MiMeDB: Showing metabocard for Steresterone A (MMDBc0025857)

Record Information

Version

2.0

Status

Detected and Quantified

Creation Date

2021-05-15 15:33:57 UTC

Update Date

2025-10-07 16:07:36 UTC

Metabolite ID

MMDBc0025857

Metabolite Identification

Common Name

Steresterone A

Description

Steresterone A is a steroid metabolite. There is little literature available on this compound, indicating a gap in the understanding of its biological significance and potential applications.

Structure

MOL SDF PDB SMILES InChI


  Mrv1652305152117332D          

 44 49  0  0  1  0            999 V2000
    8.0393    2.7219    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6845    2.6263    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0101    4.0176    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.5965    4.3936    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0680    1.2213    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.7790    1.8097    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.8145    1.6010    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.2184    2.6398    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.2814   -0.0057    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5136    1.6183    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6901    1.6271    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0148   -0.3955    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.2368    0.3689    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.9171    0.2494    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4456    3.4160    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.3577    3.6040    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.8713    1.4093    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    4.9856   -0.4833    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.4358    0.8076    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    5.7190    1.0536    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.8508   -0.4066    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.9611    0.9072    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.9221    3.0023    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.1101    2.1990    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    4.1218   -0.5326    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    6.0583    1.8056    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.8474    0.9875    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.2669    0.9111    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.6683    0.1571    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    3.5350    0.1381    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    6.3157   -1.0881    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.8024   -1.2932    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.5767    2.4754    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.8792    1.8877    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.7118    2.7634    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.0783   -0.5663    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2068    4.2056    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.6325    0.6196    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.0456   -1.3061    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.0002    0.2060    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.4115    0.2160    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.1949    2.6128    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.2856    2.2253    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.5978   -1.2063    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
  8  1  1  0  0  0  0
 11 10  1  0  0  0  0
 12  9  1  0  0  0  0
 15  2  1  0  0  0  0
 15  3  1  0  0  0  0
 16  4  1  1  0  0  0
 16 15  1  0  0  0  0
 17  5  1  6  0  0  0
 18 14  1  0  0  0  0
 19  9  1  0  0  0  0
 19 17  1  1  0  0  0
 20 13  2  0  0  0  0
 21 13  1  0  0  0  0
 21 18  1  0  0  0  0
 22 10  1  0  0  0  0
 23 16  1  6  0  0  0
 24 17  1  1  0  0  0
 24 23  1  0  0  0  0
 25 18  1  0  0  0  0
 26 20  1  0  0  0  0
 27  6  1  1  0  0  0
 27 14  1  0  0  0  0
 27 20  1  0  0  0  0
 27 22  1  0  0  0  0
 28  7  1  6  0  0  0
 28 11  1  0  0  0  0
 28 19  1  0  0  0  0
 29 12  1  0  0  0  0
 29 28  1  0  0  0  0
 30 22  1  0  0  0  0
 30 25  1  0  0  0  0
 30 29  1  0  0  0  0
 31 21  2  0  0  0  0
 25 32  1  1  0  0  0
 33 26  2  0  0  0  0
 34  8  1  0  0  0  0
 34 26  1  0  0  0  0
 35 23  1  0  0  0  0
 35 24  1  0  0  0  0
 29 36  1  6  0  0  0
 30 36  1  6  0  0  0
 16 37  1  6  0  0  0
 17 38  1  1  0  0  0
 18 39  1  1  0  0  0
 19 40  1  1  0  0  0
 22 41  1  1  0  0  0
 23 42  1  1  0  0  0
 24 43  1  6  0  0  0
 25 44  1  6  0  0  0
M  END


