MiMeDB: Showing metabocard for Aspoquinolone A (MMDBc0015253)

Record Information

Version

2.0

Status

Detected and Quantified

Creation Date

2021-05-15 06:07:28 UTC

Update Date

2025-10-07 16:06:23 UTC

Metabolite ID

MMDBc0015253

Metabolite Identification

Common Name

Aspoquinolone A

Description

Aspoquinolone A is a quinolone alkaloid. There is limited literature available on this metabolite, with few studies providing detailed insights into its properties and biological significance.

Structure

MOL SDF PDB SMILES InChI


  Mrv1652305152108072D          

 39 43  0  0  1  0            999 V2000
   -4.1199   -2.1338    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2995   -1.3951    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6585   -3.5549    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.3626   -4.0347    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5724   -1.2375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7145   -0.4125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.6771   -3.0572    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7717   -2.1387    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2074   -3.6892    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3020   -2.7707    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0000    0.0000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4289   -1.6500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4289   -2.4750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4710   -3.8520    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7145   -1.2375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9592   -2.2820    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.0198   -3.5460    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4710   -3.0270    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   -2.7565   -3.4395    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.7145   -0.4125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7145   -1.2375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0000   -1.6500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1434   -1.2375    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.1434   -0.4125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2995   -2.2201    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1434   -2.8875    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.4289   -1.6500    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.4289   -0.0000    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    0.0000   -2.4750    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.8579    0.0000    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.8986   -2.2820    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.5501   -4.1779    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.8579   -1.6500    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4790   -2.1338    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1434   -1.2375    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7145   -2.8875    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2915   -2.9408    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2716   -4.1070    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.1434   -2.0625    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
  9  7  1  0  0  0  0
 10  8  2  0  0  0  0
 11  6  2  0  0  0  0
 13 12  2  0  0  0  0
 15  6  1  0  0  0  0
 15 12  1  0  0  0  0
 16  7  2  0  0  0  0
 16  8  1  0  0  0  0
 17  9  2  0  0  0  0
 17 10  1  0  0  0  0
 18 14  1  0  0  0  0
 19 14  1  0  0  0  0
 19 18  1  0  0  0  0
 20 11  1  0  0  0  0
 21 20  2  0  0  0  0
 22 15  2  0  0  0  0
 22 21  1  0  0  0  0
 24 23  1  0  0  0  0
 25  1  1  0  0  0  0
 25  2  1  0  0  0  0
 25 18  1  0  0  0  0
 26  3  1  1  0  0  0
 26 13  1  6  0  0  0
 26 19  1  0  0  0  0
 27 16  1  1  0  0  0
 27 21  1  0  0  0  0
 27 23  1  0  0  0  0
 28 20  1  0  0  0  0
 28 24  2  0  0  0  0
 29 22  1  0  0  0  0
 30 24  1  0  0  0  0
 27 31  1  6  0  0  0
 32  4  1  0  0  0  0
 32 17  1  0  0  0  0
 33  5  1  0  0  0  0
 23 33  1  6  0  0  0
 34 25  1  0  0  0  0
 34 26  1  0  0  0  0
 35 12  1  0  0  0  0
 36 13  1  0  0  0  0
 18 37  1  6  0  0  0
 19 38  1  6  0  0  0
 23 39  1  1  0  0  0
M  END


