MiMeDB: Showing metabocard for Communesin A (MMDBc0009363)

Record Information

Version

2.0

Status

Detected and Quantified

Creation Date

2021-05-15 01:54:05 UTC

Update Date

2025-10-07 16:05:35 UTC

Metabolite ID

MMDBc0009363

Metabolite Identification

Common Name

Communesin A

Description

Communesin A is a Penicillium-derived alkaloid that belongs to the chemical class of metabolites. This compound is part of a diverse family of communesin alkaloids, which have garnered attention in recent synthetic and biological research. The total synthesis of communesin A and its related alkaloids has been explored through various innovative approaches, highlighting the compound's structural complexity and potential applications (PMID:26353936 ). Notably, the synthesis of communesin A has been achieved through P450-mediated coupling of indole fragments, showcasing the intricate chemistry involved in its formation (PMID:26963294 ). Furthermore, the producing organism, identified as Penicillium marinum, has been shown to accept modified amino acid analogues, leading to the generation of mono-fluoro-communesin analogues, which underscores the biological versatility of this metabolite (PMID:18280722 ). The production of communesin A along with other extrolites from fungal sources emphasizes its significance in both natural product chemistry and potential pharmacological applications (PMID:23173673 ). Recent collaborative syntheses have further advanced the understanding of communesin A, positioning it as a compound of interest in ongoing chemical and biological studies (PMID:31356068 ).

Structure

MOL SDF PDB SMILES InChI


  Mrv1652305152103542D          

 38 45  0  0  1  0            999 V2000
    6.0213    5.3490    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.4885    5.1894    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3154    5.6599    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.9940    0.2094    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.0109    2.3682    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.1908    1.5631    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8829    1.4385    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.1177    2.2621    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.2236    2.6149    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.5836    1.0047    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.4553    0.8249    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.9947    3.0091    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.9146    3.2915    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.4762    3.6893    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.5527    4.1563    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.7461    4.9549    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.8221    2.7635    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.6163    2.0565    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.7963    1.2513    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.0948    1.3913    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.4617    2.1784    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.3310    3.4670    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    3.8214    4.1158    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.4260    1.6390    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    6.0613    3.6394    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    3.7045    4.9324    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.1482    2.7746    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    5.2785    2.4987    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    5.9927    1.0275    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    4.8464    1.0211    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    6.7672    4.1302    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    5.2296    3.8332    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    7.4498    5.3856    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.0557    4.4229    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.5954    2.6855    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.3266    3.4556    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.1657    2.0042    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.9061    4.4496    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
  6  5  2  0  0  0  0
  8  7  2  0  0  0  0
  9  5  1  0  0  0  0
 10  6  1  0  0  0  0
 11  7  1  0  0  0  0
 14 12  1  0  0  0  0
 15 13  1  0  0  0  0
 16  1  1  0  0  0  0
 17  8  1  0  0  0  0
 18  9  2  0  0  0  0
 19 10  2  0  0  0  0
 19 18  1  0  0  0  0
 20 11  2  0  0  0  0
 21 17  2  0  0  0  0
 21 20  1  0  0  0  0
 22 17  1  0  0  0  0
 23 22  1  0  0  0  0
 26  2  1  0  0  0  0
 26  3  1  0  0  0  0
 26 23  1  0  0  0  0
 27 12  1  1  0  0  0
 27 18  1  0  0  0  0
 27 25  1  0  0  0  0
 28 13  1  0  0  0  0
 28 21  1  6  0  0  0
 28 24  1  0  0  0  0
 28 27  1  0  0  0  0
 29 19  1  0  0  0  0
 29 24  1  0  0  0  0
 30  4  1  0  0  0  0
 30 20  1  0  0  0  0
 30 24  1  0  0  0  0
 31 14  1  0  0  0  0
 31 16  1  0  0  0  0
 31 25  1  0  0  0  0
 32 15  1  0  0  0  0
 32 22  1  0  0  0  0
 32 25  1  0  0  0  0
 33 16  2  0  0  0  0
 34 23  1  0  0  0  0
 34 26  1  0  0  0  0
 22 35  1  6  0  0  0
 36 23  1  0  0  0  0
 24 37  1  1  0  0  0
 25 38  1  6  0  0  0
M  END


