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Record Information

Version

5.0

Status

Expected but not Quantified

Creation Date

2012-09-11 20:56:30 UTC

Update Date

2022-03-07 02:54:41 UTC

HMDB ID

HMDB0035895

Secondary Accession Numbers

HMDB35895

Metabolite Identification

Common Name

20-Hydroxy-3,7,11,15,23-pentaoxolanost-8-en-26-oic acid

Description

20-Hydroxy-3,7,11,15,23-pentaoxolanost-8-en-26-oic acid belongs to the class of organic compounds known as triterpenoids. These are terpene molecules containing six isoprene units. Based on a literature review a small amount of articles have been published on 20-Hydroxy-3,7,11,15,23-pentaoxolanost-8-en-26-oic acid.

Structure

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


  Mrv0541 05061308462D          

 38 41  0  0  0  0            999 V2000
   -0.4374   -2.6263    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.7119    3.0734    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.7094    2.7131    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6232    0.6018    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.1073    0.1997    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4186   -0.3656    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.9451    2.5190    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2475    0.8922    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.4354    0.7470    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5655   -1.7493    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6520    2.7844    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5867    1.7614    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3701   -0.3338    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.9990    0.3114    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2547   -2.5135    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0592   -1.0980    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
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    3.1838    2.1537    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
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    2.0914    1.2325    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5596    1.8632    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7610   -3.1648    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
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    2.9035    1.3777    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.4672    0.9421    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8637    0.3176    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
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   -0.2419   -1.2108    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.3081    3.2699    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.3429   -0.1741    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.3399    1.8134    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
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   -1.5151    0.8239    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
  9  8  1  0  0  0  0
 15  1  1  0  0  0  0
 15 10  1  0  0  0  0
 16 10  1  0  0  0  0
 16 13  1  0  0  0  0
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 23 18  1  0  0  0  0
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 24 23  2  0  0  0  0
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 26  3  1  0  0  0  0
 26 19  1  0  0  0  0
 26 21  1  0  0  0  0
 27  4  1  0  0  0  0
 27  9  1  0  0  0  0
 27 19  1  0  0  0  0
 27 23  1  0  0  0  0
 28  5  1  0  0  0  0
 28 14  1  0  0  0  0
 28 20  1  0  0  0  0
 29  6  1  0  0  0  0
 29 13  1  0  0  0  0
 29 20  1  0  0  0  0
 30  7  1  0  0  0  0
 30 22  1  0  0  0  0
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 31 16  2  0  0  0  0
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 33 18  2  0  0  0  0
 34 21  2  0  0  0  0
 35 22  2  0  0  0  0
 36 25  2  0  0  0  0
 37 25  1  0  0  0  0
 38 29  1  0  0  0  0
M  END

HMDB0035895
     RDKit          3D
20-Hydroxy-3,7,11,15,23-pentaoxolanost-8-en-26-oic acid
 78 81  0  0  0  0  0  0  0  0999 V2000
    5.6923   -2.2251   -0.7695 C   0  0  0  0  0  0  0  0  0  0  0  0
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 31 72  1  0
 31 73  1  0
 31 74  1  0
 32 75  1  0
 33 76  1  0
 33 77  1  0
 38 78  1  0
M  END


  Mrv0541 05061308462D          

 38 41  0  0  0  0            999 V2000
   -0.4374   -2.6263    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
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    0.1230    3.0489    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4501   -3.9290    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5783   -3.0519    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5151    0.8239    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
  9  8  1  0  0  0  0
 15  1  1  0  0  0  0
 15 10  1  0  0  0  0
 16 10  1  0  0  0  0
 16 13  1  0  0  0  0
 17 11  1  0  0  0  0
 18 14  1  0  0  0  0
 19 11  1  0  0  0  0
 20 12  1  0  0  0  0
 21  8  1  0  0  0  0
 22 12  1  0  0  0  0
 23 18  1  0  0  0  0
 24 17  1  0  0  0  0
 24 23  2  0  0  0  0
 25 15  1  0  0  0  0
 26  2  1  0  0  0  0
 26  3  1  0  0  0  0
 26 19  1  0  0  0  0
 26 21  1  0  0  0  0
 27  4  1  0  0  0  0
 27  9  1  0  0  0  0
 27 19  1  0  0  0  0
 27 23  1  0  0  0  0
 28  5  1  0  0  0  0
 28 14  1  0  0  0  0
 28 20  1  0  0  0  0
 29  6  1  0  0  0  0
 29 13  1  0  0  0  0
 29 20  1  0  0  0  0
 30  7  1  0  0  0  0
 30 22  1  0  0  0  0
 30 24  1  0  0  0  0
 30 28  1  0  0  0  0
 31 16  2  0  0  0  0
 32 17  2  0  0  0  0
 33 18  2  0  0  0  0
 34 21  2  0  0  0  0
 35 22  2  0  0  0  0
 36 25  2  0  0  0  0
 37 25  1  0  0  0  0
 38 29  1  0  0  0  0
M  END
> <DATABASE_ID>
HMDB0035895

> <DATABASE_NAME>
hmdb

> <SMILES>
CC(CC(=O)CC(C)(O)C1CC(=O)C2(C)C3=C(C(=O)CC12C)C1(C)CCC(=O)C(C)(C)C1CC3=O)C(O)=O

> <INCHI_IDENTIFIER>
InChI=1S/C30H40O8/c1-15(25(36)37)10-16(31)13-29(6,38)20-12-22(35)30(7)24-17(32)11-19-26(2,3)21(34)8-9-27(19,4)23(24)18(33)14-28(20,30)5/h15,19-20,38H,8-14H2,1-7H3,(H,36,37)

> <INCHI_KEY>
QXAZRJVLUHRKJT-UHFFFAOYSA-N

> <FORMULA>
C30H40O8

> <MOLECULAR_WEIGHT>
528.6338

> <EXACT_MASS>
528.272318256

> <JCHEM_ACCEPTOR_COUNT>
8

> <JCHEM_AVERAGE_POLARIZABILITY>
55.45952392952442

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
2

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
6-hydroxy-2-methyl-4-oxo-6-{2,6,6,11,15-pentamethyl-5,9,12,17-tetraoxotetracyclo[8.7.0.0²,⁷.0¹¹,¹⁵]heptadec-1(10)-en-14-yl}heptanoic acid

> <ALOGPS_LOGP>
3.27

> <JCHEM_LOGP>
3.2711375506666664

> <ALOGPS_LOGS>
-4.49

> <JCHEM_MDDR_LIKE_RULE>
1

> <JCHEM_NUMBER_OF_RINGS>
4

> <JCHEM_PHYSIOLOGICAL_CHARGE>
-1

> <JCHEM_PKA>
14.564766099549342

> <JCHEM_PKA_STRONGEST_ACIDIC>
4.211419772758079

> <JCHEM_PKA_STRONGEST_BASIC>
-2.988389683415141

> <JCHEM_POLAR_SURFACE_AREA>
142.88

> <JCHEM_REFRACTIVITY>
138.81279999999998

> <JCHEM_ROTATABLE_BOND_COUNT>
6

> <JCHEM_RULE_OF_FIVE>
0

> <ALOGPS_SOLUBILITY>
1.70e-02 g/l

> <JCHEM_TRADITIONAL_IUPAC>
6-hydroxy-2-methyl-4-oxo-6-{2,6,6,11,15-pentamethyl-5,9,12,17-tetraoxotetracyclo[8.7.0.0²,⁷.0¹¹,¹⁵]heptadec-1(10)-en-14-yl}heptanoic acid

> <JCHEM_VEBER_RULE>
0

$$$$

HMDB0035895
     RDKit          3D
20-Hydroxy-3,7,11,15,23-pentaoxolanost-8-en-26-oic acid
 78 81  0  0  0  0  0  0  0  0999 V2000
    5.6923   -2.2251   -0.7695 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.5085   -1.2356    0.0333 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.7121   -0.0351    0.4421 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.1491    0.7517   -0.6601 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.9390    1.4823   -1.2791 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.7244    0.7452   -1.0902 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8701    1.7197   -0.3311 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.4944    3.1079   -0.5960 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.0604    1.4991    1.0272 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.4695    1.8241   -0.7863 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7884    2.8562    0.1255 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5657    2.3031    0.3951 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2697    2.5574    1.3081 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8230    1.3726   -0.7322 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9829    2.2637   -1.9361 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8855    0.4027   -0.5452 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8331   -0.4388    0.4707 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5596   -0.6163    1.1335 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4174   -1.3069    2.1891 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.6806    0.0077    0.6151 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.5633    0.6775   -0.7057 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.5596   -0.2508   -1.8819 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0048   -1.2156    0.9688 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4559   -2.5832    1.4149 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4514   -0.5430    2.2426 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.3208    0.6693    2.0297 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.2482    0.5014    0.9043 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.8655    1.4358    0.4629 O   0  0  0  0  0  0  0  0  0  0  0  0
   -5.4159   -0.8444    0.3136 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.1034   -1.7899    1.2806 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.3038   -0.7438   -0.9012 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.0660   -1.4730   -0.0295 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7034   -1.0924   -1.4555 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0379    0.2579   -1.4210 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4799    1.1675   -2.1157 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.9544   -1.9371    1.2637 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.6434   -1.5045    2.4035 O   0  0  0  0  0  0  0  0  0  0  0  0
    7.7342   -3.1024    1.2325 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.4004   -3.0408   -1.0850 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.9628   -2.7135   -0.0897 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.2689   -1.8137   -1.6871 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.3997   -0.8741   -0.5156 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.9795   -0.3162    1.2350 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.4330    0.6495    0.9791 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.7093    0.8555   -2.1700 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.3622   -0.3053   -0.8787 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.9291    3.8825   -0.0373 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.5626    3.1001   -0.3537 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.3885    3.2796   -1.6821 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.5605    2.1872    1.4883 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.5008    2.1638   -1.8500 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.8103    3.8609   -0.2792 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.3022    2.8718    1.1232 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2407    3.1155   -1.8585 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9538    2.8210   -1.7605 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9150    1.7773   -2.9014 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.4637   -0.7781    0.6562 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.9103    0.8071    1.3835 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.1109   -1.2052   -1.6720 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.9099    0.2323   -2.8169 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4855   -0.6041   -2.1239 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2022   -3.3849    1.1536 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5637   -2.7935    0.7970 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2999   -2.6478    2.4899 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5360   -0.1910    2.7652 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9250   -1.2807    2.9528 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.9408    0.7621    2.9712 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7548    1.6244    1.9899 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.0660   -2.1845    0.8731 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.4929   -2.6856    1.5114 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.3584   -1.2257    2.2054 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.0918    0.1457   -1.5274 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.4062   -1.6838   -1.4617 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.3380   -0.5407   -0.4900 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.3093   -2.5792   -0.1136 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0017   -1.8547   -1.8858 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.5727   -1.0704   -2.1013 H   0  0  0  0  0  0  0  0  0  0  0  0
    8.7396   -3.0277    1.1269 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  2  0
  4  6  1  0
  6  7  1  0
  7  8  1  0
  7  9  1  0
  7 10  1  0
 10 11  1  0
 11 12  1  0
 12 13  2  0
 12 14  1  0
 14 15  1  0
 14 16  1  0
 16 17  2  0
 17 18  1  0
 18 19  2  0
 18 20  1  0
 20 21  1  0
 21 22  1  0
 17 23  1  0
 23 24  1  0
 23 25  1  0
 25 26  1  0
 26 27  1  0
 27 28  2  0
 27 29  1  0
 29 30  1  0
 29 31  1  0
 29 32  1  0
 32 33  1  0
 33 34  1  0
 34 35  2  0
  2 36  1  0
 36 37  2  0
 36 38  1  0
 21 10  1  0
 32 23  1  0
 21 14  1  0
 34 16  1  0
  1 39  1  0
  1 40  1  0
  1 41  1  0
  2 42  1  0
  3 43  1  0
  3 44  1  0
  6 45  1  0
  6 46  1  0
  8 47  1  0
  8 48  1  0
  8 49  1  0
  9 50  1  0
 10 51  1  0
 11 52  1  0
 11 53  1  0
 15 54  1  0
 15 55  1  0
 15 56  1  0
 20 57  1  0
 20 58  1  0
 22 59  1  0
 22 60  1  0
 22 61  1  0
 24 62  1  0
 24 63  1  0
 24 64  1  0
 25 65  1  0
 25 66  1  0
 26 67  1  0
 26 68  1  0
 30 69  1  0
 30 70  1  0
 30 71  1  0
 31 72  1  0
 31 73  1  0
 31 74  1  0
 32 75  1  0
 33 76  1  0
 33 77  1  0
 38 78  1  0
M  END

HEADER    PROTEIN                                 06-MAY-13   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   06-MAY-13         0                                  
HETATM    1  C   UNK     0      -0.816  -4.902   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0       6.929   5.737   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0       8.791   5.064   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0       4.897   1.123   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0       0.200   0.373   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0      -0.781  -0.682   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0       1.764   4.702   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0       7.929   1.665   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0       6.413   1.394   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0      -2.922  -3.265   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0       4.950   5.198   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0      -1.095   3.288   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0      -2.558  -0.623   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0       1.865   0.581   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0      -2.342  -4.692   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0      -1.977  -2.050   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0       3.434   4.926   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0       3.381   0.852   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0       5.943   4.020   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0      -0.667   1.809   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0       8.452   3.114   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0       0.180   4.152   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0       3.904   2.301   0.000  0.00  0.00           C+0
HETATM   24  C   UNK     0       2.911   3.478   0.000  0.00  0.00           C+0
HETATM   25  C   UNK     0      -3.287  -5.908   0.000  0.00  0.00           C+0
HETATM   26  C   UNK     0       7.459   4.291   0.000  0.00  0.00           C+0
HETATM   27  C   UNK     0       5.420   2.572   0.000  0.00  0.00           C+0
HETATM   28  C   UNK     0       0.872   1.759   0.000  0.00  0.00           C+0
HETATM   29  C   UNK     0      -1.612   0.593   0.000  0.00  0.00           C+0
HETATM   30  C   UNK     0       1.395   3.207   0.000  0.00  0.00           C+0
HETATM   31  O   UNK     0      -0.452  -2.260   0.000  0.00  0.00           O+0
HETATM   32  O   UNK     0       2.442   6.104   0.000  0.00  0.00           O+0
HETATM   33  O   UNK     0       4.373  -0.325   0.000  0.00  0.00           O+0
HETATM   34  O   UNK     0       9.968   3.385   0.000  0.00  0.00           O+0
HETATM   35  O   UNK     0       0.230   5.691   0.000  0.00  0.00           O+0
HETATM   36  O   UNK     0      -2.707  -7.334   0.000  0.00  0.00           O+0
HETATM   37  O   UNK     0      -4.813  -5.697   0.000  0.00  0.00           O+0
HETATM   38  O   UNK     0      -2.828   1.538   0.000  0.00  0.00           O+0
CONECT    1   15                                                            
CONECT    2   26                                                            
CONECT    3   26                                                            
CONECT    4   27                                                            
CONECT    5   28                                                            
CONECT    6   29                                                            
CONECT    7   30                                                            
CONECT    8    9   21                                                       
CONECT    9    8   27                                                       
CONECT   10   15   16                                                       
CONECT   11   17   19                                                       
CONECT   12   20   22                                                       
CONECT   13   16   29                                                       
CONECT   14   18   28                                                       
CONECT   15    1   10   25                                                  
CONECT   16   10   13   31                                                  
CONECT   17   11   24   32                                                  
CONECT   18   14   23   33                                                  
CONECT   19   11   26   27                                                  
CONECT   20   12   28   29                                                  
CONECT   21    8   26   34                                                  
CONECT   22   12   30   35                                                  
CONECT   23   18   24   27                                                  
CONECT   24   17   23   30                                                  
CONECT   25   15   36   37                                                  
CONECT   26    2    3   19   21                                             
CONECT   27    4    9   19   23                                             
CONECT   28    5   14   20   30                                             
CONECT   29    6   13   20   38                                             
CONECT   30    7   22   24   28                                             
CONECT   31   16                                                            
CONECT   32   17                                                            
CONECT   33   18                                                            
CONECT   34   21                                                            
CONECT   35   22                                                            
CONECT   36   25                                                            
CONECT   37   25                                                            
CONECT   38   29                                                            
MASTER        0    0    0    0    0    0    0    0   38    0   82    0
END

COMPND    HMDB0035895
HETATM    1  C1  UNL     1       5.692  -2.225  -0.770  1.00  0.00           C  
HETATM    2  C2  UNL     1       6.509  -1.236   0.033  1.00  0.00           C  
HETATM    3  C3  UNL     1       5.712  -0.035   0.442  1.00  0.00           C  
HETATM    4  C4  UNL     1       5.149   0.752  -0.660  1.00  0.00           C  
HETATM    5  O1  UNL     1       5.939   1.482  -1.279  1.00  0.00           O  
HETATM    6  C5  UNL     1       3.724   0.745  -1.090  1.00  0.00           C  
HETATM    7  C6  UNL     1       2.870   1.720  -0.331  1.00  0.00           C  
HETATM    8  C7  UNL     1       3.494   3.108  -0.596  1.00  0.00           C  
HETATM    9  O2  UNL     1       3.060   1.499   1.027  1.00  0.00           O  
HETATM   10  C8  UNL     1       1.470   1.824  -0.786  1.00  0.00           C  
HETATM   11  C9  UNL     1       0.788   2.856   0.126  1.00  0.00           C  
HETATM   12  C10 UNL     1      -0.566   2.303   0.395  1.00  0.00           C  
HETATM   13  O3  UNL     1      -1.270   2.557   1.308  1.00  0.00           O  
HETATM   14  C11 UNL     1      -0.823   1.373  -0.732  1.00  0.00           C  
HETATM   15  C12 UNL     1      -0.983   2.264  -1.936  1.00  0.00           C  
HETATM   16  C13 UNL     1      -1.885   0.403  -0.545  1.00  0.00           C  
HETATM   17  C14 UNL     1      -1.833  -0.439   0.471  1.00  0.00           C  
HETATM   18  C15 UNL     1      -0.560  -0.616   1.133  1.00  0.00           C  
HETATM   19  O4  UNL     1      -0.417  -1.307   2.189  1.00  0.00           O  
HETATM   20  C16 UNL     1       0.681   0.008   0.615  1.00  0.00           C  
HETATM   21  C17 UNL     1       0.563   0.678  -0.706  1.00  0.00           C  
HETATM   22  C18 UNL     1       0.560  -0.251  -1.882  1.00  0.00           C  
HETATM   23  C19 UNL     1      -3.005  -1.216   0.969  1.00  0.00           C  
HETATM   24  C20 UNL     1      -2.456  -2.583   1.415  1.00  0.00           C  
HETATM   25  C21 UNL     1      -3.451  -0.543   2.243  1.00  0.00           C  
HETATM   26  C22 UNL     1      -4.321   0.669   2.030  1.00  0.00           C  
HETATM   27  C23 UNL     1      -5.248   0.501   0.904  1.00  0.00           C  
HETATM   28  O5  UNL     1      -5.865   1.436   0.463  1.00  0.00           O  
HETATM   29  C24 UNL     1      -5.416  -0.844   0.314  1.00  0.00           C  
HETATM   30  C25 UNL     1      -6.103  -1.790   1.281  1.00  0.00           C  
HETATM   31  C26 UNL     1      -6.304  -0.744  -0.901  1.00  0.00           C  
HETATM   32  C27 UNL     1      -4.066  -1.473  -0.029  1.00  0.00           C  
HETATM   33  C28 UNL     1      -3.703  -1.092  -1.455  1.00  0.00           C  
HETATM   34  C29 UNL     1      -3.038   0.258  -1.421  1.00  0.00           C  
HETATM   35  O6  UNL     1      -3.480   1.168  -2.116  1.00  0.00           O  
HETATM   36  C30 UNL     1       6.954  -1.937   1.264  1.00  0.00           C  
HETATM   37  O7  UNL     1       6.643  -1.504   2.403  1.00  0.00           O  
HETATM   38  O8  UNL     1       7.734  -3.102   1.233  1.00  0.00           O  
HETATM   39  H1  UNL     1       6.400  -3.041  -1.085  1.00  0.00           H  
HETATM   40  H2  UNL     1       4.963  -2.713  -0.090  1.00  0.00           H  
HETATM   41  H3  UNL     1       5.269  -1.814  -1.687  1.00  0.00           H  
HETATM   42  H4  UNL     1       7.400  -0.874  -0.516  1.00  0.00           H  
HETATM   43  H5  UNL     1       4.980  -0.316   1.235  1.00  0.00           H  
HETATM   44  H6  UNL     1       6.433   0.650   0.979  1.00  0.00           H  
HETATM   45  H7  UNL     1       3.709   0.856  -2.170  1.00  0.00           H  
HETATM   46  H8  UNL     1       3.362  -0.305  -0.879  1.00  0.00           H  
HETATM   47  H9  UNL     1       2.929   3.883  -0.037  1.00  0.00           H  
HETATM   48  H10 UNL     1       4.563   3.100  -0.354  1.00  0.00           H  
HETATM   49  H11 UNL     1       3.389   3.280  -1.682  1.00  0.00           H  
HETATM   50  H12 UNL     1       3.561   2.187   1.488  1.00  0.00           H  
HETATM   51  H13 UNL     1       1.501   2.164  -1.850  1.00  0.00           H  
HETATM   52  H14 UNL     1       0.810   3.861  -0.279  1.00  0.00           H  
HETATM   53  H15 UNL     1       1.302   2.872   1.123  1.00  0.00           H  
HETATM   54  H16 UNL     1      -0.241   3.115  -1.858  1.00  0.00           H  
HETATM   55  H17 UNL     1      -1.954   2.821  -1.760  1.00  0.00           H  
HETATM   56  H18 UNL     1      -0.915   1.777  -2.901  1.00  0.00           H  
HETATM   57  H19 UNL     1       1.464  -0.778   0.656  1.00  0.00           H  
HETATM   58  H20 UNL     1       0.910   0.807   1.383  1.00  0.00           H  
HETATM   59  H21 UNL     1       1.111  -1.205  -1.672  1.00  0.00           H  
HETATM   60  H22 UNL     1       0.910   0.232  -2.817  1.00  0.00           H  
HETATM   61  H23 UNL     1      -0.485  -0.604  -2.124  1.00  0.00           H  
HETATM   62  H24 UNL     1      -3.202  -3.385   1.154  1.00  0.00           H  
HETATM   63  H25 UNL     1      -1.564  -2.793   0.797  1.00  0.00           H  
HETATM   64  H26 UNL     1      -2.300  -2.648   2.490  1.00  0.00           H  
HETATM   65  H27 UNL     1      -2.536  -0.191   2.765  1.00  0.00           H  
HETATM   66  H28 UNL     1      -3.925  -1.281   2.953  1.00  0.00           H  
HETATM   67  H29 UNL     1      -4.941   0.762   2.971  1.00  0.00           H  
HETATM   68  H30 UNL     1      -3.755   1.624   1.990  1.00  0.00           H  
HETATM   69  H31 UNL     1      -7.066  -2.185   0.873  1.00  0.00           H  
HETATM   70  H32 UNL     1      -5.493  -2.686   1.511  1.00  0.00           H  
HETATM   71  H33 UNL     1      -6.358  -1.226   2.205  1.00  0.00           H  
HETATM   72  H34 UNL     1      -6.092   0.146  -1.527  1.00  0.00           H  
HETATM   73  H35 UNL     1      -6.406  -1.684  -1.462  1.00  0.00           H  
HETATM   74  H36 UNL     1      -7.338  -0.541  -0.490  1.00  0.00           H  
HETATM   75  H37 UNL     1      -4.309  -2.579  -0.114  1.00  0.00           H  
HETATM   76  H38 UNL     1      -3.002  -1.855  -1.886  1.00  0.00           H  
HETATM   77  H39 UNL     1      -4.573  -1.070  -2.101  1.00  0.00           H  
HETATM   78  H40 UNL     1       8.740  -3.028   1.127  1.00  0.00           H  
CONECT    1    2   39   40   41
CONECT    2    3   36   42
CONECT    3    4   43   44
CONECT    4    5    5    6
CONECT    6    7   45   46
CONECT    7    8    9   10
CONECT    8   47   48   49
CONECT    9   50
CONECT   10   11   21   51
CONECT   11   12   52   53
CONECT   12   13   13   14
CONECT   14   15   16   21
CONECT   15   54   55   56
CONECT   16   17   17   34
CONECT   17   18   23
CONECT   18   19   19   20
CONECT   20   21   57   58
CONECT   21   22
CONECT   22   59   60   61
CONECT   23   24   25   32
CONECT   24   62   63   64
CONECT   25   26   65   66
CONECT   26   27   67   68
CONECT   27   28   28   29
CONECT   29   30   31   32
CONECT   30   69   70   71
CONECT   31   72   73   74
CONECT   32   33   75
CONECT   33   34   76   77
CONECT   34   35   35
CONECT   36   37   37   38
CONECT   38   78
END

HMDB0035895
     RDKit          3D
20-Hydroxy-3,7,11,15,23-pentaoxolanost-8-en-26-oic acid
 78 81  0  0  0  0  0  0  0  0999 V2000
    5.6923   -2.2251   -0.7695 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.5085   -1.2356    0.0333 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.7121   -0.0351    0.4421 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.1491    0.7517   -0.6601 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.9390    1.4823   -1.2791 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.7244    0.7452   -1.0902 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8701    1.7197   -0.3311 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.4944    3.1079   -0.5960 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.0604    1.4991    1.0272 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.4695    1.8241   -0.7863 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7884    2.8562    0.1255 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5657    2.3031    0.3951 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2697    2.5574    1.3081 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8230    1.3726   -0.7322 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9829    2.2637   -1.9361 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8855    0.4027   -0.5452 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8331   -0.4388    0.4707 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5596   -0.6163    1.1335 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4174   -1.3069    2.1891 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.6806    0.0077    0.6151 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.5633    0.6775   -0.7057 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.5596   -0.2508   -1.8819 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0048   -1.2156    0.9688 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4559   -2.5832    1.4149 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4514   -0.5430    2.2426 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.3208    0.6693    2.0297 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.2482    0.5014    0.9043 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.8655    1.4358    0.4629 O   0  0  0  0  0  0  0  0  0  0  0  0
   -5.4159   -0.8444    0.3136 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.1034   -1.7899    1.2806 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.3038   -0.7438   -0.9012 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.0660   -1.4730   -0.0295 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7034   -1.0924   -1.4555 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0379    0.2579   -1.4210 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4799    1.1675   -2.1157 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.9544   -1.9371    1.2637 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.6434   -1.5045    2.4035 O   0  0  0  0  0  0  0  0  0  0  0  0
    7.7342   -3.1024    1.2325 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.4004   -3.0408   -1.0850 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.9628   -2.7135   -0.0897 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.2689   -1.8137   -1.6871 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.3997   -0.8741   -0.5156 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.9795   -0.3162    1.2350 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.4330    0.6495    0.9791 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.7093    0.8555   -2.1700 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.3622   -0.3053   -0.8787 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.9291    3.8825   -0.0373 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.5626    3.1001   -0.3537 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.3885    3.2796   -1.6821 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.5605    2.1872    1.4883 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.5008    2.1638   -1.8500 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.8103    3.8609   -0.2792 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.3022    2.8718    1.1232 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2407    3.1155   -1.8585 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9538    2.8210   -1.7605 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9150    1.7773   -2.9014 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.4637   -0.7781    0.6562 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.9103    0.8071    1.3835 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.1109   -1.2052   -1.6720 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.9099    0.2323   -2.8169 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4855   -0.6041   -2.1239 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2022   -3.3849    1.1536 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5637   -2.7935    0.7970 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2999   -2.6478    2.4899 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5360   -0.1910    2.7652 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9250   -1.2807    2.9528 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.9408    0.7621    2.9712 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7548    1.6244    1.9899 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.0660   -2.1845    0.8731 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.4929   -2.6856    1.5114 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.3584   -1.2257    2.2054 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.0918    0.1457   -1.5274 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.4062   -1.6838   -1.4617 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.3380   -0.5407   -0.4900 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.3093   -2.5792   -0.1136 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0017   -1.8547   -1.8858 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.5727   -1.0704   -2.1013 H   0  0  0  0  0  0  0  0  0  0  0  0
    8.7396   -3.0277    1.1269 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  2  0
  4  6  1  0
  6  7  1  0
  7  8  1  0
  7  9  1  0
  7 10  1  0
 10 11  1  0
 11 12  1  0
 12 13  2  0
 12 14  1  0
 14 15  1  0
 14 16  1  0
 16 17  2  0
 17 18  1  0
 18 19  2  0
 18 20  1  0
 20 21  1  0
 21 22  1  0
 17 23  1  0
 23 24  1  0
 23 25  1  0
 25 26  1  0
 26 27  1  0
 27 28  2  0
 27 29  1  0
 29 30  1  0
 29 31  1  0
 29 32  1  0
 32 33  1  0
 33 34  1  0
 34 35  2  0
  2 36  1  0
 36 37  2  0
 36 38  1  0
 21 10  1  0
 32 23  1  0
 21 14  1  0
 34 16  1  0
  1 39  1  0
  1 40  1  0
  1 41  1  0
  2 42  1  0
  3 43  1  0
  3 44  1  0
  6 45  1  0
  6 46  1  0
  8 47  1  0
  8 48  1  0
  8 49  1  0
  9 50  1  0
 10 51  1  0
 11 52  1  0
 11 53  1  0
 15 54  1  0
 15 55  1  0
 15 56  1  0
 20 57  1  0
 20 58  1  0
 22 59  1  0
 22 60  1  0
 22 61  1  0
 24 62  1  0
 24 63  1  0
 24 64  1  0
 25 65  1  0
 25 66  1  0
 26 67  1  0
 26 68  1  0
 30 69  1  0
 30 70  1  0
 30 71  1  0
 31 72  1  0
 31 73  1  0
 31 74  1  0
 32 75  1  0
 33 76  1  0
 33 77  1  0
 38 78  1  0
M  END

View in JSmol View Stereo Labels

Synonyms

Value	Source
20-Hydroxy-3,7,11,15,23-pentaoxolanost-8-en-26-Oate	Generator
20-Hydroxy-3,7,11,15,23-pentaoxo-5alpha-lanost-8-en-26-Oic acid	HMDB
Ganoderic acid o??	HMDB
6-Hydroxy-2-methyl-4-oxo-6-{2,6,6,11,15-pentamethyl-5,9,12,17-tetraoxotetracyclo[8.7.0.0²,⁷.0¹¹,¹⁵]heptadec-1(10)-en-14-yl}heptanoate	Generator

Chemical Formula

C₃₀H₄₀O₈

Average Molecular Weight

528.6338

Monoisotopic Molecular Weight

528.272318256

IUPAC Name

6-hydroxy-2-methyl-4-oxo-6-{2,6,6,11,15-pentamethyl-5,9,12,17-tetraoxotetracyclo[8.7.0.0²,⁷.0¹¹,¹⁵]heptadec-1(10)-en-14-yl}heptanoic acid

Traditional Name

6-hydroxy-2-methyl-4-oxo-6-{2,6,6,11,15-pentamethyl-5,9,12,17-tetraoxotetracyclo[8.7.0.0²,⁷.0¹¹,¹⁵]heptadec-1(10)-en-14-yl}heptanoic acid

CAS Registry Number

110241-21-9

SMILES

CC(CC(=O)CC(C)(O)C1CC(=O)C2(C)C3=C(C(=O)CC12C)C1(C)CCC(=O)C(C)(C)C1CC3=O)C(O)=O

InChI Identifier

InChI=1S/C30H40O8/c1-15(25(36)37)10-16(31)13-29(6,38)20-12-22(35)30(7)24-17(32)11-19-26(2,3)21(34)8-9-27(19,4)23(24)18(33)14-28(20,30)5/h15,19-20,38H,8-14H2,1-7H3,(H,36,37)

InChI Key

QXAZRJVLUHRKJT-UHFFFAOYSA-N

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as triterpenoids. These are terpene molecules containing six isoprene units.

