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Record Information

Version

5.0

Status

Detected but not Quantified

Creation Date

2021-09-07 09:56:14 UTC

Update Date

2021-09-26 22:50:29 UTC

HMDB ID

HMDB0242754

Secondary Accession Numbers

None

Metabolite Identification

Common Name

(2R,3S,4R,5R,6S)-2-[[(1R,2R,4R,5R,6S,10R)-5-Hydroxy-2-(hydroxymethyl)-3,9-dioxatricyclo[4.4.0.02,4]dec-7-en-10-yl]oxy]-6-(hydroxymethyl)oxane-3,4,5-triol

Description

Catalpol belongs to the class of organic compounds known as o-glycosyl compounds. These are glycoside in which a sugar group is bonded through one carbon to another group via a O-glycosidic bond. Based on a literature review a significant number of articles have been published on Catalpol. This compound has been identified in human blood as reported by (PMID: 31557052 ). (2r,3s,4r,5r,6s)-2-[[(1r,2r,4r,5r,6s,10r)-5-hydroxy-2-(hydroxymethyl)-3,9-dioxatricyclo[4.4.0.02,4]dec-7-en-10-yl]oxy]-6-(hydroxymethyl)oxane-3,4,5-triol is not a naturally occurring metabolite and is only found in those individuals exposed to this compound or its derivatives. Technically (2R,3S,4R,5R,6S)-2-[[(1R,2R,4R,5R,6S,10R)-5-Hydroxy-2-(hydroxymethyl)-3,9-dioxatricyclo[4.4.0.02,4]dec-7-en-10-yl]oxy]-6-(hydroxymethyl)oxane-3,4,5-triol is part of the human exposome. The exposome can be defined as the collection of all the exposures of an individual in a lifetime and how those exposures relate to health. An individual's exposure begins before birth and includes insults from environmental and occupational sources.

Structure

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

  Mrv1533004151518222D          

 25 28  0  0  0  0            999 V2000
   -2.2647   -2.4406    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6689   -1.8700    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8768   -2.1007    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2810   -1.5300    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.5111   -1.7608    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1070   -1.1901    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.9107   -0.3888    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.1186   -0.1581    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0776    0.6432    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.5182    1.2138    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.3103    0.9831    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0118    1.4174    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0727    2.2401    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.6415    0.8845    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.1467    0.2322    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.3293    0.1208    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3547   -0.7038    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.6532   -1.1381    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.5066    0.1818    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7074   -2.5621    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4995   -2.7928    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.1115   -3.1327    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.3078   -3.9340    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6805   -2.9020    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2764   -3.4726    0.0000 O   0  0  0  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
  8  9  1  0  0  0  0
  9 10  2  0  0  0  0
 10 11  1  0  0  0  0
 11 12  1  0  0  0  0
 12 13  1  0  0  0  0
 12 14  1  0  0  0  0
 14 15  1  0  0  0  0
 15 16  1  0  0  0  0
 14 16  1  0  0  0  0
 16 17  1  0  0  0  0
 17 18  1  0  0  0  0
 16 19  1  0  0  0  0
  7 19  1  0  0  0  0
 11 19  1  0  0  0  0
  5 20  1  0  0  0  0
 20 21  1  0  0  0  0
 20 22  1  0  0  0  0
 22 23  1  0  0  0  0
 22 24  1  0  0  0  0
  3 24  1  0  0  0  0
 24 25  1  0  0  0  0
M  END

HMDB0249702
     RDKit          3D
Catalpinoside,(S)
 47 50  0  0  0  0  0  0  0  0999 V2000
    5.1914    2.1192   -0.4905 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.8956    1.8829   -0.9454 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.9912    1.4385    0.2086 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.7178    1.2033   -0.2228 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.3128   -0.1123   -0.1784 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.2055   -0.2809   -0.9731 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9304   -0.7042   -0.2629 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2215   -2.0008   -0.6944 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1615   -2.2644   -1.6514 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1657   -1.4016   -1.7661 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3163   -0.2105   -0.9411 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2441   -0.4198    0.2679 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.7978   -1.7252    0.0585 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2777   -0.4570    1.3545 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6375    0.3246    2.1795 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5259    0.8110    0.9513 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1912    2.1473    0.8329 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.5205    2.2130    1.1372 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0121    0.2829   -0.3259 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3879   -1.0855   -0.5834 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.8473   -2.3683   -0.5456 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.4787   -1.0206    0.4455 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.1052   -1.8844    1.4895 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.6109    0.3491    1.0135 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.9675    0.6260    1.1759 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.8301    2.0545   -1.2431 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.5042    2.8832   -1.2741 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.9495    1.1478   -1.7461 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.9417    2.3477    0.8810 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.0282   -0.3599    0.8637 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5927   -0.7893    0.8125 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0457   -3.1489   -2.2608 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9070   -1.6118   -2.5227 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7942    0.5811   -1.5570 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.0912    0.2448    0.2899 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.9132   -2.1074    0.9777 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6649   -1.4350    1.2469 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9322    2.6700   -0.1208 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6772    2.7986    1.6112 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.7230    2.5759    2.0366 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6862    1.1355   -0.9731 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.7466   -0.9241   -1.6160 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.4294   -2.6312   -1.4016 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.4488   -1.4176    0.0683 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.7314   -1.8445    2.2503 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.1696    0.4128    2.0505 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.5384   -0.0447    0.7466 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  2  0
 10 11  1  0
 11 12  1  0
 12 13  1  0
 12 14  1  0
 14 15  1  0
 15 16  1  0
 16 17  1  0
 17 18  1  0
 16 19  1  0
  5 20  1  0
 20 21  1  0
 20 22  1  0
 22 23  1  0
 22 24  1  0
 24 25  1  0
 24  3  1  0
 19  7  1  0
 19 11  1  0
 16 14  1  0
  1 26  1  0
  2 27  1  0
  2 28  1  0
  3 29  1  0
  5 30  1  0
  7 31  1  0
  9 32  1  0
 10 33  1  0
 11 34  1  0
 12 35  1  0
 13 36  1  0
 14 37  1  0
 17 38  1  0
 17 39  1  0
 18 40  1  0
 19 41  1  0
 20 42  1  0
 21 43  1  0
 22 44  1  0
 23 45  1  0
 24 46  1  0
 25 47  1  0
M  END

  Mrv1533004151518222D          

 25 28  0  0  0  0            999 V2000
   -2.2647   -2.4406    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6689   -1.8700    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8768   -2.1007    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2810   -1.5300    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.5111   -1.7608    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1070   -1.1901    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.9107   -0.3888    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.1186   -0.1581    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0776    0.6432    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.5182    1.2138    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.3103    0.9831    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0118    1.4174    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0727    2.2401    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.6415    0.8845    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.1467    0.2322    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.3293    0.1208    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3547   -0.7038    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.6532   -1.1381    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.5066    0.1818    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7074   -2.5621    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4995   -2.7928    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.1115   -3.1327    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.3078   -3.9340    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6805   -2.9020    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2764   -3.4726    0.0000 O   0  0  0  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
  8  9  1  0  0  0  0
  9 10  2  0  0  0  0
 10 11  1  0  0  0  0
 11 12  1  0  0  0  0
 12 13  1  0  0  0  0
 12 14  1  0  0  0  0
 14 15  1  0  0  0  0
 15 16  1  0  0  0  0
 14 16  1  0  0  0  0
 16 17  1  0  0  0  0
 17 18  1  0  0  0  0
 16 19  1  0  0  0  0
  7 19  1  0  0  0  0
 11 19  1  0  0  0  0
  5 20  1  0  0  0  0
 20 21  1  0  0  0  0
 20 22  1  0  0  0  0
 22 23  1  0  0  0  0
 22 24  1  0  0  0  0
  3 24  1  0  0  0  0
 24 25  1  0  0  0  0
M  END
> <DATABASE_ID>
HMDB0242754

> <DATABASE_NAME>
hmdb

> <SMILES>
OCC1OC(OC2OC=CC3C(O)C4OC4(CO)C23)C(O)C(O)C1O

> <INCHI_IDENTIFIER>
InChI=1S/C15H22O10/c16-3-6-9(19)10(20)11(21)14(23-6)24-13-7-5(1-2-22-13)8(18)12-15(7,4-17)25-12/h1-2,5-14,16-21H,3-4H2

> <INCHI_KEY>
LHDWRKICQLTVDL-UHFFFAOYSA-N

> <FORMULA>
C15H22O10

> <MOLECULAR_WEIGHT>
362.331

> <EXACT_MASS>
362.121296908

> <JCHEM_ACCEPTOR_COUNT>
10

> <JCHEM_ATOM_COUNT>
47

> <JCHEM_AVERAGE_POLARIZABILITY>
33.77421737486523

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
6

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
2-{[5-hydroxy-2-(hydroxymethyl)-3,9-dioxatricyclo[4.4.0.0²,⁴]dec-7-en-10-yl]oxy}-6-(hydroxymethyl)oxane-3,4,5-triol

> <ALOGPS_LOGP>
-2.19

> <JCHEM_LOGP>
-3.431803609666667

> <ALOGPS_LOGS>
-0.19

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
4

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
13.081662421196974

> <JCHEM_PKA_STRONGEST_ACIDIC>
12.19162069297514

> <JCHEM_PKA_STRONGEST_BASIC>
-2.9810847601929344

> <JCHEM_POLAR_SURFACE_AREA>
161.6

> <JCHEM_REFRACTIVITY>
77.1915

> <JCHEM_ROTATABLE_BOND_COUNT>
4

> <JCHEM_RULE_OF_FIVE>
0

> <ALOGPS_SOLUBILITY>
2.33e+02 g/l

> <JCHEM_TRADITIONAL_IUPAC>
catalpol

> <JCHEM_VEBER_RULE>
0

$$$$

HMDB0249702
     RDKit          3D
Catalpinoside,(S)
 47 50  0  0  0  0  0  0  0  0999 V2000
    5.1914    2.1192   -0.4905 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.8956    1.8829   -0.9454 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.9912    1.4385    0.2086 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.7178    1.2033   -0.2228 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.3128   -0.1123   -0.1784 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.2055   -0.2809   -0.9731 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9304   -0.7042   -0.2629 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2215   -2.0008   -0.6944 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1615   -2.2644   -1.6514 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1657   -1.4016   -1.7661 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3163   -0.2105   -0.9411 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2441   -0.4198    0.2679 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.7978   -1.7252    0.0585 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2777   -0.4570    1.3545 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6375    0.3246    2.1795 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5259    0.8110    0.9513 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1912    2.1473    0.8329 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.5205    2.2130    1.1372 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0121    0.2829   -0.3259 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3879   -1.0855   -0.5834 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.8473   -2.3683   -0.5456 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.4787   -1.0206    0.4455 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.1052   -1.8844    1.4895 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.6109    0.3491    1.0135 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.9675    0.6260    1.1759 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.8301    2.0545   -1.2431 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.5042    2.8832   -1.2741 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.9495    1.1478   -1.7461 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.9417    2.3477    0.8810 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.0282   -0.3599    0.8637 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5927   -0.7893    0.8125 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0457   -3.1489   -2.2608 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9070   -1.6118   -2.5227 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7942    0.5811   -1.5570 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.0912    0.2448    0.2899 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.9132   -2.1074    0.9777 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6649   -1.4350    1.2469 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9322    2.6700   -0.1208 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6772    2.7986    1.6112 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.7230    2.5759    2.0366 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6862    1.1355   -0.9731 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.7466   -0.9241   -1.6160 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.4294   -2.6312   -1.4016 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.4488   -1.4176    0.0683 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.7314   -1.8445    2.2503 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.1696    0.4128    2.0505 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.5384   -0.0447    0.7466 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  2  0
 10 11  1  0
 11 12  1  0
 12 13  1  0
 12 14  1  0
 14 15  1  0
 15 16  1  0
 16 17  1  0
 17 18  1  0
 16 19  1  0
  5 20  1  0
 20 21  1  0
 20 22  1  0
 22 23  1  0
 22 24  1  0
 24 25  1  0
 24  3  1  0
 19  7  1  0
 19 11  1  0
 16 14  1  0
  1 26  1  0
  2 27  1  0
  2 28  1  0
  3 29  1  0
  5 30  1  0
  7 31  1  0
  9 32  1  0
 10 33  1  0
 11 34  1  0
 12 35  1  0
 13 36  1  0
 14 37  1  0
 17 38  1  0
 17 39  1  0
 18 40  1  0
 19 41  1  0
 20 42  1  0
 21 43  1  0
 22 44  1  0
 23 45  1  0
 24 46  1  0
 25 47  1  0
M  END

HEADER    PROTEIN                                 15-APR-15   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   15-APR-15         0                                  
HETATM    1  O   UNK     0      -4.227  -4.556   0.000  0.00  0.00           O+0
HETATM    2  C   UNK     0      -3.115  -3.491   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0      -1.637  -3.921   0.000  0.00  0.00           C+0
HETATM    4  O   UNK     0      -0.524  -2.856   0.000  0.00  0.00           O+0
HETATM    5  C   UNK     0       0.954  -3.287   0.000  0.00  0.00           C+0
HETATM    6  O   UNK     0       2.066  -2.222   0.000  0.00  0.00           O+0
HETATM    7  C   UNK     0       1.700  -0.726   0.000  0.00  0.00           C+0
HETATM    8  O   UNK     0       0.221  -0.295   0.000  0.00  0.00           O+0
HETATM    9  C   UNK     0      -0.145   1.201   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0       0.967   2.266   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0       2.446   1.835   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0       3.755   2.646   0.000  0.00  0.00           C+0
HETATM   13  O   UNK     0       3.869   4.182   0.000  0.00  0.00           O+0
HETATM   14  C   UNK     0       4.931   1.651   0.000  0.00  0.00           C+0
HETATM   15  O   UNK     0       5.874   0.433   0.000  0.00  0.00           O+0
HETATM   16  C   UNK     0       4.348   0.226   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0       4.395  -1.314   0.000  0.00  0.00           C+0
HETATM   18  O   UNK     0       3.086  -2.124   0.000  0.00  0.00           O+0
HETATM   19  C   UNK     0       2.812   0.339   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0       1.320  -4.783   0.000  0.00  0.00           C+0
HETATM   21  O   UNK     0       2.799  -5.213   0.000  0.00  0.00           O+0
HETATM   22  C   UNK     0       0.208  -5.848   0.000  0.00  0.00           C+0
HETATM   23  O   UNK     0       0.575  -7.343   0.000  0.00  0.00           O+0
HETATM   24  C   UNK     0      -1.270  -5.417   0.000  0.00  0.00           C+0
HETATM   25  O   UNK     0      -2.383  -6.482   0.000  0.00  0.00           O+0
CONECT    1    2                                                            
CONECT    2    1    3                                                       
CONECT    3    2    4   24                                                  
CONECT    4    3    5                                                       
CONECT    5    4    6   20                                                  
CONECT    6    5    7                                                       
CONECT    7    6    8   19                                                  
CONECT    8    7    9                                                       
CONECT    9    8   10                                                       
CONECT   10    9   11                                                       
CONECT   11   10   12   19                                                  
CONECT   12   11   13   14                                                  
CONECT   13   12                                                            
CONECT   14   12   15   16                                                  
CONECT   15   14   16                                                       
CONECT   16   15   14   17   19                                             
CONECT   17   16   18                                                       
CONECT   18   17                                                            
CONECT   19   16    7   11                                                  
CONECT   20    5   21   22                                                  
CONECT   21   20                                                            
CONECT   22   20   23   24                                                  
CONECT   23   22                                                            
CONECT   24   22    3   25                                                  
CONECT   25   24                                                            
MASTER        0    0    0    0    0    0    0    0   25    0   56    0
END

COMPND    HMDB0249704
HETATM    1  O1  UNL     1       3.985   1.752   2.687  1.00  0.00           O  
HETATM    2  C1  UNL     1       2.800   1.268   2.172  1.00  0.00           C  
HETATM    3  C2  UNL     1       2.477   2.062   0.931  1.00  0.00           C  
HETATM    4  O2  UNL     1       1.316   1.697   0.300  1.00  0.00           O  
HETATM    5  C3  UNL     1       1.308   0.397  -0.163  1.00  0.00           C  
HETATM    6  O3  UNL     1       0.045   0.167  -0.713  1.00  0.00           O  
HETATM    7  C4  UNL     1      -0.655  -0.851  -0.081  1.00  0.00           C  
HETATM    8  O4  UNL     1      -0.897  -1.949  -0.911  1.00  0.00           O  
HETATM    9  C5  UNL     1      -1.751  -2.942  -0.462  1.00  0.00           C  
HETATM   10  C6  UNL     1      -2.507  -2.764   0.609  1.00  0.00           C  
HETATM   11  C7  UNL     1      -2.495  -1.517   1.388  1.00  0.00           C  
HETATM   12  C8  UNL     1      -3.916  -1.072   1.616  1.00  0.00           C  
HETATM   13  O5  UNL     1      -4.748  -2.177   1.787  1.00  0.00           O  
HETATM   14  C9  UNL     1      -4.242  -0.363   0.312  1.00  0.00           C  
HETATM   15  O6  UNL     1      -3.889   0.992   0.284  1.00  0.00           O  
HETATM   16  C10 UNL     1      -3.019   0.015  -0.323  1.00  0.00           C  
HETATM   17  C11 UNL     1      -2.864   0.153  -1.812  1.00  0.00           C  
HETATM   18  O7  UNL     1      -4.052   0.031  -2.495  1.00  0.00           O  
HETATM   19  C12 UNL     1      -1.909  -0.384   0.574  1.00  0.00           C  
HETATM   20  C13 UNL     1       2.410   0.124  -1.160  1.00  0.00           C  
HETATM   21  O8  UNL     1       3.259  -0.899  -0.757  1.00  0.00           O  
HETATM   22  C14 UNL     1       3.170   1.412  -1.385  1.00  0.00           C  
HETATM   23  O9  UNL     1       4.321   1.202  -2.140  1.00  0.00           O  
HETATM   24  C15 UNL     1       3.629   1.946  -0.035  1.00  0.00           C  
HETATM   25  O10 UNL     1       4.189   3.207  -0.226  1.00  0.00           O  
HETATM   26  H1  UNL     1       4.741   1.221   2.346  1.00  0.00           H  
HETATM   27  H2  UNL     1       2.964   0.218   1.882  1.00  0.00           H  
HETATM   28  H3  UNL     1       1.970   1.290   2.910  1.00  0.00           H  
HETATM   29  H4  UNL     1       2.340   3.136   1.247  1.00  0.00           H  
HETATM   30  H5  UNL     1       1.424  -0.325   0.671  1.00  0.00           H  
HETATM   31  H6  UNL     1       0.018  -1.231   0.743  1.00  0.00           H  
HETATM   32  H7  UNL     1      -1.823  -3.888  -0.973  1.00  0.00           H  
HETATM   33  H8  UNL     1      -3.179  -3.563   0.951  1.00  0.00           H  
HETATM   34  H9  UNL     1      -1.957  -1.653   2.349  1.00  0.00           H  
HETATM   35  H10 UNL     1      -3.987  -0.414   2.486  1.00  0.00           H  
HETATM   36  H11 UNL     1      -4.613  -2.516   2.704  1.00  0.00           H  
HETATM   37  H12 UNL     1      -5.158  -0.676  -0.229  1.00  0.00           H  
HETATM   38  H13 UNL     1      -2.504   1.209  -1.990  1.00  0.00           H  
HETATM   39  H14 UNL     1      -2.117  -0.499  -2.250  1.00  0.00           H  
HETATM   40  H15 UNL     1      -4.385  -0.893  -2.553  1.00  0.00           H  
HETATM   41  H16 UNL     1      -1.648   0.450   1.277  1.00  0.00           H  
HETATM   42  H17 UNL     1       1.964  -0.179  -2.135  1.00  0.00           H  
HETATM   43  H18 UNL     1       3.413  -1.565  -1.476  1.00  0.00           H  
HETATM   44  H19 UNL     1       2.476   2.133  -1.860  1.00  0.00           H  
HETATM   45  H20 UNL     1       4.527   1.931  -2.757  1.00  0.00           H  
HETATM   46  H21 UNL     1       4.405   1.233   0.336  1.00  0.00           H  
HETATM   47  H22 UNL     1       5.166   3.076  -0.314  1.00  0.00           H  
CONECT    1    2   26
CONECT    2    3   27   28
CONECT    3    4   24   29
CONECT    4    5
CONECT    5    6   20   30
CONECT    6    7
CONECT    7    8   19   31
CONECT    8    9
CONECT    9   10   10   32
CONECT   10   11   33
CONECT   11   12   19   34
CONECT   12   13   14   35
CONECT   13   36
CONECT   14   15   16   37
CONECT   15   16
CONECT   16   17   19
CONECT   17   18   38   39
CONECT   18   40
CONECT   19   41
CONECT   20   21   22   42
CONECT   21   43
CONECT   22   23   24   44
CONECT   23   45
CONECT   24   25   46
CONECT   25   47
END

HMDB0249702
     RDKit          3D
Catalpinoside,(S)
 47 50  0  0  0  0  0  0  0  0999 V2000
    5.1914    2.1192   -0.4905 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.8956    1.8829   -0.9454 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.9912    1.4385    0.2086 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.7178    1.2033   -0.2228 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.3128   -0.1123   -0.1784 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.2055   -0.2809   -0.9731 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9304   -0.7042   -0.2629 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2215   -2.0008   -0.6944 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1615   -2.2644   -1.6514 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1657   -1.4016   -1.7661 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3163   -0.2105   -0.9411 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2441   -0.4198    0.2679 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.7978   -1.7252    0.0585 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2777   -0.4570    1.3545 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6375    0.3246    2.1795 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5259    0.8110    0.9513 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1912    2.1473    0.8329 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.5205    2.2130    1.1372 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0121    0.2829   -0.3259 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3879   -1.0855   -0.5834 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.8473   -2.3683   -0.5456 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.4787   -1.0206    0.4455 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.1052   -1.8844    1.4895 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.6109    0.3491    1.0135 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.9675    0.6260    1.1759 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.8301    2.0545   -1.2431 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.5042    2.8832   -1.2741 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.9495    1.1478   -1.7461 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.9417    2.3477    0.8810 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.0282   -0.3599    0.8637 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5927   -0.7893    0.8125 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0457   -3.1489   -2.2608 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9070   -1.6118   -2.5227 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7942    0.5811   -1.5570 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.0912    0.2448    0.2899 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.9132   -2.1074    0.9777 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6649   -1.4350    1.2469 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9322    2.6700   -0.1208 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6772    2.7986    1.6112 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.7230    2.5759    2.0366 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6862    1.1355   -0.9731 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.7466   -0.9241   -1.6160 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.4294   -2.6312   -1.4016 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.4488   -1.4176    0.0683 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.7314   -1.8445    2.2503 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.1696    0.4128    2.0505 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.5384   -0.0447    0.7466 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  2  0
 10 11  1  0
 11 12  1  0
 12 13  1  0
 12 14  1  0
 14 15  1  0
 15 16  1  0
 16 17  1  0
 17 18  1  0
 16 19  1  0
  5 20  1  0
 20 21  1  0
 20 22  1  0
 22 23  1  0
 22 24  1  0
 24 25  1  0
 24  3  1  0
 19  7  1  0
 19 11  1  0
 16 14  1  0
  1 26  1  0
  2 27  1  0
  2 28  1  0
  3 29  1  0
  5 30  1  0
  7 31  1  0
  9 32  1  0
 10 33  1  0
 11 34  1  0
 12 35  1  0
 13 36  1  0
 14 37  1  0
 17 38  1  0
 17 39  1  0
 18 40  1  0
 19 41  1  0
 20 42  1  0
 21 43  1  0
 22 44  1  0
 23 45  1  0
 24 46  1  0
 25 47  1  0
M  END

View in JSmol View NMR Assignments View Stereo Labels

Synonyms

Value	Source
Catalpol	MeSH

Chemical Formula

C₁₅H₂₂O₁₀

Average Molecular Weight

362.331

Monoisotopic Molecular Weight

362.121296908

IUPAC Name

2-{[5-hydroxy-2-(hydroxymethyl)-3,9-dioxatricyclo[4.4.0.0²,⁴]dec-7-en-10-yl]oxy}-6-(hydroxymethyl)oxane-3,4,5-triol

Traditional Name

catalpol

CAS Registry Number

Not Available

SMILES

OCC1OC(OC2OC=CC3C(O)C4OC4(CO)C23)C(O)C(O)C1O

InChI Identifier

InChI=1S/C15H22O10/c16-3-6-9(19)10(20)11(21)14(23-6)24-13-7-5(1-2-22-13)8(18)12-15(7,4-17)25-12/h1-2,5-14,16-21H,3-4H2

InChI Key

LHDWRKICQLTVDL-UHFFFAOYSA-N

Chemical Taxonomy

Description

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

Kingdom

Organic compounds

Super Class

Organic oxygen compounds

Class

Organooxygen compounds

Sub Class

Carbohydrates and carbohydrate conjugates

Direct Parent

O-glycosyl compounds

Alternative Parents

Substituents

Hexose monosaccharide
O-glycosyl compound
Monosaccharide
Oxane
Cyclic alcohol
Secondary alcohol
Acetal
Dialkyl ether
Oxirane
Ether
Polyol
Organoheterocyclic compound
Oxacycle
Alcohol
Primary alcohol
Hydrocarbon derivative
Aliphatic heteropolycyclic compound

Molecular Framework

Aliphatic heteropolycyclic compounds

External Descriptors

Not Available

Ontology

Physiological effect

Not Available

Disposition

Biological location

Non-excretory biofluid

Biofluid or Excreta

Blood (PMID: 31557052)

Source

Exogenous

Exogenous (PMID: 31557052)

Process

Not Available

Role

Not Available

Physical Properties

State

Not Available

Experimental Molecular Properties

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

Experimental Chromatographic Properties

Not Available

Predicted Molecular Properties

Property	Value	Source
logP	-2.2	ALOGPS
logP	-3.4	ChemAxon
logS	-0.19	ALOGPS
pKa (Strongest Acidic)	12.19	ChemAxon
pKa (Strongest Basic)	-3	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	10	ChemAxon
Hydrogen Donor Count	6	ChemAxon
Polar Surface Area	161.6 Å²	ChemAxon
Rotatable Bond Count	4	ChemAxon
Refractivity	77.19 m³·mol⁻¹	ChemAxon
Polarizability	33.77 Å³	ChemAxon
Number of Rings	4	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-2H]-	206.601	30932474
DeepCCS	[M+Na]+	181.841	30932474
AllCCS	[M+H]+	182.2	32859911
AllCCS	[M+H-H2O]+	179.5	32859911
AllCCS	[M+NH4]+	184.8	32859911
AllCCS	[M+Na]+	185.6	32859911
AllCCS	[M-H]-	180.9	32859911
AllCCS	[M+Na-2H]-	180.0	32859911
AllCCS	[M+HCOO]-	179.2	32859911

