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Record Information

Version

5.0

Status

Expected but not Quantified

Creation Date

2012-09-11 20:10:22 UTC

Update Date

2022-03-07 02:54:25 UTC

HMDB ID

HMDB0035221

Secondary Accession Numbers

HMDB35221

Metabolite Identification

Common Name

(3beta,17alpha,23S)-17,23-Epoxy-3,28,29-trihydroxy-27-norlanost-8-en-24-one

Description

(3beta,17alpha,23S)-17,23-Epoxy-3,28,29-trihydroxy-27-norlanost-8-en-24-one 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 (3beta,17alpha,23S)-17,23-Epoxy-3,28,29-trihydroxy-27-norlanost-8-en-24-one.

Structure

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


  Mrv0541 02241212012D          

 34 38  0  0  0  0            999 V2000
    1.8828    1.1994    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.8828    2.0244    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.0991    2.2801    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.6138    1.6119    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.0991    0.9451    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5831    0.2771    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.0991   -0.3896    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.3140   -0.1340    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.3140    0.6894    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3993    1.1019    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1142    0.6894    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1142   -0.1340    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3993   -0.5465    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3993   -1.3714    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1142   -1.7838    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8292   -1.3714    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8292   -0.5465    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5427   -0.1340    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
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   -3.2576   -1.3714    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5427   -1.7838    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0734   -2.4163    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0666   -3.3112    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0134   -2.4163    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0202   -3.3292    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.1009    1.4869    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8292    0.2771    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9725   -1.7838    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1009    2.0244    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5510    2.5083    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3044    2.1715    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.9725    2.6555    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.4657    3.3292    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.3140   -0.9590    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0  0  0  0
  1  5  1  0  0  0  0
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  2 30  1  0  0  0  0
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  4  5  1  0  0  0  0
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  6  7  1  0  0  0  0
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  8 13  1  0  0  0  0
  8 34  1  0  0  0  0
  9 10  1  0  0  0  0
  9 26  1  0  0  0  0
 10 11  1  0  0  0  0
 11 12  1  0  0  0  0
 12 13  2  0  0  0  0
 12 17  1  0  0  0  0
 13 14  1  0  0  0  0
 14 15  1  0  0  0  0
 15 16  1  0  0  0  0
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 16 21  1  0  0  0  0
 17 18  1  0  0  0  0
 17 27  1  0  0  0  0
 18 19  1  0  0  0  0
 19 20  1  0  0  0  0
 20 21  1  0  0  0  0
 20 28  1  0  0  0  0
 21 22  1  0  0  0  0
 21 24  1  0  0  0  0
 22 23  1  0  0  0  0
 24 25  1  0  0  0  0
 30 31  1  0  0  0  0
 30 33  2  0  0  0  0
 31 32  1  0  0  0  0
M  END

HMDB0035221
     RDKit          3D
(3beta,17alpha,23S)-17,23-Epoxy-3,28,29-trihydroxy-27-norlanost-8-en-24-one
 80 84  0  0  0  0  0  0  0  0999 V2000
   -6.5282    3.3547   -0.9349 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.4047    1.9115   -0.5592 C   0  0  0  0  0  0  0  0  0  0  0  0
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   -1.5891   -0.6200    0.4073 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1448   -1.2674    1.7016 C   0  0  0  0  0  0  0  0  0  0  0  0
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 31 76  1  0
 32 77  1  0
 32 78  1  0
 33 79  1  0
 33 80  1  0
M  END


  Mrv0541 02241212012D          

 34 38  0  0  0  0            999 V2000
    1.8828    1.1994    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.8828    2.0244    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.0991    2.2801    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.6138    1.6119    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
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  4 29  1  0  0  0  0
  5  6  1  0  0  0  0
  5  9  1  0  0  0  0
  6  7  1  0  0  0  0
  7  8  1  0  0  0  0
  8  9  1  0  0  0  0
  8 13  1  0  0  0  0
  8 34  1  0  0  0  0
  9 10  1  0  0  0  0
  9 26  1  0  0  0  0
 10 11  1  0  0  0  0
 11 12  1  0  0  0  0
 12 13  2  0  0  0  0
 12 17  1  0  0  0  0
 13 14  1  0  0  0  0
 14 15  1  0  0  0  0
 15 16  1  0  0  0  0
 16 17  1  0  0  0  0
 16 21  1  0  0  0  0
 17 18  1  0  0  0  0
 17 27  1  0  0  0  0
 18 19  1  0  0  0  0
 19 20  1  0  0  0  0
 20 21  1  0  0  0  0
 20 28  1  0  0  0  0
 21 22  1  0  0  0  0
 21 24  1  0  0  0  0
 22 23  1  0  0  0  0
 24 25  1  0  0  0  0
 30 31  1  0  0  0  0
 30 33  2  0  0  0  0
 31 32  1  0  0  0  0
M  END
> <DATABASE_ID>
HMDB0035221

> <DATABASE_NAME>
hmdb

> <SMILES>
CCC(=O)C1CC(C)C2(CCC3(C)C4=C(CCC23C)C2(C)CCC(O)C(CO)(CO)C2CC4)O1

> <INCHI_IDENTIFIER>
InChI=1S/C29H46O5/c1-6-21(32)22-15-18(2)29(34-22)14-13-26(4)20-7-8-23-25(3,19(20)9-12-27(26,29)5)11-10-24(33)28(23,16-30)17-31/h18,22-24,30-31,33H,6-17H2,1-5H3

> <INCHI_KEY>
PGCCXLDWXXFVMP-UHFFFAOYSA-N

> <FORMULA>
C29H46O5

> <MOLECULAR_WEIGHT>
474.6725

> <EXACT_MASS>
474.334524582

> <JCHEM_ACCEPTOR_COUNT>
5

> <JCHEM_AVERAGE_POLARIZABILITY>
55.605775049768454

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
3

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
1-[5'-hydroxy-6',6'-bis(hydroxymethyl)-2',3,11',15'-tetramethylspiro[oxolane-2,14'-tetracyclo[8.7.0.0²,⁷.0¹¹,¹⁵]heptadecan]-1'(10')-en-5-yl]propan-1-one

> <ALOGPS_LOGP>
3.95

> <JCHEM_LOGP>
3.2937644839999987

> <ALOGPS_LOGS>
-4.84

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
5

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
14.92016625756398

> <JCHEM_PKA_STRONGEST_ACIDIC>
14.297359845042266

> <JCHEM_PKA_STRONGEST_BASIC>
-2.8201325690842687

> <JCHEM_POLAR_SURFACE_AREA>
86.99000000000001

> <JCHEM_REFRACTIVITY>
132.77009999999996

> <JCHEM_ROTATABLE_BOND_COUNT>
4

> <JCHEM_RULE_OF_FIVE>
1

> <ALOGPS_SOLUBILITY>
6.79e-03 g/l

> <JCHEM_TRADITIONAL_IUPAC>
1-[5'-hydroxy-6',6'-bis(hydroxymethyl)-2',3,11',15'-tetramethylspiro[oxolane-2,14'-tetracyclo[8.7.0.0²,⁷.0¹¹,¹⁵]heptadecan]-1'(10')-en-5-yl]propan-1-one