Kingdom

Organic compounds

Super Class

Lipids and lipid-like molecules

Class

Prenol lipids

Sub Class

Triterpenoids

Direct Parent

Triterpenoids

Alternative Parents

Substituents

Triterpenoid
Hydroxy bile acid, alcohol, or derivatives
Monohydroxy bile acid, alcohol, or derivatives
23-oxosteroid
Bile acid, alcohol, or derivatives
20-hydroxysteroid
Steroid acid
7-oxosteroid
3-oxosteroid
Oxosteroid
15-oxosteroid
Hydroxysteroid
11-oxosteroid
Steroid
Medium-chain keto acid
Gamma-keto acid
Cyclohexenone
Beta-hydroxy ketone
Keto acid
Tertiary alcohol
Cyclic ketone
Ketone
Monocarboxylic acid or derivatives
Carboxylic acid
Carboxylic acid derivative
Alcohol
Organic oxygen compound
Carbonyl group
Organooxygen compound
Hydrocarbon derivative
Organic oxide
Aliphatic homopolycyclic compound

Molecular Framework

Aliphatic homopolycyclic compounds

External Descriptors

Not Available

Ontology

Physiological effect

Not Available

Disposition

Biological location

Cellular substructure

Route of exposure

Enteral

Ingestion (HMDB: HMDB0035895)

Source

Endogenous

Endogenous (HMDB: HMDB0035895)

Plant

Plant (HMDB: HMDB0035895)

Animal

Animal (HMDB: HMDB0035895)

Exogenous

Food

Food (HMDB: HMDB0035895)

Vegetable

Mushroom

Exogenous (HMDB: HMDB0035895)

Process

Naturally occurring process

Biological process

Chemical reaction

Lipid Peroxidation (HMDB: HMDB0035895)

Biochemical pathway

Metabolic pathway

Fatty Acid Metabolism (HMDB: HMDB0035895)

Lipid metabolism pathway (HMDB: HMDB0035895)

Cellular process

Cell signaling (HMDB: HMDB0035895)

Biochemical process

Lipid transport (HMDB: HMDB0035895)

Role

Biological role

Energy source (HMDB: HMDB0035895)

Industrial application

Manufacturing industry

Material processing agent

Fluid processing agent

Surfactant

Surfactant (HMDB: HMDB0035895)

Physical Properties

State

Solid

Experimental Molecular Properties

Property	Value	Reference
Melting Point	168 - 171 °C	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
Water Solubility	0.017 g/L	ALOGPS
logP	3.27	ALOGPS
logP	3.27	ChemAxon
logS	-4.5	ALOGPS
pKa (Strongest Acidic)	4.21	ChemAxon
pKa (Strongest Basic)	-3	ChemAxon
Physiological Charge	-1	ChemAxon
Hydrogen Acceptor Count	8	ChemAxon
Hydrogen Donor Count	2	ChemAxon
Polar Surface Area	142.88 Å²	ChemAxon
Rotatable Bond Count	6	ChemAxon
Refractivity	138.81 m³·mol⁻¹	ChemAxon
Polarizability	55.46 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	Yes	ChemAxon

Predicted Chromatographic Properties

Predicted Collision Cross Sections

Predictor	Adduct Type	CCS Value (Å²)	Reference
DarkChem	[M+H]+	218.581	31661259
DarkChem	[M-H]-	216.506	31661259
DeepCCS	[M-2H]-	248.766	30932474
DeepCCS	[M+Na]+	224.191	30932474
AllCCS	[M+H]+	219.8	32859911
AllCCS	[M+H-H2O]+	218.3	32859911
AllCCS	[M+NH4]+	221.1	32859911
AllCCS	[M+Na]+	221.5	32859911
AllCCS	[M-H]-	225.9	32859911
AllCCS	[M+Na-2H]-	228.6	32859911
AllCCS	[M+HCOO]-	231.8	32859911

Predicted Retention Times

Underivatized

Chromatographic Method	Retention Time	Reference
Measured using a Waters Acquity ultraperformance liquid chromatography (UPLC) ethylene-bridged hybrid (BEH) C18 column (100 mm × 2.1 mm; 1.7 μmparticle diameter). Predicted by Afia on May 17, 2022.	6.51 minutes	32390414
Predicted by Siyang on May 30, 2022	13.0851 minutes	33406817
Predicted by Siyang using ReTip algorithm on June 8, 2022	2.81 minutes	32390414
AjsUoB = Accucore 150 Amide HILIC with 10mM Ammonium Formate, 0.1% Formic Acid	52.3 seconds	40023050
Fem_Long = Waters ACQUITY UPLC HSS T3 C18 with Water:MeOH and 0.1% Formic Acid	2904.7 seconds	40023050
Fem_Lipids = Ascentis Express C18 with (60:40 water:ACN):(90:10 IPA:ACN) and 10mM NH4COOH + 0.1% Formic Acid	153.0 seconds	40023050
Life_Old = Waters ACQUITY UPLC BEH C18 with Water:(20:80 acetone:ACN) and 0.1% Formic Acid	215.6 seconds	40023050
Life_New = RP Waters ACQUITY UPLC HSS T3 C18 with Water:(30:70 MeOH:ACN) and 0.1% Formic Acid	150.4 seconds	40023050
RIKEN = Waters ACQUITY UPLC BEH C18 with Water:ACN and 0.1% Formic Acid	136.4 seconds	40023050
Eawag_XBridgeC18 = XBridge C18 3.5u 2.1x50 mm with Water:MeOH and 0.1% Formic Acid	540.2 seconds	40023050
BfG_NTS_RP1 =Agilent Zorbax Eclipse Plus C18 (2.1 mm x 150 mm, 3.5 um) with Water:ACN and 0.1% Formic Acid	597.5 seconds	40023050
HILIC_BDD_2 = Merck SeQuant ZIC-HILIC with ACN(0.1% formic acid):water(16 mM ammonium formate)	83.2 seconds	40023050
UniToyama_Atlantis = RP Waters Atlantis T3 (2.1 x 150 mm, 5 um) with ACN:Water and 0.1% Formic Acid	1049.5 seconds	40023050
BDD_C18 = Hypersil Gold 1.9µm C18 with Water:ACN and 0.1% Formic Acid	541.7 seconds	40023050
UFZ_Phenomenex = Kinetex Core-Shell C18 2.6 um, 3.0 x 100 mm, Phenomenex with Water:MeOH and 0.1% Formic Acid	1474.7 seconds	40023050
SNU_RIKEN_POS = Waters ACQUITY UPLC BEH C18 with Water:ACN and 0.1% Formic Acid	308.6 seconds	40023050
RPMMFDA = Waters ACQUITY UPLC BEH C18 with Water:ACN and 0.1% Formic Acid	439.9 seconds	40023050
MTBLS87 = Merck SeQuant ZIC-pHILIC column with ACN:Water and :ammonium carbonate	191.7 seconds	40023050
KI_GIAR_zic_HILIC_pH2_7 = Merck SeQuant ZIC-HILIC with ACN:Water and 0.1% FA	188.2 seconds	40023050
Meister zic-pHILIC pH9.3 = Merck SeQuant ZIC-pHILIC column with ACN:Water 5mM NH4Ac pH9.3 and 5mM ammonium acetate in water	8.5 seconds	40023050

Predicted Kovats Retention Indices

Underivatized

Metabolite	SMILES	Kovats RI Value	Column Type	Reference
20-Hydroxy-3,7,11,15,23-pentaoxolanost-8-en-26-oic acid	CC(CC(=O)CC(C)(O)C1CC(=O)C2(C)C3=C(C(=O)CC12C)C1(C)CCC(=O)C(C)(C)C1CC3=O)C(O)=O	5267.7	Standard polar	33892256
20-Hydroxy-3,7,11,15,23-pentaoxolanost-8-en-26-oic acid	CC(CC(=O)CC(C)(O)C1CC(=O)C2(C)C3=C(C(=O)CC12C)C1(C)CCC(=O)C(C)(C)C1CC3=O)C(O)=O	3355.9	Standard non polar	33892256
20-Hydroxy-3,7,11,15,23-pentaoxolanost-8-en-26-oic acid	CC(CC(=O)CC(C)(O)C1CC(=O)C2(C)C3=C(C(=O)CC12C)C1(C)CCC(=O)C(C)(C)C1CC3=O)C(O)=O	4253.3	Semi standard non polar	33892256

