MiMeDB: Showing metabocard for Chaetoglobinol A (MMDBc0016648)

Record Information

Version

2.0

Status

Detected and Quantified

Creation Date

2021-05-15 07:14:58 UTC

Update Date

2025-10-07 16:06:35 UTC

Metabolite ID

MMDBc0016648

Metabolite Identification

Common Name

Chaetoglobinol A

Description

Chaetoglobinol A is a secondary metabolite belonging to the chemical class of indole alkaloids. It was isolated from the rice culture of the fungus Chaetomium globosum, alongside other compounds such as chaetocochin J, chetomin, and cochliodinol (PMID:26125976 ). The chemical structure of Chaetoglobinol A features a complex arrangement of carbon, nitrogen, and oxygen atoms characteristic of indole alkaloids, which often exhibit diverse biological activities. In terms of biochemical pathways, Chaetoglobinol A may be involved in various metabolic processes within the fungal organism, potentially influencing secondary metabolite production and contributing to the organism's ecological interactions. Its structural features suggest potential roles in cellular signaling or defense mechanisms, although specific biological functions require further investigation. The study of such metabolites is crucial for understanding the chemical ecology of fungi and their potential applications in pharmaceuticals and agriculture.

Structure

MOL SDF PDB SMILES InChI


  Mrv1652305152109152D          

 39 43  0  0  0  0            999 V2000
   -4.6228    0.7135    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2801    1.2022    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.8513   -0.0000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.1368   -1.2375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5282   -0.2050    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.4223   -0.0000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7157   -0.3483    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.7079   -0.4125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9639   -1.7555    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.9934    0.8250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6817   -2.5308    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.2789    1.2375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6211   -1.2668    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.2789   -0.4125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6316   -3.1741    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.2949    0.4125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8104    0.5702    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.1368   -0.4125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4336   -1.1236    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.9934    0.0000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3389   -2.0421    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5645    0.0000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5740   -2.3511    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.7798   -0.2549    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8692   -2.6740    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5645    0.8250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.1256   -1.9139    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.8540   -2.3012    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0968   -1.0894    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5537   -1.8641    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7965   -0.6522    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5249   -1.0396    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4321   -3.3737    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    1.7798    1.0799    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    0.8828   -3.1257    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6316   -0.7021    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.2821   -2.2514    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.7677    0.1723    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.3419   -1.1544    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
  7  5  1  0  0  0  0
  8  6  1  0  0  0  0
 11  9  2  0  0  0  0
 12 10  2  0  0  0  0
 17  1  1  0  0  0  0
 17  2  1  0  0  0  0
 17  5  2  0  0  0  0
 18  3  1  0  0  0  0
 18  4  1  0  0  0  0
 18  6  2  0  0  0  0
 19  7  1  0  0  0  0
 19  9  1  0  0  0  0
 19 13  2  0  0  0  0
 20  8  1  0  0  0  0
 20 10  1  0  0  0  0
 20 14  2  0  0  0  0
 21 13  1  0  0  0  0
 22 14  1  0  0  0  0
 23 15  2  0  0  0  0
 23 21  1  0  0  0  0
 24 16  2  0  0  0  0
 24 22  1  0  0  0  0
 25 11  1  0  0  0  0
 25 21  2  0  0  0  0
 26 12  1  0  0  0  0
 26 22  2  0  0  0  0
 27 23  1  0  0  0  0
 28 27  2  0  0  0  0
 29 27  1  0  0  0  0
 30 28  1  0  0  0  0
 31 29  1  0  0  0  0
 32 24  1  0  0  0  0
 32 30  1  0  0  0  0
 32 31  1  0  0  0  0
 33 15  1  0  0  0  0
 33 25  1  0  0  0  0
 34 16  1  0  0  0  0
 34 26  1  0  0  0  0
 35 28  1  0  0  0  0
 36 29  2  0  0  0  0
 37 30  2  0  0  0  0
 38 31  2  0  0  0  0
 39 32  1  0  0  0  0
M  END


