MiMeDB: Showing metabocard for Aspergillamide C (MMDBc0027010)

Record Information

Version

1.0

Status

Detected and Quantified

Creation Date

2021-05-15 16:42:12 UTC

Update Date

2022-08-31 06:52:26 UTC

Metabolite ID

MMDBc0027010

Metabolite Identification

Common Name

Aspergillamide C

Description

Aspergillamide C belongs to the class of organic compounds known as dipeptides. These are organic compounds containing a sequence of exactly two alpha-amino acids joined by a peptide bond. Based on a literature review very few articles have been published on Aspergillamide C.

Structure

MOL SDF PDB SMILES InChI


  Mrv1652305152118422D          

 41 43  0  0  1  0            999 V2000
   -5.7322   -0.3533    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.3033   -1.1783    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.0177    0.8842    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1599    0.8842    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.0177    0.0592    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3284   -3.3423    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0735   -4.1270    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7764   -2.7292    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2665   -4.2985    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0164    1.2967    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4454    1.2967    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0164    2.1217    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4454    2.1217    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.6980   -1.5908    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0164   -1.1783    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7309    0.0592    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.3655   -2.9008    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.3033   -0.3533    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   -4.3033    1.2967    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7309    0.8842    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.6980   -2.4158    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7309    2.5342    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0306   -2.9008    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.2855   -3.6854    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4454   -0.3533    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   -3.5888    0.0592    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   -1.4454   -1.1783    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8743   -0.3533    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7309   -1.5908    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    1.1105   -3.6854    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5888    0.8842    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1599    0.0592    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
   -4.3033    2.1217    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7309    3.3592    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1599   -1.5908    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8743   -1.1783    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.4125   -1.1783    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0164   -0.3533    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.0177   -0.7658    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7309   -0.7658    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5888   -0.7658    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
  5  1  1  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
 12 10  1  0  0  0  0
 13 11  2  0  0  0  0
 15 14  2  0  0  0  0
 18  2  1  1  0  0  0
 18  5  1  0  0  0  0
 19  3  1  4  0  0  0
 20 10  2  0  0  0  0
 20 11  1  0  0  0  0
 20 16  1  0  0  0  0
 21 14  1  0  0  0  0
 21 17  2  0  0  0  0
 22 12  2  0  0  0  0
 22 13  1  0  0  0  0
 23  8  2  0  0  0  0
 23 21  1  0  0  0  0
 24  9  2  0  0  0  0
 24 23  1  0  0  0  0
 25 16  1  0  0  0  0
 26 18  1  0  0  0  0
 27 25  1  0  0  0  0
 28 26  1  0  0  0  0
 29 15  1  4  0  0  0
 29 27  2  0  0  0  0
 30 17  1  0  0  0  0
 30 24  1  0  0  0  0
 31 19  2  0  0  0  0
 26 31  1  1  0  0  0
 32  4  1  0  0  0  0
 25 32  1  6  0  0  0
 32 28  1  0  0  0  0
 33 19  1  0  0  0  0
 34 22  1  0  0  0  0
 35 27  1  0  0  0  0
 36 28  2  0  0  0  0
 37 14  1  0  0  0  0
 38 15  1  0  0  0  0
 18 39  1  6  0  0  0
 25 40  1  6  0  0  0
 26 41  1  1  0  0  0
M  END