Derivatized

Derivative Name / Structure	SMILES	Kovats RI Value	Column Type	Reference
20-Hydroxy-3,7,11,15,23-pentaoxolanost-8-en-26-oic acid,1TMS,isomer #1	CC(CC(=O)CC(C)(O[Si](C)(C)C)C1CC(=O)C2(C)C3=C(C(=O)CC12C)C1(C)CCC(=O)C(C)(C)C1CC3=O)C(=O)O	4046.0	Semi standard non polar	33892256
20-Hydroxy-3,7,11,15,23-pentaoxolanost-8-en-26-oic acid,1TMS,isomer #2	CC(CC(=O)CC(C)(O)C1CC(=O)C2(C)C3=C(C(=O)CC12C)C1(C)CCC(=O)C(C)(C)C1CC3=O)C(=O)O[Si](C)(C)C	4122.0	Semi standard non polar	33892256
20-Hydroxy-3,7,11,15,23-pentaoxolanost-8-en-26-oic acid,1TMS,isomer #3	CC(CC(=CC(C)(O)C1CC(=O)C2(C)C3=C(C(=O)CC12C)C1(C)CCC(=O)C(C)(C)C1CC3=O)O[Si](C)(C)C)C(=O)O	4022.5	Semi standard non polar	33892256
20-Hydroxy-3,7,11,15,23-pentaoxolanost-8-en-26-oic acid,1TMS,isomer #4	CC(C=C(CC(C)(O)C1CC(=O)C2(C)C3=C(C(=O)CC12C)C1(C)CCC(=O)C(C)(C)C1CC3=O)O[Si](C)(C)C)C(=O)O	4129.1	Semi standard non polar	33892256
20-Hydroxy-3,7,11,15,23-pentaoxolanost-8-en-26-oic acid,1TMS,isomer #5	CC(CC(=O)CC(C)(O)C1C=C(O[Si](C)(C)C)C2(C)C3=C(C(=O)CC12C)C1(C)CCC(=O)C(C)(C)C1CC3=O)C(=O)O	3957.5	Semi standard non polar	33892256
20-Hydroxy-3,7,11,15,23-pentaoxolanost-8-en-26-oic acid,1TMS,isomer #6	CC(CC(=O)CC(C)(O)C1CC(=O)C2(C)C3=C(C(O[Si](C)(C)C)=CC12C)C1(C)CCC(=O)C(C)(C)C1CC3=O)C(=O)O	3945.6	Semi standard non polar	33892256
20-Hydroxy-3,7,11,15,23-pentaoxolanost-8-en-26-oic acid,1TMS,isomer #7	CC(CC(=O)CC(C)(O)C1CC(=O)C2(C)C3=C(C(=O)CC12C)C1(C)CC=C(O[Si](C)(C)C)C(C)(C)C1CC3=O)C(=O)O	3940.7	Semi standard non polar	33892256
20-Hydroxy-3,7,11,15,23-pentaoxolanost-8-en-26-oic acid,1TMS,isomer #8	CC(CC(=O)CC(C)(O)C1CC(=O)C2(C)C3=C(C(=O)CC12C)C1(C)CCC(=O)C(C)(C)C1C=C3O[Si](C)(C)C)C(=O)O	3930.7	Semi standard non polar	33892256
20-Hydroxy-3,7,11,15,23-pentaoxolanost-8-en-26-oic acid,2TMS,isomer #1	CC(CC(=O)CC(C)(O[Si](C)(C)C)C1CC(=O)C2(C)C3=C(C(=O)CC12C)C1(C)CCC(=O)C(C)(C)C1CC3=O)C(=O)O[Si](C)(C)C	4041.2	Semi standard non polar	33892256
20-Hydroxy-3,7,11,15,23-pentaoxolanost-8-en-26-oic acid,2TMS,isomer #10	CC(CC(=O)CC(C)(O)C1C=C(O[Si](C)(C)C)C2(C)C3=C(C(=O)CC12C)C1(C)CCC(=O)C(C)(C)C1CC3=O)C(=O)O[Si](C)(C)C	3916.2	Semi standard non polar	33892256
20-Hydroxy-3,7,11,15,23-pentaoxolanost-8-en-26-oic acid,2TMS,isomer #11	CC(CC(=O)CC(C)(O)C1CC(=O)C2(C)C3=C(C(O[Si](C)(C)C)=CC12C)C1(C)CCC(=O)C(C)(C)C1CC3=O)C(=O)O[Si](C)(C)C	3911.0	Semi standard non polar	33892256
20-Hydroxy-3,7,11,15,23-pentaoxolanost-8-en-26-oic acid,2TMS,isomer #12	CC(CC(=O)CC(C)(O)C1CC(=O)C2(C)C3=C(C(=O)CC12C)C1(C)CC=C(O[Si](C)(C)C)C(C)(C)C1CC3=O)C(=O)O[Si](C)(C)C	3894.4	Semi standard non polar	33892256
20-Hydroxy-3,7,11,15,23-pentaoxolanost-8-en-26-oic acid,2TMS,isomer #13	CC(CC(=O)CC(C)(O)C1CC(=O)C2(C)C3=C(C(=O)CC12C)C1(C)CCC(=O)C(C)(C)C1C=C3O[Si](C)(C)C)C(=O)O[Si](C)(C)C	3907.3	Semi standard non polar	33892256
20-Hydroxy-3,7,11,15,23-pentaoxolanost-8-en-26-oic acid,2TMS,isomer #14	CC(CC(=CC(C)(O)C1C=C(O[Si](C)(C)C)C2(C)C3=C(C(=O)CC12C)C1(C)CCC(=O)C(C)(C)C1CC3=O)O[Si](C)(C)C)C(=O)O	3814.5	Semi standard non polar	33892256
20-Hydroxy-3,7,11,15,23-pentaoxolanost-8-en-26-oic acid,2TMS,isomer #15	CC(CC(=CC(C)(O)C1CC(=O)C2(C)C3=C(C(O[Si](C)(C)C)=CC12C)C1(C)CCC(=O)C(C)(C)C1CC3=O)O[Si](C)(C)C)C(=O)O	3803.5	Semi standard non polar	33892256
20-Hydroxy-3,7,11,15,23-pentaoxolanost-8-en-26-oic acid,2TMS,isomer #16	CC(CC(=CC(C)(O)C1CC(=O)C2(C)C3=C(C(=O)CC12C)C1(C)CC=C(O[Si](C)(C)C)C(C)(C)C1CC3=O)O[Si](C)(C)C)C(=O)O	3782.5	Semi standard non polar	33892256
20-Hydroxy-3,7,11,15,23-pentaoxolanost-8-en-26-oic acid,2TMS,isomer #17	CC(CC(=CC(C)(O)C1CC(=O)C2(C)C3=C(C(=O)CC12C)C1(C)CCC(=O)C(C)(C)C1C=C3O[Si](C)(C)C)O[Si](C)(C)C)C(=O)O	3801.0	Semi standard non polar	33892256
20-Hydroxy-3,7,11,15,23-pentaoxolanost-8-en-26-oic acid,2TMS,isomer #18	CC(C=C(CC(C)(O)C1C=C(O[Si](C)(C)C)C2(C)C3=C(C(=O)CC12C)C1(C)CCC(=O)C(C)(C)C1CC3=O)O[Si](C)(C)C)C(=O)O	3881.4	Semi standard non polar	33892256
20-Hydroxy-3,7,11,15,23-pentaoxolanost-8-en-26-oic acid,2TMS,isomer #19	CC(C=C(CC(C)(O)C1CC(=O)C2(C)C3=C(C(O[Si](C)(C)C)=CC12C)C1(C)CCC(=O)C(C)(C)C1CC3=O)O[Si](C)(C)C)C(=O)O	3882.2	Semi standard non polar	33892256
20-Hydroxy-3,7,11,15,23-pentaoxolanost-8-en-26-oic acid,2TMS,isomer #2	CC(CC(=CC(C)(O[Si](C)(C)C)C1CC(=O)C2(C)C3=C(C(=O)CC12C)C1(C)CCC(=O)C(C)(C)C1CC3=O)O[Si](C)(C)C)C(=O)O	3964.1	Semi standard non polar	33892256
20-Hydroxy-3,7,11,15,23-pentaoxolanost-8-en-26-oic acid,2TMS,isomer #20	CC(C=C(CC(C)(O)C1CC(=O)C2(C)C3=C(C(=O)CC12C)C1(C)CC=C(O[Si](C)(C)C)C(C)(C)C1CC3=O)O[Si](C)(C)C)C(=O)O	3864.1	Semi standard non polar	33892256
20-Hydroxy-3,7,11,15,23-pentaoxolanost-8-en-26-oic acid,2TMS,isomer #21	CC(C=C(CC(C)(O)C1CC(=O)C2(C)C3=C(C(=O)CC12C)C1(C)CCC(=O)C(C)(C)C1C=C3O[Si](C)(C)C)O[Si](C)(C)C)C(=O)O	3888.4	Semi standard non polar	33892256
20-Hydroxy-3,7,11,15,23-pentaoxolanost-8-en-26-oic acid,2TMS,isomer #22	CC(CC(=O)CC(C)(O)C1C=C(O[Si](C)(C)C)C2(C)C3=C(C(O[Si](C)(C)C)=CC12C)C1(C)CCC(=O)C(C)(C)C1CC3=O)C(=O)O	3745.6	Semi standard non polar	33892256
20-Hydroxy-3,7,11,15,23-pentaoxolanost-8-en-26-oic acid,2TMS,isomer #23	CC(CC(=O)CC(C)(O)C1C=C(O[Si](C)(C)C)C2(C)C3=C(C(=O)CC12C)C1(C)CC=C(O[Si](C)(C)C)C(C)(C)C1CC3=O)C(=O)O	3736.3	Semi standard non polar	33892256
20-Hydroxy-3,7,11,15,23-pentaoxolanost-8-en-26-oic acid,2TMS,isomer #24	CC(CC(=O)CC(C)(O)C1C=C(O[Si](C)(C)C)C2(C)C3=C(C(=O)CC12C)C1(C)CCC(=O)C(C)(C)C1C=C3O[Si](C)(C)C)C(=O)O	3798.6	Semi standard non polar	33892256
20-Hydroxy-3,7,11,15,23-pentaoxolanost-8-en-26-oic acid,2TMS,isomer #25	CC(CC(=O)CC(C)(O)C1CC(=O)C2(C)C3=C(C(O[Si](C)(C)C)=CC12C)C1(C)CC=C(O[Si](C)(C)C)C(C)(C)C1CC3=O)C(=O)O	3745.7	Semi standard non polar	33892256
20-Hydroxy-3,7,11,15,23-pentaoxolanost-8-en-26-oic acid,2TMS,isomer #26	CC(CC(=O)CC(C)(O)C1CC(=O)C2(C)C3=C(C(O[Si](C)(C)C)=CC12C)C1(C)CCC(=O)C(C)(C)C1C=C3O[Si](C)(C)C)C(=O)O	3769.7	Semi standard non polar	33892256
20-Hydroxy-3,7,11,15,23-pentaoxolanost-8-en-26-oic acid,2TMS,isomer #27	CC(CC(=O)CC(C)(O)C1CC(=O)C2(C)C3=C(C(=O)CC12C)C1(C)CC=C(O[Si](C)(C)C)C(C)(C)C1C=C3O[Si](C)(C)C)C(=O)O	3768.7	Semi standard non polar	33892256
20-Hydroxy-3,7,11,15,23-pentaoxolanost-8-en-26-oic acid,2TMS,isomer #3	CC(C=C(CC(C)(O[Si](C)(C)C)C1CC(=O)C2(C)C3=C(C(=O)CC12C)C1(C)CCC(=O)C(C)(C)C1CC3=O)O[Si](C)(C)C)C(=O)O	4005.0	Semi standard non polar	33892256
20-Hydroxy-3,7,11,15,23-pentaoxolanost-8-en-26-oic acid,2TMS,isomer #4	CC(CC(=O)CC(C)(O[Si](C)(C)C)C1C=C(O[Si](C)(C)C)C2(C)C3=C(C(=O)CC12C)C1(C)CCC(=O)C(C)(C)C1CC3=O)C(=O)O	3880.8	Semi standard non polar	33892256
20-Hydroxy-3,7,11,15,23-pentaoxolanost-8-en-26-oic acid,2TMS,isomer #5	CC(CC(=O)CC(C)(O[Si](C)(C)C)C1CC(=O)C2(C)C3=C(C(O[Si](C)(C)C)=CC12C)C1(C)CCC(=O)C(C)(C)C1CC3=O)C(=O)O	3843.9	Semi standard non polar	33892256
20-Hydroxy-3,7,11,15,23-pentaoxolanost-8-en-26-oic acid,2TMS,isomer #6	CC(CC(=O)CC(C)(O[Si](C)(C)C)C1CC(=O)C2(C)C3=C(C(=O)CC12C)C1(C)CC=C(O[Si](C)(C)C)C(C)(C)C1CC3=O)C(=O)O	3833.7	Semi standard non polar	33892256
20-Hydroxy-3,7,11,15,23-pentaoxolanost-8-en-26-oic acid,2TMS,isomer #7	CC(CC(=O)CC(C)(O[Si](C)(C)C)C1CC(=O)C2(C)C3=C(C(=O)CC12C)C1(C)CCC(=O)C(C)(C)C1C=C3O[Si](C)(C)C)C(=O)O	3857.6	Semi standard non polar	33892256
20-Hydroxy-3,7,11,15,23-pentaoxolanost-8-en-26-oic acid,2TMS,isomer #8	CC(CC(=CC(C)(O)C1CC(=O)C2(C)C3=C(C(=O)CC12C)C1(C)CCC(=O)C(C)(C)C1CC3=O)O[Si](C)(C)C)C(=O)O[Si](C)(C)C	3955.8	Semi standard non polar	33892256
20-Hydroxy-3,7,11,15,23-pentaoxolanost-8-en-26-oic acid,2TMS,isomer #9	CC(C=C(CC(C)(O)C1CC(=O)C2(C)C3=C(C(=O)CC12C)C1(C)CCC(=O)C(C)(C)C1CC3=O)O[Si](C)(C)C)C(=O)O[Si](C)(C)C	4031.4	Semi standard non polar	33892256
20-Hydroxy-3,7,11,15,23-pentaoxolanost-8-en-26-oic acid,3TMS,isomer #1	CC(CC(=CC(C)(O[Si](C)(C)C)C1CC(=O)C2(C)C3=C(C(=O)CC12C)C1(C)CCC(=O)C(C)(C)C1CC3=O)O[Si](C)(C)C)C(=O)O[Si](C)(C)C	3889.5	Semi standard non polar	33892256
20-Hydroxy-3,7,11,15,23-pentaoxolanost-8-en-26-oic acid,3TMS,isomer #1	CC(CC(=CC(C)(O[Si](C)(C)C)C1CC(=O)C2(C)C3=C(C(=O)CC12C)C1(C)CCC(=O)C(C)(C)C1CC3=O)O[Si](C)(C)C)C(=O)O[Si](C)(C)C	3962.4	Standard non polar	33892256
20-Hydroxy-3,7,11,15,23-pentaoxolanost-8-en-26-oic acid,3TMS,isomer #10	CC(CC(=CC(C)(O[Si](C)(C)C)C1CC(=O)C2(C)C3=C(C(=O)CC12C)C1(C)CCC(=O)C(C)(C)C1C=C3O[Si](C)(C)C)O[Si](C)(C)C)C(=O)O	3757.1	Semi standard non polar	33892256
20-Hydroxy-3,7,11,15,23-pentaoxolanost-8-en-26-oic acid,3TMS,isomer #10	CC(CC(=CC(C)(O[Si](C)(C)C)C1CC(=O)C2(C)C3=C(C(=O)CC12C)C1(C)CCC(=O)C(C)(C)C1C=C3O[Si](C)(C)C)O[Si](C)(C)C)C(=O)O	3904.3	Standard non polar	33892256
20-Hydroxy-3,7,11,15,23-pentaoxolanost-8-en-26-oic acid,3TMS,isomer #11	CC(C=C(CC(C)(O[Si](C)(C)C)C1C=C(O[Si](C)(C)C)C2(C)C3=C(C(=O)CC12C)C1(C)CCC(=O)C(C)(C)C1CC3=O)O[Si](C)(C)C)C(=O)O	3801.3	Semi standard non polar	33892256
20-Hydroxy-3,7,11,15,23-pentaoxolanost-8-en-26-oic acid,3TMS,isomer #11	CC(C=C(CC(C)(O[Si](C)(C)C)C1C=C(O[Si](C)(C)C)C2(C)C3=C(C(=O)CC12C)C1(C)CCC(=O)C(C)(C)C1CC3=O)O[Si](C)(C)C)C(=O)O	3793.0	Standard non polar	33892256
20-Hydroxy-3,7,11,15,23-pentaoxolanost-8-en-26-oic acid,3TMS,isomer #12	CC(C=C(CC(C)(O[Si](C)(C)C)C1CC(=O)C2(C)C3=C(C(O[Si](C)(C)C)=CC12C)C1(C)CCC(=O)C(C)(C)C1CC3=O)O[Si](C)(C)C)C(=O)O	3763.7	Semi standard non polar	33892256
20-Hydroxy-3,7,11,15,23-pentaoxolanost-8-en-26-oic acid,3TMS,isomer #12	CC(C=C(CC(C)(O[Si](C)(C)C)C1CC(=O)C2(C)C3=C(C(O[Si](C)(C)C)=CC12C)C1(C)CCC(=O)C(C)(C)C1CC3=O)O[Si](C)(C)C)C(=O)O	3963.3	Standard non polar	33892256
20-Hydroxy-3,7,11,15,23-pentaoxolanost-8-en-26-oic acid,3TMS,isomer #13	CC(C=C(CC(C)(O[Si](C)(C)C)C1CC(=O)C2(C)C3=C(C(=O)CC12C)C1(C)CC=C(O[Si](C)(C)C)C(C)(C)C1CC3=O)O[Si](C)(C)C)C(=O)O	3753.6	Semi standard non polar	33892256
20-Hydroxy-3,7,11,15,23-pentaoxolanost-8-en-26-oic acid,3TMS,isomer #13	CC(C=C(CC(C)(O[Si](C)(C)C)C1CC(=O)C2(C)C3=C(C(=O)CC12C)C1(C)CC=C(O[Si](C)(C)C)C(C)(C)C1CC3=O)O[Si](C)(C)C)C(=O)O	3832.5	Standard non polar	33892256
20-Hydroxy-3,7,11,15,23-pentaoxolanost-8-en-26-oic acid,3TMS,isomer #14	CC(C=C(CC(C)(O[Si](C)(C)C)C1CC(=O)C2(C)C3=C(C(=O)CC12C)C1(C)CCC(=O)C(C)(C)C1C=C3O[Si](C)(C)C)O[Si](C)(C)C)C(=O)O	3792.2	Semi standard non polar	33892256
20-Hydroxy-3,7,11,15,23-pentaoxolanost-8-en-26-oic acid,3TMS,isomer #14	CC(C=C(CC(C)(O[Si](C)(C)C)C1CC(=O)C2(C)C3=C(C(=O)CC12C)C1(C)CCC(=O)C(C)(C)C1C=C3O[Si](C)(C)C)O[Si](C)(C)C)C(=O)O	3963.0	Standard non polar	33892256
20-Hydroxy-3,7,11,15,23-pentaoxolanost-8-en-26-oic acid,3TMS,isomer #15	CC(CC(=O)CC(C)(O[Si](C)(C)C)C1C=C(O[Si](C)(C)C)C2(C)C3=C(C(O[Si](C)(C)C)=CC12C)C1(C)CCC(=O)C(C)(C)C1CC3=O)C(=O)O	3688.2	Semi standard non polar	33892256
20-Hydroxy-3,7,11,15,23-pentaoxolanost-8-en-26-oic acid,3TMS,isomer #15	CC(CC(=O)CC(C)(O[Si](C)(C)C)C1C=C(O[Si](C)(C)C)C2(C)C3=C(C(O[Si](C)(C)C)=CC12C)C1(C)CCC(=O)C(C)(C)C1CC3=O)C(=O)O	3738.6	Standard non polar	33892256
20-Hydroxy-3,7,11,15,23-pentaoxolanost-8-en-26-oic acid,3TMS,isomer #16	CC(CC(=O)CC(C)(O[Si](C)(C)C)C1C=C(O[Si](C)(C)C)C2(C)C3=C(C(=O)CC12C)C1(C)CC=C(O[Si](C)(C)C)C(C)(C)C1CC3=O)C(=O)O	3683.8	Semi standard non polar	33892256
20-Hydroxy-3,7,11,15,23-pentaoxolanost-8-en-26-oic acid,3TMS,isomer #16	CC(CC(=O)CC(C)(O[Si](C)(C)C)C1C=C(O[Si](C)(C)C)C2(C)C3=C(C(=O)CC12C)C1(C)CC=C(O[Si](C)(C)C)C(C)(C)C1CC3=O)C(=O)O	3620.6	Standard non polar	33892256
20-Hydroxy-3,7,11,15,23-pentaoxolanost-8-en-26-oic acid,3TMS,isomer #17	CC(CC(=O)CC(C)(O[Si](C)(C)C)C1C=C(O[Si](C)(C)C)C2(C)C3=C(C(=O)CC12C)C1(C)CCC(=O)C(C)(C)C1C=C3O[Si](C)(C)C)C(=O)O	3751.6	Semi standard non polar	33892256
20-Hydroxy-3,7,11,15,23-pentaoxolanost-8-en-26-oic acid,3TMS,isomer #17	CC(CC(=O)CC(C)(O[Si](C)(C)C)C1C=C(O[Si](C)(C)C)C2(C)C3=C(C(=O)CC12C)C1(C)CCC(=O)C(C)(C)C1C=C3O[Si](C)(C)C)C(=O)O	3688.5	Standard non polar	33892256
20-Hydroxy-3,7,11,15,23-pentaoxolanost-8-en-26-oic acid,3TMS,isomer #18	CC(CC(=O)CC(C)(O[Si](C)(C)C)C1CC(=O)C2(C)C3=C(C(O[Si](C)(C)C)=CC12C)C1(C)CC=C(O[Si](C)(C)C)C(C)(C)C1CC3=O)C(=O)O	3653.6	Semi standard non polar	33892256
20-Hydroxy-3,7,11,15,23-pentaoxolanost-8-en-26-oic acid,3TMS,isomer #18	CC(CC(=O)CC(C)(O[Si](C)(C)C)C1CC(=O)C2(C)C3=C(C(O[Si](C)(C)C)=CC12C)C1(C)CC=C(O[Si](C)(C)C)C(C)(C)C1CC3=O)C(=O)O	3763.0	Standard non polar	33892256
20-Hydroxy-3,7,11,15,23-pentaoxolanost-8-en-26-oic acid,3TMS,isomer #19	CC(CC(=O)CC(C)(O[Si](C)(C)C)C1CC(=O)C2(C)C3=C(C(O[Si](C)(C)C)=CC12C)C1(C)CCC(=O)C(C)(C)C1C=C3O[Si](C)(C)C)C(=O)O	3676.8	Semi standard non polar	33892256
20-Hydroxy-3,7,11,15,23-pentaoxolanost-8-en-26-oic acid,3TMS,isomer #19	CC(CC(=O)CC(C)(O[Si](C)(C)C)C1CC(=O)C2(C)C3=C(C(O[Si](C)(C)C)=CC12C)C1(C)CCC(=O)C(C)(C)C1C=C3O[Si](C)(C)C)C(=O)O	3865.1	Standard non polar	33892256
20-Hydroxy-3,7,11,15,23-pentaoxolanost-8-en-26-oic acid,3TMS,isomer #2	CC(C=C(CC(C)(O[Si](C)(C)C)C1CC(=O)C2(C)C3=C(C(=O)CC12C)C1(C)CCC(=O)C(C)(C)C1CC3=O)O[Si](C)(C)C)C(=O)O[Si](C)(C)C	3920.8	Semi standard non polar	33892256
20-Hydroxy-3,7,11,15,23-pentaoxolanost-8-en-26-oic acid,3TMS,isomer #2	CC(C=C(CC(C)(O[Si](C)(C)C)C1CC(=O)C2(C)C3=C(C(=O)CC12C)C1(C)CCC(=O)C(C)(C)C1CC3=O)O[Si](C)(C)C)C(=O)O[Si](C)(C)C	3999.4	Standard non polar	33892256
20-Hydroxy-3,7,11,15,23-pentaoxolanost-8-en-26-oic acid,3TMS,isomer #20	CC(CC(=O)CC(C)(O[Si](C)(C)C)C1CC(=O)C2(C)C3=C(C(=O)CC12C)C1(C)CC=C(O[Si](C)(C)C)C(C)(C)C1C=C3O[Si](C)(C)C)C(=O)O	3703.4	Semi standard non polar	33892256
20-Hydroxy-3,7,11,15,23-pentaoxolanost-8-en-26-oic acid,3TMS,isomer #20	CC(CC(=O)CC(C)(O[Si](C)(C)C)C1CC(=O)C2(C)C3=C(C(=O)CC12C)C1(C)CC=C(O[Si](C)(C)C)C(C)(C)C1C=C3O[Si](C)(C)C)C(=O)O	3769.1	Standard non polar	33892256
20-Hydroxy-3,7,11,15,23-pentaoxolanost-8-en-26-oic acid,3TMS,isomer #21	CC(CC(=CC(C)(O)C1C=C(O[Si](C)(C)C)C2(C)C3=C(C(=O)CC12C)C1(C)CCC(=O)C(C)(C)C1CC3=O)O[Si](C)(C)C)C(=O)O[Si](C)(C)C	3756.4	Semi standard non polar	33892256
20-Hydroxy-3,7,11,15,23-pentaoxolanost-8-en-26-oic acid,3TMS,isomer #21	CC(CC(=CC(C)(O)C1C=C(O[Si](C)(C)C)C2(C)C3=C(C(=O)CC12C)C1(C)CCC(=O)C(C)(C)C1CC3=O)O[Si](C)(C)C)C(=O)O[Si](C)(C)C	3772.9	Standard non polar	33892256
20-Hydroxy-3,7,11,15,23-pentaoxolanost-8-en-26-oic acid,3TMS,isomer #22	CC(CC(=CC(C)(O)C1CC(=O)C2(C)C3=C(C(O[Si](C)(C)C)=CC12C)C1(C)CCC(=O)C(C)(C)C1CC3=O)O[Si](C)(C)C)C(=O)O[Si](C)(C)C	3736.3	Semi standard non polar	33892256
20-Hydroxy-3,7,11,15,23-pentaoxolanost-8-en-26-oic acid,3TMS,isomer #22	CC(CC(=CC(C)(O)C1CC(=O)C2(C)C3=C(C(O[Si](C)(C)C)=CC12C)C1(C)CCC(=O)C(C)(C)C1CC3=O)O[Si](C)(C)C)C(=O)O[Si](C)(C)C	3931.9	Standard non polar	33892256
20-Hydroxy-3,7,11,15,23-pentaoxolanost-8-en-26-oic acid,3TMS,isomer #23	CC(CC(=CC(C)(O)C1CC(=O)C2(C)C3=C(C(=O)CC12C)C1(C)CC=C(O[Si](C)(C)C)C(C)(C)C1CC3=O)O[Si](C)(C)C)C(=O)O[Si](C)(C)C	3711.0	Semi standard non polar	33892256
20-Hydroxy-3,7,11,15,23-pentaoxolanost-8-en-26-oic acid,3TMS,isomer #23	CC(CC(=CC(C)(O)C1CC(=O)C2(C)C3=C(C(=O)CC12C)C1(C)CC=C(O[Si](C)(C)C)C(C)(C)C1CC3=O)O[Si](C)(C)C)C(=O)O[Si](C)(C)C	3799.9	Standard non polar	33892256
20-Hydroxy-3,7,11,15,23-pentaoxolanost-8-en-26-oic acid,3TMS,isomer #24	CC(CC(=CC(C)(O)C1CC(=O)C2(C)C3=C(C(=O)CC12C)C1(C)CCC(=O)C(C)(C)C1C=C3O[Si](C)(C)C)O[Si](C)(C)C)C(=O)O[Si](C)(C)C	3736.0	Semi standard non polar	33892256
20-Hydroxy-3,7,11,15,23-pentaoxolanost-8-en-26-oic acid,3TMS,isomer #24	CC(CC(=CC(C)(O)C1CC(=O)C2(C)C3=C(C(=O)CC12C)C1(C)CCC(=O)C(C)(C)C1C=C3O[Si](C)(C)C)O[Si](C)(C)C)C(=O)O[Si](C)(C)C	3933.0	Standard non polar	33892256
20-Hydroxy-3,7,11,15,23-pentaoxolanost-8-en-26-oic acid,3TMS,isomer #25	CC(C=C(CC(C)(O)C1C=C(O[Si](C)(C)C)C2(C)C3=C(C(=O)CC12C)C1(C)CCC(=O)C(C)(C)C1CC3=O)O[Si](C)(C)C)C(=O)O[Si](C)(C)C	3795.8	Semi standard non polar	33892256
20-Hydroxy-3,7,11,15,23-pentaoxolanost-8-en-26-oic acid,3TMS,isomer #25	CC(C=C(CC(C)(O)C1C=C(O[Si](C)(C)C)C2(C)C3=C(C(=O)CC12C)C1(C)CCC(=O)C(C)(C)C1CC3=O)O[Si](C)(C)C)C(=O)O[Si](C)(C)C	3803.6	Standard non polar	33892256
20-Hydroxy-3,7,11,15,23-pentaoxolanost-8-en-26-oic acid,3TMS,isomer #26	CC(C=C(CC(C)(O)C1CC(=O)C2(C)C3=C(C(O[Si](C)(C)C)=CC12C)C1(C)CCC(=O)C(C)(C)C1CC3=O)O[Si](C)(C)C)C(=O)O[Si](C)(C)C	3794.7	Semi standard non polar	33892256
20-Hydroxy-3,7,11,15,23-pentaoxolanost-8-en-26-oic acid,3TMS,isomer #26	CC(C=C(CC(C)(O)C1CC(=O)C2(C)C3=C(C(O[Si](C)(C)C)=CC12C)C1(C)CCC(=O)C(C)(C)C1CC3=O)O[Si](C)(C)C)C(=O)O[Si](C)(C)C	3963.7	Standard non polar	33892256
20-Hydroxy-3,7,11,15,23-pentaoxolanost-8-en-26-oic acid,3TMS,isomer #27	CC(C=C(CC(C)(O)C1CC(=O)C2(C)C3=C(C(=O)CC12C)C1(C)CC=C(O[Si](C)(C)C)C(C)(C)C1CC3=O)O[Si](C)(C)C)C(=O)O[Si](C)(C)C	3765.0	Semi standard non polar	33892256
20-Hydroxy-3,7,11,15,23-pentaoxolanost-8-en-26-oic acid,3TMS,isomer #27	CC(C=C(CC(C)(O)C1CC(=O)C2(C)C3=C(C(=O)CC12C)C1(C)CC=C(O[Si](C)(C)C)C(C)(C)C1CC3=O)O[Si](C)(C)C)C(=O)O[Si](C)(C)C	3844.7	Standard non polar	33892256
20-Hydroxy-3,7,11,15,23-pentaoxolanost-8-en-26-oic acid,3TMS,isomer #28	CC(C=C(CC(C)(O)C1CC(=O)C2(C)C3=C(C(=O)CC12C)C1(C)CCC(=O)C(C)(C)C1C=C3O[Si](C)(C)C)O[Si](C)(C)C)C(=O)O[Si](C)(C)C	3799.6	Semi standard non polar	33892256
20-Hydroxy-3,7,11,15,23-pentaoxolanost-8-en-26-oic acid,3TMS,isomer #28	CC(C=C(CC(C)(O)C1CC(=O)C2(C)C3=C(C(=O)CC12C)C1(C)CCC(=O)C(C)(C)C1C=C3O[Si](C)(C)C)O[Si](C)(C)C)C(=O)O[Si](C)(C)C	3970.9	Standard non polar	33892256
20-Hydroxy-3,7,11,15,23-pentaoxolanost-8-en-26-oic acid,3TMS,isomer #29	CC(CC(=O)CC(C)(O)C1C=C(O[Si](C)(C)C)C2(C)C3=C(C(O[Si](C)(C)C)=CC12C)C1(C)CCC(=O)C(C)(C)C1CC3=O)C(=O)O[Si](C)(C)C	3711.8	Semi standard non polar	33892256
20-Hydroxy-3,7,11,15,23-pentaoxolanost-8-en-26-oic acid,3TMS,isomer #29	CC(CC(=O)CC(C)(O)C1C=C(O[Si](C)(C)C)C2(C)C3=C(C(O[Si](C)(C)C)=CC12C)C1(C)CCC(=O)C(C)(C)C1CC3=O)C(=O)O[Si](C)(C)C	3746.9	Standard non polar	33892256
20-Hydroxy-3,7,11,15,23-pentaoxolanost-8-en-26-oic acid,3TMS,isomer #3	CC(CC(=O)CC(C)(O[Si](C)(C)C)C1C=C(O[Si](C)(C)C)C2(C)C3=C(C(=O)CC12C)C1(C)CCC(=O)C(C)(C)C1CC3=O)C(=O)O[Si](C)(C)C	3858.5	Semi standard non polar	33892256
20-Hydroxy-3,7,11,15,23-pentaoxolanost-8-en-26-oic acid,3TMS,isomer #3	CC(CC(=O)CC(C)(O[Si](C)(C)C)C1C=C(O[Si](C)(C)C)C2(C)C3=C(C(=O)CC12C)C1(C)CCC(=O)C(C)(C)C1CC3=O)C(=O)O[Si](C)(C)C	3742.0	Standard non polar	33892256
20-Hydroxy-3,7,11,15,23-pentaoxolanost-8-en-26-oic acid,3TMS,isomer #30	CC(CC(=O)CC(C)(O)C1C=C(O[Si](C)(C)C)C2(C)C3=C(C(=O)CC12C)C1(C)CC=C(O[Si](C)(C)C)C(C)(C)C1CC3=O)C(=O)O[Si](C)(C)C	3688.5	Semi standard non polar	33892256
20-Hydroxy-3,7,11,15,23-pentaoxolanost-8-en-26-oic acid,3TMS,isomer #30	CC(CC(=O)CC(C)(O)C1C=C(O[Si](C)(C)C)C2(C)C3=C(C(=O)CC12C)C1(C)CC=C(O[Si](C)(C)C)C(C)(C)C1CC3=O)C(=O)O[Si](C)(C)C	3645.3	Standard non polar	33892256
20-Hydroxy-3,7,11,15,23-pentaoxolanost-8-en-26-oic acid,3TMS,isomer #31	CC(CC(=O)CC(C)(O)C1C=C(O[Si](C)(C)C)C2(C)C3=C(C(=O)CC12C)C1(C)CCC(=O)C(C)(C)C1C=C3O[Si](C)(C)C)C(=O)O[Si](C)(C)C	3758.9	Semi standard non polar	33892256
20-Hydroxy-3,7,11,15,23-pentaoxolanost-8-en-26-oic acid,3TMS,isomer #31	CC(CC(=O)CC(C)(O)C1C=C(O[Si](C)(C)C)C2(C)C3=C(C(=O)CC12C)C1(C)CCC(=O)C(C)(C)C1C=C3O[Si](C)(C)C)C(=O)O[Si](C)(C)C	3702.2	Standard non polar	33892256
20-Hydroxy-3,7,11,15,23-pentaoxolanost-8-en-26-oic acid,3TMS,isomer #32	CC(CC(=O)CC(C)(O)C1CC(=O)C2(C)C3=C(C(O[Si](C)(C)C)=CC12C)C1(C)CC=C(O[Si](C)(C)C)C(C)(C)C1CC3=O)C(=O)O[Si](C)(C)C	3696.7	Semi standard non polar	33892256
20-Hydroxy-3,7,11,15,23-pentaoxolanost-8-en-26-oic acid,3TMS,isomer #32	CC(CC(=O)CC(C)(O)C1CC(=O)C2(C)C3=C(C(O[Si](C)(C)C)=CC12C)C1(C)CC=C(O[Si](C)(C)C)C(C)(C)C1CC3=O)C(=O)O[Si](C)(C)C	3766.2	Standard non polar	33892256
20-Hydroxy-3,7,11,15,23-pentaoxolanost-8-en-26-oic acid,3TMS,isomer #33	CC(CC(=O)CC(C)(O)C1CC(=O)C2(C)C3=C(C(O[Si](C)(C)C)=CC12C)C1(C)CCC(=O)C(C)(C)C1C=C3O[Si](C)(C)C)C(=O)O[Si](C)(C)C	3735.8	Semi standard non polar	33892256
20-Hydroxy-3,7,11,15,23-pentaoxolanost-8-en-26-oic acid,3TMS,isomer #33	CC(CC(=O)CC(C)(O)C1CC(=O)C2(C)C3=C(C(O[Si](C)(C)C)=CC12C)C1(C)CCC(=O)C(C)(C)C1C=C3O[Si](C)(C)C)C(=O)O[Si](C)(C)C	3876.6	Standard non polar	33892256
20-Hydroxy-3,7,11,15,23-pentaoxolanost-8-en-26-oic acid,3TMS,isomer #34	CC(CC(=O)CC(C)(O)C1CC(=O)C2(C)C3=C(C(=O)CC12C)C1(C)CC=C(O[Si](C)(C)C)C(C)(C)C1C=C3O[Si](C)(C)C)C(=O)O[Si](C)(C)C	3715.9	Semi standard non polar	33892256
20-Hydroxy-3,7,11,15,23-pentaoxolanost-8-en-26-oic acid,3TMS,isomer #34	CC(CC(=O)CC(C)(O)C1CC(=O)C2(C)C3=C(C(=O)CC12C)C1(C)CC=C(O[Si](C)(C)C)C(C)(C)C1C=C3O[Si](C)(C)C)C(=O)O[Si](C)(C)C	3780.1	Standard non polar	33892256
20-Hydroxy-3,7,11,15,23-pentaoxolanost-8-en-26-oic acid,3TMS,isomer #35	CC(CC(=CC(C)(O)C1C=C(O[Si](C)(C)C)C2(C)C3=C(C(O[Si](C)(C)C)=CC12C)C1(C)CCC(=O)C(C)(C)C1CC3=O)O[Si](C)(C)C)C(=O)O	3656.3	Semi standard non polar	33892256
20-Hydroxy-3,7,11,15,23-pentaoxolanost-8-en-26-oic acid,3TMS,isomer #35	CC(CC(=CC(C)(O)C1C=C(O[Si](C)(C)C)C2(C)C3=C(C(O[Si](C)(C)C)=CC12C)C1(C)CCC(=O)C(C)(C)C1CC3=O)O[Si](C)(C)C)C(=O)O	3727.9	Standard non polar	33892256
20-Hydroxy-3,7,11,15,23-pentaoxolanost-8-en-26-oic acid,3TMS,isomer #36	CC(CC(=CC(C)(O)C1C=C(O[Si](C)(C)C)C2(C)C3=C(C(=O)CC12C)C1(C)CC=C(O[Si](C)(C)C)C(C)(C)C1CC3=O)O[Si](C)(C)C)C(=O)O	3639.3	Semi standard non polar	33892256
20-Hydroxy-3,7,11,15,23-pentaoxolanost-8-en-26-oic acid,3TMS,isomer #36	CC(CC(=CC(C)(O)C1C=C(O[Si](C)(C)C)C2(C)C3=C(C(=O)CC12C)C1(C)CC=C(O[Si](C)(C)C)C(C)(C)C1CC3=O)O[Si](C)(C)C)C(=O)O	3590.0	Standard non polar	33892256
20-Hydroxy-3,7,11,15,23-pentaoxolanost-8-en-26-oic acid,3TMS,isomer #37	CC(CC(=CC(C)(O)C1C=C(O[Si](C)(C)C)C2(C)C3=C(C(=O)CC12C)C1(C)CCC(=O)C(C)(C)C1C=C3O[Si](C)(C)C)O[Si](C)(C)C)C(=O)O	3704.7	Semi standard non polar	33892256
