MiMeDB: Showing metabocard for 3Î²-hydroxyergosta-8,14,24(28)-trien-7-one (MMDBc0026000)

Record Information

Version

2.0

Status

Detected and Quantified

Creation Date

2021-05-15 15:42:12 UTC

Update Date

2025-10-07 16:07:37 UTC

Metabolite ID

MMDBc0026000

Metabolite Identification

Common Name

3Î²-hydroxyergosta-8,14,24(28)-trien-7-one

Description

3Î²-hydroxyergosta-8,14,24(28)-trien-7-one is a sterol, a class of organic compounds characterized by a four-ring core structure. There is limited literature available on this metabolite, indicating that further research may be needed to fully understand its biological significance and potential applications.

Structure

MOL SDF PDB SMILES InChI


  Mrv1652305152117422D          

 34 37  0  0  1  0            999 V2000
    5.3818    4.3076    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.6673    3.0701    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.9529    5.1326    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.8094    3.0701    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5276    2.8443    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.9544    3.4200    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.2384    3.8951    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5239    4.3076    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.0087    5.1280    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.2018    5.2996    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1415    2.5013    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7206    3.0159    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3346    2.6728    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0864    3.1874    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4386    3.8990    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3767    4.8551    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.6673    3.8951    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.9529    4.3076    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.8094    3.8951    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   -2.6316    4.0705    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   -3.6936    3.1144    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.0950    4.3076    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   -0.2107    4.5851    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2726    3.6290    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5697    5.0267    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0177    4.4136    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0796    3.4574    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.3413    3.9720    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   -4.5005    2.9428    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3148    5.8113    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.5239    3.4826    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8247    4.2420    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2456    3.7275    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.7869    4.7569    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
  8  7  1  0  0  0  0
 10  9  1  0  0  0  0
 13 11  1  0  0  0  0
 14 12  1  0  0  0  0
 17  1  1  0  0  0  0
 17  2  1  0  0  0  0
 18  3  2  0  0  0  0
 18  7  1  0  0  0  0
 18 17  1  0  0  0  0
 19  4  1  1  0  0  0
 19  8  1  0  0  0  0
 20 15  1  0  0  0  0
 20 16  1  0  0  0  0
 21 11  1  0  0  0  0
 21 15  1  0  0  0  0
 22  9  1  0  0  0  0
 22 19  1  6  0  0  0
 23 10  2  0  0  0  0
 24 12  1  0  0  0  0
 25 16  1  0  0  0  0
 26 23  1  0  0  0  0
 26 24  2  0  0  0  0
 26 25  1  0  0  0  0
 27  5  1  6  0  0  0
 27 13  1  0  0  0  0
 27 20  1  0  0  0  0
 27 24  1  0  0  0  0
 28  6  1  6  0  0  0
 28 14  1  0  0  0  0
 28 22  1  0  0  0  0
 28 23  1  0  0  0  0
 21 29  1  6  0  0  0
 30 25  2  0  0  0  0
 19 31  1  6  0  0  0
 20 32  1  1  0  0  0
 21 33  1  1  0  0  0
 22 34  1  1  0  0  0
M  END