Predicted Kovats Retention Indices

Derivatized

Derivative Name / Structure	SMILES	Kovats RI Value	Column Type	Reference
(2R,3S,4R,5R,6S)-2-[[(1R,2R,4R,5R,6S,10R)-5-Hydroxy-2-(hydroxymethyl)-3,9-dioxatricyclo[4.4.0.02,4]dec-7-en-10-yl]oxy]-6-(hydroxymethyl)oxane-3,4,5-triol,1TMS,isomer #2	C[Si](C)(C)OC1C2C=COC(OC3OC(CO)C(O)C(O)C3O)C2C2(CO)OC12	3052.8	Semi standard non polar	33892256
(2R,3S,4R,5R,6S)-2-[[(1R,2R,4R,5R,6S,10R)-5-Hydroxy-2-(hydroxymethyl)-3,9-dioxatricyclo[4.4.0.02,4]dec-7-en-10-yl]oxy]-6-(hydroxymethyl)oxane-3,4,5-triol,1TMS,isomer #2	C[Si](C)(C)OC1C2C=COC(OC3OC(CO)C(O)C(O)C3O)C2C2(CO)OC12	2820.8	Standard non polar	33892256
(2R,3S,4R,5R,6S)-2-[[(1R,2R,4R,5R,6S,10R)-5-Hydroxy-2-(hydroxymethyl)-3,9-dioxatricyclo[4.4.0.02,4]dec-7-en-10-yl]oxy]-6-(hydroxymethyl)oxane-3,4,5-triol,1TMS,isomer #2	C[Si](C)(C)OC1C2C=COC(OC3OC(CO)C(O)C(O)C3O)C2C2(CO)OC12	4474.1	Standard polar	33892256
(2R,3S,4R,5R,6S)-2-[[(1R,2R,4R,5R,6S,10R)-5-Hydroxy-2-(hydroxymethyl)-3,9-dioxatricyclo[4.4.0.02,4]dec-7-en-10-yl]oxy]-6-(hydroxymethyl)oxane-3,4,5-triol,1TMS,isomer #3	C[Si](C)(C)OCC12OC1C(O)C1C=COC(OC3OC(CO)C(O)C(O)C3O)C12	3030.6	Semi standard non polar	33892256
(2R,3S,4R,5R,6S)-2-[[(1R,2R,4R,5R,6S,10R)-5-Hydroxy-2-(hydroxymethyl)-3,9-dioxatricyclo[4.4.0.02,4]dec-7-en-10-yl]oxy]-6-(hydroxymethyl)oxane-3,4,5-triol,1TMS,isomer #3	C[Si](C)(C)OCC12OC1C(O)C1C=COC(OC3OC(CO)C(O)C(O)C3O)C12	2905.8	Standard non polar	33892256
(2R,3S,4R,5R,6S)-2-[[(1R,2R,4R,5R,6S,10R)-5-Hydroxy-2-(hydroxymethyl)-3,9-dioxatricyclo[4.4.0.02,4]dec-7-en-10-yl]oxy]-6-(hydroxymethyl)oxane-3,4,5-triol,1TMS,isomer #3	C[Si](C)(C)OCC12OC1C(O)C1C=COC(OC3OC(CO)C(O)C(O)C3O)C12	4715.5	Standard polar	33892256
(2R,3S,4R,5R,6S)-2-[[(1R,2R,4R,5R,6S,10R)-5-Hydroxy-2-(hydroxymethyl)-3,9-dioxatricyclo[4.4.0.02,4]dec-7-en-10-yl]oxy]-6-(hydroxymethyl)oxane-3,4,5-triol,3TMS,isomer #11	C[Si](C)(C)OCC12OC1C(O[Si](C)(C)C)C1C=COC(OC3OC(CO)C(O[Si](C)(C)C)C(O)C3O)C12	2875.6	Semi standard non polar	33892256
(2R,3S,4R,5R,6S)-2-[[(1R,2R,4R,5R,6S,10R)-5-Hydroxy-2-(hydroxymethyl)-3,9-dioxatricyclo[4.4.0.02,4]dec-7-en-10-yl]oxy]-6-(hydroxymethyl)oxane-3,4,5-triol,3TMS,isomer #11	C[Si](C)(C)OCC12OC1C(O[Si](C)(C)C)C1C=COC(OC3OC(CO)C(O[Si](C)(C)C)C(O)C3O)C12	2993.4	Standard non polar	33892256
(2R,3S,4R,5R,6S)-2-[[(1R,2R,4R,5R,6S,10R)-5-Hydroxy-2-(hydroxymethyl)-3,9-dioxatricyclo[4.4.0.02,4]dec-7-en-10-yl]oxy]-6-(hydroxymethyl)oxane-3,4,5-triol,3TMS,isomer #11	C[Si](C)(C)OCC12OC1C(O[Si](C)(C)C)C1C=COC(OC3OC(CO)C(O[Si](C)(C)C)C(O)C3O)C12	3860.0	Standard polar	33892256
(2R,3S,4R,5R,6S)-2-[[(1R,2R,4R,5R,6S,10R)-5-Hydroxy-2-(hydroxymethyl)-3,9-dioxatricyclo[4.4.0.02,4]dec-7-en-10-yl]oxy]-6-(hydroxymethyl)oxane-3,4,5-triol,3TMS,isomer #12	C[Si](C)(C)OC1C(CO)OC(OC2OC=CC3C(O[Si](C)(C)C)C4OC4(CO)C23)C(O[Si](C)(C)C)C1O	2908.8	Semi standard non polar	33892256
(2R,3S,4R,5R,6S)-2-[[(1R,2R,4R,5R,6S,10R)-5-Hydroxy-2-(hydroxymethyl)-3,9-dioxatricyclo[4.4.0.02,4]dec-7-en-10-yl]oxy]-6-(hydroxymethyl)oxane-3,4,5-triol,3TMS,isomer #12	C[Si](C)(C)OC1C(CO)OC(OC2OC=CC3C(O[Si](C)(C)C)C4OC4(CO)C23)C(O[Si](C)(C)C)C1O	2983.7	Standard non polar	33892256
(2R,3S,4R,5R,6S)-2-[[(1R,2R,4R,5R,6S,10R)-5-Hydroxy-2-(hydroxymethyl)-3,9-dioxatricyclo[4.4.0.02,4]dec-7-en-10-yl]oxy]-6-(hydroxymethyl)oxane-3,4,5-triol,3TMS,isomer #12	C[Si](C)(C)OC1C(CO)OC(OC2OC=CC3C(O[Si](C)(C)C)C4OC4(CO)C23)C(O[Si](C)(C)C)C1O	3889.1	Standard polar	33892256
(2R,3S,4R,5R,6S)-2-[[(1R,2R,4R,5R,6S,10R)-5-Hydroxy-2-(hydroxymethyl)-3,9-dioxatricyclo[4.4.0.02,4]dec-7-en-10-yl]oxy]-6-(hydroxymethyl)oxane-3,4,5-triol,3TMS,isomer #13	C[Si](C)(C)OC1C(CO)OC(OC2OC=CC3C(O[Si](C)(C)C)C4OC4(CO)C23)C(O)C1O[Si](C)(C)C	2904.0	Semi standard non polar	33892256
(2R,3S,4R,5R,6S)-2-[[(1R,2R,4R,5R,6S,10R)-5-Hydroxy-2-(hydroxymethyl)-3,9-dioxatricyclo[4.4.0.02,4]dec-7-en-10-yl]oxy]-6-(hydroxymethyl)oxane-3,4,5-triol,3TMS,isomer #13	C[Si](C)(C)OC1C(CO)OC(OC2OC=CC3C(O[Si](C)(C)C)C4OC4(CO)C23)C(O)C1O[Si](C)(C)C	2969.7	Standard non polar	33892256
(2R,3S,4R,5R,6S)-2-[[(1R,2R,4R,5R,6S,10R)-5-Hydroxy-2-(hydroxymethyl)-3,9-dioxatricyclo[4.4.0.02,4]dec-7-en-10-yl]oxy]-6-(hydroxymethyl)oxane-3,4,5-triol,3TMS,isomer #13	C[Si](C)(C)OC1C(CO)OC(OC2OC=CC3C(O[Si](C)(C)C)C4OC4(CO)C23)C(O)C1O[Si](C)(C)C	3844.1	Standard polar	33892256
(2R,3S,4R,5R,6S)-2-[[(1R,2R,4R,5R,6S,10R)-5-Hydroxy-2-(hydroxymethyl)-3,9-dioxatricyclo[4.4.0.02,4]dec-7-en-10-yl]oxy]-6-(hydroxymethyl)oxane-3,4,5-triol,3TMS,isomer #14	C[Si](C)(C)OCC12OC1C(O[Si](C)(C)C)C1C=COC(OC3OC(CO)C(O)C(O[Si](C)(C)C)C3O)C12	2841.4	Semi standard non polar	33892256
(2R,3S,4R,5R,6S)-2-[[(1R,2R,4R,5R,6S,10R)-5-Hydroxy-2-(hydroxymethyl)-3,9-dioxatricyclo[4.4.0.02,4]dec-7-en-10-yl]oxy]-6-(hydroxymethyl)oxane-3,4,5-triol,3TMS,isomer #14	C[Si](C)(C)OCC12OC1C(O[Si](C)(C)C)C1C=COC(OC3OC(CO)C(O)C(O[Si](C)(C)C)C3O)C12	3009.8	Standard non polar	33892256
(2R,3S,4R,5R,6S)-2-[[(1R,2R,4R,5R,6S,10R)-5-Hydroxy-2-(hydroxymethyl)-3,9-dioxatricyclo[4.4.0.02,4]dec-7-en-10-yl]oxy]-6-(hydroxymethyl)oxane-3,4,5-triol,3TMS,isomer #14	C[Si](C)(C)OCC12OC1C(O[Si](C)(C)C)C1C=COC(OC3OC(CO)C(O)C(O[Si](C)(C)C)C3O)C12	3887.9	Standard polar	33892256
(2R,3S,4R,5R,6S)-2-[[(1R,2R,4R,5R,6S,10R)-5-Hydroxy-2-(hydroxymethyl)-3,9-dioxatricyclo[4.4.0.02,4]dec-7-en-10-yl]oxy]-6-(hydroxymethyl)oxane-3,4,5-triol,3TMS,isomer #15	C[Si](C)(C)OC1C(OC2OC=CC3C(O[Si](C)(C)C)C4OC4(CO)C23)OC(CO)C(O)C1O[Si](C)(C)C	2894.5	Semi standard non polar	33892256
(2R,3S,4R,5R,6S)-2-[[(1R,2R,4R,5R,6S,10R)-5-Hydroxy-2-(hydroxymethyl)-3,9-dioxatricyclo[4.4.0.02,4]dec-7-en-10-yl]oxy]-6-(hydroxymethyl)oxane-3,4,5-triol,3TMS,isomer #15	C[Si](C)(C)OC1C(OC2OC=CC3C(O[Si](C)(C)C)C4OC4(CO)C23)OC(CO)C(O)C1O[Si](C)(C)C	2968.7	Standard non polar	33892256
(2R,3S,4R,5R,6S)-2-[[(1R,2R,4R,5R,6S,10R)-5-Hydroxy-2-(hydroxymethyl)-3,9-dioxatricyclo[4.4.0.02,4]dec-7-en-10-yl]oxy]-6-(hydroxymethyl)oxane-3,4,5-triol,3TMS,isomer #15	C[Si](C)(C)OC1C(OC2OC=CC3C(O[Si](C)(C)C)C4OC4(CO)C23)OC(CO)C(O)C1O[Si](C)(C)C	3867.6	Standard polar	33892256
(2R,3S,4R,5R,6S)-2-[[(1R,2R,4R,5R,6S,10R)-5-Hydroxy-2-(hydroxymethyl)-3,9-dioxatricyclo[4.4.0.02,4]dec-7-en-10-yl]oxy]-6-(hydroxymethyl)oxane-3,4,5-triol,3TMS,isomer #16	C[Si](C)(C)OCC12OC1C(O[Si](C)(C)C)C1C=COC(OC3OC(CO)C(O)C(O)C3O[Si](C)(C)C)C12	2855.0	Semi standard non polar	33892256
(2R,3S,4R,5R,6S)-2-[[(1R,2R,4R,5R,6S,10R)-5-Hydroxy-2-(hydroxymethyl)-3,9-dioxatricyclo[4.4.0.02,4]dec-7-en-10-yl]oxy]-6-(hydroxymethyl)oxane-3,4,5-triol,3TMS,isomer #16	C[Si](C)(C)OCC12OC1C(O[Si](C)(C)C)C1C=COC(OC3OC(CO)C(O)C(O)C3O[Si](C)(C)C)C12	2996.2	Standard non polar	33892256
(2R,3S,4R,5R,6S)-2-[[(1R,2R,4R,5R,6S,10R)-5-Hydroxy-2-(hydroxymethyl)-3,9-dioxatricyclo[4.4.0.02,4]dec-7-en-10-yl]oxy]-6-(hydroxymethyl)oxane-3,4,5-triol,3TMS,isomer #16	C[Si](C)(C)OCC12OC1C(O[Si](C)(C)C)C1C=COC(OC3OC(CO)C(O)C(O)C3O[Si](C)(C)C)C12	3881.6	Standard polar	33892256
(2R,3S,4R,5R,6S)-2-[[(1R,2R,4R,5R,6S,10R)-5-Hydroxy-2-(hydroxymethyl)-3,9-dioxatricyclo[4.4.0.02,4]dec-7-en-10-yl]oxy]-6-(hydroxymethyl)oxane-3,4,5-triol,3TMS,isomer #17	C[Si](C)(C)OCC12OC1C(O)C1C=COC(OC3OC(CO)C(O[Si](C)(C)C)C(O[Si](C)(C)C)C3O)C12	2845.6	Semi standard non polar	33892256
(2R,3S,4R,5R,6S)-2-[[(1R,2R,4R,5R,6S,10R)-5-Hydroxy-2-(hydroxymethyl)-3,9-dioxatricyclo[4.4.0.02,4]dec-7-en-10-yl]oxy]-6-(hydroxymethyl)oxane-3,4,5-triol,3TMS,isomer #17	C[Si](C)(C)OCC12OC1C(O)C1C=COC(OC3OC(CO)C(O[Si](C)(C)C)C(O[Si](C)(C)C)C3O)C12	3020.7	Standard non polar	33892256
(2R,3S,4R,5R,6S)-2-[[(1R,2R,4R,5R,6S,10R)-5-Hydroxy-2-(hydroxymethyl)-3,9-dioxatricyclo[4.4.0.02,4]dec-7-en-10-yl]oxy]-6-(hydroxymethyl)oxane-3,4,5-triol,3TMS,isomer #17	C[Si](C)(C)OCC12OC1C(O)C1C=COC(OC3OC(CO)C(O[Si](C)(C)C)C(O[Si](C)(C)C)C3O)C12	3984.9	Standard polar	33892256
(2R,3S,4R,5R,6S)-2-[[(1R,2R,4R,5R,6S,10R)-5-Hydroxy-2-(hydroxymethyl)-3,9-dioxatricyclo[4.4.0.02,4]dec-7-en-10-yl]oxy]-6-(hydroxymethyl)oxane-3,4,5-triol,3TMS,isomer #18	C[Si](C)(C)OCC12OC1C(O)C1C=COC(OC3OC(CO)C(O[Si](C)(C)C)C(O)C3O[Si](C)(C)C)C12	2841.8	Semi standard non polar	33892256
(2R,3S,4R,5R,6S)-2-[[(1R,2R,4R,5R,6S,10R)-5-Hydroxy-2-(hydroxymethyl)-3,9-dioxatricyclo[4.4.0.02,4]dec-7-en-10-yl]oxy]-6-(hydroxymethyl)oxane-3,4,5-triol,3TMS,isomer #18	C[Si](C)(C)OCC12OC1C(O)C1C=COC(OC3OC(CO)C(O[Si](C)(C)C)C(O)C3O[Si](C)(C)C)C12	3033.3	Standard non polar	33892256
(2R,3S,4R,5R,6S)-2-[[(1R,2R,4R,5R,6S,10R)-5-Hydroxy-2-(hydroxymethyl)-3,9-dioxatricyclo[4.4.0.02,4]dec-7-en-10-yl]oxy]-6-(hydroxymethyl)oxane-3,4,5-triol,3TMS,isomer #18	C[Si](C)(C)OCC12OC1C(O)C1C=COC(OC3OC(CO)C(O[Si](C)(C)C)C(O)C3O[Si](C)(C)C)C12	4028.6	Standard polar	33892256
(2R,3S,4R,5R,6S)-2-[[(1R,2R,4R,5R,6S,10R)-5-Hydroxy-2-(hydroxymethyl)-3,9-dioxatricyclo[4.4.0.02,4]dec-7-en-10-yl]oxy]-6-(hydroxymethyl)oxane-3,4,5-triol,3TMS,isomer #19	C[Si](C)(C)OCC12OC1C(O)C1C=COC(OC3OC(CO)C(O)C(O[Si](C)(C)C)C3O[Si](C)(C)C)C12	2829.8	Semi standard non polar	33892256
(2R,3S,4R,5R,6S)-2-[[(1R,2R,4R,5R,6S,10R)-5-Hydroxy-2-(hydroxymethyl)-3,9-dioxatricyclo[4.4.0.02,4]dec-7-en-10-yl]oxy]-6-(hydroxymethyl)oxane-3,4,5-triol,3TMS,isomer #19	C[Si](C)(C)OCC12OC1C(O)C1C=COC(OC3OC(CO)C(O)C(O[Si](C)(C)C)C3O[Si](C)(C)C)C12	3022.6	Standard non polar	33892256
(2R,3S,4R,5R,6S)-2-[[(1R,2R,4R,5R,6S,10R)-5-Hydroxy-2-(hydroxymethyl)-3,9-dioxatricyclo[4.4.0.02,4]dec-7-en-10-yl]oxy]-6-(hydroxymethyl)oxane-3,4,5-triol,3TMS,isomer #19	C[Si](C)(C)OCC12OC1C(O)C1C=COC(OC3OC(CO)C(O)C(O[Si](C)(C)C)C3O[Si](C)(C)C)C12	4007.3	Standard polar	33892256
(2R,3S,4R,5R,6S)-2-[[(1R,2R,4R,5R,6S,10R)-5-Hydroxy-2-(hydroxymethyl)-3,9-dioxatricyclo[4.4.0.02,4]dec-7-en-10-yl]oxy]-6-(hydroxymethyl)oxane-3,4,5-triol,3TMS,isomer #2	C[Si](C)(C)OCC1OC(OC2OC=CC3C(O[Si](C)(C)C)C4OC4(CO)C23)C(O[Si](C)(C)C)C(O)C1O	2900.0	Semi standard non polar	33892256
(2R,3S,4R,5R,6S)-2-[[(1R,2R,4R,5R,6S,10R)-5-Hydroxy-2-(hydroxymethyl)-3,9-dioxatricyclo[4.4.0.02,4]dec-7-en-10-yl]oxy]-6-(hydroxymethyl)oxane-3,4,5-triol,3TMS,isomer #2	C[Si](C)(C)OCC1OC(OC2OC=CC3C(O[Si](C)(C)C)C4OC4(CO)C23)C(O[Si](C)(C)C)C(O)C1O	2991.8	Standard non polar	33892256
(2R,3S,4R,5R,6S)-2-[[(1R,2R,4R,5R,6S,10R)-5-Hydroxy-2-(hydroxymethyl)-3,9-dioxatricyclo[4.4.0.02,4]dec-7-en-10-yl]oxy]-6-(hydroxymethyl)oxane-3,4,5-triol,3TMS,isomer #2	C[Si](C)(C)OCC1OC(OC2OC=CC3C(O[Si](C)(C)C)C4OC4(CO)C23)C(O[Si](C)(C)C)C(O)C1O	3923.5	Standard polar	33892256
(2R,3S,4R,5R,6S)-2-[[(1R,2R,4R,5R,6S,10R)-5-Hydroxy-2-(hydroxymethyl)-3,9-dioxatricyclo[4.4.0.02,4]dec-7-en-10-yl]oxy]-6-(hydroxymethyl)oxane-3,4,5-triol,3TMS,isomer #20	C[Si](C)(C)OC1C(CO)OC(OC2OC=CC3C(O)C4OC4(CO)C23)C(O[Si](C)(C)C)C1O[Si](C)(C)C	2896.3	Semi standard non polar	33892256
(2R,3S,4R,5R,6S)-2-[[(1R,2R,4R,5R,6S,10R)-5-Hydroxy-2-(hydroxymethyl)-3,9-dioxatricyclo[4.4.0.02,4]dec-7-en-10-yl]oxy]-6-(hydroxymethyl)oxane-3,4,5-triol,3TMS,isomer #20	C[Si](C)(C)OC1C(CO)OC(OC2OC=CC3C(O)C4OC4(CO)C23)C(O[Si](C)(C)C)C1O[Si](C)(C)C	2989.9	Standard non polar	33892256
(2R,3S,4R,5R,6S)-2-[[(1R,2R,4R,5R,6S,10R)-5-Hydroxy-2-(hydroxymethyl)-3,9-dioxatricyclo[4.4.0.02,4]dec-7-en-10-yl]oxy]-6-(hydroxymethyl)oxane-3,4,5-triol,3TMS,isomer #20	C[Si](C)(C)OC1C(CO)OC(OC2OC=CC3C(O)C4OC4(CO)C23)C(O[Si](C)(C)C)C1O[Si](C)(C)C	3935.7	Standard polar	33892256
(2R,3S,4R,5R,6S)-2-[[(1R,2R,4R,5R,6S,10R)-5-Hydroxy-2-(hydroxymethyl)-3,9-dioxatricyclo[4.4.0.02,4]dec-7-en-10-yl]oxy]-6-(hydroxymethyl)oxane-3,4,5-triol,3TMS,isomer #7	C[Si](C)(C)OCC1OC(OC2OC=CC3C(O)C4OC4(CO[Si](C)(C)C)C23)C(O)C(O)C1O[Si](C)(C)C	2878.7	Semi standard non polar	33892256
(2R,3S,4R,5R,6S)-2-[[(1R,2R,4R,5R,6S,10R)-5-Hydroxy-2-(hydroxymethyl)-3,9-dioxatricyclo[4.4.0.02,4]dec-7-en-10-yl]oxy]-6-(hydroxymethyl)oxane-3,4,5-triol,3TMS,isomer #7	C[Si](C)(C)OCC1OC(OC2OC=CC3C(O)C4OC4(CO[Si](C)(C)C)C23)C(O)C(O)C1O[Si](C)(C)C	3051.7	Standard non polar	33892256
(2R,3S,4R,5R,6S)-2-[[(1R,2R,4R,5R,6S,10R)-5-Hydroxy-2-(hydroxymethyl)-3,9-dioxatricyclo[4.4.0.02,4]dec-7-en-10-yl]oxy]-6-(hydroxymethyl)oxane-3,4,5-triol,3TMS,isomer #7	C[Si](C)(C)OCC1OC(OC2OC=CC3C(O)C4OC4(CO[Si](C)(C)C)C23)C(O)C(O)C1O[Si](C)(C)C	4041.6	Standard polar	33892256
(2R,3S,4R,5R,6S)-2-[[(1R,2R,4R,5R,6S,10R)-5-Hydroxy-2-(hydroxymethyl)-3,9-dioxatricyclo[4.4.0.02,4]dec-7-en-10-yl]oxy]-6-(hydroxymethyl)oxane-3,4,5-triol,4TMS,isomer #1	C[Si](C)(C)OCC1OC(OC2OC=CC3C(O[Si](C)(C)C)C4OC4(CO[Si](C)(C)C)C23)C(O[Si](C)(C)C)C(O)C1O	2773.8	Semi standard non polar	33892256
(2R,3S,4R,5R,6S)-2-[[(1R,2R,4R,5R,6S,10R)-5-Hydroxy-2-(hydroxymethyl)-3,9-dioxatricyclo[4.4.0.02,4]dec-7-en-10-yl]oxy]-6-(hydroxymethyl)oxane-3,4,5-triol,4TMS,isomer #1	C[Si](C)(C)OCC1OC(OC2OC=CC3C(O[Si](C)(C)C)C4OC4(CO[Si](C)(C)C)C23)C(O[Si](C)(C)C)C(O)C1O	3056.9	Standard non polar	33892256
(2R,3S,4R,5R,6S)-2-[[(1R,2R,4R,5R,6S,10R)-5-Hydroxy-2-(hydroxymethyl)-3,9-dioxatricyclo[4.4.0.02,4]dec-7-en-10-yl]oxy]-6-(hydroxymethyl)oxane-3,4,5-triol,4TMS,isomer #1	C[Si](C)(C)OCC1OC(OC2OC=CC3C(O[Si](C)(C)C)C4OC4(CO[Si](C)(C)C)C23)C(O[Si](C)(C)C)C(O)C1O	3681.9	Standard polar	33892256
(2R,3S,4R,5R,6S)-2-[[(1R,2R,4R,5R,6S,10R)-5-Hydroxy-2-(hydroxymethyl)-3,9-dioxatricyclo[4.4.0.02,4]dec-7-en-10-yl]oxy]-6-(hydroxymethyl)oxane-3,4,5-triol,4TMS,isomer #10	C[Si](C)(C)OCC1OC(OC2OC=CC3C(O)C4OC4(CO)C23)C(O[Si](C)(C)C)C(O[Si](C)(C)C)C1O[Si](C)(C)C	2824.6	Semi standard non polar	33892256
(2R,3S,4R,5R,6S)-2-[[(1R,2R,4R,5R,6S,10R)-5-Hydroxy-2-(hydroxymethyl)-3,9-dioxatricyclo[4.4.0.02,4]dec-7-en-10-yl]oxy]-6-(hydroxymethyl)oxane-3,4,5-triol,4TMS,isomer #10	C[Si](C)(C)OCC1OC(OC2OC=CC3C(O)C4OC4(CO)C23)C(O[Si](C)(C)C)C(O[Si](C)(C)C)C1O[Si](C)(C)C	3058.8	Standard non polar	33892256
(2R,3S,4R,5R,6S)-2-[[(1R,2R,4R,5R,6S,10R)-5-Hydroxy-2-(hydroxymethyl)-3,9-dioxatricyclo[4.4.0.02,4]dec-7-en-10-yl]oxy]-6-(hydroxymethyl)oxane-3,4,5-triol,4TMS,isomer #10	C[Si](C)(C)OCC1OC(OC2OC=CC3C(O)C4OC4(CO)C23)C(O[Si](C)(C)C)C(O[Si](C)(C)C)C1O[Si](C)(C)C	3734.3	Standard polar	33892256