  Mrv1652305152117332D          

 44 49  0  0  1  0            999 V2000
    8.0393    2.7219    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6845    2.6263    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0101    4.0176    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.5965    4.3936    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0680    1.2213    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.7790    1.8097    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.8145    1.6010    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.2184    2.6398    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.2814   -0.0057    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5136    1.6183    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6901    1.6271    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0148   -0.3955    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.2368    0.3689    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.9171    0.2494    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4456    3.4160    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.3577    3.6040    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.8713    1.4093    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    4.9856   -0.4833    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.4358    0.8076    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    5.7190    1.0536    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.8508   -0.4066    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.9611    0.9072    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.9221    3.0023    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.1101    2.1990    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    4.1218   -0.5326    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    6.0583    1.8056    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.8474    0.9875    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.2669    0.9111    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.6683    0.1571    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    3.5350    0.1381    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    6.3157   -1.0881    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.8024   -1.2932    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.5767    2.4754    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.8792    1.8877    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.7118    2.7634    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.0783   -0.5663    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2068    4.2056    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.6325    0.6196    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.0456   -1.3061    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.0002    0.2060    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.4115    0.2160    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.1949    2.6128    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.2856    2.2253    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.5978   -1.2063    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
  8  1  1  0  0  0  0
 11 10  1  0  0  0  0
 12  9  1  0  0  0  0
 15  2  1  0  0  0  0
 15  3  1  0  0  0  0
 16  4  1  1  0  0  0
 16 15  1  0  0  0  0
 17  5  1  6  0  0  0
 18 14  1  0  0  0  0
 19  9  1  0  0  0  0
 19 17  1  1  0  0  0
 20 13  2  0  0  0  0
 21 13  1  0  0  0  0
 21 18  1  0  0  0  0
 22 10  1  0  0  0  0
 23 16  1  6  0  0  0
 24 17  1  1  0  0  0
 24 23  1  0  0  0  0
 25 18  1  0  0  0  0
 26 20  1  0  0  0  0
 27  6  1  1  0  0  0
 27 14  1  0  0  0  0
 27 20  1  0  0  0  0
 27 22  1  0  0  0  0
 28  7  1  6  0  0  0
 28 11  1  0  0  0  0
 28 19  1  0  0  0  0
 29 12  1  0  0  0  0
 29 28  1  0  0  0  0
 30 22  1  0  0  0  0
 30 25  1  0  0  0  0
 30 29  1  0  0  0  0
 31 21  2  0  0  0  0
 25 32  1  1  0  0  0
 33 26  2  0  0  0  0
 34  8  1  0  0  0  0
 34 26  1  0  0  0  0
 35 23  1  0  0  0  0
 35 24  1  0  0  0  0
 29 36  1  6  0  0  0
 30 36  1  6  0  0  0
 16 37  1  6  0  0  0
 17 38  1  1  0  0  0
 18 39  1  1  0  0  0
 19 40  1  1  0  0  0
 22 41  1  1  0  0  0
 23 42  1  1  0  0  0
 24 43  1  6  0  0  0
 25 44  1  6  0  0  0
M  END
> <DATABASE_ID>
MMDBc0025857

> <DATABASE_NAME>
MIME

> <SMILES>
[H][C@@](C)(C(C)C)[C@]1([H])O[C@@]1([H])[C@@]([H])(C)[C@@]1([H])CC[C@]23O[C@]22[C@]([H])(O)[C@]4([H])C[C@@](C)(C(=CC4=O)C(=O)OCC)[C@@]2([H])CC[C@]13C

> <INCHI_IDENTIFIER>
InChI=1S/C30H44O6/c1-8-34-26(33)20-13-21(31)18-14-27(20,6)22-10-11-28(7)19(9-12-29(28)30(22,36-29)25(18)32)17(5)24-23(35-24)16(4)15(2)3/h13,15-19,22-25,32H,8-12,14H2,1-7H3/t16-,17+,18-,19-,22-,23+,24+,25-,27+,28-,29-,30-/m1/s1

> <INCHI_KEY>
OWBPJBQKRVNNBP-NHJUSTAWSA-N

> <FORMULA>
C30H44O6

> <MOLECULAR_WEIGHT>
500.676

> <EXACT_MASS>
500.313789137

> <JCHEM_ACCEPTOR_COUNT>
5

> <JCHEM_ATOM_COUNT>
80

> <JCHEM_AVERAGE_POLARIZABILITY>
56.904797491926395

> <JCHEM_BIOAVAILABILITY>
0

> <JCHEM_DONOR_COUNT>
1

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
ethyl (1R,2R,5R,6R,9R,11R,12R,13S)-12-hydroxy-1,5-dimethyl-6-[(1S)-1-[(2S,3S)-3-[(2R)-3-methylbutan-2-yl]oxiran-2-yl]ethyl]-14-oxo-10-oxapentacyclo[11.3.1.0^{2,11}.0^{5,9}.0^{9,11}]heptadec-15-ene-16-carboxylate

