MiMeDB: Showing metabocard for Fumiquinazoline A (MMDBc0005817)

Record Information

Version

1.0

Status

Detected and Quantified

Creation Date

2021-05-14 23:16:27 UTC

Update Date

2025-10-07 16:05:04 UTC

Metabolite ID

MMDBc0005817

Metabolite Identification

Common Name

Fumiquinazoline A

Description

Fumiquinazoline A is a fungal peptidyl alkaloid that belongs to the chemical class of alkaloids. This metabolite has garnered attention in biomedical literature for its complex biosynthesis and potential biological activities. Studies have shown that the fungus FE316 produces Fumiquinazoline A along with other metabolites when cultured with coffee husk, highlighting the influence of growth conditions on its production (PMID:40036116 ). Additionally, research utilizing liquid chromatography-mass spectrometry has revealed that mutations affecting iron metabolism can lead to reduced levels of Fumiquinazoline A, indicating its sensitivity to environmental factors (PMID:28753224 ). Among various mycotoxins, Fumiquinazoline A has been identified as a significant compound produced by certain fungal species, including Aspergillus (PMID:25737146 ). The biosynthetic pathway of Fumiquinazoline A involves the oxidation of its precursor to form more complex structures, such as fumiquinazoline C, facilitated by specific enzymes (PMID:21899262 ). Furthermore, bioinformatic analyses have identified key genetic components responsible for its biosynthesis in Aspergillus fumigatus, suggesting intricate regulatory mechanisms at play (PMID:20225828 ).

Structure

MOL SDF PDB SMILES InChI


  Mrv1652305152101162D          

 37 42  0  0  1  0            999 V2000
   -0.0543   -1.4742    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9494    3.8600    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.0714   -0.5372    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5964    3.1723    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8320   -1.3266    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.3569    3.9618    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5074    0.0649    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.0323    2.5702    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0286   -1.5141    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.5535    4.1492    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0120    1.6838    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2937   -0.6847    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   -2.1700    3.5897    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   -2.7040   -0.1225    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.2289    2.7576    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4646   -0.9120    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0105    3.5471    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7725    0.8943    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   -1.0971   -0.4973    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0309    0.7069    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4931    4.0613    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1400    0.4796    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1057    2.7839    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   -0.4480    2.2859    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.2703   -0.0826    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9305    2.8002    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6611   -1.0994    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3366    0.2922    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8353    3.5633    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    0.5949    1.3090    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4768    4.8862    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3794    1.2691    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.0919    1.6621    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8577   -1.2868    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2829    4.4069    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5760    1.0817    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3761    2.0045    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
  5  3  2  0  0  0  0
  6  4  2  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
 10  6  1  0  0  0  0
 12  1  1  1  0  0  0
 13  2  1  1  0  0  0
 14  7  2  0  0  0  0
 15  8  2  0  0  0  0
 16  9  2  0  0  0  0
 16 14  1  0  0  0  0
 17 10  2  0  0  0  0
 17 15  1  0  0  0  0
 18 11  1  6  0  0  0
 19 12  1  0  0  0  0
 20 18  1  0  0  0  0
 21 13  1  0  0  0  0
 22 14  1  0  0  0  0
 24 11  1  1  0  0  0
 24 15  1  0  0  0  0
 24 23  1  0  0  0  0
 25 12  1  0  0  0  0
 25 20  2  0  0  0  0
 26 13  1  0  0  0  0
 26 23  1  0  0  0  0
 27 16  1  0  0  0  0
 27 19  2  0  0  0  0
 28 18  1  0  0  0  0
 28 19  1  0  0  0  0
 28 22  1  0  0  0  0
 29 17  1  0  0  0  0
 29 21  1  0  0  0  0
 29 23  1  0  0  0  0
 30 20  1  0  0  0  0
 31 21  2  0  0  0  0
 32 22  2  0  0  0  0
 24 33  1  6  0  0  0
 12 34  1  6  0  0  0
 13 35  1  6  0  0  0
 18 36  1  1  0  0  0
 23 37  1  6  0  0  0
M  END


