3794.7	Semi standard non polar	33892256
1-Deoxy-1-(N6-lysino)-D-fructose,5TBDMS,isomer #3	CC(C)(C)[Si](C)(C)OC[C@H]1O[C@@](CN(CCCC[C@H](N)C(=O)O[Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)(O[Si](C)(C)C(C)(C)C)[C@@H](O[Si](C)(C)C(C)(C)C)[C@@H]1O	3781.6	Semi standard non polar	33892256
1-Deoxy-1-(N6-lysino)-D-fructose,5TBDMS,isomer #30	CC(C)(C)[Si](C)(C)OC[C@H]1O[C@](O)(CNCCCC[C@@H](C(=O)O[Si](C)(C)C(C)(C)C)N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)[C@@H](O)[C@@H]1O[Si](C)(C)C(C)(C)C	3886.4	Semi standard non polar	33892256
1-Deoxy-1-(N6-lysino)-D-fructose,5TBDMS,isomer #31	CC(C)(C)[Si](C)(C)N[C@@H](CCCCN(C[C@@]1(O)O[C@H](CO[Si](C)(C)C(C)(C)C)[C@@H](O[Si](C)(C)C(C)(C)C)[C@@H]1O)[Si](C)(C)C(C)(C)C)C(=O)O[Si](C)(C)C(C)(C)C	3770.5	Semi standard non polar	33892256
1-Deoxy-1-(N6-lysino)-D-fructose,5TBDMS,isomer #32	CC(C)(C)[Si](C)(C)OC[C@H]1O[C@](O)(CN(CCCC[C@@H](C(=O)O[Si](C)(C)C(C)(C)C)N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)[C@@H](O)[C@@H]1O	3946.1	Semi standard non polar	33892256
1-Deoxy-1-(N6-lysino)-D-fructose,5TBDMS,isomer #33	CC(C)(C)[Si](C)(C)OC[C@H]1O[C@](O)(CNCCCC[C@@H](C(=O)O)N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)[C@@H](O[Si](C)(C)C(C)(C)C)[C@@H]1O[Si](C)(C)C(C)(C)C	3921.0	Semi standard non polar	33892256
1-Deoxy-1-(N6-lysino)-D-fructose,5TBDMS,isomer #34	CC(C)(C)[Si](C)(C)N[C@@H](CCCCN(C[C@@]1(O)O[C@H](CO[Si](C)(C)C(C)(C)C)[C@@H](O[Si](C)(C)C(C)(C)C)[C@@H]1O[Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)C(=O)O	3829.9	Semi standard non polar	33892256
1-Deoxy-1-(N6-lysino)-D-fructose,5TBDMS,isomer #35	CC(C)(C)[Si](C)(C)OC[C@H]1O[C@](O)(CN(CCCC[C@@H](C(=O)O)N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)[C@@H](O[Si](C)(C)C(C)(C)C)[C@@H]1O	3986.2	Semi standard non polar	33892256
1-Deoxy-1-(N6-lysino)-D-fructose,5TBDMS,isomer #36	CC(C)(C)[Si](C)(C)OC[C@H]1O[C@](O)(CN(CCCC[C@@H](C(=O)O)N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)[C@@H](O)[C@@H]1O[Si](C)(C)C(C)(C)C	3970.7	Semi standard non polar	33892256
1-Deoxy-1-(N6-lysino)-D-fructose,5TBDMS,isomer #37	CC(C)(C)[Si](C)(C)OC(=O)[C@H](CCCCNC[C@@]1(O)O[C@H](CO)[C@@H](O[Si](C)(C)C(C)(C)C)[C@@H]1O[Si](C)(C)C(C)(C)C)N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C	3879.6	Semi standard non polar	33892256
1-Deoxy-1-(N6-lysino)-D-fructose,5TBDMS,isomer #38	CC(C)(C)[Si](C)(C)N[C@@H](CCCCN(C[C@@]1(O)O[C@H](CO)[C@@H](O[Si](C)(C)C(C)(C)C)[C@@H]1O[Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)C(=O)O[Si](C)(C)C(C)(C)C	3772.2	Semi standard non polar	33892256
1-Deoxy-1-(N6-lysino)-D-fructose,5TBDMS,isomer #39	CC(C)(C)[Si](C)(C)O[C@H]1[C@H](O[Si](C)(C)C(C)(C)C)[C@@H](CO)O[C@]1(O)CN(CCCC[C@@H](C(=O)O)N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C	3964.1	Semi standard non polar	33892256
1-Deoxy-1-(N6-lysino)-D-fructose,5TBDMS,isomer #4	CC(C)(C)[Si](C)(C)N[C@@H](CCCCNC[C@@]1(O[Si](C)(C)C(C)(C)C)O[C@H](CO[Si](C)(C)C(C)(C)C)[C@@H](O[Si](C)(C)C(C)(C)C)[C@@H]1O)C(=O)O[Si](C)(C)C(C)(C)C	3677.0	Semi standard non polar	33892256
1-Deoxy-1-(N6-lysino)-D-fructose,5TBDMS,isomer #40	CC(C)(C)[Si](C)(C)OC(=O)[C@H](CCCCN(C[C@@]1(O)O[C@H](CO)[C@@H](O[Si](C)(C)C(C)(C)C)[C@@H]1O)[Si](C)(C)C(C)(C)C)N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C	3941.3	Semi standard non polar	33892256
1-Deoxy-1-(N6-lysino)-D-fructose,5TBDMS,isomer #41	CC(C)(C)[Si](C)(C)OC(=O)[C@H](CCCCN(C[C@@]1(O)O[C@H](CO)[C@@H](O)[C@@H]1O[Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C	3945.1	Semi standard non polar	33892256
1-Deoxy-1-(N6-lysino)-D-fructose,5TBDMS,isomer #5	CC(C)(C)[Si](C)(C)OC[C@H]1O[C@@](CN(CCCC[C@H](N)C(=O)O[Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)(O[Si](C)(C)C(C)(C)C)[C@@H](O)[C@@H]1O[Si](C)(C)C(C)(C)C	3773.7	Semi standard non polar	33892256
1-Deoxy-1-(N6-lysino)-D-fructose,5TBDMS,isomer #6	CC(C)(C)[Si](C)(C)OC[C@H]1O[C@@](CNCCCC[C@@H](C(=O)O[Si](C)(C)C(C)(C)C)N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)(O[Si](C)(C)C(C)(C)C)[C@@H](O)[C@@H]1O	3894.3	Semi standard non polar	33892256
1-Deoxy-1-(N6-lysino)-D-fructose,5TBDMS,isomer #7	CC(C)(C)[Si](C)(C)N[C@@H](CCCCN(C[C@@]1(O[Si](C)(C)C(C)(C)C)O[C@H](CO[Si](C)(C)C(C)(C)C)[C@@H](O)[C@@H]1O)[Si](C)(C)C(C)(C)C)C(=O)O[Si](C)(C)C(C)(C)C	3811.2	Semi standard non polar	33892256
1-Deoxy-1-(N6-lysino)-D-fructose,5TBDMS,isomer #8	CC(C)(C)[Si](C)(C)N[C@@H](CCCCNC[C@@]1(O[Si](C)(C)C(C)(C)C)O[C@H](CO)[C@@H](O[Si](C)(C)C(C)(C)C)[C@@H]1O[Si](C)(C)C(C)(C)C)C(=O)O[Si](C)(C)C(C)(C)C	3633.8	Semi standard non polar	33892256
1-Deoxy-1-(N6-lysino)-D-fructose,5TBDMS,isomer #9	CC(C)(C)[Si](C)(C)OC(=O)[C@@H](N)CCCCN(C[C@@]1(O[Si](C)(C)C(C)(C)C)O[C@H](CO)[C@@H](O[Si](C)(C)C(C)(C)C)[C@@H]1O[Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C	3749.6	Semi standard non polar	33892256

