MiMeDB: Showing metabocard for Deoxynortryptoquivaline (MMDBc0014701)

Record Information

Version

1.0

Status

Detected and Quantified

Creation Date

2021-05-15 05:41:19 UTC

Update Date

2022-08-31 06:38:02 UTC

Metabolite ID

MMDBc0014701

Metabolite Identification

Common Name

Deoxynortryptoquivaline

Description

Deoxynortryptoquivaline belongs to the class of organic compounds known as alpha amino acid esters. These are ester derivatives of alpha amino acids. Deoxynortryptoquivaline is a strong basic compound (based on its pKa).

Structure

MOL SDF PDB SMILES InChI


  Mrv1533004241510342D          

 38 43  0  0  0  0            999 V2000
    2.8096    1.4866    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5321    1.8849    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.8527    1.1248    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.0300    2.5426    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.8487    2.4403    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.1693    1.6801    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.9879    1.5777    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.6713    1.0224    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.7094    3.3028    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2074    3.9605    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    3.8868    4.7207    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.3847    5.3784    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.0641    6.1386    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.2455    6.2410    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7475    5.5832    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.0681    4.8231    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5701    4.1653    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.7515    4.2677    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.8908    3.4052    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    2.3928    2.7474    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6322    1.9579    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9554    1.4863    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.2976    1.9843    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.5680    2.7637    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.0963    3.4406    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.6131    0.9883    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.4379    0.9720    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    3.6774    0.1825    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.4568   -0.0878    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.0005   -0.2892    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.9842   -1.1140    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.3427    0.2088    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    1.5179    0.2251    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.9539   -0.3770    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.1505   -0.1896    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0890    0.5999    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.4750    1.2020    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.2785    1.0146    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0  0  0  0
  2  3  1  0  0  0  0
  2  4  1  0  0  0  0
  4  5  1  0  0  0  0
  5  6  1  0  0  0  0
  6  7  2  0  0  0  0
  6  8  1  0  0  0  0
  4  9  1  0  0  0  0
  9 10  2  0  0  0  0
 10 11  1  0  0  0  0
 11 12  2  0  0  0  0
 12 13  1  0  0  0  0
 13 14  2  0  0  0  0
 14 15  1  0  0  0  0
 15 16  2  0  0  0  0
 11 16  1  0  0  0  0
 16 17  1  0  0  0  0
 17 18  2  0  0  0  0
 17 19  1  0  0  0  0
  9 19  1  0  0  0  0
 19 20  1  0  0  0  0
 20 21  1  0  0  0  0
 21 22  1  0  0  0  0
 22 23  1  0  0  0  0
 23 24  1  0  0  0  0
 20 24  1  0  0  0  0
 24 25  2  0  0  0  0
 22 26  1  0  0  0  0
 26 27  1  0  0  0  0
 27 28  1  0  0  0  0
 28 29  1  0  0  0  0
 28 30  1  0  0  0  0
 30 31  2  0  0  0  0
 30 32  1  0  0  0  0
 26 32  1  0  0  0  0
 32 33  1  0  0  0  0
 33 34  2  0  0  0  0
 34 35  1  0  0  0  0
 35 36  2  0  0  0  0
 36 37  1  0  0  0  0
 37 38  2  0  0  0  0
 22 38  1  0  0  0  0
 33 38  1  0  0  0  0
M  END


