MiMeDB: Showing metabocard for 5Î±,8Î±-Epidioxycholesta-6,9(11),22-trien-3Î²-ol (MMDBc0015388)

Record Information

Version

2.0

Status

Detected and Quantified

Creation Date

2021-05-15 06:13:06 UTC

Update Date

2025-10-07 16:06:24 UTC

Metabolite ID

MMDBc0015388

Metabolite Identification

Common Name

5Î±,8Î±-Epidioxycholesta-6,9(11),22-trien-3Î²-ol

Description

5Î±,8Î±-Epidioxycholesta-6,9(11),22-trien-3Î²-ol is a sterol, specifically a type of cholesterol derivative. There is limited literature available on this metabolite, indicating that further research may be necessary to fully understand its biological significance and potential applications.

Structure

MOL SDF PDB SMILES InChI


  Mrv1652305152108132D          

 36 40  0  0  1  0            999 V2000
    0.3623    0.3332    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5347    1.1501    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2434   -1.4873    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.6332   -0.6768    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.8704    0.9791    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.4780   -0.2036    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.6560   -0.2736    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.9497   -0.8805    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.7237    0.6590    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2877    1.2611    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.8686   -0.1211    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.2538   -0.4495    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.4416   -0.5930    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.0479   -0.2024    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.3243    1.8505    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.3956    1.7227    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.8540    1.4366    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1843    0.4032    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.7717   -0.8104    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    9.1781    0.6661    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    4.1221   -0.0635    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    5.0347    0.9107    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    6.6063    0.3227    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.9323    0.0921    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    7.4998    0.4457    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    8.0203    1.2063    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    5.8996    0.9142    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   10.0030    0.6759    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    7.3168    1.2176    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.5739    1.1153    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.8284    0.5433    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.5993   -1.6274    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.4214   -1.5573    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
    8.3531    0.6564    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.2975   -0.0904    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.2125    1.7163    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
  7  6  1  0  0  0  0
  8  6  2  0  0  0  0
 10  9  1  0  0  0  0
 13 12  1  0  0  0  0
 14 11  1  0  0  0  0
 16 15  2  0  0  0  0
 18  1  1  0  0  0  0
 18  2  1  0  0  0  0
 18  7  1  0  0  0  0
 19  3  1  6  0  0  0
 19  8  1  0  0  0  0
 20 11  1  0  0  0  0
 20 17  1  0  0  0  0
 21  9  1  0  0  0  0
 21 19  1  1  0  0  0
 22 10  1  0  0  0  0
 23 12  2  0  0  0  0
 24  4  1  1  0  0  0
 24 13  1  0  0  0  0
 24 21  1  0  0  0  0
 24 22  1  0  0  0  0
 25  5  1  1  0  0  0
 25 14  1  0  0  0  0
 25 23  1  0  0  0  0
 26 15  1  0  0  0  0
 26 17  1  0  0  0  0
 26 25  1  0  0  0  0
 27 16  1  0  0  0  0
 27 22  1  0  0  0  0
 27 23  1  0  0  0  0
 20 28  1  6  0  0  0
 26 29  1  6  0  0  0
 27 30  1  6  0  0  0
 30 29  1  0  0  0  0
 31  6  1  0  0  0  0
 32  8  1  0  0  0  0
 19 33  1  1  0  0  0
 20 34  1  6  0  0  0
 21 35  1  6  0  0  0
 22 36  1  6  0  0  0
M  END


