MiMeDB: Showing metabocard for Penicilindole C (MMDBc0022573)

Record Information

Version

1.0

Status

Detected and Quantified

Creation Date

2021-05-15 12:39:56 UTC

Update Date

2022-08-31 06:47:43 UTC

Metabolite ID

MMDBc0022573

Metabolite Identification

Common Name

Penicilindole C

Description

Penicilindole C belongs to the class of organic compounds known as naphthofurans. Naphthofurans are compounds containing a furan ring fused to a naphthalene moiety. Furan is a 5 membered- ring aromatic ring with four carbon and one oxygen atoms. Naphthalene is a polycyclic aromatic hydrocarbon made up of two fused benzene rings. Penicilindole C is an extremely weak basic (essentially neutral) compound (based on its pKa).

Structure

MOL SDF PDB SMILES InChI


  Mrv1652305152114392D          

 35 39  0  0  1  0            999 V2000
    2.1190   -3.4491    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.8815   -2.7346    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7145    2.0625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4289    1.6500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.1401   -0.7752    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6470   -3.8682    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.4540   -4.0397    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3921   -3.0836    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.0060   -3.4266    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0000    0.8250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0000   -0.0000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1434    1.2375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8579    0.8250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1190   -2.0202    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1434   -1.2375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0118   -0.6647    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6116   -1.3144    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.7065   -2.7346    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7145    1.2375    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.8579   -1.6500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.7065   -1.3057    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.9441   -2.4705    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.7511   -2.6420    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1434   -0.4125    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.7145   -0.4125    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.4289    0.8250    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.8579   -0.0000    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.4289    0.0000    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    4.1636   -1.9275    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    3.6704    0.1433    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.8860   -1.2195    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.7145    0.4125    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.2572   -1.9976    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.8579   -0.8250    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.0470   -0.8974    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
  7  6  2  0  0  0  0
  8  6  1  0  0  0  0
  9  7  1  0  0  0  0
 11 10  1  0  0  0  0
 13 12  1  0  0  0  0
 18  1  1  0  0  0  0
 18  2  1  0  0  0  0
 18 14  2  0  0  0  0
 19  3  1  6  0  0  0
 19 10  1  0  0  0  0
 20 15  1  0  0  0  0
 20 17  2  0  0  0  0
 21 14  1  1  0  0  0
 21 16  1  0  0  0  0
 22  8  2  0  0  0  0
 22 20  1  0  0  0  0
 23  9  2  0  0  0  0
 23 22  1  0  0  0  0
 24 15  1  1  0  0  0
 25 11  1  0  0  0  0
 26  4  1  1  0  0  0
 26 12  1  0  0  0  0
 26 19  1  0  0  0  0
 27  5  1  6  0  0  0
 27 13  1  0  0  0  0
 27 24  1  0  0  0  0
 28 16  1  1  0  0  0
 28 24  1  0  0  0  0
 28 25  1  0  0  0  0
 28 26  1  0  0  0  0
 29 17  1  0  0  0  0
 29 23  1  0  0  0  0
 27 30  1  1  0  0  0
 31 21  1  0  0  0  0
 31 25  1  0  0  0  0
 19 32  1  6  0  0  0
 21 33  1  6  0  0  0
 24 34  1  6  0  0  0
 25 35  1  6  0  0  0
M  END


