MiMeDB: Showing metabocard for Erinacine A (MMDBc0017554)

Record Information

Version

1.0

Status

Detected and Quantified

Creation Date

2021-05-15 07:54:21 UTC

Update Date

2022-12-15 22:51:45 UTC

Metabolite ID

MMDBc0017554

Metabolite Identification

Common Name

Erinacine A

Description

Erinacine A 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 Erinacine A.

Structure

MOL SDF PDB SMILES InChI


  Mrv1652305152109542D          

 36 39  0  0  1  0            999 V2000
    3.5076   -1.6467    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1296   -1.2686    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6073    1.7072    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1231    1.9284    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.6603   -0.5177    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4615   -0.3210    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.9180    0.0267    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.8798    0.8509    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7141    1.8065    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.8905    1.8546    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0067    0.8109    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7304   -0.3841    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.4162    3.0488    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.9278   -1.0599    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0069   -0.0140    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.1461   -0.2643    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.8072    0.4281    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2195    3.8500    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.6298    1.3358    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.6307    0.3800    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4272    4.0802    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.8317    3.5092    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.0285    2.7080    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    3.0842    1.0692    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.4370    1.1654    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   -1.4196    0.0693    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.8149    4.4210    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.2305    4.8814    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.0395    3.7394    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.8208    2.4778    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.4330    2.1370    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.0227    4.6512    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.8266    0.5346    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.6240    3.2790    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.6350    4.3104    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.2363    2.9382    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
  6  5  1  0  0  0  0
  8  7  1  0  0  0  0
 10  9  1  0  0  0  0
 14  1  1  0  0  0  0
 14  2  1  0  0  0  0
 15  5  2  0  0  0  0
 15 11  1  0  0  0  0
 15 12  1  0  0  0  0
 16  7  1  0  0  0  0
 16 14  1  0  0  0  0
 17  6  2  0  0  0  0
 18 13  1  0  0  0  0
 19 11  1  0  0  0  0
 20 16  2  0  0  0  0
 20 17  1  0  0  0  0
 21 18  1  0  0  0  0
 22 21  1  0  0  0  0
 23 22  1  0  0  0  0
 24  3  1  6  0  0  0
 24  8  1  0  0  0  0
 24  9  1  0  0  0  0
 24 20  1  0  0  0  0
 25  4  1  1  0  0  0
 25 10  1  0  0  0  0
 25 17  1  0  0  0  0
 25 19  1  0  0  0  0
 26 12  2  0  0  0  0
 18 27  1  6  0  0  0
 21 28  1  6  0  0  0
 22 29  1  6  0  0  0
 30 13  1  0  0  0  0
 30 23  1  0  0  0  0
 19 31  1  1  0  0  0
 23 31  1  1  0  0  0
 18 32  1  1  0  0  0
 19 33  1  1  0  0  0
 21 34  1  6  0  0  0
 22 35  1  1  0  0  0
 23 36  1  6  0  0  0
M  END


  Mrv1652305152109542D          

 36 39  0  0  1  0            999 V2000
    3.5076   -1.6467    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1296   -1.2686    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6073    1.7072    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1231    1.9284    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.6603   -0.5177    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4615   -0.3210    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.9180    0.0267    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.8798    0.8509    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7141    1.8065    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.8905    1.8546    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0067    0.8109    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7304   -0.3841    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.4162    3.0488    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.9278   -1.0599    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0069   -0.0140    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.1461   -0.2643    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.8072    0.4281    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2195    3.8500    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.6298    1.3358    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.6307    0.3800    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4272    4.0802    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.8317    3.5092    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.0285    2.7080    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    3.0842    1.0692    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.4370    1.1654    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   -1.4196    0.0693    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.8149    4.4210    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.2305    4.8814    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.0395    3.7394    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.8208    2.4778    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.4330    2.1370    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.0227    4.6512    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.8266    0.5346    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.6240    3.2790    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.6350    4.3104    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.2363    2.9382    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
  6  5  1  0  0  0  0
  8  7  1  0  0  0  0
 10  9  1  0  0  0  0
 14  1  1  0  0  0  0
 14  2  1  0  0  0  0
 15  5  2  0  0  0  0
 15 11  1  0  0  0  0
 15 12  1  0  0  0  0
 16  7  1  0  0  0  0
 16 14  1  0  0  0  0
 17  6  2  0  0  0  0
 18 13  1  0  0  0  0
 19 11  1  0  0  0  0
 20 16  2  0  0  0  0
 20 17  1  0  0  0  0
 21 18  1  0  0  0  0
 22 21  1  0  0  0  0
 23 22  1  0  0  0  0
 24  3  1  6  0  0  0
 24  8  1  0  0  0  0
 24  9  1  0  0  0  0
 24 20  1  0  0  0  0
 25  4  1  1  0  0  0
 25 10  1  0  0  0  0
 25 17  1  0  0  0  0
 25 19  1  0  0  0  0
 26 12  2  0  0  0  0
 18 27  1  6  0  0  0
 21 28  1  6  0  0  0
 22 29  1  6  0  0  0
 30 13  1  0  0  0  0
 30 23  1  0  0  0  0
 19 31  1  1  0  0  0
 23 31  1  1  0  0  0
 18 32  1  1  0  0  0
 19 33  1  1  0  0  0
 21 34  1  6  0  0  0
 22 35  1  1  0  0  0
 23 36  1  6  0  0  0
M  END
> <DATABASE_ID>
MMDBc0017554