Spectra

GC-MS Spectra

Spectrum Type	Description	Splash Key	Deposition Date	Source	View
Predicted GC-MS	Predicted GC-MS Spectrum - 1-Deoxy-1-(N6-lysino)-D-fructose GC-MS (Non-derivatized) - 70eV, Positive	Not Available	2021-10-12	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 - 1-Deoxy-1-(N6-lysino)-D-fructose 10V, Positive-QTOF	splash10-0abc-0094000000-d77f3d23caad13a312c0	2021-09-22	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 1-Deoxy-1-(N6-lysino)-D-fructose 20V, Positive-QTOF	splash10-053r-2982000000-9c19ee079047920ca852	2021-09-22	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 1-Deoxy-1-(N6-lysino)-D-fructose 40V, Positive-QTOF	splash10-003r-5900000000-01fbe3f994d9a06dd7dd	2021-09-22	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 1-Deoxy-1-(N6-lysino)-D-fructose 10V, Negative-QTOF	splash10-0a4i-0039000000-45b8040e84722234d782	2021-09-23	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 1-Deoxy-1-(N6-lysino)-D-fructose 20V, Negative-QTOF	splash10-0a4r-1494000000-28cab6b1988ba64e481a	2021-09-23	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 1-Deoxy-1-(N6-lysino)-D-fructose 40V, Negative-QTOF	splash10-052g-9410000000-ecdb35da557e9f2d2748	2021-09-23	Wishart Lab	View Spectrum