  Mrv1652305152101162D          

 37 42  0  0  1  0            999 V2000
   -0.0543   -1.4742    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9494    3.8600    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.0714   -0.5372    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5964    3.1723    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8320   -1.3266    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.3569    3.9618    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5074    0.0649    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.0323    2.5702    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0286   -1.5141    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.5535    4.1492    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0120    1.6838    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2937   -0.6847    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   -2.1700    3.5897    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   -2.7040   -0.1225    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.2289    2.7576    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4646   -0.9120    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0105    3.5471    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7725    0.8943    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   -1.0971   -0.4973    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0309    0.7069    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4931    4.0613    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1400    0.4796    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1057    2.7839    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   -0.4480    2.2859    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.2703   -0.0826    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9305    2.8002    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6611   -1.0994    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3366    0.2922    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8353    3.5633    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    0.5949    1.3090    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4768    4.8862    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3794    1.2691    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.0919    1.6621    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8577   -1.2868    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2829    4.4069    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5760    1.0817    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3761    2.0045    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
  5  3  2  0  0  0  0
  6  4  2  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
 10  6  1  0  0  0  0
 12  1  1  1  0  0  0
 13  2  1  1  0  0  0
 14  7  2  0  0  0  0
 15  8  2  0  0  0  0
 16  9  2  0  0  0  0
 16 14  1  0  0  0  0
 17 10  2  0  0  0  0
 17 15  1  0  0  0  0
 18 11  1  6  0  0  0
 19 12  1  0  0  0  0
 20 18  1  0  0  0  0
 21 13  1  0  0  0  0
 22 14  1  0  0  0  0
 24 11  1  1  0  0  0
 24 15  1  0  0  0  0
 24 23  1  0  0  0  0
 25 12  1  0  0  0  0
 25 20  2  0  0  0  0
 26 13  1  0  0  0  0
 26 23  1  0  0  0  0
 27 16  1  0  0  0  0
 27 19  2  0  0  0  0
 28 18  1  0  0  0  0
 28 19  1  0  0  0  0
 28 22  1  0  0  0  0
 29 17  1  0  0  0  0
 29 21  1  0  0  0  0
 29 23  1  0  0  0  0
 30 20  1  0  0  0  0
 31 21  2  0  0  0  0
 32 22  2  0  0  0  0
 24 33  1  6  0  0  0
 12 34  1  6  0  0  0
 13 35  1  6  0  0  0
 18 36  1  1  0  0  0
 23 37  1  6  0  0  0
M  END
> <DATABASE_ID>
MMDBc0005817

> <DATABASE_NAME>
MIME

> <SMILES>
[H][C@@]1(C)N[C@@]2([H])N(C1=O)C1=CC=CC=C1[C@@]2(O)C[C@@]1([H])N2C(=O)C3=CC=CC=C3N=C2[C@]([H])(C)N=C1O

> <INCHI_IDENTIFIER>
InChI=1S/C24H23N5O4/c1-12-19-27-16-9-5-3-7-14(16)22(32)28(19)18(20(30)25-12)11-24(33)15-8-4-6-10-17(15)29-21(31)13(2)26-23(24)29/h3-10,12-13,18,23,26,33H,11H2,1-2H3,(H,25,30)/t12-,13-,18+,23-,24-/m0/s1

> <INCHI_KEY>
DQQCCKFZJNINST-VCPZKGNQSA-N

> <FORMULA>
C24H23N5O4

> <MOLECULAR_WEIGHT>
445.479

> <EXACT_MASS>
445.175004241

> <JCHEM_ACCEPTOR_COUNT>
7

> <JCHEM_ATOM_COUNT>
56

> <JCHEM_AVERAGE_POLARIZABILITY>
45.57319377978835

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
3

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
(2S,9S,9aS)-9-hydroxy-9-{[(1S,4R)-3-hydroxy-1-methyl-6-oxo-1H,4H,6H-pyrazino[2,1-b]quinazolin-4-yl]methyl}-2-methyl-1H,2H,3H,9H,9aH-imidazo[1,2-a]indol-3-one

> <ALOGPS_LOGP>
0.57

> <JCHEM_LOGP>
0.04351726616819357

> <ALOGPS_LOGS>
-3.81

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
6

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
12.93525496093595

> <JCHEM_PKA_STRONGEST_ACIDIC>
3.902932564030674

> <JCHEM_PKA_STRONGEST_BASIC>
5.182519574527406

> <JCHEM_POLAR_SURFACE_AREA>
117.83

> <JCHEM_REFRACTIVITY>
120.02869999999997

> <JCHEM_ROTATABLE_BOND_COUNT>
2

> <JCHEM_RULE_OF_FIVE>
1

> <ALOGPS_SOLUBILITY>
6.85e-02 g/l

> <JCHEM_TRADITIONAL_IUPAC>
(2S,9S,9aS)-9-hydroxy-9-{[(1S,4R)-3-hydroxy-1-methyl-6-oxo-1H,4H-pyrazino[2,1-b]quinazolin-4-yl]methyl}-2-methyl-1H,2H,9aH-imidazo[1,2-a]indol-3-one