> <JCHEM_VEBER_RULE>
0

$$$$

HMDB0035221
     RDKit          3D
(3beta,17alpha,23S)-17,23-Epoxy-3,28,29-trihydroxy-27-norlanost-8-en-24-one
 80 84  0  0  0  0  0  0  0  0999 V2000
   -6.5282    3.3547   -0.9349 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.4047    1.9115   -0.5592 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.0707    1.3574   -0.9151 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2703    2.1060   -1.4461 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.7622   -0.0663   -0.6168 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.8480   -0.2329    0.8859 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8704   -1.3991    1.0814 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.6627   -2.6583    0.9140 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8928   -1.1551   -0.0326 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5407   -2.5243   -0.6158 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0246   -2.5885   -0.6852 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6536   -1.1327   -0.6868 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9570   -0.5706   -2.0290 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7165   -0.8521   -0.2121 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.9917    0.3848    0.2150 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0573    1.1980    0.9265 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4531    0.8439    0.5379 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5891   -0.6200    0.4073 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1448   -1.2674    1.7016 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3618    0.9047   -0.0353 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.4205    2.2861    0.5607 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6577    1.0846   -1.5100 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.0098    1.6883   -1.6530 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.1214    1.0612   -0.9099 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.0271    2.0716   -0.5302 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.7919    0.2924    0.3185 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.5755   -1.0383    0.2007 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.9249   -0.5918    0.1401 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.4022    0.9050    1.5730 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0707    0.1647    2.7049 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.3521   -0.0745    0.4975 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.1444   -1.3816   -0.2439 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.7382   -1.9043   -0.2070 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4995   -0.4170   -1.0049 O   0  0  0  0  0  0  0  0  0  0  0  0
   -5.8883    3.6478   -1.7918 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.2005    3.9951   -0.0740 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.6126    3.5503   -1.1375 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.2326    1.3182   -1.0032 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.5060    1.8478    0.5617 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.5413   -0.7186   -1.1014 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.8555   -0.5223    1.2197 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.4582    0.6359    1.4296 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4370   -1.3739    2.0809 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.8586   -2.9182   -0.1571 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.6906   -2.4657    1.3412 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2712   -3.5175    1.4934 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8715   -3.3496    0.0190 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9732   -2.6349   -1.6335 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7435   -3.0046   -1.6742 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6223   -3.1544    0.1587 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0286   -0.5214   -2.6481 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4145    0.4133   -2.0524 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6410   -1.2552   -2.6118 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.0605    2.2843    0.7596 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.0474    0.9453    2.0220 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8225    1.4250   -0.3314 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1168    1.1711    1.3940 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0407   -1.2326    1.8246 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4838   -2.3048    1.8079 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5421   -0.6031    2.5241 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.7517    2.9064   -0.1195 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.9388    2.3559    1.5579 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.3845    2.7931    0.4876 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.9258    1.8824   -1.8447 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.4394    0.2243   -2.1339 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.2522    1.6445   -2.7576 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.9727    2.7847   -1.4534 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.7238    0.4367   -1.6395 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.9417    1.6840   -0.4709 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.4193   -1.5341   -0.7540 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.5004   -1.6380    1.1041 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.4804   -1.0101    0.8142 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.5336    0.8188    1.5275 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.2367    1.9890    1.6701 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.5109    0.7323    3.2945 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.1796   -0.2556    1.5805 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.5115   -1.2596   -1.2833 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.7705   -2.2106    0.1971 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.5926   -2.5286   -1.1178 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.6021   -2.6127    0.6517 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  2  3  1  0
  3  4  2  0
  3  5  1  0
  5  6  1  0
  6  7  1  0
  7  8  1  0
  7  9  1  0
  9 10  1  0
 10 11  1  0
 11 12  1  0
 12 13  1  0
 12 14  1  0
 14 15  2  0
 15 16  1  0
 16 17  1  0
 17 18  1  0
 18 19  1  0
 15 20  1  0
 20 21  1  0
 20 22  1  0
 22 23  1  0
 23 24  1  0
 24 25  1  0
 24 26  1  0
 26 27  1  0
 27 28  1  0
 26 29  1  0
 29 30  1  0
 26 31  1  0
 31 32  1  0
 32 33  1  0
  9 34  1  0
 34  5  1  0
 18  9  1  0
 31 20  1  0
 18 12  1  0
 33 14  1  0
  1 35  1  0
  1 36  1  0
  1 37  1  0
  2 38  1  0
  2 39  1  0
  5 40  1  0
  6 41  1  0
  6 42  1  0
  7 43  1  0
  8 44  1  0
  8 45  1  0
  8 46  1  0
 10 47  1  0
 10 48  1  0
 11 49  1  0
 11 50  1  0
 13 51  1  0
 13 52  1  0
 13 53  1  0
 16 54  1  0
 16 55  1  0
 17 56  1  0
 17 57  1  0
 19 58  1  0
 19 59  1  0
 19 60  1  0
 21 61  1  0
 21 62  1  0
 21 63  1  0
 22 64  1  0
 22 65  1  0
 23 66  1  0
 23 67  1  0
 24 68  1  0
 25 69  1  0
 27 70  1  0
 27 71  1  0
 28 72  1  0
 29 73  1  0
 29 74  1  0
 30 75  1  0
 31 76  1  0
 32 77  1  0
 32 78  1  0
 33 79  1  0
 33 80  1  0
M  END

HEADER    PROTEIN                                 24-FEB-12   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   24-FEB-12         0                                  
HETATM    1  O   UNK     0       3.515   2.239   0.000  0.00  0.00           O+0
HETATM    2  C   UNK     0       3.515   3.779   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0       2.052   4.256   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0       1.146   3.009   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0       2.052   1.764   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0       2.955   0.517   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0       2.052  -0.727   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0       0.586  -0.250   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0       0.586   1.287   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0      -0.745   2.057   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0      -2.080   1.287   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0      -2.080  -0.250   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0      -0.745  -1.020   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0      -0.745  -2.560   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0      -2.080  -3.330   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0      -3.415  -2.560   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0      -3.415  -1.020   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0      -4.746  -0.250   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0      -6.081  -1.020   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0      -6.081  -2.560   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0      -4.746  -3.330   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0      -5.737  -4.510   0.000  0.00  0.00           C+0
HETATM   23  O   UNK     0      -5.724  -6.181   0.000  0.00  0.00           O+0
HETATM   24  C   UNK     0      -3.758  -4.510   0.000  0.00  0.00           C+0
HETATM   25  O   UNK     0      -3.771  -6.215   0.000  0.00  0.00           O+0
HETATM   26  C   UNK     0       0.188   2.776   0.000  0.00  0.00           C+0
HETATM   27  C   UNK     0      -3.415   0.517   0.000  0.00  0.00           C+0
HETATM   28  O   UNK     0      -7.415  -3.330   0.000  0.00  0.00           O+0
HETATM   29  C   UNK     0      -0.188   3.779   0.000  0.00  0.00           C+0
HETATM   30  C   UNK     0       4.762   4.682   0.000  0.00  0.00           C+0
HETATM   31  C   UNK     0       6.168   4.053   0.000  0.00  0.00           C+0
HETATM   32  C   UNK     0       7.415   4.957   0.000  0.00  0.00           C+0
HETATM   33  O   UNK     0       4.603   6.215   0.000  0.00  0.00           O+0
HETATM   34  C   UNK     0       0.586  -1.790   0.000  0.00  0.00           C+0
CONECT    1    2    5                                                       
CONECT    2    1    3   30                                                  
CONECT    3    2    4                                                       
CONECT    4    3    5   29                                                  
CONECT    5    1    4    6    9                                             
CONECT    6    5    7                                                       
CONECT    7    6    8                                                       
CONECT    8    7    9   13   34                                             
CONECT    9    5    8   10   26                                             
CONECT   10    9   11                                                       
CONECT   11   10   12                                                       
CONECT   12   11   13   17                                                  
CONECT   13    8   12   14                                                  
CONECT   14   13   15                                                       
CONECT   15   14   16                                                       
CONECT   16   15   17   21                                                  
CONECT   17   12   16   18   27                                             
CONECT   18   17   19                                                       
CONECT   19   18   20                                                       
CONECT   20   19   21   28                                                  
CONECT   21   16   20   22   24                                             
CONECT   22   21   23                                                       
CONECT   23   22                                                            
CONECT   24   21   25                                                       
CONECT   25   24                                                            
CONECT   26    9                                                            
CONECT   27   17                                                            
CONECT   28   20                                                            
CONECT   29    4                                                            
CONECT   30    2   31   33                                                  
CONECT   31   30   32                                                       
CONECT   32   31                                                            
CONECT   33   30                                                            
CONECT   34    8                                                            
MASTER        0    0    0    0    0    0    0    0   34    0   76    0
END