  Mrv1533004241510342D          

 38 43  0  0  0  0            999 V2000
    2.8096    1.4866    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5321    1.8849    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.8527    1.1248    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.0300    2.5426    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.8487    2.4403    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.1693    1.6801    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.9879    1.5777    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.6713    1.0224    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.7094    3.3028    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2074    3.9605    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    3.8868    4.7207    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.3847    5.3784    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.0641    6.1386    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.2455    6.2410    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7475    5.5832    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.0681    4.8231    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5701    4.1653    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.7515    4.2677    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.8908    3.4052    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    2.3928    2.7474    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6322    1.9579    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9554    1.4863    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.2976    1.9843    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.5680    2.7637    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.0963    3.4406    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.6131    0.9883    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.4379    0.9720    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    3.6774    0.1825    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.4568   -0.0878    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.0005   -0.2892    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.9842   -1.1140    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.3427    0.2088    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    1.5179    0.2251    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.9539   -0.3770    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.1505   -0.1896    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0890    0.5999    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.4750    1.2020    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.2785    1.0146    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0  0  0  0
  2  3  1  0  0  0  0
  2  4  1  0  0  0  0
  4  5  1  0  0  0  0
  5  6  1  0  0  0  0
  6  7  2  0  0  0  0
  6  8  1  0  0  0  0
  4  9  1  0  0  0  0
  9 10  2  0  0  0  0
 10 11  1  0  0  0  0
 11 12  2  0  0  0  0
 12 13  1  0  0  0  0
 13 14  2  0  0  0  0
 14 15  1  0  0  0  0
 15 16  2  0  0  0  0
 11 16  1  0  0  0  0
 16 17  1  0  0  0  0
 17 18  2  0  0  0  0
 17 19  1  0  0  0  0
  9 19  1  0  0  0  0
 19 20  1  0  0  0  0
 20 21  1  0  0  0  0
 21 22  1  0  0  0  0
 22 23  1  0  0  0  0
 23 24  1  0  0  0  0
 20 24  1  0  0  0  0
 24 25  2  0  0  0  0
 22 26  1  0  0  0  0
 26 27  1  0  0  0  0
 27 28  1  0  0  0  0
 28 29  1  0  0  0  0
 28 30  1  0  0  0  0
 30 31  2  0  0  0  0
 30 32  1  0  0  0  0
 26 32  1  0  0  0  0
 32 33  1  0  0  0  0
 33 34  2  0  0  0  0
 34 35  1  0  0  0  0
 35 36  2  0  0  0  0
 36 37  1  0  0  0  0
 37 38  2  0  0  0  0
 22 38  1  0  0  0  0
 33 38  1  0  0  0  0
M  END
> <DATABASE_ID>
MMDBc0014701

> <DATABASE_NAME>
MIME

> <SMILES>
CC(C)C(OC(C)=O)C1=NC2=CC=CC=C2C(=O)N1C1CC2(OC1=O)C1NC(C)C(=O)N1C1=CC=CC=C21

> <INCHI_IDENTIFIER>
InChI=1S/C28H28N4O6/c1-14(2)22(37-16(4)33)23-30-19-11-7-5-9-17(19)25(35)31(23)21-13-28(38-26(21)36)18-10-6-8-12-20(18)32-24(34)15(3)29-27(28)32/h5-12,14-15,21-22,27,29H,13H2,1-4H3

> <INCHI_KEY>
UQWRSTHNSHDTCA-UHFFFAOYSA-N

> <FORMULA>
C28H28N4O6

> <MOLECULAR_WEIGHT>
516.554

> <EXACT_MASS>
516.200884638

> <JCHEM_ACCEPTOR_COUNT>
6

> <JCHEM_ATOM_COUNT>
66

> <JCHEM_AVERAGE_POLARIZABILITY>
53.79193526454159

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
1

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
2-methyl-1-(3-{2-methyl-3,5'-dioxo-1,2,3,9a-tetrahydrospiro[imidazolidino[1,2-a]indole-9,2'-oxolane]-4'-yl}-4-oxo-3,4-dihydroquinazolin-2-yl)propyl acetate

> <ALOGPS_LOGP>
1.87

> <JCHEM_LOGP>
2.6713501566666666

> <ALOGPS_LOGS>
-3.94

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
6

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA_STRONGEST_ACIDIC>
18.45786441712119

> <JCHEM_PKA_STRONGEST_BASIC>
3.852784576507093

> <JCHEM_POLAR_SURFACE_AREA>
117.61

> <JCHEM_REFRACTIVITY>
135.7043

> <JCHEM_ROTATABLE_BOND_COUNT>
5

> <JCHEM_RULE_OF_FIVE>
0

> <ALOGPS_SOLUBILITY>
5.96e-02 g/l

> <JCHEM_TRADITIONAL_IUPAC>
2-methyl-1-(3-{2-methyl-3,5'-dioxo-2,9a-dihydro-1H-spiro[imidazolidino[1,2-a]indole-9,2'-oxolane]-4'-yl}-4-oxoquinazolin-2-yl)propyl acetate

