MiMeDB: Showing metabocard for Gibberellin A25 (MMDBc0011521)

Record Information

Version

1.0

Status

Detected and Quantified

Creation Date

2021-05-15 03:22:03 UTC

Update Date

2022-08-31 06:33:10 UTC

Metabolite ID

MMDBc0011521

Metabolite Identification

Common Name

Gibberellin A25

Description

gibberellin A25 belongs to the class of organic compounds known as c20-gibberellin 20-carboxylic acids. These are c20-gibberellins with a carboxyl group at the 6-position. Based on a literature review very few articles have been published on gibberellin A25.

Structure

MOL SDF PDB SMILES InChI


  Mrv1652303192017232D          

 28 31  0  0  1  0            999 V2000
    8.3344   -5.4961    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.3344   -4.6806    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.0491   -4.2683    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   11.8893   -4.2683    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   12.6039   -4.6806    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   12.6039   -5.4961    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   12.4391   -6.3207    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   11.3396   -6.3207    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.7546   -4.6806    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   11.8893   -5.9083    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   11.1747   -4.6806    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   11.1747   -5.4961    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   12.9358   -6.9251    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   11.1820   -3.8978    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
    9.7565   -3.8738    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.0429   -3.4597    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   10.4719   -3.4629    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    8.3351   -6.3220    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.3364   -7.1470    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    7.6200   -5.9105    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    9.7546   -5.4961    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    9.7546   -6.3115    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
   10.4692   -5.9083    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   10.4692   -6.7238    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.7631   -7.1315    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   11.1754   -7.1315    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    9.0491   -5.9083    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    9.0491   -6.7238    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
 11  9  1  0  0  0  0
  2  3  1  0  0  0  0
  1  2  1  0  0  0  0
  4 11  1  0  0  0  0
 12 11  1  0  0  0  0
 12 10  1  0  0  0  0
 12  8  1  1  0  0  0
  5  4  1  0  0  0  0
  6  5  1  0  0  0  0
  6 10  1  0  0  0  0
  6  7  1  1  0  0  0
  7  8  1  0  0  0  0
 13  7  2  0  0  0  0
 11 14  1  1  0  0  0
  9 15  1  6  0  0  0
  3  9  1  0  0  0  0
 15 16  1  0  0  0  0
 15 17  2  0  0  0  0
 19 18  2  0  0  0  0
 20 18  1  0  0  0  0
 21 22  1  1  0  0  0
 21  9  1  0  0  0  0
 23 24  1  1  0  0  0
 24 26  2  0  0  0  0
 24 25  1  0  0  0  0
 12 23  1  0  0  0  0
 23 21  1  0  0  0  0
 27 28  1  1  0  0  0
  1 27  1  0  0  0  0
 27 18  1  0  0  0  0
 27 21  1  0  0  0  0
M  END


  Mrv1652303192017232D          

 28 31  0  0  1  0            999 V2000
    8.3344   -5.4961    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.3344   -4.6806    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.0491   -4.2683    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   11.8893   -4.2683    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   12.6039   -4.6806    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   12.6039   -5.4961    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   12.4391   -6.3207    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   11.3396   -6.3207    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.7546   -4.6806    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   11.8893   -5.9083    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   11.1747   -4.6806    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   11.1747   -5.4961    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   12.9358   -6.9251    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   11.1820   -3.8978    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
    9.7565   -3.8738    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.0429   -3.4597    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   10.4719   -3.4629    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    8.3351   -6.3220    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.3364   -7.1470    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    7.6200   -5.9105    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    9.7546   -5.4961    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    9.7546   -6.3115    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
   10.4692   -5.9083    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   10.4692   -6.7238    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.7631   -7.1315    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   11.1754   -7.1315    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    9.0491   -5.9083    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    9.0491   -6.7238    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
 11  9  1  0  0  0  0
  2  3  1  0  0  0  0
  1  2  1  0  0  0  0
  4 11  1  0  0  0  0
 12 11  1  0  0  0  0
 12 10  1  0  0  0  0
 12  8  1  1  0  0  0
  5  4  1  0  0  0  0
  6  5  1  0  0  0  0
  6 10  1  0  0  0  0
  6  7  1  1  0  0  0
  7  8  1  0  0  0  0
 13  7  2  0  0  0  0
 11 14  1  1  0  0  0
  9 15  1  6  0  0  0
  3  9  1  0  0  0  0
 15 16  1  0  0  0  0
 15 17  2  0  0  0  0
 19 18  2  0  0  0  0
 20 18  1  0  0  0  0
 21 22  1  1  0  0  0
 21  9  1  0  0  0  0
 23 24  1  1  0  0  0
 24 26  2  0  0  0  0
 24 25  1  0  0  0  0
 12 23  1  0  0  0  0
 23 21  1  0  0  0  0
 27 28  1  1  0  0  0
  1 27  1  0  0  0  0
 27 18  1  0  0  0  0
 27 21  1  0  0  0  0
M  END
> <DATABASE_ID>
MMDBc0011521