COMPND    HMDB0035221
HETATM    1  C1  UNL     1      -6.528   3.355  -0.935  1.00  0.00           C  
HETATM    2  C2  UNL     1      -6.405   1.912  -0.559  1.00  0.00           C  
HETATM    3  C3  UNL     1      -5.071   1.357  -0.915  1.00  0.00           C  
HETATM    4  O1  UNL     1      -4.270   2.106  -1.446  1.00  0.00           O  
HETATM    5  C4  UNL     1      -4.762  -0.066  -0.617  1.00  0.00           C  
HETATM    6  C5  UNL     1      -4.848  -0.233   0.886  1.00  0.00           C  
HETATM    7  C6  UNL     1      -3.870  -1.399   1.081  1.00  0.00           C  
HETATM    8  C7  UNL     1      -4.663  -2.658   0.914  1.00  0.00           C  
HETATM    9  C8  UNL     1      -2.893  -1.155  -0.033  1.00  0.00           C  
HETATM   10  C9  UNL     1      -2.541  -2.524  -0.616  1.00  0.00           C  
HETATM   11  C10 UNL     1      -1.025  -2.588  -0.685  1.00  0.00           C  
HETATM   12  C11 UNL     1      -0.654  -1.133  -0.687  1.00  0.00           C  
HETATM   13  C12 UNL     1      -0.957  -0.571  -2.029  1.00  0.00           C  
HETATM   14  C13 UNL     1       0.716  -0.852  -0.212  1.00  0.00           C  
HETATM   15  C14 UNL     1       0.992   0.385   0.215  1.00  0.00           C  
HETATM   16  C15 UNL     1      -0.057   1.198   0.926  1.00  0.00           C  
HETATM   17  C16 UNL     1      -1.453   0.844   0.538  1.00  0.00           C  
HETATM   18  C17 UNL     1      -1.589  -0.620   0.407  1.00  0.00           C  
HETATM   19  C18 UNL     1      -1.145  -1.267   1.702  1.00  0.00           C  
HETATM   20  C19 UNL     1       2.362   0.905  -0.035  1.00  0.00           C  
HETATM   21  C20 UNL     1       2.421   2.286   0.561  1.00  0.00           C  
HETATM   22  C21 UNL     1       2.658   1.085  -1.510  1.00  0.00           C  
HETATM   23  C22 UNL     1       4.010   1.688  -1.653  1.00  0.00           C  
HETATM   24  C23 UNL     1       5.121   1.061  -0.910  1.00  0.00           C  
HETATM   25  O2  UNL     1       6.027   2.072  -0.530  1.00  0.00           O  
HETATM   26  C24 UNL     1       4.792   0.292   0.319  1.00  0.00           C  
HETATM   27  C25 UNL     1       5.576  -1.038   0.201  1.00  0.00           C  
HETATM   28  O3  UNL     1       6.925  -0.592   0.140  1.00  0.00           O  
HETATM   29  C26 UNL     1       5.402   0.905   1.573  1.00  0.00           C  
HETATM   30  O4  UNL     1       5.071   0.165   2.705  1.00  0.00           O  
HETATM   31  C27 UNL     1       3.352  -0.075   0.497  1.00  0.00           C  
HETATM   32  C28 UNL     1       3.144  -1.382  -0.244  1.00  0.00           C  
HETATM   33  C29 UNL     1       1.738  -1.904  -0.207  1.00  0.00           C  
HETATM   34  O5  UNL     1      -3.500  -0.417  -1.005  1.00  0.00           O  
HETATM   35  H1  UNL     1      -5.888   3.648  -1.792  1.00  0.00           H  
HETATM   36  H2  UNL     1      -6.201   3.995  -0.074  1.00  0.00           H  
HETATM   37  H3  UNL     1      -7.613   3.550  -1.138  1.00  0.00           H  
HETATM   38  H4  UNL     1      -7.233   1.318  -1.003  1.00  0.00           H  
HETATM   39  H5  UNL     1      -6.506   1.848   0.562  1.00  0.00           H  
HETATM   40  H6  UNL     1      -5.541  -0.719  -1.101  1.00  0.00           H  
HETATM   41  H7  UNL     1      -5.855  -0.522   1.220  1.00  0.00           H  
HETATM   42  H8  UNL     1      -4.458   0.636   1.430  1.00  0.00           H  
HETATM   43  H9  UNL     1      -3.437  -1.374   2.081  1.00  0.00           H  
HETATM   44  H10 UNL     1      -4.859  -2.918  -0.157  1.00  0.00           H  
HETATM   45  H11 UNL     1      -5.691  -2.466   1.341  1.00  0.00           H  
HETATM   46  H12 UNL     1      -4.271  -3.518   1.493  1.00  0.00           H  
HETATM   47  H13 UNL     1      -2.871  -3.350   0.019  1.00  0.00           H  
HETATM   48  H14 UNL     1      -2.973  -2.635  -1.634  1.00  0.00           H  
HETATM   49  H15 UNL     1      -0.744  -3.005  -1.674  1.00  0.00           H  
HETATM   50  H16 UNL     1      -0.622  -3.154   0.159  1.00  0.00           H  
HETATM   51  H17 UNL     1      -0.029  -0.521  -2.648  1.00  0.00           H  
HETATM   52  H18 UNL     1      -1.414   0.413  -2.052  1.00  0.00           H  
HETATM   53  H19 UNL     1      -1.641  -1.255  -2.612  1.00  0.00           H  
HETATM   54  H20 UNL     1       0.061   2.284   0.760  1.00  0.00           H  
HETATM   55  H21 UNL     1       0.047   0.945   2.022  1.00  0.00           H  
HETATM   56  H22 UNL     1      -1.823   1.425  -0.331  1.00  0.00           H  
HETATM   57  H23 UNL     1      -2.117   1.171   1.394  1.00  0.00           H  
HETATM   58  H24 UNL     1      -0.041  -1.233   1.825  1.00  0.00           H  
HETATM   59  H25 UNL     1      -1.484  -2.305   1.808  1.00  0.00           H  
HETATM   60  H26 UNL     1      -1.542  -0.603   2.524  1.00  0.00           H  
HETATM   61  H27 UNL     1       1.752   2.906  -0.119  1.00  0.00           H  
HETATM   62  H28 UNL     1       1.939   2.356   1.558  1.00  0.00           H  
HETATM   63  H29 UNL     1       3.385   2.793   0.488  1.00  0.00           H  
HETATM   64  H30 UNL     1       1.926   1.882  -1.845  1.00  0.00           H  
HETATM   65  H31 UNL     1       2.439   0.224  -2.134  1.00  0.00           H  
HETATM   66  H32 UNL     1       4.252   1.645  -2.758  1.00  0.00           H  
HETATM   67  H33 UNL     1       3.973   2.785  -1.453  1.00  0.00           H  
HETATM   68  H34 UNL     1       5.724   0.437  -1.640  1.00  0.00           H  
HETATM   69  H35 UNL     1       6.942   1.684  -0.471  1.00  0.00           H  
HETATM   70  H36 UNL     1       5.419  -1.534  -0.754  1.00  0.00           H  
HETATM   71  H37 UNL     1       5.500  -1.638   1.104  1.00  0.00           H  
HETATM   72  H38 UNL     1       7.480  -1.010   0.814  1.00  0.00           H  
HETATM   73  H39 UNL     1       6.534   0.819   1.527  1.00  0.00           H  
HETATM   74  H40 UNL     1       5.237   1.989   1.670  1.00  0.00           H  
HETATM   75  H41 UNL     1       4.511   0.732   3.295  1.00  0.00           H  
HETATM   76  H42 UNL     1       3.180  -0.256   1.581  1.00  0.00           H  
HETATM   77  H43 UNL     1       3.511  -1.260  -1.283  1.00  0.00           H  
HETATM   78  H44 UNL     1       3.770  -2.211   0.197  1.00  0.00           H  
HETATM   79  H45 UNL     1       1.593  -2.529  -1.118  1.00  0.00           H  
HETATM   80  H46 UNL     1       1.602  -2.613   0.652  1.00  0.00           H  
CONECT    1    2   35   36   37
CONECT    2    3   38   39
CONECT    3    4    4    5
CONECT    5    6   34   40
CONECT    6    7   41   42
CONECT    7    8    9   43
CONECT    8   44   45   46
CONECT    9   10   18   34
CONECT   10   11   47   48
CONECT   11   12   49   50
CONECT   12   13   14   18
CONECT   13   51   52   53
CONECT   14   15   15   33
CONECT   15   16   20
CONECT   16   17   54   55
CONECT   17   18   56   57
CONECT   18   19
CONECT   19   58   59   60
CONECT   20   21   22   31
CONECT   21   61   62   63
CONECT   22   23   64   65
CONECT   23   24   66   67
CONECT   24   25   26   68
CONECT   25   69
CONECT   26   27   29   31
CONECT   27   28   70   71
CONECT   28   72
CONECT   29   30   73   74
CONECT   30   75
CONECT   31   32   76
CONECT   32   33   77   78
CONECT   33   79   80
END