  Mrv1652305152103542D          

 38 45  0  0  1  0            999 V2000
    6.0213    5.3490    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.4885    5.1894    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3154    5.6599    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.9940    0.2094    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.0109    2.3682    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.1908    1.5631    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8829    1.4385    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.1177    2.2621    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.2236    2.6149    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.5836    1.0047    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.4553    0.8249    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.9947    3.0091    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.9146    3.2915    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.4762    3.6893    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.5527    4.1563    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.7461    4.9549    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.8221    2.7635    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.6163    2.0565    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.7963    1.2513    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.0948    1.3913    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.4617    2.1784    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.3310    3.4670    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    3.8214    4.1158    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.4260    1.6390    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    6.0613    3.6394    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    3.7045    4.9324    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.1482    2.7746    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    5.2785    2.4987    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    5.9927    1.0275    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    4.8464    1.0211    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    6.7672    4.1302    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    5.2296    3.8332    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    7.4498    5.3856    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.0557    4.4229    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.5954    2.6855    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.3266    3.4556    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.1657    2.0042    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.9061    4.4496    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
  6  5  2  0  0  0  0
  8  7  2  0  0  0  0
  9  5  1  0  0  0  0
 10  6  1  0  0  0  0
 11  7  1  0  0  0  0
 14 12  1  0  0  0  0
 15 13  1  0  0  0  0
 16  1  1  0  0  0  0
 17  8  1  0  0  0  0
 18  9  2  0  0  0  0
 19 10  2  0  0  0  0
 19 18  1  0  0  0  0
 20 11  2  0  0  0  0
 21 17  2  0  0  0  0
 21 20  1  0  0  0  0
 22 17  1  0  0  0  0
 23 22  1  0  0  0  0
 26  2  1  0  0  0  0
 26  3  1  0  0  0  0
 26 23  1  0  0  0  0
 27 12  1  1  0  0  0
 27 18  1  0  0  0  0
 27 25  1  0  0  0  0
 28 13  1  0  0  0  0
 28 21  1  6  0  0  0
 28 24  1  0  0  0  0
 28 27  1  0  0  0  0
 29 19  1  0  0  0  0
 29 24  1  0  0  0  0
 30  4  1  0  0  0  0
 30 20  1  0  0  0  0
 30 24  1  0  0  0  0
 31 14  1  0  0  0  0
 31 16  1  0  0  0  0
 31 25  1  0  0  0  0
 32 15  1  0  0  0  0
 32 22  1  0  0  0  0
 32 25  1  0  0  0  0
 33 16  2  0  0  0  0
 34 23  1  0  0  0  0
 34 26  1  0  0  0  0
 22 35  1  6  0  0  0
 36 23  1  0  0  0  0
 24 37  1  1  0  0  0
 25 38  1  6  0  0  0
M  END
> <DATABASE_ID>
MMDBc0009363

> <DATABASE_NAME>
MIME

> <SMILES>
[H]C1(OC1(C)C)[C@@]1([H])N2CC[C@]34C5=C1C=CC=C5N(C)[C@@]3([H])NC1=CC=CC=C1[C@]41CCN(C(C)=O)[C@]21[H]

> <INCHI_IDENTIFIER>
InChI=1S/C28H32N4O2/c1-16(33)31-14-12-27-18-9-5-6-10-19(18)29-24-28(27)13-15-32(25(27)31)22(23-26(2,3)34-23)17-8-7-11-20(21(17)28)30(24)4/h5-11,22-25,29H,12-15H2,1-4H3/t22-,23?,24+,25+,27-,28-/m0/s1

> <INCHI_KEY>
QKUUVGNHUMKUAN-CBRPJXDCSA-N

> <FORMULA>
C28H32N4O2

> <MOLECULAR_WEIGHT>
456.59

> <EXACT_MASS>
456.252526286

> <JCHEM_ACCEPTOR_COUNT>
5

> <JCHEM_ATOM_COUNT>
66

> <JCHEM_AVERAGE_POLARIZABILITY>
50.17893544746474

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
1

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
1-[(2S,6R,14R,22R,25S)-25-(3,3-dimethyloxiran-2-yl)-15-methyl-1,3,13,15-tetraazaheptacyclo[18.4.1.0^{2,6}.0^{6,22}.0^{7,12}.0^{14,22}.0^{16,21}]pentacosa-7,9,11,16,18,20-hexaen-3-yl]ethan-1-one

> <ALOGPS_LOGP>
3.48

> <JCHEM_LOGP>
3.0584611903333325

> <ALOGPS_LOGS>
-3.90

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
8

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA_STRONGEST_ACIDIC>
15.41075073337715

