MiMeDB: Showing metabocard for Arisugacin C (MMDBc0014417)

Record Information

Version

2.0

Status

Detected and Quantified

Creation Date

2021-05-15 05:26:51 UTC

Update Date

2025-10-07 16:06:16 UTC

Metabolite ID

MMDBc0014417

Metabolite Identification

Common Name

Arisugacin C

Description

Arisugacin C is a meroterpene, a chemical class that typically combines elements of terpenes and other natural products. It was identified as a metabolite produced by the endophytic fungus Penicillium echinulatum pt-4, which was isolated from the marine red alga Chondrus ocellatus. This discovery highlights the potential of marine-derived fungi as sources of novel bioactive compounds. The isolation of arisugacin C, along with other related meroterpenes such as arisugacin J, arisugacin G, and territrem C, suggests that these compounds may have unique structural features and biological activities worth investigating further. The study of arisugacin C and its analogs could provide insights into their roles in the ecological interactions within their marine environments and their potential applications in pharmaceuticals or biotechnology. The relevance of such metabolites in drug discovery underscores the importance of exploring marine biodiversity for novel chemical entities. (PMID:24482051 )

Structure

MOL SDF PDB SMILES InChI

Arisugacin C
  Mrv1652309242002282D          

 33 37  0  0  0  0            999 V2000
    1.2375   -0.7144    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.4125   -0.7144    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.8250    0.0000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.4125    0.7144    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4125    0.7144    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8250    1.4290    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8250    0.0000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4125   -0.7144    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   -0.8250   -1.4290    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4125   -2.1434    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.4125   -2.1434    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.8250   -1.4290    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.6500   -1.4290    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0625   -2.1434    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.6500   -2.8579    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.8250   -2.8579    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.0625   -3.5724    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8875   -3.5724    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3000   -2.8579    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.8875   -2.1434    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3000   -1.4290    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.3000   -4.2868    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8875   -5.0013    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3000   -5.7158    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.1250   -5.7158    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.5375   -5.0013    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.1250   -4.2868    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.5375   -6.4302    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.1250   -7.1447    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0000   -2.8579    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2313   -0.8150    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5169   -0.4493    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4570    0.5303    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
  2  1  1  1  0  0  0
  2  3  1  0  0  0  0
  3  4  1  0  0  0  0
  4  5  1  0  0  0  0
  5  6  2  0  0  0  0
  5  7  1  0  0  0  0
  7  8  1  0  0  0  0
  8  9  1  0  0  0  0
  9 10  1  0  0  0  0
 10 11  1  0  0  0  0
 11 12  1  0  0  0  0
 12 13  1  1  0  0  0
 13 14  1  0  0  0  0
 14 15  2  0  0  0  0
 15 16  1  0  0  0  0
 15 17  1  0  0  0  0
 17 18  2  0  0  0  0
 18 19  1  0  0  0  0
 19 20  1  0  0  0  0
 20 21  2  0  0  0  0
 18 22  1  0  0  0  0
 22 23  2  0  0  0  0
 23 24  1  0  0  0  0
 24 25  2  0  0  0  0
 25 26  1  0  0  0  0
 26 27  2  0  0  0  0
 25 28  1  0  0  0  0
 28 29  1  0  0  0  0
 11 30  1  1  0  0  0
  8 31  1  6  0  0  0
  7 32  1  0  0  0  0
  7 33  1  0  0  0  0
  8  2  1  0  0  0  0
 12  2  1  0  0  0  0
 16 11  1  0  0  0  0
 20 14  1  0  0  0  0
 27 22  1  0  0  0  0
M  END