20-Hydroxy-3,7,11,15,23-pentaoxolanost-8-en-26-oic acid,3TMS,isomer #37	CC(CC(=CC(C)(O)C1C=C(O[Si](C)(C)C)C2(C)C3=C(C(=O)CC12C)C1(C)CCC(=O)C(C)(C)C1C=C3O[Si](C)(C)C)O[Si](C)(C)C)C(=O)O	3671.7	Standard non polar	33892256
20-Hydroxy-3,7,11,15,23-pentaoxolanost-8-en-26-oic acid,3TMS,isomer #38	CC(CC(=CC(C)(O)C1CC(=O)C2(C)C3=C(C(O[Si](C)(C)C)=CC12C)C1(C)CC=C(O[Si](C)(C)C)C(C)(C)C1CC3=O)O[Si](C)(C)C)C(=O)O	3644.3	Semi standard non polar	33892256
20-Hydroxy-3,7,11,15,23-pentaoxolanost-8-en-26-oic acid,3TMS,isomer #38	CC(CC(=CC(C)(O)C1CC(=O)C2(C)C3=C(C(O[Si](C)(C)C)=CC12C)C1(C)CC=C(O[Si](C)(C)C)C(C)(C)C1CC3=O)O[Si](C)(C)C)C(=O)O	3723.7	Standard non polar	33892256
20-Hydroxy-3,7,11,15,23-pentaoxolanost-8-en-26-oic acid,3TMS,isomer #39	CC(CC(=CC(C)(O)C1CC(=O)C2(C)C3=C(C(O[Si](C)(C)C)=CC12C)C1(C)CCC(=O)C(C)(C)C1C=C3O[Si](C)(C)C)O[Si](C)(C)C)C(=O)O	3683.0	Semi standard non polar	33892256
20-Hydroxy-3,7,11,15,23-pentaoxolanost-8-en-26-oic acid,3TMS,isomer #39	CC(CC(=CC(C)(O)C1CC(=O)C2(C)C3=C(C(O[Si](C)(C)C)=CC12C)C1(C)CCC(=O)C(C)(C)C1C=C3O[Si](C)(C)C)O[Si](C)(C)C)C(=O)O	3836.5	Standard non polar	33892256
20-Hydroxy-3,7,11,15,23-pentaoxolanost-8-en-26-oic acid,3TMS,isomer #4	CC(CC(=O)CC(C)(O[Si](C)(C)C)C1CC(=O)C2(C)C3=C(C(O[Si](C)(C)C)=CC12C)C1(C)CCC(=O)C(C)(C)C1CC3=O)C(=O)O[Si](C)(C)C	3815.4	Semi standard non polar	33892256
20-Hydroxy-3,7,11,15,23-pentaoxolanost-8-en-26-oic acid,3TMS,isomer #4	CC(CC(=O)CC(C)(O[Si](C)(C)C)C1CC(=O)C2(C)C3=C(C(O[Si](C)(C)C)=CC12C)C1(C)CCC(=O)C(C)(C)C1CC3=O)C(=O)O[Si](C)(C)C	3925.5	Standard non polar	33892256
20-Hydroxy-3,7,11,15,23-pentaoxolanost-8-en-26-oic acid,3TMS,isomer #40	CC(CC(=CC(C)(O)C1CC(=O)C2(C)C3=C(C(=O)CC12C)C1(C)CC=C(O[Si](C)(C)C)C(C)(C)C1C=C3O[Si](C)(C)C)O[Si](C)(C)C)C(=O)O	3658.4	Semi standard non polar	33892256
20-Hydroxy-3,7,11,15,23-pentaoxolanost-8-en-26-oic acid,3TMS,isomer #40	CC(CC(=CC(C)(O)C1CC(=O)C2(C)C3=C(C(=O)CC12C)C1(C)CC=C(O[Si](C)(C)C)C(C)(C)C1C=C3O[Si](C)(C)C)O[Si](C)(C)C)C(=O)O	3735.5	Standard non polar	33892256
20-Hydroxy-3,7,11,15,23-pentaoxolanost-8-en-26-oic acid,3TMS,isomer #41	CC(C=C(CC(C)(O)C1C=C(O[Si](C)(C)C)C2(C)C3=C(C(O[Si](C)(C)C)=CC12C)C1(C)CCC(=O)C(C)(C)C1CC3=O)O[Si](C)(C)C)C(=O)O	3693.7	Semi standard non polar	33892256
20-Hydroxy-3,7,11,15,23-pentaoxolanost-8-en-26-oic acid,3TMS,isomer #41	CC(C=C(CC(C)(O)C1C=C(O[Si](C)(C)C)C2(C)C3=C(C(O[Si](C)(C)C)=CC12C)C1(C)CCC(=O)C(C)(C)C1CC3=O)O[Si](C)(C)C)C(=O)O	3780.0	Standard non polar	33892256
20-Hydroxy-3,7,11,15,23-pentaoxolanost-8-en-26-oic acid,3TMS,isomer #42	CC(C=C(CC(C)(O)C1C=C(O[Si](C)(C)C)C2(C)C3=C(C(=O)CC12C)C1(C)CC=C(O[Si](C)(C)C)C(C)(C)C1CC3=O)O[Si](C)(C)C)C(=O)O	3677.4	Semi standard non polar	33892256
20-Hydroxy-3,7,11,15,23-pentaoxolanost-8-en-26-oic acid,3TMS,isomer #42	CC(C=C(CC(C)(O)C1C=C(O[Si](C)(C)C)C2(C)C3=C(C(=O)CC12C)C1(C)CC=C(O[Si](C)(C)C)C(C)(C)C1CC3=O)O[Si](C)(C)C)C(=O)O	3654.6	Standard non polar	33892256
20-Hydroxy-3,7,11,15,23-pentaoxolanost-8-en-26-oic acid,3TMS,isomer #43	CC(C=C(CC(C)(O)C1C=C(O[Si](C)(C)C)C2(C)C3=C(C(=O)CC12C)C1(C)CCC(=O)C(C)(C)C1C=C3O[Si](C)(C)C)O[Si](C)(C)C)C(=O)O	3762.5	Semi standard non polar	33892256
20-Hydroxy-3,7,11,15,23-pentaoxolanost-8-en-26-oic acid,3TMS,isomer #43	CC(C=C(CC(C)(O)C1C=C(O[Si](C)(C)C)C2(C)C3=C(C(=O)CC12C)C1(C)CCC(=O)C(C)(C)C1C=C3O[Si](C)(C)C)O[Si](C)(C)C)C(=O)O	3730.4	Standard non polar	33892256
20-Hydroxy-3,7,11,15,23-pentaoxolanost-8-en-26-oic acid,3TMS,isomer #44	CC(C=C(CC(C)(O)C1CC(=O)C2(C)C3=C(C(O[Si](C)(C)C)=CC12C)C1(C)CC=C(O[Si](C)(C)C)C(C)(C)C1CC3=O)O[Si](C)(C)C)C(=O)O	3693.7	Semi standard non polar	33892256
20-Hydroxy-3,7,11,15,23-pentaoxolanost-8-en-26-oic acid,3TMS,isomer #44	CC(C=C(CC(C)(O)C1CC(=O)C2(C)C3=C(C(O[Si](C)(C)C)=CC12C)C1(C)CC=C(O[Si](C)(C)C)C(C)(C)C1CC3=O)O[Si](C)(C)C)C(=O)O	3795.9	Standard non polar	33892256
20-Hydroxy-3,7,11,15,23-pentaoxolanost-8-en-26-oic acid,3TMS,isomer #45	CC(C=C(CC(C)(O)C1CC(=O)C2(C)C3=C(C(O[Si](C)(C)C)=CC12C)C1(C)CCC(=O)C(C)(C)C1C=C3O[Si](C)(C)C)O[Si](C)(C)C)C(=O)O	3737.6	Semi standard non polar	33892256
20-Hydroxy-3,7,11,15,23-pentaoxolanost-8-en-26-oic acid,3TMS,isomer #45	CC(C=C(CC(C)(O)C1CC(=O)C2(C)C3=C(C(O[Si](C)(C)C)=CC12C)C1(C)CCC(=O)C(C)(C)C1C=C3O[Si](C)(C)C)O[Si](C)(C)C)C(=O)O	3904.6	Standard non polar	33892256
20-Hydroxy-3,7,11,15,23-pentaoxolanost-8-en-26-oic acid,3TMS,isomer #46	CC(C=C(CC(C)(O)C1CC(=O)C2(C)C3=C(C(=O)CC12C)C1(C)CC=C(O[Si](C)(C)C)C(C)(C)C1C=C3O[Si](C)(C)C)O[Si](C)(C)C)C(=O)O	3722.6	Semi standard non polar	33892256
20-Hydroxy-3,7,11,15,23-pentaoxolanost-8-en-26-oic acid,3TMS,isomer #46	CC(C=C(CC(C)(O)C1CC(=O)C2(C)C3=C(C(=O)CC12C)C1(C)CC=C(O[Si](C)(C)C)C(C)(C)C1C=C3O[Si](C)(C)C)O[Si](C)(C)C)C(=O)O	3810.4	Standard non polar	33892256
20-Hydroxy-3,7,11,15,23-pentaoxolanost-8-en-26-oic acid,3TMS,isomer #47	CC(CC(=O)CC(C)(O)C1C=C(O[Si](C)(C)C)C2(C)C3=C(C(O[Si](C)(C)C)=CC12C)C1(C)CC=C(O[Si](C)(C)C)C(C)(C)C1CC3=O)C(=O)O	3614.2	Semi standard non polar	33892256
20-Hydroxy-3,7,11,15,23-pentaoxolanost-8-en-26-oic acid,3TMS,isomer #47	CC(CC(=O)CC(C)(O)C1C=C(O[Si](C)(C)C)C2(C)C3=C(C(O[Si](C)(C)C)=CC12C)C1(C)CC=C(O[Si](C)(C)C)C(C)(C)C1CC3=O)C(=O)O	3631.1	Standard non polar	33892256
20-Hydroxy-3,7,11,15,23-pentaoxolanost-8-en-26-oic acid,3TMS,isomer #48	CC(CC(=O)CC(C)(O)C1C=C(O[Si](C)(C)C)C2(C)C3=C(C(O[Si](C)(C)C)=CC12C)C1(C)CCC(=O)C(C)(C)C1C=C3O[Si](C)(C)C)C(=O)O	3686.9	Semi standard non polar	33892256
20-Hydroxy-3,7,11,15,23-pentaoxolanost-8-en-26-oic acid,3TMS,isomer #48	CC(CC(=O)CC(C)(O)C1C=C(O[Si](C)(C)C)C2(C)C3=C(C(O[Si](C)(C)C)=CC12C)C1(C)CCC(=O)C(C)(C)C1C=C3O[Si](C)(C)C)C(=O)O	3685.2	Standard non polar	33892256
20-Hydroxy-3,7,11,15,23-pentaoxolanost-8-en-26-oic acid,3TMS,isomer #49	CC(CC(=O)CC(C)(O)C1C=C(O[Si](C)(C)C)C2(C)C3=C(C(=O)CC12C)C1(C)CC=C(O[Si](C)(C)C)C(C)(C)C1C=C3O[Si](C)(C)C)C(=O)O	3675.1	Semi standard non polar	33892256
20-Hydroxy-3,7,11,15,23-pentaoxolanost-8-en-26-oic acid,3TMS,isomer #49	CC(CC(=O)CC(C)(O)C1C=C(O[Si](C)(C)C)C2(C)C3=C(C(=O)CC12C)C1(C)CC=C(O[Si](C)(C)C)C(C)(C)C1C=C3O[Si](C)(C)C)C(=O)O	3588.8	Standard non polar	33892256
20-Hydroxy-3,7,11,15,23-pentaoxolanost-8-en-26-oic acid,3TMS,isomer #5	CC(CC(=O)CC(C)(O[Si](C)(C)C)C1CC(=O)C2(C)C3=C(C(=O)CC12C)C1(C)CC=C(O[Si](C)(C)C)C(C)(C)C1CC3=O)C(=O)O[Si](C)(C)C	3798.7	Semi standard non polar	33892256
20-Hydroxy-3,7,11,15,23-pentaoxolanost-8-en-26-oic acid,3TMS,isomer #5	CC(CC(=O)CC(C)(O[Si](C)(C)C)C1CC(=O)C2(C)C3=C(C(=O)CC12C)C1(C)CC=C(O[Si](C)(C)C)C(C)(C)C1CC3=O)C(=O)O[Si](C)(C)C	3788.0	Standard non polar	33892256
20-Hydroxy-3,7,11,15,23-pentaoxolanost-8-en-26-oic acid,3TMS,isomer #50	CC(CC(=O)CC(C)(O)C1CC(=O)C2(C)C3=C(C(O[Si](C)(C)C)=CC12C)C1(C)CC=C(O[Si](C)(C)C)C(C)(C)C1C=C3O[Si](C)(C)C)C(=O)O	3656.2	Semi standard non polar	33892256
20-Hydroxy-3,7,11,15,23-pentaoxolanost-8-en-26-oic acid,3TMS,isomer #50	CC(CC(=O)CC(C)(O)C1CC(=O)C2(C)C3=C(C(O[Si](C)(C)C)=CC12C)C1(C)CC=C(O[Si](C)(C)C)C(C)(C)C1C=C3O[Si](C)(C)C)C(=O)O	3735.5	Standard non polar	33892256
20-Hydroxy-3,7,11,15,23-pentaoxolanost-8-en-26-oic acid,3TMS,isomer #6	CC(CC(=O)CC(C)(O[Si](C)(C)C)C1CC(=O)C2(C)C3=C(C(=O)CC12C)C1(C)CCC(=O)C(C)(C)C1C=C3O[Si](C)(C)C)C(=O)O[Si](C)(C)C	3837.0	Semi standard non polar	33892256
20-Hydroxy-3,7,11,15,23-pentaoxolanost-8-en-26-oic acid,3TMS,isomer #6	CC(CC(=O)CC(C)(O[Si](C)(C)C)C1CC(=O)C2(C)C3=C(C(=O)CC12C)C1(C)CCC(=O)C(C)(C)C1C=C3O[Si](C)(C)C)C(=O)O[Si](C)(C)C	3928.2	Standard non polar	33892256
20-Hydroxy-3,7,11,15,23-pentaoxolanost-8-en-26-oic acid,3TMS,isomer #7	CC(CC(=CC(C)(O[Si](C)(C)C)C1C=C(O[Si](C)(C)C)C2(C)C3=C(C(=O)CC12C)C1(C)CCC(=O)C(C)(C)C1CC3=O)O[Si](C)(C)C)C(=O)O	3782.6	Semi standard non polar	33892256
20-Hydroxy-3,7,11,15,23-pentaoxolanost-8-en-26-oic acid,3TMS,isomer #7	CC(CC(=CC(C)(O[Si](C)(C)C)C1C=C(O[Si](C)(C)C)C2(C)C3=C(C(=O)CC12C)C1(C)CCC(=O)C(C)(C)C1CC3=O)O[Si](C)(C)C)C(=O)O	3741.8	Standard non polar	33892256
20-Hydroxy-3,7,11,15,23-pentaoxolanost-8-en-26-oic acid,3TMS,isomer #8	CC(CC(=CC(C)(O[Si](C)(C)C)C1CC(=O)C2(C)C3=C(C(O[Si](C)(C)C)=CC12C)C1(C)CCC(=O)C(C)(C)C1CC3=O)O[Si](C)(C)C)C(=O)O	3739.0	Semi standard non polar	33892256
20-Hydroxy-3,7,11,15,23-pentaoxolanost-8-en-26-oic acid,3TMS,isomer #8	CC(CC(=CC(C)(O[Si](C)(C)C)C1CC(=O)C2(C)C3=C(C(O[Si](C)(C)C)=CC12C)C1(C)CCC(=O)C(C)(C)C1CC3=O)O[Si](C)(C)C)C(=O)O	3906.8	Standard non polar	33892256
20-Hydroxy-3,7,11,15,23-pentaoxolanost-8-en-26-oic acid,3TMS,isomer #9	CC(CC(=CC(C)(O[Si](C)(C)C)C1CC(=O)C2(C)C3=C(C(=O)CC12C)C1(C)CC=C(O[Si](C)(C)C)C(C)(C)C1CC3=O)O[Si](C)(C)C)C(=O)O	3721.9	Semi standard non polar	33892256
20-Hydroxy-3,7,11,15,23-pentaoxolanost-8-en-26-oic acid,3TMS,isomer #9	CC(CC(=CC(C)(O[Si](C)(C)C)C1CC(=O)C2(C)C3=C(C(=O)CC12C)C1(C)CC=C(O[Si](C)(C)C)C(C)(C)C1CC3=O)O[Si](C)(C)C)C(=O)O	3766.4	Standard non polar	33892256
20-Hydroxy-3,7,11,15,23-pentaoxolanost-8-en-26-oic acid,4TMS,isomer #1	CC(CC(=CC(C)(O[Si](C)(C)C)C1C=C(O[Si](C)(C)C)C2(C)C3=C(C(=O)CC12C)C1(C)CCC(=O)C(C)(C)C1CC3=O)O[Si](C)(C)C)C(=O)O[Si](C)(C)C	3715.1	Semi standard non polar	33892256
20-Hydroxy-3,7,11,15,23-pentaoxolanost-8-en-26-oic acid,4TMS,isomer #1	CC(CC(=CC(C)(O[Si](C)(C)C)C1C=C(O[Si](C)(C)C)C2(C)C3=C(C(=O)CC12C)C1(C)CCC(=O)C(C)(C)C1CC3=O)O[Si](C)(C)C)C(=O)O[Si](C)(C)C	3777.8	Standard non polar	33892256
20-Hydroxy-3,7,11,15,23-pentaoxolanost-8-en-26-oic acid,4TMS,isomer #10	CC(CC(=O)CC(C)(O[Si](C)(C)C)C1C=C(O[Si](C)(C)C)C2(C)C3=C(C(=O)CC12C)C1(C)CC=C(O[Si](C)(C)C)C(C)(C)C1CC3=O)C(=O)O[Si](C)(C)C	3644.8	Semi standard non polar	33892256
20-Hydroxy-3,7,11,15,23-pentaoxolanost-8-en-26-oic acid,4TMS,isomer #10	CC(CC(=O)CC(C)(O[Si](C)(C)C)C1C=C(O[Si](C)(C)C)C2(C)C3=C(C(=O)CC12C)C1(C)CC=C(O[Si](C)(C)C)C(C)(C)C1CC3=O)C(=O)O[Si](C)(C)C	3643.1	Standard non polar	33892256
20-Hydroxy-3,7,11,15,23-pentaoxolanost-8-en-26-oic acid,4TMS,isomer #11	CC(CC(=O)CC(C)(O[Si](C)(C)C)C1C=C(O[Si](C)(C)C)C2(C)C3=C(C(=O)CC12C)C1(C)CCC(=O)C(C)(C)C1C=C3O[Si](C)(C)C)C(=O)O[Si](C)(C)C	3730.3	Semi standard non polar	33892256
20-Hydroxy-3,7,11,15,23-pentaoxolanost-8-en-26-oic acid,4TMS,isomer #11	CC(CC(=O)CC(C)(O[Si](C)(C)C)C1C=C(O[Si](C)(C)C)C2(C)C3=C(C(=O)CC12C)C1(C)CCC(=O)C(C)(C)C1C=C3O[Si](C)(C)C)C(=O)O[Si](C)(C)C	3714.8	Standard non polar	33892256
20-Hydroxy-3,7,11,15,23-pentaoxolanost-8-en-26-oic acid,4TMS,isomer #12	CC(CC(=O)CC(C)(O[Si](C)(C)C)C1CC(=O)C2(C)C3=C(C(O[Si](C)(C)C)=CC12C)C1(C)CC=C(O[Si](C)(C)C)C(C)(C)C1CC3=O)C(=O)O[Si](C)(C)C	3613.0	Semi standard non polar	33892256
20-Hydroxy-3,7,11,15,23-pentaoxolanost-8-en-26-oic acid,4TMS,isomer #12	CC(CC(=O)CC(C)(O[Si](C)(C)C)C1CC(=O)C2(C)C3=C(C(O[Si](C)(C)C)=CC12C)C1(C)CC=C(O[Si](C)(C)C)C(C)(C)C1CC3=O)C(=O)O[Si](C)(C)C	3799.0	Standard non polar	33892256
20-Hydroxy-3,7,11,15,23-pentaoxolanost-8-en-26-oic acid,4TMS,isomer #13	CC(CC(=O)CC(C)(O[Si](C)(C)C)C1CC(=O)C2(C)C3=C(C(O[Si](C)(C)C)=CC12C)C1(C)CCC(=O)C(C)(C)C1C=C3O[Si](C)(C)C)C(=O)O[Si](C)(C)C	3672.5	Semi standard non polar	33892256
20-Hydroxy-3,7,11,15,23-pentaoxolanost-8-en-26-oic acid,4TMS,isomer #13	CC(CC(=O)CC(C)(O[Si](C)(C)C)C1CC(=O)C2(C)C3=C(C(O[Si](C)(C)C)=CC12C)C1(C)CCC(=O)C(C)(C)C1C=C3O[Si](C)(C)C)C(=O)O[Si](C)(C)C	3910.6	Standard non polar	33892256
20-Hydroxy-3,7,11,15,23-pentaoxolanost-8-en-26-oic acid,4TMS,isomer #14	CC(CC(=O)CC(C)(O[Si](C)(C)C)C1CC(=O)C2(C)C3=C(C(=O)CC12C)C1(C)CC=C(O[Si](C)(C)C)C(C)(C)C1C=C3O[Si](C)(C)C)C(=O)O[Si](C)(C)C	3671.8	Semi standard non polar	33892256
20-Hydroxy-3,7,11,15,23-pentaoxolanost-8-en-26-oic acid,4TMS,isomer #14	CC(CC(=O)CC(C)(O[Si](C)(C)C)C1CC(=O)C2(C)C3=C(C(=O)CC12C)C1(C)CC=C(O[Si](C)(C)C)C(C)(C)C1C=C3O[Si](C)(C)C)C(=O)O[Si](C)(C)C	3799.4	Standard non polar	33892256
20-Hydroxy-3,7,11,15,23-pentaoxolanost-8-en-26-oic acid,4TMS,isomer #15	CC(CC(=CC(C)(O[Si](C)(C)C)C1C=C(O[Si](C)(C)C)C2(C)C3=C(C(O[Si](C)(C)C)=CC12C)C1(C)CCC(=O)C(C)(C)C1CC3=O)O[Si](C)(C)C)C(=O)O	3634.6	Semi standard non polar	33892256
20-Hydroxy-3,7,11,15,23-pentaoxolanost-8-en-26-oic acid,4TMS,isomer #15	CC(CC(=CC(C)(O[Si](C)(C)C)C1C=C(O[Si](C)(C)C)C2(C)C3=C(C(O[Si](C)(C)C)=CC12C)C1(C)CCC(=O)C(C)(C)C1CC3=O)O[Si](C)(C)C)C(=O)O	3750.4	Standard non polar	33892256
20-Hydroxy-3,7,11,15,23-pentaoxolanost-8-en-26-oic acid,4TMS,isomer #16	CC(CC(=CC(C)(O[Si](C)(C)C)C1C=C(O[Si](C)(C)C)C2(C)C3=C(C(=O)CC12C)C1(C)CC=C(O[Si](C)(C)C)C(C)(C)C1CC3=O)O[Si](C)(C)C)C(=O)O	3619.2	Semi standard non polar	33892256
20-Hydroxy-3,7,11,15,23-pentaoxolanost-8-en-26-oic acid,4TMS,isomer #16	CC(CC(=CC(C)(O[Si](C)(C)C)C1C=C(O[Si](C)(C)C)C2(C)C3=C(C(=O)CC12C)C1(C)CC=C(O[Si](C)(C)C)C(C)(C)C1CC3=O)O[Si](C)(C)C)C(=O)O	3598.0	Standard non polar	33892256
20-Hydroxy-3,7,11,15,23-pentaoxolanost-8-en-26-oic acid,4TMS,isomer #17	CC(CC(=CC(C)(O[Si](C)(C)C)C1C=C(O[Si](C)(C)C)C2(C)C3=C(C(=O)CC12C)C1(C)CCC(=O)C(C)(C)C1C=C3O[Si](C)(C)C)O[Si](C)(C)C)C(=O)O	3693.5	Semi standard non polar	33892256
20-Hydroxy-3,7,11,15,23-pentaoxolanost-8-en-26-oic acid,4TMS,isomer #17	CC(CC(=CC(C)(O[Si](C)(C)C)C1C=C(O[Si](C)(C)C)C2(C)C3=C(C(=O)CC12C)C1(C)CCC(=O)C(C)(C)C1C=C3O[Si](C)(C)C)O[Si](C)(C)C)C(=O)O	3680.9	Standard non polar	33892256
20-Hydroxy-3,7,11,15,23-pentaoxolanost-8-en-26-oic acid,4TMS,isomer #18	CC(CC(=CC(C)(O[Si](C)(C)C)C1CC(=O)C2(C)C3=C(C(O[Si](C)(C)C)=CC12C)C1(C)CC=C(O[Si](C)(C)C)C(C)(C)C1CC3=O)O[Si](C)(C)C)C(=O)O	3599.4	Semi standard non polar	33892256
20-Hydroxy-3,7,11,15,23-pentaoxolanost-8-en-26-oic acid,4TMS,isomer #18	CC(CC(=CC(C)(O[Si](C)(C)C)C1CC(=O)C2(C)C3=C(C(O[Si](C)(C)C)=CC12C)C1(C)CC=C(O[Si](C)(C)C)C(C)(C)C1CC3=O)O[Si](C)(C)C)C(=O)O	3750.7	Standard non polar	33892256
20-Hydroxy-3,7,11,15,23-pentaoxolanost-8-en-26-oic acid,4TMS,isomer #19	CC(CC(=CC(C)(O[Si](C)(C)C)C1CC(=O)C2(C)C3=C(C(O[Si](C)(C)C)=CC12C)C1(C)CCC(=O)C(C)(C)C1C=C3O[Si](C)(C)C)O[Si](C)(C)C)C(=O)O	3643.5	Semi standard non polar	33892256
20-Hydroxy-3,7,11,15,23-pentaoxolanost-8-en-26-oic acid,4TMS,isomer #19	CC(CC(=CC(C)(O[Si](C)(C)C)C1CC(=O)C2(C)C3=C(C(O[Si](C)(C)C)=CC12C)C1(C)CCC(=O)C(C)(C)C1C=C3O[Si](C)(C)C)O[Si](C)(C)C)C(=O)O	3873.2	Standard non polar	33892256
20-Hydroxy-3,7,11,15,23-pentaoxolanost-8-en-26-oic acid,4TMS,isomer #2	CC(CC(=CC(C)(O[Si](C)(C)C)C1CC(=O)C2(C)C3=C(C(O[Si](C)(C)C)=CC12C)C1(C)CCC(=O)C(C)(C)C1CC3=O)O[Si](C)(C)C)C(=O)O[Si](C)(C)C	3670.9	Semi standard non polar	33892256
20-Hydroxy-3,7,11,15,23-pentaoxolanost-8-en-26-oic acid,4TMS,isomer #2	CC(CC(=CC(C)(O[Si](C)(C)C)C1CC(=O)C2(C)C3=C(C(O[Si](C)(C)C)=CC12C)C1(C)CCC(=O)C(C)(C)C1CC3=O)O[Si](C)(C)C)C(=O)O[Si](C)(C)C	3963.8	Standard non polar	33892256
20-Hydroxy-3,7,11,15,23-pentaoxolanost-8-en-26-oic acid,4TMS,isomer #20	CC(CC(=CC(C)(O[Si](C)(C)C)C1CC(=O)C2(C)C3=C(C(=O)CC12C)C1(C)CC=C(O[Si](C)(C)C)C(C)(C)C1C=C3O[Si](C)(C)C)O[Si](C)(C)C)C(=O)O	3639.1	Semi standard non polar	33892256
20-Hydroxy-3,7,11,15,23-pentaoxolanost-8-en-26-oic acid,4TMS,isomer #20	CC(CC(=CC(C)(O[Si](C)(C)C)C1CC(=O)C2(C)C3=C(C(=O)CC12C)C1(C)CC=C(O[Si](C)(C)C)C(C)(C)C1C=C3O[Si](C)(C)C)O[Si](C)(C)C)C(=O)O	3752.8	Standard non polar	33892256
20-Hydroxy-3,7,11,15,23-pentaoxolanost-8-en-26-oic acid,4TMS,isomer #21	CC(C=C(CC(C)(O[Si](C)(C)C)C1C=C(O[Si](C)(C)C)C2(C)C3=C(C(O[Si](C)(C)C)=CC12C)C1(C)CCC(=O)C(C)(C)C1CC3=O)O[Si](C)(C)C)C(=O)O	3658.9	Semi standard non polar	33892256
20-Hydroxy-3,7,11,15,23-pentaoxolanost-8-en-26-oic acid,4TMS,isomer #21	CC(C=C(CC(C)(O[Si](C)(C)C)C1C=C(O[Si](C)(C)C)C2(C)C3=C(C(O[Si](C)(C)C)=CC12C)C1(C)CCC(=O)C(C)(C)C1CC3=O)O[Si](C)(C)C)C(=O)O	3791.6	Standard non polar	33892256
20-Hydroxy-3,7,11,15,23-pentaoxolanost-8-en-26-oic acid,4TMS,isomer #22	CC(C=C(CC(C)(O[Si](C)(C)C)C1C=C(O[Si](C)(C)C)C2(C)C3=C(C(=O)CC12C)C1(C)CC=C(O[Si](C)(C)C)C(C)(C)C1CC3=O)O[Si](C)(C)C)C(=O)O	3639.7	Semi standard non polar	33892256
20-Hydroxy-3,7,11,15,23-pentaoxolanost-8-en-26-oic acid,4TMS,isomer #22	CC(C=C(CC(C)(O[Si](C)(C)C)C1C=C(O[Si](C)(C)C)C2(C)C3=C(C(=O)CC12C)C1(C)CC=C(O[Si](C)(C)C)C(C)(C)C1CC3=O)O[Si](C)(C)C)C(=O)O	3643.5	Standard non polar	33892256
20-Hydroxy-3,7,11,15,23-pentaoxolanost-8-en-26-oic acid,4TMS,isomer #23	CC(C=C(CC(C)(O[Si](C)(C)C)C1C=C(O[Si](C)(C)C)C2(C)C3=C(C(=O)CC12C)C1(C)CCC(=O)C(C)(C)C1C=C3O[Si](C)(C)C)O[Si](C)(C)C)C(=O)O	3728.0	Semi standard non polar	33892256
20-Hydroxy-3,7,11,15,23-pentaoxolanost-8-en-26-oic acid,4TMS,isomer #23	CC(C=C(CC(C)(O[Si](C)(C)C)C1C=C(O[Si](C)(C)C)C2(C)C3=C(C(=O)CC12C)C1(C)CCC(=O)C(C)(C)C1C=C3O[Si](C)(C)C)O[Si](C)(C)C)C(=O)O	3727.6	Standard non polar	33892256
20-Hydroxy-3,7,11,15,23-pentaoxolanost-8-en-26-oic acid,4TMS,isomer #24	CC(C=C(CC(C)(O[Si](C)(C)C)C1CC(=O)C2(C)C3=C(C(O[Si](C)(C)C)=CC12C)C1(C)CC=C(O[Si](C)(C)C)C(C)(C)C1CC3=O)O[Si](C)(C)C)C(=O)O	3619.8	Semi standard non polar	33892256
20-Hydroxy-3,7,11,15,23-pentaoxolanost-8-en-26-oic acid,4TMS,isomer #24	CC(C=C(CC(C)(O[Si](C)(C)C)C1CC(=O)C2(C)C3=C(C(O[Si](C)(C)C)=CC12C)C1(C)CC=C(O[Si](C)(C)C)C(C)(C)C1CC3=O)O[Si](C)(C)C)C(=O)O	3812.2	Standard non polar	33892256
20-Hydroxy-3,7,11,15,23-pentaoxolanost-8-en-26-oic acid,4TMS,isomer #25	CC(C=C(CC(C)(O[Si](C)(C)C)C1CC(=O)C2(C)C3=C(C(O[Si](C)(C)C)=CC12C)C1(C)CCC(=O)C(C)(C)C1C=C3O[Si](C)(C)C)O[Si](C)(C)C)C(=O)O	3674.8	Semi standard non polar	33892256
20-Hydroxy-3,7,11,15,23-pentaoxolanost-8-en-26-oic acid,4TMS,isomer #25	CC(C=C(CC(C)(O[Si](C)(C)C)C1CC(=O)C2(C)C3=C(C(O[Si](C)(C)C)=CC12C)C1(C)CCC(=O)C(C)(C)C1C=C3O[Si](C)(C)C)O[Si](C)(C)C)C(=O)O	3941.8	Standard non polar	33892256
20-Hydroxy-3,7,11,15,23-pentaoxolanost-8-en-26-oic acid,4TMS,isomer #26	CC(C=C(CC(C)(O[Si](C)(C)C)C1CC(=O)C2(C)C3=C(C(=O)CC12C)C1(C)CC=C(O[Si](C)(C)C)C(C)(C)C1C=C3O[Si](C)(C)C)O[Si](C)(C)C)C(=O)O	3674.8	Semi standard non polar	33892256
20-Hydroxy-3,7,11,15,23-pentaoxolanost-8-en-26-oic acid,4TMS,isomer #26	CC(C=C(CC(C)(O[Si](C)(C)C)C1CC(=O)C2(C)C3=C(C(=O)CC12C)C1(C)CC=C(O[Si](C)(C)C)C(C)(C)C1C=C3O[Si](C)(C)C)O[Si](C)(C)C)C(=O)O	3814.6	Standard non polar	33892256
20-Hydroxy-3,7,11,15,23-pentaoxolanost-8-en-26-oic acid,4TMS,isomer #27	CC(CC(=O)CC(C)(O[Si](C)(C)C)C1C=C(O[Si](C)(C)C)C2(C)C3=C(C(O[Si](C)(C)C)=CC12C)C1(C)CC=C(O[Si](C)(C)C)C(C)(C)C1CC3=O)C(=O)O	3581.4	Semi standard non polar	33892256
20-Hydroxy-3,7,11,15,23-pentaoxolanost-8-en-26-oic acid,4TMS,isomer #27	CC(CC(=O)CC(C)(O[Si](C)(C)C)C1C=C(O[Si](C)(C)C)C2(C)C3=C(C(O[Si](C)(C)C)=CC12C)C1(C)CC=C(O[Si](C)(C)C)C(C)(C)C1CC3=O)C(=O)O	3652.8	Standard non polar	33892256
20-Hydroxy-3,7,11,15,23-pentaoxolanost-8-en-26-oic acid,4TMS,isomer #28	CC(CC(=O)CC(C)(O[Si](C)(C)C)C1C=C(O[Si](C)(C)C)C2(C)C3=C(C(O[Si](C)(C)C)=CC12C)C1(C)CCC(=O)C(C)(C)C1C=C3O[Si](C)(C)C)C(=O)O	3651.4	Semi standard non polar	33892256
20-Hydroxy-3,7,11,15,23-pentaoxolanost-8-en-26-oic acid,4TMS,isomer #28	CC(CC(=O)CC(C)(O[Si](C)(C)C)C1C=C(O[Si](C)(C)C)C2(C)C3=C(C(O[Si](C)(C)C)=CC12C)C1(C)CCC(=O)C(C)(C)C1C=C3O[Si](C)(C)C)C(=O)O	3705.4	Standard non polar	33892256
20-Hydroxy-3,7,11,15,23-pentaoxolanost-8-en-26-oic acid,4TMS,isomer #29	CC(CC(=O)CC(C)(O[Si](C)(C)C)C1C=C(O[Si](C)(C)C)C2(C)C3=C(C(=O)CC12C)C1(C)CC=C(O[Si](C)(C)C)C(C)(C)C1C=C3O[Si](C)(C)C)C(=O)O	3649.4	Semi standard non polar	33892256
20-Hydroxy-3,7,11,15,23-pentaoxolanost-8-en-26-oic acid,4TMS,isomer #29	CC(CC(=O)CC(C)(O[Si](C)(C)C)C1C=C(O[Si](C)(C)C)C2(C)C3=C(C(=O)CC12C)C1(C)CC=C(O[Si](C)(C)C)C(C)(C)C1C=C3O[Si](C)(C)C)C(=O)O	3606.9	Standard non polar	33892256
20-Hydroxy-3,7,11,15,23-pentaoxolanost-8-en-26-oic acid,4TMS,isomer #3	CC(CC(=CC(C)(O[Si](C)(C)C)C1CC(=O)C2(C)C3=C(C(=O)CC12C)C1(C)CC=C(O[Si](C)(C)C)C(C)(C)C1CC3=O)O[Si](C)(C)C)C(=O)O[Si](C)(C)C	3647.0	Semi standard non polar	33892256
20-Hydroxy-3,7,11,15,23-pentaoxolanost-8-en-26-oic acid,4TMS,isomer #3	CC(CC(=CC(C)(O[Si](C)(C)C)C1CC(=O)C2(C)C3=C(C(=O)CC12C)C1(C)CC=C(O[Si](C)(C)C)C(C)(C)C1CC3=O)O[Si](C)(C)C)C(=O)O[Si](C)(C)C	3806.5	Standard non polar	33892256
20-Hydroxy-3,7,11,15,23-pentaoxolanost-8-en-26-oic acid,4TMS,isomer #30	CC(CC(=O)CC(C)(O[Si](C)(C)C)C1CC(=O)C2(C)C3=C(C(O[Si](C)(C)C)=CC12C)C1(C)CC=C(O[Si](C)(C)C)C(C)(C)C1C=C3O[Si](C)(C)C)C(=O)O	3598.9	Semi standard non polar	33892256
20-Hydroxy-3,7,11,15,23-pentaoxolanost-8-en-26-oic acid,4TMS,isomer #30	CC(CC(=O)CC(C)(O[Si](C)(C)C)C1CC(=O)C2(C)C3=C(C(O[Si](C)(C)C)=CC12C)C1(C)CC=C(O[Si](C)(C)C)C(C)(C)C1C=C3O[Si](C)(C)C)C(=O)O	3761.1	Standard non polar	33892256
20-Hydroxy-3,7,11,15,23-pentaoxolanost-8-en-26-oic acid,4TMS,isomer #31	CC(CC(=CC(C)(O)C1C=C(O[Si](C)(C)C)C2(C)C3=C(C(O[Si](C)(C)C)=CC12C)C1(C)CCC(=O)C(C)(C)C1CC3=O)O[Si](C)(C)C)C(=O)O[Si](C)(C)C	3599.7	Semi standard non polar	33892256
20-Hydroxy-3,7,11,15,23-pentaoxolanost-8-en-26-oic acid,4TMS,isomer #31	CC(CC(=CC(C)(O)C1C=C(O[Si](C)(C)C)C2(C)C3=C(C(O[Si](C)(C)C)=CC12C)C1(C)CCC(=O)C(C)(C)C1CC3=O)O[Si](C)(C)C)C(=O)O[Si](C)(C)C	3784.3	Standard non polar	33892256
20-Hydroxy-3,7,11,15,23-pentaoxolanost-8-en-26-oic acid,4TMS,isomer #32	CC(CC(=CC(C)(O)C1C=C(O[Si](C)(C)C)C2(C)C3=C(C(=O)CC12C)C1(C)CC=C(O[Si](C)(C)C)C(C)(C)C1CC3=O)O[Si](C)(C)C)C(=O)O[Si](C)(C)C	3561.3	Semi standard non polar	33892256
20-Hydroxy-3,7,11,15,23-pentaoxolanost-8-en-26-oic acid,4TMS,isomer #32	CC(CC(=CC(C)(O)C1C=C(O[Si](C)(C)C)C2(C)C3=C(C(=O)CC12C)C1(C)CC=C(O[Si](C)(C)C)C(C)(C)C1CC3=O)O[Si](C)(C)C)C(=O)O[Si](C)(C)C	3645.1	Standard non polar	33892256
20-Hydroxy-3,7,11,15,23-pentaoxolanost-8-en-26-oic acid,4TMS,isomer #33	CC(CC(=CC(C)(O)C1C=C(O[Si](C)(C)C)C2(C)C3=C(C(=O)CC12C)C1(C)CCC(=O)C(C)(C)C1C=C3O[Si](C)(C)C)O[Si](C)(C)C)C(=O)O[Si](C)(C)C	3643.0	Semi standard non polar	33892256