> <JCHEM_PKA_STRONGEST_BASIC>
6.289318981809924

> <JCHEM_POLAR_SURFACE_AREA>
51.35

> <JCHEM_REFRACTIVITY>
132.44069999999996

> <JCHEM_ROTATABLE_BOND_COUNT>
1

> <JCHEM_RULE_OF_FIVE>
1

> <ALOGPS_SOLUBILITY>
5.80e-02 g/l

> <JCHEM_TRADITIONAL_IUPAC>
1-[(2S,6R,14R,22R,25S)-25-(3,3-dimethyloxiran-2-yl)-15-methyl-1,3,13,15-tetraazaheptacyclo[18.4.1.0^{2,6}.0^{6,22}.0^{7,12}.0^{14,22}.0^{16,21}]pentacosa-7,9,11,16,18,20-hexaen-3-yl]ethanone

> <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      11.240   9.985   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0       8.379   9.687   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0       6.189  10.565   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0       9.322   0.391   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0      14.954   4.421   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0      15.290   2.918   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0       5.381   2.685   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0       5.820   4.223   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0      13.484   4.881   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0      14.156   1.875   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0       6.450   1.540   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0      13.057   5.617   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0       9.174   6.144   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0      13.956   6.887   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0       8.498   7.758   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0      12.593   9.249   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0       7.135   5.159   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0      12.350   3.839   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0      12.686   2.336   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0       7.644   2.597   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0       8.328   4.066   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0       8.085   6.472   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0       7.133   7.683   0.000  0.00  0.00           C+0
HETATM   24  C   UNK     0      10.128   3.059   0.000  0.00  0.00           C+0
HETATM   25  C   UNK     0      11.314   6.794   0.000  0.00  0.00           C+0
HETATM   26  C   UNK     0       6.915   9.207   0.000  0.00  0.00           C+0
HETATM   27  C   UNK     0      11.477   5.179   0.000  0.00  0.00           C+0
HETATM   28  C   UNK     0       9.853   4.664   0.000  0.00  0.00           C+0
HETATM   29  N   UNK     0      11.186   1.918   0.000  0.00  0.00           N+0
HETATM   30  N   UNK     0       9.047   1.906   0.000  0.00  0.00           N+0
HETATM   31  N   UNK     0      12.632   7.710   0.000  0.00  0.00           N+0
HETATM   32  N   UNK     0       9.762   7.155   0.000  0.00  0.00           N+0
HETATM   33  O   UNK     0      13.906  10.053   0.000  0.00  0.00           O+0
HETATM   34  O   UNK     0       5.704   8.256   0.000  0.00  0.00           O+0
HETATM   35  H   UNK     0       8.578   5.013   0.000  0.00  0.00           H+0
HETATM   36  H   UNK     0       6.210   6.451   0.000  0.00  0.00           H+0
HETATM   37  H   UNK     0      11.509   3.741   0.000  0.00  0.00           H+0
HETATM   38  H   UNK     0      11.025   8.306   0.000  0.00  0.00           H+0
CONECT    1   16                                                            
CONECT    2   26                                                            
CONECT    3   26                                                            
CONECT    4   30                                                            
CONECT    5    6    9                                                       
CONECT    6    5   10                                                       
CONECT    7    8   11                                                       
CONECT    8    7   17                                                       
CONECT    9    5   18                                                       
CONECT   10    6   19                                                       
CONECT   11    7   20                                                       
CONECT   12   14   27                                                       
CONECT   13   15   28                                                       
CONECT   14   12   31                                                       
CONECT   15   13   32                                                       
CONECT   16    1   31   33                                                  
CONECT   17    8   21   22                                                  
CONECT   18    9   19   27                                                  
CONECT   19   10   18   29                                                  
CONECT   20   11   21   30                                                  
CONECT   21   17   20   28                                                  
CONECT   22   17   23   32   35                                             
CONECT   23   22   26   34   36                                             
CONECT   24   28   29   30   37                                             
CONECT   25   27   31   32   38                                             
CONECT   26    2    3   23   34                                             
CONECT   27   12   18   25   28                                             
CONECT   28   13   21   24   27                                             
CONECT   29   19   24                                                       
CONECT   30    4   20   24                                                  
CONECT   31   14   16   25                                                  
CONECT   32   15   22   25                                                  
CONECT   33   16                                                            
CONECT   34   23   26                                                       
CONECT   35   22                                                            
CONECT   36   23                                                            
CONECT   37   24                                                            
CONECT   38   25                                                            
MASTER        0    0    0    0    0    0    0    0   38    0   90    0
END

