MiMeDB: Showing metabocard for Chaetominine (MMDBc0015280)

Record Information

Version

1.0

Status

Detected and Quantified

Creation Date

2021-05-15 06:08:37 UTC

Update Date

2022-08-31 06:39:05 UTC

Metabolite ID

MMDBc0015280

Metabolite Identification

Common Name

Chaetominine

Description

Chaetominine belongs to the class of organic compounds known as pyridoindolones. These are pyridoindoles with a structure that contains an indole moiety bearing a ketone. Indole is a bicyclic compound consisting of a six-membered benzene ring fused to a five-membered nitrogen-containing pyrrole ring. Chaetominine is a moderately basic compound (based on its pKa).

Structure

MOL SDF PDB SMILES InChI


  Mrv1652305152108082D          

 33 38  0  0  1  0            999 V2000
   -0.1635    4.1894    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5267   -2.3896    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.1625    1.0189    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3337   -2.2181    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.4174    1.8035    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9747   -1.7766    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3555    0.8474    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5886   -1.4335    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8654    2.4166    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.4265    0.8474    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7395    0.5773    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.3111    3.5146    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   -1.2296   -0.9919    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.8035    1.4604    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0366   -0.8204    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0584    2.2451    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3805    1.0189    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.1361    3.5146    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6776   -0.3788    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6354    1.8035    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7236    2.2451    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.9785    1.4604    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   -2.2915   -0.0358    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9325    0.4058    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0834    2.4166    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    1.3910    2.7300    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    1.6210    4.1820    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.1294   -0.5504    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4424    1.9750    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.3141    0.7068    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.6912    4.2468    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1875    1.1904    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.5520    3.0520    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
  4  2  2  0  0  0  0
  5  3  2  0  0  0  0
  6  2  1  0  0  0  0
  7  3  1  0  0  0  0
  8  4  1  0  0  0  0
  9  5  1  0  0  0  0
 12  1  1  1  0  0  0
 13  6  2  0  0  0  0
 14  7  2  0  0  0  0
 15  8  2  0  0  0  0
 15 13  1  0  0  0  0
 16  9  2  0  0  0  0
 16 14  1  0  0  0  0
 17 10  1  0  0  0  0
 18 12  1  0  0  0  0
 19 13  1  0  0  0  0
 20 17  1  0  0  0  0
 22 10  1  0  0  0  0
 22 14  1  0  0  0  0
 22 21  1  0  0  0  0
 23 11  2  0  0  0  0
 23 15  1  0  0  0  0
 24 11  1  0  0  0  0
 17 24  1  1  0  0  0
 24 19  1  0  0  0  0
 25 12  1  0  0  0  0
 25 20  1  0  0  0  0
 25 21  1  0  0  0  0
 26 16  1  0  0  0  0
 26 18  1  0  0  0  0
 26 21  1  0  0  0  0
 27 18  2  0  0  0  0
 28 19  2  0  0  0  0
 29 20  2  0  0  0  0
 22 30  1  6  0  0  0
 12 31  1  6  0  0  0
 17 32  1  6  0  0  0
 21 33  1  6  0  0  0
M  END