> <ALOGPS_LOGP>
4.55

> <JCHEM_LOGP>
5.007257615

> <ALOGPS_LOGS>
-5.73

> <JCHEM_MDDR_LIKE_RULE>
1

> <JCHEM_NUMBER_OF_RINGS>
6

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
15.968847634001918

> <JCHEM_PKA_STRONGEST_ACIDIC>
13.476693091821652

> <JCHEM_PKA_STRONGEST_BASIC>
-3.458236021448827

> <JCHEM_POLAR_SURFACE_AREA>
88.66

> <JCHEM_REFRACTIVITY>
135.21159999999998

> <JCHEM_ROTATABLE_BOND_COUNT>
7

> <JCHEM_RULE_OF_FIVE>
0

> <ALOGPS_SOLUBILITY>
9.33e-04 g/l

> <JCHEM_TRADITIONAL_IUPAC>
ethyl (1R,2R,5R,6R,9R,11R,12R,13S)-12-hydroxy-1,5-dimethyl-6-[(1S)-1-[(2S,3S)-3-[(2R)-3-methylbutan-2-yl]oxiran-2-yl]ethyl]-14-oxo-10-oxapentacyclo[11.3.1.0^{2,11}.0^{5,9}.0^{9,11}]heptadec-15-ene-16-carboxylate

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 15-MAY-21   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   15-MAY-21         0                                  
HETATM    1  C   UNK     0      15.007   5.081   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0      -1.278   4.902   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0      -1.885   7.500   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0       1.113   8.201   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0       0.127   2.280   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0       8.921   3.378   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0       3.387   2.988   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0      13.474   4.928   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0       2.392  -0.011   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0       6.559   3.021   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0       5.021   3.037   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0       3.761  -0.738   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0      11.642   0.689   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0       9.179   0.466   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0      -0.832   6.376   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0       0.668   6.727   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0       1.626   2.631   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0       9.306  -0.902   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0       2.680   1.508   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0      10.675   1.967   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0      10.921  -0.759   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0       7.394   1.693   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0       1.721   5.604   0.000  0.00  0.00           C+0
HETATM   24  C   UNK     0       2.072   4.105   0.000  0.00  0.00           C+0
HETATM   25  C   UNK     0       7.694  -0.994   0.000  0.00  0.00           C+0
HETATM   26  C   UNK     0      11.309   3.370   0.000  0.00  0.00           C+0
HETATM   27  C   UNK     0       9.048   1.843   0.000  0.00  0.00           C+0
HETATM   28  C   UNK     0       4.231   1.701   0.000  0.00  0.00           C+0
HETATM   29  C   UNK     0       4.981   0.293   0.000  0.00  0.00           C+0
HETATM   30  C   UNK     0       6.599   0.258   0.000  0.00  0.00           C+0
HETATM   31  O   UNK     0      11.789  -2.031   0.000  0.00  0.00           O+0
HETATM   32  O   UNK     0       7.098  -2.414   0.000  0.00  0.00           O+0
HETATM   33  O   UNK     0      10.410   4.621   0.000  0.00  0.00           O+0
HETATM   34  O   UNK     0      12.841   3.524   0.000  0.00  0.00           O+0
HETATM   35  O   UNK     0       3.195   5.158   0.000  0.00  0.00           O+0
HETATM   36  O   UNK     0       5.746  -1.057   0.000  0.00  0.00           O+0
HETATM   37  H   UNK     0      -0.386   7.850   0.000  0.00  0.00           H+0
HETATM   38  H   UNK     0       1.181   1.157   0.000  0.00  0.00           H+0
HETATM   39  H   UNK     0       9.418  -2.438   0.000  0.00  0.00           H+0
HETATM   40  H   UNK     0       3.734   0.384   0.000  0.00  0.00           H+0
HETATM   41  H   UNK     0       8.235   0.403   0.000  0.00  0.00           H+0
HETATM   42  H   UNK     0       0.364   4.877   0.000  0.00  0.00           H+0
HETATM   43  H   UNK     0       0.533   4.154   0.000  0.00  0.00           H+0
HETATM   44  H   UNK     0       8.583  -2.252   0.000  0.00  0.00           H+0
CONECT    1    8                                                            
CONECT    2   15                                                            
CONECT    3   15                                                            
CONECT    4   16                                                            
CONECT    5   17                                                            
CONECT    6   27                                                            
CONECT    7   28                                                            
CONECT    8    1   34                                                       
CONECT    9   12   19                                                       
CONECT   10   11   22                                                       
CONECT   11   10   28                                                       
CONECT   12    9   29                                                       
CONECT   13   20   21                                                       
CONECT   14   18   27                                                       
CONECT   15    2    3   16                                                  
CONECT   16    4   15   23   37                                             
CONECT   17    5   19   24   38                                             
CONECT   18   14   21   25   39                                             
CONECT   19    9   17   28   40                                             
CONECT   20   13   26   27                                                  
CONECT   21   13   18   31                                                  
CONECT   22   10   27   30   41                                             
CONECT   23   16   24   35   42                                             
CONECT   24   17   23   35   43                                             
CONECT   25   18   30   32   44                                             
CONECT   26   20   33   34                                                  
CONECT   27    6   14   20   22                                             
CONECT   28    7   11   19   29                                             
CONECT   29   12   28   30   36                                             
CONECT   30   22   25   29   36                                             
CONECT   31   21                                                            
CONECT   32   25                                                            
CONECT   33   26                                                            
CONECT   34    8   26                                                       
CONECT   35   23   24                                                       
CONECT   36   29   30                                                       
CONECT   37   16                                                            
CONECT   38   17                                                            
CONECT   39   18                                                            
CONECT   40   19                                                            
CONECT   41   22                                                            
CONECT   42   23                                                            
CONECT   43   24                                                            
CONECT   44   25                                                            
MASTER        0    0    0    0    0    0    0    0   44    0   98    0
END