Synonyms

Not Available

Molecular Formula

C₂₈H₃₂N₄O₂

Average Mass

456.59

Monoisotopic Mass

456.252526286

IUPAC Name

1-[(2S,6R,14R,22R,25S)-25-(3,3-dimethyloxiran-2-yl)-15-methyl-1,3,13,15-tetraazaheptacyclo[18.4.1.0^{2,6}.0^{6,22}.0^{7,12}.0^{14,22}.0^{16,21}]pentacosa-7,9,11,16,18,20-hexaen-3-yl]ethan-1-one

Traditional Name

1-[(2S,6R,14R,22R,25S)-25-(3,3-dimethyloxiran-2-yl)-15-methyl-1,3,13,15-tetraazaheptacyclo[18.4.1.0^{2,6}.0^{6,22}.0^{7,12}.0^{14,22}.0^{16,21}]pentacosa-7,9,11,16,18,20-hexaen-3-yl]ethanone

CAS Registry Number

Not Available

SMILES

[H]C1(OC1(C)C)[C@@]1([H])N2CC[C@]34C5=C1C=CC=C5N(C)[C@@]3([H])NC1=CC=CC=C1[C@]41CCN(C(C)=O)[C@]21[H]

InChI Identifier

InChI=1S/C28H32N4O2/c1-16(33)31-14-12-27-18-9-5-6-10-19(18)29-24-28(27)13-15-32(25(27)31)22(23-26(2,3)34-23)17-8-7-11-20(21(17)28)30(24)4/h5-11,22-25,29H,12-15H2,1-4H3/t22-,23?,24+,25+,27-,28-/m0/s1

InChI Key

QKUUVGNHUMKUAN-CBRPJXDCSA-N

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as alpha carbolines. These are organic compounds containing a pyrido[2,3-b]indole core (which is a pyridine fused to an indole).

Kingdom

Organic compounds

Super Class

Organoheterocyclic compounds

Class

Indoles and derivatives

Sub Class

Pyridoindoles

Direct Parent

Alpha carbolines

Alternative Parents

Substituents

Alpha-carboline
Benzazepine
Aminoquinoline
Diazanaphthalene
Naphthyridine
Tetrahydroquinoline
Dialkylarylamine
N-acylpyrrolidine
Secondary aliphatic/aromatic amine
Azepine
Benzenoid
Piperidine
Acetamide
Tertiary carboxylic acid amide
Pyrrolidine
Carboxamide group
Amino acid or derivatives
Oxacycle
Azacycle
Secondary amine
Ether
Oxirane
Dialkyl ether
Carboxylic acid derivative
Organic nitrogen compound
Organic oxygen compound
Organopnictogen compound
Organic oxide
Hydrocarbon derivative
Organooxygen compound
Organonitrogen compound
Carbonyl group
Amine
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	0.058 g/L	ALOGPS
logP	3.48	ALOGPS
logP	3.06	ChemAxon
logS	-3.9	ALOGPS
pKa (Strongest Acidic)	15.41	ChemAxon
pKa (Strongest Basic)	6.29	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	5	ChemAxon
Hydrogen Donor Count	1	ChemAxon
Polar Surface Area	51.35 Å²	ChemAxon
Rotatable Bond Count	1	ChemAxon
Refractivity	132.44 m³·mol⁻¹	ChemAxon
Polarizability	50.18 Å³	ChemAxon
Number of Rings	8	ChemAxon
Bioavailability	Yes	ChemAxon
Rule of Five	Yes	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

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 feces; Human supragingival plaque	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

74095765

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

135011754

PDB ID

Not Available

ChEBI ID

Not Available

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 Communesin A (MMDBc0009363)

MOL for #<Metabolite:0x00007f2a9ed356b0>

3D MOL for #<Metabolite:0x00007f2a9ed356b0>

3D SDF for #<Metabolite:0x00007f2a9ed356b0>

3D-SDF for #<Metabolite:0x00007f2a9ed356b0>

PDB for #<Metabolite:0x00007f2a9ed356b0>

3D PDB for #<Metabolite:0x00007f2a9ed356b0>

SMILES for #<Metabolite:0x00007f2a9ed356b0>

INCHI for #<Metabolite:0x00007f2a9ed356b0>

Structure for #<Metabolite:0x00007f2a9ed356b0>

3D Structure for #<Metabolite:0x00007f2a9ed356b0>