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 24-APR-15   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   24-APR-15         0                                  
HETATM    1  C   UNK     0       5.245   2.775   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0       6.593   3.518   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0       7.192   2.100   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0       7.523   4.746   0.000  0.00  0.00           C+0
HETATM    5  O   UNK     0       9.051   4.555   0.000  0.00  0.00           O+0
HETATM    6  C   UNK     0       9.649   3.136   0.000  0.00  0.00           C+0
HETATM    7  O   UNK     0      11.177   2.945   0.000  0.00  0.00           O+0
HETATM    8  C   UNK     0       8.720   1.908   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0       6.924   6.165   0.000  0.00  0.00           C+0
HETATM   10  N   UNK     0       7.854   7.393   0.000  0.00  0.00           N+0
HETATM   11  C   UNK     0       7.255   8.812   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0       8.185  10.040   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0       7.586  11.459   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0       6.058  11.650   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0       5.129  10.422   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0       5.727   9.003   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0       4.798   7.775   0.000  0.00  0.00           C+0
HETATM   18  O   UNK     0       3.270   7.966   0.000  0.00  0.00           O+0
HETATM   19  N   UNK     0       5.396   6.356   0.000  0.00  0.00           N+0
HETATM   20  C   UNK     0       4.467   5.129   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0       4.913   3.655   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0       3.650   2.774   0.000  0.00  0.00           C+0
HETATM   23  O   UNK     0       2.422   3.704   0.000  0.00  0.00           O+0
HETATM   24  C   UNK     0       2.927   5.159   0.000  0.00  0.00           C+0
HETATM   25  O   UNK     0       2.046   6.422   0.000  0.00  0.00           O+0
HETATM   26  C   UNK     0       4.878   1.845   0.000  0.00  0.00           C+0
HETATM   27  N   UNK     0       6.417   1.814   0.000  0.00  0.00           N+0
HETATM   28  C   UNK     0       6.864   0.341   0.000  0.00  0.00           C+0
HETATM   29  C   UNK     0       8.319  -0.164   0.000  0.00  0.00           C+0
HETATM   30  C   UNK     0       5.601  -0.540   0.000  0.00  0.00           C+0
HETATM   31  O   UNK     0       5.571  -2.079   0.000  0.00  0.00           O+0
HETATM   32  N   UNK     0       4.373   0.390   0.000  0.00  0.00           N+0
HETATM   33  C   UNK     0       2.833   0.420   0.000  0.00  0.00           C+0
HETATM   34  C   UNK     0       1.781  -0.704   0.000  0.00  0.00           C+0
HETATM   35  C   UNK     0       0.281  -0.354   0.000  0.00  0.00           C+0
HETATM   36  C   UNK     0      -0.166   1.120   0.000  0.00  0.00           C+0
HETATM   37  C   UNK     0       0.887   2.244   0.000  0.00  0.00           C+0
HETATM   38  C   UNK     0       2.387   1.894   0.000  0.00  0.00           C+0
CONECT    1    2                                                            
CONECT    2    1    3    4                                                  
CONECT    3    2                                                            
CONECT    4    2    5    9                                                  
CONECT    5    4    6                                                       
CONECT    6    5    7    8                                                  
CONECT    7    6                                                            
CONECT    8    6                                                            
CONECT    9    4   10   19                                                  
CONECT   10    9   11                                                       
CONECT   11   10   12   16                                                  
CONECT   12   11   13                                                       
CONECT   13   12   14                                                       
CONECT   14   13   15                                                       
CONECT   15   14   16                                                       
CONECT   16   15   11   17                                                  
CONECT   17   16   18   19                                                  
CONECT   18   17                                                            
CONECT   19   17    9   20                                                  
CONECT   20   19   21   24                                                  
CONECT   21   20   22                                                       
CONECT   22   21   23   26   38                                             
CONECT   23   22   24                                                       
CONECT   24   23   20   25                                                  
CONECT   25   24                                                            
CONECT   26   22   27   32                                                  
CONECT   27   26   28                                                       
CONECT   28   27   29   30                                                  
CONECT   29   28                                                            
CONECT   30   28   31   32                                                  
CONECT   31   30                                                            
CONECT   32   30   26   33                                                  
CONECT   33   32   34   38                                                  
CONECT   34   33   35                                                       
CONECT   35   34   36                                                       
CONECT   36   35   37                                                       
CONECT   37   36   38                                                       
CONECT   38   37   22   33                                                  
MASTER        0    0    0    0    0    0    0    0   38    0   86    0
END