(2R,3S,4R,5R,6S)-2-[[(1R,2R,4R,5R,6S,10R)-5-Hydroxy-2-(hydroxymethyl)-3,9-dioxatricyclo[4.4.0.02,4]dec-7-en-10-yl]oxy]-6-(hydroxymethyl)oxane-3,4,5-triol,4TMS,isomer #11	C[Si](C)(C)OCC12OC1C(O[Si](C)(C)C)C1C=COC(OC3OC(CO)C(O[Si](C)(C)C)C(O[Si](C)(C)C)C3O)C12	2736.9	Semi standard non polar	33892256
(2R,3S,4R,5R,6S)-2-[[(1R,2R,4R,5R,6S,10R)-5-Hydroxy-2-(hydroxymethyl)-3,9-dioxatricyclo[4.4.0.02,4]dec-7-en-10-yl]oxy]-6-(hydroxymethyl)oxane-3,4,5-triol,4TMS,isomer #11	C[Si](C)(C)OCC12OC1C(O[Si](C)(C)C)C1C=COC(OC3OC(CO)C(O[Si](C)(C)C)C(O[Si](C)(C)C)C3O)C12	3026.2	Standard non polar	33892256
(2R,3S,4R,5R,6S)-2-[[(1R,2R,4R,5R,6S,10R)-5-Hydroxy-2-(hydroxymethyl)-3,9-dioxatricyclo[4.4.0.02,4]dec-7-en-10-yl]oxy]-6-(hydroxymethyl)oxane-3,4,5-triol,4TMS,isomer #11	C[Si](C)(C)OCC12OC1C(O[Si](C)(C)C)C1C=COC(OC3OC(CO)C(O[Si](C)(C)C)C(O[Si](C)(C)C)C3O)C12	3628.3	Standard polar	33892256
(2R,3S,4R,5R,6S)-2-[[(1R,2R,4R,5R,6S,10R)-5-Hydroxy-2-(hydroxymethyl)-3,9-dioxatricyclo[4.4.0.02,4]dec-7-en-10-yl]oxy]-6-(hydroxymethyl)oxane-3,4,5-triol,4TMS,isomer #12	C[Si](C)(C)OCC12OC1C(O[Si](C)(C)C)C1C=COC(OC3OC(CO)C(O[Si](C)(C)C)C(O)C3O[Si](C)(C)C)C12	2739.6	Semi standard non polar	33892256
(2R,3S,4R,5R,6S)-2-[[(1R,2R,4R,5R,6S,10R)-5-Hydroxy-2-(hydroxymethyl)-3,9-dioxatricyclo[4.4.0.02,4]dec-7-en-10-yl]oxy]-6-(hydroxymethyl)oxane-3,4,5-triol,4TMS,isomer #12	C[Si](C)(C)OCC12OC1C(O[Si](C)(C)C)C1C=COC(OC3OC(CO)C(O[Si](C)(C)C)C(O)C3O[Si](C)(C)C)C12	3052.8	Standard non polar	33892256
(2R,3S,4R,5R,6S)-2-[[(1R,2R,4R,5R,6S,10R)-5-Hydroxy-2-(hydroxymethyl)-3,9-dioxatricyclo[4.4.0.02,4]dec-7-en-10-yl]oxy]-6-(hydroxymethyl)oxane-3,4,5-triol,4TMS,isomer #12	C[Si](C)(C)OCC12OC1C(O[Si](C)(C)C)C1C=COC(OC3OC(CO)C(O[Si](C)(C)C)C(O)C3O[Si](C)(C)C)C12	3672.1	Standard polar	33892256
(2R,3S,4R,5R,6S)-2-[[(1R,2R,4R,5R,6S,10R)-5-Hydroxy-2-(hydroxymethyl)-3,9-dioxatricyclo[4.4.0.02,4]dec-7-en-10-yl]oxy]-6-(hydroxymethyl)oxane-3,4,5-triol,4TMS,isomer #13	C[Si](C)(C)OC1C(CO)OC(OC2OC=CC3C(O[Si](C)(C)C)C4OC4(CO)C23)C(O[Si](C)(C)C)C1O[Si](C)(C)C	2810.4	Semi standard non polar	33892256
(2R,3S,4R,5R,6S)-2-[[(1R,2R,4R,5R,6S,10R)-5-Hydroxy-2-(hydroxymethyl)-3,9-dioxatricyclo[4.4.0.02,4]dec-7-en-10-yl]oxy]-6-(hydroxymethyl)oxane-3,4,5-triol,4TMS,isomer #13	C[Si](C)(C)OC1C(CO)OC(OC2OC=CC3C(O[Si](C)(C)C)C4OC4(CO)C23)C(O[Si](C)(C)C)C1O[Si](C)(C)C	2981.2	Standard non polar	33892256
(2R,3S,4R,5R,6S)-2-[[(1R,2R,4R,5R,6S,10R)-5-Hydroxy-2-(hydroxymethyl)-3,9-dioxatricyclo[4.4.0.02,4]dec-7-en-10-yl]oxy]-6-(hydroxymethyl)oxane-3,4,5-triol,4TMS,isomer #13	C[Si](C)(C)OC1C(CO)OC(OC2OC=CC3C(O[Si](C)(C)C)C4OC4(CO)C23)C(O[Si](C)(C)C)C1O[Si](C)(C)C	3606.5	Standard polar	33892256
(2R,3S,4R,5R,6S)-2-[[(1R,2R,4R,5R,6S,10R)-5-Hydroxy-2-(hydroxymethyl)-3,9-dioxatricyclo[4.4.0.02,4]dec-7-en-10-yl]oxy]-6-(hydroxymethyl)oxane-3,4,5-triol,4TMS,isomer #14	C[Si](C)(C)OCC12OC1C(O[Si](C)(C)C)C1C=COC(OC3OC(CO)C(O)C(O[Si](C)(C)C)C3O[Si](C)(C)C)C12	2709.3	Semi standard non polar	33892256
(2R,3S,4R,5R,6S)-2-[[(1R,2R,4R,5R,6S,10R)-5-Hydroxy-2-(hydroxymethyl)-3,9-dioxatricyclo[4.4.0.02,4]dec-7-en-10-yl]oxy]-6-(hydroxymethyl)oxane-3,4,5-triol,4TMS,isomer #14	C[Si](C)(C)OCC12OC1C(O[Si](C)(C)C)C1C=COC(OC3OC(CO)C(O)C(O[Si](C)(C)C)C3O[Si](C)(C)C)C12	3030.3	Standard non polar	33892256
(2R,3S,4R,5R,6S)-2-[[(1R,2R,4R,5R,6S,10R)-5-Hydroxy-2-(hydroxymethyl)-3,9-dioxatricyclo[4.4.0.02,4]dec-7-en-10-yl]oxy]-6-(hydroxymethyl)oxane-3,4,5-triol,4TMS,isomer #14	C[Si](C)(C)OCC12OC1C(O[Si](C)(C)C)C1C=COC(OC3OC(CO)C(O)C(O[Si](C)(C)C)C3O[Si](C)(C)C)C12	3649.6	Standard polar	33892256
(2R,3S,4R,5R,6S)-2-[[(1R,2R,4R,5R,6S,10R)-5-Hydroxy-2-(hydroxymethyl)-3,9-dioxatricyclo[4.4.0.02,4]dec-7-en-10-yl]oxy]-6-(hydroxymethyl)oxane-3,4,5-triol,4TMS,isomer #15	C[Si](C)(C)OCC12OC1C(O)C1C=COC(OC3OC(CO)C(O[Si](C)(C)C)C(O[Si](C)(C)C)C3O[Si](C)(C)C)C12	2728.1	Semi standard non polar	33892256
(2R,3S,4R,5R,6S)-2-[[(1R,2R,4R,5R,6S,10R)-5-Hydroxy-2-(hydroxymethyl)-3,9-dioxatricyclo[4.4.0.02,4]dec-7-en-10-yl]oxy]-6-(hydroxymethyl)oxane-3,4,5-triol,4TMS,isomer #15	C[Si](C)(C)OCC12OC1C(O)C1C=COC(OC3OC(CO)C(O[Si](C)(C)C)C(O[Si](C)(C)C)C3O[Si](C)(C)C)C12	3031.6	Standard non polar	33892256
(2R,3S,4R,5R,6S)-2-[[(1R,2R,4R,5R,6S,10R)-5-Hydroxy-2-(hydroxymethyl)-3,9-dioxatricyclo[4.4.0.02,4]dec-7-en-10-yl]oxy]-6-(hydroxymethyl)oxane-3,4,5-triol,4TMS,isomer #15	C[Si](C)(C)OCC12OC1C(O)C1C=COC(OC3OC(CO)C(O[Si](C)(C)C)C(O[Si](C)(C)C)C3O[Si](C)(C)C)C12	3740.2	Standard polar	33892256
(2R,3S,4R,5R,6S)-2-[[(1R,2R,4R,5R,6S,10R)-5-Hydroxy-2-(hydroxymethyl)-3,9-dioxatricyclo[4.4.0.02,4]dec-7-en-10-yl]oxy]-6-(hydroxymethyl)oxane-3,4,5-triol,4TMS,isomer #2	C[Si](C)(C)OCC1OC(OC2OC=CC3C(O[Si](C)(C)C)C4OC4(CO[Si](C)(C)C)C23)C(O)C(O[Si](C)(C)C)C1O	2760.4	Semi standard non polar	33892256
(2R,3S,4R,5R,6S)-2-[[(1R,2R,4R,5R,6S,10R)-5-Hydroxy-2-(hydroxymethyl)-3,9-dioxatricyclo[4.4.0.02,4]dec-7-en-10-yl]oxy]-6-(hydroxymethyl)oxane-3,4,5-triol,4TMS,isomer #2	C[Si](C)(C)OCC1OC(OC2OC=CC3C(O[Si](C)(C)C)C4OC4(CO[Si](C)(C)C)C23)C(O)C(O[Si](C)(C)C)C1O	3071.6	Standard non polar	33892256
(2R,3S,4R,5R,6S)-2-[[(1R,2R,4R,5R,6S,10R)-5-Hydroxy-2-(hydroxymethyl)-3,9-dioxatricyclo[4.4.0.02,4]dec-7-en-10-yl]oxy]-6-(hydroxymethyl)oxane-3,4,5-triol,4TMS,isomer #2	C[Si](C)(C)OCC1OC(OC2OC=CC3C(O[Si](C)(C)C)C4OC4(CO[Si](C)(C)C)C23)C(O)C(O[Si](C)(C)C)C1O	3692.8	Standard polar	33892256
(2R,3S,4R,5R,6S)-2-[[(1R,2R,4R,5R,6S,10R)-5-Hydroxy-2-(hydroxymethyl)-3,9-dioxatricyclo[4.4.0.02,4]dec-7-en-10-yl]oxy]-6-(hydroxymethyl)oxane-3,4,5-triol,4TMS,isomer #3	C[Si](C)(C)OCC1OC(OC2OC=CC3C(O[Si](C)(C)C)C4OC4(CO[Si](C)(C)C)C23)C(O)C(O)C1O[Si](C)(C)C	2793.7	Semi standard non polar	33892256
(2R,3S,4R,5R,6S)-2-[[(1R,2R,4R,5R,6S,10R)-5-Hydroxy-2-(hydroxymethyl)-3,9-dioxatricyclo[4.4.0.02,4]dec-7-en-10-yl]oxy]-6-(hydroxymethyl)oxane-3,4,5-triol,4TMS,isomer #3	C[Si](C)(C)OCC1OC(OC2OC=CC3C(O[Si](C)(C)C)C4OC4(CO[Si](C)(C)C)C23)C(O)C(O)C1O[Si](C)(C)C	3055.6	Standard non polar	33892256
(2R,3S,4R,5R,6S)-2-[[(1R,2R,4R,5R,6S,10R)-5-Hydroxy-2-(hydroxymethyl)-3,9-dioxatricyclo[4.4.0.02,4]dec-7-en-10-yl]oxy]-6-(hydroxymethyl)oxane-3,4,5-triol,4TMS,isomer #3	C[Si](C)(C)OCC1OC(OC2OC=CC3C(O[Si](C)(C)C)C4OC4(CO[Si](C)(C)C)C23)C(O)C(O)C1O[Si](C)(C)C	3662.0	Standard polar	33892256
(2R,3S,4R,5R,6S)-2-[[(1R,2R,4R,5R,6S,10R)-5-Hydroxy-2-(hydroxymethyl)-3,9-dioxatricyclo[4.4.0.02,4]dec-7-en-10-yl]oxy]-6-(hydroxymethyl)oxane-3,4,5-triol,4TMS,isomer #4	C[Si](C)(C)OCC1OC(OC2OC=CC3C(O[Si](C)(C)C)C4OC4(CO)C23)C(O[Si](C)(C)C)C(O[Si](C)(C)C)C1O	2776.4	Semi standard non polar	33892256
(2R,3S,4R,5R,6S)-2-[[(1R,2R,4R,5R,6S,10R)-5-Hydroxy-2-(hydroxymethyl)-3,9-dioxatricyclo[4.4.0.02,4]dec-7-en-10-yl]oxy]-6-(hydroxymethyl)oxane-3,4,5-triol,4TMS,isomer #4	C[Si](C)(C)OCC1OC(OC2OC=CC3C(O[Si](C)(C)C)C4OC4(CO)C23)C(O[Si](C)(C)C)C(O[Si](C)(C)C)C1O	3034.2	Standard non polar	33892256
(2R,3S,4R,5R,6S)-2-[[(1R,2R,4R,5R,6S,10R)-5-Hydroxy-2-(hydroxymethyl)-3,9-dioxatricyclo[4.4.0.02,4]dec-7-en-10-yl]oxy]-6-(hydroxymethyl)oxane-3,4,5-triol,4TMS,isomer #4	C[Si](C)(C)OCC1OC(OC2OC=CC3C(O[Si](C)(C)C)C4OC4(CO)C23)C(O[Si](C)(C)C)C(O[Si](C)(C)C)C1O	3681.6	Standard polar	33892256
(2R,3S,4R,5R,6S)-2-[[(1R,2R,4R,5R,6S,10R)-5-Hydroxy-2-(hydroxymethyl)-3,9-dioxatricyclo[4.4.0.02,4]dec-7-en-10-yl]oxy]-6-(hydroxymethyl)oxane-3,4,5-triol,4TMS,isomer #5	C[Si](C)(C)OCC1OC(OC2OC=CC3C(O[Si](C)(C)C)C4OC4(CO)C23)C(O[Si](C)(C)C)C(O)C1O[Si](C)(C)C	2804.4	Semi standard non polar	33892256
(2R,3S,4R,5R,6S)-2-[[(1R,2R,4R,5R,6S,10R)-5-Hydroxy-2-(hydroxymethyl)-3,9-dioxatricyclo[4.4.0.02,4]dec-7-en-10-yl]oxy]-6-(hydroxymethyl)oxane-3,4,5-triol,4TMS,isomer #5	C[Si](C)(C)OCC1OC(OC2OC=CC3C(O[Si](C)(C)C)C4OC4(CO)C23)C(O[Si](C)(C)C)C(O)C1O[Si](C)(C)C	3064.4	Standard non polar	33892256
(2R,3S,4R,5R,6S)-2-[[(1R,2R,4R,5R,6S,10R)-5-Hydroxy-2-(hydroxymethyl)-3,9-dioxatricyclo[4.4.0.02,4]dec-7-en-10-yl]oxy]-6-(hydroxymethyl)oxane-3,4,5-triol,4TMS,isomer #5	C[Si](C)(C)OCC1OC(OC2OC=CC3C(O[Si](C)(C)C)C4OC4(CO)C23)C(O[Si](C)(C)C)C(O)C1O[Si](C)(C)C	3703.7	Standard polar	33892256
(2R,3S,4R,5R,6S)-2-[[(1R,2R,4R,5R,6S,10R)-5-Hydroxy-2-(hydroxymethyl)-3,9-dioxatricyclo[4.4.0.02,4]dec-7-en-10-yl]oxy]-6-(hydroxymethyl)oxane-3,4,5-triol,4TMS,isomer #6	C[Si](C)(C)OCC1OC(OC2OC=CC3C(O[Si](C)(C)C)C4OC4(CO)C23)C(O)C(O[Si](C)(C)C)C1O[Si](C)(C)C	2800.9	Semi standard non polar	33892256
(2R,3S,4R,5R,6S)-2-[[(1R,2R,4R,5R,6S,10R)-5-Hydroxy-2-(hydroxymethyl)-3,9-dioxatricyclo[4.4.0.02,4]dec-7-en-10-yl]oxy]-6-(hydroxymethyl)oxane-3,4,5-triol,4TMS,isomer #6	C[Si](C)(C)OCC1OC(OC2OC=CC3C(O[Si](C)(C)C)C4OC4(CO)C23)C(O)C(O[Si](C)(C)C)C1O[Si](C)(C)C	3031.8	Standard non polar	33892256
(2R,3S,4R,5R,6S)-2-[[(1R,2R,4R,5R,6S,10R)-5-Hydroxy-2-(hydroxymethyl)-3,9-dioxatricyclo[4.4.0.02,4]dec-7-en-10-yl]oxy]-6-(hydroxymethyl)oxane-3,4,5-triol,4TMS,isomer #6	C[Si](C)(C)OCC1OC(OC2OC=CC3C(O[Si](C)(C)C)C4OC4(CO)C23)C(O)C(O[Si](C)(C)C)C1O[Si](C)(C)C	3660.8	Standard polar	33892256
(2R,3S,4R,5R,6S)-2-[[(1R,2R,4R,5R,6S,10R)-5-Hydroxy-2-(hydroxymethyl)-3,9-dioxatricyclo[4.4.0.02,4]dec-7-en-10-yl]oxy]-6-(hydroxymethyl)oxane-3,4,5-triol,4TMS,isomer #7	C[Si](C)(C)OCC1OC(OC2OC=CC3C(O)C4OC4(CO[Si](C)(C)C)C23)C(O[Si](C)(C)C)C(O[Si](C)(C)C)C1O	2765.4	Semi standard non polar	33892256
(2R,3S,4R,5R,6S)-2-[[(1R,2R,4R,5R,6S,10R)-5-Hydroxy-2-(hydroxymethyl)-3,9-dioxatricyclo[4.4.0.02,4]dec-7-en-10-yl]oxy]-6-(hydroxymethyl)oxane-3,4,5-triol,4TMS,isomer #7	C[Si](C)(C)OCC1OC(OC2OC=CC3C(O)C4OC4(CO[Si](C)(C)C)C23)C(O[Si](C)(C)C)C(O[Si](C)(C)C)C1O	3085.4	Standard non polar	33892256
(2R,3S,4R,5R,6S)-2-[[(1R,2R,4R,5R,6S,10R)-5-Hydroxy-2-(hydroxymethyl)-3,9-dioxatricyclo[4.4.0.02,4]dec-7-en-10-yl]oxy]-6-(hydroxymethyl)oxane-3,4,5-triol,4TMS,isomer #7	C[Si](C)(C)OCC1OC(OC2OC=CC3C(O)C4OC4(CO[Si](C)(C)C)C23)C(O[Si](C)(C)C)C(O[Si](C)(C)C)C1O	3805.4	Standard polar	33892256
(2R,3S,4R,5R,6S)-2-[[(1R,2R,4R,5R,6S,10R)-5-Hydroxy-2-(hydroxymethyl)-3,9-dioxatricyclo[4.4.0.02,4]dec-7-en-10-yl]oxy]-6-(hydroxymethyl)oxane-3,4,5-triol,4TMS,isomer #8	C[Si](C)(C)OCC1OC(OC2OC=CC3C(O)C4OC4(CO[Si](C)(C)C)C23)C(O[Si](C)(C)C)C(O)C1O[Si](C)(C)C	2786.9	Semi standard non polar	33892256
(2R,3S,4R,5R,6S)-2-[[(1R,2R,4R,5R,6S,10R)-5-Hydroxy-2-(hydroxymethyl)-3,9-dioxatricyclo[4.4.0.02,4]dec-7-en-10-yl]oxy]-6-(hydroxymethyl)oxane-3,4,5-triol,4TMS,isomer #8	C[Si](C)(C)OCC1OC(OC2OC=CC3C(O)C4OC4(CO[Si](C)(C)C)C23)C(O[Si](C)(C)C)C(O)C1O[Si](C)(C)C	3113.8	Standard non polar	33892256
(2R,3S,4R,5R,6S)-2-[[(1R,2R,4R,5R,6S,10R)-5-Hydroxy-2-(hydroxymethyl)-3,9-dioxatricyclo[4.4.0.02,4]dec-7-en-10-yl]oxy]-6-(hydroxymethyl)oxane-3,4,5-triol,4TMS,isomer #8	C[Si](C)(C)OCC1OC(OC2OC=CC3C(O)C4OC4(CO[Si](C)(C)C)C23)C(O[Si](C)(C)C)C(O)C1O[Si](C)(C)C	3826.5	Standard polar	33892256
(2R,3S,4R,5R,6S)-2-[[(1R,2R,4R,5R,6S,10R)-5-Hydroxy-2-(hydroxymethyl)-3,9-dioxatricyclo[4.4.0.02,4]dec-7-en-10-yl]oxy]-6-(hydroxymethyl)oxane-3,4,5-triol,4TMS,isomer #9	C[Si](C)(C)OCC1OC(OC2OC=CC3C(O)C4OC4(CO[Si](C)(C)C)C23)C(O)C(O[Si](C)(C)C)C1O[Si](C)(C)C	2793.3	Semi standard non polar	33892256
(2R,3S,4R,5R,6S)-2-[[(1R,2R,4R,5R,6S,10R)-5-Hydroxy-2-(hydroxymethyl)-3,9-dioxatricyclo[4.4.0.02,4]dec-7-en-10-yl]oxy]-6-(hydroxymethyl)oxane-3,4,5-triol,4TMS,isomer #9	C[Si](C)(C)OCC1OC(OC2OC=CC3C(O)C4OC4(CO[Si](C)(C)C)C23)C(O)C(O[Si](C)(C)C)C1O[Si](C)(C)C	3082.3	Standard non polar	33892256
(2R,3S,4R,5R,6S)-2-[[(1R,2R,4R,5R,6S,10R)-5-Hydroxy-2-(hydroxymethyl)-3,9-dioxatricyclo[4.4.0.02,4]dec-7-en-10-yl]oxy]-6-(hydroxymethyl)oxane-3,4,5-triol,4TMS,isomer #9	C[Si](C)(C)OCC1OC(OC2OC=CC3C(O)C4OC4(CO[Si](C)(C)C)C23)C(O)C(O[Si](C)(C)C)C1O[Si](C)(C)C	3783.9	Standard polar	33892256
(2R,3S,4R,5R,6S)-2-[[(1R,2R,4R,5R,6S,10R)-5-Hydroxy-2-(hydroxymethyl)-3,9-dioxatricyclo[4.4.0.02,4]dec-7-en-10-yl]oxy]-6-(hydroxymethyl)oxane-3,4,5-triol,5TMS,isomer #1	C[Si](C)(C)OCC1OC(OC2OC=CC3C(O[Si](C)(C)C)C4OC4(CO[Si](C)(C)C)C23)C(O[Si](C)(C)C)C(O[Si](C)(C)C)C1O	2646.6	Semi standard non polar	33892256
(2R,3S,4R,5R,6S)-2-[[(1R,2R,4R,5R,6S,10R)-5-Hydroxy-2-(hydroxymethyl)-3,9-dioxatricyclo[4.4.0.02,4]dec-7-en-10-yl]oxy]-6-(hydroxymethyl)oxane-3,4,5-triol,5TMS,isomer #1	C[Si](C)(C)OCC1OC(OC2OC=CC3C(O[Si](C)(C)C)C4OC4(CO[Si](C)(C)C)C23)C(O[Si](C)(C)C)C(O[Si](C)(C)C)C1O	3065.2	Standard non polar	33892256
(2R,3S,4R,5R,6S)-2-[[(1R,2R,4R,5R,6S,10R)-5-Hydroxy-2-(hydroxymethyl)-3,9-dioxatricyclo[4.4.0.02,4]dec-7-en-10-yl]oxy]-6-(hydroxymethyl)oxane-3,4,5-triol,5TMS,isomer #1	C[Si](C)(C)OCC1OC(OC2OC=CC3C(O[Si](C)(C)C)C4OC4(CO[Si](C)(C)C)C23)C(O[Si](C)(C)C)C(O[Si](C)(C)C)C1O	3453.0	Standard polar	33892256
(2R,3S,4R,5R,6S)-2-[[(1R,2R,4R,5R,6S,10R)-5-Hydroxy-2-(hydroxymethyl)-3,9-dioxatricyclo[4.4.0.02,4]dec-7-en-10-yl]oxy]-6-(hydroxymethyl)oxane-3,4,5-triol,5TMS,isomer #2	C[Si](C)(C)OCC1OC(OC2OC=CC3C(O[Si](C)(C)C)C4OC4(CO[Si](C)(C)C)C23)C(O[Si](C)(C)C)C(O)C1O[Si](C)(C)C	2667.2	Semi standard non polar	33892256
(2R,3S,4R,5R,6S)-2-[[(1R,2R,4R,5R,6S,10R)-5-Hydroxy-2-(hydroxymethyl)-3,9-dioxatricyclo[4.4.0.02,4]dec-7-en-10-yl]oxy]-6-(hydroxymethyl)oxane-3,4,5-triol,5TMS,isomer #2	C[Si](C)(C)OCC1OC(OC2OC=CC3C(O[Si](C)(C)C)C4OC4(CO[Si](C)(C)C)C23)C(O[Si](C)(C)C)C(O)C1O[Si](C)(C)C	3098.4	Standard non polar	33892256
(2R,3S,4R,5R,6S)-2-[[(1R,2R,4R,5R,6S,10R)-5-Hydroxy-2-(hydroxymethyl)-3,9-dioxatricyclo[4.4.0.02,4]dec-7-en-10-yl]oxy]-6-(hydroxymethyl)oxane-3,4,5-triol,5TMS,isomer #2	C[Si](C)(C)OCC1OC(OC2OC=CC3C(O[Si](C)(C)C)C4OC4(CO[Si](C)(C)C)C23)C(O[Si](C)(C)C)C(O)C1O[Si](C)(C)C	3475.0	Standard polar	33892256
(2R,3S,4R,5R,6S)-2-[[(1R,2R,4R,5R,6S,10R)-5-Hydroxy-2-(hydroxymethyl)-3,9-dioxatricyclo[4.4.0.02,4]dec-7-en-10-yl]oxy]-6-(hydroxymethyl)oxane-3,4,5-triol,5TMS,isomer #3	C[Si](C)(C)OCC1OC(OC2OC=CC3C(O[Si](C)(C)C)C4OC4(CO[Si](C)(C)C)C23)C(O)C(O[Si](C)(C)C)C1O[Si](C)(C)C	2656.9	Semi standard non polar	33892256
(2R,3S,4R,5R,6S)-2-[[(1R,2R,4R,5R,6S,10R)-5-Hydroxy-2-(hydroxymethyl)-3,9-dioxatricyclo[4.4.0.02,4]dec-7-en-10-yl]oxy]-6-(hydroxymethyl)oxane-3,4,5-triol,5TMS,isomer #3	C[Si](C)(C)OCC1OC(OC2OC=CC3C(O[Si](C)(C)C)C4OC4(CO[Si](C)(C)C)C23)C(O)C(O[Si](C)(C)C)C1O[Si](C)(C)C	3057.7	Standard non polar	33892256