Arisugacin C
  Mrv1652309242002282D          

 33 37  0  0  0  0            999 V2000
    1.2375   -0.7144    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.4125   -0.7144    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.8250    0.0000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.4125    0.7144    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4125    0.7144    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8250    1.4290    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8250    0.0000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4125   -0.7144    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   -0.8250   -1.4290    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4125   -2.1434    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.4125   -2.1434    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.8250   -1.4290    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.6500   -1.4290    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0625   -2.1434    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.6500   -2.8579    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.8250   -2.8579    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.0625   -3.5724    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8875   -3.5724    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3000   -2.8579    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.8875   -2.1434    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3000   -1.4290    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.3000   -4.2868    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8875   -5.0013    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3000   -5.7158    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.1250   -5.7158    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.5375   -5.0013    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.1250   -4.2868    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.5375   -6.4302    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.1250   -7.1447    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0000   -2.8579    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2313   -0.8150    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5169   -0.4493    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4570    0.5303    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
  2  1  1  1  0  0  0
  2  3  1  0  0  0  0
  3  4  1  0  0  0  0
  4  5  1  0  0  0  0
  5  6  2  0  0  0  0
  5  7  1  0  0  0  0
  7  8  1  0  0  0  0
  8  9  1  0  0  0  0
  9 10  1  0  0  0  0
 10 11  1  0  0  0  0
 11 12  1  0  0  0  0
 12 13  1  1  0  0  0
 13 14  1  0  0  0  0
 14 15  2  0  0  0  0
 15 16  1  0  0  0  0
 15 17  1  0  0  0  0
 17 18  2  0  0  0  0
 18 19  1  0  0  0  0
 19 20  1  0  0  0  0
 20 21  2  0  0  0  0
 18 22  1  0  0  0  0
 22 23  2  0  0  0  0
 23 24  1  0  0  0  0
 24 25  2  0  0  0  0
 25 26  1  0  0  0  0
 26 27  2  0  0  0  0
 25 28  1  0  0  0  0
 28 29  1  0  0  0  0
 11 30  1  1  0  0  0
  8 31  1  6  0  0  0
  7 32  1  0  0  0  0
  7 33  1  0  0  0  0
  8  2  1  0  0  0  0
 12  2  1  0  0  0  0
 16 11  1  0  0  0  0
 20 14  1  0  0  0  0
 27 22  1  0  0  0  0
M  END
> <DATABASE_ID>
MMDBc0014417

> <DATABASE_NAME>
MIME

> <SMILES>
COC1=CC=C(C=C1)C1=CC2=C(C[C@H]3[C@@](C)(CC[C@@]4(O)C(C)(C)C(=O)CC[C@]34C)O2)C(=O)O1

> <INCHI_IDENTIFIER>
InChI=1S/C27H32O6/c1-24(2)22(28)10-11-25(3)21-14-18-20(33-26(21,4)12-13-27(24,25)30)15-19(32-23(18)29)16-6-8-17(31-5)9-7-16/h6-9,15,21,30H,10-14H2,1-5H3/t21-,25-,26-,27-/m1/s1

> <INCHI_KEY>
XKDGQMPLQPRTCS-HHPVDLARSA-N

> <FORMULA>
C27H32O6

> <MOLECULAR_WEIGHT>
452.547

> <EXACT_MASS>
452.21988875

> <JCHEM_ACCEPTOR_COUNT>
5

> <JCHEM_ATOM_COUNT>
65

> <JCHEM_AVERAGE_POLARIZABILITY>
50.209909505177535

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
1

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
(5aR,7aS,11aR,11bR)-7a-hydroxy-3-(4-methoxyphenyl)-5a,8,8,11a-tetramethyl-1,5a,6,7,7a,8,9,10,11,11a,11b,12-dodecahydro-2,5-dioxatetraphene-1,9-dione

> <ALOGPS_LOGP>
4.17

> <JCHEM_LOGP>
3.748032840666667

> <ALOGPS_LOGS>
-5.29

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
5

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
19.36276492983811

> <JCHEM_PKA_STRONGEST_ACIDIC>
13.860574501824502

> <JCHEM_PKA_STRONGEST_BASIC>
-3.2971815900431913

> <JCHEM_POLAR_SURFACE_AREA>
82.06

> <JCHEM_REFRACTIVITY>
125.0263

> <JCHEM_ROTATABLE_BOND_COUNT>
2

> <JCHEM_RULE_OF_FIVE>
1

> <ALOGPS_SOLUBILITY>
2.31e-03 g/l

> <JCHEM_TRADITIONAL_IUPAC>
(5aR,7aS,11aR,11bR)-7a-hydroxy-3-(4-methoxyphenyl)-5a,8,8,11a-tetramethyl-6,7,10,11,11b,12-hexahydro-2,5-dioxatetraphene-1,9-dione