20-Hydroxy-3,7,11,15,23-pentaoxolanost-8-en-26-oic acid,4TMS,isomer #33	CC(CC(=CC(C)(O)C1C=C(O[Si](C)(C)C)C2(C)C3=C(C(=O)CC12C)C1(C)CCC(=O)C(C)(C)C1C=C3O[Si](C)(C)C)O[Si](C)(C)C)C(=O)O[Si](C)(C)C	3719.8	Standard non polar	33892256
20-Hydroxy-3,7,11,15,23-pentaoxolanost-8-en-26-oic acid,4TMS,isomer #34	CC(CC(=CC(C)(O)C1CC(=O)C2(C)C3=C(C(O[Si](C)(C)C)=CC12C)C1(C)CC=C(O[Si](C)(C)C)C(C)(C)C1CC3=O)O[Si](C)(C)C)C(=O)O[Si](C)(C)C	3569.8	Semi standard non polar	33892256
20-Hydroxy-3,7,11,15,23-pentaoxolanost-8-en-26-oic acid,4TMS,isomer #34	CC(CC(=CC(C)(O)C1CC(=O)C2(C)C3=C(C(O[Si](C)(C)C)=CC12C)C1(C)CC=C(O[Si](C)(C)C)C(C)(C)C1CC3=O)O[Si](C)(C)C)C(=O)O[Si](C)(C)C	3777.6	Standard non polar	33892256
20-Hydroxy-3,7,11,15,23-pentaoxolanost-8-en-26-oic acid,4TMS,isomer #35	CC(CC(=CC(C)(O)C1CC(=O)C2(C)C3=C(C(O[Si](C)(C)C)=CC12C)C1(C)CCC(=O)C(C)(C)C1C=C3O[Si](C)(C)C)O[Si](C)(C)C)C(=O)O[Si](C)(C)C	3619.0	Semi standard non polar	33892256
20-Hydroxy-3,7,11,15,23-pentaoxolanost-8-en-26-oic acid,4TMS,isomer #35	CC(CC(=CC(C)(O)C1CC(=O)C2(C)C3=C(C(O[Si](C)(C)C)=CC12C)C1(C)CCC(=O)C(C)(C)C1C=C3O[Si](C)(C)C)O[Si](C)(C)C)C(=O)O[Si](C)(C)C	3908.9	Standard non polar	33892256
20-Hydroxy-3,7,11,15,23-pentaoxolanost-8-en-26-oic acid,4TMS,isomer #36	CC(CC(=CC(C)(O)C1CC(=O)C2(C)C3=C(C(=O)CC12C)C1(C)CC=C(O[Si](C)(C)C)C(C)(C)C1C=C3O[Si](C)(C)C)O[Si](C)(C)C)C(=O)O[Si](C)(C)C	3581.6	Semi standard non polar	33892256
20-Hydroxy-3,7,11,15,23-pentaoxolanost-8-en-26-oic acid,4TMS,isomer #36	CC(CC(=CC(C)(O)C1CC(=O)C2(C)C3=C(C(=O)CC12C)C1(C)CC=C(O[Si](C)(C)C)C(C)(C)C1C=C3O[Si](C)(C)C)O[Si](C)(C)C)C(=O)O[Si](C)(C)C	3786.7	Standard non polar	33892256
20-Hydroxy-3,7,11,15,23-pentaoxolanost-8-en-26-oic acid,4TMS,isomer #37	CC(C=C(CC(C)(O)C1C=C(O[Si](C)(C)C)C2(C)C3=C(C(O[Si](C)(C)C)=CC12C)C1(C)CCC(=O)C(C)(C)C1CC3=O)O[Si](C)(C)C)C(=O)O[Si](C)(C)C	3625.9	Semi standard non polar	33892256
20-Hydroxy-3,7,11,15,23-pentaoxolanost-8-en-26-oic acid,4TMS,isomer #37	CC(C=C(CC(C)(O)C1C=C(O[Si](C)(C)C)C2(C)C3=C(C(O[Si](C)(C)C)=CC12C)C1(C)CCC(=O)C(C)(C)C1CC3=O)O[Si](C)(C)C)C(=O)O[Si](C)(C)C	3801.2	Standard non polar	33892256
20-Hydroxy-3,7,11,15,23-pentaoxolanost-8-en-26-oic acid,4TMS,isomer #38	CC(C=C(CC(C)(O)C1C=C(O[Si](C)(C)C)C2(C)C3=C(C(=O)CC12C)C1(C)CC=C(O[Si](C)(C)C)C(C)(C)C1CC3=O)O[Si](C)(C)C)C(=O)O[Si](C)(C)C	3597.5	Semi standard non polar	33892256
20-Hydroxy-3,7,11,15,23-pentaoxolanost-8-en-26-oic acid,4TMS,isomer #38	CC(C=C(CC(C)(O)C1C=C(O[Si](C)(C)C)C2(C)C3=C(C(=O)CC12C)C1(C)CC=C(O[Si](C)(C)C)C(C)(C)C1CC3=O)O[Si](C)(C)C)C(=O)O[Si](C)(C)C	3677.2	Standard non polar	33892256
20-Hydroxy-3,7,11,15,23-pentaoxolanost-8-en-26-oic acid,4TMS,isomer #39	CC(C=C(CC(C)(O)C1C=C(O[Si](C)(C)C)C2(C)C3=C(C(=O)CC12C)C1(C)CCC(=O)C(C)(C)C1C=C3O[Si](C)(C)C)O[Si](C)(C)C)C(=O)O[Si](C)(C)C	3689.1	Semi standard non polar	33892256
20-Hydroxy-3,7,11,15,23-pentaoxolanost-8-en-26-oic acid,4TMS,isomer #39	CC(C=C(CC(C)(O)C1C=C(O[Si](C)(C)C)C2(C)C3=C(C(=O)CC12C)C1(C)CCC(=O)C(C)(C)C1C=C3O[Si](C)(C)C)O[Si](C)(C)C)C(=O)O[Si](C)(C)C	3740.5	Standard non polar	33892256
20-Hydroxy-3,7,11,15,23-pentaoxolanost-8-en-26-oic acid,4TMS,isomer #4	CC(CC(=CC(C)(O[Si](C)(C)C)C1CC(=O)C2(C)C3=C(C(=O)CC12C)C1(C)CCC(=O)C(C)(C)C1C=C3O[Si](C)(C)C)O[Si](C)(C)C)C(=O)O[Si](C)(C)C	3697.8	Semi standard non polar	33892256
20-Hydroxy-3,7,11,15,23-pentaoxolanost-8-en-26-oic acid,4TMS,isomer #4	CC(CC(=CC(C)(O[Si](C)(C)C)C1CC(=O)C2(C)C3=C(C(=O)CC12C)C1(C)CCC(=O)C(C)(C)C1C=C3O[Si](C)(C)C)O[Si](C)(C)C)C(=O)O[Si](C)(C)C	3961.3	Standard non polar	33892256
20-Hydroxy-3,7,11,15,23-pentaoxolanost-8-en-26-oic acid,4TMS,isomer #40	CC(C=C(CC(C)(O)C1CC(=O)C2(C)C3=C(C(O[Si](C)(C)C)=CC12C)C1(C)CC=C(O[Si](C)(C)C)C(C)(C)C1CC3=O)O[Si](C)(C)C)C(=O)O[Si](C)(C)C	3602.8	Semi standard non polar	33892256
20-Hydroxy-3,7,11,15,23-pentaoxolanost-8-en-26-oic acid,4TMS,isomer #40	CC(C=C(CC(C)(O)C1CC(=O)C2(C)C3=C(C(O[Si](C)(C)C)=CC12C)C1(C)CC=C(O[Si](C)(C)C)C(C)(C)C1CC3=O)O[Si](C)(C)C)C(=O)O[Si](C)(C)C	3814.5	Standard non polar	33892256
20-Hydroxy-3,7,11,15,23-pentaoxolanost-8-en-26-oic acid,4TMS,isomer #41	CC(C=C(CC(C)(O)C1CC(=O)C2(C)C3=C(C(O[Si](C)(C)C)=CC12C)C1(C)CCC(=O)C(C)(C)C1C=C3O[Si](C)(C)C)O[Si](C)(C)C)C(=O)O[Si](C)(C)C	3661.6	Semi standard non polar	33892256
20-Hydroxy-3,7,11,15,23-pentaoxolanost-8-en-26-oic acid,4TMS,isomer #41	CC(C=C(CC(C)(O)C1CC(=O)C2(C)C3=C(C(O[Si](C)(C)C)=CC12C)C1(C)CCC(=O)C(C)(C)C1C=C3O[Si](C)(C)C)O[Si](C)(C)C)C(=O)O[Si](C)(C)C	3943.1	Standard non polar	33892256
20-Hydroxy-3,7,11,15,23-pentaoxolanost-8-en-26-oic acid,4TMS,isomer #42	CC(C=C(CC(C)(O)C1CC(=O)C2(C)C3=C(C(=O)CC12C)C1(C)CC=C(O[Si](C)(C)C)C(C)(C)C1C=C3O[Si](C)(C)C)O[Si](C)(C)C)C(=O)O[Si](C)(C)C	3628.2	Semi standard non polar	33892256
20-Hydroxy-3,7,11,15,23-pentaoxolanost-8-en-26-oic acid,4TMS,isomer #42	CC(C=C(CC(C)(O)C1CC(=O)C2(C)C3=C(C(=O)CC12C)C1(C)CC=C(O[Si](C)(C)C)C(C)(C)C1C=C3O[Si](C)(C)C)O[Si](C)(C)C)C(=O)O[Si](C)(C)C	3824.8	Standard non polar	33892256
20-Hydroxy-3,7,11,15,23-pentaoxolanost-8-en-26-oic acid,4TMS,isomer #43	CC(CC(=O)CC(C)(O)C1C=C(O[Si](C)(C)C)C2(C)C3=C(C(O[Si](C)(C)C)=CC12C)C1(C)CC=C(O[Si](C)(C)C)C(C)(C)C1CC3=O)C(=O)O[Si](C)(C)C	3561.6	Semi standard non polar	33892256
20-Hydroxy-3,7,11,15,23-pentaoxolanost-8-en-26-oic acid,4TMS,isomer #43	CC(CC(=O)CC(C)(O)C1C=C(O[Si](C)(C)C)C2(C)C3=C(C(O[Si](C)(C)C)=CC12C)C1(C)CC=C(O[Si](C)(C)C)C(C)(C)C1CC3=O)C(=O)O[Si](C)(C)C	3669.8	Standard non polar	33892256
20-Hydroxy-3,7,11,15,23-pentaoxolanost-8-en-26-oic acid,4TMS,isomer #44	CC(CC(=O)CC(C)(O)C1C=C(O[Si](C)(C)C)C2(C)C3=C(C(O[Si](C)(C)C)=CC12C)C1(C)CCC(=O)C(C)(C)C1C=C3O[Si](C)(C)C)C(=O)O[Si](C)(C)C	3649.4	Semi standard non polar	33892256
20-Hydroxy-3,7,11,15,23-pentaoxolanost-8-en-26-oic acid,4TMS,isomer #44	CC(CC(=O)CC(C)(O)C1C=C(O[Si](C)(C)C)C2(C)C3=C(C(O[Si](C)(C)C)=CC12C)C1(C)CCC(=O)C(C)(C)C1C=C3O[Si](C)(C)C)C(=O)O[Si](C)(C)C	3721.0	Standard non polar	33892256
20-Hydroxy-3,7,11,15,23-pentaoxolanost-8-en-26-oic acid,4TMS,isomer #45	CC(CC(=O)CC(C)(O)C1C=C(O[Si](C)(C)C)C2(C)C3=C(C(=O)CC12C)C1(C)CC=C(O[Si](C)(C)C)C(C)(C)C1C=C3O[Si](C)(C)C)C(=O)O[Si](C)(C)C	3623.7	Semi standard non polar	33892256
20-Hydroxy-3,7,11,15,23-pentaoxolanost-8-en-26-oic acid,4TMS,isomer #45	CC(CC(=O)CC(C)(O)C1C=C(O[Si](C)(C)C)C2(C)C3=C(C(=O)CC12C)C1(C)CC=C(O[Si](C)(C)C)C(C)(C)C1C=C3O[Si](C)(C)C)C(=O)O[Si](C)(C)C	3627.4	Standard non polar	33892256
20-Hydroxy-3,7,11,15,23-pentaoxolanost-8-en-26-oic acid,4TMS,isomer #46	CC(CC(=O)CC(C)(O)C1CC(=O)C2(C)C3=C(C(O[Si](C)(C)C)=CC12C)C1(C)CC=C(O[Si](C)(C)C)C(C)(C)C1C=C3O[Si](C)(C)C)C(=O)O[Si](C)(C)C	3602.8	Semi standard non polar	33892256
20-Hydroxy-3,7,11,15,23-pentaoxolanost-8-en-26-oic acid,4TMS,isomer #46	CC(CC(=O)CC(C)(O)C1CC(=O)C2(C)C3=C(C(O[Si](C)(C)C)=CC12C)C1(C)CC=C(O[Si](C)(C)C)C(C)(C)C1C=C3O[Si](C)(C)C)C(=O)O[Si](C)(C)C	3770.6	Standard non polar	33892256
20-Hydroxy-3,7,11,15,23-pentaoxolanost-8-en-26-oic acid,4TMS,isomer #47	CC(CC(=CC(C)(O)C1C=C(O[Si](C)(C)C)C2(C)C3=C(C(O[Si](C)(C)C)=CC12C)C1(C)CC=C(O[Si](C)(C)C)C(C)(C)C1CC3=O)O[Si](C)(C)C)C(=O)O	3561.3	Semi standard non polar	33892256
20-Hydroxy-3,7,11,15,23-pentaoxolanost-8-en-26-oic acid,4TMS,isomer #47	CC(CC(=CC(C)(O)C1C=C(O[Si](C)(C)C)C2(C)C3=C(C(O[Si](C)(C)C)=CC12C)C1(C)CC=C(O[Si](C)(C)C)C(C)(C)C1CC3=O)O[Si](C)(C)C)C(=O)O	3607.0	Standard non polar	33892256
20-Hydroxy-3,7,11,15,23-pentaoxolanost-8-en-26-oic acid,4TMS,isomer #48	CC(CC(=CC(C)(O)C1C=C(O[Si](C)(C)C)C2(C)C3=C(C(O[Si](C)(C)C)=CC12C)C1(C)CCC(=O)C(C)(C)C1C=C3O[Si](C)(C)C)O[Si](C)(C)C)C(=O)O	3634.3	Semi standard non polar	33892256
20-Hydroxy-3,7,11,15,23-pentaoxolanost-8-en-26-oic acid,4TMS,isomer #48	CC(CC(=CC(C)(O)C1C=C(O[Si](C)(C)C)C2(C)C3=C(C(O[Si](C)(C)C)=CC12C)C1(C)CCC(=O)C(C)(C)C1C=C3O[Si](C)(C)C)O[Si](C)(C)C)C(=O)O	3678.9	Standard non polar	33892256
20-Hydroxy-3,7,11,15,23-pentaoxolanost-8-en-26-oic acid,4TMS,isomer #49	CC(CC(=CC(C)(O)C1C=C(O[Si](C)(C)C)C2(C)C3=C(C(=O)CC12C)C1(C)CC=C(O[Si](C)(C)C)C(C)(C)C1C=C3O[Si](C)(C)C)O[Si](C)(C)C)C(=O)O	3601.5	Semi standard non polar	33892256
20-Hydroxy-3,7,11,15,23-pentaoxolanost-8-en-26-oic acid,4TMS,isomer #49	CC(CC(=CC(C)(O)C1C=C(O[Si](C)(C)C)C2(C)C3=C(C(=O)CC12C)C1(C)CC=C(O[Si](C)(C)C)C(C)(C)C1C=C3O[Si](C)(C)C)O[Si](C)(C)C)C(=O)O	3553.9	Standard non polar	33892256
20-Hydroxy-3,7,11,15,23-pentaoxolanost-8-en-26-oic acid,4TMS,isomer #5	CC(C=C(CC(C)(O[Si](C)(C)C)C1C=C(O[Si](C)(C)C)C2(C)C3=C(C(=O)CC12C)C1(C)CCC(=O)C(C)(C)C1CC3=O)O[Si](C)(C)C)C(=O)O[Si](C)(C)C	3737.9	Semi standard non polar	33892256
20-Hydroxy-3,7,11,15,23-pentaoxolanost-8-en-26-oic acid,4TMS,isomer #5	CC(C=C(CC(C)(O[Si](C)(C)C)C1C=C(O[Si](C)(C)C)C2(C)C3=C(C(=O)CC12C)C1(C)CCC(=O)C(C)(C)C1CC3=O)O[Si](C)(C)C)C(=O)O[Si](C)(C)C	3791.1	Standard non polar	33892256
20-Hydroxy-3,7,11,15,23-pentaoxolanost-8-en-26-oic acid,4TMS,isomer #50	CC(CC(=CC(C)(O)C1CC(=O)C2(C)C3=C(C(O[Si](C)(C)C)=CC12C)C1(C)CC=C(O[Si](C)(C)C)C(C)(C)C1C=C3O[Si](C)(C)C)O[Si](C)(C)C)C(=O)O	3588.1	Semi standard non polar	33892256
20-Hydroxy-3,7,11,15,23-pentaoxolanost-8-en-26-oic acid,4TMS,isomer #50	CC(CC(=CC(C)(O)C1CC(=O)C2(C)C3=C(C(O[Si](C)(C)C)=CC12C)C1(C)CC=C(O[Si](C)(C)C)C(C)(C)C1C=C3O[Si](C)(C)C)O[Si](C)(C)C)C(=O)O	3704.4	Standard non polar	33892256
20-Hydroxy-3,7,11,15,23-pentaoxolanost-8-en-26-oic acid,4TMS,isomer #51	CC(C=C(CC(C)(O)C1C=C(O[Si](C)(C)C)C2(C)C3=C(C(O[Si](C)(C)C)=CC12C)C1(C)CC=C(O[Si](C)(C)C)C(C)(C)C1CC3=O)O[Si](C)(C)C)C(=O)O	3572.1	Semi standard non polar	33892256
20-Hydroxy-3,7,11,15,23-pentaoxolanost-8-en-26-oic acid,4TMS,isomer #51	CC(C=C(CC(C)(O)C1C=C(O[Si](C)(C)C)C2(C)C3=C(C(O[Si](C)(C)C)=CC12C)C1(C)CC=C(O[Si](C)(C)C)C(C)(C)C1CC3=O)O[Si](C)(C)C)C(=O)O	3658.3	Standard non polar	33892256
20-Hydroxy-3,7,11,15,23-pentaoxolanost-8-en-26-oic acid,4TMS,isomer #52	CC(C=C(CC(C)(O)C1C=C(O[Si](C)(C)C)C2(C)C3=C(C(O[Si](C)(C)C)=CC12C)C1(C)CCC(=O)C(C)(C)C1C=C3O[Si](C)(C)C)O[Si](C)(C)C)C(=O)O	3660.9	Semi standard non polar	33892256
20-Hydroxy-3,7,11,15,23-pentaoxolanost-8-en-26-oic acid,4TMS,isomer #52	CC(C=C(CC(C)(O)C1C=C(O[Si](C)(C)C)C2(C)C3=C(C(O[Si](C)(C)C)=CC12C)C1(C)CCC(=O)C(C)(C)C1C=C3O[Si](C)(C)C)O[Si](C)(C)C)C(=O)O	3722.8	Standard non polar	33892256
20-Hydroxy-3,7,11,15,23-pentaoxolanost-8-en-26-oic acid,4TMS,isomer #53	CC(C=C(CC(C)(O)C1C=C(O[Si](C)(C)C)C2(C)C3=C(C(=O)CC12C)C1(C)CC=C(O[Si](C)(C)C)C(C)(C)C1C=C3O[Si](C)(C)C)O[Si](C)(C)C)C(=O)O	3643.9	Semi standard non polar	33892256
20-Hydroxy-3,7,11,15,23-pentaoxolanost-8-en-26-oic acid,4TMS,isomer #53	CC(C=C(CC(C)(O)C1C=C(O[Si](C)(C)C)C2(C)C3=C(C(=O)CC12C)C1(C)CC=C(O[Si](C)(C)C)C(C)(C)C1C=C3O[Si](C)(C)C)O[Si](C)(C)C)C(=O)O	3607.4	Standard non polar	33892256
20-Hydroxy-3,7,11,15,23-pentaoxolanost-8-en-26-oic acid,4TMS,isomer #54	CC(C=C(CC(C)(O)C1CC(=O)C2(C)C3=C(C(O[Si](C)(C)C)=CC12C)C1(C)CC=C(O[Si](C)(C)C)C(C)(C)C1C=C3O[Si](C)(C)C)O[Si](C)(C)C)C(=O)O	3621.7	Semi standard non polar	33892256
20-Hydroxy-3,7,11,15,23-pentaoxolanost-8-en-26-oic acid,4TMS,isomer #54	CC(C=C(CC(C)(O)C1CC(=O)C2(C)C3=C(C(O[Si](C)(C)C)=CC12C)C1(C)CC=C(O[Si](C)(C)C)C(C)(C)C1C=C3O[Si](C)(C)C)O[Si](C)(C)C)C(=O)O	3774.6	Standard non polar	33892256
20-Hydroxy-3,7,11,15,23-pentaoxolanost-8-en-26-oic acid,4TMS,isomer #55	CC(CC(=O)CC(C)(O)C1C=C(O[Si](C)(C)C)C2(C)C3=C(C(O[Si](C)(C)C)=CC12C)C1(C)CC=C(O[Si](C)(C)C)C(C)(C)C1C=C3O[Si](C)(C)C)C(=O)O	3593.6	Semi standard non polar	33892256
20-Hydroxy-3,7,11,15,23-pentaoxolanost-8-en-26-oic acid,4TMS,isomer #55	CC(CC(=O)CC(C)(O)C1C=C(O[Si](C)(C)C)C2(C)C3=C(C(O[Si](C)(C)C)=CC12C)C1(C)CC=C(O[Si](C)(C)C)C(C)(C)C1C=C3O[Si](C)(C)C)C(=O)O	3622.3	Standard non polar	33892256
20-Hydroxy-3,7,11,15,23-pentaoxolanost-8-en-26-oic acid,4TMS,isomer #6	CC(C=C(CC(C)(O[Si](C)(C)C)C1CC(=O)C2(C)C3=C(C(O[Si](C)(C)C)=CC12C)C1(C)CCC(=O)C(C)(C)C1CC3=O)O[Si](C)(C)C)C(=O)O[Si](C)(C)C	3701.6	Semi standard non polar	33892256
20-Hydroxy-3,7,11,15,23-pentaoxolanost-8-en-26-oic acid,4TMS,isomer #6	CC(C=C(CC(C)(O[Si](C)(C)C)C1CC(=O)C2(C)C3=C(C(O[Si](C)(C)C)=CC12C)C1(C)CCC(=O)C(C)(C)C1CC3=O)O[Si](C)(C)C)C(=O)O[Si](C)(C)C	3990.1	Standard non polar	33892256
20-Hydroxy-3,7,11,15,23-pentaoxolanost-8-en-26-oic acid,4TMS,isomer #7	CC(C=C(CC(C)(O[Si](C)(C)C)C1CC(=O)C2(C)C3=C(C(=O)CC12C)C1(C)CC=C(O[Si](C)(C)C)C(C)(C)C1CC3=O)O[Si](C)(C)C)C(=O)O[Si](C)(C)C	3681.6	Semi standard non polar	33892256
20-Hydroxy-3,7,11,15,23-pentaoxolanost-8-en-26-oic acid,4TMS,isomer #7	CC(C=C(CC(C)(O[Si](C)(C)C)C1CC(=O)C2(C)C3=C(C(=O)CC12C)C1(C)CC=C(O[Si](C)(C)C)C(C)(C)C1CC3=O)O[Si](C)(C)C)C(=O)O[Si](C)(C)C	3835.8	Standard non polar	33892256
20-Hydroxy-3,7,11,15,23-pentaoxolanost-8-en-26-oic acid,4TMS,isomer #8	CC(C=C(CC(C)(O[Si](C)(C)C)C1CC(=O)C2(C)C3=C(C(=O)CC12C)C1(C)CCC(=O)C(C)(C)C1C=C3O[Si](C)(C)C)O[Si](C)(C)C)C(=O)O[Si](C)(C)C	3740.1	Semi standard non polar	33892256
20-Hydroxy-3,7,11,15,23-pentaoxolanost-8-en-26-oic acid,4TMS,isomer #8	CC(C=C(CC(C)(O[Si](C)(C)C)C1CC(=O)C2(C)C3=C(C(=O)CC12C)C1(C)CCC(=O)C(C)(C)C1C=C3O[Si](C)(C)C)O[Si](C)(C)C)C(=O)O[Si](C)(C)C	3991.7	Standard non polar	33892256
20-Hydroxy-3,7,11,15,23-pentaoxolanost-8-en-26-oic acid,4TMS,isomer #9	CC(CC(=O)CC(C)(O[Si](C)(C)C)C1C=C(O[Si](C)(C)C)C2(C)C3=C(C(O[Si](C)(C)C)=CC12C)C1(C)CCC(=O)C(C)(C)C1CC3=O)C(=O)O[Si](C)(C)C	3666.9	Semi standard non polar	33892256
20-Hydroxy-3,7,11,15,23-pentaoxolanost-8-en-26-oic acid,4TMS,isomer #9	CC(CC(=O)CC(C)(O[Si](C)(C)C)C1C=C(O[Si](C)(C)C)C2(C)C3=C(C(O[Si](C)(C)C)=CC12C)C1(C)CCC(=O)C(C)(C)C1CC3=O)C(=O)O[Si](C)(C)C	3774.8	Standard non polar	33892256
20-Hydroxy-3,7,11,15,23-pentaoxolanost-8-en-26-oic acid,5TMS,isomer #1	CC(CC(=CC(C)(O[Si](C)(C)C)C1C=C(O[Si](C)(C)C)C2(C)C3=C(C(O[Si](C)(C)C)=CC12C)C1(C)CCC(=O)C(C)(C)C1CC3=O)O[Si](C)(C)C)C(=O)O[Si](C)(C)C	3590.7	Semi standard non polar	33892256
20-Hydroxy-3,7,11,15,23-pentaoxolanost-8-en-26-oic acid,5TMS,isomer #1	CC(CC(=CC(C)(O[Si](C)(C)C)C1C=C(O[Si](C)(C)C)C2(C)C3=C(C(O[Si](C)(C)C)=CC12C)C1(C)CCC(=O)C(C)(C)C1CC3=O)O[Si](C)(C)C)C(=O)O[Si](C)(C)C	3799.4	Standard non polar	33892256
20-Hydroxy-3,7,11,15,23-pentaoxolanost-8-en-26-oic acid,5TMS,isomer #10	CC(C=C(CC(C)(O[Si](C)(C)C)C1CC(=O)C2(C)C3=C(C(O[Si](C)(C)C)=CC12C)C1(C)CC=C(O[Si](C)(C)C)C(C)(C)C1CC3=O)O[Si](C)(C)C)C(=O)O[Si](C)(C)C	3559.9	Semi standard non polar	33892256
20-Hydroxy-3,7,11,15,23-pentaoxolanost-8-en-26-oic acid,5TMS,isomer #10	CC(C=C(CC(C)(O[Si](C)(C)C)C1CC(=O)C2(C)C3=C(C(O[Si](C)(C)C)=CC12C)C1(C)CC=C(O[Si](C)(C)C)C(C)(C)C1CC3=O)O[Si](C)(C)C)C(=O)O[Si](C)(C)C	3821.5	Standard non polar	33892256
20-Hydroxy-3,7,11,15,23-pentaoxolanost-8-en-26-oic acid,5TMS,isomer #11	CC(C=C(CC(C)(O[Si](C)(C)C)C1CC(=O)C2(C)C3=C(C(O[Si](C)(C)C)=CC12C)C1(C)CCC(=O)C(C)(C)C1C=C3O[Si](C)(C)C)O[Si](C)(C)C)C(=O)O[Si](C)(C)C	3627.5	Semi standard non polar	33892256
20-Hydroxy-3,7,11,15,23-pentaoxolanost-8-en-26-oic acid,5TMS,isomer #11	CC(C=C(CC(C)(O[Si](C)(C)C)C1CC(=O)C2(C)C3=C(C(O[Si](C)(C)C)=CC12C)C1(C)CCC(=O)C(C)(C)C1C=C3O[Si](C)(C)C)O[Si](C)(C)C)C(=O)O[Si](C)(C)C	3944.8	Standard non polar	33892256
20-Hydroxy-3,7,11,15,23-pentaoxolanost-8-en-26-oic acid,5TMS,isomer #12	CC(C=C(CC(C)(O[Si](C)(C)C)C1CC(=O)C2(C)C3=C(C(=O)CC12C)C1(C)CC=C(O[Si](C)(C)C)C(C)(C)C1C=C3O[Si](C)(C)C)O[Si](C)(C)C)C(=O)O[Si](C)(C)C	3617.7	Semi standard non polar	33892256
20-Hydroxy-3,7,11,15,23-pentaoxolanost-8-en-26-oic acid,5TMS,isomer #12	CC(C=C(CC(C)(O[Si](C)(C)C)C1CC(=O)C2(C)C3=C(C(=O)CC12C)C1(C)CC=C(O[Si](C)(C)C)C(C)(C)C1C=C3O[Si](C)(C)C)O[Si](C)(C)C)C(=O)O[Si](C)(C)C	3821.6	Standard non polar	33892256
20-Hydroxy-3,7,11,15,23-pentaoxolanost-8-en-26-oic acid,5TMS,isomer #13	CC(CC(=O)CC(C)(O[Si](C)(C)C)C1C=C(O[Si](C)(C)C)C2(C)C3=C(C(O[Si](C)(C)C)=CC12C)C1(C)CC=C(O[Si](C)(C)C)C(C)(C)C1CC3=O)C(=O)O[Si](C)(C)C	3539.2	Semi standard non polar	33892256
20-Hydroxy-3,7,11,15,23-pentaoxolanost-8-en-26-oic acid,5TMS,isomer #13	CC(CC(=O)CC(C)(O[Si](C)(C)C)C1C=C(O[Si](C)(C)C)C2(C)C3=C(C(O[Si](C)(C)C)=CC12C)C1(C)CC=C(O[Si](C)(C)C)C(C)(C)C1CC3=O)C(=O)O[Si](C)(C)C	3688.6	Standard non polar	33892256
20-Hydroxy-3,7,11,15,23-pentaoxolanost-8-en-26-oic acid,5TMS,isomer #14	CC(CC(=O)CC(C)(O[Si](C)(C)C)C1C=C(O[Si](C)(C)C)C2(C)C3=C(C(O[Si](C)(C)C)=CC12C)C1(C)CCC(=O)C(C)(C)C1C=C3O[Si](C)(C)C)C(=O)O[Si](C)(C)C	3622.3	Semi standard non polar	33892256
20-Hydroxy-3,7,11,15,23-pentaoxolanost-8-en-26-oic acid,5TMS,isomer #14	CC(CC(=O)CC(C)(O[Si](C)(C)C)C1C=C(O[Si](C)(C)C)C2(C)C3=C(C(O[Si](C)(C)C)=CC12C)C1(C)CCC(=O)C(C)(C)C1C=C3O[Si](C)(C)C)C(=O)O[Si](C)(C)C	3736.6	Standard non polar	33892256
20-Hydroxy-3,7,11,15,23-pentaoxolanost-8-en-26-oic acid,5TMS,isomer #15	CC(CC(=O)CC(C)(O[Si](C)(C)C)C1C=C(O[Si](C)(C)C)C2(C)C3=C(C(=O)CC12C)C1(C)CC=C(O[Si](C)(C)C)C(C)(C)C1C=C3O[Si](C)(C)C)C(=O)O[Si](C)(C)C	3606.1	Semi standard non polar	33892256
20-Hydroxy-3,7,11,15,23-pentaoxolanost-8-en-26-oic acid,5TMS,isomer #15	CC(CC(=O)CC(C)(O[Si](C)(C)C)C1C=C(O[Si](C)(C)C)C2(C)C3=C(C(=O)CC12C)C1(C)CC=C(O[Si](C)(C)C)C(C)(C)C1C=C3O[Si](C)(C)C)C(=O)O[Si](C)(C)C	3635.9	Standard non polar	33892256
20-Hydroxy-3,7,11,15,23-pentaoxolanost-8-en-26-oic acid,5TMS,isomer #16	CC(CC(=O)CC(C)(O[Si](C)(C)C)C1CC(=O)C2(C)C3=C(C(O[Si](C)(C)C)=CC12C)C1(C)CC=C(O[Si](C)(C)C)C(C)(C)C1C=C3O[Si](C)(C)C)C(=O)O[Si](C)(C)C	3558.5	Semi standard non polar	33892256
20-Hydroxy-3,7,11,15,23-pentaoxolanost-8-en-26-oic acid,5TMS,isomer #16	CC(CC(=O)CC(C)(O[Si](C)(C)C)C1CC(=O)C2(C)C3=C(C(O[Si](C)(C)C)=CC12C)C1(C)CC=C(O[Si](C)(C)C)C(C)(C)C1C=C3O[Si](C)(C)C)C(=O)O[Si](C)(C)C	3784.1	Standard non polar	33892256
20-Hydroxy-3,7,11,15,23-pentaoxolanost-8-en-26-oic acid,5TMS,isomer #17	CC(CC(=CC(C)(O[Si](C)(C)C)C1C=C(O[Si](C)(C)C)C2(C)C3=C(C(O[Si](C)(C)C)=CC12C)C1(C)CC=C(O[Si](C)(C)C)C(C)(C)C1CC3=O)O[Si](C)(C)C)C(=O)O	3531.9	Semi standard non polar	33892256
20-Hydroxy-3,7,11,15,23-pentaoxolanost-8-en-26-oic acid,5TMS,isomer #17	CC(CC(=CC(C)(O[Si](C)(C)C)C1C=C(O[Si](C)(C)C)C2(C)C3=C(C(O[Si](C)(C)C)=CC12C)C1(C)CC=C(O[Si](C)(C)C)C(C)(C)C1CC3=O)O[Si](C)(C)C)C(=O)O	3620.4	Standard non polar	33892256
20-Hydroxy-3,7,11,15,23-pentaoxolanost-8-en-26-oic acid,5TMS,isomer #18	CC(CC(=CC(C)(O[Si](C)(C)C)C1C=C(O[Si](C)(C)C)C2(C)C3=C(C(O[Si](C)(C)C)=CC12C)C1(C)CCC(=O)C(C)(C)C1C=C3O[Si](C)(C)C)O[Si](C)(C)C)C(=O)O	3618.7	Semi standard non polar	33892256
20-Hydroxy-3,7,11,15,23-pentaoxolanost-8-en-26-oic acid,5TMS,isomer #18	CC(CC(=CC(C)(O[Si](C)(C)C)C1C=C(O[Si](C)(C)C)C2(C)C3=C(C(O[Si](C)(C)C)=CC12C)C1(C)CCC(=O)C(C)(C)C1C=C3O[Si](C)(C)C)O[Si](C)(C)C)C(=O)O	3688.2	Standard non polar	33892256
20-Hydroxy-3,7,11,15,23-pentaoxolanost-8-en-26-oic acid,5TMS,isomer #19	CC(CC(=CC(C)(O[Si](C)(C)C)C1C=C(O[Si](C)(C)C)C2(C)C3=C(C(=O)CC12C)C1(C)CC=C(O[Si](C)(C)C)C(C)(C)C1C=C3O[Si](C)(C)C)O[Si](C)(C)C)C(=O)O	3589.7	Semi standard non polar	33892256
20-Hydroxy-3,7,11,15,23-pentaoxolanost-8-en-26-oic acid,5TMS,isomer #19	CC(CC(=CC(C)(O[Si](C)(C)C)C1C=C(O[Si](C)(C)C)C2(C)C3=C(C(=O)CC12C)C1(C)CC=C(O[Si](C)(C)C)C(C)(C)C1C=C3O[Si](C)(C)C)O[Si](C)(C)C)C(=O)O	3557.5	Standard non polar	33892256
20-Hydroxy-3,7,11,15,23-pentaoxolanost-8-en-26-oic acid,5TMS,isomer #2	CC(CC(=CC(C)(O[Si](C)(C)C)C1C=C(O[Si](C)(C)C)C2(C)C3=C(C(=O)CC12C)C1(C)CC=C(O[Si](C)(C)C)C(C)(C)C1CC3=O)O[Si](C)(C)C)C(=O)O[Si](C)(C)C	3554.5	Semi standard non polar	33892256
20-Hydroxy-3,7,11,15,23-pentaoxolanost-8-en-26-oic acid,5TMS,isomer #2	CC(CC(=CC(C)(O[Si](C)(C)C)C1C=C(O[Si](C)(C)C)C2(C)C3=C(C(=O)CC12C)C1(C)CC=C(O[Si](C)(C)C)C(C)(C)C1CC3=O)O[Si](C)(C)C)C(=O)O[Si](C)(C)C	3638.4	Standard non polar	33892256
20-Hydroxy-3,7,11,15,23-pentaoxolanost-8-en-26-oic acid,5TMS,isomer #20	CC(CC(=CC(C)(O[Si](C)(C)C)C1CC(=O)C2(C)C3=C(C(O[Si](C)(C)C)=CC12C)C1(C)CC=C(O[Si](C)(C)C)C(C)(C)C1C=C3O[Si](C)(C)C)O[Si](C)(C)C)C(=O)O	3553.0	Semi standard non polar	33892256
20-Hydroxy-3,7,11,15,23-pentaoxolanost-8-en-26-oic acid,5TMS,isomer #20	CC(CC(=CC(C)(O[Si](C)(C)C)C1CC(=O)C2(C)C3=C(C(O[Si](C)(C)C)=CC12C)C1(C)CC=C(O[Si](C)(C)C)C(C)(C)C1C=C3O[Si](C)(C)C)O[Si](C)(C)C)C(=O)O	3716.7	Standard non polar	33892256
20-Hydroxy-3,7,11,15,23-pentaoxolanost-8-en-26-oic acid,5TMS,isomer #21	CC(C=C(CC(C)(O[Si](C)(C)C)C1C=C(O[Si](C)(C)C)C2(C)C3=C(C(O[Si](C)(C)C)=CC12C)C1(C)CC=C(O[Si](C)(C)C)C(C)(C)C1CC3=O)O[Si](C)(C)C)C(=O)O	3540.7	Semi standard non polar	33892256
20-Hydroxy-3,7,11,15,23-pentaoxolanost-8-en-26-oic acid,5TMS,isomer #21	CC(C=C(CC(C)(O[Si](C)(C)C)C1C=C(O[Si](C)(C)C)C2(C)C3=C(C(O[Si](C)(C)C)=CC12C)C1(C)CC=C(O[Si](C)(C)C)C(C)(C)C1CC3=O)O[Si](C)(C)C)C(=O)O	3662.6	Standard non polar	33892256
20-Hydroxy-3,7,11,15,23-pentaoxolanost-8-en-26-oic acid,5TMS,isomer #22	CC(C=C(CC(C)(O[Si](C)(C)C)C1C=C(O[Si](C)(C)C)C2(C)C3=C(C(O[Si](C)(C)C)=CC12C)C1(C)CCC(=O)C(C)(C)C1C=C3O[Si](C)(C)C)O[Si](C)(C)C)C(=O)O	3635.7	Semi standard non polar	33892256
20-Hydroxy-3,7,11,15,23-pentaoxolanost-8-en-26-oic acid,5TMS,isomer #22	CC(C=C(CC(C)(O[Si](C)(C)C)C1C=C(O[Si](C)(C)C)C2(C)C3=C(C(O[Si](C)(C)C)=CC12C)C1(C)CCC(=O)C(C)(C)C1C=C3O[Si](C)(C)C)O[Si](C)(C)C)C(=O)O	3715.4	Standard non polar	33892256
20-Hydroxy-3,7,11,15,23-pentaoxolanost-8-en-26-oic acid,5TMS,isomer #23	CC(C=C(CC(C)(O[Si](C)(C)C)C1C=C(O[Si](C)(C)C)C2(C)C3=C(C(=O)CC12C)C1(C)CC=C(O[Si](C)(C)C)C(C)(C)C1C=C3O[Si](C)(C)C)O[Si](C)(C)C)C(=O)O	3611.3	Semi standard non polar	33892256
20-Hydroxy-3,7,11,15,23-pentaoxolanost-8-en-26-oic acid,5TMS,isomer #23	CC(C=C(CC(C)(O[Si](C)(C)C)C1C=C(O[Si](C)(C)C)C2(C)C3=C(C(=O)CC12C)C1(C)CC=C(O[Si](C)(C)C)C(C)(C)C1C=C3O[Si](C)(C)C)O[Si](C)(C)C)C(=O)O	3604.0	Standard non polar	33892256