  Mrv1652305152108082D          

 33 38  0  0  1  0            999 V2000
   -0.1635    4.1894    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5267   -2.3896    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.1625    1.0189    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3337   -2.2181    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.4174    1.8035    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9747   -1.7766    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3555    0.8474    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5886   -1.4335    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8654    2.4166    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.4265    0.8474    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7395    0.5773    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.3111    3.5146    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   -1.2296   -0.9919    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.8035    1.4604    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0366   -0.8204    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0584    2.2451    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3805    1.0189    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.1361    3.5146    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6776   -0.3788    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6354    1.8035    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7236    2.2451    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.9785    1.4604    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   -2.2915   -0.0358    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9325    0.4058    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0834    2.4166    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    1.3910    2.7300    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    1.6210    4.1820    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.1294   -0.5504    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4424    1.9750    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.3141    0.7068    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.6912    4.2468    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1875    1.1904    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.5520    3.0520    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
  4  2  2  0  0  0  0
  5  3  2  0  0  0  0
  6  2  1  0  0  0  0
  7  3  1  0  0  0  0
  8  4  1  0  0  0  0
  9  5  1  0  0  0  0
 12  1  1  1  0  0  0
 13  6  2  0  0  0  0
 14  7  2  0  0  0  0
 15  8  2  0  0  0  0
 15 13  1  0  0  0  0
 16  9  2  0  0  0  0
 16 14  1  0  0  0  0
 17 10  1  0  0  0  0
 18 12  1  0  0  0  0
 19 13  1  0  0  0  0
 20 17  1  0  0  0  0
 22 10  1  0  0  0  0
 22 14  1  0  0  0  0
 22 21  1  0  0  0  0
 23 11  2  0  0  0  0
 23 15  1  0  0  0  0
 24 11  1  0  0  0  0
 17 24  1  1  0  0  0
 24 19  1  0  0  0  0
 25 12  1  0  0  0  0
 25 20  1  0  0  0  0
 25 21  1  0  0  0  0
 26 16  1  0  0  0  0
 26 18  1  0  0  0  0
 26 21  1  0  0  0  0
 27 18  2  0  0  0  0
 28 19  2  0  0  0  0
 29 20  2  0  0  0  0
 22 30  1  6  0  0  0
 12 31  1  6  0  0  0
 17 32  1  6  0  0  0
 21 33  1  6  0  0  0
M  END
> <DATABASE_ID>
MMDBc0015280

> <DATABASE_NAME>
MIME

> <SMILES>
[H][C@@]1(C)N2C(=O)[C@@]([H])(C[C@]3(O)C4=CC=CC=C4N(C1=O)[C@]23[H])N1C=NC2=CC=CC=C2C1=O

> <INCHI_IDENTIFIER>
InChI=1S/C22H18N4O4/c1-12-18(27)26-16-9-5-3-7-14(16)22(30)10-17(20(29)25(12)21(22)26)24-11-23-15-8-4-2-6-13(15)19(24)28/h2-9,11-12,17,21,30H,10H2,1H3/t12-,17+,21-,22-/m0/s1

> <INCHI_KEY>
GEURDGODABUDHB-TYTLQBBQSA-N

> <FORMULA>
C22H18N4O4

> <MOLECULAR_WEIGHT>
402.41

> <EXACT_MASS>
402.132805076

> <JCHEM_ACCEPTOR_COUNT>
5

> <JCHEM_ATOM_COUNT>
48

> <JCHEM_AVERAGE_POLARIZABILITY>
40.0372609811095

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
1

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
(1S,10S,13R,15S)-1-hydroxy-10-methyl-13-(4-oxo-3,4-dihydroquinazolin-3-yl)-8,11-diazatetracyclo[6.6.1.0^{2,7}.0^{11,15}]pentadeca-2,4,6-triene-9,12-dione