HMDB0035221
     RDKit          3D
(3beta,17alpha,23S)-17,23-Epoxy-3,28,29-trihydroxy-27-norlanost-8-en-24-one
 80 84  0  0  0  0  0  0  0  0999 V2000
   -6.5282    3.3547   -0.9349 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.4047    1.9115   -0.5592 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.0707    1.3574   -0.9151 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2703    2.1060   -1.4461 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.7622   -0.0663   -0.6168 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.8480   -0.2329    0.8859 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8704   -1.3991    1.0814 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.6627   -2.6583    0.9140 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8928   -1.1551   -0.0326 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5407   -2.5243   -0.6158 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0246   -2.5885   -0.6852 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6536   -1.1327   -0.6868 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9570   -0.5706   -2.0290 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7165   -0.8521   -0.2121 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.9917    0.3848    0.2150 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0573    1.1980    0.9265 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4531    0.8439    0.5379 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5891   -0.6200    0.4073 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1448   -1.2674    1.7016 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3618    0.9047   -0.0353 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.4205    2.2861    0.5607 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6577    1.0846   -1.5100 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.0098    1.6883   -1.6530 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.1214    1.0612   -0.9099 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.0271    2.0716   -0.5302 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.7919    0.2924    0.3185 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.5755   -1.0383    0.2007 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.9249   -0.5918    0.1401 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.4022    0.9050    1.5730 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0707    0.1647    2.7049 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.3521   -0.0745    0.4975 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.1444   -1.3816   -0.2439 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.7382   -1.9043   -0.2070 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4995   -0.4170   -1.0049 O   0  0  0  0  0  0  0  0  0  0  0  0
   -5.8883    3.6478   -1.7918 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.2005    3.9951   -0.0740 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.6126    3.5503   -1.1375 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.2326    1.3182   -1.0032 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.5060    1.8478    0.5617 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.5413   -0.7186   -1.1014 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.8555   -0.5223    1.2197 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.4582    0.6359    1.4296 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4370   -1.3739    2.0809 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.8586   -2.9182   -0.1571 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.6906   -2.4657    1.3412 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2712   -3.5175    1.4934 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8715   -3.3496    0.0190 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9732   -2.6349   -1.6335 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7435   -3.0046   -1.6742 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6223   -3.1544    0.1587 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0286   -0.5214   -2.6481 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4145    0.4133   -2.0524 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6410   -1.2552   -2.6118 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.0605    2.2843    0.7596 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.0474    0.9453    2.0220 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8225    1.4250   -0.3314 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1168    1.1711    1.3940 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0407   -1.2326    1.8246 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4838   -2.3048    1.8079 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5421   -0.6031    2.5241 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.7517    2.9064   -0.1195 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.9388    2.3559    1.5579 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.3845    2.7931    0.4876 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.9258    1.8824   -1.8447 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.4394    0.2243   -2.1339 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.2522    1.6445   -2.7576 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.9727    2.7847   -1.4534 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.7238    0.4367   -1.6395 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.9417    1.6840   -0.4709 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.4193   -1.5341   -0.7540 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.5004   -1.6380    1.1041 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.4804   -1.0101    0.8142 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.5336    0.8188    1.5275 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.2367    1.9890    1.6701 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.5109    0.7323    3.2945 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.1796   -0.2556    1.5805 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.5115   -1.2596   -1.2833 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.7705   -2.2106    0.1971 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.5926   -2.5286   -1.1178 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.6021   -2.6127    0.6517 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  2  3  1  0
  3  4  2  0
  3  5  1  0
  5  6  1  0
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  9 10  1  0
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 12 14  1  0
 14 15  2  0
 15 16  1  0
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 18 19  1  0
 15 20  1  0
 20 21  1  0
 20 22  1  0
 22 23  1  0
 23 24  1  0
 24 25  1  0
 24 26  1  0
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 26 29  1  0
 29 30  1  0
 26 31  1  0
 31 32  1  0
 32 33  1  0
  9 34  1  0
 34  5  1  0
 18  9  1  0
 31 20  1  0
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 33 14  1  0
  1 35  1  0
  1 36  1  0
  1 37  1  0
  2 38  1  0
  2 39  1  0
  5 40  1  0
  6 41  1  0
  6 42  1  0
  7 43  1  0
  8 44  1  0
  8 45  1  0
  8 46  1  0
 10 47  1  0
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 25 69  1  0
 27 70  1  0
 27 71  1  0
 28 72  1  0
 29 73  1  0
 29 74  1  0
 30 75  1  0
 31 76  1  0
 32 77  1  0
 32 78  1  0
 33 79  1  0
 33 80  1  0
M  END