(2R,3S,4R,5R,6S)-2-[[(1R,2R,4R,5R,6S,10R)-5-Hydroxy-2-(hydroxymethyl)-3,9-dioxatricyclo[4.4.0.02,4]dec-7-en-10-yl]oxy]-6-(hydroxymethyl)oxane-3,4,5-triol,5TMS,isomer #3	C[Si](C)(C)OCC1OC(OC2OC=CC3C(O[Si](C)(C)C)C4OC4(CO[Si](C)(C)C)C23)C(O)C(O[Si](C)(C)C)C1O[Si](C)(C)C	3434.2	Standard polar	33892256
(2R,3S,4R,5R,6S)-2-[[(1R,2R,4R,5R,6S,10R)-5-Hydroxy-2-(hydroxymethyl)-3,9-dioxatricyclo[4.4.0.02,4]dec-7-en-10-yl]oxy]-6-(hydroxymethyl)oxane-3,4,5-triol,5TMS,isomer #4	C[Si](C)(C)OCC1OC(OC2OC=CC3C(O[Si](C)(C)C)C4OC4(CO)C23)C(O[Si](C)(C)C)C(O[Si](C)(C)C)C1O[Si](C)(C)C	2675.9	Semi standard non polar	33892256
(2R,3S,4R,5R,6S)-2-[[(1R,2R,4R,5R,6S,10R)-5-Hydroxy-2-(hydroxymethyl)-3,9-dioxatricyclo[4.4.0.02,4]dec-7-en-10-yl]oxy]-6-(hydroxymethyl)oxane-3,4,5-triol,5TMS,isomer #4	C[Si](C)(C)OCC1OC(OC2OC=CC3C(O[Si](C)(C)C)C4OC4(CO)C23)C(O[Si](C)(C)C)C(O[Si](C)(C)C)C1O[Si](C)(C)C	3023.3	Standard non polar	33892256
(2R,3S,4R,5R,6S)-2-[[(1R,2R,4R,5R,6S,10R)-5-Hydroxy-2-(hydroxymethyl)-3,9-dioxatricyclo[4.4.0.02,4]dec-7-en-10-yl]oxy]-6-(hydroxymethyl)oxane-3,4,5-triol,5TMS,isomer #4	C[Si](C)(C)OCC1OC(OC2OC=CC3C(O[Si](C)(C)C)C4OC4(CO)C23)C(O[Si](C)(C)C)C(O[Si](C)(C)C)C1O[Si](C)(C)C	3403.1	Standard polar	33892256
(2R,3S,4R,5R,6S)-2-[[(1R,2R,4R,5R,6S,10R)-5-Hydroxy-2-(hydroxymethyl)-3,9-dioxatricyclo[4.4.0.02,4]dec-7-en-10-yl]oxy]-6-(hydroxymethyl)oxane-3,4,5-triol,5TMS,isomer #5	C[Si](C)(C)OCC1OC(OC2OC=CC3C(O)C4OC4(CO[Si](C)(C)C)C23)C(O[Si](C)(C)C)C(O[Si](C)(C)C)C1O[Si](C)(C)C	2675.0	Semi standard non polar	33892256
(2R,3S,4R,5R,6S)-2-[[(1R,2R,4R,5R,6S,10R)-5-Hydroxy-2-(hydroxymethyl)-3,9-dioxatricyclo[4.4.0.02,4]dec-7-en-10-yl]oxy]-6-(hydroxymethyl)oxane-3,4,5-triol,5TMS,isomer #5	C[Si](C)(C)OCC1OC(OC2OC=CC3C(O)C4OC4(CO[Si](C)(C)C)C23)C(O[Si](C)(C)C)C(O[Si](C)(C)C)C1O[Si](C)(C)C	3080.5	Standard non polar	33892256
(2R,3S,4R,5R,6S)-2-[[(1R,2R,4R,5R,6S,10R)-5-Hydroxy-2-(hydroxymethyl)-3,9-dioxatricyclo[4.4.0.02,4]dec-7-en-10-yl]oxy]-6-(hydroxymethyl)oxane-3,4,5-triol,5TMS,isomer #5	C[Si](C)(C)OCC1OC(OC2OC=CC3C(O)C4OC4(CO[Si](C)(C)C)C23)C(O[Si](C)(C)C)C(O[Si](C)(C)C)C1O[Si](C)(C)C	3527.4	Standard polar	33892256
(2R,3S,4R,5R,6S)-2-[[(1R,2R,4R,5R,6S,10R)-5-Hydroxy-2-(hydroxymethyl)-3,9-dioxatricyclo[4.4.0.02,4]dec-7-en-10-yl]oxy]-6-(hydroxymethyl)oxane-3,4,5-triol,5TMS,isomer #6	C[Si](C)(C)OCC12OC1C(O[Si](C)(C)C)C1C=COC(OC3OC(CO)C(O[Si](C)(C)C)C(O[Si](C)(C)C)C3O[Si](C)(C)C)C12	2572.5	Semi standard non polar	33892256
(2R,3S,4R,5R,6S)-2-[[(1R,2R,4R,5R,6S,10R)-5-Hydroxy-2-(hydroxymethyl)-3,9-dioxatricyclo[4.4.0.02,4]dec-7-en-10-yl]oxy]-6-(hydroxymethyl)oxane-3,4,5-triol,5TMS,isomer #6	C[Si](C)(C)OCC12OC1C(O[Si](C)(C)C)C1C=COC(OC3OC(CO)C(O[Si](C)(C)C)C(O[Si](C)(C)C)C3O[Si](C)(C)C)C12	3011.5	Standard non polar	33892256
(2R,3S,4R,5R,6S)-2-[[(1R,2R,4R,5R,6S,10R)-5-Hydroxy-2-(hydroxymethyl)-3,9-dioxatricyclo[4.4.0.02,4]dec-7-en-10-yl]oxy]-6-(hydroxymethyl)oxane-3,4,5-triol,5TMS,isomer #6	C[Si](C)(C)OCC12OC1C(O[Si](C)(C)C)C1C=COC(OC3OC(CO)C(O[Si](C)(C)C)C(O[Si](C)(C)C)C3O[Si](C)(C)C)C12	3392.6	Standard polar	33892256
(2R,3S,4R,5R,6S)-2-[[(1R,2R,4R,5R,6S,10R)-5-Hydroxy-2-(hydroxymethyl)-3,9-dioxatricyclo[4.4.0.02,4]dec-7-en-10-yl]oxy]-6-(hydroxymethyl)oxane-3,4,5-triol,6TMS,isomer #1	C[Si](C)(C)OCC1OC(OC2OC=CC3C(O[Si](C)(C)C)C4OC4(CO[Si](C)(C)C)C23)C(O[Si](C)(C)C)C(O[Si](C)(C)C)C1O[Si](C)(C)C	2574.4	Semi standard non polar	33892256
(2R,3S,4R,5R,6S)-2-[[(1R,2R,4R,5R,6S,10R)-5-Hydroxy-2-(hydroxymethyl)-3,9-dioxatricyclo[4.4.0.02,4]dec-7-en-10-yl]oxy]-6-(hydroxymethyl)oxane-3,4,5-triol,6TMS,isomer #1	C[Si](C)(C)OCC1OC(OC2OC=CC3C(O[Si](C)(C)C)C4OC4(CO[Si](C)(C)C)C23)C(O[Si](C)(C)C)C(O[Si](C)(C)C)C1O[Si](C)(C)C	3051.4	Standard non polar	33892256
(2R,3S,4R,5R,6S)-2-[[(1R,2R,4R,5R,6S,10R)-5-Hydroxy-2-(hydroxymethyl)-3,9-dioxatricyclo[4.4.0.02,4]dec-7-en-10-yl]oxy]-6-(hydroxymethyl)oxane-3,4,5-triol,6TMS,isomer #1	C[Si](C)(C)OCC1OC(OC2OC=CC3C(O[Si](C)(C)C)C4OC4(CO[Si](C)(C)C)C23)C(O[Si](C)(C)C)C(O[Si](C)(C)C)C1O[Si](C)(C)C	3218.3	Standard polar	33892256
(2R,3S,4R,5R,6S)-2-[[(1R,2R,4R,5R,6S,10R)-5-Hydroxy-2-(hydroxymethyl)-3,9-dioxatricyclo[4.4.0.02,4]dec-7-en-10-yl]oxy]-6-(hydroxymethyl)oxane-3,4,5-triol,1TBDMS,isomer #1	CC(C)(C)[Si](C)(C)OCC1OC(OC2OC=CC3C(O)C4OC4(CO)C23)C(O)C(O)C1O	3284.0	Semi standard non polar	33892256
(2R,3S,4R,5R,6S)-2-[[(1R,2R,4R,5R,6S,10R)-5-Hydroxy-2-(hydroxymethyl)-3,9-dioxatricyclo[4.4.0.02,4]dec-7-en-10-yl]oxy]-6-(hydroxymethyl)oxane-3,4,5-triol,1TBDMS,isomer #1	CC(C)(C)[Si](C)(C)OCC1OC(OC2OC=CC3C(O)C4OC4(CO)C23)C(O)C(O)C1O	3205.8	Standard non polar	33892256
(2R,3S,4R,5R,6S)-2-[[(1R,2R,4R,5R,6S,10R)-5-Hydroxy-2-(hydroxymethyl)-3,9-dioxatricyclo[4.4.0.02,4]dec-7-en-10-yl]oxy]-6-(hydroxymethyl)oxane-3,4,5-triol,1TBDMS,isomer #1	CC(C)(C)[Si](C)(C)OCC1OC(OC2OC=CC3C(O)C4OC4(CO)C23)C(O)C(O)C1O	4726.9	Standard polar	33892256
(2R,3S,4R,5R,6S)-2-[[(1R,2R,4R,5R,6S,10R)-5-Hydroxy-2-(hydroxymethyl)-3,9-dioxatricyclo[4.4.0.02,4]dec-7-en-10-yl]oxy]-6-(hydroxymethyl)oxane-3,4,5-triol,1TBDMS,isomer #2	CC(C)(C)[Si](C)(C)OC1C2C=COC(OC3OC(CO)C(O)C(O)C3O)C2C2(CO)OC12	3304.8	Semi standard non polar	33892256
(2R,3S,4R,5R,6S)-2-[[(1R,2R,4R,5R,6S,10R)-5-Hydroxy-2-(hydroxymethyl)-3,9-dioxatricyclo[4.4.0.02,4]dec-7-en-10-yl]oxy]-6-(hydroxymethyl)oxane-3,4,5-triol,1TBDMS,isomer #2	CC(C)(C)[Si](C)(C)OC1C2C=COC(OC3OC(CO)C(O)C(O)C3O)C2C2(CO)OC12	3114.2	Standard non polar	33892256
(2R,3S,4R,5R,6S)-2-[[(1R,2R,4R,5R,6S,10R)-5-Hydroxy-2-(hydroxymethyl)-3,9-dioxatricyclo[4.4.0.02,4]dec-7-en-10-yl]oxy]-6-(hydroxymethyl)oxane-3,4,5-triol,1TBDMS,isomer #2	CC(C)(C)[Si](C)(C)OC1C2C=COC(OC3OC(CO)C(O)C(O)C3O)C2C2(CO)OC12	4538.0	Standard polar	33892256
(2R,3S,4R,5R,6S)-2-[[(1R,2R,4R,5R,6S,10R)-5-Hydroxy-2-(hydroxymethyl)-3,9-dioxatricyclo[4.4.0.02,4]dec-7-en-10-yl]oxy]-6-(hydroxymethyl)oxane-3,4,5-triol,1TBDMS,isomer #3	CC(C)(C)[Si](C)(C)OCC12OC1C(O)C1C=COC(OC3OC(CO)C(O)C(O)C3O)C12	3252.1	Semi standard non polar	33892256
(2R,3S,4R,5R,6S)-2-[[(1R,2R,4R,5R,6S,10R)-5-Hydroxy-2-(hydroxymethyl)-3,9-dioxatricyclo[4.4.0.02,4]dec-7-en-10-yl]oxy]-6-(hydroxymethyl)oxane-3,4,5-triol,1TBDMS,isomer #3	CC(C)(C)[Si](C)(C)OCC12OC1C(O)C1C=COC(OC3OC(CO)C(O)C(O)C3O)C12	3208.2	Standard non polar	33892256
(2R,3S,4R,5R,6S)-2-[[(1R,2R,4R,5R,6S,10R)-5-Hydroxy-2-(hydroxymethyl)-3,9-dioxatricyclo[4.4.0.02,4]dec-7-en-10-yl]oxy]-6-(hydroxymethyl)oxane-3,4,5-triol,1TBDMS,isomer #3	CC(C)(C)[Si](C)(C)OCC12OC1C(O)C1C=COC(OC3OC(CO)C(O)C(O)C3O)C12	4763.4	Standard polar	33892256
(2R,3S,4R,5R,6S)-2-[[(1R,2R,4R,5R,6S,10R)-5-Hydroxy-2-(hydroxymethyl)-3,9-dioxatricyclo[4.4.0.02,4]dec-7-en-10-yl]oxy]-6-(hydroxymethyl)oxane-3,4,5-triol,1TBDMS,isomer #4	CC(C)(C)[Si](C)(C)OC1C(OC2OC=CC3C(O)C4OC4(CO)C23)OC(CO)C(O)C1O	3286.2	Semi standard non polar	33892256
(2R,3S,4R,5R,6S)-2-[[(1R,2R,4R,5R,6S,10R)-5-Hydroxy-2-(hydroxymethyl)-3,9-dioxatricyclo[4.4.0.02,4]dec-7-en-10-yl]oxy]-6-(hydroxymethyl)oxane-3,4,5-triol,1TBDMS,isomer #4	CC(C)(C)[Si](C)(C)OC1C(OC2OC=CC3C(O)C4OC4(CO)C23)OC(CO)C(O)C1O	3126.0	Standard non polar	33892256
(2R,3S,4R,5R,6S)-2-[[(1R,2R,4R,5R,6S,10R)-5-Hydroxy-2-(hydroxymethyl)-3,9-dioxatricyclo[4.4.0.02,4]dec-7-en-10-yl]oxy]-6-(hydroxymethyl)oxane-3,4,5-triol,1TBDMS,isomer #4	CC(C)(C)[Si](C)(C)OC1C(OC2OC=CC3C(O)C4OC4(CO)C23)OC(CO)C(O)C1O	4666.4	Standard polar	33892256
(2R,3S,4R,5R,6S)-2-[[(1R,2R,4R,5R,6S,10R)-5-Hydroxy-2-(hydroxymethyl)-3,9-dioxatricyclo[4.4.0.02,4]dec-7-en-10-yl]oxy]-6-(hydroxymethyl)oxane-3,4,5-triol,1TBDMS,isomer #5	CC(C)(C)[Si](C)(C)OC1C(O)C(CO)OC(OC2OC=CC3C(O)C4OC4(CO)C23)C1O	3279.4	Semi standard non polar	33892256
(2R,3S,4R,5R,6S)-2-[[(1R,2R,4R,5R,6S,10R)-5-Hydroxy-2-(hydroxymethyl)-3,9-dioxatricyclo[4.4.0.02,4]dec-7-en-10-yl]oxy]-6-(hydroxymethyl)oxane-3,4,5-triol,1TBDMS,isomer #5	CC(C)(C)[Si](C)(C)OC1C(O)C(CO)OC(OC2OC=CC3C(O)C4OC4(CO)C23)C1O	3116.9	Standard non polar	33892256
(2R,3S,4R,5R,6S)-2-[[(1R,2R,4R,5R,6S,10R)-5-Hydroxy-2-(hydroxymethyl)-3,9-dioxatricyclo[4.4.0.02,4]dec-7-en-10-yl]oxy]-6-(hydroxymethyl)oxane-3,4,5-triol,1TBDMS,isomer #5	CC(C)(C)[Si](C)(C)OC1C(O)C(CO)OC(OC2OC=CC3C(O)C4OC4(CO)C23)C1O	4647.2	Standard polar	33892256
(2R,3S,4R,5R,6S)-2-[[(1R,2R,4R,5R,6S,10R)-5-Hydroxy-2-(hydroxymethyl)-3,9-dioxatricyclo[4.4.0.02,4]dec-7-en-10-yl]oxy]-6-(hydroxymethyl)oxane-3,4,5-triol,1TBDMS,isomer #6	CC(C)(C)[Si](C)(C)OC1C(CO)OC(OC2OC=CC3C(O)C4OC4(CO)C23)C(O)C1O	3288.7	Semi standard non polar	33892256
(2R,3S,4R,5R,6S)-2-[[(1R,2R,4R,5R,6S,10R)-5-Hydroxy-2-(hydroxymethyl)-3,9-dioxatricyclo[4.4.0.02,4]dec-7-en-10-yl]oxy]-6-(hydroxymethyl)oxane-3,4,5-triol,1TBDMS,isomer #6	CC(C)(C)[Si](C)(C)OC1C(CO)OC(OC2OC=CC3C(O)C4OC4(CO)C23)C(O)C1O	3120.0	Standard non polar	33892256
(2R,3S,4R,5R,6S)-2-[[(1R,2R,4R,5R,6S,10R)-5-Hydroxy-2-(hydroxymethyl)-3,9-dioxatricyclo[4.4.0.02,4]dec-7-en-10-yl]oxy]-6-(hydroxymethyl)oxane-3,4,5-triol,1TBDMS,isomer #6	CC(C)(C)[Si](C)(C)OC1C(CO)OC(OC2OC=CC3C(O)C4OC4(CO)C23)C(O)C1O	4646.5	Standard polar	33892256
(2R,3S,4R,5R,6S)-2-[[(1R,2R,4R,5R,6S,10R)-5-Hydroxy-2-(hydroxymethyl)-3,9-dioxatricyclo[4.4.0.02,4]dec-7-en-10-yl]oxy]-6-(hydroxymethyl)oxane-3,4,5-triol,2TBDMS,isomer #1	CC(C)(C)[Si](C)(C)OCC1OC(OC2OC=CC3C(O[Si](C)(C)C(C)(C)C)C4OC4(CO)C23)C(O)C(O)C1O	3430.2	Semi standard non polar	33892256
(2R,3S,4R,5R,6S)-2-[[(1R,2R,4R,5R,6S,10R)-5-Hydroxy-2-(hydroxymethyl)-3,9-dioxatricyclo[4.4.0.02,4]dec-7-en-10-yl]oxy]-6-(hydroxymethyl)oxane-3,4,5-triol,2TBDMS,isomer #1	CC(C)(C)[Si](C)(C)OCC1OC(OC2OC=CC3C(O[Si](C)(C)C(C)(C)C)C4OC4(CO)C23)C(O)C(O)C1O	3452.2	Standard non polar	33892256
(2R,3S,4R,5R,6S)-2-[[(1R,2R,4R,5R,6S,10R)-5-Hydroxy-2-(hydroxymethyl)-3,9-dioxatricyclo[4.4.0.02,4]dec-7-en-10-yl]oxy]-6-(hydroxymethyl)oxane-3,4,5-triol,2TBDMS,isomer #1	CC(C)(C)[Si](C)(C)OCC1OC(OC2OC=CC3C(O[Si](C)(C)C(C)(C)C)C4OC4(CO)C23)C(O)C(O)C1O	4301.5	Standard polar	33892256
(2R,3S,4R,5R,6S)-2-[[(1R,2R,4R,5R,6S,10R)-5-Hydroxy-2-(hydroxymethyl)-3,9-dioxatricyclo[4.4.0.02,4]dec-7-en-10-yl]oxy]-6-(hydroxymethyl)oxane-3,4,5-triol,2TBDMS,isomer #10	CC(C)(C)[Si](C)(C)OCC12OC1C(O)C1C=COC(OC3OC(CO)C(O[Si](C)(C)C(C)(C)C)C(O)C3O)C12	3405.1	Semi standard non polar	33892256
(2R,3S,4R,5R,6S)-2-[[(1R,2R,4R,5R,6S,10R)-5-Hydroxy-2-(hydroxymethyl)-3,9-dioxatricyclo[4.4.0.02,4]dec-7-en-10-yl]oxy]-6-(hydroxymethyl)oxane-3,4,5-triol,2TBDMS,isomer #10	CC(C)(C)[Si](C)(C)OCC12OC1C(O)C1C=COC(OC3OC(CO)C(O[Si](C)(C)C(C)(C)C)C(O)C3O)C12	3468.3	Standard non polar	33892256
(2R,3S,4R,5R,6S)-2-[[(1R,2R,4R,5R,6S,10R)-5-Hydroxy-2-(hydroxymethyl)-3,9-dioxatricyclo[4.4.0.02,4]dec-7-en-10-yl]oxy]-6-(hydroxymethyl)oxane-3,4,5-triol,2TBDMS,isomer #10	CC(C)(C)[Si](C)(C)OCC12OC1C(O)C1C=COC(OC3OC(CO)C(O[Si](C)(C)C(C)(C)C)C(O)C3O)C12	4402.7	Standard polar	33892256
(2R,3S,4R,5R,6S)-2-[[(1R,2R,4R,5R,6S,10R)-5-Hydroxy-2-(hydroxymethyl)-3,9-dioxatricyclo[4.4.0.02,4]dec-7-en-10-yl]oxy]-6-(hydroxymethyl)oxane-3,4,5-triol,2TBDMS,isomer #11	CC(C)(C)[Si](C)(C)OCC12OC1C(O)C1C=COC(OC3OC(CO)C(O)C(O[Si](C)(C)C(C)(C)C)C3O)C12	3395.6	Semi standard non polar	33892256
(2R,3S,4R,5R,6S)-2-[[(1R,2R,4R,5R,6S,10R)-5-Hydroxy-2-(hydroxymethyl)-3,9-dioxatricyclo[4.4.0.02,4]dec-7-en-10-yl]oxy]-6-(hydroxymethyl)oxane-3,4,5-triol,2TBDMS,isomer #11	CC(C)(C)[Si](C)(C)OCC12OC1C(O)C1C=COC(OC3OC(CO)C(O)C(O[Si](C)(C)C(C)(C)C)C3O)C12	3471.4	Standard non polar	33892256
(2R,3S,4R,5R,6S)-2-[[(1R,2R,4R,5R,6S,10R)-5-Hydroxy-2-(hydroxymethyl)-3,9-dioxatricyclo[4.4.0.02,4]dec-7-en-10-yl]oxy]-6-(hydroxymethyl)oxane-3,4,5-triol,2TBDMS,isomer #11	CC(C)(C)[Si](C)(C)OCC12OC1C(O)C1C=COC(OC3OC(CO)C(O)C(O[Si](C)(C)C(C)(C)C)C3O)C12	4414.0	Standard polar	33892256
(2R,3S,4R,5R,6S)-2-[[(1R,2R,4R,5R,6S,10R)-5-Hydroxy-2-(hydroxymethyl)-3,9-dioxatricyclo[4.4.0.02,4]dec-7-en-10-yl]oxy]-6-(hydroxymethyl)oxane-3,4,5-triol,2TBDMS,isomer #12	CC(C)(C)[Si](C)(C)OCC12OC1C(O)C1C=COC(OC3OC(CO)C(O)C(O)C3O[Si](C)(C)C(C)(C)C)C12	3402.5	Semi standard non polar	33892256
(2R,3S,4R,5R,6S)-2-[[(1R,2R,4R,5R,6S,10R)-5-Hydroxy-2-(hydroxymethyl)-3,9-dioxatricyclo[4.4.0.02,4]dec-7-en-10-yl]oxy]-6-(hydroxymethyl)oxane-3,4,5-triol,2TBDMS,isomer #12	CC(C)(C)[Si](C)(C)OCC12OC1C(O)C1C=COC(OC3OC(CO)C(O)C(O)C3O[Si](C)(C)C(C)(C)C)C12	3473.9	Standard non polar	33892256
(2R,3S,4R,5R,6S)-2-[[(1R,2R,4R,5R,6S,10R)-5-Hydroxy-2-(hydroxymethyl)-3,9-dioxatricyclo[4.4.0.02,4]dec-7-en-10-yl]oxy]-6-(hydroxymethyl)oxane-3,4,5-triol,2TBDMS,isomer #12	CC(C)(C)[Si](C)(C)OCC12OC1C(O)C1C=COC(OC3OC(CO)C(O)C(O)C3O[Si](C)(C)C(C)(C)C)C12	4423.4	Standard polar	33892256
(2R,3S,4R,5R,6S)-2-[[(1R,2R,4R,5R,6S,10R)-5-Hydroxy-2-(hydroxymethyl)-3,9-dioxatricyclo[4.4.0.02,4]dec-7-en-10-yl]oxy]-6-(hydroxymethyl)oxane-3,4,5-triol,2TBDMS,isomer #13	CC(C)(C)[Si](C)(C)OC1C(CO)OC(OC2OC=CC3C(O)C4OC4(CO)C23)C(O[Si](C)(C)C(C)(C)C)C1O	3441.4	Semi standard non polar	33892256
(2R,3S,4R,5R,6S)-2-[[(1R,2R,4R,5R,6S,10R)-5-Hydroxy-2-(hydroxymethyl)-3,9-dioxatricyclo[4.4.0.02,4]dec-7-en-10-yl]oxy]-6-(hydroxymethyl)oxane-3,4,5-triol,2TBDMS,isomer #13	CC(C)(C)[Si](C)(C)OC1C(CO)OC(OC2OC=CC3C(O)C4OC4(CO)C23)C(O[Si](C)(C)C(C)(C)C)C1O	3415.4	Standard non polar	33892256
(2R,3S,4R,5R,6S)-2-[[(1R,2R,4R,5R,6S,10R)-5-Hydroxy-2-(hydroxymethyl)-3,9-dioxatricyclo[4.4.0.02,4]dec-7-en-10-yl]oxy]-6-(hydroxymethyl)oxane-3,4,5-triol,2TBDMS,isomer #13	CC(C)(C)[Si](C)(C)OC1C(CO)OC(OC2OC=CC3C(O)C4OC4(CO)C23)C(O[Si](C)(C)C(C)(C)C)C1O	4377.6	Standard polar	33892256
(2R,3S,4R,5R,6S)-2-[[(1R,2R,4R,5R,6S,10R)-5-Hydroxy-2-(hydroxymethyl)-3,9-dioxatricyclo[4.4.0.02,4]dec-7-en-10-yl]oxy]-6-(hydroxymethyl)oxane-3,4,5-triol,2TBDMS,isomer #14	CC(C)(C)[Si](C)(C)OC1C(OC2OC=CC3C(O)C4OC4(CO)C23)OC(CO)C(O)C1O[Si](C)(C)C(C)(C)C	3458.4	Semi standard non polar	33892256