> <DATABASE_NAME>
MIME

> <SMILES>
[H][C@@]1(O)CO[C@@]([H])(O[C@@]2([H])CC(C=O)=CC=C3C4=C(CC[C@]4(C)CC[C@@]23C)C(C)C)[C@]([H])(O)[C@@]1([H])O

> <INCHI_IDENTIFIER>
InChI=1S/C25H36O6/c1-14(2)16-7-8-24(3)9-10-25(4)17(20(16)24)6-5-15(12-26)11-19(25)31-23-22(29)21(28)18(27)13-30-23/h5-6,12,14,18-19,21-23,27-29H,7-11,13H2,1-4H3/t18-,19+,21+,22-,23+,24-,25-/m1/s1

> <INCHI_KEY>
LPPCHLAEVDUIIW-NLLUTMDRSA-N

> <FORMULA>
C25H36O6

> <MOLECULAR_WEIGHT>
432.557

> <EXACT_MASS>
432.251188879

> <JCHEM_ACCEPTOR_COUNT>
6

> <JCHEM_ATOM_COUNT>
67

> <JCHEM_AVERAGE_POLARIZABILITY>
46.86744636906536

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
3

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
(3aR,5aR,6S)-3a,5a-dimethyl-1-(propan-2-yl)-6-{[(2S,3R,4S,5R)-3,4,5-trihydroxyoxan-2-yl]oxy}-2H,3H,3aH,4H,5H,5aH,6H,7H-cyclohepta[e]indene-8-carbaldehyde

> <ALOGPS_LOGP>
2.98

> <JCHEM_LOGP>
1.9733997313333345

> <ALOGPS_LOGS>
-3.88

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
4

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
13.403212287166475

> <JCHEM_PKA_STRONGEST_ACIDIC>
12.246231746121753

> <JCHEM_PKA_STRONGEST_BASIC>
-3.52658062854581

> <JCHEM_POLAR_SURFACE_AREA>
96.22000000000001

> <JCHEM_REFRACTIVITY>
118.83849999999995

> <JCHEM_ROTATABLE_BOND_COUNT>
4

> <JCHEM_RULE_OF_FIVE>
1

> <ALOGPS_SOLUBILITY>
5.66e-02 g/l

> <JCHEM_TRADITIONAL_IUPAC>
(3aR,5aR,6S)-1-isopropyl-3a,5a-dimethyl-6-{[(2S,3R,4S,5R)-3,4,5-trihydroxyoxan-2-yl]oxy}-2H,3H,4H,5H,6H,7H-cyclohepta[e]indene-8-carbaldehyde

> <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       6.548  -3.074   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0       3.975  -2.368   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0       6.734   3.187   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0       2.096   3.600   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0       1.232  -0.966   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0       2.728  -0.599   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0       7.314   0.050   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0       7.242   1.588   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0       5.066   3.372   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0       3.529   3.462   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0      -0.012   1.514   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0      -1.363  -0.717   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0       4.510   5.691   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0       5.465  -1.978   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0       0.013  -0.026   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0       5.873  -0.493   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0       3.373   0.799   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0       4.143   7.187   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0       1.176   2.493   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0       4.911   0.709   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0       2.664   7.616   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0       1.553   6.550   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0       1.920   5.055   0.000  0.00  0.00           C+0
HETATM   24  C   UNK     0       5.757   1.996   0.000  0.00  0.00           C+0
HETATM   25  C   UNK     0       2.682   2.175   0.000  0.00  0.00           C+0
HETATM   26  O   UNK     0      -2.650   0.129   0.000  0.00  0.00           O+0
HETATM   27  O   UNK     0       5.255   8.252   0.000  0.00  0.00           O+0
HETATM   28  O   UNK     0       2.297   9.112   0.000  0.00  0.00           O+0
HETATM   29  O   UNK     0       0.074   6.980   0.000  0.00  0.00           O+0
HETATM   30  O   UNK     0       3.399   4.625   0.000  0.00  0.00           O+0
HETATM   31  O   UNK     0       0.808   3.989   0.000  0.00  0.00           O+0
HETATM   32  H   UNK     0       3.776   8.682   0.000  0.00  0.00           H+0
HETATM   33  H   UNK     0       1.543   0.998   0.000  0.00  0.00           H+0
HETATM   34  H   UNK     0       3.031   6.121   0.000  0.00  0.00           H+0
HETATM   35  H   UNK     0       1.185   8.046   0.000  0.00  0.00           H+0
HETATM   36  H   UNK     0       0.441   5.485   0.000  0.00  0.00           H+0
CONECT    1   14                                                            
CONECT    2   14                                                            
CONECT    3   24                                                            
CONECT    4   25                                                            
CONECT    5    6   15                                                       
CONECT    6    5   17                                                       
CONECT    7    8   16                                                       
CONECT    8    7   24                                                       
CONECT    9   10   24                                                       
CONECT   10    9   25                                                       
CONECT   11   15   19                                                       
CONECT   12   15   26                                                       
CONECT   13   18   30                                                       
CONECT   14    1    2   16                                                  
CONECT   15    5   11   12                                                  
CONECT   16    7   14   20                                                  
CONECT   17    6   20   25                                                  
CONECT   18   13   21   27   32                                             
CONECT   19   11   25   31   33                                             
CONECT   20   16   17   24                                                  
CONECT   21   18   22   28   34                                             
CONECT   22   21   23   29   35                                             
CONECT   23   22   30   31   36                                             
CONECT   24    3    8    9   20                                             
CONECT   25    4   10   17   19                                             
CONECT   26   12                                                            
CONECT   27   18                                                            
CONECT   28   21                                                            
CONECT   29   22                                                            
CONECT   30   13   23                                                       
CONECT   31   19   23                                                       
CONECT   32   18                                                            
CONECT   33   19                                                            
CONECT   34   21                                                            
CONECT   35   22                                                            
CONECT   36   23                                                            
MASTER        0    0    0    0    0    0    0    0   36    0   78    0
END