  Mrv1652305152118422D          

 41 43  0  0  1  0            999 V2000
   -5.7322   -0.3533    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.3033   -1.1783    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.0177    0.8842    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1599    0.8842    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.0177    0.0592    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3284   -3.3423    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0735   -4.1270    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7764   -2.7292    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2665   -4.2985    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0164    1.2967    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4454    1.2967    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0164    2.1217    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4454    2.1217    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.6980   -1.5908    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0164   -1.1783    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7309    0.0592    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.3655   -2.9008    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.3033   -0.3533    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   -4.3033    1.2967    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7309    0.8842    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.6980   -2.4158    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7309    2.5342    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0306   -2.9008    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.2855   -3.6854    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4454   -0.3533    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   -3.5888    0.0592    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   -1.4454   -1.1783    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8743   -0.3533    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7309   -1.5908    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    1.1105   -3.6854    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5888    0.8842    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1599    0.0592    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
   -4.3033    2.1217    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7309    3.3592    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1599   -1.5908    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8743   -1.1783    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.4125   -1.1783    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0164   -0.3533    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.0177   -0.7658    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7309   -0.7658    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5888   -0.7658    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
  5  1  1  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
 12 10  1  0  0  0  0
 13 11  2  0  0  0  0
 15 14  2  0  0  0  0
 18  2  1  1  0  0  0
 18  5  1  0  0  0  0
 19  3  1  4  0  0  0
 20 10  2  0  0  0  0
 20 11  1  0  0  0  0
 20 16  1  0  0  0  0
 21 14  1  0  0  0  0
 21 17  2  0  0  0  0
 22 12  2  0  0  0  0
 22 13  1  0  0  0  0
 23  8  2  0  0  0  0
 23 21  1  0  0  0  0
 24  9  2  0  0  0  0
 24 23  1  0  0  0  0
 25 16  1  0  0  0  0
 26 18  1  0  0  0  0
 27 25  1  0  0  0  0
 28 26  1  0  0  0  0
 29 15  1  4  0  0  0
 29 27  2  0  0  0  0
 30 17  1  0  0  0  0
 30 24  1  0  0  0  0
 31 19  2  0  0  0  0
 26 31  1  1  0  0  0
 32  4  1  0  0  0  0
 25 32  1  6  0  0  0
 32 28  1  0  0  0  0
 33 19  1  0  0  0  0
 34 22  1  0  0  0  0
 35 27  1  0  0  0  0
 36 28  2  0  0  0  0
 37 14  1  0  0  0  0
 38 15  1  0  0  0  0
 18 39  1  6  0  0  0
 25 40  1  6  0  0  0
 26 41  1  1  0  0  0
M  END
> <DATABASE_ID>
MMDBc0027010

> <DATABASE_NAME>
MIME

> <SMILES>
[H]\C(N=C(O)[C@]([H])(CC1=CC=C(O)C=C1)N(C)C(=O)[C@@]([H])(N=C(C)O)[C@@]([H])(C)CC)=C(/[H])C1=CNC2=CC=CC=C12

> <INCHI_IDENTIFIER>
InChI=1S/C28H34N4O4/c1-5-18(2)26(31-19(3)33)28(36)32(4)25(16-20-10-12-22(34)13-11-20)27(35)29-15-14-21-17-30-24-9-7-6-8-23(21)24/h6-15,17-18,25-26,30,34H,5,16H2,1-4H3,(H,29,35)(H,31,33)/b15-14-/t18-,25-,26-/m0/s1

> <INCHI_KEY>
NZRQIPUGMHEHIL-AQFPYVEVSA-N

> <FORMULA>
C28H34N4O4

> <MOLECULAR_WEIGHT>
490.604

> <EXACT_MASS>
490.258005591

> <JCHEM_ACCEPTOR_COUNT>
6

> <JCHEM_ATOM_COUNT>
70

> <JCHEM_AVERAGE_POLARIZABILITY>
53.15004820047905

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
4

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
(2S)-2-[(2S,3S)-2-[(1-hydroxyethylidene)amino]-N,3-dimethylpentanamido]-3-(4-hydroxyphenyl)-N-[(Z)-2-(1H-indol-3-yl)ethenyl]propanimidic acid

> <ALOGPS_LOGP>
4.23

> <JCHEM_LOGP>
3.5761801735430137

> <ALOGPS_LOGS>
-5.23

> <JCHEM_MDDR_LIKE_RULE>
1

> <JCHEM_NUMBER_OF_RINGS>
3

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
6.250445464998659

> <JCHEM_PKA_STRONGEST_ACIDIC>
3.3441888013477716

> <JCHEM_PKA_STRONGEST_BASIC>
5.629649603722625

> <JCHEM_POLAR_SURFACE_AREA>
121.51000000000002

> <JCHEM_REFRACTIVITY>
140.64120000000005

> <JCHEM_ROTATABLE_BOND_COUNT>
10

> <JCHEM_RULE_OF_FIVE>
1

> <ALOGPS_SOLUBILITY>
2.87e-03 g/l

> <JCHEM_TRADITIONAL_IUPAC>
(2S)-2-[(2S,3S)-2-[(1-hydroxyethylidene)amino]-N,3-dimethylpentanamido]-3-(4-hydroxyphenyl)-N-[(Z)-2-(1H-indol-3-yl)ethenyl]propanimidic acid