  Mrv1652305152114392D          

 35 39  0  0  1  0            999 V2000
    2.1190   -3.4491    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.8815   -2.7346    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7145    2.0625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4289    1.6500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.1401   -0.7752    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6470   -3.8682    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.4540   -4.0397    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3921   -3.0836    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.0060   -3.4266    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0000    0.8250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0000   -0.0000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1434    1.2375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8579    0.8250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1190   -2.0202    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1434   -1.2375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0118   -0.6647    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6116   -1.3144    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.7065   -2.7346    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7145    1.2375    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.8579   -1.6500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.7065   -1.3057    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.9441   -2.4705    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.7511   -2.6420    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1434   -0.4125    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.7145   -0.4125    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.4289    0.8250    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.8579   -0.0000    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.4289    0.0000    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    4.1636   -1.9275    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    3.6704    0.1433    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.8860   -1.2195    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.7145    0.4125    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.2572   -1.9976    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.8579   -0.8250    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.0470   -0.8974    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
  7  6  2  0  0  0  0
  8  6  1  0  0  0  0
  9  7  1  0  0  0  0
 11 10  1  0  0  0  0
 13 12  1  0  0  0  0
 18  1  1  0  0  0  0
 18  2  1  0  0  0  0
 18 14  2  0  0  0  0
 19  3  1  6  0  0  0
 19 10  1  0  0  0  0
 20 15  1  0  0  0  0
 20 17  2  0  0  0  0
 21 14  1  1  0  0  0
 21 16  1  0  0  0  0
 22  8  2  0  0  0  0
 22 20  1  0  0  0  0
 23  9  2  0  0  0  0
 23 22  1  0  0  0  0
 24 15  1  1  0  0  0
 25 11  1  0  0  0  0
 26  4  1  1  0  0  0
 26 12  1  0  0  0  0
 26 19  1  0  0  0  0
 27  5  1  6  0  0  0
 27 13  1  0  0  0  0
 27 24  1  0  0  0  0
 28 16  1  1  0  0  0
 28 24  1  0  0  0  0
 28 25  1  0  0  0  0
 28 26  1  0  0  0  0
 29 17  1  0  0  0  0
 29 23  1  0  0  0  0
 27 30  1  1  0  0  0
 31 21  1  0  0  0  0
 31 25  1  0  0  0  0
 19 32  1  6  0  0  0
 21 33  1  6  0  0  0
 24 34  1  6  0  0  0
 25 35  1  6  0  0  0
M  END
> <DATABASE_ID>
MMDBc0022573

> <DATABASE_NAME>
MIME

> <SMILES>
[H][C@]1(C[C@@]23[C@]([H])(CC[C@@]([H])(C)[C@]2(C)CC[C@@](C)(O)[C@@]3([H])CC2=CNC3=CC=CC=C23)O1)C=C(C)C

> <INCHI_IDENTIFIER>
InChI=1S/C28H39NO2/c1-18(2)14-21-16-28-24(15-20-17-29-23-9-7-6-8-22(20)23)27(5,30)13-12-26(28,4)19(3)10-11-25(28)31-21/h6-9,14,17,19,21,24-25,29-30H,10-13,15-16H2,1-5H3/t19-,21-,24-,25+,26+,27-,28-/m1/s1

> <INCHI_KEY>
XHGDWOIUBXSXIP-JTACFZARSA-N

> <FORMULA>
C28H39NO2

> <MOLECULAR_WEIGHT>
421.625

> <EXACT_MASS>
421.2980795

> <JCHEM_ACCEPTOR_COUNT>
2

> <JCHEM_ATOM_COUNT>
70

> <JCHEM_AVERAGE_POLARIZABILITY>
49.88764891660674

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
2

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
(2S,6R,6aS,9R,10S,10aS,10bS)-10-[(1H-indol-3-yl)methyl]-6,6a,9-trimethyl-2-(2-methylprop-1-en-1-yl)-decahydro-1H-naphtho[1,8a-b]furan-9-ol

> <ALOGPS_LOGP>
5.88

> <JCHEM_LOGP>
5.849736257999998

> <ALOGPS_LOGS>
-6.75

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
5

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
17.286294667957286

> <JCHEM_PKA_STRONGEST_ACIDIC>
14.75393997287614

> <JCHEM_PKA_STRONGEST_BASIC>
-2.9058159099136995

> <JCHEM_POLAR_SURFACE_AREA>
45.25

> <JCHEM_REFRACTIVITY>
127.48709999999997

> <JCHEM_ROTATABLE_BOND_COUNT>
3

> <JCHEM_RULE_OF_FIVE>
0

> <ALOGPS_SOLUBILITY>
7.43e-05 g/l

> <JCHEM_TRADITIONAL_IUPAC>
(2S,6R,6aS,9R,10S,10aS,10bS)-10-(1H-indol-3-ylmethyl)-6,6a,9-trimethyl-2-(2-methylprop-1-en-1-yl)-octahydro-1H-naphtho[1,8a-b]furan-9-ol