Synonyms

Not Available

Molecular Formula

C₃₀H₄₄O₆

Average Mass

500.676

Monoisotopic Mass

500.313789137

IUPAC Name

ethyl (1R,2R,5R,6R,9R,11R,12R,13S)-12-hydroxy-1,5-dimethyl-6-[(1S)-1-[(2S,3S)-3-[(2R)-3-methylbutan-2-yl]oxiran-2-yl]ethyl]-14-oxo-10-oxapentacyclo[11.3.1.0^{2,11}.0^{5,9}.0^{9,11}]heptadec-15-ene-16-carboxylate

Traditional Name

CAS Registry Number

Not Available

SMILES

[H][C@@](C)(C(C)C)[C@]1([H])O[C@@]1([H])[C@@]([H])(C)[C@@]1([H])CC[C@]23O[C@]22[C@]([H])(O)[C@]4([H])C[C@@](C)(C(=CC4=O)C(=O)OCC)[C@@]2([H])CC[C@]13C

InChI Identifier

InChI=1S/C30H44O6/c1-8-34-26(33)20-13-21(31)18-14-27(20,6)22-10-11-28(7)19(9-12-29(28)30(22,36-29)25(18)32)17(5)24-23(35-24)16(4)15(2)3/h13,15-19,22-25,32H,8-12,14H2,1-7H3/t16-,17+,18-,19-,22-,23+,24+,25-,27+,28-,29-,30-/m1/s1

InChI Key

OWBPJBQKRVNNBP-NHJUSTAWSA-N

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as prostaglandins and related compounds. These are unsaturated carboxylic acids consisting of a 20 carbon skeleton that also contains a five member ring, and are based upon the fatty acid arachidonic acid.

Kingdom

Organic compounds

Super Class

Lipids and lipid-like molecules

Class

Fatty Acyls

Sub Class

Eicosanoids

Direct Parent

Prostaglandins and related compounds

Alternative Parents

Substituents

Prostaglandin skeleton
Sesquiterpenoid
Cyclohexenone
Oxepane
Alpha,beta-unsaturated carboxylic ester
Enoate ester
Cyclic alcohol
Secondary alcohol
Ketone
Carboxylic acid ester
Oxacycle
Organoheterocyclic compound
Monocarboxylic acid or derivatives
Ether
Oxirane
Dialkyl ether
Carboxylic acid derivative
Organic oxygen compound
Organic oxide
Hydrocarbon derivative
Organooxygen compound
Carbonyl group
Alcohol
Aliphatic heteropolycyclic compound

Molecular Framework

Aliphatic heteropolycyclic compounds

External Descriptors

Not Available

Functional Ontology

Not Available

Physical Properties

State

Expected Solid

Predicted Properties

Property	Value	Source
Water Solubility	0.00093 g/L	ALOGPS
logP	4.55	ALOGPS
logP	5.01	ChemAxon
logS	-5.7	ALOGPS
pKa (Strongest Acidic)	13.48	ChemAxon
pKa (Strongest Basic)	-3.5	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	5	ChemAxon
Hydrogen Donor Count	1	ChemAxon
Polar Surface Area	88.66 Å²	ChemAxon
Rotatable Bond Count	7	ChemAxon
Refractivity	135.21 m³·mol⁻¹	ChemAxon
Polarizability	56.9 Å³	ChemAxon
Number of Rings	6	ChemAxon
Bioavailability	No	ChemAxon
Rule of Five	No	ChemAxon
Ghose Filter	No	ChemAxon
Veber's Rule	No	ChemAxon
MDDR-like Rule	Yes	ChemAxon