  Mrv1652305152108132D          

 36 40  0  0  1  0            999 V2000
    0.3623    0.3332    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5347    1.1501    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2434   -1.4873    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.6332   -0.6768    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.8704    0.9791    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.4780   -0.2036    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.6560   -0.2736    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.9497   -0.8805    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.7237    0.6590    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2877    1.2611    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.8686   -0.1211    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.2538   -0.4495    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.4416   -0.5930    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.0479   -0.2024    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.3243    1.8505    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.3956    1.7227    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.8540    1.4366    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1843    0.4032    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.7717   -0.8104    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    9.1781    0.6661    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    4.1221   -0.0635    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    5.0347    0.9107    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    6.6063    0.3227    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.9323    0.0921    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    7.4998    0.4457    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    8.0203    1.2063    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    5.8996    0.9142    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   10.0030    0.6759    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    7.3168    1.2176    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.5739    1.1153    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.8284    0.5433    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.5993   -1.6274    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.4214   -1.5573    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
    8.3531    0.6564    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.2975   -0.0904    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.2125    1.7163    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
  7  6  1  0  0  0  0
  8  6  2  0  0  0  0
 10  9  1  0  0  0  0
 13 12  1  0  0  0  0
 14 11  1  0  0  0  0
 16 15  2  0  0  0  0
 18  1  1  0  0  0  0
 18  2  1  0  0  0  0
 18  7  1  0  0  0  0
 19  3  1  6  0  0  0
 19  8  1  0  0  0  0
 20 11  1  0  0  0  0
 20 17  1  0  0  0  0
 21  9  1  0  0  0  0
 21 19  1  1  0  0  0
 22 10  1  0  0  0  0
 23 12  2  0  0  0  0
 24  4  1  1  0  0  0
 24 13  1  0  0  0  0
 24 21  1  0  0  0  0
 24 22  1  0  0  0  0
 25  5  1  1  0  0  0
 25 14  1  0  0  0  0
 25 23  1  0  0  0  0
 26 15  1  0  0  0  0
 26 17  1  0  0  0  0
 26 25  1  0  0  0  0
 27 16  1  0  0  0  0
 27 22  1  0  0  0  0
 27 23  1  0  0  0  0
 20 28  1  6  0  0  0
 26 29  1  6  0  0  0
 27 30  1  6  0  0  0
 30 29  1  0  0  0  0
 31  6  1  0  0  0  0
 32  8  1  0  0  0  0
 19 33  1  1  0  0  0
 20 34  1  6  0  0  0
 21 35  1  6  0  0  0
 22 36  1  6  0  0  0
M  END
> <DATABASE_ID>
MMDBc0015388

> <DATABASE_NAME>
MIME

> <SMILES>
[H]\C(CC(C)C)=C(\[H])[C@@]([H])(C)[C@@]1([H])CC[C@]2([H])[C@]1(C)CC=C1[C@@]3(C)CC[C@]([H])(O)C[C@@]33OO[C@@]21C=C3

> <INCHI_IDENTIFIER>
InChI=1S/C27H40O3/c1-18(2)7-6-8-19(3)21-9-10-22-24(21,4)13-12-23-25(5)14-11-20(28)17-26(25)15-16-27(22,23)30-29-26/h6,8,12,15-16,18-22,28H,7,9-11,13-14,17H2,1-5H3/b8-6+/t19-,20+,21-,22-,24-,25-,26-,27+/m1/s1

> <INCHI_KEY>
CAUMZAZCOGASOU-LRCFNPBWSA-N

> <FORMULA>
C27H40O3

> <MOLECULAR_WEIGHT>
412.614

> <EXACT_MASS>
412.297745148

> <JCHEM_ACCEPTOR_COUNT>
3

> <JCHEM_ATOM_COUNT>
70

> <JCHEM_AVERAGE_POLARIZABILITY>
49.94147484525008

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
1

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
(1S,2R,5R,6R,10R,13S,15S)-6,10-dimethyl-5-[(2R,3E)-6-methylhept-3-en-2-yl]-16,17-dioxapentacyclo[13.2.2.0^{1,9}.0^{2,6}.0^{10,15}]nonadeca-8,18-dien-13-ol

> <ALOGPS_LOGP>
6.65

> <JCHEM_LOGP>
5.733294

> <ALOGPS_LOGS>
-6.20

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
5

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA_STRONGEST_ACIDIC>
15.14787838866792

> <JCHEM_PKA_STRONGEST_BASIC>
-2.7341179927966524

> <JCHEM_POLAR_SURFACE_AREA>
38.69

> <JCHEM_REFRACTIVITY>
123.04849999999998

> <JCHEM_ROTATABLE_BOND_COUNT>
4

> <JCHEM_RULE_OF_FIVE>
0

> <ALOGPS_SOLUBILITY>
2.59e-04 g/l

> <JCHEM_TRADITIONAL_IUPAC>
(1S,2R,5R,6R,10R,13S,15S)-6,10-dimethyl-5-[(2R,3E)-6-methylhept-3-en-2-yl]-16,17-dioxapentacyclo[13.2.2.0^{1,9}.0^{2,6}.0^{10,15}]nonadeca-8,18-dien-13-ol