  Mrv1652305152109152D          

 39 43  0  0  0  0            999 V2000
   -4.6228    0.7135    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2801    1.2022    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.8513   -0.0000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.1368   -1.2375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5282   -0.2050    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.4223   -0.0000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7157   -0.3483    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.7079   -0.4125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9639   -1.7555    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.9934    0.8250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6817   -2.5308    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.2789    1.2375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6211   -1.2668    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.2789   -0.4125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6316   -3.1741    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.2949    0.4125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8104    0.5702    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.1368   -0.4125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4336   -1.1236    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.9934    0.0000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3389   -2.0421    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5645    0.0000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5740   -2.3511    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.7798   -0.2549    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8692   -2.6740    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5645    0.8250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.1256   -1.9139    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.8540   -2.3012    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0968   -1.0894    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5537   -1.8641    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7965   -0.6522    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5249   -1.0396    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4321   -3.3737    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    1.7798    1.0799    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    0.8828   -3.1257    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6316   -0.7021    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.2821   -2.2514    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.7677    0.1723    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.3419   -1.1544    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
  7  5  1  0  0  0  0
  8  6  1  0  0  0  0
 11  9  2  0  0  0  0
 12 10  2  0  0  0  0
 17  1  1  0  0  0  0
 17  2  1  0  0  0  0
 17  5  2  0  0  0  0
 18  3  1  0  0  0  0
 18  4  1  0  0  0  0
 18  6  2  0  0  0  0
 19  7  1  0  0  0  0
 19  9  1  0  0  0  0
 19 13  2  0  0  0  0
 20  8  1  0  0  0  0
 20 10  1  0  0  0  0
 20 14  2  0  0  0  0
 21 13  1  0  0  0  0
 22 14  1  0  0  0  0
 23 15  2  0  0  0  0
 23 21  1  0  0  0  0
 24 16  2  0  0  0  0
 24 22  1  0  0  0  0
 25 11  1  0  0  0  0
 25 21  2  0  0  0  0
 26 12  1  0  0  0  0
 26 22  2  0  0  0  0
 27 23  1  0  0  0  0
 28 27  2  0  0  0  0
 29 27  1  0  0  0  0
 30 28  1  0  0  0  0
 31 29  1  0  0  0  0
 32 24  1  0  0  0  0
 32 30  1  0  0  0  0
 32 31  1  0  0  0  0
 33 15  1  0  0  0  0
 33 25  1  0  0  0  0
 34 16  1  0  0  0  0
 34 26  1  0  0  0  0
 35 28  1  0  0  0  0
 36 29  2  0  0  0  0
 37 30  2  0  0  0  0
 38 31  2  0  0  0  0
 39 32  1  0  0  0  0
M  END
> <DATABASE_ID>
MMDBc0016648

> <DATABASE_NAME>
MIME

> <SMILES>
CC(C)=CCC1=CC2=C(NC=C2C2=C(O)C(=O)C(O)(C3=CNC4=C3C=C(CC=C(C)C)C=C4)C(=O)C2=O)C=C1

> <INCHI_IDENTIFIER>
InChI=1S/C32H30N2O5/c1-17(2)5-7-19-9-11-25-21(13-19)23(15-33-25)27-28(35)30(37)32(39,31(38)29(27)36)24-16-34-26-12-10-20(14-22(24)26)8-6-18(3)4/h5-6,9-16,33-35,39H,7-8H2,1-4H3

> <INCHI_KEY>
QOAPGRJTTCYFMV-UHFFFAOYSA-N

> <FORMULA>
C32H30N2O5

> <MOLECULAR_WEIGHT>
522.601

> <EXACT_MASS>
522.215472074

> <JCHEM_ACCEPTOR_COUNT>
5

> <JCHEM_ATOM_COUNT>
69

> <JCHEM_AVERAGE_POLARIZABILITY>
57.75657760266297

> <JCHEM_BIOAVAILABILITY>
0

> <JCHEM_DONOR_COUNT>
4

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
3,5-dihydroxy-3,6-bis[5-(3-methylbut-2-en-1-yl)-1H-indol-3-yl]cyclohex-5-ene-1,2,4-trione

> <ALOGPS_LOGP>
4.47

> <JCHEM_LOGP>
6.912491228666664

> <ALOGPS_LOGS>
-6.42

> <JCHEM_MDDR_LIKE_RULE>
1

> <JCHEM_NUMBER_OF_RINGS>
5

> <JCHEM_PHYSIOLOGICAL_CHARGE>
-1

> <JCHEM_PKA>
10.84186627872142

> <JCHEM_PKA_STRONGEST_ACIDIC>
4.5584078867169096

> <JCHEM_PKA_STRONGEST_BASIC>
-4.770956810034396

> <JCHEM_POLAR_SURFACE_AREA>
123.25

> <JCHEM_REFRACTIVITY>
153.74920000000003

> <JCHEM_ROTATABLE_BOND_COUNT>
6

> <JCHEM_RULE_OF_FIVE>
0

> <ALOGPS_SOLUBILITY>
1.99e-04 g/l

> <JCHEM_TRADITIONAL_IUPAC>
3,5-dihydroxy-3,6-bis[5-(3-methylbut-2-en-1-yl)-1H-indol-3-yl]cyclohex-5-ene-1,2,4-trione