> <ALOGPS_LOGP>
0.86

> <JCHEM_LOGP>
0.7113314853333338

> <ALOGPS_LOGS>
-3.15

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
6

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
15.529926100222998

> <JCHEM_PKA_STRONGEST_ACIDIC>
12.880888687034588

> <JCHEM_PKA_STRONGEST_BASIC>
2.735949537233905

> <JCHEM_POLAR_SURFACE_AREA>
93.52000000000001

> <JCHEM_REFRACTIVITY>
107.28500000000003

> <JCHEM_ROTATABLE_BOND_COUNT>
1

> <JCHEM_RULE_OF_FIVE>
1

> <ALOGPS_SOLUBILITY>
2.85e-01 g/l

> <JCHEM_TRADITIONAL_IUPAC>
(1S,10S,13R,15S)-1-hydroxy-10-methyl-13-(4-oxoquinazolin-3-yl)-8,11-diazatetracyclo[6.6.1.0^{2,7}.0^{11,15}]pentadeca-2,4,6-triene-9,12-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      -0.305   7.820   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0      -2.850  -4.461   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0       5.903   1.902   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0      -4.356  -4.140   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0       6.379   3.367   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0      -1.819  -3.316   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0       4.397   1.582   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0      -4.832  -2.676   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0       5.349   4.511   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0       0.796   1.582   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0      -3.247   1.078   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0       0.581   6.561   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0      -2.295  -1.852   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0       3.367   2.726   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0      -3.802  -1.531   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0       3.842   4.191   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0      -0.710   1.902   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0       2.121   6.561   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0      -1.265  -0.707   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0      -1.186   3.367   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0       1.351   4.191   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0       1.827   2.726   0.000  0.00  0.00           C+0
HETATM   23  N   UNK     0      -4.278  -0.067   0.000  0.00  0.00           N+0
HETATM   24  N   UNK     0      -1.741   0.757   0.000  0.00  0.00           N+0
HETATM   25  N   UNK     0      -0.156   4.511   0.000  0.00  0.00           N+0
HETATM   26  N   UNK     0       2.597   5.096   0.000  0.00  0.00           N+0
HETATM   27  O   UNK     0       3.026   7.806   0.000  0.00  0.00           O+0
HETATM   28  O   UNK     0       0.241  -1.027   0.000  0.00  0.00           O+0
HETATM   29  O   UNK     0      -2.693   3.687   0.000  0.00  0.00           O+0
HETATM   30  O   UNK     0       2.453   1.319   0.000  0.00  0.00           O+0
HETATM   31  H   UNK     0       1.290   7.927   0.000  0.00  0.00           H+0
HETATM   32  H   UNK     0      -2.217   2.222   0.000  0.00  0.00           H+0
HETATM   33  H   UNK     0       1.030   5.697   0.000  0.00  0.00           H+0
CONECT    1   12                                                            
CONECT    2    4    6                                                       
CONECT    3    5    7                                                       
CONECT    4    2    8                                                       
CONECT    5    3    9                                                       
CONECT    6    2   13                                                       
CONECT    7    3   14                                                       
CONECT    8    4   15                                                       
CONECT    9    5   16                                                       
CONECT   10   17   22                                                       
CONECT   11   23   24                                                       
CONECT   12    1   18   25   31                                             
CONECT   13    6   15   19                                                  
CONECT   14    7   16   22                                                  
CONECT   15    8   13   23                                                  
CONECT   16    9   14   26                                                  
CONECT   17   10   20   24   32                                             
CONECT   18   12   26   27                                                  
CONECT   19   13   24   28                                                  
CONECT   20   17   25   29                                                  
CONECT   21   22   25   26   33                                             
CONECT   22   10   14   21   30                                             
CONECT   23   11   15                                                       
CONECT   24   11   17   19                                                  
CONECT   25   12   20   21                                                  
CONECT   26   16   18   21                                                  
CONECT   27   18                                                            
CONECT   28   19                                                            
CONECT   29   20                                                            
CONECT   30   22                                                            
CONECT   31   12                                                            
CONECT   32   17                                                            
CONECT   33   21                                                            
MASTER        0    0    0    0    0    0    0    0   33    0   76    0
END

Synonyms

Not Available

Molecular Formula

C₂₂H₁₈N₄O₄

Average Mass

402.41

Monoisotopic Mass

402.132805076

IUPAC Name

(1S,10S,13R,15S)-1-hydroxy-10-methyl-13-(4-oxo-3,4-dihydroquinazolin-3-yl)-8,11-diazatetracyclo[6.6.1.0^{2,7}.0^{11,15}]pentadeca-2,4,6-triene-9,12-dione

Traditional Name

(1S,10S,13R,15S)-1-hydroxy-10-methyl-13-(4-oxoquinazolin-3-yl)-8,11-diazatetracyclo[6.6.1.0^{2,7}.0^{11,15}]pentadeca-2,4,6-triene-9,12-dione

CAS Registry Number

Not Available

SMILES

[H][C@@]1(C)N2C(=O)[C@@]([H])(C[C@]3(O)C4=CC=CC=C4N(C1=O)[C@]23[H])N1C=NC2=CC=CC=C2C1=O

InChI Identifier

InChI=1S/C22H18N4O4/c1-12-18(27)26-16-9-5-3-7-14(16)22(30)10-17(20(29)25(12)21(22)26)24-11-23-15-8-4-2-6-13(15)19(24)28/h2-9,11-12,17,21,30H,10H2,1H3/t12-,17+,21-,22-/m0/s1

InChI Key

GEURDGODABUDHB-TYTLQBBQSA-N

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as pyridoindolones. These are pyridoindoles with a structure that contains an indole moiety bearing a ketone. Indole is a bicyclic compound consisting of a six-membered benzene ring fused to a five-membered nitrogen-containing pyrrole ring.