> <JCHEM_VEBER_RULE>
1

$$$$

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       0.676   0.622   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0       2.865   2.147   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0       7.921  -2.776   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0       8.649  -1.263   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0      12.825   1.828   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0       4.626  -0.380   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0       3.091  -0.511   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0       5.506  -1.644   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0       6.951   1.230   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0       8.004   2.354   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0      16.555  -0.226   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0      11.674  -0.839   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0      10.158  -1.107   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0      15.023  -0.378   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0      13.672   3.454   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0      11.939   3.216   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0      16.528   2.682   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0       2.211   0.753   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0       7.041  -1.513   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0      17.132   1.243   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0       7.695  -0.119   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0       9.398   1.700   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0      12.332   0.602   0.000  0.00  0.00           C+0
HETATM   24  C   UNK     0       9.207   0.172   0.000  0.00  0.00           C+0
HETATM   25  C   UNK     0      14.000   0.832   0.000  0.00  0.00           C+0
HETATM   26  C   UNK     0      14.971   2.252   0.000  0.00  0.00           C+0
HETATM   27  C   UNK     0      11.013   1.707   0.000  0.00  0.00           C+0
HETATM   28  O   UNK     0      18.672   1.262   0.000  0.00  0.00           O+0
HETATM   29  O   UNK     0      13.658   2.273   0.000  0.00  0.00           O+0
HETATM   30  O   UNK     0      12.271   2.082   0.000  0.00  0.00           O+0
HETATM   31  H   UNK     0       5.280   1.014   0.000  0.00  0.00           H+0
HETATM   32  H   UNK     0       4.852  -3.038   0.000  0.00  0.00           H+0
HETATM   33  H   UNK     0       6.387  -2.907   0.000  0.00  0.00           H+0
HETATM   34  H   UNK     0      15.593   1.225   0.000  0.00  0.00           H+0
HETATM   35  H   UNK     0       6.155  -0.169   0.000  0.00  0.00           H+0
HETATM   36  H   UNK     0       9.730   3.204   0.000  0.00  0.00           H+0
CONECT    1   18                                                            
CONECT    2   18                                                            
CONECT    3   19                                                            
CONECT    4   24                                                            
CONECT    5   25                                                            
CONECT    6    7    8   31                                                  
CONECT    7    6   18                                                       
CONECT    8    6   19   32                                                  
CONECT    9   10   21                                                       
CONECT   10    9   22                                                       
CONECT   11   14   20                                                       
CONECT   12   13   23                                                       
CONECT   13   12   24                                                       
CONECT   14   11   25                                                       
CONECT   15   16   26                                                       
CONECT   16   15   27                                                       
CONECT   17   20   26                                                       
CONECT   18    1    2    7                                                  
CONECT   19    3    8   21   33                                             
CONECT   20   11   17   28   34                                             
CONECT   21    9   19   24   35                                             
CONECT   22   10   24   27   36                                             
CONECT   23   12   25   27                                                  
CONECT   24    4   13   21   22                                             
CONECT   25    5   14   23   26                                             
CONECT   26   15   17   25   29                                             
CONECT   27   16   22   23   30                                             
CONECT   28   20                                                            
CONECT   29   26   30                                                       
CONECT   30   27   29                                                       
CONECT   31    6                                                            
CONECT   32    8                                                            
CONECT   33   19                                                            
CONECT   34   20                                                            
CONECT   35   21                                                            
CONECT   36   22                                                            
MASTER        0    0    0    0    0    0    0    0   36    0   80    0
END

Synonyms

Not Available

Molecular Formula

C₂₇H₄₀O₃

Average Mass

412.614

Monoisotopic Mass

412.297745148

IUPAC Name

(1S,2R,5R,6R,10R,13S,15S)-6,10-dimethyl-5-[(2R,3E)-6-methylhept-3-en-2-yl]-16,17-dioxapentacyclo[13.2.2.0^{1,9}.0^{2,6}.0^{10,15}]nonadeca-8,18-dien-13-ol

Traditional Name

(1S,2R,5R,6R,10R,13S,15S)-6,10-dimethyl-5-[(2R,3E)-6-methylhept-3-en-2-yl]-16,17-dioxapentacyclo[13.2.2.0^{1,9}.0^{2,6}.0^{10,15}]nonadeca-8,18-dien-13-ol

CAS Registry Number

Not Available

SMILES

[H]\C(CC(C)C)=C(\[H])[C@@]([H])(C)[C@@]1([H])CC[C@]2([H])[C@]1(C)CC=C1[C@@]3(C)CC[C@]([H])(O)C[C@@]33OO[C@@]21C=C3

InChI Identifier

InChI=1S/C27H40O3/c1-18(2)7-6-8-19(3)21-9-10-22-24(21,4)13-12-23-25(5)14-11-20(28)17-26(25)15-16-27(22,23)30-29-26/h6,8,12,15-16,18-22,28H,7,9-11,13-14,17H2,1-5H3/b8-6+/t19-,20+,21-,22-,24-,25-,26-,27+/m1/s1

InChI Key

CAUMZAZCOGASOU-LRCFNPBWSA-N

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as steroids and steroid derivatives. Steroids and steroid derivatives are compounds based on the cyclopenta[a]phenanthrene carbon skeleton, partially or completely hydrogenated; there are usually methyl groups at C-10 and C-13, and often an alkyl group at C-17. By extension, one or more bond scissions, ring expansions and/or ring contractions of the skeleton may have occurred.