View in JSmol View Stereo Labels

Synonyms

Value	Source
(3b,17a,23S)-17,23-Epoxy-3,28,29-trihydroxy-27-norlanost-8-en-24-one	Generator
(3Β,17α,23S)-17,23-epoxy-3,28,29-trihydroxy-27-norlanost-8-en-24-one	Generator

Chemical Formula

C₂₉H₄₆O₅

Average Molecular Weight

474.6725

Monoisotopic Molecular Weight

474.334524582

IUPAC Name

1-[5'-hydroxy-6',6'-bis(hydroxymethyl)-2',3,11',15'-tetramethylspiro[oxolane-2,14'-tetracyclo[8.7.0.0²,⁷.0¹¹,¹⁵]heptadecan]-1'(10')-en-5-yl]propan-1-one

Traditional Name

1-[5'-hydroxy-6',6'-bis(hydroxymethyl)-2',3,11',15'-tetramethylspiro[oxolane-2,14'-tetracyclo[8.7.0.0²,⁷.0¹¹,¹⁵]heptadecan]-1'(10')-en-5-yl]propan-1-one

CAS Registry Number

Not Available

SMILES

CCC(=O)C1CC(C)C2(CCC3(C)C4=C(CCC23C)C2(C)CCC(O)C(CO)(CO)C2CC4)O1

InChI Identifier

InChI=1S/C29H46O5/c1-6-21(32)22-15-18(2)29(34-22)14-13-26(4)20-7-8-23-25(3,19(20)9-12-27(26,29)5)11-10-24(33)28(23,16-30)17-31/h18,22-24,30-31,33H,6-17H2,1-5H3

InChI Key

PGCCXLDWXXFVMP-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
3-hydroxysteroid
Hydroxysteroid
Steroid
Cyclic alcohol
Tetrahydrofuran
Ketone
Secondary alcohol
Dialkyl ether
Ether
Oxacycle
Organoheterocyclic compound
Hydrocarbon derivative
Alcohol
Organic oxygen compound
Organic oxide
Organooxygen compound
Primary alcohol
Carbonyl group
Aliphatic heteropolycyclic compound

Molecular Framework

Aliphatic heteropolycyclic compounds

External Descriptors

Not Available

Ontology

Physiological effect

Not Available

Disposition

Biological location

Cellular substructure

Membrane (HMDB: HMDB0035221)

Route of exposure

Enteral

Ingestion (HMDB: HMDB0035221)

Source

Endogenous

Endogenous (HMDB: HMDB0035221)

Plant

Plant (HMDB: HMDB0035221)

Exogenous

Food

Food (HMDB: HMDB0035221)

Herb and spice

Herbs and Spices (FooDB: FOOD00866)

Process

Naturally occurring process

Biological process

Chemical reaction

Lipid peroxidation (HMDB: HMDB0035221)

Biochemical process

Fatty acid metabolism (HMDB: HMDB0035221)

Cellular process

Cell signaling (HMDB: HMDB0035221)

Biochemical pathway

Lipid metabolism pathway (HMDB: HMDB0035221)

Role

Biological role

Membrane stabilizer (HMDB: HMDB0035221)

Nutrient

Nutrient (HMDB: HMDB0035221)

Industrial application

Manufacturing industry

Material processing agent

Fluid processing agent

Surfactant

Surfactant (HMDB: HMDB0035221)

Emulsifier (HMDB: HMDB0035221)

Physical Properties

State

Not Available

Experimental Molecular Properties

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

Experimental Chromatographic Properties

Not Available

Predicted Molecular Properties

Property	Value	Source
Water Solubility	0.0068 g/L	ALOGPS
logP	3.95	ALOGPS
logP	3.29	ChemAxon
logS	-4.8	ALOGPS
pKa (Strongest Acidic)	14.3	ChemAxon
pKa (Strongest Basic)	-2.8	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	5	ChemAxon
Hydrogen Donor Count	3	ChemAxon
Polar Surface Area	86.99 Å²	ChemAxon
Rotatable Bond Count	4	ChemAxon
Refractivity	132.77 m³·mol⁻¹	ChemAxon
Polarizability	55.61 Å³	ChemAxon
Number of Rings	5	ChemAxon
Bioavailability	Yes	ChemAxon
Rule of Five	Yes	ChemAxon
Ghose Filter	No	ChemAxon
Veber's Rule	No	ChemAxon
MDDR-like Rule	No	ChemAxon

Predicted Chromatographic Properties

Predicted Collision Cross Sections

Predictor	Adduct Type	CCS Value (Å²)	Reference
DarkChem	[M+H]+	209.646	31661259
DarkChem	[M-H]-	203.568	31661259
DeepCCS	[M-2H]-	244.754	30932474
DeepCCS	[M+Na]+	220.112	30932474
AllCCS	[M+H]+	214.3	32859911
AllCCS	[M+H-H2O]+	212.6	32859911
AllCCS	[M+NH4]+	215.9	32859911
AllCCS	[M+Na]+	216.3	32859911
AllCCS	[M-H]-	214.6	32859911
AllCCS	[M+Na-2H]-	216.9	32859911
AllCCS	[M+HCOO]-	219.6	32859911

Predicted Kovats Retention Indices

Underivatized

Metabolite	SMILES	Kovats RI Value	Column Type	Reference
(3beta,17alpha,23S)-17,23-Epoxy-3,28,29-trihydroxy-27-norlanost-8-en-24-one	CCC(=O)C1CC(C)C2(CCC3(C)C4=C(CCC23C)C2(C)CCC(O)C(CO)(CO)C2CC4)O1	3106.4	Standard polar	33892256
(3beta,17alpha,23S)-17,23-Epoxy-3,28,29-trihydroxy-27-norlanost-8-en-24-one	CCC(=O)C1CC(C)C2(CCC3(C)C4=C(CCC23C)C2(C)CCC(O)C(CO)(CO)C2CC4)O1	3749.8	Standard non polar	33892256
(3beta,17alpha,23S)-17,23-Epoxy-3,28,29-trihydroxy-27-norlanost-8-en-24-one	CCC(=O)C1CC(C)C2(CCC3(C)C4=C(CCC23C)C2(C)CCC(O)C(CO)(CO)C2CC4)O1	4165.8	Semi standard non polar	33892256