NMR Spectra

Spectrum Type	Description	Deposition Date	Source	View
Predicted 1D NMR	¹H NMR Spectrum (1D, 100 MHz, D₂O, predicted)	2021-09-24	Wishart Lab	View Spectrum
Predicted 1D NMR	¹³C NMR Spectrum (1D, 100 MHz, D₂O, predicted)	2021-09-24	Wishart Lab	View Spectrum
Predicted 1D NMR	¹H NMR Spectrum (1D, 1000 MHz, D₂O, predicted)	2021-09-24	Wishart Lab	View Spectrum
Predicted 1D NMR	¹³C NMR Spectrum (1D, 1000 MHz, D₂O, predicted)	2021-09-24	Wishart Lab	View Spectrum
Predicted 1D NMR	¹H NMR Spectrum (1D, 200 MHz, D₂O, predicted)	2021-09-24	Wishart Lab	View Spectrum
Predicted 1D NMR	¹³C NMR Spectrum (1D, 200 MHz, D₂O, predicted)	2021-09-24	Wishart Lab	View Spectrum
Predicted 1D NMR	¹H NMR Spectrum (1D, 300 MHz, D₂O, predicted)	2021-09-24	Wishart Lab	View Spectrum
Predicted 1D NMR	¹³C NMR Spectrum (1D, 300 MHz, D₂O, predicted)	2021-09-24	Wishart Lab	View Spectrum
Predicted 1D NMR	¹H NMR Spectrum (1D, 400 MHz, D₂O, predicted)	2021-09-24	Wishart Lab	View Spectrum
Predicted 1D NMR	¹³C NMR Spectrum (1D, 400 MHz, D₂O, predicted)	2021-09-24	Wishart Lab	View Spectrum
Predicted 1D NMR	¹H NMR Spectrum (1D, 500 MHz, D₂O, predicted)	2021-09-24	Wishart Lab	View Spectrum
Predicted 1D NMR	¹³C NMR Spectrum (1D, 500 MHz, D₂O, predicted)	2021-09-24	Wishart Lab	View Spectrum
Predicted 1D NMR	¹H NMR Spectrum (1D, 600 MHz, D₂O, predicted)	2021-09-24	Wishart Lab	View Spectrum
Predicted 1D NMR	¹³C NMR Spectrum (1D, 600 MHz, D₂O, predicted)	2021-09-24	Wishart Lab	View Spectrum
Predicted 1D NMR	¹H NMR Spectrum (1D, 700 MHz, D₂O, predicted)	2021-09-24	Wishart Lab	View Spectrum
Predicted 1D NMR	¹³C NMR Spectrum (1D, 700 MHz, D₂O, predicted)	2021-09-24	Wishart Lab	View Spectrum
Predicted 1D NMR	¹H NMR Spectrum (1D, 800 MHz, D₂O, predicted)	2021-09-24	Wishart Lab	View Spectrum
Predicted 1D NMR	¹³C NMR Spectrum (1D, 800 MHz, D₂O, predicted)	2021-09-24	Wishart Lab	View Spectrum
Predicted 1D NMR	¹H NMR Spectrum (1D, 900 MHz, D₂O, predicted)	2021-09-24	Wishart Lab	View Spectrum
Predicted 1D NMR	¹³C NMR Spectrum (1D, 900 MHz, D₂O, predicted)	2021-09-24	Wishart Lab	View Spectrum

Biological Properties

Cellular Locations

Not Available

Biospecimen Locations

Sweat

Tissue Locations

Not Available

Pathways

Not Available

Name	SMPDB/PathBank	KEGG

Normal Concentrations

Biospecimen	Status	Value	Age	Sex	Condition	Reference	Details
Sweat	Detected but not Quantified	Not Quantified	Adult	Both	Normal	26755145	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

Not Available

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

Not Available

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

Not Available

Showing metabocard for 1-Deoxy-1-(N6-lysino)-D-fructose (HMDB0062186)

MOL for HMDB0062186 (1-Deoxy-1-(N6-lysino)-D-fructose)

3D MOL for HMDB0062186 (1-Deoxy-1-(N6-lysino)-D-fructose)

3D SDF for HMDB0062186 (1-Deoxy-1-(N6-lysino)-D-fructose)

3D-SDF for HMDB0062186 (1-Deoxy-1-(N6-lysino)-D-fructose)

PDB for HMDB0062186 (1-Deoxy-1-(N6-lysino)-D-fructose)

3D PDB for HMDB0062186 (1-Deoxy-1-(N6-lysino)-D-fructose)

SMILES for HMDB0062186 (1-Deoxy-1-(N6-lysino)-D-fructose)

INCHI for HMDB0062186 (1-Deoxy-1-(N6-lysino)-D-fructose)

Structure for HMDB0062186 (1-Deoxy-1-(N6-lysino)-D-fructose)

3D Structure for HMDB0062186 (1-Deoxy-1-(N6-lysino)-D-fructose)

Predicted Collision Cross Sections

Predicted Kovats Retention Indices

Underivatized

Derivatized

GC-MS Spectra

MS/MS Spectra

NMR Spectra