> <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       3.955  -6.438   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0       1.645  -5.105   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0       1.334   3.850   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0       2.667   3.080   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0       5.861  -1.447   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0       4.941  -7.221   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0       6.447  -7.541   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0       4.465  -5.756   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0       7.478  -6.396   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0       0.000   1.540   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0       0.000  -0.000   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0       4.001   2.310   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0       5.335   1.540   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0       3.955  -3.771   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0       4.001  -2.310   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0       3.755  -1.241   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0       6.742  -2.454   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0       3.185  -5.105   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0       1.334   2.310   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0       5.335  -3.080   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0       3.185  -2.437   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0       5.496  -4.612   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0       7.002  -4.932   0.000  0.00  0.00           C+0
HETATM   24  C   UNK     0       4.001  -0.770   0.000  0.00  0.00           C+0
HETATM   25  C   UNK     0       1.334  -0.770   0.000  0.00  0.00           C+0
HETATM   26  C   UNK     0       2.667   1.540   0.000  0.00  0.00           C+0
HETATM   27  C   UNK     0       5.335  -0.000   0.000  0.00  0.00           C+0
HETATM   28  C   UNK     0       2.667   0.000   0.000  0.00  0.00           C+0
HETATM   29  N   UNK     0       7.772  -3.598   0.000  0.00  0.00           N+0
HETATM   30  O   UNK     0       6.851   0.267   0.000  0.00  0.00           O+0
HETATM   31  O   UNK     0       1.654  -2.276   0.000  0.00  0.00           O+0
HETATM   32  H   UNK     0       1.334   0.770   0.000  0.00  0.00           H+0
HETATM   33  H   UNK     0       2.347  -3.729   0.000  0.00  0.00           H+0
HETATM   34  H   UNK     0       5.335  -1.540   0.000  0.00  0.00           H+0
HETATM   35  H   UNK     0       0.088  -1.675   0.000  0.00  0.00           H+0
CONECT    1   18                                                            
CONECT    2   18                                                            
CONECT    3   19                                                            
CONECT    4   26                                                            
CONECT    5   27                                                            
CONECT    6    7    8                                                       
CONECT    7    6    9                                                       
CONECT    8    6   22                                                       
CONECT    9    7   23                                                       
CONECT   10   11   19                                                       
CONECT   11   10   25                                                       
CONECT   12   13   26                                                       
CONECT   13   12   27                                                       
CONECT   14   18   21                                                       
CONECT   15   20   24                                                       
CONECT   16   21   28                                                       
CONECT   17   20   29                                                       
CONECT   18    1    2   14                                                  
CONECT   19    3   10   26   32                                             
CONECT   20   15   17   22                                                  
CONECT   21   14   16   31   33                                             
CONECT   22    8   20   23                                                  
CONECT   23    9   22   29                                                  
CONECT   24   15   27   28   34                                             
CONECT   25   11   28   31   35                                             
CONECT   26    4   12   19   28                                             
CONECT   27    5   13   24   30                                             
CONECT   28   16   24   25   26                                             
CONECT   29   17   23                                                       
CONECT   30   27                                                            
CONECT   31   21   25                                                       
CONECT   32   19                                                            
CONECT   33   21                                                            
CONECT   34   24                                                            
CONECT   35   25                                                            
MASTER        0    0    0    0    0    0    0    0   35    0   78    0
END

Synonyms

Not Available

Molecular Formula

C₂₈H₃₉NO₂

Average Mass

421.625

Monoisotopic Mass

421.2980795

IUPAC Name

(2S,6R,6aS,9R,10S,10aS,10bS)-10-[(1H-indol-3-yl)methyl]-6,6a,9-trimethyl-2-(2-methylprop-1-en-1-yl)-decahydro-1H-naphtho[1,8a-b]furan-9-ol