Derivatized

Derivative Name / Structure	SMILES	Kovats RI Value	Column Type	Reference
(3beta,17alpha,23S)-17,23-Epoxy-3,28,29-trihydroxy-27-norlanost-8-en-24-one,1TMS,isomer #1	CCC(=O)C1CC(C)C2(CCC3(C)C4=C(CCC32C)C2(C)CCC(O[Si](C)(C)C)C(CO)(CO)C2CC4)O1	3856.5	Semi standard non polar	33892256
(3beta,17alpha,23S)-17,23-Epoxy-3,28,29-trihydroxy-27-norlanost-8-en-24-one,1TMS,isomer #2	CCC(=O)C1CC(C)C2(CCC3(C)C4=C(CCC32C)C2(C)CCC(O)C(CO)(CO[Si](C)(C)C)C2CC4)O1	3827.4	Semi standard non polar	33892256
(3beta,17alpha,23S)-17,23-Epoxy-3,28,29-trihydroxy-27-norlanost-8-en-24-one,1TMS,isomer #3	CCC(O[Si](C)(C)C)=C1CC(C)C2(CCC3(C)C4=C(CCC32C)C2(C)CCC(O)C(CO)(CO)C2CC4)O1	3878.5	Semi standard non polar	33892256
(3beta,17alpha,23S)-17,23-Epoxy-3,28,29-trihydroxy-27-norlanost-8-en-24-one,1TMS,isomer #4	CC=C(O[Si](C)(C)C)C1CC(C)C2(CCC3(C)C4=C(CCC32C)C2(C)CCC(O)C(CO)(CO)C2CC4)O1	3827.8	Semi standard non polar	33892256
(3beta,17alpha,23S)-17,23-Epoxy-3,28,29-trihydroxy-27-norlanost-8-en-24-one,2TMS,isomer #1	CCC(=O)C1CC(C)C2(CCC3(C)C4=C(CCC32C)C2(C)CCC(O[Si](C)(C)C)C(CO)(CO[Si](C)(C)C)C2CC4)O1	3818.9	Semi standard non polar	33892256
(3beta,17alpha,23S)-17,23-Epoxy-3,28,29-trihydroxy-27-norlanost-8-en-24-one,2TMS,isomer #2	CCC(O[Si](C)(C)C)=C1CC(C)C2(CCC3(C)C4=C(CCC32C)C2(C)CCC(O[Si](C)(C)C)C(CO)(CO)C2CC4)O1	3866.5	Semi standard non polar	33892256
(3beta,17alpha,23S)-17,23-Epoxy-3,28,29-trihydroxy-27-norlanost-8-en-24-one,2TMS,isomer #3	CC=C(O[Si](C)(C)C)C1CC(C)C2(CCC3(C)C4=C(CCC32C)C2(C)CCC(O[Si](C)(C)C)C(CO)(CO)C2CC4)O1	3814.5	Semi standard non polar	33892256
(3beta,17alpha,23S)-17,23-Epoxy-3,28,29-trihydroxy-27-norlanost-8-en-24-one,2TMS,isomer #4	CCC(=O)C1CC(C)C2(CCC3(C)C4=C(CCC32C)C2(C)CCC(O)C(CO[Si](C)(C)C)(CO[Si](C)(C)C)C2CC4)O1	3829.3	Semi standard non polar	33892256
(3beta,17alpha,23S)-17,23-Epoxy-3,28,29-trihydroxy-27-norlanost-8-en-24-one,2TMS,isomer #5	CCC(O[Si](C)(C)C)=C1CC(C)C2(CCC3(C)C4=C(CCC32C)C2(C)CCC(O)C(CO)(CO[Si](C)(C)C)C2CC4)O1	3826.1	Semi standard non polar	33892256
(3beta,17alpha,23S)-17,23-Epoxy-3,28,29-trihydroxy-27-norlanost-8-en-24-one,2TMS,isomer #6	CC=C(O[Si](C)(C)C)C1CC(C)C2(CCC3(C)C4=C(CCC32C)C2(C)CCC(O)C(CO)(CO[Si](C)(C)C)C2CC4)O1	3778.7	Semi standard non polar	33892256
(3beta,17alpha,23S)-17,23-Epoxy-3,28,29-trihydroxy-27-norlanost-8-en-24-one,3TMS,isomer #1	CCC(=O)C1CC(C)C2(CCC3(C)C4=C(CCC32C)C2(C)CCC(O[Si](C)(C)C)C(CO[Si](C)(C)C)(CO[Si](C)(C)C)C2CC4)O1	3795.1	Semi standard non polar	33892256
(3beta,17alpha,23S)-17,23-Epoxy-3,28,29-trihydroxy-27-norlanost-8-en-24-one,3TMS,isomer #2	CCC(O[Si](C)(C)C)=C1CC(C)C2(CCC3(C)C4=C(CCC32C)C2(C)CCC(O[Si](C)(C)C)C(CO)(CO[Si](C)(C)C)C2CC4)O1	3796.0	Semi standard non polar	33892256
(3beta,17alpha,23S)-17,23-Epoxy-3,28,29-trihydroxy-27-norlanost-8-en-24-one,3TMS,isomer #3	CC=C(O[Si](C)(C)C)C1CC(C)C2(CCC3(C)C4=C(CCC32C)C2(C)CCC(O[Si](C)(C)C)C(CO)(CO[Si](C)(C)C)C2CC4)O1	3757.0	Semi standard non polar	33892256
(3beta,17alpha,23S)-17,23-Epoxy-3,28,29-trihydroxy-27-norlanost-8-en-24-one,3TMS,isomer #4	CCC(O[Si](C)(C)C)=C1CC(C)C2(CCC3(C)C4=C(CCC32C)C2(C)CCC(O)C(CO[Si](C)(C)C)(CO[Si](C)(C)C)C2CC4)O1	3795.5	Semi standard non polar	33892256
(3beta,17alpha,23S)-17,23-Epoxy-3,28,29-trihydroxy-27-norlanost-8-en-24-one,3TMS,isomer #5	CC=C(O[Si](C)(C)C)C1CC(C)C2(CCC3(C)C4=C(CCC32C)C2(C)CCC(O)C(CO[Si](C)(C)C)(CO[Si](C)(C)C)C2CC4)O1	3759.3	Semi standard non polar	33892256
(3beta,17alpha,23S)-17,23-Epoxy-3,28,29-trihydroxy-27-norlanost-8-en-24-one,4TMS,isomer #1	CCC(O[Si](C)(C)C)=C1CC(C)C2(CCC3(C)C4=C(CCC32C)C2(C)CCC(O[Si](C)(C)C)C(CO[Si](C)(C)C)(CO[Si](C)(C)C)C2CC4)O1	3787.6	Semi standard non polar	33892256
(3beta,17alpha,23S)-17,23-Epoxy-3,28,29-trihydroxy-27-norlanost-8-en-24-one,4TMS,isomer #1	CCC(O[Si](C)(C)C)=C1CC(C)C2(CCC3(C)C4=C(CCC32C)C2(C)CCC(O[Si](C)(C)C)C(CO[Si](C)(C)C)(CO[Si](C)(C)C)C2CC4)O1	3720.9	Standard non polar	33892256