(2R,3S,4R,5R,6S)-2-[[(1R,2R,4R,5R,6S,10R)-5-Hydroxy-2-(hydroxymethyl)-3,9-dioxatricyclo[4.4.0.02,4]dec-7-en-10-yl]oxy]-6-(hydroxymethyl)oxane-3,4,5-triol,2TBDMS,isomer #14	CC(C)(C)[Si](C)(C)OC1C(OC2OC=CC3C(O)C4OC4(CO)C23)OC(CO)C(O)C1O[Si](C)(C)C(C)(C)C	3409.8	Standard non polar	33892256
(2R,3S,4R,5R,6S)-2-[[(1R,2R,4R,5R,6S,10R)-5-Hydroxy-2-(hydroxymethyl)-3,9-dioxatricyclo[4.4.0.02,4]dec-7-en-10-yl]oxy]-6-(hydroxymethyl)oxane-3,4,5-triol,2TBDMS,isomer #14	CC(C)(C)[Si](C)(C)OC1C(OC2OC=CC3C(O)C4OC4(CO)C23)OC(CO)C(O)C1O[Si](C)(C)C(C)(C)C	4359.6	Standard polar	33892256
(2R,3S,4R,5R,6S)-2-[[(1R,2R,4R,5R,6S,10R)-5-Hydroxy-2-(hydroxymethyl)-3,9-dioxatricyclo[4.4.0.02,4]dec-7-en-10-yl]oxy]-6-(hydroxymethyl)oxane-3,4,5-triol,2TBDMS,isomer #15	CC(C)(C)[Si](C)(C)OC1C(CO)OC(OC2OC=CC3C(O)C4OC4(CO)C23)C(O)C1O[Si](C)(C)C(C)(C)C	3449.4	Semi standard non polar	33892256
(2R,3S,4R,5R,6S)-2-[[(1R,2R,4R,5R,6S,10R)-5-Hydroxy-2-(hydroxymethyl)-3,9-dioxatricyclo[4.4.0.02,4]dec-7-en-10-yl]oxy]-6-(hydroxymethyl)oxane-3,4,5-triol,2TBDMS,isomer #15	CC(C)(C)[Si](C)(C)OC1C(CO)OC(OC2OC=CC3C(O)C4OC4(CO)C23)C(O)C1O[Si](C)(C)C(C)(C)C	3403.9	Standard non polar	33892256
(2R,3S,4R,5R,6S)-2-[[(1R,2R,4R,5R,6S,10R)-5-Hydroxy-2-(hydroxymethyl)-3,9-dioxatricyclo[4.4.0.02,4]dec-7-en-10-yl]oxy]-6-(hydroxymethyl)oxane-3,4,5-triol,2TBDMS,isomer #15	CC(C)(C)[Si](C)(C)OC1C(CO)OC(OC2OC=CC3C(O)C4OC4(CO)C23)C(O)C1O[Si](C)(C)C(C)(C)C	4337.3	Standard polar	33892256
(2R,3S,4R,5R,6S)-2-[[(1R,2R,4R,5R,6S,10R)-5-Hydroxy-2-(hydroxymethyl)-3,9-dioxatricyclo[4.4.0.02,4]dec-7-en-10-yl]oxy]-6-(hydroxymethyl)oxane-3,4,5-triol,2TBDMS,isomer #2	CC(C)(C)[Si](C)(C)OCC1OC(OC2OC=CC3C(O)C4OC4(CO[Si](C)(C)C(C)(C)C)C23)C(O)C(O)C1O	3396.5	Semi standard non polar	33892256
(2R,3S,4R,5R,6S)-2-[[(1R,2R,4R,5R,6S,10R)-5-Hydroxy-2-(hydroxymethyl)-3,9-dioxatricyclo[4.4.0.02,4]dec-7-en-10-yl]oxy]-6-(hydroxymethyl)oxane-3,4,5-triol,2TBDMS,isomer #2	CC(C)(C)[Si](C)(C)OCC1OC(OC2OC=CC3C(O)C4OC4(CO[Si](C)(C)C(C)(C)C)C23)C(O)C(O)C1O	3541.2	Standard non polar	33892256
(2R,3S,4R,5R,6S)-2-[[(1R,2R,4R,5R,6S,10R)-5-Hydroxy-2-(hydroxymethyl)-3,9-dioxatricyclo[4.4.0.02,4]dec-7-en-10-yl]oxy]-6-(hydroxymethyl)oxane-3,4,5-triol,2TBDMS,isomer #2	CC(C)(C)[Si](C)(C)OCC1OC(OC2OC=CC3C(O)C4OC4(CO[Si](C)(C)C(C)(C)C)C23)C(O)C(O)C1O	4460.5	Standard polar	33892256
(2R,3S,4R,5R,6S)-2-[[(1R,2R,4R,5R,6S,10R)-5-Hydroxy-2-(hydroxymethyl)-3,9-dioxatricyclo[4.4.0.02,4]dec-7-en-10-yl]oxy]-6-(hydroxymethyl)oxane-3,4,5-triol,2TBDMS,isomer #3	CC(C)(C)[Si](C)(C)OCC1OC(OC2OC=CC3C(O)C4OC4(CO)C23)C(O[Si](C)(C)C(C)(C)C)C(O)C1O	3432.8	Semi standard non polar	33892256
(2R,3S,4R,5R,6S)-2-[[(1R,2R,4R,5R,6S,10R)-5-Hydroxy-2-(hydroxymethyl)-3,9-dioxatricyclo[4.4.0.02,4]dec-7-en-10-yl]oxy]-6-(hydroxymethyl)oxane-3,4,5-triol,2TBDMS,isomer #3	CC(C)(C)[Si](C)(C)OCC1OC(OC2OC=CC3C(O)C4OC4(CO)C23)C(O[Si](C)(C)C(C)(C)C)C(O)C1O	3470.3	Standard non polar	33892256
(2R,3S,4R,5R,6S)-2-[[(1R,2R,4R,5R,6S,10R)-5-Hydroxy-2-(hydroxymethyl)-3,9-dioxatricyclo[4.4.0.02,4]dec-7-en-10-yl]oxy]-6-(hydroxymethyl)oxane-3,4,5-triol,2TBDMS,isomer #3	CC(C)(C)[Si](C)(C)OCC1OC(OC2OC=CC3C(O)C4OC4(CO)C23)C(O[Si](C)(C)C(C)(C)C)C(O)C1O	4435.2	Standard polar	33892256
(2R,3S,4R,5R,6S)-2-[[(1R,2R,4R,5R,6S,10R)-5-Hydroxy-2-(hydroxymethyl)-3,9-dioxatricyclo[4.4.0.02,4]dec-7-en-10-yl]oxy]-6-(hydroxymethyl)oxane-3,4,5-triol,2TBDMS,isomer #4	CC(C)(C)[Si](C)(C)OCC1OC(OC2OC=CC3C(O)C4OC4(CO)C23)C(O)C(O[Si](C)(C)C(C)(C)C)C1O	3436.2	Semi standard non polar	33892256
(2R,3S,4R,5R,6S)-2-[[(1R,2R,4R,5R,6S,10R)-5-Hydroxy-2-(hydroxymethyl)-3,9-dioxatricyclo[4.4.0.02,4]dec-7-en-10-yl]oxy]-6-(hydroxymethyl)oxane-3,4,5-triol,2TBDMS,isomer #4	CC(C)(C)[Si](C)(C)OCC1OC(OC2OC=CC3C(O)C4OC4(CO)C23)C(O)C(O[Si](C)(C)C(C)(C)C)C1O	3472.1	Standard non polar	33892256
(2R,3S,4R,5R,6S)-2-[[(1R,2R,4R,5R,6S,10R)-5-Hydroxy-2-(hydroxymethyl)-3,9-dioxatricyclo[4.4.0.02,4]dec-7-en-10-yl]oxy]-6-(hydroxymethyl)oxane-3,4,5-triol,2TBDMS,isomer #4	CC(C)(C)[Si](C)(C)OCC1OC(OC2OC=CC3C(O)C4OC4(CO)C23)C(O)C(O[Si](C)(C)C(C)(C)C)C1O	4425.5	Standard polar	33892256
(2R,3S,4R,5R,6S)-2-[[(1R,2R,4R,5R,6S,10R)-5-Hydroxy-2-(hydroxymethyl)-3,9-dioxatricyclo[4.4.0.02,4]dec-7-en-10-yl]oxy]-6-(hydroxymethyl)oxane-3,4,5-triol,2TBDMS,isomer #5	CC(C)(C)[Si](C)(C)OCC1OC(OC2OC=CC3C(O)C4OC4(CO)C23)C(O)C(O)C1O[Si](C)(C)C(C)(C)C	3431.6	Semi standard non polar	33892256
(2R,3S,4R,5R,6S)-2-[[(1R,2R,4R,5R,6S,10R)-5-Hydroxy-2-(hydroxymethyl)-3,9-dioxatricyclo[4.4.0.02,4]dec-7-en-10-yl]oxy]-6-(hydroxymethyl)oxane-3,4,5-triol,2TBDMS,isomer #5	CC(C)(C)[Si](C)(C)OCC1OC(OC2OC=CC3C(O)C4OC4(CO)C23)C(O)C(O)C1O[Si](C)(C)C(C)(C)C	3471.9	Standard non polar	33892256
(2R,3S,4R,5R,6S)-2-[[(1R,2R,4R,5R,6S,10R)-5-Hydroxy-2-(hydroxymethyl)-3,9-dioxatricyclo[4.4.0.02,4]dec-7-en-10-yl]oxy]-6-(hydroxymethyl)oxane-3,4,5-triol,2TBDMS,isomer #5	CC(C)(C)[Si](C)(C)OCC1OC(OC2OC=CC3C(O)C4OC4(CO)C23)C(O)C(O)C1O[Si](C)(C)C(C)(C)C	4417.3	Standard polar	33892256
(2R,3S,4R,5R,6S)-2-[[(1R,2R,4R,5R,6S,10R)-5-Hydroxy-2-(hydroxymethyl)-3,9-dioxatricyclo[4.4.0.02,4]dec-7-en-10-yl]oxy]-6-(hydroxymethyl)oxane-3,4,5-triol,2TBDMS,isomer #6	CC(C)(C)[Si](C)(C)OC1C(CO)OC(OC2OC=CC3C(O[Si](C)(C)C(C)(C)C)C4OC4(CO)C23)C(O)C1O	3447.3	Semi standard non polar	33892256
(2R,3S,4R,5R,6S)-2-[[(1R,2R,4R,5R,6S,10R)-5-Hydroxy-2-(hydroxymethyl)-3,9-dioxatricyclo[4.4.0.02,4]dec-7-en-10-yl]oxy]-6-(hydroxymethyl)oxane-3,4,5-triol,2TBDMS,isomer #6	CC(C)(C)[Si](C)(C)OC1C(CO)OC(OC2OC=CC3C(O[Si](C)(C)C(C)(C)C)C4OC4(CO)C23)C(O)C1O	3379.9	Standard non polar	33892256
(2R,3S,4R,5R,6S)-2-[[(1R,2R,4R,5R,6S,10R)-5-Hydroxy-2-(hydroxymethyl)-3,9-dioxatricyclo[4.4.0.02,4]dec-7-en-10-yl]oxy]-6-(hydroxymethyl)oxane-3,4,5-triol,2TBDMS,isomer #6	CC(C)(C)[Si](C)(C)OC1C(CO)OC(OC2OC=CC3C(O[Si](C)(C)C(C)(C)C)C4OC4(CO)C23)C(O)C1O	4243.1	Standard polar	33892256
(2R,3S,4R,5R,6S)-2-[[(1R,2R,4R,5R,6S,10R)-5-Hydroxy-2-(hydroxymethyl)-3,9-dioxatricyclo[4.4.0.02,4]dec-7-en-10-yl]oxy]-6-(hydroxymethyl)oxane-3,4,5-triol,2TBDMS,isomer #7	CC(C)(C)[Si](C)(C)OC1C(O)C(CO)OC(OC2OC=CC3C(O[Si](C)(C)C(C)(C)C)C4OC4(CO)C23)C1O	3454.8	Semi standard non polar	33892256
(2R,3S,4R,5R,6S)-2-[[(1R,2R,4R,5R,6S,10R)-5-Hydroxy-2-(hydroxymethyl)-3,9-dioxatricyclo[4.4.0.02,4]dec-7-en-10-yl]oxy]-6-(hydroxymethyl)oxane-3,4,5-triol,2TBDMS,isomer #7	CC(C)(C)[Si](C)(C)OC1C(O)C(CO)OC(OC2OC=CC3C(O[Si](C)(C)C(C)(C)C)C4OC4(CO)C23)C1O	3383.9	Standard non polar	33892256
(2R,3S,4R,5R,6S)-2-[[(1R,2R,4R,5R,6S,10R)-5-Hydroxy-2-(hydroxymethyl)-3,9-dioxatricyclo[4.4.0.02,4]dec-7-en-10-yl]oxy]-6-(hydroxymethyl)oxane-3,4,5-triol,2TBDMS,isomer #7	CC(C)(C)[Si](C)(C)OC1C(O)C(CO)OC(OC2OC=CC3C(O[Si](C)(C)C(C)(C)C)C4OC4(CO)C23)C1O	4256.8	Standard polar	33892256
(2R,3S,4R,5R,6S)-2-[[(1R,2R,4R,5R,6S,10R)-5-Hydroxy-2-(hydroxymethyl)-3,9-dioxatricyclo[4.4.0.02,4]dec-7-en-10-yl]oxy]-6-(hydroxymethyl)oxane-3,4,5-triol,2TBDMS,isomer #8	CC(C)(C)[Si](C)(C)OC1C(OC2OC=CC3C(O[Si](C)(C)C(C)(C)C)C4OC4(CO)C23)OC(CO)C(O)C1O	3445.4	Semi standard non polar	33892256
(2R,3S,4R,5R,6S)-2-[[(1R,2R,4R,5R,6S,10R)-5-Hydroxy-2-(hydroxymethyl)-3,9-dioxatricyclo[4.4.0.02,4]dec-7-en-10-yl]oxy]-6-(hydroxymethyl)oxane-3,4,5-triol,2TBDMS,isomer #8	CC(C)(C)[Si](C)(C)OC1C(OC2OC=CC3C(O[Si](C)(C)C(C)(C)C)C4OC4(CO)C23)OC(CO)C(O)C1O	3383.9	Standard non polar	33892256
(2R,3S,4R,5R,6S)-2-[[(1R,2R,4R,5R,6S,10R)-5-Hydroxy-2-(hydroxymethyl)-3,9-dioxatricyclo[4.4.0.02,4]dec-7-en-10-yl]oxy]-6-(hydroxymethyl)oxane-3,4,5-triol,2TBDMS,isomer #8	CC(C)(C)[Si](C)(C)OC1C(OC2OC=CC3C(O[Si](C)(C)C(C)(C)C)C4OC4(CO)C23)OC(CO)C(O)C1O	4263.3	Standard polar	33892256
(2R,3S,4R,5R,6S)-2-[[(1R,2R,4R,5R,6S,10R)-5-Hydroxy-2-(hydroxymethyl)-3,9-dioxatricyclo[4.4.0.02,4]dec-7-en-10-yl]oxy]-6-(hydroxymethyl)oxane-3,4,5-triol,2TBDMS,isomer #9	CC(C)(C)[Si](C)(C)OCC12OC1C(O[Si](C)(C)C(C)(C)C)C1C=COC(OC3OC(CO)C(O)C(O)C3O)C12	3405.8	Semi standard non polar	33892256
(2R,3S,4R,5R,6S)-2-[[(1R,2R,4R,5R,6S,10R)-5-Hydroxy-2-(hydroxymethyl)-3,9-dioxatricyclo[4.4.0.02,4]dec-7-en-10-yl]oxy]-6-(hydroxymethyl)oxane-3,4,5-triol,2TBDMS,isomer #9	CC(C)(C)[Si](C)(C)OCC12OC1C(O[Si](C)(C)C(C)(C)C)C1C=COC(OC3OC(CO)C(O)C(O)C3O)C12	3461.3	Standard non polar	33892256
(2R,3S,4R,5R,6S)-2-[[(1R,2R,4R,5R,6S,10R)-5-Hydroxy-2-(hydroxymethyl)-3,9-dioxatricyclo[4.4.0.02,4]dec-7-en-10-yl]oxy]-6-(hydroxymethyl)oxane-3,4,5-triol,2TBDMS,isomer #9	CC(C)(C)[Si](C)(C)OCC12OC1C(O[Si](C)(C)C(C)(C)C)C1C=COC(OC3OC(CO)C(O)C(O)C3O)C12	4272.7	Standard polar	33892256
(2R,3S,4R,5R,6S)-2-[[(1R,2R,4R,5R,6S,10R)-5-Hydroxy-2-(hydroxymethyl)-3,9-dioxatricyclo[4.4.0.02,4]dec-7-en-10-yl]oxy]-6-(hydroxymethyl)oxane-3,4,5-triol,3TBDMS,isomer #1	CC(C)(C)[Si](C)(C)OCC1OC(OC2OC=CC3C(O[Si](C)(C)C(C)(C)C)C4OC4(CO[Si](C)(C)C(C)(C)C)C23)C(O)C(O)C1O	3545.0	Semi standard non polar	33892256
(2R,3S,4R,5R,6S)-2-[[(1R,2R,4R,5R,6S,10R)-5-Hydroxy-2-(hydroxymethyl)-3,9-dioxatricyclo[4.4.0.02,4]dec-7-en-10-yl]oxy]-6-(hydroxymethyl)oxane-3,4,5-triol,3TBDMS,isomer #1	CC(C)(C)[Si](C)(C)OCC1OC(OC2OC=CC3C(O[Si](C)(C)C(C)(C)C)C4OC4(CO[Si](C)(C)C(C)(C)C)C23)C(O)C(O)C1O	3733.3	Standard non polar	33892256
(2R,3S,4R,5R,6S)-2-[[(1R,2R,4R,5R,6S,10R)-5-Hydroxy-2-(hydroxymethyl)-3,9-dioxatricyclo[4.4.0.02,4]dec-7-en-10-yl]oxy]-6-(hydroxymethyl)oxane-3,4,5-triol,3TBDMS,isomer #1	CC(C)(C)[Si](C)(C)OCC1OC(OC2OC=CC3C(O[Si](C)(C)C(C)(C)C)C4OC4(CO[Si](C)(C)C(C)(C)C)C23)C(O)C(O)C1O	4085.3	Standard polar	33892256
(2R,3S,4R,5R,6S)-2-[[(1R,2R,4R,5R,6S,10R)-5-Hydroxy-2-(hydroxymethyl)-3,9-dioxatricyclo[4.4.0.02,4]dec-7-en-10-yl]oxy]-6-(hydroxymethyl)oxane-3,4,5-triol,3TBDMS,isomer #10	CC(C)(C)[Si](C)(C)OCC1OC(OC2OC=CC3C(O)C4OC4(CO)C23)C(O)C(O[Si](C)(C)C(C)(C)C)C1O[Si](C)(C)C(C)(C)C	3589.7	Semi standard non polar	33892256
(2R,3S,4R,5R,6S)-2-[[(1R,2R,4R,5R,6S,10R)-5-Hydroxy-2-(hydroxymethyl)-3,9-dioxatricyclo[4.4.0.02,4]dec-7-en-10-yl]oxy]-6-(hydroxymethyl)oxane-3,4,5-triol,3TBDMS,isomer #10	CC(C)(C)[Si](C)(C)OCC1OC(OC2OC=CC3C(O)C4OC4(CO)C23)C(O)C(O[Si](C)(C)C(C)(C)C)C1O[Si](C)(C)C(C)(C)C	3682.0	Standard non polar	33892256
(2R,3S,4R,5R,6S)-2-[[(1R,2R,4R,5R,6S,10R)-5-Hydroxy-2-(hydroxymethyl)-3,9-dioxatricyclo[4.4.0.02,4]dec-7-en-10-yl]oxy]-6-(hydroxymethyl)oxane-3,4,5-triol,3TBDMS,isomer #10	CC(C)(C)[Si](C)(C)OCC1OC(OC2OC=CC3C(O)C4OC4(CO)C23)C(O)C(O[Si](C)(C)C(C)(C)C)C1O[Si](C)(C)C(C)(C)C	4169.8	Standard polar	33892256
(2R,3S,4R,5R,6S)-2-[[(1R,2R,4R,5R,6S,10R)-5-Hydroxy-2-(hydroxymethyl)-3,9-dioxatricyclo[4.4.0.02,4]dec-7-en-10-yl]oxy]-6-(hydroxymethyl)oxane-3,4,5-triol,3TBDMS,isomer #11	CC(C)(C)[Si](C)(C)OCC12OC1C(O[Si](C)(C)C(C)(C)C)C1C=COC(OC3OC(CO)C(O[Si](C)(C)C(C)(C)C)C(O)C3O)C12	3537.7	Semi standard non polar	33892256
(2R,3S,4R,5R,6S)-2-[[(1R,2R,4R,5R,6S,10R)-5-Hydroxy-2-(hydroxymethyl)-3,9-dioxatricyclo[4.4.0.02,4]dec-7-en-10-yl]oxy]-6-(hydroxymethyl)oxane-3,4,5-triol,3TBDMS,isomer #11	CC(C)(C)[Si](C)(C)OCC12OC1C(O[Si](C)(C)C(C)(C)C)C1C=COC(OC3OC(CO)C(O[Si](C)(C)C(C)(C)C)C(O)C3O)C12	3669.7	Standard non polar	33892256
(2R,3S,4R,5R,6S)-2-[[(1R,2R,4R,5R,6S,10R)-5-Hydroxy-2-(hydroxymethyl)-3,9-dioxatricyclo[4.4.0.02,4]dec-7-en-10-yl]oxy]-6-(hydroxymethyl)oxane-3,4,5-triol,3TBDMS,isomer #11	CC(C)(C)[Si](C)(C)OCC12OC1C(O[Si](C)(C)C(C)(C)C)C1C=COC(OC3OC(CO)C(O[Si](C)(C)C(C)(C)C)C(O)C3O)C12	4049.7	Standard polar	33892256
(2R,3S,4R,5R,6S)-2-[[(1R,2R,4R,5R,6S,10R)-5-Hydroxy-2-(hydroxymethyl)-3,9-dioxatricyclo[4.4.0.02,4]dec-7-en-10-yl]oxy]-6-(hydroxymethyl)oxane-3,4,5-triol,3TBDMS,isomer #12	CC(C)(C)[Si](C)(C)OC1C(CO)OC(OC2OC=CC3C(O[Si](C)(C)C(C)(C)C)C4OC4(CO)C23)C(O[Si](C)(C)C(C)(C)C)C1O	3575.2	Semi standard non polar	33892256
(2R,3S,4R,5R,6S)-2-[[(1R,2R,4R,5R,6S,10R)-5-Hydroxy-2-(hydroxymethyl)-3,9-dioxatricyclo[4.4.0.02,4]dec-7-en-10-yl]oxy]-6-(hydroxymethyl)oxane-3,4,5-triol,3TBDMS,isomer #12	CC(C)(C)[Si](C)(C)OC1C(CO)OC(OC2OC=CC3C(O[Si](C)(C)C(C)(C)C)C4OC4(CO)C23)C(O[Si](C)(C)C(C)(C)C)C1O	3620.9	Standard non polar	33892256
(2R,3S,4R,5R,6S)-2-[[(1R,2R,4R,5R,6S,10R)-5-Hydroxy-2-(hydroxymethyl)-3,9-dioxatricyclo[4.4.0.02,4]dec-7-en-10-yl]oxy]-6-(hydroxymethyl)oxane-3,4,5-triol,3TBDMS,isomer #12	CC(C)(C)[Si](C)(C)OC1C(CO)OC(OC2OC=CC3C(O[Si](C)(C)C(C)(C)C)C4OC4(CO)C23)C(O[Si](C)(C)C(C)(C)C)C1O	4068.9	Standard polar	33892256
(2R,3S,4R,5R,6S)-2-[[(1R,2R,4R,5R,6S,10R)-5-Hydroxy-2-(hydroxymethyl)-3,9-dioxatricyclo[4.4.0.02,4]dec-7-en-10-yl]oxy]-6-(hydroxymethyl)oxane-3,4,5-triol,3TBDMS,isomer #13	CC(C)(C)[Si](C)(C)OC1C(CO)OC(OC2OC=CC3C(O[Si](C)(C)C(C)(C)C)C4OC4(CO)C23)C(O)C1O[Si](C)(C)C(C)(C)C	3573.1	Semi standard non polar	33892256
(2R,3S,4R,5R,6S)-2-[[(1R,2R,4R,5R,6S,10R)-5-Hydroxy-2-(hydroxymethyl)-3,9-dioxatricyclo[4.4.0.02,4]dec-7-en-10-yl]oxy]-6-(hydroxymethyl)oxane-3,4,5-triol,3TBDMS,isomer #13	CC(C)(C)[Si](C)(C)OC1C(CO)OC(OC2OC=CC3C(O[Si](C)(C)C(C)(C)C)C4OC4(CO)C23)C(O)C1O[Si](C)(C)C(C)(C)C	3588.4	Standard non polar	33892256
(2R,3S,4R,5R,6S)-2-[[(1R,2R,4R,5R,6S,10R)-5-Hydroxy-2-(hydroxymethyl)-3,9-dioxatricyclo[4.4.0.02,4]dec-7-en-10-yl]oxy]-6-(hydroxymethyl)oxane-3,4,5-triol,3TBDMS,isomer #13	CC(C)(C)[Si](C)(C)OC1C(CO)OC(OC2OC=CC3C(O[Si](C)(C)C(C)(C)C)C4OC4(CO)C23)C(O)C1O[Si](C)(C)C(C)(C)C	4031.7	Standard polar	33892256
(2R,3S,4R,5R,6S)-2-[[(1R,2R,4R,5R,6S,10R)-5-Hydroxy-2-(hydroxymethyl)-3,9-dioxatricyclo[4.4.0.02,4]dec-7-en-10-yl]oxy]-6-(hydroxymethyl)oxane-3,4,5-triol,3TBDMS,isomer #14	CC(C)(C)[Si](C)(C)OCC12OC1C(O[Si](C)(C)C(C)(C)C)C1C=COC(OC3OC(CO)C(O)C(O[Si](C)(C)C(C)(C)C)C3O)C12	3542.0	Semi standard non polar	33892256
(2R,3S,4R,5R,6S)-2-[[(1R,2R,4R,5R,6S,10R)-5-Hydroxy-2-(hydroxymethyl)-3,9-dioxatricyclo[4.4.0.02,4]dec-7-en-10-yl]oxy]-6-(hydroxymethyl)oxane-3,4,5-triol,3TBDMS,isomer #14	CC(C)(C)[Si](C)(C)OCC12OC1C(O[Si](C)(C)C(C)(C)C)C1C=COC(OC3OC(CO)C(O)C(O[Si](C)(C)C(C)(C)C)C3O)C12	3661.2	Standard non polar	33892256
(2R,3S,4R,5R,6S)-2-[[(1R,2R,4R,5R,6S,10R)-5-Hydroxy-2-(hydroxymethyl)-3,9-dioxatricyclo[4.4.0.02,4]dec-7-en-10-yl]oxy]-6-(hydroxymethyl)oxane-3,4,5-triol,3TBDMS,isomer #14	CC(C)(C)[Si](C)(C)OCC12OC1C(O[Si](C)(C)C(C)(C)C)C1C=COC(OC3OC(CO)C(O)C(O[Si](C)(C)C(C)(C)C)C3O)C12	4065.3	Standard polar	33892256