> <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      -8.629   1.332   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0      -6.123   2.244   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0      12.789  -0.000   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0      11.455  -2.310   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0      -6.586  -0.383   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0      10.122  -0.000   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0      -5.069  -0.650   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0       8.788  -0.770   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0      -5.533  -3.277   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0       7.454   1.540   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0      -5.006  -4.724   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0       6.121   2.310   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0      -3.026  -2.365   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0       6.121  -0.770   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0      -1.179  -5.925   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0       2.417   0.770   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0      -7.113   1.064   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0      11.455  -0.770   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0      -4.543  -2.097   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0       7.454   0.000   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0      -2.499  -3.812   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0       4.787   0.000   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0      -1.072  -4.389   0.000  0.00  0.00           C+0
HETATM   24  C   UNK     0       3.322  -0.476   0.000  0.00  0.00           C+0
HETATM   25  C   UNK     0      -3.489  -4.992   0.000  0.00  0.00           C+0
HETATM   26  C   UNK     0       4.787   1.540   0.000  0.00  0.00           C+0
HETATM   27  C   UNK     0       0.234  -3.573   0.000  0.00  0.00           C+0
HETATM   28  C   UNK     0       1.594  -4.296   0.000  0.00  0.00           C+0
HETATM   29  C   UNK     0       0.181  -2.034   0.000  0.00  0.00           C+0
HETATM   30  C   UNK     0       2.900  -3.480   0.000  0.00  0.00           C+0
HETATM   31  C   UNK     0       1.487  -1.218   0.000  0.00  0.00           C+0
HETATM   32  C   UNK     0       2.846  -1.941   0.000  0.00  0.00           C+0
HETATM   33  N   UNK     0      -2.673  -6.298   0.000  0.00  0.00           N+0
HETATM   34  N   UNK     0       3.322   2.016   0.000  0.00  0.00           N+0
HETATM   35  O   UNK     0       1.648  -5.835   0.000  0.00  0.00           O+0
HETATM   36  O   UNK     0      -1.179  -1.311   0.000  0.00  0.00           O+0
HETATM   37  O   UNK     0       4.260  -4.203   0.000  0.00  0.00           O+0
HETATM   38  O   UNK     0       1.433   0.322   0.000  0.00  0.00           O+0
HETATM   39  O   UNK     0       4.371  -2.155   0.000  0.00  0.00           O+0
CONECT    1   17                                                            
CONECT    2   17                                                            
CONECT    3   18                                                            
CONECT    4   18                                                            
CONECT    5    7   17                                                       
CONECT    6    8   18                                                       
CONECT    7    5   19                                                       
CONECT    8    6   20                                                       
CONECT    9   11   19                                                       
CONECT   10   12   20                                                       
CONECT   11    9   25                                                       
CONECT   12   10   26                                                       
CONECT   13   19   21                                                       
CONECT   14   20   22                                                       
CONECT   15   23   33                                                       
CONECT   16   24   34                                                       
CONECT   17    1    2    5                                                  
CONECT   18    3    4    6                                                  
CONECT   19    7    9   13                                                  
CONECT   20    8   10   14                                                  
CONECT   21   13   23   25                                                  
CONECT   22   14   24   26                                                  
CONECT   23   15   21   27                                                  
CONECT   24   16   22   32                                                  
CONECT   25   11   21   33                                                  
CONECT   26   12   22   34                                                  
CONECT   27   23   28   29                                                  
CONECT   28   27   30   35                                                  
CONECT   29   27   31   36                                                  
CONECT   30   28   32   37                                                  
CONECT   31   29   32   38                                                  
CONECT   32   24   30   31   39                                             
CONECT   33   15   25                                                       
CONECT   34   16   26                                                       
CONECT   35   28                                                            
CONECT   36   29                                                            
CONECT   37   30                                                            
CONECT   38   31                                                            
CONECT   39   32                                                            
MASTER        0    0    0    0    0    0    0    0   39    0   86    0
END

Synonyms

Not Available

Molecular Formula

C₃₂H₃₀N₂O₅

Average Mass

522.601

Monoisotopic Mass

522.215472074

IUPAC Name

3,5-dihydroxy-3,6-bis[5-(3-methylbut-2-en-1-yl)-1H-indol-3-yl]cyclohex-5-ene-1,2,4-trione

