MiMeDB: Showing metabocard for 1beta,7beta-Dihydroxydehydroabietic acid (MMDBc0019271)

Record Information

Version

1.0

Status

Detected and Quantified

Creation Date

2021-05-15 09:21:29 UTC

Update Date

2022-08-31 06:45:08 UTC

Metabolite ID

MMDBc0019271

Metabolite Identification

Common Name

1beta,7beta-Dihydroxydehydroabietic acid

Description

1beta,7beta-Dihydroxydehydroabietic acid, also known as 1β,7β-dihydroxydehydroabietate, belongs to the class of organic compounds known as diterpenoids. These are terpene compounds formed by four isoprene units. Based on a literature review a significant number of articles have been published on 1beta,7beta-Dihydroxydehydroabietic acid.

Structure

MOL SDF PDB SMILES InChI


  Mrv1652305152111212D          

 27 29  0  0  1  0            999 V2000
    4.5375    2.3645    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.5375    0.9355    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2692    0.1231    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.2375    2.3645    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8875    2.3645    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0625    2.3645    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4125    2.3645    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8250    1.6500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8875    0.9355    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.8250    0.2211    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.1250    1.6500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3000    1.6500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0625    0.9355    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.6500    1.6500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.6500    0.2211    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.4125    0.9355    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.4125    2.3645    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   -1.1877    0.6534    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4125    0.9355    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.8250    1.6500    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.0625   -0.4934    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.8250    3.0789    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3310   -0.1591    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8197    1.1837    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.4750    0.2211    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0000    0.2211    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0000    1.6500    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
  6  5  2  0  0  0  0
  8  7  1  0  0  0  0
 11  1  1  0  0  0  0
 11  2  1  0  0  0  0
 12  5  1  0  0  0  0
 12  9  2  0  0  0  0
 12 11  1  0  0  0  0
 13  9  1  0  0  0  0
 14  6  1  0  0  0  0
 14 13  2  0  0  0  0
 15 10  1  0  0  0  0
 15 13  1  0  0  0  0
 16 10  1  0  0  0  0
 17  7  1  0  0  0  0
 19  3  1  1  0  0  0
 19  8  1  0  0  0  0
 19 16  1  0  0  0  0
 19 18  1  6  0  0  0
 20  4  1  1  0  0  0
 20 14  1  0  0  0  0
 20 16  1  0  0  0  0
 20 17  1  0  0  0  0
 15 21  1  1  0  0  0
 17 22  1  6  0  0  0
 23 18  2  0  0  0  0
 24 18  1  0  0  0  0
 15 25  1  6  0  0  0
 16 26  1  6  0  0  0
 17 27  1  6  0  0  0
M  END


  Mrv1652305152111212D          

 27 29  0  0  1  0            999 V2000
    4.5375    2.3645    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.5375    0.9355    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2692    0.1231    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.2375    2.3645    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8875    2.3645    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0625    2.3645    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4125    2.3645    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8250    1.6500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8875    0.9355    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.8250    0.2211    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.1250    1.6500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3000    1.6500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0625    0.9355    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.6500    1.6500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.6500    0.2211    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.4125    0.9355    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.4125    2.3645    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   -1.1877    0.6534    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4125    0.9355    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.8250    1.6500    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.0625   -0.4934    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.8250    3.0789    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3310   -0.1591    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8197    1.1837    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.4750    0.2211    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0000    0.2211    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0000    1.6500    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
  6  5  2  0  0  0  0
  8  7  1  0  0  0  0
 11  1  1  0  0  0  0
 11  2  1  0  0  0  0
 12  5  1  0  0  0  0
 12  9  2  0  0  0  0
 12 11  1  0  0  0  0
 13  9  1  0  0  0  0
 14  6  1  0  0  0  0
 14 13  2  0  0  0  0
 15 10  1  0  0  0  0
 15 13  1  0  0  0  0
 16 10  1  0  0  0  0
 17  7  1  0  0  0  0
 19  3  1  1  0  0  0
 19  8  1  0  0  0  0
 19 16  1  0  0  0  0
 19 18  1  6  0  0  0
 20  4  1  1  0  0  0
 20 14  1  0  0  0  0
 20 16  1  0  0  0  0
 20 17  1  0  0  0  0
 15 21  1  1  0  0  0
 17 22  1  6  0  0  0
 23 18  2  0  0  0  0
 24 18  1  0  0  0  0
 15 25  1  6  0  0  0
 16 26  1  6  0  0  0
 17 27  1  6  0  0  0
M  END
> <DATABASE_ID>
MMDBc0019271

> <DATABASE_NAME>
MIME

> <SMILES>
[H][C@]1(O)C[C@@]2([H])[C@@](C)(CC[C@@]([H])(O)[C@]2(C)C2=C1C=C(C=C2)C(C)C)C(O)=O

> <INCHI_IDENTIFIER>
InChI=1S/C20H28O4/c1-11(2)12-5-6-14-13(9-12)15(21)10-16-19(3,18(23)24)8-7-17(22)20(14,16)4/h5-6,9,11,15-17,21-22H,7-8,10H2,1-4H3,(H,23,24)/t15-,16-,17+,19+,20+/m0/s1