Synonyms

Not Available

Molecular Formula

C₂₅H₃₆O₆

Average Mass

432.557

Monoisotopic Mass

432.251188879

IUPAC Name

(3aR,5aR,6S)-3a,5a-dimethyl-1-(propan-2-yl)-6-{[(2S,3R,4S,5R)-3,4,5-trihydroxyoxan-2-yl]oxy}-2H,3H,3aH,4H,5H,5aH,6H,7H-cyclohepta[e]indene-8-carbaldehyde

Traditional Name

(3aR,5aR,6S)-1-isopropyl-3a,5a-dimethyl-6-{[(2S,3R,4S,5R)-3,4,5-trihydroxyoxan-2-yl]oxy}-2H,3H,4H,5H,6H,7H-cyclohepta[e]indene-8-carbaldehyde

CAS Registry Number

Not Available

SMILES

[H][C@@]1(O)CO[C@@]([H])(O[C@@]2([H])CC(C=O)=CC=C3C4=C(CC[C@]4(C)CC[C@@]23C)C(C)C)[C@]([H])(O)[C@@]1([H])O

InChI Identifier

InChI=1S/C25H36O6/c1-14(2)16-7-8-24(3)9-10-25(4)17(20(16)24)6-5-15(12-26)11-19(25)31-23-22(29)21(28)18(27)13-30-23/h5-6,12,14,18-19,21-23,27-29H,7-11,13H2,1-4H3/t18-,19+,21+,22-,23+,24-,25-/m1/s1

InChI Key

LPPCHLAEVDUIIW-NLLUTMDRSA-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

Diterpenoid
Glycosyl compound
O-glycosyl compound
Oxane
Monosaccharide
Secondary alcohol
Acetal
Oxacycle
Organoheterocyclic compound
Polyol
Organic oxygen compound
Organooxygen compound
Hydrocarbon derivative
Organic oxide
Carbonyl group
Aldehyde
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	0.057 g/L	ALOGPS
logP	2.98	ALOGPS
logP	1.97	ChemAxon
logS	-3.9	ALOGPS
pKa (Strongest Acidic)	12.25	ChemAxon
pKa (Strongest Basic)	-3.5	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	6	ChemAxon
Hydrogen Donor Count	3	ChemAxon
Polar Surface Area	96.22 Å²	ChemAxon
Rotatable Bond Count	4	ChemAxon
Refractivity	118.84 m³·mol⁻¹	ChemAxon
Polarizability	46.87 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

Not Available

Biological Properties

Cellular Locations

Extracellular
Membrane

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	Basidiomycota	3	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

8586005

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

10410568

PDB ID

Not Available

ChEBI ID

175499

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 Erinacine A (MMDBc0017554)

MOL for #<Metabolite:0x00007fecf01efbd8>

3D MOL for #<Metabolite:0x00007fecf01efbd8>

3D SDF for #<Metabolite:0x00007fecf01efbd8>

3D-SDF for #<Metabolite:0x00007fecf01efbd8>

PDB for #<Metabolite:0x00007fecf01efbd8>

3D PDB for #<Metabolite:0x00007fecf01efbd8>

SMILES for #<Metabolite:0x00007fecf01efbd8>

INCHI for #<Metabolite:0x00007fecf01efbd8>

Structure for #<Metabolite:0x00007fecf01efbd8>

3D Structure for #<Metabolite:0x00007fecf01efbd8>