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 24-SEP-20   NONE
TITLE     NULL                                                        
COMPND    MOLECULE: Arisugacin C                                      
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   24-SEP-20         0                                  
HETATM    1  C   UNK     0       2.310  -1.334   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0       0.770  -1.334   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0       1.540   0.000   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0       0.770   1.334   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0      -0.770   1.334   0.000  0.00  0.00           C+0
HETATM    6  O   UNK     0      -1.540   2.667   0.000  0.00  0.00           O+0
HETATM    7  C   UNK     0      -1.540   0.000   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0      -0.770  -1.334   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0      -1.540  -2.667   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0      -0.770  -4.001   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0       0.770  -4.001   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0       1.540  -2.667   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0       3.080  -2.667   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0       3.850  -4.001   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0       3.080  -5.335   0.000  0.00  0.00           C+0
HETATM   16  O   UNK     0       1.540  -5.335   0.000  0.00  0.00           O+0
HETATM   17  C   UNK     0       3.850  -6.668   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0       5.390  -6.668   0.000  0.00  0.00           C+0
HETATM   19  O   UNK     0       6.160  -5.335   0.000  0.00  0.00           O+0
HETATM   20  C   UNK     0       5.390  -4.001   0.000  0.00  0.00           C+0
HETATM   21  O   UNK     0       6.160  -2.667   0.000  0.00  0.00           O+0
HETATM   22  C   UNK     0       6.160  -8.002   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0       5.390  -9.336   0.000  0.00  0.00           C+0
HETATM   24  C   UNK     0       6.160 -10.669   0.000  0.00  0.00           C+0
HETATM   25  C   UNK     0       7.700 -10.669   0.000  0.00  0.00           C+0
HETATM   26  C   UNK     0       8.470  -9.336   0.000  0.00  0.00           C+0
HETATM   27  C   UNK     0       7.700  -8.002   0.000  0.00  0.00           C+0
HETATM   28  O   UNK     0       8.470 -12.003   0.000  0.00  0.00           O+0
HETATM   29  C   UNK     0       7.700 -13.337   0.000  0.00  0.00           C+0
HETATM   30  C   UNK     0       0.000  -5.335   0.000  0.00  0.00           C+0
HETATM   31  O   UNK     0      -2.299  -1.521   0.000  0.00  0.00           O+0
HETATM   32  C   UNK     0      -2.832  -0.839   0.000  0.00  0.00           C+0
HETATM   33  C   UNK     0      -2.720   0.990   0.000  0.00  0.00           C+0
CONECT    1    2                                                            
CONECT    2    1    3    8   12                                             
CONECT    3    2    4                                                       
CONECT    4    3    5                                                       
CONECT    5    4    6    7                                                  
CONECT    6    5                                                            
CONECT    7    5    8   32   33                                             
CONECT    8    7    9   31    2                                             
CONECT    9    8   10                                                       
CONECT   10    9   11                                                       
CONECT   11   10   12   30   16                                             
CONECT   12   11   13    2                                                  
CONECT   13   12   14                                                       
CONECT   14   13   15   20                                                  
CONECT   15   14   16   17                                                  
CONECT   16   15   11                                                       
CONECT   17   15   18                                                       
CONECT   18   17   19   22                                                  
CONECT   19   18   20                                                       
CONECT   20   19   21   14                                                  
CONECT   21   20                                                            
CONECT   22   18   23   27                                                  
CONECT   23   22   24                                                       
CONECT   24   23   25                                                       
CONECT   25   24   26   28                                                  
CONECT   26   25   27                                                       
CONECT   27   26   22                                                       
CONECT   28   25   29                                                       
CONECT   29   28                                                            
CONECT   30   11                                                            
CONECT   31    8                                                            
CONECT   32    7                                                            
CONECT   33    7                                                            
MASTER        0    0    0    0    0    0    0    0   33    0   74    0
END