(2R,3S,4R,5R,6S)-2-[[(1R,2R,4R,5R,6S,10R)-5-Hydroxy-2-(hydroxymethyl)-3,9-dioxatricyclo[4.4.0.02,4]dec-7-en-10-yl]oxy]-6-(hydroxymethyl)oxane-3,4,5-triol,3TBDMS,isomer #15	CC(C)(C)[Si](C)(C)OC1C(OC2OC=CC3C(O[Si](C)(C)C(C)(C)C)C4OC4(CO)C23)OC(CO)C(O)C1O[Si](C)(C)C(C)(C)C	3575.6	Semi standard non polar	33892256
(2R,3S,4R,5R,6S)-2-[[(1R,2R,4R,5R,6S,10R)-5-Hydroxy-2-(hydroxymethyl)-3,9-dioxatricyclo[4.4.0.02,4]dec-7-en-10-yl]oxy]-6-(hydroxymethyl)oxane-3,4,5-triol,3TBDMS,isomer #15	CC(C)(C)[Si](C)(C)OC1C(OC2OC=CC3C(O[Si](C)(C)C(C)(C)C)C4OC4(CO)C23)OC(CO)C(O)C1O[Si](C)(C)C(C)(C)C	3595.9	Standard non polar	33892256
(2R,3S,4R,5R,6S)-2-[[(1R,2R,4R,5R,6S,10R)-5-Hydroxy-2-(hydroxymethyl)-3,9-dioxatricyclo[4.4.0.02,4]dec-7-en-10-yl]oxy]-6-(hydroxymethyl)oxane-3,4,5-triol,3TBDMS,isomer #15	CC(C)(C)[Si](C)(C)OC1C(OC2OC=CC3C(O[Si](C)(C)C(C)(C)C)C4OC4(CO)C23)OC(CO)C(O)C1O[Si](C)(C)C(C)(C)C	4050.8	Standard polar	33892256
(2R,3S,4R,5R,6S)-2-[[(1R,2R,4R,5R,6S,10R)-5-Hydroxy-2-(hydroxymethyl)-3,9-dioxatricyclo[4.4.0.02,4]dec-7-en-10-yl]oxy]-6-(hydroxymethyl)oxane-3,4,5-triol,3TBDMS,isomer #16	CC(C)(C)[Si](C)(C)OCC12OC1C(O[Si](C)(C)C(C)(C)C)C1C=COC(OC3OC(CO)C(O)C(O)C3O[Si](C)(C)C(C)(C)C)C12	3526.2	Semi standard non polar	33892256
(2R,3S,4R,5R,6S)-2-[[(1R,2R,4R,5R,6S,10R)-5-Hydroxy-2-(hydroxymethyl)-3,9-dioxatricyclo[4.4.0.02,4]dec-7-en-10-yl]oxy]-6-(hydroxymethyl)oxane-3,4,5-triol,3TBDMS,isomer #16	CC(C)(C)[Si](C)(C)OCC12OC1C(O[Si](C)(C)C(C)(C)C)C1C=COC(OC3OC(CO)C(O)C(O)C3O[Si](C)(C)C(C)(C)C)C12	3678.9	Standard non polar	33892256
(2R,3S,4R,5R,6S)-2-[[(1R,2R,4R,5R,6S,10R)-5-Hydroxy-2-(hydroxymethyl)-3,9-dioxatricyclo[4.4.0.02,4]dec-7-en-10-yl]oxy]-6-(hydroxymethyl)oxane-3,4,5-triol,3TBDMS,isomer #16	CC(C)(C)[Si](C)(C)OCC12OC1C(O[Si](C)(C)C(C)(C)C)C1C=COC(OC3OC(CO)C(O)C(O)C3O[Si](C)(C)C(C)(C)C)C12	4069.1	Standard polar	33892256
(2R,3S,4R,5R,6S)-2-[[(1R,2R,4R,5R,6S,10R)-5-Hydroxy-2-(hydroxymethyl)-3,9-dioxatricyclo[4.4.0.02,4]dec-7-en-10-yl]oxy]-6-(hydroxymethyl)oxane-3,4,5-triol,3TBDMS,isomer #17	CC(C)(C)[Si](C)(C)OCC12OC1C(O)C1C=COC(OC3OC(CO)C(O[Si](C)(C)C(C)(C)C)C(O[Si](C)(C)C(C)(C)C)C3O)C12	3534.3	Semi standard non polar	33892256
(2R,3S,4R,5R,6S)-2-[[(1R,2R,4R,5R,6S,10R)-5-Hydroxy-2-(hydroxymethyl)-3,9-dioxatricyclo[4.4.0.02,4]dec-7-en-10-yl]oxy]-6-(hydroxymethyl)oxane-3,4,5-triol,3TBDMS,isomer #17	CC(C)(C)[Si](C)(C)OCC12OC1C(O)C1C=COC(OC3OC(CO)C(O[Si](C)(C)C(C)(C)C)C(O[Si](C)(C)C(C)(C)C)C3O)C12	3676.1	Standard non polar	33892256
(2R,3S,4R,5R,6S)-2-[[(1R,2R,4R,5R,6S,10R)-5-Hydroxy-2-(hydroxymethyl)-3,9-dioxatricyclo[4.4.0.02,4]dec-7-en-10-yl]oxy]-6-(hydroxymethyl)oxane-3,4,5-triol,3TBDMS,isomer #17	CC(C)(C)[Si](C)(C)OCC12OC1C(O)C1C=COC(OC3OC(CO)C(O[Si](C)(C)C(C)(C)C)C(O[Si](C)(C)C(C)(C)C)C3O)C12	4159.0	Standard polar	33892256
(2R,3S,4R,5R,6S)-2-[[(1R,2R,4R,5R,6S,10R)-5-Hydroxy-2-(hydroxymethyl)-3,9-dioxatricyclo[4.4.0.02,4]dec-7-en-10-yl]oxy]-6-(hydroxymethyl)oxane-3,4,5-triol,3TBDMS,isomer #18	CC(C)(C)[Si](C)(C)OCC12OC1C(O)C1C=COC(OC3OC(CO)C(O[Si](C)(C)C(C)(C)C)C(O)C3O[Si](C)(C)C(C)(C)C)C12	3531.5	Semi standard non polar	33892256
(2R,3S,4R,5R,6S)-2-[[(1R,2R,4R,5R,6S,10R)-5-Hydroxy-2-(hydroxymethyl)-3,9-dioxatricyclo[4.4.0.02,4]dec-7-en-10-yl]oxy]-6-(hydroxymethyl)oxane-3,4,5-triol,3TBDMS,isomer #18	CC(C)(C)[Si](C)(C)OCC12OC1C(O)C1C=COC(OC3OC(CO)C(O[Si](C)(C)C(C)(C)C)C(O)C3O[Si](C)(C)C(C)(C)C)C12	3704.5	Standard non polar	33892256
(2R,3S,4R,5R,6S)-2-[[(1R,2R,4R,5R,6S,10R)-5-Hydroxy-2-(hydroxymethyl)-3,9-dioxatricyclo[4.4.0.02,4]dec-7-en-10-yl]oxy]-6-(hydroxymethyl)oxane-3,4,5-triol,3TBDMS,isomer #18	CC(C)(C)[Si](C)(C)OCC12OC1C(O)C1C=COC(OC3OC(CO)C(O[Si](C)(C)C(C)(C)C)C(O)C3O[Si](C)(C)C(C)(C)C)C12	4197.8	Standard polar	33892256
(2R,3S,4R,5R,6S)-2-[[(1R,2R,4R,5R,6S,10R)-5-Hydroxy-2-(hydroxymethyl)-3,9-dioxatricyclo[4.4.0.02,4]dec-7-en-10-yl]oxy]-6-(hydroxymethyl)oxane-3,4,5-triol,3TBDMS,isomer #19	CC(C)(C)[Si](C)(C)OCC12OC1C(O)C1C=COC(OC3OC(CO)C(O)C(O[Si](C)(C)C(C)(C)C)C3O[Si](C)(C)C(C)(C)C)C12	3538.1	Semi standard non polar	33892256
(2R,3S,4R,5R,6S)-2-[[(1R,2R,4R,5R,6S,10R)-5-Hydroxy-2-(hydroxymethyl)-3,9-dioxatricyclo[4.4.0.02,4]dec-7-en-10-yl]oxy]-6-(hydroxymethyl)oxane-3,4,5-triol,3TBDMS,isomer #19	CC(C)(C)[Si](C)(C)OCC12OC1C(O)C1C=COC(OC3OC(CO)C(O)C(O[Si](C)(C)C(C)(C)C)C3O[Si](C)(C)C(C)(C)C)C12	3684.9	Standard non polar	33892256
(2R,3S,4R,5R,6S)-2-[[(1R,2R,4R,5R,6S,10R)-5-Hydroxy-2-(hydroxymethyl)-3,9-dioxatricyclo[4.4.0.02,4]dec-7-en-10-yl]oxy]-6-(hydroxymethyl)oxane-3,4,5-triol,3TBDMS,isomer #19	CC(C)(C)[Si](C)(C)OCC12OC1C(O)C1C=COC(OC3OC(CO)C(O)C(O[Si](C)(C)C(C)(C)C)C3O[Si](C)(C)C(C)(C)C)C12	4179.0	Standard polar	33892256
(2R,3S,4R,5R,6S)-2-[[(1R,2R,4R,5R,6S,10R)-5-Hydroxy-2-(hydroxymethyl)-3,9-dioxatricyclo[4.4.0.02,4]dec-7-en-10-yl]oxy]-6-(hydroxymethyl)oxane-3,4,5-triol,3TBDMS,isomer #2	CC(C)(C)[Si](C)(C)OCC1OC(OC2OC=CC3C(O[Si](C)(C)C(C)(C)C)C4OC4(CO)C23)C(O[Si](C)(C)C(C)(C)C)C(O)C1O	3562.7	Semi standard non polar	33892256
(2R,3S,4R,5R,6S)-2-[[(1R,2R,4R,5R,6S,10R)-5-Hydroxy-2-(hydroxymethyl)-3,9-dioxatricyclo[4.4.0.02,4]dec-7-en-10-yl]oxy]-6-(hydroxymethyl)oxane-3,4,5-triol,3TBDMS,isomer #2	CC(C)(C)[Si](C)(C)OCC1OC(OC2OC=CC3C(O[Si](C)(C)C(C)(C)C)C4OC4(CO)C23)C(O[Si](C)(C)C(C)(C)C)C(O)C1O	3659.6	Standard non polar	33892256
(2R,3S,4R,5R,6S)-2-[[(1R,2R,4R,5R,6S,10R)-5-Hydroxy-2-(hydroxymethyl)-3,9-dioxatricyclo[4.4.0.02,4]dec-7-en-10-yl]oxy]-6-(hydroxymethyl)oxane-3,4,5-triol,3TBDMS,isomer #2	CC(C)(C)[Si](C)(C)OCC1OC(OC2OC=CC3C(O[Si](C)(C)C(C)(C)C)C4OC4(CO)C23)C(O[Si](C)(C)C(C)(C)C)C(O)C1O	4100.9	Standard polar	33892256
(2R,3S,4R,5R,6S)-2-[[(1R,2R,4R,5R,6S,10R)-5-Hydroxy-2-(hydroxymethyl)-3,9-dioxatricyclo[4.4.0.02,4]dec-7-en-10-yl]oxy]-6-(hydroxymethyl)oxane-3,4,5-triol,3TBDMS,isomer #20	CC(C)(C)[Si](C)(C)OC1C(CO)OC(OC2OC=CC3C(O)C4OC4(CO)C23)C(O[Si](C)(C)C(C)(C)C)C1O[Si](C)(C)C(C)(C)C	3573.9	Semi standard non polar	33892256
(2R,3S,4R,5R,6S)-2-[[(1R,2R,4R,5R,6S,10R)-5-Hydroxy-2-(hydroxymethyl)-3,9-dioxatricyclo[4.4.0.02,4]dec-7-en-10-yl]oxy]-6-(hydroxymethyl)oxane-3,4,5-triol,3TBDMS,isomer #20	CC(C)(C)[Si](C)(C)OC1C(CO)OC(OC2OC=CC3C(O)C4OC4(CO)C23)C(O[Si](C)(C)C(C)(C)C)C1O[Si](C)(C)C(C)(C)C	3621.6	Standard non polar	33892256
(2R,3S,4R,5R,6S)-2-[[(1R,2R,4R,5R,6S,10R)-5-Hydroxy-2-(hydroxymethyl)-3,9-dioxatricyclo[4.4.0.02,4]dec-7-en-10-yl]oxy]-6-(hydroxymethyl)oxane-3,4,5-triol,3TBDMS,isomer #20	CC(C)(C)[Si](C)(C)OC1C(CO)OC(OC2OC=CC3C(O)C4OC4(CO)C23)C(O[Si](C)(C)C(C)(C)C)C1O[Si](C)(C)C(C)(C)C	4119.8	Standard polar	33892256
(2R,3S,4R,5R,6S)-2-[[(1R,2R,4R,5R,6S,10R)-5-Hydroxy-2-(hydroxymethyl)-3,9-dioxatricyclo[4.4.0.02,4]dec-7-en-10-yl]oxy]-6-(hydroxymethyl)oxane-3,4,5-triol,3TBDMS,isomer #3	CC(C)(C)[Si](C)(C)OCC1OC(OC2OC=CC3C(O[Si](C)(C)C(C)(C)C)C4OC4(CO)C23)C(O)C(O[Si](C)(C)C(C)(C)C)C1O	3581.3	Semi standard non polar	33892256
(2R,3S,4R,5R,6S)-2-[[(1R,2R,4R,5R,6S,10R)-5-Hydroxy-2-(hydroxymethyl)-3,9-dioxatricyclo[4.4.0.02,4]dec-7-en-10-yl]oxy]-6-(hydroxymethyl)oxane-3,4,5-triol,3TBDMS,isomer #3	CC(C)(C)[Si](C)(C)OCC1OC(OC2OC=CC3C(O[Si](C)(C)C(C)(C)C)C4OC4(CO)C23)C(O)C(O[Si](C)(C)C(C)(C)C)C1O	3655.0	Standard non polar	33892256
(2R,3S,4R,5R,6S)-2-[[(1R,2R,4R,5R,6S,10R)-5-Hydroxy-2-(hydroxymethyl)-3,9-dioxatricyclo[4.4.0.02,4]dec-7-en-10-yl]oxy]-6-(hydroxymethyl)oxane-3,4,5-triol,3TBDMS,isomer #3	CC(C)(C)[Si](C)(C)OCC1OC(OC2OC=CC3C(O[Si](C)(C)C(C)(C)C)C4OC4(CO)C23)C(O)C(O[Si](C)(C)C(C)(C)C)C1O	4099.5	Standard polar	33892256
(2R,3S,4R,5R,6S)-2-[[(1R,2R,4R,5R,6S,10R)-5-Hydroxy-2-(hydroxymethyl)-3,9-dioxatricyclo[4.4.0.02,4]dec-7-en-10-yl]oxy]-6-(hydroxymethyl)oxane-3,4,5-triol,3TBDMS,isomer #4	CC(C)(C)[Si](C)(C)OCC1OC(OC2OC=CC3C(O[Si](C)(C)C(C)(C)C)C4OC4(CO)C23)C(O)C(O)C1O[Si](C)(C)C(C)(C)C	3563.5	Semi standard non polar	33892256
(2R,3S,4R,5R,6S)-2-[[(1R,2R,4R,5R,6S,10R)-5-Hydroxy-2-(hydroxymethyl)-3,9-dioxatricyclo[4.4.0.02,4]dec-7-en-10-yl]oxy]-6-(hydroxymethyl)oxane-3,4,5-triol,3TBDMS,isomer #4	CC(C)(C)[Si](C)(C)OCC1OC(OC2OC=CC3C(O[Si](C)(C)C(C)(C)C)C4OC4(CO)C23)C(O)C(O)C1O[Si](C)(C)C(C)(C)C	3660.0	Standard non polar	33892256
(2R,3S,4R,5R,6S)-2-[[(1R,2R,4R,5R,6S,10R)-5-Hydroxy-2-(hydroxymethyl)-3,9-dioxatricyclo[4.4.0.02,4]dec-7-en-10-yl]oxy]-6-(hydroxymethyl)oxane-3,4,5-triol,3TBDMS,isomer #4	CC(C)(C)[Si](C)(C)OCC1OC(OC2OC=CC3C(O[Si](C)(C)C(C)(C)C)C4OC4(CO)C23)C(O)C(O)C1O[Si](C)(C)C(C)(C)C	4084.3	Standard polar	33892256
(2R,3S,4R,5R,6S)-2-[[(1R,2R,4R,5R,6S,10R)-5-Hydroxy-2-(hydroxymethyl)-3,9-dioxatricyclo[4.4.0.02,4]dec-7-en-10-yl]oxy]-6-(hydroxymethyl)oxane-3,4,5-triol,3TBDMS,isomer #5	CC(C)(C)[Si](C)(C)OCC1OC(OC2OC=CC3C(O)C4OC4(CO[Si](C)(C)C(C)(C)C)C23)C(O[Si](C)(C)C(C)(C)C)C(O)C1O	3559.0	Semi standard non polar	33892256
(2R,3S,4R,5R,6S)-2-[[(1R,2R,4R,5R,6S,10R)-5-Hydroxy-2-(hydroxymethyl)-3,9-dioxatricyclo[4.4.0.02,4]dec-7-en-10-yl]oxy]-6-(hydroxymethyl)oxane-3,4,5-triol,3TBDMS,isomer #5	CC(C)(C)[Si](C)(C)OCC1OC(OC2OC=CC3C(O)C4OC4(CO[Si](C)(C)C(C)(C)C)C23)C(O[Si](C)(C)C(C)(C)C)C(O)C1O	3738.8	Standard non polar	33892256
(2R,3S,4R,5R,6S)-2-[[(1R,2R,4R,5R,6S,10R)-5-Hydroxy-2-(hydroxymethyl)-3,9-dioxatricyclo[4.4.0.02,4]dec-7-en-10-yl]oxy]-6-(hydroxymethyl)oxane-3,4,5-triol,3TBDMS,isomer #5	CC(C)(C)[Si](C)(C)OCC1OC(OC2OC=CC3C(O)C4OC4(CO[Si](C)(C)C(C)(C)C)C23)C(O[Si](C)(C)C(C)(C)C)C(O)C1O	4225.9	Standard polar	33892256
(2R,3S,4R,5R,6S)-2-[[(1R,2R,4R,5R,6S,10R)-5-Hydroxy-2-(hydroxymethyl)-3,9-dioxatricyclo[4.4.0.02,4]dec-7-en-10-yl]oxy]-6-(hydroxymethyl)oxane-3,4,5-triol,3TBDMS,isomer #6	CC(C)(C)[Si](C)(C)OCC1OC(OC2OC=CC3C(O)C4OC4(CO[Si](C)(C)C(C)(C)C)C23)C(O)C(O[Si](C)(C)C(C)(C)C)C1O	3568.2	Semi standard non polar	33892256
(2R,3S,4R,5R,6S)-2-[[(1R,2R,4R,5R,6S,10R)-5-Hydroxy-2-(hydroxymethyl)-3,9-dioxatricyclo[4.4.0.02,4]dec-7-en-10-yl]oxy]-6-(hydroxymethyl)oxane-3,4,5-triol,3TBDMS,isomer #6	CC(C)(C)[Si](C)(C)OCC1OC(OC2OC=CC3C(O)C4OC4(CO[Si](C)(C)C(C)(C)C)C23)C(O)C(O[Si](C)(C)C(C)(C)C)C1O	3733.1	Standard non polar	33892256
(2R,3S,4R,5R,6S)-2-[[(1R,2R,4R,5R,6S,10R)-5-Hydroxy-2-(hydroxymethyl)-3,9-dioxatricyclo[4.4.0.02,4]dec-7-en-10-yl]oxy]-6-(hydroxymethyl)oxane-3,4,5-triol,3TBDMS,isomer #6	CC(C)(C)[Si](C)(C)OCC1OC(OC2OC=CC3C(O)C4OC4(CO[Si](C)(C)C(C)(C)C)C23)C(O)C(O[Si](C)(C)C(C)(C)C)C1O	4224.4	Standard polar	33892256
(2R,3S,4R,5R,6S)-2-[[(1R,2R,4R,5R,6S,10R)-5-Hydroxy-2-(hydroxymethyl)-3,9-dioxatricyclo[4.4.0.02,4]dec-7-en-10-yl]oxy]-6-(hydroxymethyl)oxane-3,4,5-triol,3TBDMS,isomer #7	CC(C)(C)[Si](C)(C)OCC1OC(OC2OC=CC3C(O)C4OC4(CO[Si](C)(C)C(C)(C)C)C23)C(O)C(O)C1O[Si](C)(C)C(C)(C)C	3558.2	Semi standard non polar	33892256
(2R,3S,4R,5R,6S)-2-[[(1R,2R,4R,5R,6S,10R)-5-Hydroxy-2-(hydroxymethyl)-3,9-dioxatricyclo[4.4.0.02,4]dec-7-en-10-yl]oxy]-6-(hydroxymethyl)oxane-3,4,5-triol,3TBDMS,isomer #7	CC(C)(C)[Si](C)(C)OCC1OC(OC2OC=CC3C(O)C4OC4(CO[Si](C)(C)C(C)(C)C)C23)C(O)C(O)C1O[Si](C)(C)C(C)(C)C	3738.3	Standard non polar	33892256
(2R,3S,4R,5R,6S)-2-[[(1R,2R,4R,5R,6S,10R)-5-Hydroxy-2-(hydroxymethyl)-3,9-dioxatricyclo[4.4.0.02,4]dec-7-en-10-yl]oxy]-6-(hydroxymethyl)oxane-3,4,5-triol,3TBDMS,isomer #7	CC(C)(C)[Si](C)(C)OCC1OC(OC2OC=CC3C(O)C4OC4(CO[Si](C)(C)C(C)(C)C)C23)C(O)C(O)C1O[Si](C)(C)C(C)(C)C	4208.4	Standard polar	33892256
(2R,3S,4R,5R,6S)-2-[[(1R,2R,4R,5R,6S,10R)-5-Hydroxy-2-(hydroxymethyl)-3,9-dioxatricyclo[4.4.0.02,4]dec-7-en-10-yl]oxy]-6-(hydroxymethyl)oxane-3,4,5-triol,3TBDMS,isomer #8	CC(C)(C)[Si](C)(C)OCC1OC(OC2OC=CC3C(O)C4OC4(CO)C23)C(O[Si](C)(C)C(C)(C)C)C(O[Si](C)(C)C(C)(C)C)C1O	3580.4	Semi standard non polar	33892256
(2R,3S,4R,5R,6S)-2-[[(1R,2R,4R,5R,6S,10R)-5-Hydroxy-2-(hydroxymethyl)-3,9-dioxatricyclo[4.4.0.02,4]dec-7-en-10-yl]oxy]-6-(hydroxymethyl)oxane-3,4,5-triol,3TBDMS,isomer #8	CC(C)(C)[Si](C)(C)OCC1OC(OC2OC=CC3C(O)C4OC4(CO)C23)C(O[Si](C)(C)C(C)(C)C)C(O[Si](C)(C)C(C)(C)C)C1O	3682.4	Standard non polar	33892256
(2R,3S,4R,5R,6S)-2-[[(1R,2R,4R,5R,6S,10R)-5-Hydroxy-2-(hydroxymethyl)-3,9-dioxatricyclo[4.4.0.02,4]dec-7-en-10-yl]oxy]-6-(hydroxymethyl)oxane-3,4,5-triol,3TBDMS,isomer #8	CC(C)(C)[Si](C)(C)OCC1OC(OC2OC=CC3C(O)C4OC4(CO)C23)C(O[Si](C)(C)C(C)(C)C)C(O[Si](C)(C)C(C)(C)C)C1O	4187.9	Standard polar	33892256
(2R,3S,4R,5R,6S)-2-[[(1R,2R,4R,5R,6S,10R)-5-Hydroxy-2-(hydroxymethyl)-3,9-dioxatricyclo[4.4.0.02,4]dec-7-en-10-yl]oxy]-6-(hydroxymethyl)oxane-3,4,5-triol,3TBDMS,isomer #9	CC(C)(C)[Si](C)(C)OCC1OC(OC2OC=CC3C(O)C4OC4(CO)C23)C(O[Si](C)(C)C(C)(C)C)C(O)C1O[Si](C)(C)C(C)(C)C	3582.1	Semi standard non polar	33892256
(2R,3S,4R,5R,6S)-2-[[(1R,2R,4R,5R,6S,10R)-5-Hydroxy-2-(hydroxymethyl)-3,9-dioxatricyclo[4.4.0.02,4]dec-7-en-10-yl]oxy]-6-(hydroxymethyl)oxane-3,4,5-triol,3TBDMS,isomer #9	CC(C)(C)[Si](C)(C)OCC1OC(OC2OC=CC3C(O)C4OC4(CO)C23)C(O[Si](C)(C)C(C)(C)C)C(O)C1O[Si](C)(C)C(C)(C)C	3708.6	Standard non polar	33892256
(2R,3S,4R,5R,6S)-2-[[(1R,2R,4R,5R,6S,10R)-5-Hydroxy-2-(hydroxymethyl)-3,9-dioxatricyclo[4.4.0.02,4]dec-7-en-10-yl]oxy]-6-(hydroxymethyl)oxane-3,4,5-triol,3TBDMS,isomer #9	CC(C)(C)[Si](C)(C)OCC1OC(OC2OC=CC3C(O)C4OC4(CO)C23)C(O[Si](C)(C)C(C)(C)C)C(O)C1O[Si](C)(C)C(C)(C)C	4207.9	Standard polar	33892256
(2R,3S,4R,5R,6S)-2-[[(1R,2R,4R,5R,6S,10R)-5-Hydroxy-2-(hydroxymethyl)-3,9-dioxatricyclo[4.4.0.02,4]dec-7-en-10-yl]oxy]-6-(hydroxymethyl)oxane-3,4,5-triol,4TBDMS,isomer #1	CC(C)(C)[Si](C)(C)OCC1OC(OC2OC=CC3C(O[Si](C)(C)C(C)(C)C)C4OC4(CO[Si](C)(C)C(C)(C)C)C23)C(O[Si](C)(C)C(C)(C)C)C(O)C1O	3695.2	Semi standard non polar	33892256
(2R,3S,4R,5R,6S)-2-[[(1R,2R,4R,5R,6S,10R)-5-Hydroxy-2-(hydroxymethyl)-3,9-dioxatricyclo[4.4.0.02,4]dec-7-en-10-yl]oxy]-6-(hydroxymethyl)oxane-3,4,5-triol,4TBDMS,isomer #1	CC(C)(C)[Si](C)(C)OCC1OC(OC2OC=CC3C(O[Si](C)(C)C(C)(C)C)C4OC4(CO[Si](C)(C)C(C)(C)C)C23)C(O[Si](C)(C)C(C)(C)C)C(O)C1O	3860.9	Standard non polar	33892256
(2R,3S,4R,5R,6S)-2-[[(1R,2R,4R,5R,6S,10R)-5-Hydroxy-2-(hydroxymethyl)-3,9-dioxatricyclo[4.4.0.02,4]dec-7-en-10-yl]oxy]-6-(hydroxymethyl)oxane-3,4,5-triol,4TBDMS,isomer #1	CC(C)(C)[Si](C)(C)OCC1OC(OC2OC=CC3C(O[Si](C)(C)C(C)(C)C)C4OC4(CO[Si](C)(C)C(C)(C)C)C23)C(O[Si](C)(C)C(C)(C)C)C(O)C1O	3915.7	Standard polar	33892256