> <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      -0.101  -2.752   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0      -5.506   7.205   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0      -7.600  -1.003   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0       2.980   5.922   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0      -7.153  -2.476   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0       2.533   7.395   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0      -6.547   0.121   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0       1.927   4.798   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0      -5.653  -2.826   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0       1.033   7.745   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0      -1.889   3.143   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0      -0.548  -1.278   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0      -4.051   6.701   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0      -5.047  -0.229   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0       0.427   5.147   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0      -4.601  -1.702   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0      -0.020   6.621   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0      -1.442   1.669   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0      -2.048  -0.928   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0       0.058   1.320   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0      -2.787   7.581   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0      -3.995   0.895   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0      -2.064   5.197   0.000  0.00  0.00           C+0
HETATM   24  C   UNK     0      -0.836   4.267   0.000  0.00  0.00           C+0
HETATM   25  N   UNK     0       0.505  -0.154   0.000  0.00  0.00           N+0
HETATM   26  N   UNK     0      -3.604   5.227   0.000  0.00  0.00           N+0
HETATM   27  N   UNK     0      -3.101  -2.052   0.000  0.00  0.00           N+0
HETATM   28  N   UNK     0      -2.495   0.545   0.000  0.00  0.00           N+0
HETATM   29  N   UNK     0      -1.559   6.652   0.000  0.00  0.00           N+0
HETATM   30  O   UNK     0       1.110   2.443   0.000  0.00  0.00           O+0
HETATM   31  O   UNK     0      -2.757   9.121   0.000  0.00  0.00           O+0
HETATM   32  O   UNK     0      -4.442   2.369   0.000  0.00  0.00           O+0
HETATM   33  O   UNK     0       0.172   3.102   0.000  0.00  0.00           O+0
HETATM   34  H   UNK     0      -1.601  -2.402   0.000  0.00  0.00           H+0
HETATM   35  H   UNK     0      -4.261   8.226   0.000  0.00  0.00           H+0
HETATM   36  H   UNK     0      -2.942   2.019   0.000  0.00  0.00           H+0
HETATM   37  H   UNK     0      -2.569   3.742   0.000  0.00  0.00           H+0
CONECT    1   12                                                            
CONECT    2   13                                                            
CONECT    3    5    7                                                       
CONECT    4    6    8                                                       
CONECT    5    3    9                                                       
CONECT    6    4   10                                                       
CONECT    7    3   14                                                       
CONECT    8    4   15                                                       
CONECT    9    5   16                                                       
CONECT   10    6   17                                                       
CONECT   11   18   24                                                       
CONECT   12    1   19   25   34                                             
CONECT   13    2   21   26   35                                             
CONECT   14    7   16   22                                                  
CONECT   15    8   17   24                                                  
CONECT   16    9   14   27                                                  
CONECT   17   10   15   29                                                  
CONECT   18   11   20   28   36                                             
CONECT   19   12   27   28                                                  
CONECT   20   18   25   30                                                  
CONECT   21   13   29   31                                                  
CONECT   22   14   28   32                                                  
CONECT   23   24   26   29   37                                             
CONECT   24   11   15   23   33                                             
CONECT   25   12   20                                                       
CONECT   26   13   23                                                       
CONECT   27   16   19                                                       
CONECT   28   18   19   22                                                  
CONECT   29   17   21   23                                                  
CONECT   30   20                                                            
CONECT   31   21                                                            
CONECT   32   22                                                            
CONECT   33   24                                                            
CONECT   34   12                                                            
CONECT   35   13                                                            
CONECT   36   18                                                            
CONECT   37   23                                                            
MASTER        0    0    0    0    0    0    0    0   37    0   84    0
END