> <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     -10.700  -0.660   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0      -8.033  -2.200   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0      -9.366   1.650   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0      -4.032   1.650   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0      -9.366   0.110   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0      -2.480  -6.239   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0      -2.004  -7.704   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0      -1.449  -5.095   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0      -0.497  -8.024   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0      -0.031   2.420   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0      -2.698   2.420   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0      -0.031   3.960   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0      -2.698   3.960   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0       1.303  -2.970   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0      -0.031  -2.200   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0      -1.364   0.110   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0       2.549  -5.415   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0      -8.033  -0.660   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0      -8.033   2.420   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0      -1.364   1.650   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0       1.303  -4.510   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0      -1.364   4.730   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0       0.057  -5.415   0.000  0.00  0.00           C+0
HETATM   24  C   UNK     0       0.533  -6.879   0.000  0.00  0.00           C+0
HETATM   25  C   UNK     0      -2.698  -0.660   0.000  0.00  0.00           C+0
HETATM   26  C   UNK     0      -6.699   0.110   0.000  0.00  0.00           C+0
HETATM   27  C   UNK     0      -2.698  -2.200   0.000  0.00  0.00           C+0
HETATM   28  C   UNK     0      -5.365  -0.660   0.000  0.00  0.00           C+0
HETATM   29  N   UNK     0      -1.364  -2.970   0.000  0.00  0.00           N+0
HETATM   30  N   UNK     0       2.073  -6.879   0.000  0.00  0.00           N+0
HETATM   31  N   UNK     0      -6.699   1.650   0.000  0.00  0.00           N+0
HETATM   32  N   UNK     0      -4.032   0.110   0.000  0.00  0.00           N+0
HETATM   33  O   UNK     0      -8.033   3.960   0.000  0.00  0.00           O+0
HETATM   34  O   UNK     0      -1.364   6.270   0.000  0.00  0.00           O+0
HETATM   35  O   UNK     0      -4.032  -2.970   0.000  0.00  0.00           O+0
HETATM   36  O   UNK     0      -5.365  -2.200   0.000  0.00  0.00           O+0
HETATM   37  H   UNK     0       2.637  -2.200   0.000  0.00  0.00           H+0
HETATM   38  H   UNK     0      -0.031  -0.660   0.000  0.00  0.00           H+0
HETATM   39  H   UNK     0      -9.366  -1.430   0.000  0.00  0.00           H+0
HETATM   40  H   UNK     0      -1.364  -1.430   0.000  0.00  0.00           H+0
HETATM   41  H   UNK     0      -6.699  -1.430   0.000  0.00  0.00           H+0
CONECT    1    5                                                            
CONECT    2   18                                                            
CONECT    3   19                                                            
CONECT    4   32                                                            
CONECT    5    1   18                                                       
CONECT    6    7    8                                                       
CONECT    7    6    9                                                       
CONECT    8    6   23                                                       
CONECT    9    7   24                                                       
CONECT   10   12   20                                                       
CONECT   11   13   20                                                       
CONECT   12   10   22                                                       
CONECT   13   11   22                                                       
CONECT   14   15   21   37                                                  
CONECT   15   14   29   38                                                  
CONECT   16   20   25                                                       
CONECT   17   21   30                                                       
CONECT   18    2    5   26   39                                             
CONECT   19    3   31   33                                                  
CONECT   20   10   11   16                                                  
CONECT   21   14   17   23                                                  
CONECT   22   12   13   34                                                  
CONECT   23    8   21   24                                                  
CONECT   24    9   23   30                                                  
CONECT   25   16   27   32   40                                             
CONECT   26   18   28   31   41                                             
CONECT   27   25   29   35                                                  
CONECT   28   26   32   36                                                  
CONECT   29   15   27                                                       
CONECT   30   17   24                                                       
CONECT   31   19   26                                                       
CONECT   32    4   25   28                                                  
CONECT   33   19                                                            
CONECT   34   22                                                            
CONECT   35   27                                                            
CONECT   36   28                                                            
CONECT   37   14                                                            
CONECT   38   15                                                            
CONECT   39   18                                                            
CONECT   40   25                                                            
CONECT   41   26                                                            
MASTER        0    0    0    0    0    0    0    0   41    0   86    0
END