Synonyms

Not Available

Molecular Formula

C₂₇H₃₂O₆

Average Mass

452.547

Monoisotopic Mass

452.21988875

IUPAC Name

(5aR,7aS,11aR,11bR)-7a-hydroxy-3-(4-methoxyphenyl)-5a,8,8,11a-tetramethyl-1,5a,6,7,7a,8,9,10,11,11a,11b,12-dodecahydro-2,5-dioxatetraphene-1,9-dione

Traditional Name

(5aR,7aS,11aR,11bR)-7a-hydroxy-3-(4-methoxyphenyl)-5a,8,8,11a-tetramethyl-6,7,10,11,11b,12-hexahydro-2,5-dioxatetraphene-1,9-dione

CAS Registry Number

Not Available

SMILES

COC1=CC=C(C=C1)C1=CC2=C(C[C@H]3[C@@](C)(CC[C@@]4(O)C(C)(C)C(=O)CC[C@]34C)O2)C(=O)O1

InChI Identifier

InChI=1S/C27H32O6/c1-24(2)22(28)10-11-25(3)21-14-18-20(33-26(21,4)12-13-27(24,25)30)15-19(32-23(18)29)16-6-8-17(31-5)9-7-16/h6-9,15,21,30H,10-14H2,1-5H3/t21-,25-,26-,27-/m1/s1

InChI Key

XKDGQMPLQPRTCS-HHPVDLARSA-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
Anisole
Methoxybenzene
Phenol ether
Alkyl aryl ether
Pyranone
Monocyclic benzene moiety
Benzenoid
Pyran
Cyclic alcohol
Heteroaromatic compound
Vinylogous ester
Tertiary alcohol
Lactone
Ketone
Cyclic ketone
Oxacycle
Ether
Organic oxygen compound
Alcohol
Carbonyl group
Hydrocarbon derivative
Organooxygen compound
Organic oxide
Aromatic heteropolycyclic compound

Molecular Framework

Aromatic heteropolycyclic compounds

External Descriptors

cyclic ketone (CHEBI:65437 )
tertiary alcohol (CHEBI:65437 )
aromatic ether (CHEBI:65437 )
organic heterotetracyclic compound (CHEBI:65437 )
delta-lactone (CHEBI:65437 )

Functional Ontology

Not Available

Physical Properties

State

Expected Solid

Predicted Properties

Property	Value	Source
Water Solubility	0.0023 g/L	ALOGPS
logP	4.17	ALOGPS
logP	3.75	ChemAxon
logS	-5.3	ALOGPS
pKa (Strongest Acidic)	13.86	ChemAxon
pKa (Strongest Basic)	-3.3	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	5	ChemAxon
Hydrogen Donor Count	1	ChemAxon
Polar Surface Area	82.06 Å²	ChemAxon
Rotatable Bond Count	2	ChemAxon
Refractivity	125.03 m³·mol⁻¹	ChemAxon
Polarizability	50.21 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

This table shows at most 5 pathways. For the full list of associated pathways:

See All Associated Bacterial Pathways

Name	SMPDB/PathBank	Species

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	2	Human sputum; Human ; 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

8679213

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

10503812

PDB ID

Not Available

ChEBI ID

65437

Food Biomarker Ontology

Not Available

CMMC Knowledgebase

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 Arisugacin C (MMDBc0014417)

MOL for #<Metabolite:0x00007f287c42fa08>

3D MOL for #<Metabolite:0x00007f287c42fa08>

3D SDF for #<Metabolite:0x00007f287c42fa08>

3D-SDF for #<Metabolite:0x00007f287c42fa08>

PDB for #<Metabolite:0x00007f287c42fa08>

3D PDB for #<Metabolite:0x00007f287c42fa08>

SMILES for #<Metabolite:0x00007f287c42fa08>

INCHI for #<Metabolite:0x00007f287c42fa08>

Structure for #<Metabolite:0x00007f287c42fa08>

3D Structure for #<Metabolite:0x00007f287c42fa08>