20-Hydroxy-3,7,11,15,23-pentaoxolanost-8-en-26-oic acid,5TMS,isomer #24	CC(C=C(CC(C)(O[Si](C)(C)C)C1CC(=O)C2(C)C3=C(C(O[Si](C)(C)C)=CC12C)C1(C)CC=C(O[Si](C)(C)C)C(C)(C)C1C=C3O[Si](C)(C)C)O[Si](C)(C)C)C(=O)O	3576.6	Semi standard non polar	33892256
20-Hydroxy-3,7,11,15,23-pentaoxolanost-8-en-26-oic acid,5TMS,isomer #24	CC(C=C(CC(C)(O[Si](C)(C)C)C1CC(=O)C2(C)C3=C(C(O[Si](C)(C)C)=CC12C)C1(C)CC=C(O[Si](C)(C)C)C(C)(C)C1C=C3O[Si](C)(C)C)O[Si](C)(C)C)C(=O)O	3766.3	Standard non polar	33892256
20-Hydroxy-3,7,11,15,23-pentaoxolanost-8-en-26-oic acid,5TMS,isomer #25	CC(CC(=O)CC(C)(O[Si](C)(C)C)C1C=C(O[Si](C)(C)C)C2(C)C3=C(C(O[Si](C)(C)C)=CC12C)C1(C)CC=C(O[Si](C)(C)C)C(C)(C)C1C=C3O[Si](C)(C)C)C(=O)O	3574.7	Semi standard non polar	33892256
20-Hydroxy-3,7,11,15,23-pentaoxolanost-8-en-26-oic acid,5TMS,isomer #25	CC(CC(=O)CC(C)(O[Si](C)(C)C)C1C=C(O[Si](C)(C)C)C2(C)C3=C(C(O[Si](C)(C)C)=CC12C)C1(C)CC=C(O[Si](C)(C)C)C(C)(C)C1C=C3O[Si](C)(C)C)C(=O)O	3629.0	Standard non polar	33892256
20-Hydroxy-3,7,11,15,23-pentaoxolanost-8-en-26-oic acid,5TMS,isomer #26	CC(CC(=CC(C)(O)C1C=C(O[Si](C)(C)C)C2(C)C3=C(C(O[Si](C)(C)C)=CC12C)C1(C)CC=C(O[Si](C)(C)C)C(C)(C)C1CC3=O)O[Si](C)(C)C)C(=O)O[Si](C)(C)C	3485.4	Semi standard non polar	33892256
20-Hydroxy-3,7,11,15,23-pentaoxolanost-8-en-26-oic acid,5TMS,isomer #26	CC(CC(=CC(C)(O)C1C=C(O[Si](C)(C)C)C2(C)C3=C(C(O[Si](C)(C)C)=CC12C)C1(C)CC=C(O[Si](C)(C)C)C(C)(C)C1CC3=O)O[Si](C)(C)C)C(=O)O[Si](C)(C)C	3668.2	Standard non polar	33892256
20-Hydroxy-3,7,11,15,23-pentaoxolanost-8-en-26-oic acid,5TMS,isomer #27	CC(CC(=CC(C)(O)C1C=C(O[Si](C)(C)C)C2(C)C3=C(C(O[Si](C)(C)C)=CC12C)C1(C)CCC(=O)C(C)(C)C1C=C3O[Si](C)(C)C)O[Si](C)(C)C)C(=O)O[Si](C)(C)C	3572.7	Semi standard non polar	33892256
20-Hydroxy-3,7,11,15,23-pentaoxolanost-8-en-26-oic acid,5TMS,isomer #27	CC(CC(=CC(C)(O)C1C=C(O[Si](C)(C)C)C2(C)C3=C(C(O[Si](C)(C)C)=CC12C)C1(C)CCC(=O)C(C)(C)C1C=C3O[Si](C)(C)C)O[Si](C)(C)C)C(=O)O[Si](C)(C)C	3733.6	Standard non polar	33892256
20-Hydroxy-3,7,11,15,23-pentaoxolanost-8-en-26-oic acid,5TMS,isomer #28	CC(CC(=CC(C)(O)C1C=C(O[Si](C)(C)C)C2(C)C3=C(C(=O)CC12C)C1(C)CC=C(O[Si](C)(C)C)C(C)(C)C1C=C3O[Si](C)(C)C)O[Si](C)(C)C)C(=O)O[Si](C)(C)C	3528.5	Semi standard non polar	33892256
20-Hydroxy-3,7,11,15,23-pentaoxolanost-8-en-26-oic acid,5TMS,isomer #28	CC(CC(=CC(C)(O)C1C=C(O[Si](C)(C)C)C2(C)C3=C(C(=O)CC12C)C1(C)CC=C(O[Si](C)(C)C)C(C)(C)C1C=C3O[Si](C)(C)C)O[Si](C)(C)C)C(=O)O[Si](C)(C)C	3611.6	Standard non polar	33892256
20-Hydroxy-3,7,11,15,23-pentaoxolanost-8-en-26-oic acid,5TMS,isomer #29	CC(CC(=CC(C)(O)C1CC(=O)C2(C)C3=C(C(O[Si](C)(C)C)=CC12C)C1(C)CC=C(O[Si](C)(C)C)C(C)(C)C1C=C3O[Si](C)(C)C)O[Si](C)(C)C)C(=O)O[Si](C)(C)C	3507.8	Semi standard non polar	33892256
20-Hydroxy-3,7,11,15,23-pentaoxolanost-8-en-26-oic acid,5TMS,isomer #29	CC(CC(=CC(C)(O)C1CC(=O)C2(C)C3=C(C(O[Si](C)(C)C)=CC12C)C1(C)CC=C(O[Si](C)(C)C)C(C)(C)C1C=C3O[Si](C)(C)C)O[Si](C)(C)C)C(=O)O[Si](C)(C)C	3754.3	Standard non polar	33892256
20-Hydroxy-3,7,11,15,23-pentaoxolanost-8-en-26-oic acid,5TMS,isomer #3	CC(CC(=CC(C)(O[Si](C)(C)C)C1C=C(O[Si](C)(C)C)C2(C)C3=C(C(=O)CC12C)C1(C)CCC(=O)C(C)(C)C1C=C3O[Si](C)(C)C)O[Si](C)(C)C)C(=O)O[Si](C)(C)C	3638.5	Semi standard non polar	33892256
20-Hydroxy-3,7,11,15,23-pentaoxolanost-8-en-26-oic acid,5TMS,isomer #3	CC(CC(=CC(C)(O[Si](C)(C)C)C1C=C(O[Si](C)(C)C)C2(C)C3=C(C(=O)CC12C)C1(C)CCC(=O)C(C)(C)C1C=C3O[Si](C)(C)C)O[Si](C)(C)C)C(=O)O[Si](C)(C)C	3725.0	Standard non polar	33892256
20-Hydroxy-3,7,11,15,23-pentaoxolanost-8-en-26-oic acid,5TMS,isomer #30	CC(C=C(CC(C)(O)C1C=C(O[Si](C)(C)C)C2(C)C3=C(C(O[Si](C)(C)C)=CC12C)C1(C)CC=C(O[Si](C)(C)C)C(C)(C)C1CC3=O)O[Si](C)(C)C)C(=O)O[Si](C)(C)C	3507.8	Semi standard non polar	33892256
20-Hydroxy-3,7,11,15,23-pentaoxolanost-8-en-26-oic acid,5TMS,isomer #30	CC(C=C(CC(C)(O)C1C=C(O[Si](C)(C)C)C2(C)C3=C(C(O[Si](C)(C)C)=CC12C)C1(C)CC=C(O[Si](C)(C)C)C(C)(C)C1CC3=O)O[Si](C)(C)C)C(=O)O[Si](C)(C)C	3693.2	Standard non polar	33892256
20-Hydroxy-3,7,11,15,23-pentaoxolanost-8-en-26-oic acid,5TMS,isomer #31	CC(C=C(CC(C)(O)C1C=C(O[Si](C)(C)C)C2(C)C3=C(C(O[Si](C)(C)C)=CC12C)C1(C)CCC(=O)C(C)(C)C1C=C3O[Si](C)(C)C)O[Si](C)(C)C)C(=O)O[Si](C)(C)C	3604.0	Semi standard non polar	33892256
20-Hydroxy-3,7,11,15,23-pentaoxolanost-8-en-26-oic acid,5TMS,isomer #31	CC(C=C(CC(C)(O)C1C=C(O[Si](C)(C)C)C2(C)C3=C(C(O[Si](C)(C)C)=CC12C)C1(C)CCC(=O)C(C)(C)C1C=C3O[Si](C)(C)C)O[Si](C)(C)C)C(=O)O[Si](C)(C)C	3746.0	Standard non polar	33892256
20-Hydroxy-3,7,11,15,23-pentaoxolanost-8-en-26-oic acid,5TMS,isomer #32	CC(C=C(CC(C)(O)C1C=C(O[Si](C)(C)C)C2(C)C3=C(C(=O)CC12C)C1(C)CC=C(O[Si](C)(C)C)C(C)(C)C1C=C3O[Si](C)(C)C)O[Si](C)(C)C)C(=O)O[Si](C)(C)C	3568.3	Semi standard non polar	33892256
20-Hydroxy-3,7,11,15,23-pentaoxolanost-8-en-26-oic acid,5TMS,isomer #32	CC(C=C(CC(C)(O)C1C=C(O[Si](C)(C)C)C2(C)C3=C(C(=O)CC12C)C1(C)CC=C(O[Si](C)(C)C)C(C)(C)C1C=C3O[Si](C)(C)C)O[Si](C)(C)C)C(=O)O[Si](C)(C)C	3638.8	Standard non polar	33892256
20-Hydroxy-3,7,11,15,23-pentaoxolanost-8-en-26-oic acid,5TMS,isomer #33	CC(C=C(CC(C)(O)C1CC(=O)C2(C)C3=C(C(O[Si](C)(C)C)=CC12C)C1(C)CC=C(O[Si](C)(C)C)C(C)(C)C1C=C3O[Si](C)(C)C)O[Si](C)(C)C)C(=O)O[Si](C)(C)C	3544.0	Semi standard non polar	33892256
20-Hydroxy-3,7,11,15,23-pentaoxolanost-8-en-26-oic acid,5TMS,isomer #33	CC(C=C(CC(C)(O)C1CC(=O)C2(C)C3=C(C(O[Si](C)(C)C)=CC12C)C1(C)CC=C(O[Si](C)(C)C)C(C)(C)C1C=C3O[Si](C)(C)C)O[Si](C)(C)C)C(=O)O[Si](C)(C)C	3791.8	Standard non polar	33892256
20-Hydroxy-3,7,11,15,23-pentaoxolanost-8-en-26-oic acid,5TMS,isomer #34	CC(CC(=O)CC(C)(O)C1C=C(O[Si](C)(C)C)C2(C)C3=C(C(O[Si](C)(C)C)=CC12C)C1(C)CC=C(O[Si](C)(C)C)C(C)(C)C1C=C3O[Si](C)(C)C)C(=O)O[Si](C)(C)C	3546.5	Semi standard non polar	33892256
20-Hydroxy-3,7,11,15,23-pentaoxolanost-8-en-26-oic acid,5TMS,isomer #34	CC(CC(=O)CC(C)(O)C1C=C(O[Si](C)(C)C)C2(C)C3=C(C(O[Si](C)(C)C)=CC12C)C1(C)CC=C(O[Si](C)(C)C)C(C)(C)C1C=C3O[Si](C)(C)C)C(=O)O[Si](C)(C)C	3662.6	Standard non polar	33892256
20-Hydroxy-3,7,11,15,23-pentaoxolanost-8-en-26-oic acid,5TMS,isomer #35	CC(CC(=CC(C)(O)C1C=C(O[Si](C)(C)C)C2(C)C3=C(C(O[Si](C)(C)C)=CC12C)C1(C)CC=C(O[Si](C)(C)C)C(C)(C)C1C=C3O[Si](C)(C)C)O[Si](C)(C)C)C(=O)O	3540.2	Semi standard non polar	33892256
20-Hydroxy-3,7,11,15,23-pentaoxolanost-8-en-26-oic acid,5TMS,isomer #35	CC(CC(=CC(C)(O)C1C=C(O[Si](C)(C)C)C2(C)C3=C(C(O[Si](C)(C)C)=CC12C)C1(C)CC=C(O[Si](C)(C)C)C(C)(C)C1C=C3O[Si](C)(C)C)O[Si](C)(C)C)C(=O)O	3575.5	Standard non polar	33892256
20-Hydroxy-3,7,11,15,23-pentaoxolanost-8-en-26-oic acid,5TMS,isomer #36	CC(C=C(CC(C)(O)C1C=C(O[Si](C)(C)C)C2(C)C3=C(C(O[Si](C)(C)C)=CC12C)C1(C)CC=C(O[Si](C)(C)C)C(C)(C)C1C=C3O[Si](C)(C)C)O[Si](C)(C)C)C(=O)O	3551.9	Semi standard non polar	33892256
20-Hydroxy-3,7,11,15,23-pentaoxolanost-8-en-26-oic acid,5TMS,isomer #36	CC(C=C(CC(C)(O)C1C=C(O[Si](C)(C)C)C2(C)C3=C(C(O[Si](C)(C)C)=CC12C)C1(C)CC=C(O[Si](C)(C)C)C(C)(C)C1C=C3O[Si](C)(C)C)O[Si](C)(C)C)C(=O)O	3621.8	Standard non polar	33892256
20-Hydroxy-3,7,11,15,23-pentaoxolanost-8-en-26-oic acid,5TMS,isomer #4	CC(CC(=CC(C)(O[Si](C)(C)C)C1CC(=O)C2(C)C3=C(C(O[Si](C)(C)C)=CC12C)C1(C)CC=C(O[Si](C)(C)C)C(C)(C)C1CC3=O)O[Si](C)(C)C)C(=O)O[Si](C)(C)C	3537.1	Semi standard non polar	33892256
20-Hydroxy-3,7,11,15,23-pentaoxolanost-8-en-26-oic acid,5TMS,isomer #4	CC(CC(=CC(C)(O[Si](C)(C)C)C1CC(=O)C2(C)C3=C(C(O[Si](C)(C)C)=CC12C)C1(C)CC=C(O[Si](C)(C)C)C(C)(C)C1CC3=O)O[Si](C)(C)C)C(=O)O[Si](C)(C)C	3795.1	Standard non polar	33892256
20-Hydroxy-3,7,11,15,23-pentaoxolanost-8-en-26-oic acid,5TMS,isomer #5	CC(CC(=CC(C)(O[Si](C)(C)C)C1CC(=O)C2(C)C3=C(C(O[Si](C)(C)C)=CC12C)C1(C)CCC(=O)C(C)(C)C1C=C3O[Si](C)(C)C)O[Si](C)(C)C)C(=O)O[Si](C)(C)C	3598.2	Semi standard non polar	33892256
20-Hydroxy-3,7,11,15,23-pentaoxolanost-8-en-26-oic acid,5TMS,isomer #5	CC(CC(=CC(C)(O[Si](C)(C)C)C1CC(=O)C2(C)C3=C(C(O[Si](C)(C)C)=CC12C)C1(C)CCC(=O)C(C)(C)C1C=C3O[Si](C)(C)C)O[Si](C)(C)C)C(=O)O[Si](C)(C)C	3916.4	Standard non polar	33892256
20-Hydroxy-3,7,11,15,23-pentaoxolanost-8-en-26-oic acid,5TMS,isomer #6	CC(CC(=CC(C)(O[Si](C)(C)C)C1CC(=O)C2(C)C3=C(C(=O)CC12C)C1(C)CC=C(O[Si](C)(C)C)C(C)(C)C1C=C3O[Si](C)(C)C)O[Si](C)(C)C)C(=O)O[Si](C)(C)C	3576.7	Semi standard non polar	33892256
20-Hydroxy-3,7,11,15,23-pentaoxolanost-8-en-26-oic acid,5TMS,isomer #6	CC(CC(=CC(C)(O[Si](C)(C)C)C1CC(=O)C2(C)C3=C(C(=O)CC12C)C1(C)CC=C(O[Si](C)(C)C)C(C)(C)C1C=C3O[Si](C)(C)C)O[Si](C)(C)C)C(=O)O[Si](C)(C)C	3792.0	Standard non polar	33892256
20-Hydroxy-3,7,11,15,23-pentaoxolanost-8-en-26-oic acid,5TMS,isomer #7	CC(C=C(CC(C)(O[Si](C)(C)C)C1C=C(O[Si](C)(C)C)C2(C)C3=C(C(O[Si](C)(C)C)=CC12C)C1(C)CCC(=O)C(C)(C)C1CC3=O)O[Si](C)(C)C)C(=O)O[Si](C)(C)C	3606.8	Semi standard non polar	33892256
20-Hydroxy-3,7,11,15,23-pentaoxolanost-8-en-26-oic acid,5TMS,isomer #7	CC(C=C(CC(C)(O[Si](C)(C)C)C1C=C(O[Si](C)(C)C)C2(C)C3=C(C(O[Si](C)(C)C)=CC12C)C1(C)CCC(=O)C(C)(C)C1CC3=O)O[Si](C)(C)C)C(=O)O[Si](C)(C)C	3810.4	Standard non polar	33892256
20-Hydroxy-3,7,11,15,23-pentaoxolanost-8-en-26-oic acid,5TMS,isomer #8	CC(C=C(CC(C)(O[Si](C)(C)C)C1C=C(O[Si](C)(C)C)C2(C)C3=C(C(=O)CC12C)C1(C)CC=C(O[Si](C)(C)C)C(C)(C)C1CC3=O)O[Si](C)(C)C)C(=O)O[Si](C)(C)C	3578.4	Semi standard non polar	33892256
20-Hydroxy-3,7,11,15,23-pentaoxolanost-8-en-26-oic acid,5TMS,isomer #8	CC(C=C(CC(C)(O[Si](C)(C)C)C1C=C(O[Si](C)(C)C)C2(C)C3=C(C(=O)CC12C)C1(C)CC=C(O[Si](C)(C)C)C(C)(C)C1CC3=O)O[Si](C)(C)C)C(=O)O[Si](C)(C)C	3657.4	Standard non polar	33892256
20-Hydroxy-3,7,11,15,23-pentaoxolanost-8-en-26-oic acid,5TMS,isomer #9	CC(C=C(CC(C)(O[Si](C)(C)C)C1C=C(O[Si](C)(C)C)C2(C)C3=C(C(=O)CC12C)C1(C)CCC(=O)C(C)(C)C1C=C3O[Si](C)(C)C)O[Si](C)(C)C)C(=O)O[Si](C)(C)C	3669.3	Semi standard non polar	33892256
20-Hydroxy-3,7,11,15,23-pentaoxolanost-8-en-26-oic acid,5TMS,isomer #9	CC(C=C(CC(C)(O[Si](C)(C)C)C1C=C(O[Si](C)(C)C)C2(C)C3=C(C(=O)CC12C)C1(C)CCC(=O)C(C)(C)C1C=C3O[Si](C)(C)C)O[Si](C)(C)C)C(=O)O[Si](C)(C)C	3736.3	Standard non polar	33892256
20-Hydroxy-3,7,11,15,23-pentaoxolanost-8-en-26-oic acid,1TBDMS,isomer #1	CC(CC(=O)CC(C)(O[Si](C)(C)C(C)(C)C)C1CC(=O)C2(C)C3=C(C(=O)CC12C)C1(C)CCC(=O)C(C)(C)C1CC3=O)C(=O)O	4305.0	Semi standard non polar	33892256
20-Hydroxy-3,7,11,15,23-pentaoxolanost-8-en-26-oic acid,1TBDMS,isomer #2	CC(CC(=O)CC(C)(O)C1CC(=O)C2(C)C3=C(C(=O)CC12C)C1(C)CCC(=O)C(C)(C)C1CC3=O)C(=O)O[Si](C)(C)C(C)(C)C	4396.1	Semi standard non polar	33892256
20-Hydroxy-3,7,11,15,23-pentaoxolanost-8-en-26-oic acid,1TBDMS,isomer #3	CC(CC(=CC(C)(O)C1CC(=O)C2(C)C3=C(C(=O)CC12C)C1(C)CCC(=O)C(C)(C)C1CC3=O)O[Si](C)(C)C(C)(C)C)C(=O)O	4277.0	Semi standard non polar	33892256
20-Hydroxy-3,7,11,15,23-pentaoxolanost-8-en-26-oic acid,1TBDMS,isomer #4	CC(C=C(CC(C)(O)C1CC(=O)C2(C)C3=C(C(=O)CC12C)C1(C)CCC(=O)C(C)(C)C1CC3=O)O[Si](C)(C)C(C)(C)C)C(=O)O	4385.4	Semi standard non polar	33892256
20-Hydroxy-3,7,11,15,23-pentaoxolanost-8-en-26-oic acid,1TBDMS,isomer #5	CC(CC(=O)CC(C)(O)C1C=C(O[Si](C)(C)C(C)(C)C)C2(C)C3=C(C(=O)CC12C)C1(C)CCC(=O)C(C)(C)C1CC3=O)C(=O)O	4199.7	Semi standard non polar	33892256
20-Hydroxy-3,7,11,15,23-pentaoxolanost-8-en-26-oic acid,1TBDMS,isomer #6	CC(CC(=O)CC(C)(O)C1CC(=O)C2(C)C3=C(C(O[Si](C)(C)C(C)(C)C)=CC12C)C1(C)CCC(=O)C(C)(C)C1CC3=O)C(=O)O	4216.6	Semi standard non polar	33892256
20-Hydroxy-3,7,11,15,23-pentaoxolanost-8-en-26-oic acid,1TBDMS,isomer #7	CC(CC(=O)CC(C)(O)C1CC(=O)C2(C)C3=C(C(=O)CC12C)C1(C)CC=C(O[Si](C)(C)C(C)(C)C)C(C)(C)C1CC3=O)C(=O)O	4194.5	Semi standard non polar	33892256
20-Hydroxy-3,7,11,15,23-pentaoxolanost-8-en-26-oic acid,1TBDMS,isomer #8	CC(CC(=O)CC(C)(O)C1CC(=O)C2(C)C3=C(C(=O)CC12C)C1(C)CCC(=O)C(C)(C)C1C=C3O[Si](C)(C)C(C)(C)C)C(=O)O	4195.8	Semi standard non polar	33892256
20-Hydroxy-3,7,11,15,23-pentaoxolanost-8-en-26-oic acid,2TBDMS,isomer #1	CC(CC(=O)CC(C)(O[Si](C)(C)C(C)(C)C)C1CC(=O)C2(C)C3=C(C(=O)CC12C)C1(C)CCC(=O)C(C)(C)C1CC3=O)C(=O)O[Si](C)(C)C(C)(C)C	4562.0	Semi standard non polar	33892256
20-Hydroxy-3,7,11,15,23-pentaoxolanost-8-en-26-oic acid,2TBDMS,isomer #10	CC(CC(=O)CC(C)(O)C1C=C(O[Si](C)(C)C(C)(C)C)C2(C)C3=C(C(=O)CC12C)C1(C)CCC(=O)C(C)(C)C1CC3=O)C(=O)O[Si](C)(C)C(C)(C)C	4395.4	Semi standard non polar	33892256
20-Hydroxy-3,7,11,15,23-pentaoxolanost-8-en-26-oic acid,2TBDMS,isomer #11	CC(CC(=O)CC(C)(O)C1CC(=O)C2(C)C3=C(C(O[Si](C)(C)C(C)(C)C)=CC12C)C1(C)CCC(=O)C(C)(C)C1CC3=O)C(=O)O[Si](C)(C)C(C)(C)C	4396.2	Semi standard non polar	33892256
20-Hydroxy-3,7,11,15,23-pentaoxolanost-8-en-26-oic acid,2TBDMS,isomer #12	CC(CC(=O)CC(C)(O)C1CC(=O)C2(C)C3=C(C(=O)CC12C)C1(C)CC=C(O[Si](C)(C)C(C)(C)C)C(C)(C)C1CC3=O)C(=O)O[Si](C)(C)C(C)(C)C	4382.6	Semi standard non polar	33892256
20-Hydroxy-3,7,11,15,23-pentaoxolanost-8-en-26-oic acid,2TBDMS,isomer #13	CC(CC(=O)CC(C)(O)C1CC(=O)C2(C)C3=C(C(=O)CC12C)C1(C)CCC(=O)C(C)(C)C1C=C3O[Si](C)(C)C(C)(C)C)C(=O)O[Si](C)(C)C(C)(C)C	4370.2	Semi standard non polar	33892256
20-Hydroxy-3,7,11,15,23-pentaoxolanost-8-en-26-oic acid,2TBDMS,isomer #14	CC(CC(=CC(C)(O)C1C=C(O[Si](C)(C)C(C)(C)C)C2(C)C3=C(C(=O)CC12C)C1(C)CCC(=O)C(C)(C)C1CC3=O)O[Si](C)(C)C(C)(C)C)C(=O)O	4284.8	Semi standard non polar	33892256
20-Hydroxy-3,7,11,15,23-pentaoxolanost-8-en-26-oic acid,2TBDMS,isomer #15	CC(CC(=CC(C)(O)C1CC(=O)C2(C)C3=C(C(O[Si](C)(C)C(C)(C)C)=CC12C)C1(C)CCC(=O)C(C)(C)C1CC3=O)O[Si](C)(C)C(C)(C)C)C(=O)O	4284.7	Semi standard non polar	33892256
20-Hydroxy-3,7,11,15,23-pentaoxolanost-8-en-26-oic acid,2TBDMS,isomer #16	CC(CC(=CC(C)(O)C1CC(=O)C2(C)C3=C(C(=O)CC12C)C1(C)CC=C(O[Si](C)(C)C(C)(C)C)C(C)(C)C1CC3=O)O[Si](C)(C)C(C)(C)C)C(=O)O	4268.0	Semi standard non polar	33892256
20-Hydroxy-3,7,11,15,23-pentaoxolanost-8-en-26-oic acid,2TBDMS,isomer #17	CC(CC(=CC(C)(O)C1CC(=O)C2(C)C3=C(C(=O)CC12C)C1(C)CCC(=O)C(C)(C)C1C=C3O[Si](C)(C)C(C)(C)C)O[Si](C)(C)C(C)(C)C)C(=O)O	4275.9	Semi standard non polar	33892256
20-Hydroxy-3,7,11,15,23-pentaoxolanost-8-en-26-oic acid,2TBDMS,isomer #18	CC(C=C(CC(C)(O)C1C=C(O[Si](C)(C)C(C)(C)C)C2(C)C3=C(C(=O)CC12C)C1(C)CCC(=O)C(C)(C)C1CC3=O)O[Si](C)(C)C(C)(C)C)C(=O)O	4370.2	Semi standard non polar	33892256
20-Hydroxy-3,7,11,15,23-pentaoxolanost-8-en-26-oic acid,2TBDMS,isomer #19	CC(C=C(CC(C)(O)C1CC(=O)C2(C)C3=C(C(O[Si](C)(C)C(C)(C)C)=CC12C)C1(C)CCC(=O)C(C)(C)C1CC3=O)O[Si](C)(C)C(C)(C)C)C(=O)O	4386.8	Semi standard non polar	33892256
20-Hydroxy-3,7,11,15,23-pentaoxolanost-8-en-26-oic acid,2TBDMS,isomer #2	CC(CC(=CC(C)(O[Si](C)(C)C(C)(C)C)C1CC(=O)C2(C)C3=C(C(=O)CC12C)C1(C)CCC(=O)C(C)(C)C1CC3=O)O[Si](C)(C)C(C)(C)C)C(=O)O	4455.4	Semi standard non polar	33892256
20-Hydroxy-3,7,11,15,23-pentaoxolanost-8-en-26-oic acid,2TBDMS,isomer #20	CC(C=C(CC(C)(O)C1CC(=O)C2(C)C3=C(C(=O)CC12C)C1(C)CC=C(O[Si](C)(C)C(C)(C)C)C(C)(C)C1CC3=O)O[Si](C)(C)C(C)(C)C)C(=O)O	4367.7	Semi standard non polar	33892256
20-Hydroxy-3,7,11,15,23-pentaoxolanost-8-en-26-oic acid,2TBDMS,isomer #21	CC(C=C(CC(C)(O)C1CC(=O)C2(C)C3=C(C(=O)CC12C)C1(C)CCC(=O)C(C)(C)C1C=C3O[Si](C)(C)C(C)(C)C)O[Si](C)(C)C(C)(C)C)C(=O)O	4370.4	Semi standard non polar	33892256
20-Hydroxy-3,7,11,15,23-pentaoxolanost-8-en-26-oic acid,2TBDMS,isomer #22	CC(CC(=O)CC(C)(O)C1C=C(O[Si](C)(C)C(C)(C)C)C2(C)C3=C(C(O[Si](C)(C)C(C)(C)C)=CC12C)C1(C)CCC(=O)C(C)(C)C1CC3=O)C(=O)O	4224.4	Semi standard non polar	33892256
20-Hydroxy-3,7,11,15,23-pentaoxolanost-8-en-26-oic acid,2TBDMS,isomer #23	CC(CC(=O)CC(C)(O)C1C=C(O[Si](C)(C)C(C)(C)C)C2(C)C3=C(C(=O)CC12C)C1(C)CC=C(O[Si](C)(C)C(C)(C)C)C(C)(C)C1CC3=O)C(=O)O	4216.3	Semi standard non polar	33892256
20-Hydroxy-3,7,11,15,23-pentaoxolanost-8-en-26-oic acid,2TBDMS,isomer #24	CC(CC(=O)CC(C)(O)C1C=C(O[Si](C)(C)C(C)(C)C)C2(C)C3=C(C(=O)CC12C)C1(C)CCC(=O)C(C)(C)C1C=C3O[Si](C)(C)C(C)(C)C)C(=O)O	4269.9	Semi standard non polar	33892256
20-Hydroxy-3,7,11,15,23-pentaoxolanost-8-en-26-oic acid,2TBDMS,isomer #25	CC(CC(=O)CC(C)(O)C1CC(=O)C2(C)C3=C(C(O[Si](C)(C)C(C)(C)C)=CC12C)C1(C)CC=C(O[Si](C)(C)C(C)(C)C)C(C)(C)C1CC3=O)C(=O)O	4227.9	Semi standard non polar	33892256
20-Hydroxy-3,7,11,15,23-pentaoxolanost-8-en-26-oic acid,2TBDMS,isomer #26	CC(CC(=O)CC(C)(O)C1CC(=O)C2(C)C3=C(C(O[Si](C)(C)C(C)(C)C)=CC12C)C1(C)CCC(=O)C(C)(C)C1C=C3O[Si](C)(C)C(C)(C)C)C(=O)O	4235.1	Semi standard non polar	33892256
20-Hydroxy-3,7,11,15,23-pentaoxolanost-8-en-26-oic acid,2TBDMS,isomer #27	CC(CC(=O)CC(C)(O)C1CC(=O)C2(C)C3=C(C(=O)CC12C)C1(C)CC=C(O[Si](C)(C)C(C)(C)C)C(C)(C)C1C=C3O[Si](C)(C)C(C)(C)C)C(=O)O	4229.5	Semi standard non polar	33892256
20-Hydroxy-3,7,11,15,23-pentaoxolanost-8-en-26-oic acid,2TBDMS,isomer #3	CC(C=C(CC(C)(O[Si](C)(C)C(C)(C)C)C1CC(=O)C2(C)C3=C(C(=O)CC12C)C1(C)CCC(=O)C(C)(C)C1CC3=O)O[Si](C)(C)C(C)(C)C)C(=O)O	4510.6	Semi standard non polar	33892256
20-Hydroxy-3,7,11,15,23-pentaoxolanost-8-en-26-oic acid,2TBDMS,isomer #4	CC(CC(=O)CC(C)(O[Si](C)(C)C(C)(C)C)C1C=C(O[Si](C)(C)C(C)(C)C)C2(C)C3=C(C(=O)CC12C)C1(C)CCC(=O)C(C)(C)C1CC3=O)C(=O)O	4367.5	Semi standard non polar	33892256
20-Hydroxy-3,7,11,15,23-pentaoxolanost-8-en-26-oic acid,2TBDMS,isomer #5	CC(CC(=O)CC(C)(O[Si](C)(C)C(C)(C)C)C1CC(=O)C2(C)C3=C(C(O[Si](C)(C)C(C)(C)C)=CC12C)C1(C)CCC(=O)C(C)(C)C1CC3=O)C(=O)O	4346.2	Semi standard non polar	33892256
20-Hydroxy-3,7,11,15,23-pentaoxolanost-8-en-26-oic acid,2TBDMS,isomer #6	CC(CC(=O)CC(C)(O[Si](C)(C)C(C)(C)C)C1CC(=O)C2(C)C3=C(C(=O)CC12C)C1(C)CC=C(O[Si](C)(C)C(C)(C)C)C(C)(C)C1CC3=O)C(=O)O	4332.1	Semi standard non polar	33892256
20-Hydroxy-3,7,11,15,23-pentaoxolanost-8-en-26-oic acid,2TBDMS,isomer #7	CC(CC(=O)CC(C)(O[Si](C)(C)C(C)(C)C)C1CC(=O)C2(C)C3=C(C(=O)CC12C)C1(C)CCC(=O)C(C)(C)C1C=C3O[Si](C)(C)C(C)(C)C)C(=O)O	4341.7	Semi standard non polar	33892256
20-Hydroxy-3,7,11,15,23-pentaoxolanost-8-en-26-oic acid,2TBDMS,isomer #8	CC(CC(=CC(C)(O)C1CC(=O)C2(C)C3=C(C(=O)CC12C)C1(C)CCC(=O)C(C)(C)C1CC3=O)O[Si](C)(C)C(C)(C)C)C(=O)O[Si](C)(C)C(C)(C)C	4447.7	Semi standard non polar	33892256
20-Hydroxy-3,7,11,15,23-pentaoxolanost-8-en-26-oic acid,2TBDMS,isomer #9	CC(C=C(CC(C)(O)C1CC(=O)C2(C)C3=C(C(=O)CC12C)C1(C)CCC(=O)C(C)(C)C1CC3=O)O[Si](C)(C)C(C)(C)C)C(=O)O[Si](C)(C)C(C)(C)C	4535.3	Semi standard non polar	33892256
20-Hydroxy-3,7,11,15,23-pentaoxolanost-8-en-26-oic acid,3TBDMS,isomer #1	CC(CC(=CC(C)(O[Si](C)(C)C(C)(C)C)C1CC(=O)C2(C)C3=C(C(=O)CC12C)C1(C)CCC(=O)C(C)(C)C1CC3=O)O[Si](C)(C)C(C)(C)C)C(=O)O[Si](C)(C)C(C)(C)C	4596.9	Semi standard non polar	33892256
20-Hydroxy-3,7,11,15,23-pentaoxolanost-8-en-26-oic acid,3TBDMS,isomer #1	CC(CC(=CC(C)(O[Si](C)(C)C(C)(C)C)C1CC(=O)C2(C)C3=C(C(=O)CC12C)C1(C)CCC(=O)C(C)(C)C1CC3=O)O[Si](C)(C)C(C)(C)C)C(=O)O[Si](C)(C)C(C)(C)C	4557.6	Standard non polar	33892256
20-Hydroxy-3,7,11,15,23-pentaoxolanost-8-en-26-oic acid,3TBDMS,isomer #10	CC(CC(=CC(C)(O[Si](C)(C)C(C)(C)C)C1CC(=O)C2(C)C3=C(C(=O)CC12C)C1(C)CCC(=O)C(C)(C)C1C=C3O[Si](C)(C)C(C)(C)C)O[Si](C)(C)C(C)(C)C)C(=O)O	4434.0	Semi standard non polar	33892256
20-Hydroxy-3,7,11,15,23-pentaoxolanost-8-en-26-oic acid,3TBDMS,isomer #10	CC(CC(=CC(C)(O[Si](C)(C)C(C)(C)C)C1CC(=O)C2(C)C3=C(C(=O)CC12C)C1(C)CCC(=O)C(C)(C)C1C=C3O[Si](C)(C)C(C)(C)C)O[Si](C)(C)C(C)(C)C)C(=O)O	4437.5	Standard non polar	33892256
20-Hydroxy-3,7,11,15,23-pentaoxolanost-8-en-26-oic acid,3TBDMS,isomer #11	CC(C=C(CC(C)(O[Si](C)(C)C(C)(C)C)C1C=C(O[Si](C)(C)C(C)(C)C)C2(C)C3=C(C(=O)CC12C)C1(C)CCC(=O)C(C)(C)C1CC3=O)O[Si](C)(C)C(C)(C)C)C(=O)O	4512.7	Semi standard non polar	33892256
20-Hydroxy-3,7,11,15,23-pentaoxolanost-8-en-26-oic acid,3TBDMS,isomer #11	CC(C=C(CC(C)(O[Si](C)(C)C(C)(C)C)C1C=C(O[Si](C)(C)C(C)(C)C)C2(C)C3=C(C(=O)CC12C)C1(C)CCC(=O)C(C)(C)C1CC3=O)O[Si](C)(C)C(C)(C)C)C(=O)O	4330.1	Standard non polar	33892256
20-Hydroxy-3,7,11,15,23-pentaoxolanost-8-en-26-oic acid,3TBDMS,isomer #12	CC(C=C(CC(C)(O[Si](C)(C)C(C)(C)C)C1CC(=O)C2(C)C3=C(C(O[Si](C)(C)C(C)(C)C)=CC12C)C1(C)CCC(=O)C(C)(C)C1CC3=O)O[Si](C)(C)C(C)(C)C)C(=O)O	4495.2	Semi standard non polar	33892256
20-Hydroxy-3,7,11,15,23-pentaoxolanost-8-en-26-oic acid,3TBDMS,isomer #12	CC(C=C(CC(C)(O[Si](C)(C)C(C)(C)C)C1CC(=O)C2(C)C3=C(C(O[Si](C)(C)C(C)(C)C)=CC12C)C1(C)CCC(=O)C(C)(C)C1CC3=O)O[Si](C)(C)C(C)(C)C)C(=O)O	4505.6	Standard non polar	33892256
20-Hydroxy-3,7,11,15,23-pentaoxolanost-8-en-26-oic acid,3TBDMS,isomer #13	CC(C=C(CC(C)(O[Si](C)(C)C(C)(C)C)C1CC(=O)C2(C)C3=C(C(=O)CC12C)C1(C)CC=C(O[Si](C)(C)C(C)(C)C)C(C)(C)C1CC3=O)O[Si](C)(C)C(C)(C)C)C(=O)O	4477.8	Semi standard non polar	33892256
20-Hydroxy-3,7,11,15,23-pentaoxolanost-8-en-26-oic acid,3TBDMS,isomer #13	CC(C=C(CC(C)(O[Si](C)(C)C(C)(C)C)C1CC(=O)C2(C)C3=C(C(=O)CC12C)C1(C)CC=C(O[Si](C)(C)C(C)(C)C)C(C)(C)C1CC3=O)O[Si](C)(C)C(C)(C)C)C(=O)O	4358.2	Standard non polar	33892256
20-Hydroxy-3,7,11,15,23-pentaoxolanost-8-en-26-oic acid,3TBDMS,isomer #14	CC(C=C(CC(C)(O[Si](C)(C)C(C)(C)C)C1CC(=O)C2(C)C3=C(C(=O)CC12C)C1(C)CCC(=O)C(C)(C)C1C=C3O[Si](C)(C)C(C)(C)C)O[Si](C)(C)C(C)(C)C)C(=O)O	4489.9	Semi standard non polar	33892256
20-Hydroxy-3,7,11,15,23-pentaoxolanost-8-en-26-oic acid,3TBDMS,isomer #14	CC(C=C(CC(C)(O[Si](C)(C)C(C)(C)C)C1CC(=O)C2(C)C3=C(C(=O)CC12C)C1(C)CCC(=O)C(C)(C)C1C=C3O[Si](C)(C)C(C)(C)C)O[Si](C)(C)C(C)(C)C)C(=O)O	4502.1	Standard non polar	33892256
20-Hydroxy-3,7,11,15,23-pentaoxolanost-8-en-26-oic acid,3TBDMS,isomer #15	CC(CC(=O)CC(C)(O[Si](C)(C)C(C)(C)C)C1C=C(O[Si](C)(C)C(C)(C)C)C2(C)C3=C(C(O[Si](C)(C)C(C)(C)C)=CC12C)C1(C)CCC(=O)C(C)(C)C1CC3=O)C(=O)O	4388.3	Semi standard non polar	33892256
20-Hydroxy-3,7,11,15,23-pentaoxolanost-8-en-26-oic acid,3TBDMS,isomer #15	CC(CC(=O)CC(C)(O[Si](C)(C)C(C)(C)C)C1C=C(O[Si](C)(C)C(C)(C)C)C2(C)C3=C(C(O[Si](C)(C)C(C)(C)C)=CC12C)C1(C)CCC(=O)C(C)(C)C1CC3=O)C(=O)O	4235.8	Standard non polar	33892256