> <DATABASE_NAME>
MIME

> <SMILES>
[H][C@@]12CC[C@@H]3C[C@]1(CC3=C)[C@@H](C(O)=O)[C@@]1([H])[C@]2(CCC[C@@]1(C)C(O)=O)C(O)=O

> <INCHI_IDENTIFIER>
InChI=1S/C20H26O6/c1-10-8-19-9-11(10)4-5-12(19)20(17(25)26)7-3-6-18(2,16(23)24)14(20)13(19)15(21)22/h11-14H,1,3-9H2,2H3,(H,21,22)(H,23,24)(H,25,26)/t11-,12-,13-,14-,18-,19+,20-/m1/s1

> <INCHI_KEY>
XOUJCIPAKFLTCI-POPXMCHDSA-N

> <FORMULA>
C20H26O6

> <MOLECULAR_WEIGHT>
362.422

> <EXACT_MASS>
362.172938557

> <JCHEM_ACCEPTOR_COUNT>
6

> <JCHEM_ATOM_COUNT>
52

> <JCHEM_AVERAGE_POLARIZABILITY>
37.04728493832086

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
3

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
(1R,2S,3R,4R,8R,9R,12R)-4-methyl-13-methylidenetetracyclo[10.2.1.0^{1,9}.0^{3,8}]pentadecane-2,4,8-tricarboxylic acid

> <ALOGPS_LOGP>
1.60

> <JCHEM_LOGP>
2.7776992116666666

> <ALOGPS_LOGS>
-2.57

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
4

> <JCHEM_PHYSIOLOGICAL_CHARGE>
-3

> <JCHEM_PKA>
4.299298842914303

> <JCHEM_PKA_STRONGEST_ACIDIC>
3.754905528717394

> <JCHEM_POLAR_SURFACE_AREA>
111.9

> <JCHEM_REFRACTIVITY>
90.71969999999997

> <JCHEM_ROTATABLE_BOND_COUNT>
3

> <JCHEM_RULE_OF_FIVE>
1

> <ALOGPS_SOLUBILITY>
9.72e-01 g/l

> <JCHEM_TRADITIONAL_IUPAC>
(1R,2S,3R,4R,8R,9R,12R)-4-methyl-13-methylidenetetracyclo[10.2.1.0^{1,9}.0^{3,8}]pentadecane-2,4,8-tricarboxylic acid

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 19-MAR-20   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   19-MAR-20         0                                  
HETATM    1  C   UNK     0      15.558 -10.259   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0      15.558  -8.737   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0      16.892  -7.967   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0      22.193  -7.967   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0      23.527  -8.737   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0      23.527 -10.259   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0      23.220 -11.799   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0      21.167 -11.799   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0      18.209  -8.737   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0      22.193 -11.029   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0      20.859  -8.737   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0      20.859 -10.259   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0      24.147 -12.927   0.000  0.00  0.00           C+0
HETATM   14  H   UNK     0      20.873  -7.276   0.000  0.00  0.00           H+0
HETATM   15  C   UNK     0      18.212  -7.231   0.000  0.00  0.00           C+0
HETATM   16  O   UNK     0      16.880  -6.458   0.000  0.00  0.00           O+0
HETATM   17  O   UNK     0      19.548  -6.464   0.000  0.00  0.00           O+0
HETATM   18  C   UNK     0      15.559 -11.801   0.000  0.00  0.00           C+0
HETATM   19  O   UNK     0      15.561 -13.341   0.000  0.00  0.00           O+0
HETATM   20  O   UNK     0      14.224 -11.033   0.000  0.00  0.00           O+0
HETATM   21  C   UNK     0      18.209 -10.259   0.000  0.00  0.00           C+0
HETATM   22  H   UNK     0      18.209 -11.781   0.000  0.00  0.00           H+0
HETATM   23  C   UNK     0      19.543 -11.029   0.000  0.00  0.00           C+0
HETATM   24  C   UNK     0      19.543 -12.551   0.000  0.00  0.00           C+0
HETATM   25  O   UNK     0      18.224 -13.312   0.000  0.00  0.00           O+0
HETATM   26  O   UNK     0      20.861 -13.312   0.000  0.00  0.00           O+0
HETATM   27  C   UNK     0      16.892 -11.029   0.000  0.00  0.00           C+0
HETATM   28  C   UNK     0      16.892 -12.551   0.000  0.00  0.00           C+0
CONECT    1    2   27                                                       
CONECT    2    3    1                                                       
CONECT    3    2    9                                                       
CONECT    4   11    5                                                       
CONECT    5    4    6                                                       
CONECT    6    5   10    7                                                  
CONECT    7    6    8   13                                                  
CONECT    8   12    7                                                       
CONECT    9   11   15    3   21                                             
CONECT   10   12    6                                                       
CONECT   11    9    4   12   14                                             
CONECT   12   11   10    8   23                                             
CONECT   13    7                                                            
CONECT   14   11                                                            
CONECT   15    9   16   17                                                  
CONECT   16   15                                                            
CONECT   17   15                                                            
CONECT   18   19   20   27                                                  
CONECT   19   18                                                            
CONECT   20   18                                                            
CONECT   21   22    9   23   27                                             
CONECT   22   21                                                            
CONECT   23   24   12   21                                                  
CONECT   24   23   26   25                                                  
CONECT   25   24                                                            
CONECT   26   24                                                            
CONECT   27   28    1   18   21                                             
CONECT   28   27                                                            
MASTER        0    0    0    0    0    0    0    0   28    0   62    0
END