(3beta,17alpha,23S)-17,23-Epoxy-3,28,29-trihydroxy-27-norlanost-8-en-24-one,4TMS,isomer #2	CC=C(O[Si](C)(C)C)C1CC(C)C2(CCC3(C)C4=C(CCC32C)C2(C)CCC(O[Si](C)(C)C)C(CO[Si](C)(C)C)(CO[Si](C)(C)C)C2CC4)O1	3740.6	Semi standard non polar	33892256
(3beta,17alpha,23S)-17,23-Epoxy-3,28,29-trihydroxy-27-norlanost-8-en-24-one,4TMS,isomer #2	CC=C(O[Si](C)(C)C)C1CC(C)C2(CCC3(C)C4=C(CCC32C)C2(C)CCC(O[Si](C)(C)C)C(CO[Si](C)(C)C)(CO[Si](C)(C)C)C2CC4)O1	3733.3	Standard non polar	33892256
(3beta,17alpha,23S)-17,23-Epoxy-3,28,29-trihydroxy-27-norlanost-8-en-24-one,1TBDMS,isomer #1	CCC(=O)C1CC(C)C2(CCC3(C)C4=C(CCC32C)C2(C)CCC(O[Si](C)(C)C(C)(C)C)C(CO)(CO)C2CC4)O1	4092.0	Semi standard non polar	33892256
(3beta,17alpha,23S)-17,23-Epoxy-3,28,29-trihydroxy-27-norlanost-8-en-24-one,1TBDMS,isomer #2	CCC(=O)C1CC(C)C2(CCC3(C)C4=C(CCC32C)C2(C)CCC(O)C(CO)(CO[Si](C)(C)C(C)(C)C)C2CC4)O1	4073.4	Semi standard non polar	33892256
(3beta,17alpha,23S)-17,23-Epoxy-3,28,29-trihydroxy-27-norlanost-8-en-24-one,1TBDMS,isomer #3	CCC(O[Si](C)(C)C(C)(C)C)=C1CC(C)C2(CCC3(C)C4=C(CCC32C)C2(C)CCC(O)C(CO)(CO)C2CC4)O1	4122.9	Semi standard non polar	33892256
(3beta,17alpha,23S)-17,23-Epoxy-3,28,29-trihydroxy-27-norlanost-8-en-24-one,1TBDMS,isomer #4	CC=C(O[Si](C)(C)C(C)(C)C)C1CC(C)C2(CCC3(C)C4=C(CCC32C)C2(C)CCC(O)C(CO)(CO)C2CC4)O1	4066.9	Semi standard non polar	33892256
(3beta,17alpha,23S)-17,23-Epoxy-3,28,29-trihydroxy-27-norlanost-8-en-24-one,2TBDMS,isomer #1	CCC(=O)C1CC(C)C2(CCC3(C)C4=C(CCC32C)C2(C)CCC(O[Si](C)(C)C(C)(C)C)C(CO)(CO[Si](C)(C)C(C)(C)C)C2CC4)O1	4283.9	Semi standard non polar	33892256
(3beta,17alpha,23S)-17,23-Epoxy-3,28,29-trihydroxy-27-norlanost-8-en-24-one,2TBDMS,isomer #2	CCC(O[Si](C)(C)C(C)(C)C)=C1CC(C)C2(CCC3(C)C4=C(CCC32C)C2(C)CCC(O[Si](C)(C)C(C)(C)C)C(CO)(CO)C2CC4)O1	4324.1	Semi standard non polar	33892256
(3beta,17alpha,23S)-17,23-Epoxy-3,28,29-trihydroxy-27-norlanost-8-en-24-one,2TBDMS,isomer #3	CC=C(O[Si](C)(C)C(C)(C)C)C1CC(C)C2(CCC3(C)C4=C(CCC32C)C2(C)CCC(O[Si](C)(C)C(C)(C)C)C(CO)(CO)C2CC4)O1	4268.6	Semi standard non polar	33892256
(3beta,17alpha,23S)-17,23-Epoxy-3,28,29-trihydroxy-27-norlanost-8-en-24-one,2TBDMS,isomer #4	CCC(=O)C1CC(C)C2(CCC3(C)C4=C(CCC32C)C2(C)CCC(O)C(CO[Si](C)(C)C(C)(C)C)(CO[Si](C)(C)C(C)(C)C)C2CC4)O1	4310.7	Semi standard non polar	33892256
(3beta,17alpha,23S)-17,23-Epoxy-3,28,29-trihydroxy-27-norlanost-8-en-24-one,2TBDMS,isomer #5	CCC(O[Si](C)(C)C(C)(C)C)=C1CC(C)C2(CCC3(C)C4=C(CCC32C)C2(C)CCC(O)C(CO)(CO[Si](C)(C)C(C)(C)C)C2CC4)O1	4290.0	Semi standard non polar	33892256
(3beta,17alpha,23S)-17,23-Epoxy-3,28,29-trihydroxy-27-norlanost-8-en-24-one,2TBDMS,isomer #6	CC=C(O[Si](C)(C)C(C)(C)C)C1CC(C)C2(CCC3(C)C4=C(CCC32C)C2(C)CCC(O)C(CO)(CO[Si](C)(C)C(C)(C)C)C2CC4)O1	4236.1	Semi standard non polar	33892256
(3beta,17alpha,23S)-17,23-Epoxy-3,28,29-trihydroxy-27-norlanost-8-en-24-one,3TBDMS,isomer #1	CCC(=O)C1CC(C)C2(CCC3(C)C4=C(CCC32C)C2(C)CCC(O[Si](C)(C)C(C)(C)C)C(CO[Si](C)(C)C(C)(C)C)(CO[Si](C)(C)C(C)(C)C)C2CC4)O1	4502.1	Semi standard non polar	33892256
(3beta,17alpha,23S)-17,23-Epoxy-3,28,29-trihydroxy-27-norlanost-8-en-24-one,3TBDMS,isomer #2	CCC(O[Si](C)(C)C(C)(C)C)=C1CC(C)C2(CCC3(C)C4=C(CCC32C)C2(C)CCC(O[Si](C)(C)C(C)(C)C)C(CO)(CO[Si](C)(C)C(C)(C)C)C2CC4)O1	4483.5	Semi standard non polar	33892256
(3beta,17alpha,23S)-17,23-Epoxy-3,28,29-trihydroxy-27-norlanost-8-en-24-one,3TBDMS,isomer #3	CC=C(O[Si](C)(C)C(C)(C)C)C1CC(C)C2(CCC3(C)C4=C(CCC32C)C2(C)CCC(O[Si](C)(C)C(C)(C)C)C(CO)(CO[Si](C)(C)C(C)(C)C)C2CC4)O1	4436.3	Semi standard non polar	33892256
(3beta,17alpha,23S)-17,23-Epoxy-3,28,29-trihydroxy-27-norlanost-8-en-24-one,3TBDMS,isomer #4	CCC(O[Si](C)(C)C(C)(C)C)=C1CC(C)C2(CCC3(C)C4=C(CCC32C)C2(C)CCC(O)C(CO[Si](C)(C)C(C)(C)C)(CO[Si](C)(C)C(C)(C)C)C2CC4)O1	4493.8	Semi standard non polar	33892256
(3beta,17alpha,23S)-17,23-Epoxy-3,28,29-trihydroxy-27-norlanost-8-en-24-one,3TBDMS,isomer #5	CC=C(O[Si](C)(C)C(C)(C)C)C1CC(C)C2(CCC3(C)C4=C(CCC32C)C2(C)CCC(O)C(CO[Si](C)(C)C(C)(C)C)(CO[Si](C)(C)C(C)(C)C)C2CC4)O1	4444.4	Semi standard non polar	33892256