20-Hydroxy-3,7,11,15,23-pentaoxolanost-8-en-26-oic acid,3TBDMS,isomer #16	CC(CC(=O)CC(C)(O[Si](C)(C)C(C)(C)C)C1C=C(O[Si](C)(C)C(C)(C)C)C2(C)C3=C(C(=O)CC12C)C1(C)CC=C(O[Si](C)(C)C(C)(C)C)C(C)(C)C1CC3=O)C(=O)O	4378.2	Semi standard non polar	33892256
20-Hydroxy-3,7,11,15,23-pentaoxolanost-8-en-26-oic acid,3TBDMS,isomer #16	CC(CC(=O)CC(C)(O[Si](C)(C)C(C)(C)C)C1C=C(O[Si](C)(C)C(C)(C)C)C2(C)C3=C(C(=O)CC12C)C1(C)CC=C(O[Si](C)(C)C(C)(C)C)C(C)(C)C1CC3=O)C(=O)O	4079.8	Standard non polar	33892256
20-Hydroxy-3,7,11,15,23-pentaoxolanost-8-en-26-oic acid,3TBDMS,isomer #17	CC(CC(=O)CC(C)(O[Si](C)(C)C(C)(C)C)C1C=C(O[Si](C)(C)C(C)(C)C)C2(C)C3=C(C(=O)CC12C)C1(C)CCC(=O)C(C)(C)C1C=C3O[Si](C)(C)C(C)(C)C)C(=O)O	4432.2	Semi standard non polar	33892256
20-Hydroxy-3,7,11,15,23-pentaoxolanost-8-en-26-oic acid,3TBDMS,isomer #17	CC(CC(=O)CC(C)(O[Si](C)(C)C(C)(C)C)C1C=C(O[Si](C)(C)C(C)(C)C)C2(C)C3=C(C(=O)CC12C)C1(C)CCC(=O)C(C)(C)C1C=C3O[Si](C)(C)C(C)(C)C)C(=O)O	4183.9	Standard non polar	33892256
20-Hydroxy-3,7,11,15,23-pentaoxolanost-8-en-26-oic acid,3TBDMS,isomer #18	CC(CC(=O)CC(C)(O[Si](C)(C)C(C)(C)C)C1CC(=O)C2(C)C3=C(C(O[Si](C)(C)C(C)(C)C)=CC12C)C1(C)CC=C(O[Si](C)(C)C(C)(C)C)C(C)(C)C1CC3=O)C(=O)O	4357.8	Semi standard non polar	33892256
20-Hydroxy-3,7,11,15,23-pentaoxolanost-8-en-26-oic acid,3TBDMS,isomer #18	CC(CC(=O)CC(C)(O[Si](C)(C)C(C)(C)C)C1CC(=O)C2(C)C3=C(C(O[Si](C)(C)C(C)(C)C)=CC12C)C1(C)CC=C(O[Si](C)(C)C(C)(C)C)C(C)(C)C1CC3=O)C(=O)O	4258.7	Standard non polar	33892256
20-Hydroxy-3,7,11,15,23-pentaoxolanost-8-en-26-oic acid,3TBDMS,isomer #19	CC(CC(=O)CC(C)(O[Si](C)(C)C(C)(C)C)C1CC(=O)C2(C)C3=C(C(O[Si](C)(C)C(C)(C)C)=CC12C)C1(C)CCC(=O)C(C)(C)C1C=C3O[Si](C)(C)C(C)(C)C)C(=O)O	4360.6	Semi standard non polar	33892256
20-Hydroxy-3,7,11,15,23-pentaoxolanost-8-en-26-oic acid,3TBDMS,isomer #19	CC(CC(=O)CC(C)(O[Si](C)(C)C(C)(C)C)C1CC(=O)C2(C)C3=C(C(O[Si](C)(C)C(C)(C)C)=CC12C)C1(C)CCC(=O)C(C)(C)C1C=C3O[Si](C)(C)C(C)(C)C)C(=O)O	4369.5	Standard non polar	33892256
20-Hydroxy-3,7,11,15,23-pentaoxolanost-8-en-26-oic acid,3TBDMS,isomer #2	CC(C=C(CC(C)(O[Si](C)(C)C(C)(C)C)C1CC(=O)C2(C)C3=C(C(=O)CC12C)C1(C)CCC(=O)C(C)(C)C1CC3=O)O[Si](C)(C)C(C)(C)C)C(=O)O[Si](C)(C)C(C)(C)C	4647.4	Semi standard non polar	33892256
20-Hydroxy-3,7,11,15,23-pentaoxolanost-8-en-26-oic acid,3TBDMS,isomer #2	CC(C=C(CC(C)(O[Si](C)(C)C(C)(C)C)C1CC(=O)C2(C)C3=C(C(=O)CC12C)C1(C)CCC(=O)C(C)(C)C1CC3=O)O[Si](C)(C)C(C)(C)C)C(=O)O[Si](C)(C)C(C)(C)C	4590.8	Standard non polar	33892256
20-Hydroxy-3,7,11,15,23-pentaoxolanost-8-en-26-oic acid,3TBDMS,isomer #20	CC(CC(=O)CC(C)(O[Si](C)(C)C(C)(C)C)C1CC(=O)C2(C)C3=C(C(=O)CC12C)C1(C)CC=C(O[Si](C)(C)C(C)(C)C)C(C)(C)C1C=C3O[Si](C)(C)C(C)(C)C)C(=O)O	4368.9	Semi standard non polar	33892256
20-Hydroxy-3,7,11,15,23-pentaoxolanost-8-en-26-oic acid,3TBDMS,isomer #20	CC(CC(=O)CC(C)(O[Si](C)(C)C(C)(C)C)C1CC(=O)C2(C)C3=C(C(=O)CC12C)C1(C)CC=C(O[Si](C)(C)C(C)(C)C)C(C)(C)C1C=C3O[Si](C)(C)C(C)(C)C)C(=O)O	4267.9	Standard non polar	33892256
20-Hydroxy-3,7,11,15,23-pentaoxolanost-8-en-26-oic acid,3TBDMS,isomer #21	CC(CC(=CC(C)(O)C1C=C(O[Si](C)(C)C(C)(C)C)C2(C)C3=C(C(=O)CC12C)C1(C)CCC(=O)C(C)(C)C1CC3=O)O[Si](C)(C)C(C)(C)C)C(=O)O[Si](C)(C)C(C)(C)C	4434.9	Semi standard non polar	33892256
20-Hydroxy-3,7,11,15,23-pentaoxolanost-8-en-26-oic acid,3TBDMS,isomer #21	CC(CC(=CC(C)(O)C1C=C(O[Si](C)(C)C(C)(C)C)C2(C)C3=C(C(=O)CC12C)C1(C)CCC(=O)C(C)(C)C1CC3=O)O[Si](C)(C)C(C)(C)C)C(=O)O[Si](C)(C)C(C)(C)C	4327.6	Standard non polar	33892256
20-Hydroxy-3,7,11,15,23-pentaoxolanost-8-en-26-oic acid,3TBDMS,isomer #22	CC(CC(=CC(C)(O)C1CC(=O)C2(C)C3=C(C(O[Si](C)(C)C(C)(C)C)=CC12C)C1(C)CCC(=O)C(C)(C)C1CC3=O)O[Si](C)(C)C(C)(C)C)C(=O)O[Si](C)(C)C(C)(C)C	4411.3	Semi standard non polar	33892256
20-Hydroxy-3,7,11,15,23-pentaoxolanost-8-en-26-oic acid,3TBDMS,isomer #22	CC(CC(=CC(C)(O)C1CC(=O)C2(C)C3=C(C(O[Si](C)(C)C(C)(C)C)=CC12C)C1(C)CCC(=O)C(C)(C)C1CC3=O)O[Si](C)(C)C(C)(C)C)C(=O)O[Si](C)(C)C(C)(C)C	4478.9	Standard non polar	33892256
20-Hydroxy-3,7,11,15,23-pentaoxolanost-8-en-26-oic acid,3TBDMS,isomer #23	CC(CC(=CC(C)(O)C1CC(=O)C2(C)C3=C(C(=O)CC12C)C1(C)CC=C(O[Si](C)(C)C(C)(C)C)C(C)(C)C1CC3=O)O[Si](C)(C)C(C)(C)C)C(=O)O[Si](C)(C)C(C)(C)C	4404.5	Semi standard non polar	33892256
20-Hydroxy-3,7,11,15,23-pentaoxolanost-8-en-26-oic acid,3TBDMS,isomer #23	CC(CC(=CC(C)(O)C1CC(=O)C2(C)C3=C(C(=O)CC12C)C1(C)CC=C(O[Si](C)(C)C(C)(C)C)C(C)(C)C1CC3=O)O[Si](C)(C)C(C)(C)C)C(=O)O[Si](C)(C)C(C)(C)C	4337.2	Standard non polar	33892256
20-Hydroxy-3,7,11,15,23-pentaoxolanost-8-en-26-oic acid,3TBDMS,isomer #24	CC(CC(=CC(C)(O)C1CC(=O)C2(C)C3=C(C(=O)CC12C)C1(C)CCC(=O)C(C)(C)C1C=C3O[Si](C)(C)C(C)(C)C)O[Si](C)(C)C(C)(C)C)C(=O)O[Si](C)(C)C(C)(C)C	4409.7	Semi standard non polar	33892256
20-Hydroxy-3,7,11,15,23-pentaoxolanost-8-en-26-oic acid,3TBDMS,isomer #24	CC(CC(=CC(C)(O)C1CC(=O)C2(C)C3=C(C(=O)CC12C)C1(C)CCC(=O)C(C)(C)C1C=C3O[Si](C)(C)C(C)(C)C)O[Si](C)(C)C(C)(C)C)C(=O)O[Si](C)(C)C(C)(C)C	4479.6	Standard non polar	33892256
20-Hydroxy-3,7,11,15,23-pentaoxolanost-8-en-26-oic acid,3TBDMS,isomer #25	CC(C=C(CC(C)(O)C1C=C(O[Si](C)(C)C(C)(C)C)C2(C)C3=C(C(=O)CC12C)C1(C)CCC(=O)C(C)(C)C1CC3=O)O[Si](C)(C)C(C)(C)C)C(=O)O[Si](C)(C)C(C)(C)C	4498.8	Semi standard non polar	33892256
20-Hydroxy-3,7,11,15,23-pentaoxolanost-8-en-26-oic acid,3TBDMS,isomer #25	CC(C=C(CC(C)(O)C1C=C(O[Si](C)(C)C(C)(C)C)C2(C)C3=C(C(=O)CC12C)C1(C)CCC(=O)C(C)(C)C1CC3=O)O[Si](C)(C)C(C)(C)C)C(=O)O[Si](C)(C)C(C)(C)C	4353.3	Standard non polar	33892256
20-Hydroxy-3,7,11,15,23-pentaoxolanost-8-en-26-oic acid,3TBDMS,isomer #26	CC(C=C(CC(C)(O)C1CC(=O)C2(C)C3=C(C(O[Si](C)(C)C(C)(C)C)=CC12C)C1(C)CCC(=O)C(C)(C)C1CC3=O)O[Si](C)(C)C(C)(C)C)C(=O)O[Si](C)(C)C(C)(C)C	4492.2	Semi standard non polar	33892256
20-Hydroxy-3,7,11,15,23-pentaoxolanost-8-en-26-oic acid,3TBDMS,isomer #26	CC(C=C(CC(C)(O)C1CC(=O)C2(C)C3=C(C(O[Si](C)(C)C(C)(C)C)=CC12C)C1(C)CCC(=O)C(C)(C)C1CC3=O)O[Si](C)(C)C(C)(C)C)C(=O)O[Si](C)(C)C(C)(C)C	4512.0	Standard non polar	33892256
20-Hydroxy-3,7,11,15,23-pentaoxolanost-8-en-26-oic acid,3TBDMS,isomer #27	CC(C=C(CC(C)(O)C1CC(=O)C2(C)C3=C(C(=O)CC12C)C1(C)CC=C(O[Si](C)(C)C(C)(C)C)C(C)(C)C1CC3=O)O[Si](C)(C)C(C)(C)C)C(=O)O[Si](C)(C)C(C)(C)C	4481.3	Semi standard non polar	33892256
20-Hydroxy-3,7,11,15,23-pentaoxolanost-8-en-26-oic acid,3TBDMS,isomer #27	CC(C=C(CC(C)(O)C1CC(=O)C2(C)C3=C(C(=O)CC12C)C1(C)CC=C(O[Si](C)(C)C(C)(C)C)C(C)(C)C1CC3=O)O[Si](C)(C)C(C)(C)C)C(=O)O[Si](C)(C)C(C)(C)C	4382.3	Standard non polar	33892256
20-Hydroxy-3,7,11,15,23-pentaoxolanost-8-en-26-oic acid,3TBDMS,isomer #28	CC(C=C(CC(C)(O)C1CC(=O)C2(C)C3=C(C(=O)CC12C)C1(C)CCC(=O)C(C)(C)C1C=C3O[Si](C)(C)C(C)(C)C)O[Si](C)(C)C(C)(C)C)C(=O)O[Si](C)(C)C(C)(C)C	4477.9	Semi standard non polar	33892256
20-Hydroxy-3,7,11,15,23-pentaoxolanost-8-en-26-oic acid,3TBDMS,isomer #28	CC(C=C(CC(C)(O)C1CC(=O)C2(C)C3=C(C(=O)CC12C)C1(C)CCC(=O)C(C)(C)C1C=C3O[Si](C)(C)C(C)(C)C)O[Si](C)(C)C(C)(C)C)C(=O)O[Si](C)(C)C(C)(C)C	4517.1	Standard non polar	33892256
20-Hydroxy-3,7,11,15,23-pentaoxolanost-8-en-26-oic acid,3TBDMS,isomer #29	CC(CC(=O)CC(C)(O)C1C=C(O[Si](C)(C)C(C)(C)C)C2(C)C3=C(C(O[Si](C)(C)C(C)(C)C)=CC12C)C1(C)CCC(=O)C(C)(C)C1CC3=O)C(=O)O[Si](C)(C)C(C)(C)C	4385.6	Semi standard non polar	33892256
20-Hydroxy-3,7,11,15,23-pentaoxolanost-8-en-26-oic acid,3TBDMS,isomer #29	CC(CC(=O)CC(C)(O)C1C=C(O[Si](C)(C)C(C)(C)C)C2(C)C3=C(C(O[Si](C)(C)C(C)(C)C)=CC12C)C1(C)CCC(=O)C(C)(C)C1CC3=O)C(=O)O[Si](C)(C)C(C)(C)C	4263.2	Standard non polar	33892256
20-Hydroxy-3,7,11,15,23-pentaoxolanost-8-en-26-oic acid,3TBDMS,isomer #3	CC(CC(=O)CC(C)(O[Si](C)(C)C(C)(C)C)C1C=C(O[Si](C)(C)C(C)(C)C)C2(C)C3=C(C(=O)CC12C)C1(C)CCC(=O)C(C)(C)C1CC3=O)C(=O)O[Si](C)(C)C(C)(C)C	4556.2	Semi standard non polar	33892256
20-Hydroxy-3,7,11,15,23-pentaoxolanost-8-en-26-oic acid,3TBDMS,isomer #3	CC(CC(=O)CC(C)(O[Si](C)(C)C(C)(C)C)C1C=C(O[Si](C)(C)C(C)(C)C)C2(C)C3=C(C(=O)CC12C)C1(C)CCC(=O)C(C)(C)C1CC3=O)C(=O)O[Si](C)(C)C(C)(C)C	4286.2	Standard non polar	33892256
20-Hydroxy-3,7,11,15,23-pentaoxolanost-8-en-26-oic acid,3TBDMS,isomer #30	CC(CC(=O)CC(C)(O)C1C=C(O[Si](C)(C)C(C)(C)C)C2(C)C3=C(C(=O)CC12C)C1(C)CC=C(O[Si](C)(C)C(C)(C)C)C(C)(C)C1CC3=O)C(=O)O[Si](C)(C)C(C)(C)C	4374.2	Semi standard non polar	33892256
20-Hydroxy-3,7,11,15,23-pentaoxolanost-8-en-26-oic acid,3TBDMS,isomer #30	CC(CC(=O)CC(C)(O)C1C=C(O[Si](C)(C)C(C)(C)C)C2(C)C3=C(C(=O)CC12C)C1(C)CC=C(O[Si](C)(C)C(C)(C)C)C(C)(C)C1CC3=O)C(=O)O[Si](C)(C)C(C)(C)C	4120.8	Standard non polar	33892256
20-Hydroxy-3,7,11,15,23-pentaoxolanost-8-en-26-oic acid,3TBDMS,isomer #31	CC(CC(=O)CC(C)(O)C1C=C(O[Si](C)(C)C(C)(C)C)C2(C)C3=C(C(=O)CC12C)C1(C)CCC(=O)C(C)(C)C1C=C3O[Si](C)(C)C(C)(C)C)C(=O)O[Si](C)(C)C(C)(C)C	4423.4	Semi standard non polar	33892256
20-Hydroxy-3,7,11,15,23-pentaoxolanost-8-en-26-oic acid,3TBDMS,isomer #31	CC(CC(=O)CC(C)(O)C1C=C(O[Si](C)(C)C(C)(C)C)C2(C)C3=C(C(=O)CC12C)C1(C)CCC(=O)C(C)(C)C1C=C3O[Si](C)(C)C(C)(C)C)C(=O)O[Si](C)(C)C(C)(C)C	4215.4	Standard non polar	33892256
20-Hydroxy-3,7,11,15,23-pentaoxolanost-8-en-26-oic acid,3TBDMS,isomer #32	CC(CC(=O)CC(C)(O)C1CC(=O)C2(C)C3=C(C(O[Si](C)(C)C(C)(C)C)=CC12C)C1(C)CC=C(O[Si](C)(C)C(C)(C)C)C(C)(C)C1CC3=O)C(=O)O[Si](C)(C)C(C)(C)C	4372.2	Semi standard non polar	33892256
20-Hydroxy-3,7,11,15,23-pentaoxolanost-8-en-26-oic acid,3TBDMS,isomer #32	CC(CC(=O)CC(C)(O)C1CC(=O)C2(C)C3=C(C(O[Si](C)(C)C(C)(C)C)=CC12C)C1(C)CC=C(O[Si](C)(C)C(C)(C)C)C(C)(C)C1CC3=O)C(=O)O[Si](C)(C)C(C)(C)C	4280.4	Standard non polar	33892256
20-Hydroxy-3,7,11,15,23-pentaoxolanost-8-en-26-oic acid,3TBDMS,isomer #33	CC(CC(=O)CC(C)(O)C1CC(=O)C2(C)C3=C(C(O[Si](C)(C)C(C)(C)C)=CC12C)C1(C)CCC(=O)C(C)(C)C1C=C3O[Si](C)(C)C(C)(C)C)C(=O)O[Si](C)(C)C(C)(C)C	4383.5	Semi standard non polar	33892256
20-Hydroxy-3,7,11,15,23-pentaoxolanost-8-en-26-oic acid,3TBDMS,isomer #33	CC(CC(=O)CC(C)(O)C1CC(=O)C2(C)C3=C(C(O[Si](C)(C)C(C)(C)C)=CC12C)C1(C)CCC(=O)C(C)(C)C1C=C3O[Si](C)(C)C(C)(C)C)C(=O)O[Si](C)(C)C(C)(C)C	4396.5	Standard non polar	33892256
20-Hydroxy-3,7,11,15,23-pentaoxolanost-8-en-26-oic acid,3TBDMS,isomer #34	CC(CC(=O)CC(C)(O)C1CC(=O)C2(C)C3=C(C(=O)CC12C)C1(C)CC=C(O[Si](C)(C)C(C)(C)C)C(C)(C)C1C=C3O[Si](C)(C)C(C)(C)C)C(=O)O[Si](C)(C)C(C)(C)C	4369.6	Semi standard non polar	33892256
20-Hydroxy-3,7,11,15,23-pentaoxolanost-8-en-26-oic acid,3TBDMS,isomer #34	CC(CC(=O)CC(C)(O)C1CC(=O)C2(C)C3=C(C(=O)CC12C)C1(C)CC=C(O[Si](C)(C)C(C)(C)C)C(C)(C)C1C=C3O[Si](C)(C)C(C)(C)C)C(=O)O[Si](C)(C)C(C)(C)C	4294.5	Standard non polar	33892256
20-Hydroxy-3,7,11,15,23-pentaoxolanost-8-en-26-oic acid,3TBDMS,isomer #35	CC(CC(=CC(C)(O)C1C=C(O[Si](C)(C)C(C)(C)C)C2(C)C3=C(C(O[Si](C)(C)C(C)(C)C)=CC12C)C1(C)CCC(=O)C(C)(C)C1CC3=O)O[Si](C)(C)C(C)(C)C)C(=O)O	4296.1	Semi standard non polar	33892256
20-Hydroxy-3,7,11,15,23-pentaoxolanost-8-en-26-oic acid,3TBDMS,isomer #35	CC(CC(=CC(C)(O)C1C=C(O[Si](C)(C)C(C)(C)C)C2(C)C3=C(C(O[Si](C)(C)C(C)(C)C)=CC12C)C1(C)CCC(=O)C(C)(C)C1CC3=O)O[Si](C)(C)C(C)(C)C)C(=O)O	4237.8	Standard non polar	33892256
20-Hydroxy-3,7,11,15,23-pentaoxolanost-8-en-26-oic acid,3TBDMS,isomer #36	CC(CC(=CC(C)(O)C1C=C(O[Si](C)(C)C(C)(C)C)C2(C)C3=C(C(=O)CC12C)C1(C)CC=C(O[Si](C)(C)C(C)(C)C)C(C)(C)C1CC3=O)O[Si](C)(C)C(C)(C)C)C(=O)O	4296.2	Semi standard non polar	33892256
20-Hydroxy-3,7,11,15,23-pentaoxolanost-8-en-26-oic acid,3TBDMS,isomer #36	CC(CC(=CC(C)(O)C1C=C(O[Si](C)(C)C(C)(C)C)C2(C)C3=C(C(=O)CC12C)C1(C)CC=C(O[Si](C)(C)C(C)(C)C)C(C)(C)C1CC3=O)O[Si](C)(C)C(C)(C)C)C(=O)O	4083.4	Standard non polar	33892256
20-Hydroxy-3,7,11,15,23-pentaoxolanost-8-en-26-oic acid,3TBDMS,isomer #37	CC(CC(=CC(C)(O)C1C=C(O[Si](C)(C)C(C)(C)C)C2(C)C3=C(C(=O)CC12C)C1(C)CCC(=O)C(C)(C)C1C=C3O[Si](C)(C)C(C)(C)C)O[Si](C)(C)C(C)(C)C)C(=O)O	4349.2	Semi standard non polar	33892256
20-Hydroxy-3,7,11,15,23-pentaoxolanost-8-en-26-oic acid,3TBDMS,isomer #37	CC(CC(=CC(C)(O)C1C=C(O[Si](C)(C)C(C)(C)C)C2(C)C3=C(C(=O)CC12C)C1(C)CCC(=O)C(C)(C)C1C=C3O[Si](C)(C)C(C)(C)C)O[Si](C)(C)C(C)(C)C)C(=O)O	4181.0	Standard non polar	33892256
20-Hydroxy-3,7,11,15,23-pentaoxolanost-8-en-26-oic acid,3TBDMS,isomer #38	CC(CC(=CC(C)(O)C1CC(=O)C2(C)C3=C(C(O[Si](C)(C)C(C)(C)C)=CC12C)C1(C)CC=C(O[Si](C)(C)C(C)(C)C)C(C)(C)C1CC3=O)O[Si](C)(C)C(C)(C)C)C(=O)O	4279.5	Semi standard non polar	33892256
20-Hydroxy-3,7,11,15,23-pentaoxolanost-8-en-26-oic acid,3TBDMS,isomer #38	CC(CC(=CC(C)(O)C1CC(=O)C2(C)C3=C(C(O[Si](C)(C)C(C)(C)C)=CC12C)C1(C)CC=C(O[Si](C)(C)C(C)(C)C)C(C)(C)C1CC3=O)O[Si](C)(C)C(C)(C)C)C(=O)O	4224.9	Standard non polar	33892256
20-Hydroxy-3,7,11,15,23-pentaoxolanost-8-en-26-oic acid,3TBDMS,isomer #39	CC(CC(=CC(C)(O)C1CC(=O)C2(C)C3=C(C(O[Si](C)(C)C(C)(C)C)=CC12C)C1(C)CCC(=O)C(C)(C)C1C=C3O[Si](C)(C)C(C)(C)C)O[Si](C)(C)C(C)(C)C)C(=O)O	4304.8	Semi standard non polar	33892256
20-Hydroxy-3,7,11,15,23-pentaoxolanost-8-en-26-oic acid,3TBDMS,isomer #39	CC(CC(=CC(C)(O)C1CC(=O)C2(C)C3=C(C(O[Si](C)(C)C(C)(C)C)=CC12C)C1(C)CCC(=O)C(C)(C)C1C=C3O[Si](C)(C)C(C)(C)C)O[Si](C)(C)C(C)(C)C)C(=O)O	4340.9	Standard non polar	33892256
20-Hydroxy-3,7,11,15,23-pentaoxolanost-8-en-26-oic acid,3TBDMS,isomer #4	CC(CC(=O)CC(C)(O[Si](C)(C)C(C)(C)C)C1CC(=O)C2(C)C3=C(C(O[Si](C)(C)C(C)(C)C)=CC12C)C1(C)CCC(=O)C(C)(C)C1CC3=O)C(=O)O[Si](C)(C)C(C)(C)C	4517.2	Semi standard non polar	33892256
20-Hydroxy-3,7,11,15,23-pentaoxolanost-8-en-26-oic acid,3TBDMS,isomer #4	CC(CC(=O)CC(C)(O[Si](C)(C)C(C)(C)C)C1CC(=O)C2(C)C3=C(C(O[Si](C)(C)C(C)(C)C)=CC12C)C1(C)CCC(=O)C(C)(C)C1CC3=O)C(=O)O[Si](C)(C)C(C)(C)C	4476.9	Standard non polar	33892256
20-Hydroxy-3,7,11,15,23-pentaoxolanost-8-en-26-oic acid,3TBDMS,isomer #40	CC(CC(=CC(C)(O)C1CC(=O)C2(C)C3=C(C(=O)CC12C)C1(C)CC=C(O[Si](C)(C)C(C)(C)C)C(C)(C)C1C=C3O[Si](C)(C)C(C)(C)C)O[Si](C)(C)C(C)(C)C)C(=O)O	4292.0	Semi standard non polar	33892256
20-Hydroxy-3,7,11,15,23-pentaoxolanost-8-en-26-oic acid,3TBDMS,isomer #40	CC(CC(=CC(C)(O)C1CC(=O)C2(C)C3=C(C(=O)CC12C)C1(C)CC=C(O[Si](C)(C)C(C)(C)C)C(C)(C)C1C=C3O[Si](C)(C)C(C)(C)C)O[Si](C)(C)C(C)(C)C)C(=O)O	4230.4	Standard non polar	33892256
20-Hydroxy-3,7,11,15,23-pentaoxolanost-8-en-26-oic acid,3TBDMS,isomer #41	CC(C=C(CC(C)(O)C1C=C(O[Si](C)(C)C(C)(C)C)C2(C)C3=C(C(O[Si](C)(C)C(C)(C)C)=CC12C)C1(C)CCC(=O)C(C)(C)C1CC3=O)O[Si](C)(C)C(C)(C)C)C(=O)O	4353.3	Semi standard non polar	33892256
20-Hydroxy-3,7,11,15,23-pentaoxolanost-8-en-26-oic acid,3TBDMS,isomer #41	CC(C=C(CC(C)(O)C1C=C(O[Si](C)(C)C(C)(C)C)C2(C)C3=C(C(O[Si](C)(C)C(C)(C)C)=CC12C)C1(C)CCC(=O)C(C)(C)C1CC3=O)O[Si](C)(C)C(C)(C)C)C(=O)O	4301.1	Standard non polar	33892256
20-Hydroxy-3,7,11,15,23-pentaoxolanost-8-en-26-oic acid,3TBDMS,isomer #42	CC(C=C(CC(C)(O)C1C=C(O[Si](C)(C)C(C)(C)C)C2(C)C3=C(C(=O)CC12C)C1(C)CC=C(O[Si](C)(C)C(C)(C)C)C(C)(C)C1CC3=O)O[Si](C)(C)C(C)(C)C)C(=O)O	4352.9	Semi standard non polar	33892256
20-Hydroxy-3,7,11,15,23-pentaoxolanost-8-en-26-oic acid,3TBDMS,isomer #42	CC(C=C(CC(C)(O)C1C=C(O[Si](C)(C)C(C)(C)C)C2(C)C3=C(C(=O)CC12C)C1(C)CC=C(O[Si](C)(C)C(C)(C)C)C(C)(C)C1CC3=O)O[Si](C)(C)C(C)(C)C)C(=O)O	4151.4	Standard non polar	33892256
20-Hydroxy-3,7,11,15,23-pentaoxolanost-8-en-26-oic acid,3TBDMS,isomer #43	CC(C=C(CC(C)(O)C1C=C(O[Si](C)(C)C(C)(C)C)C2(C)C3=C(C(=O)CC12C)C1(C)CCC(=O)C(C)(C)C1C=C3O[Si](C)(C)C(C)(C)C)O[Si](C)(C)C(C)(C)C)C(=O)O	4415.7	Semi standard non polar	33892256
20-Hydroxy-3,7,11,15,23-pentaoxolanost-8-en-26-oic acid,3TBDMS,isomer #43	CC(C=C(CC(C)(O)C1C=C(O[Si](C)(C)C(C)(C)C)C2(C)C3=C(C(=O)CC12C)C1(C)CCC(=O)C(C)(C)C1C=C3O[Si](C)(C)C(C)(C)C)O[Si](C)(C)C(C)(C)C)C(=O)O	4247.3	Standard non polar	33892256
20-Hydroxy-3,7,11,15,23-pentaoxolanost-8-en-26-oic acid,3TBDMS,isomer #44	CC(C=C(CC(C)(O)C1CC(=O)C2(C)C3=C(C(O[Si](C)(C)C(C)(C)C)=CC12C)C1(C)CC=C(O[Si](C)(C)C(C)(C)C)C(C)(C)C1CC3=O)O[Si](C)(C)C(C)(C)C)C(=O)O	4355.5	Semi standard non polar	33892256
20-Hydroxy-3,7,11,15,23-pentaoxolanost-8-en-26-oic acid,3TBDMS,isomer #44	CC(C=C(CC(C)(O)C1CC(=O)C2(C)C3=C(C(O[Si](C)(C)C(C)(C)C)=CC12C)C1(C)CC=C(O[Si](C)(C)C(C)(C)C)C(C)(C)C1CC3=O)O[Si](C)(C)C(C)(C)C)C(=O)O	4313.0	Standard non polar	33892256
20-Hydroxy-3,7,11,15,23-pentaoxolanost-8-en-26-oic acid,3TBDMS,isomer #45	CC(C=C(CC(C)(O)C1CC(=O)C2(C)C3=C(C(O[Si](C)(C)C(C)(C)C)=CC12C)C1(C)CCC(=O)C(C)(C)C1C=C3O[Si](C)(C)C(C)(C)C)O[Si](C)(C)C(C)(C)C)C(=O)O	4374.8	Semi standard non polar	33892256
20-Hydroxy-3,7,11,15,23-pentaoxolanost-8-en-26-oic acid,3TBDMS,isomer #45	CC(C=C(CC(C)(O)C1CC(=O)C2(C)C3=C(C(O[Si](C)(C)C(C)(C)C)=CC12C)C1(C)CCC(=O)C(C)(C)C1C=C3O[Si](C)(C)C(C)(C)C)O[Si](C)(C)C(C)(C)C)C(=O)O	4417.0	Standard non polar	33892256
20-Hydroxy-3,7,11,15,23-pentaoxolanost-8-en-26-oic acid,3TBDMS,isomer #46	CC(C=C(CC(C)(O)C1CC(=O)C2(C)C3=C(C(=O)CC12C)C1(C)CC=C(O[Si](C)(C)C(C)(C)C)C(C)(C)C1C=C3O[Si](C)(C)C(C)(C)C)O[Si](C)(C)C(C)(C)C)C(=O)O	4369.0	Semi standard non polar	33892256
20-Hydroxy-3,7,11,15,23-pentaoxolanost-8-en-26-oic acid,3TBDMS,isomer #46	CC(C=C(CC(C)(O)C1CC(=O)C2(C)C3=C(C(=O)CC12C)C1(C)CC=C(O[Si](C)(C)C(C)(C)C)C(C)(C)C1C=C3O[Si](C)(C)C(C)(C)C)O[Si](C)(C)C(C)(C)C)C(=O)O	4319.1	Standard non polar	33892256
20-Hydroxy-3,7,11,15,23-pentaoxolanost-8-en-26-oic acid,3TBDMS,isomer #47	CC(CC(=O)CC(C)(O)C1C=C(O[Si](C)(C)C(C)(C)C)C2(C)C3=C(C(O[Si](C)(C)C(C)(C)C)=CC12C)C1(C)CC=C(O[Si](C)(C)C(C)(C)C)C(C)(C)C1CC3=O)C(=O)O	4239.8	Semi standard non polar	33892256
20-Hydroxy-3,7,11,15,23-pentaoxolanost-8-en-26-oic acid,3TBDMS,isomer #47	CC(CC(=O)CC(C)(O)C1C=C(O[Si](C)(C)C(C)(C)C)C2(C)C3=C(C(O[Si](C)(C)C(C)(C)C)=CC12C)C1(C)CC=C(O[Si](C)(C)C(C)(C)C)C(C)(C)C1CC3=O)C(=O)O	4078.5	Standard non polar	33892256
20-Hydroxy-3,7,11,15,23-pentaoxolanost-8-en-26-oic acid,3TBDMS,isomer #48	CC(CC(=O)CC(C)(O)C1C=C(O[Si](C)(C)C(C)(C)C)C2(C)C3=C(C(O[Si](C)(C)C(C)(C)C)=CC12C)C1(C)CCC(=O)C(C)(C)C1C=C3O[Si](C)(C)C(C)(C)C)C(=O)O	4305.0	Semi standard non polar	33892256
20-Hydroxy-3,7,11,15,23-pentaoxolanost-8-en-26-oic acid,3TBDMS,isomer #48	CC(CC(=O)CC(C)(O)C1C=C(O[Si](C)(C)C(C)(C)C)C2(C)C3=C(C(O[Si](C)(C)C(C)(C)C)=CC12C)C1(C)CCC(=O)C(C)(C)C1C=C3O[Si](C)(C)C(C)(C)C)C(=O)O	4158.0	Standard non polar	33892256
20-Hydroxy-3,7,11,15,23-pentaoxolanost-8-en-26-oic acid,3TBDMS,isomer #49	CC(CC(=O)CC(C)(O)C1C=C(O[Si](C)(C)C(C)(C)C)C2(C)C3=C(C(=O)CC12C)C1(C)CC=C(O[Si](C)(C)C(C)(C)C)C(C)(C)C1C=C3O[Si](C)(C)C(C)(C)C)C(=O)O	4300.5	Semi standard non polar	33892256
20-Hydroxy-3,7,11,15,23-pentaoxolanost-8-en-26-oic acid,3TBDMS,isomer #49	CC(CC(=O)CC(C)(O)C1C=C(O[Si](C)(C)C(C)(C)C)C2(C)C3=C(C(=O)CC12C)C1(C)CC=C(O[Si](C)(C)C(C)(C)C)C(C)(C)C1C=C3O[Si](C)(C)C(C)(C)C)C(=O)O	4027.8	Standard non polar	33892256
20-Hydroxy-3,7,11,15,23-pentaoxolanost-8-en-26-oic acid,3TBDMS,isomer #5	CC(CC(=O)CC(C)(O[Si](C)(C)C(C)(C)C)C1CC(=O)C2(C)C3=C(C(=O)CC12C)C1(C)CC=C(O[Si](C)(C)C(C)(C)C)C(C)(C)C1CC3=O)C(=O)O[Si](C)(C)C(C)(C)C	4508.2	Semi standard non polar	33892256
20-Hydroxy-3,7,11,15,23-pentaoxolanost-8-en-26-oic acid,3TBDMS,isomer #5	CC(CC(=O)CC(C)(O[Si](C)(C)C(C)(C)C)C1CC(=O)C2(C)C3=C(C(=O)CC12C)C1(C)CC=C(O[Si](C)(C)C(C)(C)C)C(C)(C)C1CC3=O)C(=O)O[Si](C)(C)C(C)(C)C	4322.0	Standard non polar	33892256
20-Hydroxy-3,7,11,15,23-pentaoxolanost-8-en-26-oic acid,3TBDMS,isomer #50	CC(CC(=O)CC(C)(O)C1CC(=O)C2(C)C3=C(C(O[Si](C)(C)C(C)(C)C)=CC12C)C1(C)CC=C(O[Si](C)(C)C(C)(C)C)C(C)(C)C1C=C3O[Si](C)(C)C(C)(C)C)C(=O)O	4261.3	Semi standard non polar	33892256
20-Hydroxy-3,7,11,15,23-pentaoxolanost-8-en-26-oic acid,3TBDMS,isomer #50	CC(CC(=O)CC(C)(O)C1CC(=O)C2(C)C3=C(C(O[Si](C)(C)C(C)(C)C)=CC12C)C1(C)CC=C(O[Si](C)(C)C(C)(C)C)C(C)(C)C1C=C3O[Si](C)(C)C(C)(C)C)C(=O)O	4215.1	Standard non polar	33892256
20-Hydroxy-3,7,11,15,23-pentaoxolanost-8-en-26-oic acid,3TBDMS,isomer #6	CC(CC(=O)CC(C)(O[Si](C)(C)C(C)(C)C)C1CC(=O)C2(C)C3=C(C(=O)CC12C)C1(C)CCC(=O)C(C)(C)C1C=C3O[Si](C)(C)C(C)(C)C)C(=O)O[Si](C)(C)C(C)(C)C	4511.0	Semi standard non polar	33892256
20-Hydroxy-3,7,11,15,23-pentaoxolanost-8-en-26-oic acid,3TBDMS,isomer #6	CC(CC(=O)CC(C)(O[Si](C)(C)C(C)(C)C)C1CC(=O)C2(C)C3=C(C(=O)CC12C)C1(C)CCC(=O)C(C)(C)C1C=C3O[Si](C)(C)C(C)(C)C)C(=O)O[Si](C)(C)C(C)(C)C	4479.1	Standard non polar	33892256
20-Hydroxy-3,7,11,15,23-pentaoxolanost-8-en-26-oic acid,3TBDMS,isomer #7	CC(CC(=CC(C)(O[Si](C)(C)C(C)(C)C)C1C=C(O[Si](C)(C)C(C)(C)C)C2(C)C3=C(C(=O)CC12C)C1(C)CCC(=O)C(C)(C)C1CC3=O)O[Si](C)(C)C(C)(C)C)C(=O)O	4461.1	Semi standard non polar	33892256
20-Hydroxy-3,7,11,15,23-pentaoxolanost-8-en-26-oic acid,3TBDMS,isomer #7	CC(CC(=CC(C)(O[Si](C)(C)C(C)(C)C)C1C=C(O[Si](C)(C)C(C)(C)C)C2(C)C3=C(C(=O)CC12C)C1(C)CCC(=O)C(C)(C)C1CC3=O)O[Si](C)(C)C(C)(C)C)C(=O)O	4284.6	Standard non polar	33892256
20-Hydroxy-3,7,11,15,23-pentaoxolanost-8-en-26-oic acid,3TBDMS,isomer #8	CC(CC(=CC(C)(O[Si](C)(C)C(C)(C)C)C1CC(=O)C2(C)C3=C(C(O[Si](C)(C)C(C)(C)C)=CC12C)C1(C)CCC(=O)C(C)(C)C1CC3=O)O[Si](C)(C)C(C)(C)C)C(=O)O	4429.1	Semi standard non polar	33892256
20-Hydroxy-3,7,11,15,23-pentaoxolanost-8-en-26-oic acid,3TBDMS,isomer #8	CC(CC(=CC(C)(O[Si](C)(C)C(C)(C)C)C1CC(=O)C2(C)C3=C(C(O[Si](C)(C)C(C)(C)C)=CC12C)C1(C)CCC(=O)C(C)(C)C1CC3=O)O[Si](C)(C)C(C)(C)C)C(=O)O	4442.4	Standard non polar	33892256
20-Hydroxy-3,7,11,15,23-pentaoxolanost-8-en-26-oic acid,3TBDMS,isomer #9	CC(CC(=CC(C)(O[Si](C)(C)C(C)(C)C)C1CC(=O)C2(C)C3=C(C(=O)CC12C)C1(C)CC=C(O[Si](C)(C)C(C)(C)C)C(C)(C)C1CC3=O)O[Si](C)(C)C(C)(C)C)C(=O)O	4416.0	Semi standard non polar	33892256
20-Hydroxy-3,7,11,15,23-pentaoxolanost-8-en-26-oic acid,3TBDMS,isomer #9	CC(CC(=CC(C)(O[Si](C)(C)C(C)(C)C)C1CC(=O)C2(C)C3=C(C(=O)CC12C)C1(C)CC=C(O[Si](C)(C)C(C)(C)C)C(C)(C)C1CC3=O)O[Si](C)(C)C(C)(C)C)C(=O)O	4287.0	Standard non polar	33892256