  Mrv1652305152108072D          

 39 43  0  0  1  0            999 V2000
   -4.1199   -2.1338    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2995   -1.3951    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6585   -3.5549    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.3626   -4.0347    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5724   -1.2375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7145   -0.4125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.6771   -3.0572    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7717   -2.1387    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2074   -3.6892    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3020   -2.7707    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0000    0.0000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4289   -1.6500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4289   -2.4750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4710   -3.8520    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7145   -1.2375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9592   -2.2820    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.0198   -3.5460    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4710   -3.0270    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   -2.7565   -3.4395    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.7145   -0.4125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7145   -1.2375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0000   -1.6500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1434   -1.2375    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.1434   -0.4125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2995   -2.2201    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1434   -2.8875    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.4289   -1.6500    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.4289   -0.0000    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    0.0000   -2.4750    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.8579    0.0000    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.8986   -2.2820    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.5501   -4.1779    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.8579   -1.6500    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4790   -2.1338    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1434   -1.2375    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7145   -2.8875    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2915   -2.9408    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2716   -4.1070    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.1434   -2.0625    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
  9  7  1  0  0  0  0
 10  8  2  0  0  0  0
 11  6  2  0  0  0  0
 13 12  2  0  0  0  0
 15  6  1  0  0  0  0
 15 12  1  0  0  0  0
 16  7  2  0  0  0  0
 16  8  1  0  0  0  0
 17  9  2  0  0  0  0
 17 10  1  0  0  0  0
 18 14  1  0  0  0  0
 19 14  1  0  0  0  0
 19 18  1  0  0  0  0
 20 11  1  0  0  0  0
 21 20  2  0  0  0  0
 22 15  2  0  0  0  0
 22 21  1  0  0  0  0
 24 23  1  0  0  0  0
 25  1  1  0  0  0  0
 25  2  1  0  0  0  0
 25 18  1  0  0  0  0
 26  3  1  1  0  0  0
 26 13  1  6  0  0  0
 26 19  1  0  0  0  0
 27 16  1  1  0  0  0
 27 21  1  0  0  0  0
 27 23  1  0  0  0  0
 28 20  1  0  0  0  0
 28 24  2  0  0  0  0
 29 22  1  0  0  0  0
 30 24  1  0  0  0  0
 27 31  1  6  0  0  0
 32  4  1  0  0  0  0
 32 17  1  0  0  0  0
 33  5  1  0  0  0  0
 23 33  1  6  0  0  0
 34 25  1  0  0  0  0
 34 26  1  0  0  0  0
 35 12  1  0  0  0  0
 36 13  1  0  0  0  0
 18 37  1  6  0  0  0
 19 38  1  6  0  0  0
 23 39  1  1  0  0  0
M  END
> <DATABASE_ID>
MMDBc0015253

> <DATABASE_NAME>
MIME

> <SMILES>
[H]\C(=C(\[H])[C@@]1(C)OC(C)(C)[C@]2([H])C[C@]12[H])C1=C(O)C2=C(C=C1)N=C(O)[C@]([H])(OC)[C@@]2(O)C1=CC=C(OC)C=C1

> <INCHI_IDENTIFIER>
InChI=1S/C27H31NO6/c1-25(2)18-14-19(18)26(3,34-25)13-12-15-6-11-20-21(22(15)29)27(31,23(33-5)24(30)28-20)16-7-9-17(32-4)10-8-16/h6-13,18-19,23,29,31H,14H2,1-5H3,(H,28,30)/b13-12+/t18-,19+,23+,26-,27-/m1/s1

> <INCHI_KEY>
AISVMTZASACEBH-RSVMIURYSA-N

> <FORMULA>
C27H31NO6

> <MOLECULAR_WEIGHT>
465.546

> <EXACT_MASS>
465.215137722

> <JCHEM_ACCEPTOR_COUNT>
7

> <JCHEM_ATOM_COUNT>
65

> <JCHEM_AVERAGE_POLARIZABILITY>
50.014691689458814

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
3

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
(3R,4R)-3-methoxy-4-(4-methoxyphenyl)-6-[(E)-2-[(1S,2R,5R)-2,4,4-trimethyl-3-oxabicyclo[3.1.0]hexan-2-yl]ethenyl]-3,4-dihydroquinoline-2,4,5-triol

> <ALOGPS_LOGP>
3.92

> <JCHEM_LOGP>
3.8960619893333344

> <ALOGPS_LOGS>
-5.02

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
5

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
9.547299397659675

> <JCHEM_PKA_STRONGEST_ACIDIC>
2.5109133294180417

> <JCHEM_PKA_STRONGEST_BASIC>
-0.3524222496896591

> <JCHEM_POLAR_SURFACE_AREA>
100.74000000000002

> <JCHEM_REFRACTIVITY>
130.8713

> <JCHEM_ROTATABLE_BOND_COUNT>
5

> <JCHEM_RULE_OF_FIVE>
1

> <ALOGPS_SOLUBILITY>
4.42e-03 g/l

> <JCHEM_TRADITIONAL_IUPAC>
(3R,4R)-3-methoxy-4-(4-methoxyphenyl)-6-[(E)-2-[(1S,2R,5R)-2,4,4-trimethyl-3-oxabicyclo[3.1.0]hexan-2-yl]ethenyl]-3H-quinoline-2,4,5-triol