> <INCHI_KEY>
VBGYFFVTLRYZMI-OCBLOMHFSA-N

> <FORMULA>
C20H28O4

> <MOLECULAR_WEIGHT>
332.44

> <EXACT_MASS>
332.198759382

> <JCHEM_ACCEPTOR_COUNT>
4

> <JCHEM_ATOM_COUNT>
52

> <JCHEM_AVERAGE_POLARIZABILITY>
37.47378137484631

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
3

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
(1R,4R,4aS,9S,10aR)-4,9-dihydroxy-1,4a-dimethyl-7-(propan-2-yl)-1,2,3,4,4a,9,10,10a-octahydrophenanthrene-1-carboxylic acid

> <ALOGPS_LOGP>
3.02

> <JCHEM_LOGP>
3.287142593999999

> <ALOGPS_LOGS>
-3.26

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
3

> <JCHEM_PHYSIOLOGICAL_CHARGE>
-1

> <JCHEM_PKA>
14.215832799534088

> <JCHEM_PKA_STRONGEST_ACIDIC>
4.243490417361668

> <JCHEM_PKA_STRONGEST_BASIC>
-2.9722517117810936

> <JCHEM_POLAR_SURFACE_AREA>
77.76

> <JCHEM_REFRACTIVITY>
92.475

> <JCHEM_ROTATABLE_BOND_COUNT>
2

> <JCHEM_RULE_OF_FIVE>
1

> <ALOGPS_SOLUBILITY>
1.83e-01 g/l

> <JCHEM_TRADITIONAL_IUPAC>
(1R,4R,4aS,9S,10aR)-4,9-dihydroxy-7-isopropyl-1,4a-dimethyl-2,3,4,9,10,10a-hexahydrophenanthrene-1-carboxylic acid

> <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       8.470   4.414   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0       8.470   1.746   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0      -0.503   0.230   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0       2.310   4.414   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0       5.390   4.414   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0       3.850   4.414   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0      -0.770   4.414   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0      -1.540   3.080   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0       5.390   1.746   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0       1.540   0.413   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0       7.700   3.080   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0       6.160   3.080   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0       3.850   1.746   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0       3.080   3.080   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0       3.080   0.413   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0       0.770   1.746   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0       0.770   4.414   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0      -2.217   1.220   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0      -0.770   1.746   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0       1.540   3.080   0.000  0.00  0.00           C+0
HETATM   21  O   UNK     0       3.850  -0.921   0.000  0.00  0.00           O+0
HETATM   22  O   UNK     0       1.540   5.747   0.000  0.00  0.00           O+0
HETATM   23  O   UNK     0      -2.485  -0.297   0.000  0.00  0.00           O+0
HETATM   24  O   UNK     0      -3.397   2.210   0.000  0.00  0.00           O+0
HETATM   25  H   UNK     0       4.620   0.413   0.000  0.00  0.00           H+0
HETATM   26  H   UNK     0      -0.000   0.413   0.000  0.00  0.00           H+0
HETATM   27  H   UNK     0      -0.000   3.080   0.000  0.00  0.00           H+0
CONECT    1   11                                                            
CONECT    2   11                                                            
CONECT    3   19                                                            
CONECT    4   20                                                            
CONECT    5    6   12                                                       
CONECT    6    5   14                                                       
CONECT    7    8   17                                                       
CONECT    8    7   19                                                       
CONECT    9   12   13                                                       
CONECT   10   15   16                                                       
CONECT   11    1    2   12                                                  
CONECT   12    5    9   11                                                  
CONECT   13    9   14   15                                                  
CONECT   14    6   13   20                                                  
CONECT   15   10   13   21   25                                             
CONECT   16   10   19   20   26                                             
CONECT   17    7   20   22   27                                             
CONECT   18   19   23   24                                                  
CONECT   19    3    8   16   18                                             
CONECT   20    4   14   16   17                                             
CONECT   21   15                                                            
CONECT   22   17                                                            
CONECT   23   18                                                            
CONECT   24   18                                                            
CONECT   25   15                                                            
CONECT   26   16                                                            
CONECT   27   17                                                            
MASTER        0    0    0    0    0    0    0    0   27    0   58    0
END

Synonyms

Value	Source
1b,7b-Dihydroxydehydroabietate	Generator
1b,7b-Dihydroxydehydroabietic acid	Generator
1beta,7beta-Dihydroxydehydroabietate	Generator
1Β,7β-dihydroxydehydroabietate	Generator
1Β,7β-dihydroxydehydroabietic acid	Generator