Spectra

Spectrum Type	Description	Splash Key	Deposition Date	View
Predicted GC-MS	Predicted GC-MS Spectrum - GC-MS (TMS_2_1) - 70eV, Positive	Not Available	2022-08-08	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 10V, Positive	Not Available	2022-08-09	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 20V, Positive	Not Available	2022-08-09	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 40V, Positive	Not Available	2022-08-09	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 10V, Negative	Not Available	2022-08-09	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 20V, Negative	Not Available	2022-08-09	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 40V, Negative	Not Available	2022-08-09	View Spectrum
MS	Mass Spectrum (Electron Ionization)	Not Available	2022-08-06	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 100 MHz, H₂O, predicted)		2022-08-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 100 MHz, H₂O, predicted)		2022-08-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 1000 MHz, H₂O, predicted)		2022-08-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 1000 MHz, H₂O, predicted)		2022-08-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 200 MHz, H₂O, predicted)		2022-08-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 200 MHz, H₂O, predicted)		2022-08-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 300 MHz, H₂O, predicted)		2022-08-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 300 MHz, H₂O, predicted)		2022-08-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 400 MHz, H₂O, predicted)		2022-08-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 400 MHz, H₂O, predicted)		2022-08-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 500 MHz, H₂O, predicted)		2022-08-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 500 MHz, H₂O, predicted)		2022-08-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 600 MHz, H₂O, predicted)		2022-08-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 600 MHz, H₂O, predicted)		2022-08-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 700 MHz, H₂O, predicted)		2022-08-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 700 MHz, H₂O, predicted)		2022-08-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 800 MHz, H₂O, predicted)		2022-08-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 800 MHz, H₂O, predicted)		2022-08-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 900 MHz, H₂O, predicted)		2022-08-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 900 MHz, H₂O, predicted)		2022-08-20	View Spectrum

Biological Properties

Cellular Locations

Not Available

Biospecimen Locations

Not Available

Tissue Locations

Not Available

Associated OMIM IDs

114500 (Colorectal cancer)
610247 (Eosinophilic esophagitis)

Human Proteins and Enzymes

Protein ID	Protein Name	Protein Type	Uniprot ID	Species

Human Pathways

Pathways

Name	SMPDB/PathBank

Microbial Pathways

Pathways

Not Available

Metabolic Reactions

Reactions

This table shows at most 20 reactions. For the full list of associated reactions:

See All Associated Reactions

Reaction ID	Precursor	Product	Enzyme	Reaction Type	Data Source	Reference

Health Effects and Bioactivity

Health Outcome/Bioactivity	Metabolite Response/Effect	Evidence Type	Host and Biospecimen	Data Source	Reference

Microbial Sources

Superkingdom/Kingdom	Phylum	Total species	Hosts and Body Sites	Microbial Links
Eukaryota/Fungi	Basidiomycota	1	Human feces	Metabolic reconstruction

Exposure Sources

Other Exposures

Source Type	Data Source	Reference

Host Biospecimen and Location

Host and Biospecimen	Status	Mean	Std	Min	Max	Units	Age	Sex	Health Condition	Data Source	Reference

External Links

HMDB ID

Not Available

DrugBank ID

Not Available

Phenol Explorer Compound ID

Not Available

FooDB ID

Not Available

KNApSAcK ID

Not Available

Chemspider ID

Not Available

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

146682482

PDB ID

Not Available

ChEBI ID

Not Available

Food Biomarker Ontology

Not Available

CMMC Knowledgebase

Not Available

General References

van Santen JA, Poynton EF, Iskakova D, McMann E, Alsup TA, Clark TN, Fergusson CH, Fewer DP, Hughes AH, McCadden CA, Parra J, Soldatou S, Rudolf JD, Janssen EM, Duncan KR, Linington RG: The Natural Products Atlas 2.0: a database of microbially-derived natural products. Nucleic Acids Res. 2022 Jan 7;50(D1):D1317-D1323. doi: 10.1093/nar/gkab941. [PubMed:34718710 ]

Showing metabocard for Steresterone A (MMDBc0025857)

MOL for #<Metabolite:0x00007f8db9d73608>

3D MOL for #<Metabolite:0x00007f8db9d73608>

3D SDF for #<Metabolite:0x00007f8db9d73608>

3D-SDF for #<Metabolite:0x00007f8db9d73608>

PDB for #<Metabolite:0x00007f8db9d73608>

3D PDB for #<Metabolite:0x00007f8db9d73608>

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INCHI for #<Metabolite:0x00007f8db9d73608>

Structure for #<Metabolite:0x00007f8db9d73608>

3D Structure for #<Metabolite:0x00007f8db9d73608>