Synonyms

Not Available

Molecular Formula

C₂₀H₂₆O₆

Average Mass

362.422

Monoisotopic Mass

362.172938557

IUPAC Name

(1R,2S,3R,4R,8R,9R,12R)-4-methyl-13-methylidenetetracyclo[10.2.1.0^{1,9}.0^{3,8}]pentadecane-2,4,8-tricarboxylic acid

Traditional Name

(1R,2S,3R,4R,8R,9R,12R)-4-methyl-13-methylidenetetracyclo[10.2.1.0^{1,9}.0^{3,8}]pentadecane-2,4,8-tricarboxylic acid

CAS Registry Number

Not Available

SMILES

[H][C@@]12CC[C@@H]3C[C@]1(CC3=C)[C@@H](C(O)=O)[C@@]1([H])[C@]2(CCC[C@@]1(C)C(O)=O)C(O)=O

InChI Identifier

InChI=1S/C20H26O6/c1-10-8-19-9-11(10)4-5-12(19)20(17(25)26)7-3-6-18(2,16(23)24)14(20)13(19)15(21)22/h11-14H,1,3-9H2,2H3,(H,21,22)(H,23,24)(H,25,26)/t11-,12-,13-,14-,18-,19+,20-/m1/s1

InChI Key

XOUJCIPAKFLTCI-POPXMCHDSA-N

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as c20-gibberellin 20-carboxylic acids. These are c20-gibberellins with a carboxyl group at the 6-position.

Kingdom

Organic compounds

Super Class

Lipids and lipid-like molecules

Class

Prenol lipids

Sub Class

Diterpenoids

Direct Parent

C20-gibberellin 20-carboxylic acids

Alternative Parents

Substituents

Gibberellane-20-carboxylic acid
Gibberellane-6-carboxylic acid
Tricarboxylic acid or derivatives
Carboxylic acid
Carboxylic acid derivative
Organic oxygen compound
Organic oxide
Hydrocarbon derivative
Organooxygen compound
Carbonyl group
Aliphatic homopolycyclic compound

Molecular Framework

Aliphatic homopolycyclic compounds

External Descriptors

tricarboxylic acid (CHEBI:72601 )
C20-gibberellin (CHEBI:72601 )

Functional Ontology

Not Available

Physical Properties

State

Expected Solid

Predicted Properties

Property	Value	Source
Water Solubility	0.97 g/L	ALOGPS
logP	1.6	ALOGPS
logP	2.78	ChemAxon
logS	-2.6	ALOGPS
pKa (Strongest Acidic)	3.75	ChemAxon
Physiological Charge	-3	ChemAxon
Hydrogen Acceptor Count	6	ChemAxon
Hydrogen Donor Count	3	ChemAxon
Polar Surface Area	111.9 Å²	ChemAxon
Rotatable Bond Count	3	ChemAxon
Refractivity	90.72 m³·mol⁻¹	ChemAxon
Polarizability	37.05 Å³	ChemAxon
Number of Rings	4	ChemAxon
Bioavailability	Yes	ChemAxon
Rule of Five	Yes	ChemAxon
Ghose Filter	Yes	ChemAxon
Veber's Rule	No	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_3) - 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
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

Metabolic Reactions

Not Available

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	Metabolic reconstruction

Exposure Sources

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

28639068

KEGG Compound ID

Not Available

BioCyc ID

CPD1F-84

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

14464358

PDB ID

Not Available

ChEBI ID

72601

Food Biomarker Ontology

Not Available

References

Synthesis Reference

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 Gibberellin A25 (MMDBc0011521)

MOL for #<Metabolite:0x00007fdb04bffae0>

3D MOL for #<Metabolite:0x00007fdb04bffae0>

3D SDF for #<Metabolite:0x00007fdb04bffae0>

3D-SDF for #<Metabolite:0x00007fdb04bffae0>

PDB for #<Metabolite:0x00007fdb04bffae0>

3D PDB for #<Metabolite:0x00007fdb04bffae0>

SMILES for #<Metabolite:0x00007fdb04bffae0>

INCHI for #<Metabolite:0x00007fdb04bffae0>

Structure for #<Metabolite:0x00007fdb04bffae0>

3D Structure for #<Metabolite:0x00007fdb04bffae0>