  Mrv1652305152117422D          

 34 37  0  0  1  0            999 V2000
    5.3818    4.3076    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.6673    3.0701    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.9529    5.1326    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.8094    3.0701    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5276    2.8443    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.9544    3.4200    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.2384    3.8951    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5239    4.3076    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.0087    5.1280    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.2018    5.2996    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1415    2.5013    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7206    3.0159    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3346    2.6728    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0864    3.1874    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4386    3.8990    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3767    4.8551    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.6673    3.8951    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.9529    4.3076    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.8094    3.8951    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   -2.6316    4.0705    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   -3.6936    3.1144    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.0950    4.3076    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   -0.2107    4.5851    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2726    3.6290    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5697    5.0267    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0177    4.4136    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0796    3.4574    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.3413    3.9720    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   -4.5005    2.9428    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3148    5.8113    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.5239    3.4826    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8247    4.2420    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2456    3.7275    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.7869    4.7569    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
  8  7  1  0  0  0  0
 10  9  1  0  0  0  0
 13 11  1  0  0  0  0
 14 12  1  0  0  0  0
 17  1  1  0  0  0  0
 17  2  1  0  0  0  0
 18  3  2  0  0  0  0
 18  7  1  0  0  0  0
 18 17  1  0  0  0  0
 19  4  1  1  0  0  0
 19  8  1  0  0  0  0
 20 15  1  0  0  0  0
 20 16  1  0  0  0  0
 21 11  1  0  0  0  0
 21 15  1  0  0  0  0
 22  9  1  0  0  0  0
 22 19  1  6  0  0  0
 23 10  2  0  0  0  0
 24 12  1  0  0  0  0
 25 16  1  0  0  0  0
 26 23  1  0  0  0  0
 26 24  2  0  0  0  0
 26 25  1  0  0  0  0
 27  5  1  6  0  0  0
 27 13  1  0  0  0  0
 27 20  1  0  0  0  0
 27 24  1  0  0  0  0
 28  6  1  6  0  0  0
 28 14  1  0  0  0  0
 28 22  1  0  0  0  0
 28 23  1  0  0  0  0
 21 29  1  6  0  0  0
 30 25  2  0  0  0  0
 19 31  1  6  0  0  0
 20 32  1  1  0  0  0
 21 33  1  1  0  0  0
 22 34  1  1  0  0  0
M  END
> <DATABASE_ID>
MMDBc0026000

> <DATABASE_NAME>
MIME

> <SMILES>
[H][C@@](C)(CCC(=C)C(C)C)[C@@]1([H])CC=C2C3=C(CC[C@]12C)[C@@]1(C)CC[C@]([H])(O)C[C@]1([H])CC3=O

> <INCHI_IDENTIFIER>
InChI=1S/C28H42O2/c1-17(2)18(3)7-8-19(4)22-9-10-23-26-24(12-14-28(22,23)6)27(5)13-11-21(29)15-20(27)16-25(26)30/h10,17,19-22,29H,3,7-9,11-16H2,1-2,4-6H3/t19-,20-,21+,22-,27+,28-/m1/s1

> <INCHI_KEY>
RSKIYANMYYETSH-JCUDMMKQSA-N

> <FORMULA>
C28H42O2

> <MOLECULAR_WEIGHT>
410.642

> <EXACT_MASS>
410.318480592

> <JCHEM_ACCEPTOR_COUNT>
2

> <JCHEM_ATOM_COUNT>
72

> <JCHEM_AVERAGE_POLARIZABILITY>
50.92005354781972

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
1

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
(2S,5S,7R,14R,15R)-5-hydroxy-2,15-dimethyl-14-[(2R)-6-methyl-5-methylideneheptan-2-yl]tetracyclo[8.7.0.0^{2,7}.0^{11,15}]heptadeca-1(10),11-dien-9-one

> <ALOGPS_LOGP>
6.19

> <JCHEM_LOGP>
5.935741648666667

> <ALOGPS_LOGS>
-5.08

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
4

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA_STRONGEST_ACIDIC>
18.427018813168576

> <JCHEM_PKA_STRONGEST_BASIC>
-1.2997482302037922

> <JCHEM_POLAR_SURFACE_AREA>
37.3

> <JCHEM_REFRACTIVITY>
126.21919999999994

> <JCHEM_ROTATABLE_BOND_COUNT>
5

> <JCHEM_RULE_OF_FIVE>
0

> <ALOGPS_SOLUBILITY>
3.41e-03 g/l

> <JCHEM_TRADITIONAL_IUPAC>
(2S,5S,7R,14R,15R)-5-hydroxy-2,15-dimethyl-14-[(2R)-6-methyl-5-methylideneheptan-2-yl]tetracyclo[8.7.0.0^{2,7}.0^{11,15}]heptadeca-1(10),11-dien-9-one