Kingdom

Organic compounds

Super Class

Lipids and lipid-like molecules

Class

Steroids and steroid derivatives

Sub Class

Not Available

Direct Parent

Steroids and steroid derivatives

Alternative Parents

Substituents

Cholane-skeleton
Ortho-dioxane
Cyclic alcohol
Dialkyl peroxide
Secondary alcohol
Oxacycle
Organoheterocyclic compound
Organic oxygen compound
Hydrocarbon derivative
Organooxygen compound
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	0.00026 g/L	ALOGPS
logP	6.65	ALOGPS
logP	5.73	ChemAxon
logS	-6.2	ALOGPS
pKa (Strongest Acidic)	15.15	ChemAxon
pKa (Strongest Basic)	-2.7	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	3	ChemAxon
Hydrogen Donor Count	1	ChemAxon
Polar Surface Area	38.69 Å²	ChemAxon
Rotatable Bond Count	4	ChemAxon
Refractivity	123.05 m³·mol⁻¹	ChemAxon
Polarizability	49.94 Å³	ChemAxon
Number of Rings	5	ChemAxon
Bioavailability	Yes	ChemAxon
Rule of Five	No	ChemAxon
Ghose Filter	No	ChemAxon
Veber's Rule	Yes	ChemAxon
MDDR-like Rule	No	ChemAxon

Spectra

Spectrum Type	Description	Splash Key	Deposition Date	View
Predicted GC-MS	Predicted GC-MS Spectrum - GC-MS (TMS_1_1) - 70eV, Positive	Not Available	2022-08-08	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 10V, Positive	Not Available	2022-08-10	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 20V, Positive	Not Available	2022-08-10	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 40V, Positive	Not Available	2022-08-10	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 10V, Negative	Not Available	2022-08-10	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 20V, Negative	Not Available	2022-08-10	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 40V, Negative	Not Available	2022-08-10	View Spectrum
MS	Mass Spectrum (Electron Ionization)	Not Available	2022-08-06	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 100 MHz, H₂O, predicted)		2022-08-23	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 100 MHz, H₂O, predicted)		2022-08-23	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 1000 MHz, H₂O, predicted)		2022-08-23	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 1000 MHz, H₂O, predicted)		2022-08-23	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 200 MHz, H₂O, predicted)		2022-08-23	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 200 MHz, H₂O, predicted)		2022-08-23	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 300 MHz, H₂O, predicted)		2022-08-23	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 300 MHz, H₂O, predicted)		2022-08-23	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 400 MHz, H₂O, predicted)		2022-08-23	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 400 MHz, H₂O, predicted)		2022-08-23	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 500 MHz, H₂O, predicted)		2022-08-23	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 500 MHz, H₂O, predicted)		2022-08-23	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 600 MHz, H₂O, predicted)		2022-08-23	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 600 MHz, H₂O, predicted)		2022-08-23	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 700 MHz, H₂O, predicted)		2022-08-23	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 700 MHz, H₂O, predicted)		2022-08-23	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 800 MHz, H₂O, predicted)		2022-08-23	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 800 MHz, H₂O, predicted)		2022-08-23	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 900 MHz, H₂O, predicted)		2022-08-23	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 900 MHz, H₂O, predicted)		2022-08-23	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

23306468

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

15454717

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 5Î±,8Î±-Epidioxycholesta-6,9(11),22-trien-3Î²-ol (MMDBc0015388)

MOL for #<Metabolite:0x00007f8dd153ff28>

3D MOL for #<Metabolite:0x00007f8dd153ff28>

3D SDF for #<Metabolite:0x00007f8dd153ff28>

3D-SDF for #<Metabolite:0x00007f8dd153ff28>

PDB for #<Metabolite:0x00007f8dd153ff28>

3D PDB for #<Metabolite:0x00007f8dd153ff28>

SMILES for #<Metabolite:0x00007f8dd153ff28>

INCHI for #<Metabolite:0x00007f8dd153ff28>

Structure for #<Metabolite:0x00007f8dd153ff28>

3D Structure for #<Metabolite:0x00007f8dd153ff28>