Spectra

GC-MS Spectra

Spectrum Type	Description	Splash Key	Deposition Date	Source	View
Predicted GC-MS	Predicted GC-MS Spectrum - (3beta,17alpha,23S)-17,23-Epoxy-3,28,29-trihydroxy-27-norlanost-8-en-24-one GC-MS (Non-derivatized) - 70eV, Positive	splash10-0a4j-2003900000-83c403f8d3c2f203a293	2017-09-01	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - (3beta,17alpha,23S)-17,23-Epoxy-3,28,29-trihydroxy-27-norlanost-8-en-24-one GC-MS (3 TMS) - 70eV, Positive	splash10-01t9-3100019000-7de4099e52ec6703a3c2	2017-10-06	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - (3beta,17alpha,23S)-17,23-Epoxy-3,28,29-trihydroxy-27-norlanost-8-en-24-one GC-MS (Non-derivatized) - 70eV, Positive	Not Available	2021-10-12	Wishart Lab	View Spectrum

MS/MS Spectra

Spectrum Type	Description	Splash Key	Deposition Date	Source	View
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - (3beta,17alpha,23S)-17,23-Epoxy-3,28,29-trihydroxy-27-norlanost-8-en-24-one 10V, Positive-QTOF	splash10-0a4i-0002900000-323021f5e2f09c93f492	2016-08-01	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - (3beta,17alpha,23S)-17,23-Epoxy-3,28,29-trihydroxy-27-norlanost-8-en-24-one 20V, Positive-QTOF	splash10-0a4r-1023900000-bc006ebeef1a457682bc	2016-08-01	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - (3beta,17alpha,23S)-17,23-Epoxy-3,28,29-trihydroxy-27-norlanost-8-en-24-one 40V, Positive-QTOF	splash10-000i-0049000000-f6d5fa832338fa134192	2016-08-01	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - (3beta,17alpha,23S)-17,23-Epoxy-3,28,29-trihydroxy-27-norlanost-8-en-24-one 10V, Negative-QTOF	splash10-00di-0000900000-0fa0f1bfbf107cc2aa1c	2016-08-03	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - (3beta,17alpha,23S)-17,23-Epoxy-3,28,29-trihydroxy-27-norlanost-8-en-24-one 20V, Negative-QTOF	splash10-0adl-0000900000-d75ca516b55bb1191e8e	2016-08-03	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - (3beta,17alpha,23S)-17,23-Epoxy-3,28,29-trihydroxy-27-norlanost-8-en-24-one 40V, Negative-QTOF	splash10-052r-2009300000-fc13b34f9b9709f8dbc8	2016-08-03	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - (3beta,17alpha,23S)-17,23-Epoxy-3,28,29-trihydroxy-27-norlanost-8-en-24-one 10V, Positive-QTOF	splash10-004i-0001900000-aba354fdc291a801c6c9	2021-09-23	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - (3beta,17alpha,23S)-17,23-Epoxy-3,28,29-trihydroxy-27-norlanost-8-en-24-one 20V, Positive-QTOF	splash10-00p1-0234900000-005f3badb1b04de269a3	2021-09-23	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - (3beta,17alpha,23S)-17,23-Epoxy-3,28,29-trihydroxy-27-norlanost-8-en-24-one 40V, Positive-QTOF	splash10-0006-9256400000-ebb1b9a73137af69a75a	2021-09-23	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - (3beta,17alpha,23S)-17,23-Epoxy-3,28,29-trihydroxy-27-norlanost-8-en-24-one 10V, Negative-QTOF	splash10-00di-0000900000-221edc4136d4fc255e65	2021-09-25	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - (3beta,17alpha,23S)-17,23-Epoxy-3,28,29-trihydroxy-27-norlanost-8-en-24-one 20V, Negative-QTOF	splash10-000i-1009200000-7be6ca4dbaade3e6f01a	2021-09-25	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - (3beta,17alpha,23S)-17,23-Epoxy-3,28,29-trihydroxy-27-norlanost-8-en-24-one 40V, Negative-QTOF	splash10-03di-0000900000-2366b5e46ef4d0e98cba	2021-09-25	Wishart Lab	View Spectrum

Biological Properties

Cellular Locations

Membrane

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

FDB013870

KNApSAcK ID

C00010787

Chemspider ID

Not Available

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

131751686

PDB ID

Not Available

ChEBI ID

167967

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 ]
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Showing metabocard for (3beta,17alpha,23S)-17,23-Epoxy-3,28,29-trihydroxy-27-norlanost-8-en-24-one (HMDB0035221)

MOL for HMDB0035221 ((3beta,17alpha,23S)-17,23-Epoxy-3,28,29-trihydroxy-27-norlanost-8-en-24-one)

3D MOL for HMDB0035221 ((3beta,17alpha,23S)-17,23-Epoxy-3,28,29-trihydroxy-27-norlanost-8-en-24-one)

3D SDF for HMDB0035221 ((3beta,17alpha,23S)-17,23-Epoxy-3,28,29-trihydroxy-27-norlanost-8-en-24-one)

3D-SDF for HMDB0035221 ((3beta,17alpha,23S)-17,23-Epoxy-3,28,29-trihydroxy-27-norlanost-8-en-24-one)

PDB for HMDB0035221 ((3beta,17alpha,23S)-17,23-Epoxy-3,28,29-trihydroxy-27-norlanost-8-en-24-one)

3D PDB for HMDB0035221 ((3beta,17alpha,23S)-17,23-Epoxy-3,28,29-trihydroxy-27-norlanost-8-en-24-one)

SMILES for HMDB0035221 ((3beta,17alpha,23S)-17,23-Epoxy-3,28,29-trihydroxy-27-norlanost-8-en-24-one)

INCHI for HMDB0035221 ((3beta,17alpha,23S)-17,23-Epoxy-3,28,29-trihydroxy-27-norlanost-8-en-24-one)

Structure for HMDB0035221 ((3beta,17alpha,23S)-17,23-Epoxy-3,28,29-trihydroxy-27-norlanost-8-en-24-one)

3D Structure for HMDB0035221 ((3beta,17alpha,23S)-17,23-Epoxy-3,28,29-trihydroxy-27-norlanost-8-en-24-one)

Predicted Collision Cross Sections

Predicted Kovats Retention Indices

Underivatized

Derivatized

GC-MS Spectra

MS/MS Spectra