MiMeDB: Showing metabocard for Arisugacin P (MMDBc0025292)

Record Information

Version

2.0

Status

Detected and Quantified

Creation Date

2021-05-15 15:01:28 UTC

Update Date

2025-10-07 16:07:31 UTC

Metabolite ID

MMDBc0025292

Metabolite Identification

Common Name

Arisugacin P

Description

Arisugacin P is a member of the chemical class of 4-hydroxy-6-phenyl-2H-pyran-2-one (HPPO) derived meroterpenoids. Its chemical structure features a pyranone core, which is characteristic of this class, contributing to its reactivity and potential biological activities. Arisugacin P is involved in various biosynthetic pathways, including those related to secondary metabolites in fungi, which may play roles in ecological interactions and defense mechanisms. The compound has been identified alongside other related metabolites, such as 4a-hydroxyarisugacin P, in studies exploring the diversity of meroterpenoids (PMID: 36743349 ). These compounds are often investigated for their potential pharmacological properties, as they may exhibit antimicrobial or anti-inflammatory activities, although specific biological significance for Arisugacin P remains to be fully elucidated. The structural complexity and the presence of hydroxyl groups in Arisugacin P may influence its interaction with biological targets, making it a subject of interest in natural product chemistry and drug discovery.

Structure

MOL SDF PDB SMILES InChI


  Mrv1652305152117012D          

 34 38  0  0  1  0            999 V2000
   -0.5530    2.6765    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3547    3.3708    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.3502    4.5927    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1604    2.2541    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.3714    3.9691    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.6709    3.0336    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.9410    4.4368    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.4811    2.8777    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.7511    4.2809    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.5401    2.5659    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2700    4.9046    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.5401    4.7486    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.3502    2.4100    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1604    4.4368    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.0507    3.3454    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.4009    3.8132    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.0212    3.5014    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.9705    4.2809    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.5908    3.9691    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.2405    3.5014    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.2700    3.3454    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.6203    3.8132    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   -0.8101    4.2809    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5106    4.9046    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5401    3.5014    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.8101    3.9691    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.8903    3.0336    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   -1.6203    4.4368    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.2405    5.6841    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    7.8313    3.3454    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.3207    4.7486    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.7004    2.8777    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0000    4.1250    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.4304    3.6573    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
  8  6  1  0  0  0  0
  9  7  2  0  0  0  0
 12 11  2  0  0  0  0
 13 10  1  0  0  0  0
 16  6  2  0  0  0  0
 16  7  1  0  0  0  0
 17  8  2  0  0  0  0
 17  9  1  0  0  0  0
 18 14  1  0  0  0  0
 19 15  2  0  0  0  0
 19 16  1  0  0  0  0
 20 15  1  0  0  0  0
 20 18  2  0  0  0  0
 21 10  1  0  0  0  0
 22 14  1  0  0  0  0
 23 11  1  0  0  0  0
 24 18  1  0  0  0  0
 25  1  1  0  0  0  0
 25  2  1  0  0  0  0
 25 21  1  0  0  0  0
 25 23  1  0  0  0  0
 26  3  1  1  0  0  0
 26 12  1  0  0  0  0
 26 21  1  0  0  0  0
 26 22  1  0  0  0  0
 27  4  1  1  0  0  0
 27 13  1  0  0  0  0
 27 22  1  0  0  0  0
 28 23  2  0  0  0  0
 29 24  2  0  0  0  0
 30  5  1  0  0  0  0
 30 17  1  0  0  0  0
 31 19  1  0  0  0  0
 31 24  1  0  0  0  0
 32 20  1  0  0  0  0
 32 27  1  0  0  0  0
 21 33  1  6  0  0  0
 22 34  1  6  0  0  0
M  END


  Mrv1652305152117012D          

 34 38  0  0  1  0            999 V2000
   -0.5530    2.6765    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3547    3.3708    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.3502    4.5927    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1604    2.2541    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.3714    3.9691    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.6709    3.0336    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.9410    4.4368    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.4811    2.8777    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.7511    4.2809    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.5401    2.5659    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2700    4.9046    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.5401    4.7486    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.3502    2.4100    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1604    4.4368    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.0507    3.3454    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.4009    3.8132    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.0212    3.5014    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.9705    4.2809    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.5908    3.9691    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.2405    3.5014    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.2700    3.3454    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.6203    3.8132    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   -0.8101    4.2809    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5106    4.9046    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5401    3.5014    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.8101    3.9691    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.8903    3.0336    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   -1.6203    4.4368    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.2405    5.6841    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    7.8313    3.3454    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.3207    4.7486    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.7004    2.8777    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0000    4.1250    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.4304    3.6573    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
  8  6  1  0  0  0  0
  9  7  2  0  0  0  0
 12 11  2  0  0  0  0
 13 10  1  0  0  0  0
 16  6  2  0  0  0  0
 16  7  1  0  0  0  0
 17  8  2  0  0  0  0
 17  9  1  0  0  0  0
 18 14  1  0  0  0  0
 19 15  2  0  0  0  0
 19 16  1  0  0  0  0
 20 15  1  0  0  0  0
 20 18  2  0  0  0  0
 21 10  1  0  0  0  0
 22 14  1  0  0  0  0
 23 11  1  0  0  0  0
 24 18  1  0  0  0  0
 25  1  1  0  0  0  0
 25  2  1  0  0  0  0
 25 21  1  0  0  0  0
 25 23  1  0  0  0  0
 26  3  1  1  0  0  0
 26 12  1  0  0  0  0
 26 21  1  0  0  0  0
 26 22  1  0  0  0  0
 27  4  1  1  0  0  0
 27 13  1  0  0  0  0
 27 22  1  0  0  0  0
 28 23  2  0  0  0  0
 29 24  2  0  0  0  0
 30  5  1  0  0  0  0
 30 17  1  0  0  0  0
 31 19  1  0  0  0  0
 31 24  1  0  0  0  0
 32 20  1  0  0  0  0
 32 27  1  0  0  0  0
 21 33  1  6  0  0  0
 22 34  1  6  0  0  0
M  END
> <DATABASE_ID>
MMDBc0025292