(2R,3S,4R,5R,6S)-2-[[(1R,2R,4R,5R,6S,10R)-5-Hydroxy-2-(hydroxymethyl)-3,9-dioxatricyclo[4.4.0.02,4]dec-7-en-10-yl]oxy]-6-(hydroxymethyl)oxane-3,4,5-triol,4TBDMS,isomer #10	CC(C)(C)[Si](C)(C)OCC1OC(OC2OC=CC3C(O)C4OC4(CO)C23)C(O[Si](C)(C)C(C)(C)C)C(O[Si](C)(C)C(C)(C)C)C1O[Si](C)(C)C(C)(C)C	3714.7	Semi standard non polar	33892256
(2R,3S,4R,5R,6S)-2-[[(1R,2R,4R,5R,6S,10R)-5-Hydroxy-2-(hydroxymethyl)-3,9-dioxatricyclo[4.4.0.02,4]dec-7-en-10-yl]oxy]-6-(hydroxymethyl)oxane-3,4,5-triol,4TBDMS,isomer #10	CC(C)(C)[Si](C)(C)OCC1OC(OC2OC=CC3C(O)C4OC4(CO)C23)C(O[Si](C)(C)C(C)(C)C)C(O[Si](C)(C)C(C)(C)C)C1O[Si](C)(C)C(C)(C)C	3821.5	Standard non polar	33892256
(2R,3S,4R,5R,6S)-2-[[(1R,2R,4R,5R,6S,10R)-5-Hydroxy-2-(hydroxymethyl)-3,9-dioxatricyclo[4.4.0.02,4]dec-7-en-10-yl]oxy]-6-(hydroxymethyl)oxane-3,4,5-triol,4TBDMS,isomer #10	CC(C)(C)[Si](C)(C)OCC1OC(OC2OC=CC3C(O)C4OC4(CO)C23)C(O[Si](C)(C)C(C)(C)C)C(O[Si](C)(C)C(C)(C)C)C1O[Si](C)(C)C(C)(C)C	3963.2	Standard polar	33892256
(2R,3S,4R,5R,6S)-2-[[(1R,2R,4R,5R,6S,10R)-5-Hydroxy-2-(hydroxymethyl)-3,9-dioxatricyclo[4.4.0.02,4]dec-7-en-10-yl]oxy]-6-(hydroxymethyl)oxane-3,4,5-triol,4TBDMS,isomer #11	CC(C)(C)[Si](C)(C)OCC12OC1C(O[Si](C)(C)C(C)(C)C)C1C=COC(OC3OC(CO)C(O[Si](C)(C)C(C)(C)C)C(O[Si](C)(C)C(C)(C)C)C3O)C12	3664.2	Semi standard non polar	33892256
(2R,3S,4R,5R,6S)-2-[[(1R,2R,4R,5R,6S,10R)-5-Hydroxy-2-(hydroxymethyl)-3,9-dioxatricyclo[4.4.0.02,4]dec-7-en-10-yl]oxy]-6-(hydroxymethyl)oxane-3,4,5-triol,4TBDMS,isomer #11	CC(C)(C)[Si](C)(C)OCC12OC1C(O[Si](C)(C)C(C)(C)C)C1C=COC(OC3OC(CO)C(O[Si](C)(C)C(C)(C)C)C(O[Si](C)(C)C(C)(C)C)C3O)C12	3784.7	Standard non polar	33892256
(2R,3S,4R,5R,6S)-2-[[(1R,2R,4R,5R,6S,10R)-5-Hydroxy-2-(hydroxymethyl)-3,9-dioxatricyclo[4.4.0.02,4]dec-7-en-10-yl]oxy]-6-(hydroxymethyl)oxane-3,4,5-triol,4TBDMS,isomer #11	CC(C)(C)[Si](C)(C)OCC12OC1C(O[Si](C)(C)C(C)(C)C)C1C=COC(OC3OC(CO)C(O[Si](C)(C)C(C)(C)C)C(O[Si](C)(C)C(C)(C)C)C3O)C12	3852.1	Standard polar	33892256
(2R,3S,4R,5R,6S)-2-[[(1R,2R,4R,5R,6S,10R)-5-Hydroxy-2-(hydroxymethyl)-3,9-dioxatricyclo[4.4.0.02,4]dec-7-en-10-yl]oxy]-6-(hydroxymethyl)oxane-3,4,5-triol,4TBDMS,isomer #12	CC(C)(C)[Si](C)(C)OCC12OC1C(O[Si](C)(C)C(C)(C)C)C1C=COC(OC3OC(CO)C(O[Si](C)(C)C(C)(C)C)C(O)C3O[Si](C)(C)C(C)(C)C)C12	3648.7	Semi standard non polar	33892256
(2R,3S,4R,5R,6S)-2-[[(1R,2R,4R,5R,6S,10R)-5-Hydroxy-2-(hydroxymethyl)-3,9-dioxatricyclo[4.4.0.02,4]dec-7-en-10-yl]oxy]-6-(hydroxymethyl)oxane-3,4,5-triol,4TBDMS,isomer #12	CC(C)(C)[Si](C)(C)OCC12OC1C(O[Si](C)(C)C(C)(C)C)C1C=COC(OC3OC(CO)C(O[Si](C)(C)C(C)(C)C)C(O)C3O[Si](C)(C)C(C)(C)C)C12	3828.8	Standard non polar	33892256
(2R,3S,4R,5R,6S)-2-[[(1R,2R,4R,5R,6S,10R)-5-Hydroxy-2-(hydroxymethyl)-3,9-dioxatricyclo[4.4.0.02,4]dec-7-en-10-yl]oxy]-6-(hydroxymethyl)oxane-3,4,5-triol,4TBDMS,isomer #12	CC(C)(C)[Si](C)(C)OCC12OC1C(O[Si](C)(C)C(C)(C)C)C1C=COC(OC3OC(CO)C(O[Si](C)(C)C(C)(C)C)C(O)C3O[Si](C)(C)C(C)(C)C)C12	3896.7	Standard polar	33892256
(2R,3S,4R,5R,6S)-2-[[(1R,2R,4R,5R,6S,10R)-5-Hydroxy-2-(hydroxymethyl)-3,9-dioxatricyclo[4.4.0.02,4]dec-7-en-10-yl]oxy]-6-(hydroxymethyl)oxane-3,4,5-triol,4TBDMS,isomer #13	CC(C)(C)[Si](C)(C)OC1C(CO)OC(OC2OC=CC3C(O[Si](C)(C)C(C)(C)C)C4OC4(CO)C23)C(O[Si](C)(C)C(C)(C)C)C1O[Si](C)(C)C(C)(C)C	3670.9	Semi standard non polar	33892256
(2R,3S,4R,5R,6S)-2-[[(1R,2R,4R,5R,6S,10R)-5-Hydroxy-2-(hydroxymethyl)-3,9-dioxatricyclo[4.4.0.02,4]dec-7-en-10-yl]oxy]-6-(hydroxymethyl)oxane-3,4,5-triol,4TBDMS,isomer #13	CC(C)(C)[Si](C)(C)OC1C(CO)OC(OC2OC=CC3C(O[Si](C)(C)C(C)(C)C)C4OC4(CO)C23)C(O[Si](C)(C)C(C)(C)C)C1O[Si](C)(C)C(C)(C)C	3728.1	Standard non polar	33892256
(2R,3S,4R,5R,6S)-2-[[(1R,2R,4R,5R,6S,10R)-5-Hydroxy-2-(hydroxymethyl)-3,9-dioxatricyclo[4.4.0.02,4]dec-7-en-10-yl]oxy]-6-(hydroxymethyl)oxane-3,4,5-triol,4TBDMS,isomer #13	CC(C)(C)[Si](C)(C)OC1C(CO)OC(OC2OC=CC3C(O[Si](C)(C)C(C)(C)C)C4OC4(CO)C23)C(O[Si](C)(C)C(C)(C)C)C1O[Si](C)(C)C(C)(C)C	3839.5	Standard polar	33892256
(2R,3S,4R,5R,6S)-2-[[(1R,2R,4R,5R,6S,10R)-5-Hydroxy-2-(hydroxymethyl)-3,9-dioxatricyclo[4.4.0.02,4]dec-7-en-10-yl]oxy]-6-(hydroxymethyl)oxane-3,4,5-triol,4TBDMS,isomer #14	CC(C)(C)[Si](C)(C)OCC12OC1C(O[Si](C)(C)C(C)(C)C)C1C=COC(OC3OC(CO)C(O)C(O[Si](C)(C)C(C)(C)C)C3O[Si](C)(C)C(C)(C)C)C12	3658.6	Semi standard non polar	33892256
(2R,3S,4R,5R,6S)-2-[[(1R,2R,4R,5R,6S,10R)-5-Hydroxy-2-(hydroxymethyl)-3,9-dioxatricyclo[4.4.0.02,4]dec-7-en-10-yl]oxy]-6-(hydroxymethyl)oxane-3,4,5-triol,4TBDMS,isomer #14	CC(C)(C)[Si](C)(C)OCC12OC1C(O[Si](C)(C)C(C)(C)C)C1C=COC(OC3OC(CO)C(O)C(O[Si](C)(C)C(C)(C)C)C3O[Si](C)(C)C(C)(C)C)C12	3798.1	Standard non polar	33892256
(2R,3S,4R,5R,6S)-2-[[(1R,2R,4R,5R,6S,10R)-5-Hydroxy-2-(hydroxymethyl)-3,9-dioxatricyclo[4.4.0.02,4]dec-7-en-10-yl]oxy]-6-(hydroxymethyl)oxane-3,4,5-triol,4TBDMS,isomer #14	CC(C)(C)[Si](C)(C)OCC12OC1C(O[Si](C)(C)C(C)(C)C)C1C=COC(OC3OC(CO)C(O)C(O[Si](C)(C)C(C)(C)C)C3O[Si](C)(C)C(C)(C)C)C12	3873.0	Standard polar	33892256
(2R,3S,4R,5R,6S)-2-[[(1R,2R,4R,5R,6S,10R)-5-Hydroxy-2-(hydroxymethyl)-3,9-dioxatricyclo[4.4.0.02,4]dec-7-en-10-yl]oxy]-6-(hydroxymethyl)oxane-3,4,5-triol,4TBDMS,isomer #15	CC(C)(C)[Si](C)(C)OCC12OC1C(O)C1C=COC(OC3OC(CO)C(O[Si](C)(C)C(C)(C)C)C(O[Si](C)(C)C(C)(C)C)C3O[Si](C)(C)C(C)(C)C)C12	3650.9	Semi standard non polar	33892256
(2R,3S,4R,5R,6S)-2-[[(1R,2R,4R,5R,6S,10R)-5-Hydroxy-2-(hydroxymethyl)-3,9-dioxatricyclo[4.4.0.02,4]dec-7-en-10-yl]oxy]-6-(hydroxymethyl)oxane-3,4,5-triol,4TBDMS,isomer #15	CC(C)(C)[Si](C)(C)OCC12OC1C(O)C1C=COC(OC3OC(CO)C(O[Si](C)(C)C(C)(C)C)C(O[Si](C)(C)C(C)(C)C)C3O[Si](C)(C)C(C)(C)C)C12	3803.4	Standard non polar	33892256
(2R,3S,4R,5R,6S)-2-[[(1R,2R,4R,5R,6S,10R)-5-Hydroxy-2-(hydroxymethyl)-3,9-dioxatricyclo[4.4.0.02,4]dec-7-en-10-yl]oxy]-6-(hydroxymethyl)oxane-3,4,5-triol,4TBDMS,isomer #15	CC(C)(C)[Si](C)(C)OCC12OC1C(O)C1C=COC(OC3OC(CO)C(O[Si](C)(C)C(C)(C)C)C(O[Si](C)(C)C(C)(C)C)C3O[Si](C)(C)C(C)(C)C)C12	3972.2	Standard polar	33892256
(2R,3S,4R,5R,6S)-2-[[(1R,2R,4R,5R,6S,10R)-5-Hydroxy-2-(hydroxymethyl)-3,9-dioxatricyclo[4.4.0.02,4]dec-7-en-10-yl]oxy]-6-(hydroxymethyl)oxane-3,4,5-triol,4TBDMS,isomer #2	CC(C)(C)[Si](C)(C)OCC1OC(OC2OC=CC3C(O[Si](C)(C)C(C)(C)C)C4OC4(CO[Si](C)(C)C(C)(C)C)C23)C(O)C(O[Si](C)(C)C(C)(C)C)C1O	3730.0	Semi standard non polar	33892256
(2R,3S,4R,5R,6S)-2-[[(1R,2R,4R,5R,6S,10R)-5-Hydroxy-2-(hydroxymethyl)-3,9-dioxatricyclo[4.4.0.02,4]dec-7-en-10-yl]oxy]-6-(hydroxymethyl)oxane-3,4,5-triol,4TBDMS,isomer #2	CC(C)(C)[Si](C)(C)OCC1OC(OC2OC=CC3C(O[Si](C)(C)C(C)(C)C)C4OC4(CO[Si](C)(C)C(C)(C)C)C23)C(O)C(O[Si](C)(C)C(C)(C)C)C1O	3842.7	Standard non polar	33892256
(2R,3S,4R,5R,6S)-2-[[(1R,2R,4R,5R,6S,10R)-5-Hydroxy-2-(hydroxymethyl)-3,9-dioxatricyclo[4.4.0.02,4]dec-7-en-10-yl]oxy]-6-(hydroxymethyl)oxane-3,4,5-triol,4TBDMS,isomer #2	CC(C)(C)[Si](C)(C)OCC1OC(OC2OC=CC3C(O[Si](C)(C)C(C)(C)C)C4OC4(CO[Si](C)(C)C(C)(C)C)C23)C(O)C(O[Si](C)(C)C(C)(C)C)C1O	3912.7	Standard polar	33892256
(2R,3S,4R,5R,6S)-2-[[(1R,2R,4R,5R,6S,10R)-5-Hydroxy-2-(hydroxymethyl)-3,9-dioxatricyclo[4.4.0.02,4]dec-7-en-10-yl]oxy]-6-(hydroxymethyl)oxane-3,4,5-triol,4TBDMS,isomer #3	CC(C)(C)[Si](C)(C)OCC1OC(OC2OC=CC3C(O[Si](C)(C)C(C)(C)C)C4OC4(CO[Si](C)(C)C(C)(C)C)C23)C(O)C(O)C1O[Si](C)(C)C(C)(C)C	3696.1	Semi standard non polar	33892256
(2R,3S,4R,5R,6S)-2-[[(1R,2R,4R,5R,6S,10R)-5-Hydroxy-2-(hydroxymethyl)-3,9-dioxatricyclo[4.4.0.02,4]dec-7-en-10-yl]oxy]-6-(hydroxymethyl)oxane-3,4,5-triol,4TBDMS,isomer #3	CC(C)(C)[Si](C)(C)OCC1OC(OC2OC=CC3C(O[Si](C)(C)C(C)(C)C)C4OC4(CO[Si](C)(C)C(C)(C)C)C23)C(O)C(O)C1O[Si](C)(C)C(C)(C)C	3857.5	Standard non polar	33892256
(2R,3S,4R,5R,6S)-2-[[(1R,2R,4R,5R,6S,10R)-5-Hydroxy-2-(hydroxymethyl)-3,9-dioxatricyclo[4.4.0.02,4]dec-7-en-10-yl]oxy]-6-(hydroxymethyl)oxane-3,4,5-triol,4TBDMS,isomer #3	CC(C)(C)[Si](C)(C)OCC1OC(OC2OC=CC3C(O[Si](C)(C)C(C)(C)C)C4OC4(CO[Si](C)(C)C(C)(C)C)C23)C(O)C(O)C1O[Si](C)(C)C(C)(C)C	3900.1	Standard polar	33892256
(2R,3S,4R,5R,6S)-2-[[(1R,2R,4R,5R,6S,10R)-5-Hydroxy-2-(hydroxymethyl)-3,9-dioxatricyclo[4.4.0.02,4]dec-7-en-10-yl]oxy]-6-(hydroxymethyl)oxane-3,4,5-triol,4TBDMS,isomer #4	CC(C)(C)[Si](C)(C)OCC1OC(OC2OC=CC3C(O[Si](C)(C)C(C)(C)C)C4OC4(CO)C23)C(O[Si](C)(C)C(C)(C)C)C(O[Si](C)(C)C(C)(C)C)C1O	3708.2	Semi standard non polar	33892256
(2R,3S,4R,5R,6S)-2-[[(1R,2R,4R,5R,6S,10R)-5-Hydroxy-2-(hydroxymethyl)-3,9-dioxatricyclo[4.4.0.02,4]dec-7-en-10-yl]oxy]-6-(hydroxymethyl)oxane-3,4,5-triol,4TBDMS,isomer #4	CC(C)(C)[Si](C)(C)OCC1OC(OC2OC=CC3C(O[Si](C)(C)C(C)(C)C)C4OC4(CO)C23)C(O[Si](C)(C)C(C)(C)C)C(O[Si](C)(C)C(C)(C)C)C1O	3787.2	Standard non polar	33892256
(2R,3S,4R,5R,6S)-2-[[(1R,2R,4R,5R,6S,10R)-5-Hydroxy-2-(hydroxymethyl)-3,9-dioxatricyclo[4.4.0.02,4]dec-7-en-10-yl]oxy]-6-(hydroxymethyl)oxane-3,4,5-triol,4TBDMS,isomer #4	CC(C)(C)[Si](C)(C)OCC1OC(OC2OC=CC3C(O[Si](C)(C)C(C)(C)C)C4OC4(CO)C23)C(O[Si](C)(C)C(C)(C)C)C(O[Si](C)(C)C(C)(C)C)C1O	3904.4	Standard polar	33892256
(2R,3S,4R,5R,6S)-2-[[(1R,2R,4R,5R,6S,10R)-5-Hydroxy-2-(hydroxymethyl)-3,9-dioxatricyclo[4.4.0.02,4]dec-7-en-10-yl]oxy]-6-(hydroxymethyl)oxane-3,4,5-triol,4TBDMS,isomer #5	CC(C)(C)[Si](C)(C)OCC1OC(OC2OC=CC3C(O[Si](C)(C)C(C)(C)C)C4OC4(CO)C23)C(O[Si](C)(C)C(C)(C)C)C(O)C1O[Si](C)(C)C(C)(C)C	3698.0	Semi standard non polar	33892256
(2R,3S,4R,5R,6S)-2-[[(1R,2R,4R,5R,6S,10R)-5-Hydroxy-2-(hydroxymethyl)-3,9-dioxatricyclo[4.4.0.02,4]dec-7-en-10-yl]oxy]-6-(hydroxymethyl)oxane-3,4,5-triol,4TBDMS,isomer #5	CC(C)(C)[Si](C)(C)OCC1OC(OC2OC=CC3C(O[Si](C)(C)C(C)(C)C)C4OC4(CO)C23)C(O[Si](C)(C)C(C)(C)C)C(O)C1O[Si](C)(C)C(C)(C)C	3828.2	Standard non polar	33892256
(2R,3S,4R,5R,6S)-2-[[(1R,2R,4R,5R,6S,10R)-5-Hydroxy-2-(hydroxymethyl)-3,9-dioxatricyclo[4.4.0.02,4]dec-7-en-10-yl]oxy]-6-(hydroxymethyl)oxane-3,4,5-triol,4TBDMS,isomer #5	CC(C)(C)[Si](C)(C)OCC1OC(OC2OC=CC3C(O[Si](C)(C)C(C)(C)C)C4OC4(CO)C23)C(O[Si](C)(C)C(C)(C)C)C(O)C1O[Si](C)(C)C(C)(C)C	3926.3	Standard polar	33892256
(2R,3S,4R,5R,6S)-2-[[(1R,2R,4R,5R,6S,10R)-5-Hydroxy-2-(hydroxymethyl)-3,9-dioxatricyclo[4.4.0.02,4]dec-7-en-10-yl]oxy]-6-(hydroxymethyl)oxane-3,4,5-triol,4TBDMS,isomer #6	CC(C)(C)[Si](C)(C)OCC1OC(OC2OC=CC3C(O[Si](C)(C)C(C)(C)C)C4OC4(CO)C23)C(O)C(O[Si](C)(C)C(C)(C)C)C1O[Si](C)(C)C(C)(C)C	3713.3	Semi standard non polar	33892256
(2R,3S,4R,5R,6S)-2-[[(1R,2R,4R,5R,6S,10R)-5-Hydroxy-2-(hydroxymethyl)-3,9-dioxatricyclo[4.4.0.02,4]dec-7-en-10-yl]oxy]-6-(hydroxymethyl)oxane-3,4,5-triol,4TBDMS,isomer #6	CC(C)(C)[Si](C)(C)OCC1OC(OC2OC=CC3C(O[Si](C)(C)C(C)(C)C)C4OC4(CO)C23)C(O)C(O[Si](C)(C)C(C)(C)C)C1O[Si](C)(C)C(C)(C)C	3785.6	Standard non polar	33892256
(2R,3S,4R,5R,6S)-2-[[(1R,2R,4R,5R,6S,10R)-5-Hydroxy-2-(hydroxymethyl)-3,9-dioxatricyclo[4.4.0.02,4]dec-7-en-10-yl]oxy]-6-(hydroxymethyl)oxane-3,4,5-triol,4TBDMS,isomer #6	CC(C)(C)[Si](C)(C)OCC1OC(OC2OC=CC3C(O[Si](C)(C)C(C)(C)C)C4OC4(CO)C23)C(O)C(O[Si](C)(C)C(C)(C)C)C1O[Si](C)(C)C(C)(C)C	3886.5	Standard polar	33892256
(2R,3S,4R,5R,6S)-2-[[(1R,2R,4R,5R,6S,10R)-5-Hydroxy-2-(hydroxymethyl)-3,9-dioxatricyclo[4.4.0.02,4]dec-7-en-10-yl]oxy]-6-(hydroxymethyl)oxane-3,4,5-triol,4TBDMS,isomer #7	CC(C)(C)[Si](C)(C)OCC1OC(OC2OC=CC3C(O)C4OC4(CO[Si](C)(C)C(C)(C)C)C23)C(O[Si](C)(C)C(C)(C)C)C(O[Si](C)(C)C(C)(C)C)C1O	3718.2	Semi standard non polar	33892256
(2R,3S,4R,5R,6S)-2-[[(1R,2R,4R,5R,6S,10R)-5-Hydroxy-2-(hydroxymethyl)-3,9-dioxatricyclo[4.4.0.02,4]dec-7-en-10-yl]oxy]-6-(hydroxymethyl)oxane-3,4,5-triol,4TBDMS,isomer #7	CC(C)(C)[Si](C)(C)OCC1OC(OC2OC=CC3C(O)C4OC4(CO[Si](C)(C)C(C)(C)C)C23)C(O[Si](C)(C)C(C)(C)C)C(O[Si](C)(C)C(C)(C)C)C1O	3854.9	Standard non polar	33892256
(2R,3S,4R,5R,6S)-2-[[(1R,2R,4R,5R,6S,10R)-5-Hydroxy-2-(hydroxymethyl)-3,9-dioxatricyclo[4.4.0.02,4]dec-7-en-10-yl]oxy]-6-(hydroxymethyl)oxane-3,4,5-triol,4TBDMS,isomer #7	CC(C)(C)[Si](C)(C)OCC1OC(OC2OC=CC3C(O)C4OC4(CO[Si](C)(C)C(C)(C)C)C23)C(O[Si](C)(C)C(C)(C)C)C(O[Si](C)(C)C(C)(C)C)C1O	4034.5	Standard polar	33892256
(2R,3S,4R,5R,6S)-2-[[(1R,2R,4R,5R,6S,10R)-5-Hydroxy-2-(hydroxymethyl)-3,9-dioxatricyclo[4.4.0.02,4]dec-7-en-10-yl]oxy]-6-(hydroxymethyl)oxane-3,4,5-triol,4TBDMS,isomer #8	CC(C)(C)[Si](C)(C)OCC1OC(OC2OC=CC3C(O)C4OC4(CO[Si](C)(C)C(C)(C)C)C23)C(O[Si](C)(C)C(C)(C)C)C(O)C1O[Si](C)(C)C(C)(C)C	3715.2	Semi standard non polar	33892256
(2R,3S,4R,5R,6S)-2-[[(1R,2R,4R,5R,6S,10R)-5-Hydroxy-2-(hydroxymethyl)-3,9-dioxatricyclo[4.4.0.02,4]dec-7-en-10-yl]oxy]-6-(hydroxymethyl)oxane-3,4,5-triol,4TBDMS,isomer #8	CC(C)(C)[Si](C)(C)OCC1OC(OC2OC=CC3C(O)C4OC4(CO[Si](C)(C)C(C)(C)C)C23)C(O[Si](C)(C)C(C)(C)C)C(O)C1O[Si](C)(C)C(C)(C)C	3897.5	Standard non polar	33892256
(2R,3S,4R,5R,6S)-2-[[(1R,2R,4R,5R,6S,10R)-5-Hydroxy-2-(hydroxymethyl)-3,9-dioxatricyclo[4.4.0.02,4]dec-7-en-10-yl]oxy]-6-(hydroxymethyl)oxane-3,4,5-triol,4TBDMS,isomer #8	CC(C)(C)[Si](C)(C)OCC1OC(OC2OC=CC3C(O)C4OC4(CO[Si](C)(C)C(C)(C)C)C23)C(O[Si](C)(C)C(C)(C)C)C(O)C1O[Si](C)(C)C(C)(C)C	4057.1	Standard polar	33892256
(2R,3S,4R,5R,6S)-2-[[(1R,2R,4R,5R,6S,10R)-5-Hydroxy-2-(hydroxymethyl)-3,9-dioxatricyclo[4.4.0.02,4]dec-7-en-10-yl]oxy]-6-(hydroxymethyl)oxane-3,4,5-triol,4TBDMS,isomer #9	CC(C)(C)[Si](C)(C)OCC1OC(OC2OC=CC3C(O)C4OC4(CO[Si](C)(C)C(C)(C)C)C23)C(O)C(O[Si](C)(C)C(C)(C)C)C1O[Si](C)(C)C(C)(C)C	3722.0	Semi standard non polar	33892256
(2R,3S,4R,5R,6S)-2-[[(1R,2R,4R,5R,6S,10R)-5-Hydroxy-2-(hydroxymethyl)-3,9-dioxatricyclo[4.4.0.02,4]dec-7-en-10-yl]oxy]-6-(hydroxymethyl)oxane-3,4,5-triol,4TBDMS,isomer #9	CC(C)(C)[Si](C)(C)OCC1OC(OC2OC=CC3C(O)C4OC4(CO[Si](C)(C)C(C)(C)C)C23)C(O)C(O[Si](C)(C)C(C)(C)C)C1O[Si](C)(C)C(C)(C)C	3852.9	Standard non polar	33892256
(2R,3S,4R,5R,6S)-2-[[(1R,2R,4R,5R,6S,10R)-5-Hydroxy-2-(hydroxymethyl)-3,9-dioxatricyclo[4.4.0.02,4]dec-7-en-10-yl]oxy]-6-(hydroxymethyl)oxane-3,4,5-triol,4TBDMS,isomer #9	CC(C)(C)[Si](C)(C)OCC1OC(OC2OC=CC3C(O)C4OC4(CO[Si](C)(C)C(C)(C)C)C23)C(O)C(O[Si](C)(C)C(C)(C)C)C1O[Si](C)(C)C(C)(C)C	4015.9	Standard polar	33892256