Synonyms

Value	Source
2-Methyl-1-(3-{2-methyl-3,5'-dioxo-1,2,3,9a-tetrahydrospiro[imidazo[1,2-a]indole-9,2'-oxolane]-4'-yl}-4-oxo-3,4-dihydroquinazolin-2-yl)propyl acetic acid	Generator

Molecular Formula

C₂₈H₂₈N₄O₆

Average Mass

516.554

Monoisotopic Mass

516.200884638

IUPAC Name

2-methyl-1-(3-{2-methyl-3,5'-dioxo-1,2,3,9a-tetrahydrospiro[imidazolidino[1,2-a]indole-9,2'-oxolane]-4'-yl}-4-oxo-3,4-dihydroquinazolin-2-yl)propyl acetate

Traditional Name

2-methyl-1-(3-{2-methyl-3,5'-dioxo-2,9a-dihydro-1H-spiro[imidazolidino[1,2-a]indole-9,2'-oxolane]-4'-yl}-4-oxoquinazolin-2-yl)propyl acetate

CAS Registry Number

Not Available

SMILES

CC(C)C(OC(C)=O)C1=NC2=CC=CC=C2C(=O)N1C1CC2(OC1=O)C1NC(C)C(=O)N1C1=CC=CC=C21

InChI Identifier

InChI=1S/C28H28N4O6/c1-14(2)22(37-16(4)33)23-30-19-11-7-5-9-17(19)25(35)31(23)21-13-28(38-26(21)36)18-10-6-8-12-20(18)32-24(34)15(3)29-27(28)32/h5-12,14-15,21-22,27,29H,13H2,1-4H3

InChI Key

UQWRSTHNSHDTCA-UHFFFAOYSA-N

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as alpha amino acid esters. These are ester derivatives of alpha amino acids.

Kingdom

Organic compounds

Super Class

Organic acids and derivatives

Class

Carboxylic acids and derivatives

Sub Class

Amino acids, peptides, and analogues

Direct Parent

Alpha amino acid esters

Alternative Parents

Substituents

Alpha-amino acid ester
Diazanaphthalene
Quinazoline
Indole or derivatives
Pyrimidone
Dicarboxylic acid or derivatives
Gamma butyrolactone
Imidazolidinone
Pyrimidine
Benzenoid
Tetrahydrofuran
Tertiary carboxylic acid amide
Heteroaromatic compound
Imidazolidine
Carboxamide group
Carboxylic acid ester
Lactone
Lactam
Secondary amine
Oxacycle
Azacycle
Organoheterocyclic compound
Secondary aliphatic amine
Hydrocarbon derivative
Amine
Organic nitrogen compound
Organic oxygen compound
Organonitrogen compound
Organooxygen compound
Carbonyl group
Organopnictogen compound
Organic oxide
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	0.06 g/L	ALOGPS
logP	1.87	ALOGPS
logP	2.67	ChemAxon
logS	-3.9	ALOGPS
pKa (Strongest Acidic)	18.46	ChemAxon
pKa (Strongest Basic)	3.85	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	6	ChemAxon
Hydrogen Donor Count	1	ChemAxon
Polar Surface Area	117.61 Å²	ChemAxon
Rotatable Bond Count	5	ChemAxon
Refractivity	135.7 m³·mol⁻¹	ChemAxon
Polarizability	53.79 Å³	ChemAxon
Number of Rings	6	ChemAxon
Bioavailability	Yes	ChemAxon
Rule of Five	No	ChemAxon
Ghose Filter	No	ChemAxon
Veber's Rule	No	ChemAxon
MDDR-like Rule	No	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

185989

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 Deoxynortryptoquivaline (MMDBc0014701)

MOL for #<Metabolite:0x00007f1241462238>

3D MOL for #<Metabolite:0x00007f1241462238>

3D SDF for #<Metabolite:0x00007f1241462238>

3D-SDF for #<Metabolite:0x00007f1241462238>

PDB for #<Metabolite:0x00007f1241462238>

3D PDB for #<Metabolite:0x00007f1241462238>

SMILES for #<Metabolite:0x00007f1241462238>

INCHI for #<Metabolite:0x00007f1241462238>

Structure for #<Metabolite:0x00007f1241462238>

3D Structure for #<Metabolite:0x00007f1241462238>