Kingdom

Organic compounds

Super Class

Organoheterocyclic compounds

Class

Indoles and derivatives

Sub Class

Pyridoindoles

Direct Parent

Pyridoindolones

Alternative Parents

Substituents

Pyridoindolone
Alpha-carboline
Diazanaphthalene
Alpha-amino acid or derivatives
Quinazoline
Imidazopyridine
Indole
Delta-lactam
Piperidinone
Pyrimidone
Imidazolidinone
Piperidine
Pyridine
Pyrimidine
Benzenoid
Tertiary alcohol
Heteroaromatic compound
Tertiary carboxylic acid amide
Imidazolidine
Carboxamide group
Lactam
Azacycle
Carboxylic acid derivative
Organic oxygen compound
Alcohol
Organic oxide
Organopnictogen compound
Hydrocarbon derivative
Organonitrogen compound
Organooxygen compound
Carbonyl group
Organic nitrogen compound
Aromatic heteropolycyclic compound

Molecular Framework

Aromatic heteropolycyclic compounds

External Descriptors

organic heterotetracyclic compound (CHEBI:65610 )
indole alkaloid (CHEBI:65610 )
lactam (CHEBI:65610 )
quinazolines (CHEBI:65610 )

Functional Ontology

Not Available

Physical Properties

State

Expected Solid

Predicted Properties

Property	Value	Source
Water Solubility	0.28 g/L	ALOGPS
logP	0.86	ALOGPS
logP	0.71	ChemAxon
logS	-3.2	ALOGPS
pKa (Strongest Acidic)	12.88	ChemAxon
pKa (Strongest Basic)	2.74	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	5	ChemAxon
Hydrogen Donor Count	1	ChemAxon
Polar Surface Area	93.52 Å²	ChemAxon
Rotatable Bond Count	1	ChemAxon
Refractivity	107.28 m³·mol⁻¹	ChemAxon
Polarizability	40.04 Å³	ChemAxon
Number of Rings	6	ChemAxon
Bioavailability	Yes	ChemAxon
Rule of Five	Yes	ChemAxon
Ghose Filter	Yes	ChemAxon
Veber's Rule	No	ChemAxon
MDDR-like Rule	No	ChemAxon

Spectra

Spectrum Type	Description	Splash Key	Deposition Date	View
Predicted GC-MS	Predicted GC-MS Spectrum - GC-MS (TMS_1_1) - 70eV, Positive	Not Available	2022-08-08	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 10V, Positive	Not Available	2022-08-09	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 20V, Positive	Not Available	2022-08-09	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 40V, Positive	Not Available	2022-08-09	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 10V, Negative	Not Available	2022-08-09	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 20V, Negative	Not Available	2022-08-09	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 40V, Negative	Not Available	2022-08-09	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

Metabolic Reactions

Not Available

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	3	Human feces	Metabolic reconstruction

Exposure Sources

Source Type	Source Sub-type	Species	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

17253564

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

16095273

PDB ID

Not Available

ChEBI ID

65610

Food Biomarker Ontology

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 Chaetominine (MMDBc0015280)

MOL for #<Metabolite:0x00005634c2831038>

3D MOL for #<Metabolite:0x00005634c2831038>

3D SDF for #<Metabolite:0x00005634c2831038>

3D-SDF for #<Metabolite:0x00005634c2831038>

PDB for #<Metabolite:0x00005634c2831038>

3D PDB for #<Metabolite:0x00005634c2831038>

SMILES for #<Metabolite:0x00005634c2831038>

INCHI for #<Metabolite:0x00005634c2831038>

Structure for #<Metabolite:0x00005634c2831038>

3D Structure for #<Metabolite:0x00005634c2831038>