> <DATABASE_NAME>
MIME

> <SMILES>
[H][C@@]12CC[C@@]3(C)OC4=C(C[C@]3([H])[C@@]1(C)C=CC(=O)C2(C)C)C(=O)OC(=C4)C1=CC=C(OC)C=C1

> <INCHI_IDENTIFIER>
InChI=1S/C27H30O5/c1-25(2)21-10-13-27(4)22(26(21,3)12-11-23(25)28)14-18-20(32-27)15-19(31-24(18)29)16-6-8-17(30-5)9-7-16/h6-9,11-12,15,21-22H,10,13-14H2,1-5H3/t21-,22+,26-,27+/m0/s1

> <INCHI_KEY>
BOMYZLARCFYSCM-HXABMTEBSA-N

> <FORMULA>
C27H30O5

> <MOLECULAR_WEIGHT>
434.532

> <EXACT_MASS>
434.209324066

> <JCHEM_ACCEPTOR_COUNT>
4

> <JCHEM_ATOM_COUNT>
62

> <JCHEM_AVERAGE_POLARIZABILITY>
48.564693436994766

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
0

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
(5aR,7aR,11aS,11bR)-3-(4-methoxyphenyl)-5a,8,8,11a-tetramethyl-1,5a,6,7,7a,8,9,11a,11b,12-decahydro-2,5-dioxatetraphene-1,9-dione

> <ALOGPS_LOGP>
5.38

> <JCHEM_LOGP>
4.749248635333334

> <ALOGPS_LOGS>
-5.47

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
5

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA_STRONGEST_BASIC>
-4.4401438066854135

> <JCHEM_POLAR_SURFACE_AREA>
61.83000000000001

> <JCHEM_REFRACTIVITY>
124.74549999999996

> <JCHEM_ROTATABLE_BOND_COUNT>
2

> <JCHEM_RULE_OF_FIVE>
1

> <ALOGPS_SOLUBILITY>
1.46e-03 g/l

> <JCHEM_TRADITIONAL_IUPAC>
(5aR,7aR,11aS,11bR)-3-(4-methoxyphenyl)-5a,8,8,11a-tetramethyl-7,7a,11b,12-tetrahydro-6H-2,5-dioxatetraphene-1,9-dione

> <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      -1.032   4.996   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0      -2.529   6.292   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0       2.520   8.573   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0       4.033   4.208   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0      15.627   7.409   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0      10.586   5.663   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0      11.090   8.282   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0      12.098   5.372   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0      12.602   7.991   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0       1.008   4.790   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0      -0.504   9.155   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0       1.008   8.864   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0       2.520   4.499   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0       4.033   8.282   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0       7.561   6.245   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0      10.082   7.118   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0      13.106   6.536   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0       5.545   7.991   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0       8.569   7.409   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0       6.049   6.536   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0       0.504   6.245   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0       3.024   7.118   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0      -1.512   7.991   0.000  0.00  0.00           C+0
HETATM   24  C   UNK     0       6.553   9.155   0.000  0.00  0.00           C+0
HETATM   25  C   UNK     0      -1.008   6.536   0.000  0.00  0.00           C+0
HETATM   26  C   UNK     0       1.512   7.409   0.000  0.00  0.00           C+0
HETATM   27  C   UNK     0       3.529   5.663   0.000  0.00  0.00           C+0
HETATM   28  O   UNK     0      -3.024   8.282   0.000  0.00  0.00           O+0
HETATM   29  O   UNK     0       6.049  10.610   0.000  0.00  0.00           O+0
HETATM   30  O   UNK     0      14.618   6.245   0.000  0.00  0.00           O+0
HETATM   31  O   UNK     0       8.065   8.864   0.000  0.00  0.00           O+0
HETATM   32  O   UNK     0       5.041   5.372   0.000  0.00  0.00           O+0
HETATM   33  H   UNK     0      -0.000   7.700   0.000  0.00  0.00           H+0
HETATM   34  H   UNK     0       4.537   6.827   0.000  0.00  0.00           H+0
CONECT    1   25                                                            
CONECT    2   25                                                            
CONECT    3   26                                                            
CONECT    4   27                                                            
CONECT    5   30                                                            
CONECT    6    8   16                                                       
CONECT    7    9   16                                                       
CONECT    8    6   17                                                       
CONECT    9    7   17                                                       
CONECT   10   13   21                                                       
CONECT   11   12   23                                                       
CONECT   12   11   26                                                       
CONECT   13   10   27                                                       
CONECT   14   18   22                                                       
CONECT   15   19   20                                                       
CONECT   16    6    7   19                                                  
CONECT   17    8    9   30                                                  
CONECT   18   14   20   24                                                  
CONECT   19   15   16   31                                                  
CONECT   20   15   18   32                                                  
CONECT   21   10   25   26   33                                             
CONECT   22   14   26   27   34                                             
CONECT   23   11   25   28                                                  
CONECT   24   18   29   31                                                  
CONECT   25    1    2   21   23                                             
CONECT   26    3   12   21   22                                             
CONECT   27    4   13   22   32                                             
CONECT   28   23                                                            
CONECT   29   24                                                            
CONECT   30    5   17                                                       
CONECT   31   19   24                                                       
CONECT   32   20   27                                                       
CONECT   33   21                                                            
CONECT   34   22                                                            
MASTER        0    0    0    0    0    0    0    0   34    0   76    0
END