> <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      -7.691  -3.983   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0      -6.159  -2.604   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0      -3.096  -6.636   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0       8.144  -7.531   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0       6.668  -2.310   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0      -1.334  -0.770   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0       3.131  -5.707   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0       5.174  -3.992   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0       4.120  -6.887   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0       6.164  -5.172   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0       0.000   0.000   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0      -2.667  -3.080   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0      -2.667  -4.620   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0      -6.479  -7.190   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0      -1.334  -2.310   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0       3.657  -4.260   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0       5.637  -6.619   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0      -6.479  -5.650   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0      -5.145  -6.420   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0       1.334  -0.770   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0       1.334  -2.310   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0       0.000  -3.080   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0       4.001  -2.310   0.000  0.00  0.00           C+0
HETATM   24  C   UNK     0       4.001  -0.770   0.000  0.00  0.00           C+0
HETATM   25  C   UNK     0      -6.159  -4.144   0.000  0.00  0.00           C+0
HETATM   26  C   UNK     0      -4.001  -5.390   0.000  0.00  0.00           C+0
HETATM   27  C   UNK     0       2.667  -3.080   0.000  0.00  0.00           C+0
HETATM   28  N   UNK     0       2.667  -0.000   0.000  0.00  0.00           N+0
HETATM   29  O   UNK     0       0.000  -4.620   0.000  0.00  0.00           O+0
HETATM   30  O   UNK     0       5.335   0.000   0.000  0.00  0.00           O+0
HETATM   31  O   UNK     0       1.677  -4.260   0.000  0.00  0.00           O+0
HETATM   32  O   UNK     0       6.627  -7.799   0.000  0.00  0.00           O+0
HETATM   33  O   UNK     0       5.335  -3.080   0.000  0.00  0.00           O+0
HETATM   34  O   UNK     0      -4.627  -3.983   0.000  0.00  0.00           O+0
HETATM   35  H   UNK     0      -4.001  -2.310   0.000  0.00  0.00           H+0
HETATM   36  H   UNK     0      -1.334  -5.390   0.000  0.00  0.00           H+0
HETATM   37  H   UNK     0      -8.011  -5.489   0.000  0.00  0.00           H+0
HETATM   38  H   UNK     0      -4.240  -7.666   0.000  0.00  0.00           H+0
HETATM   39  H   UNK     0       4.001  -3.850   0.000  0.00  0.00           H+0
CONECT    1   25                                                            
CONECT    2   25                                                            
CONECT    3   26                                                            
CONECT    4   32                                                            
CONECT    5   33                                                            
CONECT    6   11   15                                                       
CONECT    7    9   16                                                       
CONECT    8   10   16                                                       
CONECT    9    7   17                                                       
CONECT   10    8   17                                                       
CONECT   11    6   20                                                       
CONECT   12   13   15   35                                                  
CONECT   13   12   26   36                                                  
CONECT   14   18   19                                                       
CONECT   15    6   12   22                                                  
CONECT   16    7    8   27                                                  
CONECT   17    9   10   32                                                  
CONECT   18   14   19   25   37                                             
CONECT   19   14   18   26   38                                             
CONECT   20   11   21   28                                                  
CONECT   21   20   22   27                                                  
CONECT   22   15   21   29                                                  
CONECT   23   24   27   33   39                                             
CONECT   24   23   28   30                                                  
CONECT   25    1    2   18   34                                             
CONECT   26    3   13   19   34                                             
CONECT   27   16   21   23   31                                             
CONECT   28   20   24                                                       
CONECT   29   22                                                            
CONECT   30   24                                                            
CONECT   31   27                                                            
CONECT   32    4   17                                                       
CONECT   33    5   23                                                       
CONECT   34   25   26                                                       
CONECT   35   12                                                            
CONECT   36   13                                                            
CONECT   37   18                                                            
CONECT   38   19                                                            
CONECT   39   23                                                            
MASTER        0    0    0    0    0    0    0    0   39    0   86    0
END