> <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      10.046   8.041   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0       8.712   5.731   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0       7.379   9.581   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0       3.378   5.731   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0      -2.851   5.309   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0       1.782   6.384   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0       6.045   7.271   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0       4.711   8.041   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0       1.883   9.572   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0       0.377   9.893   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0      -5.864   4.669   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0      -1.345   5.630   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0      -4.358   4.989   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0       0.161   5.950   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0      -6.419   7.278   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0      -4.437   9.063   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0       8.712   7.271   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0       7.379   8.041   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0       3.378   7.271   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0      -4.912   7.598   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0      -6.895   5.813   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0       2.044   8.041   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0      -0.393   8.559   0.000  0.00  0.00           C+0
HETATM   24  C   UNK     0      -2.376   6.774   0.000  0.00  0.00           C+0
HETATM   25  C   UNK     0      -2.930   9.383   0.000  0.00  0.00           C+0
HETATM   26  C   UNK     0      -1.900   8.239   0.000  0.00  0.00           C+0
HETATM   27  C   UNK     0      -3.882   6.454   0.000  0.00  0.00           C+0
HETATM   28  C   UNK     0       0.637   7.414   0.000  0.00  0.00           C+0
HETATM   29  O   UNK     0      -8.401   5.493   0.000  0.00  0.00           O+0
HETATM   30  O   UNK     0      -2.454  10.848   0.000  0.00  0.00           O+0
HETATM   31  H   UNK     0       4.711   6.501   0.000  0.00  0.00           H+0
HETATM   32  H   UNK     0      -3.406   7.918   0.000  0.00  0.00           H+0
HETATM   33  H   UNK     0      -7.925   6.958   0.000  0.00  0.00           H+0
HETATM   34  H   UNK     0       3.336   8.880   0.000  0.00  0.00           H+0
CONECT    1   17                                                            
CONECT    2   17                                                            
CONECT    3   18                                                            
CONECT    4   19                                                            
CONECT    5   27                                                            
CONECT    6   28                                                            
CONECT    7    8   18                                                       
CONECT    8    7   19                                                       
CONECT    9   10   22                                                       
CONECT   10    9   23                                                       
CONECT   11   13   21                                                       
CONECT   12   14   24                                                       
CONECT   13   11   27                                                       
CONECT   14   12   28                                                       
CONECT   15   20   21                                                       
CONECT   16   20   25                                                       
CONECT   17    1    2   18                                                  
CONECT   18    3    7   17                                                  
CONECT   19    4    8   22   31                                             
CONECT   20   15   16   27   32                                             
CONECT   21   11   15   29   33                                             
CONECT   22    9   19   28   34                                             
CONECT   23   10   26   28                                                  
CONECT   24   12   26   27                                                  
CONECT   25   16   26   30                                                  
CONECT   26   23   24   25                                                  
CONECT   27    5   13   20   24                                             
CONECT   28    6   14   22   23                                             
CONECT   29   21                                                            
CONECT   30   25                                                            
CONECT   31   19                                                            
CONECT   32   20                                                            
CONECT   33   21                                                            
CONECT   34   22                                                            
MASTER        0    0    0    0    0    0    0    0   34    0   74    0
END

Synonyms

Value	Source
3b-Hydroxyergosta-8,14,24(28)-trien-7-one	Generator
3Β-hydroxyergosta-8,14,24(28)-trien-7-one	Generator

Molecular Formula

C₂₈H₄₂O₂

Average Mass

410.642

Monoisotopic Mass

410.318480592

IUPAC Name

(2S,5S,7R,14R,15R)-5-hydroxy-2,15-dimethyl-14-[(2R)-6-methyl-5-methylideneheptan-2-yl]tetracyclo[8.7.0.0^{2,7}.0^{11,15}]heptadeca-1(10),11-dien-9-one