Traditional Name

3,5-dihydroxy-3,6-bis[5-(3-methylbut-2-en-1-yl)-1H-indol-3-yl]cyclohex-5-ene-1,2,4-trione

CAS Registry Number

Not Available

SMILES

CC(C)=CCC1=CC2=C(NC=C2C2=C(O)C(=O)C(O)(C3=CNC4=C3C=C(CC=C(C)C)C=C4)C(=O)C2=O)C=C1

InChI Identifier

InChI=1S/C32H30N2O5/c1-17(2)5-7-19-9-11-25-21(13-19)23(15-33-25)27-28(35)30(37)32(39,31(38)29(27)36)24-16-34-26-12-10-20(14-22(24)26)8-6-18(3)4/h5-6,9-16,33-35,39H,7-8H2,1-4H3

InChI Key

QOAPGRJTTCYFMV-UHFFFAOYSA-N

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as 3-alkylindoles. 3-Alkylindoles are compounds containing an indole moiety that carries an alkyl chain at the 3-position.

Kingdom

Organic compounds

Super Class

Organoheterocyclic compounds

Class

Indoles and derivatives

Sub Class

Indoles

Direct Parent

3-alkylindoles

Alternative Parents

Substituents

3-alkylindole
M-benzoquinone
Quinone
Cyclohexenone
Acyloin
Substituted pyrrole
Benzenoid
Pyrrole
Tertiary alcohol
Heteroaromatic compound
Vinylogous acid
Ketone
Cyclic ketone
Enol
Azacycle
Hydrocarbon derivative
Alcohol
Organic oxide
Organopnictogen compound
Organic nitrogen compound
Organooxygen compound
Organonitrogen compound
Organic oxygen 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	0.0002 g/L	ALOGPS
logP	4.47	ALOGPS
logP	6.91	ChemAxon
logS	-6.4	ALOGPS
pKa (Strongest Acidic)	4.56	ChemAxon
pKa (Strongest Basic)	-4.8	ChemAxon
Physiological Charge	-1	ChemAxon
Hydrogen Acceptor Count	5	ChemAxon
Hydrogen Donor Count	4	ChemAxon
Polar Surface Area	123.25 Å²	ChemAxon
Rotatable Bond Count	6	ChemAxon
Refractivity	153.75 m³·mol⁻¹	ChemAxon
Polarizability	57.76 Å³	ChemAxon
Number of Rings	5	ChemAxon
Bioavailability	No	ChemAxon
Rule of Five	No	ChemAxon
Ghose Filter	No	ChemAxon
Veber's Rule	No	ChemAxon
MDDR-like Rule	Yes	ChemAxon

Spectra

Spectrum Type	Description	Splash Key	Deposition Date	View
Predicted GC-MS	Predicted GC-MS Spectrum - GC-MS (TMS_2_4) - 70eV, Positive	Not Available	2022-08-08	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 10V, Positive	Not Available	2022-08-10	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 20V, Positive	Not Available	2022-08-10	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 40V, Positive	Not Available	2022-08-10	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 10V, Negative	Not Available	2022-08-10	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 20V, Negative	Not Available	2022-08-10	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 40V, Negative	Not Available	2022-08-10	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 100 MHz, H₂O, predicted)		2022-08-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 100 MHz, H₂O, predicted)		2022-08-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 1000 MHz, H₂O, predicted)		2022-08-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 1000 MHz, H₂O, predicted)		2022-08-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 200 MHz, H₂O, predicted)		2022-08-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 200 MHz, H₂O, predicted)		2022-08-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 300 MHz, H₂O, predicted)		2022-08-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 300 MHz, H₂O, predicted)		2022-08-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 400 MHz, H₂O, predicted)		2022-08-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 400 MHz, H₂O, predicted)		2022-08-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 500 MHz, H₂O, predicted)		2022-08-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 500 MHz, H₂O, predicted)		2022-08-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 600 MHz, H₂O, predicted)		2022-08-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 600 MHz, H₂O, predicted)		2022-08-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 700 MHz, H₂O, predicted)		2022-08-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 700 MHz, H₂O, predicted)		2022-08-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 800 MHz, H₂O, predicted)		2022-08-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 800 MHz, H₂O, predicted)		2022-08-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 900 MHz, H₂O, predicted)		2022-08-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 900 MHz, H₂O, predicted)		2022-08-20	View Spectrum

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

59000440

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

122181663

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 Chaetoglobinol A (MMDBc0016648)

MOL for #<Metabolite:0x00005560b11b8fe8>

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Structure for #<Metabolite:0x00005560b11b8fe8>

3D Structure for #<Metabolite:0x00005560b11b8fe8>