Synonyms

Not Available

Molecular Formula

C₂₄H₂₃N₅O₄

Average Mass

445.479

Monoisotopic Mass

445.175004241

IUPAC Name

(2S,9S,9aS)-9-hydroxy-9-{[(1S,4R)-3-hydroxy-1-methyl-6-oxo-1H,4H,6H-pyrazino[2,1-b]quinazolin-4-yl]methyl}-2-methyl-1H,2H,3H,9H,9aH-imidazo[1,2-a]indol-3-one

Traditional Name

(2S,9S,9aS)-9-hydroxy-9-{[(1S,4R)-3-hydroxy-1-methyl-6-oxo-1H,4H-pyrazino[2,1-b]quinazolin-4-yl]methyl}-2-methyl-1H,2H,9aH-imidazo[1,2-a]indol-3-one

CAS Registry Number

Not Available

SMILES

[H][C@@]1(C)N[C@@]2([H])N(C1=O)C1=CC=CC=C1[C@@]2(O)C[C@@]1([H])N2C(=O)C3=CC=CC=C3N=C2[C@]([H])(C)N=C1O

InChI Identifier

InChI=1S/C24H23N5O4/c1-12-19-27-16-9-5-3-7-14(16)22(32)28(19)18(20(30)25-12)11-24(33)15-8-4-6-10-17(15)29-21(31)13(2)26-23(24)29/h3-10,12-13,18,23,26,33H,11H2,1-2H3,(H,25,30)/t12-,13-,18+,23-,24-/m0/s1

InChI Key

DQQCCKFZJNINST-VCPZKGNQSA-N

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as quinazolines. Quinazolines are compounds containing a quinazoline moiety, which is made up of two fused six-member aromatic rings, a benzene ring and a pyrimidine ring.

Kingdom

Organic compounds

Super Class

Organoheterocyclic compounds

Class

Diazanaphthalenes

Sub Class

Benzodiazines

Direct Parent

Quinazolines

Alternative Parents

Substituents

Alpha-amino acid or derivatives
Quinazoline
Indole or derivatives
Pyrimidone
Imidazolidinone
Pyrimidine
Benzenoid
Heteroaromatic compound
Tertiary carboxylic acid amide
Tertiary alcohol
Imidazolidine
Secondary carboxylic acid amide
Amino acid or derivatives
Carboxamide group
Lactam
Secondary amine
Azacycle
Carboxylic acid derivative
Secondary aliphatic amine
Hydrocarbon derivative
Alcohol
Organic oxygen compound
Organonitrogen compound
Organooxygen compound
Organic nitrogen compound
Carbonyl group
Organopnictogen compound
Organic oxide
Amine
Aromatic heteropolycyclic compound

Molecular Framework

Aromatic heteropolycyclic compounds

External Descriptors

pyrazinoquinazoline (CHEBI:64546 )
fumiquinazoline (CHEBI:64546 )
imidazoindole (CHEBI:64546 )

Functional Ontology

Not Available

Physical Properties

State

Expected Solid

Predicted Properties

Property	Value	Source
Water Solubility	0.068 g/L	ALOGPS
logP	0.57	ALOGPS
logP	0.044	ChemAxon
logS	-3.8	ALOGPS
pKa (Strongest Acidic)	3.9	ChemAxon
pKa (Strongest Basic)	5.18	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	7	ChemAxon
Hydrogen Donor Count	3	ChemAxon
Polar Surface Area	117.83 Å²	ChemAxon
Rotatable Bond Count	2	ChemAxon
Refractivity	120.03 m³·mol⁻¹	ChemAxon
Polarizability	45.57 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_2_2) - 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

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	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

C00028284

Chemspider ID

9422835

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

11247802

PDB ID

Not Available

ChEBI ID

64546

Food Biomarker Ontology

Not Available

CMMC Knowledgebase

DQQCCKFZJNINST-VCPZKGNQSA-N

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 Fumiquinazoline A (MMDBc0005817)

MOL for #<Metabolite:0x0000557999eeacb0>

3D MOL for #<Metabolite:0x0000557999eeacb0>

3D SDF for #<Metabolite:0x0000557999eeacb0>

3D-SDF for #<Metabolite:0x0000557999eeacb0>

PDB for #<Metabolite:0x0000557999eeacb0>

3D PDB for #<Metabolite:0x0000557999eeacb0>

SMILES for #<Metabolite:0x0000557999eeacb0>

INCHI for #<Metabolite:0x0000557999eeacb0>

Structure for #<Metabolite:0x0000557999eeacb0>

3D Structure for #<Metabolite:0x0000557999eeacb0>