Traditional Name

(2S,5S,7R,14R,15R)-5-hydroxy-2,15-dimethyl-14-[(2R)-6-methyl-5-methylideneheptan-2-yl]tetracyclo[8.7.0.0^{2,7}.0^{11,15}]heptadeca-1(10),11-dien-9-one

CAS Registry Number

Not Available

SMILES

[H][C@@](C)(CCC(=C)C(C)C)[C@@]1([H])CC=C2C3=C(CC[C@]12C)[C@@]1(C)CC[C@]([H])(O)C[C@]1([H])CC3=O

InChI Identifier

InChI=1S/C28H42O2/c1-17(2)18(3)7-8-19(4)22-9-10-23-26-24(12-14-28(22,23)6)27(5)13-11-21(29)15-20(27)16-25(26)30/h10,17,19-22,29H,3,7-9,11-16H2,1-2,4-6H3/t19-,20-,21+,22-,27+,28-/m1/s1

InChI Key

RSKIYANMYYETSH-JCUDMMKQSA-N

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as ergosterols and derivatives. These are steroids containing ergosta-5,7,22-trien-3beta-ol or a derivative thereof, which is based on the 3beta-hydroxylated ergostane skeleton.

Kingdom

Organic compounds

Super Class

Lipids and lipid-like molecules

Class

Steroids and steroid derivatives

Sub Class

Ergostane steroids

Direct Parent

Ergosterols and derivatives

Alternative Parents

Substituents

Ergosterol-skeleton
7-oxosteroid
3-beta-hydroxysteroid
Oxosteroid
Hydroxysteroid
3-hydroxysteroid
Cyclohexenone
Cyclic alcohol
Secondary alcohol
Ketone
Organic oxygen compound
Organic oxide
Hydrocarbon derivative
Organooxygen compound
Carbonyl group
Alcohol
Aliphatic homopolycyclic compound

Molecular Framework

Aliphatic homopolycyclic compounds

External Descriptors

Not Available

Functional Ontology

Not Available

Physical Properties

State

Expected Solid

Predicted Properties

Property	Value	Source
Water Solubility	0.0034 g/L	ALOGPS
logP	6.19	ALOGPS
logP	5.94	ChemAxon
logS	-5.1	ALOGPS
pKa (Strongest Acidic)	18.43	ChemAxon
pKa (Strongest Basic)	-1.3	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	2	ChemAxon
Hydrogen Donor Count	1	ChemAxon
Polar Surface Area	37.3 Å²	ChemAxon
Rotatable Bond Count	5	ChemAxon
Refractivity	126.22 m³·mol⁻¹	ChemAxon
Polarizability	50.92 Å³	ChemAxon
Number of Rings	4	ChemAxon
Bioavailability	Yes	ChemAxon
Rule of Five	No	ChemAxon
Ghose Filter	No	ChemAxon
Veber's Rule	Yes	ChemAxon
MDDR-like Rule	No	ChemAxon

Spectra

Not Available

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	Ascomycota	2	Human feces; Human sputum; Human	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

77005956

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

146682636

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 3Î²-hydroxyergosta-8,14,24(28)-trien-7-one (MMDBc0026000)

MOL for #<Metabolite:0x00007f8dbd9b3258>

3D MOL for #<Metabolite:0x00007f8dbd9b3258>

3D SDF for #<Metabolite:0x00007f8dbd9b3258>

3D-SDF for #<Metabolite:0x00007f8dbd9b3258>

PDB for #<Metabolite:0x00007f8dbd9b3258>

3D PDB for #<Metabolite:0x00007f8dbd9b3258>

SMILES for #<Metabolite:0x00007f8dbd9b3258>

INCHI for #<Metabolite:0x00007f8dbd9b3258>

Structure for #<Metabolite:0x00007f8dbd9b3258>

3D Structure for #<Metabolite:0x00007f8dbd9b3258>