Spectra

GC-MS Spectra

Spectrum Type	Description	Splash Key	Deposition Date	Source	View
Predicted GC-MS	Predicted GC-MS Spectrum - 20-Hydroxy-3,7,11,15,23-pentaoxolanost-8-en-26-oic acid GC-MS (Non-derivatized) - 70eV, Positive	splash10-0f6w-5128960000-24a292f38fcc2732ad18	2017-09-01	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - 20-Hydroxy-3,7,11,15,23-pentaoxolanost-8-en-26-oic acid GC-MS (2 TMS) - 70eV, Positive	splash10-0a4i-4002139000-7183f288648adb74511b	2017-10-06	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - 20-Hydroxy-3,7,11,15,23-pentaoxolanost-8-en-26-oic acid GC-MS (TMS_1_1) - 70eV, Positive	Not Available	2021-10-12	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - 20-Hydroxy-3,7,11,15,23-pentaoxolanost-8-en-26-oic acid GC-MS (TMS_1_2) - 70eV, Positive	Not Available	2021-10-12	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - 20-Hydroxy-3,7,11,15,23-pentaoxolanost-8-en-26-oic acid GC-MS (TMS_1_3) - 70eV, Positive	Not Available	2021-10-12	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - 20-Hydroxy-3,7,11,15,23-pentaoxolanost-8-en-26-oic acid GC-MS (TMS_1_4) - 70eV, Positive	Not Available	2021-10-12	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - 20-Hydroxy-3,7,11,15,23-pentaoxolanost-8-en-26-oic acid GC-MS (TMS_1_5) - 70eV, Positive	Not Available	2021-10-12	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - 20-Hydroxy-3,7,11,15,23-pentaoxolanost-8-en-26-oic acid GC-MS (TMS_1_6) - 70eV, Positive	Not Available	2021-10-12	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - 20-Hydroxy-3,7,11,15,23-pentaoxolanost-8-en-26-oic acid GC-MS (TMS_1_7) - 70eV, Positive	Not Available	2021-10-12	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - 20-Hydroxy-3,7,11,15,23-pentaoxolanost-8-en-26-oic acid GC-MS (TMS_1_8) - 70eV, Positive	Not Available	2021-10-12	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - 20-Hydroxy-3,7,11,15,23-pentaoxolanost-8-en-26-oic acid GC-MS (TMS_2_2) - 70eV, Positive	Not Available	2021-10-12	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - 20-Hydroxy-3,7,11,15,23-pentaoxolanost-8-en-26-oic acid GC-MS (TMS_2_3) - 70eV, Positive	Not Available	2021-10-12	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - 20-Hydroxy-3,7,11,15,23-pentaoxolanost-8-en-26-oic acid GC-MS (TMS_2_4) - 70eV, Positive	Not Available	2021-10-12	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - 20-Hydroxy-3,7,11,15,23-pentaoxolanost-8-en-26-oic acid GC-MS (TMS_2_5) - 70eV, Positive	Not Available	2021-10-12	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - 20-Hydroxy-3,7,11,15,23-pentaoxolanost-8-en-26-oic acid GC-MS (TMS_2_6) - 70eV, Positive	Not Available	2021-10-12	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - 20-Hydroxy-3,7,11,15,23-pentaoxolanost-8-en-26-oic acid GC-MS (TMS_2_7) - 70eV, Positive	Not Available	2021-10-12	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - 20-Hydroxy-3,7,11,15,23-pentaoxolanost-8-en-26-oic acid GC-MS (TMS_2_8) - 70eV, Positive	Not Available	2021-10-12	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - 20-Hydroxy-3,7,11,15,23-pentaoxolanost-8-en-26-oic acid GC-MS (TMS_2_9) - 70eV, Positive	Not Available	2021-10-12	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - 20-Hydroxy-3,7,11,15,23-pentaoxolanost-8-en-26-oic acid GC-MS (TMS_2_10) - 70eV, Positive	Not Available	2021-10-12	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - 20-Hydroxy-3,7,11,15,23-pentaoxolanost-8-en-26-oic acid GC-MS (TMS_2_11) - 70eV, Positive	Not Available	2021-10-12	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - 20-Hydroxy-3,7,11,15,23-pentaoxolanost-8-en-26-oic acid GC-MS (TMS_2_12) - 70eV, Positive	Not Available	2021-10-12	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - 20-Hydroxy-3,7,11,15,23-pentaoxolanost-8-en-26-oic acid GC-MS (TMS_2_13) - 70eV, Positive	Not Available	2021-10-12	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - 20-Hydroxy-3,7,11,15,23-pentaoxolanost-8-en-26-oic acid GC-MS (TMS_2_14) - 70eV, Positive	Not Available	2021-10-12	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - 20-Hydroxy-3,7,11,15,23-pentaoxolanost-8-en-26-oic acid GC-MS (TMS_2_15) - 70eV, Positive	Not Available	2021-10-12	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - 20-Hydroxy-3,7,11,15,23-pentaoxolanost-8-en-26-oic acid GC-MS (TMS_2_16) - 70eV, Positive	Not Available	2021-10-12	Wishart Lab	View Spectrum

MS/MS Spectra

Spectrum Type	Description	Splash Key	Deposition Date	Source	View
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 20-Hydroxy-3,7,11,15,23-pentaoxolanost-8-en-26-oic acid 10V, Positive-QTOF	splash10-03fu-1201790000-24721d9de913900fb933	2016-08-03	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 20-Hydroxy-3,7,11,15,23-pentaoxolanost-8-en-26-oic acid 20V, Positive-QTOF	splash10-014l-4113910000-446dbe27bb9d8c05805c	2016-08-03	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 20-Hydroxy-3,7,11,15,23-pentaoxolanost-8-en-26-oic acid 40V, Positive-QTOF	splash10-014i-9400400000-075828cea3562bcfc3e7	2016-08-03	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 20-Hydroxy-3,7,11,15,23-pentaoxolanost-8-en-26-oic acid 10V, Negative-QTOF	splash10-004i-0201190000-24522cbcf6571be6e8be	2016-08-04	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 20-Hydroxy-3,7,11,15,23-pentaoxolanost-8-en-26-oic acid 20V, Negative-QTOF	splash10-0adj-9407560000-bc3cf6bbad8811bb57bb	2016-08-04	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 20-Hydroxy-3,7,11,15,23-pentaoxolanost-8-en-26-oic acid 40V, Negative-QTOF	splash10-0a4i-9023320000-e3d34fc2637ba55b7bf4	2016-08-04	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 20-Hydroxy-3,7,11,15,23-pentaoxolanost-8-en-26-oic acid 10V, Positive-QTOF	splash10-052f-2402930000-e9adece466e6f7eda9f4	2021-09-24	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 20-Hydroxy-3,7,11,15,23-pentaoxolanost-8-en-26-oic acid 20V, Positive-QTOF	splash10-0pb9-7902210000-12dd368c2ecbc07bcf1b	2021-09-24	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 20-Hydroxy-3,7,11,15,23-pentaoxolanost-8-en-26-oic acid 40V, Positive-QTOF	splash10-014m-9113000000-f4ae0ed7507d6e180862	2021-09-24	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 20-Hydroxy-3,7,11,15,23-pentaoxolanost-8-en-26-oic acid 10V, Negative-QTOF	splash10-004i-0000090000-a966ada09238864f8f68	2021-09-24	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 20-Hydroxy-3,7,11,15,23-pentaoxolanost-8-en-26-oic acid 20V, Negative-QTOF	splash10-014i-1000920000-95590b18a4f08668ad06	2021-09-24	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 20-Hydroxy-3,7,11,15,23-pentaoxolanost-8-en-26-oic acid 40V, Negative-QTOF	splash10-05ui-6003910000-15f1555e2ad58211b54b	2021-09-24	Wishart Lab	View Spectrum

Biological Properties

Cellular Locations

Extracellular

Biospecimen Locations

Not Available

Tissue Locations

Not Available

Pathways

Not Available

Name	SMPDB/PathBank	KEGG

Normal Concentrations

Not Available

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

FDB014680

KNApSAcK ID

Not Available

Chemspider ID

2788145

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

131751880

PDB ID

Not Available

ChEBI ID

175951

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

Simons K, Toomre D: Lipid rafts and signal transduction. Nat Rev Mol Cell Biol. 2000 Oct;1(1):31-9. [PubMed:11413487 ]
Watson AD: Thematic review series: systems biology approaches to metabolic and cardiovascular disorders. Lipidomics: a global approach to lipid analysis in biological systems. J Lipid Res. 2006 Oct;47(10):2101-11. Epub 2006 Aug 10. [PubMed:16902246 ]
Sethi JK, Vidal-Puig AJ: Thematic review series: adipocyte biology. Adipose tissue function and plasticity orchestrate nutritional adaptation. J Lipid Res. 2007 Jun;48(6):1253-62. Epub 2007 Mar 20. [PubMed:17374880 ]
Lingwood D, Simons K: Lipid rafts as a membrane-organizing principle. Science. 2010 Jan 1;327(5961):46-50. doi: 10.1126/science.1174621. [PubMed:20044567 ]
(). Yannai, Shmuel. (2004) Dictionary of food compounds with CD-ROM: Additives, flavors, and ingredients. Boca Raton: Chapman & Hall/CRC.. .
Gunstone, Frank D., John L. Harwood, and Albert J. Dijkstra (2007). The lipid handbook with CD-ROM. CRC Press.

Showing metabocard for 20-Hydroxy-3,7,11,15,23-pentaoxolanost-8-en-26-oic acid (HMDB0035895)

MOL for HMDB0035895 (20-Hydroxy-3,7,11,15,23-pentaoxolanost-8-en-26-oic acid)

3D MOL for HMDB0035895 (20-Hydroxy-3,7,11,15,23-pentaoxolanost-8-en-26-oic acid)

3D SDF for HMDB0035895 (20-Hydroxy-3,7,11,15,23-pentaoxolanost-8-en-26-oic acid)

3D-SDF for HMDB0035895 (20-Hydroxy-3,7,11,15,23-pentaoxolanost-8-en-26-oic acid)

PDB for HMDB0035895 (20-Hydroxy-3,7,11,15,23-pentaoxolanost-8-en-26-oic acid)

3D PDB for HMDB0035895 (20-Hydroxy-3,7,11,15,23-pentaoxolanost-8-en-26-oic acid)

SMILES for HMDB0035895 (20-Hydroxy-3,7,11,15,23-pentaoxolanost-8-en-26-oic acid)

INCHI for HMDB0035895 (20-Hydroxy-3,7,11,15,23-pentaoxolanost-8-en-26-oic acid)

Structure for HMDB0035895 (20-Hydroxy-3,7,11,15,23-pentaoxolanost-8-en-26-oic acid)

3D Structure for HMDB0035895 (20-Hydroxy-3,7,11,15,23-pentaoxolanost-8-en-26-oic acid)

Predicted Collision Cross Sections

Predicted Retention Times

Underivatized

Predicted Kovats Retention Indices

Underivatized

Derivatized

GC-MS Spectra

MS/MS Spectra