Molecular Formula

C₂₀H₂₈O₄

Average Mass

332.44

Monoisotopic Mass

332.198759382

IUPAC Name

(1R,4R,4aS,9S,10aR)-4,9-dihydroxy-1,4a-dimethyl-7-(propan-2-yl)-1,2,3,4,4a,9,10,10a-octahydrophenanthrene-1-carboxylic acid

Traditional Name

(1R,4R,4aS,9S,10aR)-4,9-dihydroxy-7-isopropyl-1,4a-dimethyl-2,3,4,9,10,10a-hexahydrophenanthrene-1-carboxylic acid

CAS Registry Number

Not Available

SMILES

[H][C@]1(O)C[C@@]2([H])[C@@](C)(CC[C@@]([H])(O)[C@]2(C)C2=C1C=C(C=C2)C(C)C)C(O)=O

InChI Identifier

InChI=1S/C20H28O4/c1-11(2)12-5-6-14-13(9-12)15(21)10-16-19(3,18(23)24)8-7-17(22)20(14,16)4/h5-6,9,11,15-17,21-22H,7-8,10H2,1-4H3,(H,23,24)/t15-,16-,17+,19+,20+/m0/s1

InChI Key

VBGYFFVTLRYZMI-OCBLOMHFSA-N

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as diterpenoids. These are terpene compounds formed by four isoprene units.

Kingdom

Organic compounds

Super Class

Lipids and lipid-like molecules

Class

Prenol lipids

Sub Class

Diterpenoids

Direct Parent

Diterpenoids

Alternative Parents

Substituents

Abietane diterpenoid
Diterpenoid
Phenanthrene
Hydrophenanthrene
Tetralin
Benzenoid
Cyclic alcohol
Secondary alcohol
Carboxylic acid derivative
Carboxylic acid
Monocarboxylic acid or derivatives
Organic oxide
Organic oxygen compound
Alcohol
Hydrocarbon derivative
Organooxygen compound
Carbonyl group
Aromatic homopolycyclic compound

Molecular Framework

Aromatic homopolycyclic compounds

External Descriptors

Not Available

Functional Ontology

Not Available

Physical Properties

State

Expected Solid

Predicted Properties

Property	Value	Source
Water Solubility	0.18 g/L	ALOGPS
logP	3.02	ALOGPS
logP	3.29	ChemAxon
logS	-3.3	ALOGPS
pKa (Strongest Acidic)	4.24	ChemAxon
pKa (Strongest Basic)	-3	ChemAxon
Physiological Charge	-1	ChemAxon
Hydrogen Acceptor Count	4	ChemAxon
Hydrogen Donor Count	3	ChemAxon
Polar Surface Area	77.76 Å²	ChemAxon
Rotatable Bond Count	2	ChemAxon
Refractivity	92.48 m³·mol⁻¹	ChemAxon
Polarizability	37.47 Å³	ChemAxon
Number of Rings	3	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_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)		2022-08-18	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 100 MHz, H₂O, predicted)		2022-08-18	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 1000 MHz, H₂O, predicted)		2022-08-18	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 1000 MHz, H₂O, predicted)		2022-08-18	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 200 MHz, H₂O, predicted)		2022-08-18	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 200 MHz, H₂O, predicted)		2022-08-18	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 300 MHz, H₂O, predicted)		2022-08-18	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 300 MHz, H₂O, predicted)		2022-08-18	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 400 MHz, H₂O, predicted)		2022-08-18	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 400 MHz, H₂O, predicted)		2022-08-18	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 500 MHz, H₂O, predicted)		2022-08-18	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 500 MHz, H₂O, predicted)		2022-08-18	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 600 MHz, H₂O, predicted)		2022-08-18	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 600 MHz, H₂O, predicted)		2022-08-18	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 700 MHz, H₂O, predicted)		2022-08-18	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 700 MHz, H₂O, predicted)		2022-08-18	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 800 MHz, H₂O, predicted)		2022-08-18	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 800 MHz, H₂O, predicted)		2022-08-18	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 900 MHz, H₂O, predicted)		2022-08-18	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 900 MHz, H₂O, predicted)		2022-08-18	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	1	Human feces	Metabolic reconstruction

Exposure Sources

Source Type	Source Sub-type	Species	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

78441962

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

101733039

PDB ID

Not Available

ChEBI ID

Not Available

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 1beta,7beta-Dihydroxydehydroabietic acid (MMDBc0019271)

MOL for #<Metabolite:0x00007fecf046e9e0>

3D MOL for #<Metabolite:0x00007fecf046e9e0>

3D SDF for #<Metabolite:0x00007fecf046e9e0>

3D-SDF for #<Metabolite:0x00007fecf046e9e0>

PDB for #<Metabolite:0x00007fecf046e9e0>

3D PDB for #<Metabolite:0x00007fecf046e9e0>

SMILES for #<Metabolite:0x00007fecf046e9e0>

INCHI for #<Metabolite:0x00007fecf046e9e0>

Structure for #<Metabolite:0x00007fecf046e9e0>

3D Structure for #<Metabolite:0x00007fecf046e9e0>