Synonyms

Value	Source
Aspoquinolone D	MeSH

Molecular Formula

C₂₇H₃₁NO₆

Average Mass

465.546

Monoisotopic Mass

465.215137722

IUPAC Name

(3R,4R)-3-methoxy-4-(4-methoxyphenyl)-6-[(E)-2-[(1S,2R,5R)-2,4,4-trimethyl-3-oxabicyclo[3.1.0]hexan-2-yl]ethenyl]-3,4-dihydroquinoline-2,4,5-triol

Traditional Name

(3R,4R)-3-methoxy-4-(4-methoxyphenyl)-6-[(E)-2-[(1S,2R,5R)-2,4,4-trimethyl-3-oxabicyclo[3.1.0]hexan-2-yl]ethenyl]-3H-quinoline-2,4,5-triol

CAS Registry Number

Not Available

SMILES

[H]\C(=C(\[H])[C@@]1(C)OC(C)(C)[C@]2([H])C[C@]12[H])C1=C(O)C2=C(C=C1)N=C(O)[C@]([H])(OC)[C@@]2(O)C1=CC=C(OC)C=C1

InChI Identifier

InChI=1S/C27H31NO6/c1-25(2)18-14-19(18)26(3,34-25)13-12-15-6-11-20-21(22(15)29)27(31,23(33-5)24(30)28-20)16-7-9-17(32-4)10-8-16/h6-13,18-19,23,29,31H,14H2,1-5H3,(H,28,30)/b13-12+/t18-,19+,23+,26-,27-/m1/s1

InChI Key

AISVMTZASACEBH-RSVMIURYSA-N

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as phenylquinolines. These are heterocyclic compounds containing a quinoline moiety substituted with a phenyl group.

Kingdom

Organic compounds

Super Class

Organoheterocyclic compounds

Class

Quinolines and derivatives

Sub Class

Phenylquinolines

Direct Parent

Phenylquinolines

Alternative Parents

Substituents

Phenylquinoline
Tetrahydroquinolone
Quinolone
Tetrahydroquinoline
Anisole
Phenoxy compound
Phenol ether
Styrene
Methoxybenzene
Alkyl aryl ether
1-hydroxy-4-unsubstituted benzenoid
Phenol
Benzenoid
Monocyclic benzene moiety
Oxane
Tertiary alcohol
Oxolane
Carboxamide group
Secondary carboxylic acid amide
Lactam
Oxacycle
Ether
Dialkyl ether
Carboxylic acid derivative
Azacycle
Organonitrogen compound
Hydrocarbon derivative
Organic nitrogen compound
Organic oxide
Carbonyl group
Organooxygen compound
Organic oxygen compound
Alcohol
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	0.0044 g/L	ALOGPS
logP	3.92	ALOGPS
logP	3.9	ChemAxon
logS	-5	ALOGPS
pKa (Strongest Acidic)	2.51	ChemAxon
pKa (Strongest Basic)	-0.35	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	7	ChemAxon
Hydrogen Donor Count	3	ChemAxon
Polar Surface Area	100.74 Å²	ChemAxon
Rotatable Bond Count	5	ChemAxon
Refractivity	130.87 m³·mol⁻¹	ChemAxon
Polarizability	50.01 Å³	ChemAxon
Number of Rings	5	ChemAxon
Bioavailability	Yes	ChemAxon
Rule of Five	Yes	ChemAxon
Ghose Filter	No	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

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

C00052199

Chemspider ID

17243758

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

16085089

PDB ID

Not Available

ChEBI ID

177743

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 Aspoquinolone A (MMDBc0015253)

MOL for #<Metabolite:0x00007f8dd0854f20>

3D MOL for #<Metabolite:0x00007f8dd0854f20>

3D SDF for #<Metabolite:0x00007f8dd0854f20>

3D-SDF for #<Metabolite:0x00007f8dd0854f20>

PDB for #<Metabolite:0x00007f8dd0854f20>

3D PDB for #<Metabolite:0x00007f8dd0854f20>

SMILES for #<Metabolite:0x00007f8dd0854f20>

INCHI for #<Metabolite:0x00007f8dd0854f20>

Structure for #<Metabolite:0x00007f8dd0854f20>

3D Structure for #<Metabolite:0x00007f8dd0854f20>