Traditional Name

(2S,6R,6aS,9R,10S,10aS,10bS)-10-(1H-indol-3-ylmethyl)-6,6a,9-trimethyl-2-(2-methylprop-1-en-1-yl)-octahydro-1H-naphtho[1,8a-b]furan-9-ol

CAS Registry Number

Not Available

SMILES

[H][C@]1(C[C@@]23[C@]([H])(CC[C@@]([H])(C)[C@]2(C)CC[C@@](C)(O)[C@@]3([H])CC2=CNC3=CC=CC=C23)O1)C=C(C)C

InChI Identifier

InChI=1S/C28H39NO2/c1-18(2)14-21-16-28-24(15-20-17-29-23-9-7-6-8-22(20)23)27(5,30)13-12-26(28,4)19(3)10-11-25(28)31-21/h6-9,14,17,19,21,24-25,29-30H,10-13,15-16H2,1-5H3/t19-,21-,24-,25+,26+,27-,28-/m1/s1

InChI Key

XHGDWOIUBXSXIP-JTACFZARSA-N

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as naphthofurans. Naphthofurans are compounds containing a furan ring fused to a naphthalene moiety. Furan is a 5 membered- ring aromatic ring with four carbon and one oxygen atoms. Naphthalene is a polycyclic aromatic hydrocarbon made up of two fused benzene rings.

Kingdom

Organic compounds

Super Class

Organoheterocyclic compounds

Class

Naphthofurans

Sub Class

Not Available

Direct Parent

Naphthofurans

Alternative Parents

Substituents

Naphthofuran
3-alkylindole
Indole or derivatives
Indole
Benzenoid
Substituted pyrrole
Heteroaromatic compound
Tetrahydrofuran
Tertiary alcohol
Pyrrole
Cyclic alcohol
Oxacycle
Azacycle
Ether
Dialkyl ether
Organic nitrogen compound
Organic oxygen compound
Organopnictogen compound
Hydrocarbon derivative
Organooxygen compound
Organonitrogen compound
Alcohol
Aromatic heteropolycyclic compound

Molecular Framework

Aromatic heteropolycyclic compounds

External Descriptors

Not Available

Functional Ontology

Not Available

Physical Properties

State

Expected Solid

Predicted Properties

Property	Value	Source
Water Solubility	7.4e-05 g/L	ALOGPS
logP	5.88	ALOGPS
logP	5.85	ChemAxon
logS	-6.8	ALOGPS
pKa (Strongest Acidic)	14.75	ChemAxon
pKa (Strongest Basic)	-2.9	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	2	ChemAxon
Hydrogen Donor Count	2	ChemAxon
Polar Surface Area	45.25 Å²	ChemAxon
Rotatable Bond Count	3	ChemAxon
Refractivity	127.49 m³·mol⁻¹	ChemAxon
Polarizability	49.89 Å³	ChemAxon
Number of Rings	5	ChemAxon
Bioavailability	Yes	ChemAxon
Rule of Five	No	ChemAxon
Ghose Filter	No	ChemAxon
Veber's Rule	No	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

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

65323289

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

139589955

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 Penicilindole C (MMDBc0022573)

MOL for #<Metabolite:0x00007fecac17d4c8>

3D MOL for #<Metabolite:0x00007fecac17d4c8>

3D SDF for #<Metabolite:0x00007fecac17d4c8>

3D-SDF for #<Metabolite:0x00007fecac17d4c8>

PDB for #<Metabolite:0x00007fecac17d4c8>

3D PDB for #<Metabolite:0x00007fecac17d4c8>

SMILES for #<Metabolite:0x00007fecac17d4c8>

INCHI for #<Metabolite:0x00007fecac17d4c8>

Structure for #<Metabolite:0x00007fecac17d4c8>

3D Structure for #<Metabolite:0x00007fecac17d4c8>