Synonyms

Not Available

Molecular Formula

C₂₇H₃₀O₅

Average Mass

434.532

Monoisotopic Mass

434.209324066

IUPAC Name

(5aR,7aR,11aS,11bR)-3-(4-methoxyphenyl)-5a,8,8,11a-tetramethyl-1,5a,6,7,7a,8,9,11a,11b,12-decahydro-2,5-dioxatetraphene-1,9-dione

Traditional Name

(5aR,7aR,11aS,11bR)-3-(4-methoxyphenyl)-5a,8,8,11a-tetramethyl-7,7a,11b,12-tetrahydro-6H-2,5-dioxatetraphene-1,9-dione

CAS Registry Number

Not Available

SMILES

[H][C@@]12CC[C@@]3(C)OC4=C(C[C@]3([H])[C@@]1(C)C=CC(=O)C2(C)C)C(=O)OC(=C4)C1=CC=C(OC)C=C1

InChI Identifier

InChI=1S/C27H30O5/c1-25(2)21-10-13-27(4)22(26(21,3)12-11-23(25)28)14-18-20(32-27)15-19(31-24(18)29)16-6-8-17(30-5)9-7-16/h6-9,11-12,15,21-22H,10,13-14H2,1-5H3/t21-,22+,26-,27+/m0/s1

InChI Key

BOMYZLARCFYSCM-HXABMTEBSA-N

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as naphthopyrans. Naphthopyrans are compounds containing a pyran ring fused to a naphthalene moiety. Furan is a 6 membered-ring non-aromatic ring with five 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

Naphthopyrans

Sub Class

Not Available

Direct Parent

Naphthopyrans

Alternative Parents

Substituents

Naphthopyran
Naphthalene
Phenoxy compound
Methoxybenzene
Phenol ether
Anisole
Cyclohexenone
Pyranone
Alkyl aryl ether
Benzenoid
Pyran
Monocyclic benzene moiety
Heteroaromatic compound
Vinylogous ester
Cyclic ketone
Lactone
Ketone
Oxacycle
Ether
Organic oxygen compound
Organic oxide
Hydrocarbon derivative
Organooxygen compound
Carbonyl group
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	0.0015 g/L	ALOGPS
logP	5.38	ALOGPS
logP	4.75	ChemAxon
logS	-5.5	ALOGPS
pKa (Strongest Basic)	-4.4	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	4	ChemAxon
Hydrogen Donor Count	0	ChemAxon
Polar Surface Area	61.83 Å²	ChemAxon
Rotatable Bond Count	2	ChemAxon
Refractivity	124.75 m³·mol⁻¹	ChemAxon
Polarizability	48.56 Å³	ChemAxon
Number of Rings	5	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

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	1	Human feces	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

Not Available

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

145721182

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 Arisugacin P (MMDBc0025292)

MOL for #<Metabolite:0x00007f8dbd1b7720>

3D MOL for #<Metabolite:0x00007f8dbd1b7720>

3D SDF for #<Metabolite:0x00007f8dbd1b7720>

3D-SDF for #<Metabolite:0x00007f8dbd1b7720>

PDB for #<Metabolite:0x00007f8dbd1b7720>

3D PDB for #<Metabolite:0x00007f8dbd1b7720>

SMILES for #<Metabolite:0x00007f8dbd1b7720>

INCHI for #<Metabolite:0x00007f8dbd1b7720>

Structure for #<Metabolite:0x00007f8dbd1b7720>

3D Structure for #<Metabolite:0x00007f8dbd1b7720>