Synonyms

Not Available

Molecular Formula

C₂₈H₃₄N₄O₄

Average Mass

490.604

Monoisotopic Mass

490.258005591

IUPAC Name

(2S)-2-[(2S,3S)-2-[(1-hydroxyethylidene)amino]-N,3-dimethylpentanamido]-3-(4-hydroxyphenyl)-N-[(Z)-2-(1H-indol-3-yl)ethenyl]propanimidic acid

Traditional Name

(2S)-2-[(2S,3S)-2-[(1-hydroxyethylidene)amino]-N,3-dimethylpentanamido]-3-(4-hydroxyphenyl)-N-[(Z)-2-(1H-indol-3-yl)ethenyl]propanimidic acid

CAS Registry Number

Not Available

SMILES

[H]\C(N=C(O)[C@]([H])(CC1=CC=C(O)C=C1)N(C)C(=O)[C@@]([H])(N=C(C)O)[C@@]([H])(C)CC)=C(/[H])C1=CNC2=CC=CC=C12

InChI Identifier

InChI=1S/C28H34N4O4/c1-5-18(2)26(31-19(3)33)28(36)32(4)25(16-20-10-12-22(34)13-11-20)27(35)29-15-14-21-17-30-24-9-7-6-8-23(21)24/h6-15,17-18,25-26,30,34H,5,16H2,1-4H3,(H,29,35)(H,31,33)/b15-14-/t18-,25-,26-/m0/s1

InChI Key

NZRQIPUGMHEHIL-AQFPYVEVSA-N

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as dipeptides. These are organic compounds containing a sequence of exactly two alpha-amino acids joined by a peptide bond.

Kingdom

Organic compounds

Super Class

Organic acids and derivatives

Class

Carboxylic acids and derivatives

Sub Class

Amino acids, peptides, and analogues

Direct Parent

Dipeptides

Alternative Parents

Substituents

Alpha-dipeptide
Tyrosine or derivatives
Phenylalanine or derivatives
Isoleucine or derivatives
N-acyl-alpha amino acid or derivatives
Alpha-amino acid amide
Amphetamine or derivatives
Alpha-amino acid or derivatives
Indole or derivatives
Indole
1-hydroxy-2-unsubstituted benzenoid
Phenol
Fatty acyl
Benzenoid
Substituted pyrrole
N-acyl-amine
Fatty amide
Monocyclic benzene moiety
Heteroaromatic compound
Acetamide
Tertiary carboxylic acid amide
Pyrrole
Secondary carboxylic acid amide
Carboxamide group
Azacycle
Organoheterocyclic compound
Organic nitrogen compound
Organic oxygen compound
Organopnictogen compound
Organic oxide
Hydrocarbon derivative
Organooxygen compound
Organonitrogen 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	0.0029 g/L	ALOGPS
logP	4.23	ALOGPS
logP	3.58	ChemAxon
logS	-5.2	ALOGPS
pKa (Strongest Acidic)	3.34	ChemAxon
pKa (Strongest Basic)	5.63	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	6	ChemAxon
Hydrogen Donor Count	4	ChemAxon
Polar Surface Area	121.51 Å²	ChemAxon
Rotatable Bond Count	10	ChemAxon
Refractivity	140.64 m³·mol⁻¹	ChemAxon
Polarizability	53.15 Å³	ChemAxon
Number of Rings	3	ChemAxon
Bioavailability	Yes	ChemAxon
Rule of Five	Yes	ChemAxon
Ghose Filter	No	ChemAxon
Veber's Rule	No	ChemAxon
MDDR-like Rule	Yes	ChemAxon

Spectra

Chromatographic Retention Times and Retention Indices

Retention Times

Not Available

Retention Indices

Not Available

Chromatographic Retention Times and Retention Indices

Retention Times

Not Available

Retention Indices

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

146683613

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 Aspergillamide C (MMDBc0027010)

MOL for #<Metabolite:0x00007f1240c71b50>

3D MOL for #<Metabolite:0x00007f1240c71b50>

3D SDF for #<Metabolite:0x00007f1240c71b50>

3D-SDF for #<Metabolite:0x00007f1240c71b50>

PDB for #<Metabolite:0x00007f1240c71b50>

3D PDB for #<Metabolite:0x00007f1240c71b50>

SMILES for #<Metabolite:0x00007f1240c71b50>

INCHI for #<Metabolite:0x00007f1240c71b50>

Structure for #<Metabolite:0x00007f1240c71b50>

3D Structure for #<Metabolite:0x00007f1240c71b50>