Spectra

GC-MS Spectra

Spectrum Type	Description	Splash Key	Deposition Date	Source	View
Predicted GC-MS	Predicted GC-MS Spectrum - (2R,3S,4R,5R,6S)-2-[[(1R,2R,4R,5R,6S,10R)-5-Hydroxy-2-(hydroxymethyl)-3,9-dioxatricyclo[4.4.0.02,4]dec-7-en-10-yl]oxy]-6-(hydroxymethyl)oxane-3,4,5-triol GC-MS (Non-derivatized) - 70eV, Positive	splash10-0544-6697000000-fff628c29715d322c1b2	2021-09-23	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - (2R,3S,4R,5R,6S)-2-[[(1R,2R,4R,5R,6S,10R)-5-Hydroxy-2-(hydroxymethyl)-3,9-dioxatricyclo[4.4.0.02,4]dec-7-en-10-yl]oxy]-6-(hydroxymethyl)oxane-3,4,5-triol GC-MS (Non-derivatized) - 70eV, Positive	Not Available	2021-10-12	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - (2R,3S,4R,5R,6S)-2-[[(1R,2R,4R,5R,6S,10R)-5-Hydroxy-2-(hydroxymethyl)-3,9-dioxatricyclo[4.4.0.02,4]dec-7-en-10-yl]oxy]-6-(hydroxymethyl)oxane-3,4,5-triol GC-MS (Non-derivatized) - 70eV, Positive	Not Available	2021-10-12	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - (2R,3S,4R,5R,6S)-2-[[(1R,2R,4R,5R,6S,10R)-5-Hydroxy-2-(hydroxymethyl)-3,9-dioxatricyclo[4.4.0.02,4]dec-7-en-10-yl]oxy]-6-(hydroxymethyl)oxane-3,4,5-triol GC-MS (Non-derivatized) - 70eV, Positive	Not Available	2021-10-12	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - (2R,3S,4R,5R,6S)-2-[[(1R,2R,4R,5R,6S,10R)-5-Hydroxy-2-(hydroxymethyl)-3,9-dioxatricyclo[4.4.0.02,4]dec-7-en-10-yl]oxy]-6-(hydroxymethyl)oxane-3,4,5-triol GC-MS (Non-derivatized) - 70eV, Positive	Not Available	2021-10-12	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - (2R,3S,4R,5R,6S)-2-[[(1R,2R,4R,5R,6S,10R)-5-Hydroxy-2-(hydroxymethyl)-3,9-dioxatricyclo[4.4.0.02,4]dec-7-en-10-yl]oxy]-6-(hydroxymethyl)oxane-3,4,5-triol GC-MS (TMS_1_1) - 70eV, Positive	Not Available	2021-11-03	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - (2R,3S,4R,5R,6S)-2-[[(1R,2R,4R,5R,6S,10R)-5-Hydroxy-2-(hydroxymethyl)-3,9-dioxatricyclo[4.4.0.02,4]dec-7-en-10-yl]oxy]-6-(hydroxymethyl)oxane-3,4,5-triol GC-MS (TMS_1_4) - 70eV, Positive	Not Available	2021-11-03	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - (2R,3S,4R,5R,6S)-2-[[(1R,2R,4R,5R,6S,10R)-5-Hydroxy-2-(hydroxymethyl)-3,9-dioxatricyclo[4.4.0.02,4]dec-7-en-10-yl]oxy]-6-(hydroxymethyl)oxane-3,4,5-triol GC-MS (TMS_1_5) - 70eV, Positive	Not Available	2021-11-03	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - (2R,3S,4R,5R,6S)-2-[[(1R,2R,4R,5R,6S,10R)-5-Hydroxy-2-(hydroxymethyl)-3,9-dioxatricyclo[4.4.0.02,4]dec-7-en-10-yl]oxy]-6-(hydroxymethyl)oxane-3,4,5-triol GC-MS (TMS_1_6) - 70eV, Positive	Not Available	2021-11-03	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - (2R,3S,4R,5R,6S)-2-[[(1R,2R,4R,5R,6S,10R)-5-Hydroxy-2-(hydroxymethyl)-3,9-dioxatricyclo[4.4.0.02,4]dec-7-en-10-yl]oxy]-6-(hydroxymethyl)oxane-3,4,5-triol GC-MS (TMS_2_1) - 70eV, Positive	Not Available	2021-11-03	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - (2R,3S,4R,5R,6S)-2-[[(1R,2R,4R,5R,6S,10R)-5-Hydroxy-2-(hydroxymethyl)-3,9-dioxatricyclo[4.4.0.02,4]dec-7-en-10-yl]oxy]-6-(hydroxymethyl)oxane-3,4,5-triol GC-MS (TMS_2_2) - 70eV, Positive	Not Available	2021-11-03	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - (2R,3S,4R,5R,6S)-2-[[(1R,2R,4R,5R,6S,10R)-5-Hydroxy-2-(hydroxymethyl)-3,9-dioxatricyclo[4.4.0.02,4]dec-7-en-10-yl]oxy]-6-(hydroxymethyl)oxane-3,4,5-triol GC-MS (TMS_2_3) - 70eV, Positive	Not Available	2021-11-03	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - (2R,3S,4R,5R,6S)-2-[[(1R,2R,4R,5R,6S,10R)-5-Hydroxy-2-(hydroxymethyl)-3,9-dioxatricyclo[4.4.0.02,4]dec-7-en-10-yl]oxy]-6-(hydroxymethyl)oxane-3,4,5-triol GC-MS (TMS_2_4) - 70eV, Positive	Not Available	2021-11-03	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - (2R,3S,4R,5R,6S)-2-[[(1R,2R,4R,5R,6S,10R)-5-Hydroxy-2-(hydroxymethyl)-3,9-dioxatricyclo[4.4.0.02,4]dec-7-en-10-yl]oxy]-6-(hydroxymethyl)oxane-3,4,5-triol GC-MS (TMS_2_5) - 70eV, Positive	Not Available	2021-11-03	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - (2R,3S,4R,5R,6S)-2-[[(1R,2R,4R,5R,6S,10R)-5-Hydroxy-2-(hydroxymethyl)-3,9-dioxatricyclo[4.4.0.02,4]dec-7-en-10-yl]oxy]-6-(hydroxymethyl)oxane-3,4,5-triol GC-MS (TMS_2_6) - 70eV, Positive	Not Available	2021-11-03	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - (2R,3S,4R,5R,6S)-2-[[(1R,2R,4R,5R,6S,10R)-5-Hydroxy-2-(hydroxymethyl)-3,9-dioxatricyclo[4.4.0.02,4]dec-7-en-10-yl]oxy]-6-(hydroxymethyl)oxane-3,4,5-triol GC-MS (TMS_2_7) - 70eV, Positive	Not Available	2021-11-03	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - (2R,3S,4R,5R,6S)-2-[[(1R,2R,4R,5R,6S,10R)-5-Hydroxy-2-(hydroxymethyl)-3,9-dioxatricyclo[4.4.0.02,4]dec-7-en-10-yl]oxy]-6-(hydroxymethyl)oxane-3,4,5-triol GC-MS (TMS_2_8) - 70eV, Positive	Not Available	2021-11-03	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - (2R,3S,4R,5R,6S)-2-[[(1R,2R,4R,5R,6S,10R)-5-Hydroxy-2-(hydroxymethyl)-3,9-dioxatricyclo[4.4.0.02,4]dec-7-en-10-yl]oxy]-6-(hydroxymethyl)oxane-3,4,5-triol GC-MS (TMS_2_9) - 70eV, Positive	Not Available	2021-11-03	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - (2R,3S,4R,5R,6S)-2-[[(1R,2R,4R,5R,6S,10R)-5-Hydroxy-2-(hydroxymethyl)-3,9-dioxatricyclo[4.4.0.02,4]dec-7-en-10-yl]oxy]-6-(hydroxymethyl)oxane-3,4,5-triol GC-MS (TMS_2_10) - 70eV, Positive	Not Available	2021-11-03	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - (2R,3S,4R,5R,6S)-2-[[(1R,2R,4R,5R,6S,10R)-5-Hydroxy-2-(hydroxymethyl)-3,9-dioxatricyclo[4.4.0.02,4]dec-7-en-10-yl]oxy]-6-(hydroxymethyl)oxane-3,4,5-triol GC-MS (TMS_2_11) - 70eV, Positive	Not Available	2021-11-03	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - (2R,3S,4R,5R,6S)-2-[[(1R,2R,4R,5R,6S,10R)-5-Hydroxy-2-(hydroxymethyl)-3,9-dioxatricyclo[4.4.0.02,4]dec-7-en-10-yl]oxy]-6-(hydroxymethyl)oxane-3,4,5-triol GC-MS (TMS_2_12) - 70eV, Positive	Not Available	2021-11-03	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - (2R,3S,4R,5R,6S)-2-[[(1R,2R,4R,5R,6S,10R)-5-Hydroxy-2-(hydroxymethyl)-3,9-dioxatricyclo[4.4.0.02,4]dec-7-en-10-yl]oxy]-6-(hydroxymethyl)oxane-3,4,5-triol GC-MS (TMS_2_13) - 70eV, Positive	Not Available	2021-11-03	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - (2R,3S,4R,5R,6S)-2-[[(1R,2R,4R,5R,6S,10R)-5-Hydroxy-2-(hydroxymethyl)-3,9-dioxatricyclo[4.4.0.02,4]dec-7-en-10-yl]oxy]-6-(hydroxymethyl)oxane-3,4,5-triol GC-MS (TMS_2_14) - 70eV, Positive	Not Available	2021-11-03	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - (2R,3S,4R,5R,6S)-2-[[(1R,2R,4R,5R,6S,10R)-5-Hydroxy-2-(hydroxymethyl)-3,9-dioxatricyclo[4.4.0.02,4]dec-7-en-10-yl]oxy]-6-(hydroxymethyl)oxane-3,4,5-triol GC-MS (TMS_2_15) - 70eV, Positive	Not Available	2021-11-03	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - (2R,3S,4R,5R,6S)-2-[[(1R,2R,4R,5R,6S,10R)-5-Hydroxy-2-(hydroxymethyl)-3,9-dioxatricyclo[4.4.0.02,4]dec-7-en-10-yl]oxy]-6-(hydroxymethyl)oxane-3,4,5-triol GC-MS (TMS_3_1) - 70eV, Positive	Not Available	2021-11-03	Wishart Lab	View Spectrum

MS/MS Spectra

Spectrum Type	Description	Splash Key	Deposition Date	Source	View
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - (2R,3S,4R,5R,6S)-2-[[(1R,2R,4R,5R,6S,10R)-5-Hydroxy-2-(hydroxymethyl)-3,9-dioxatricyclo[4.4.0.02,4]dec-7-en-10-yl]oxy]-6-(hydroxymethyl)oxane-3,4,5-triol 10V, Positive-QTOF	splash10-03di-0009000000-ea9a84ff40ae6dd4dc4d	2021-10-12	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - (2R,3S,4R,5R,6S)-2-[[(1R,2R,4R,5R,6S,10R)-5-Hydroxy-2-(hydroxymethyl)-3,9-dioxatricyclo[4.4.0.02,4]dec-7-en-10-yl]oxy]-6-(hydroxymethyl)oxane-3,4,5-triol 20V, Positive-QTOF	splash10-02ai-1925000000-1d555c54509031353934	2021-10-12	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - (2R,3S,4R,5R,6S)-2-[[(1R,2R,4R,5R,6S,10R)-5-Hydroxy-2-(hydroxymethyl)-3,9-dioxatricyclo[4.4.0.02,4]dec-7-en-10-yl]oxy]-6-(hydroxymethyl)oxane-3,4,5-triol 40V, Positive-QTOF	splash10-0avr-8941000000-1f9653b8af4767212e0f	2021-10-12	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - (2R,3S,4R,5R,6S)-2-[[(1R,2R,4R,5R,6S,10R)-5-Hydroxy-2-(hydroxymethyl)-3,9-dioxatricyclo[4.4.0.02,4]dec-7-en-10-yl]oxy]-6-(hydroxymethyl)oxane-3,4,5-triol 10V, Negative-QTOF	splash10-03di-0209000000-d7c813fcfa5adfe5c3d8	2021-10-12	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - (2R,3S,4R,5R,6S)-2-[[(1R,2R,4R,5R,6S,10R)-5-Hydroxy-2-(hydroxymethyl)-3,9-dioxatricyclo[4.4.0.02,4]dec-7-en-10-yl]oxy]-6-(hydroxymethyl)oxane-3,4,5-triol 20V, Negative-QTOF	splash10-03di-4449000000-5353fafa4669ca563a15	2021-10-12	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - (2R,3S,4R,5R,6S)-2-[[(1R,2R,4R,5R,6S,10R)-5-Hydroxy-2-(hydroxymethyl)-3,9-dioxatricyclo[4.4.0.02,4]dec-7-en-10-yl]oxy]-6-(hydroxymethyl)oxane-3,4,5-triol 40V, Negative-QTOF	splash10-0a4i-9533000000-dfd0f766f3bfbcb9eaf6	2021-10-12	Wishart Lab	View Spectrum

NMR Spectra

Spectrum Type	Description	Deposition Date	Source	View
Predicted 1D NMR	¹³C NMR Spectrum (1D, 100 MHz, D₂O, predicted)	2021-10-12	Wishart Lab	View Spectrum
Predicted 1D NMR	¹H NMR Spectrum (1D, 100 MHz, D₂O, predicted)	2021-10-12	Wishart Lab	View Spectrum
Predicted 1D NMR	¹³C NMR Spectrum (1D, 1000 MHz, D₂O, predicted)	2021-10-12	Wishart Lab	View Spectrum
Predicted 1D NMR	¹H NMR Spectrum (1D, 1000 MHz, D₂O, predicted)	2021-10-12	Wishart Lab	View Spectrum
Predicted 1D NMR	¹³C NMR Spectrum (1D, 200 MHz, D₂O, predicted)	2021-10-12	Wishart Lab	View Spectrum
Predicted 1D NMR	¹H NMR Spectrum (1D, 200 MHz, D₂O, predicted)	2021-10-12	Wishart Lab	View Spectrum
Predicted 1D NMR	¹³C NMR Spectrum (1D, 300 MHz, D₂O, predicted)	2021-10-12	Wishart Lab	View Spectrum
Predicted 1D NMR	¹H NMR Spectrum (1D, 300 MHz, D₂O, predicted)	2021-10-12	Wishart Lab	View Spectrum
Predicted 1D NMR	¹³C NMR Spectrum (1D, 400 MHz, D₂O, predicted)	2021-10-12	Wishart Lab	View Spectrum
Predicted 1D NMR	¹H NMR Spectrum (1D, 400 MHz, D₂O, predicted)	2021-10-12	Wishart Lab	View Spectrum
Predicted 1D NMR	¹³C NMR Spectrum (1D, 500 MHz, D₂O, predicted)	2021-10-12	Wishart Lab	View Spectrum
Predicted 1D NMR	¹H NMR Spectrum (1D, 500 MHz, D₂O, predicted)	2021-10-12	Wishart Lab	View Spectrum
Predicted 1D NMR	¹³C NMR Spectrum (1D, 600 MHz, D₂O, predicted)	2021-10-12	Wishart Lab	View Spectrum
Predicted 1D NMR	¹H NMR Spectrum (1D, 600 MHz, D₂O, predicted)	2021-10-12	Wishart Lab	View Spectrum
Predicted 1D NMR	¹³C NMR Spectrum (1D, 700 MHz, D₂O, predicted)	2021-10-12	Wishart Lab	View Spectrum
Predicted 1D NMR	¹H NMR Spectrum (1D, 700 MHz, D₂O, predicted)	2021-10-12	Wishart Lab	View Spectrum
Predicted 1D NMR	¹³C NMR Spectrum (1D, 800 MHz, D₂O, predicted)	2021-10-12	Wishart Lab	View Spectrum
Predicted 1D NMR	¹H NMR Spectrum (1D, 800 MHz, D₂O, predicted)	2021-10-12	Wishart Lab	View Spectrum
Predicted 1D NMR	¹³C NMR Spectrum (1D, 900 MHz, D₂O, predicted)	2021-10-12	Wishart Lab	View Spectrum
Predicted 1D NMR	¹H NMR Spectrum (1D, 900 MHz, D₂O, predicted)	2021-10-12	Wishart Lab	View Spectrum

Biological Properties

Cellular Locations

Not Available

Biospecimen Locations

Blood

Tissue Locations

Not Available

Pathways

Not Available

Name	SMPDB/PathBank	KEGG

Normal Concentrations

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

Abnormal Concentrations

Not Available

Associated Disorders and Diseases

Disease References

None

Associated OMIM IDs

None

External Links

DrugBank ID

Not Available

Phenol Explorer Compound ID

Not Available

FooDB ID

Not Available

KNApSAcK ID

C00003075

Chemspider ID

3140410

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Catalpol

METLIN ID

Not Available

PubChem Compound

3917786

PDB ID

Not Available

ChEBI ID

Not Available

Food Biomarker Ontology

Not Available

VMH ID

Not Available

MarkerDB ID

Not Available

Good Scents ID

Not Available

References

Synthesis Reference

Not Available

Material Safety Data Sheet (MSDS)

Not Available

General References

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

Showing metabocard for (2R,3S,4R,5R,6S)-2-[[(1R,2R,4R,5R,6S,10R)-5-Hydroxy-2-(hydroxymethyl)-3,9-dioxatricyclo[4.4.0.02,4]dec-7-en-10-yl]oxy]-6-(hydroxymethyl)oxane-3,4,5-triol (HMDB0242754)

MOL for HMDB0242754 ((2R,3S,4R,5R,6S)-2-[[(1R,2R,4R,5R,6S,10R)-5-Hydroxy-2-(hydroxymethyl)-3,9-dioxatricyclo[4.4.0.02,4]dec-7-en-10-yl]oxy]-6-(hydroxymethyl)oxane-3,4,5-triol)

3D MOL for HMDB0242754 ((2R,3S,4R,5R,6S)-2-[[(1R,2R,4R,5R,6S,10R)-5-Hydroxy-2-(hydroxymethyl)-3,9-dioxatricyclo[4.4.0.02,4]dec-7-en-10-yl]oxy]-6-(hydroxymethyl)oxane-3,4,5-triol)

3D SDF for HMDB0242754 ((2R,3S,4R,5R,6S)-2-[[(1R,2R,4R,5R,6S,10R)-5-Hydroxy-2-(hydroxymethyl)-3,9-dioxatricyclo[4.4.0.02,4]dec-7-en-10-yl]oxy]-6-(hydroxymethyl)oxane-3,4,5-triol)

3D-SDF for HMDB0242754 ((2R,3S,4R,5R,6S)-2-[[(1R,2R,4R,5R,6S,10R)-5-Hydroxy-2-(hydroxymethyl)-3,9-dioxatricyclo[4.4.0.02,4]dec-7-en-10-yl]oxy]-6-(hydroxymethyl)oxane-3,4,5-triol)

PDB for HMDB0242754 ((2R,3S,4R,5R,6S)-2-[[(1R,2R,4R,5R,6S,10R)-5-Hydroxy-2-(hydroxymethyl)-3,9-dioxatricyclo[4.4.0.02,4]dec-7-en-10-yl]oxy]-6-(hydroxymethyl)oxane-3,4,5-triol)

3D PDB for HMDB0242754 ((2R,3S,4R,5R,6S)-2-[[(1R,2R,4R,5R,6S,10R)-5-Hydroxy-2-(hydroxymethyl)-3,9-dioxatricyclo[4.4.0.02,4]dec-7-en-10-yl]oxy]-6-(hydroxymethyl)oxane-3,4,5-triol)

SMILES for HMDB0242754 ((2R,3S,4R,5R,6S)-2-[[(1R,2R,4R,5R,6S,10R)-5-Hydroxy-2-(hydroxymethyl)-3,9-dioxatricyclo[4.4.0.02,4]dec-7-en-10-yl]oxy]-6-(hydroxymethyl)oxane-3,4,5-triol)

INCHI for HMDB0242754 ((2R,3S,4R,5R,6S)-2-[[(1R,2R,4R,5R,6S,10R)-5-Hydroxy-2-(hydroxymethyl)-3,9-dioxatricyclo[4.4.0.02,4]dec-7-en-10-yl]oxy]-6-(hydroxymethyl)oxane-3,4,5-triol)

Structure for HMDB0242754 ((2R,3S,4R,5R,6S)-2-[[(1R,2R,4R,5R,6S,10R)-5-Hydroxy-2-(hydroxymethyl)-3,9-dioxatricyclo[4.4.0.02,4]dec-7-en-10-yl]oxy]-6-(hydroxymethyl)oxane-3,4,5-triol)

3D Structure for HMDB0242754 ((2R,3S,4R,5R,6S)-2-[[(1R,2R,4R,5R,6S,10R)-5-Hydroxy-2-(hydroxymethyl)-3,9-dioxatricyclo[4.4.0.02,4]dec-7-en-10-yl]oxy]-6-(hydroxymethyl)oxane-3,4,5-triol)

Predicted Collision Cross Sections

Predicted Kovats Retention Indices

Derivatized

GC-MS Spectra

MS/MS Spectra

NMR Spectra