MiMeDB: Showing metabocard for Flavasperone (MMDBc0006724)

Record Information

Version

1.0

Status

Detected and Quantified

Creation Date

2021-05-15 00:09:50 UTC

Update Date

2025-01-16 00:58:29 UTC

Metabolite ID

MMDBc0006724

Metabolite Identification

Common Name

Flavasperone

Description

Asperxanthone is found in fruits. Asperxanthone is a constituent of Aspergillus niger, Aspergillus awamori and Aspergillus fonsecaeus. It is isolated from A. niger infected mango fruits and peanuts

Structure

MOL 3D MOL SDF 3D SDF PDB 3D PDB SMILES InChI

HMDB0030852
     RDKit          3D
Asperxanthone
 35 37  0  0  0  0  0  0  0  0999 V2000
    5.2115    0.4613    0.0332 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.3016   -0.6146    0.1233 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.9523   -0.3651    0.1603 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0727   -1.4119    0.2478 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.6923   -1.2006    0.2879 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2320   -2.2265    0.3760 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.1519   -3.5867    0.4328 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.2423    0.1088    0.2360 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1100    1.1711    0.1482 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.4989    0.9241    0.1096 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.6934    2.4544    0.0964 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6785    2.7685    0.1309 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0985    4.0492    0.0794 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5758    1.7146    0.2194 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9414    1.8698    0.2620 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4405    2.9959    0.2215 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8175    0.7811    0.3515 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2396   -0.4669    0.3954 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1159   -1.6667    0.4907 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9405   -0.6242    0.3554 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1135    0.4032    0.2709 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.1992    0.0273   -0.2387 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.9426    1.1707   -0.7885 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.2562    1.0610    0.9680 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.3897   -2.4438    0.2902 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.5124   -3.8617    1.4449 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.9700   -3.7715   -0.3213 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6954   -4.2671    0.2098 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.1771    1.7798    0.0396 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.3609    3.2995    0.0274 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9456    4.4897    0.0878 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.8727    0.8671    0.3861 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.1693   -1.3869    0.6127 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.0493   -2.2789   -0.4432 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8094   -2.2239    1.3885 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  2  3  1  0
  3  4  2  0
  4  5  1  0
  5  6  1  0
  6  7  1  0
  5  8  2  0
  8  9  1  0
  9 10  2  0
  9 11  1  0
 11 12  2  0
 12 13  1  0
 12 14  1  0
 14 15  1  0
 15 16  2  0
 15 17  1  0
 17 18  2  0
 18 19  1  0
 18 20  1  0
 20 21  1  0
 10  3  1  0
 21 14  2  0
 21  8  1  0
  1 22  1  0
  1 23  1  0
  1 24  1  0
  4 25  1  0
  7 26  1  0
  7 27  1  0
  7 28  1  0
 10 29  1  0
 11 30  1  0
 13 31  1  0
 17 32  1  0
 19 33  1  0
 19 34  1  0
 19 35  1  0
M  END


  Mrv0541 05061305332D          

 21 23  0  0  0  0            999 V2000
    0.6039    3.0789    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.9664    2.3645    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2539    3.0789    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.6039    1.6500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.3164    0.9355    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.0789    0.2211    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.3164    2.3645    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.0164    2.3645    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.4914    0.9355    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.7289    1.6500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.0164    0.9355    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2539    0.2211    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.4914    2.3645    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.0789    1.6500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.8414    0.9355    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2539    1.6500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.6039    0.2211    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.8414   -0.4934    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.5539    1.6500    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.0789    3.0789    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.8414    2.3645    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
  8  1  1  0  0  0  0
  8  4  2  0  0  0  0
  9  5  2  0  0  0  0
  9  6  1  0  0  0  0
 10  5  1  0  0  0  0
 10  7  2  0  0  0  0
 11  4  1  0  0  0  0
 12  6  2  0  0  0  0
 13  7  1  0  0  0  0
 14  9  1  0  0  0  0
 14 13  2  0  0  0  0
 15 11  1  0  0  0  0
 15 12  1  0  0  0  0
 16 14  1  0  0  0  0
 16 15  2  0  0  0  0
 17 11  2  0  0  0  0
 18 12  1  0  0  0  0
 19  2  1  0  0  0  0
 19 10  1  0  0  0  0
 20  3  1  0  0  0  0
 20 13  1  0  0  0  0
 21  8  1  0  0  0  0
 21 16  1  0  0  0  0
M  END
> <DATABASE_ID>
MMDBc0006724

> <DATABASE_NAME>
MIME

> <SMILES>
COC1=CC(OC)=C2C(C=C(O)C3=C2OC(C)=CC3=O)=C1

> <INCHI_IDENTIFIER>
InChI=1S/C16H14O5/c1-8-4-11(17)15-12(18)6-9-5-10(19-2)7-13(20-3)14(9)16(15)21-8/h4-7,18H,1-3H3

> <INCHI_KEY>
ARXPDHLVDOYIPX-UHFFFAOYSA-N

> <FORMULA>
C16H14O5

> <MOLECULAR_WEIGHT>
286.2794

> <EXACT_MASS>
286.084123558

> <JCHEM_ACCEPTOR_COUNT>
5

> <JCHEM_AVERAGE_POLARIZABILITY>
29.240617625656768

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
1

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
5-hydroxy-8,10-dimethoxy-2-methyl-4H-benzo[h]chromen-4-one

> <ALOGPS_LOGP>
2.95

> <JCHEM_LOGP>
2.8921221729999997

> <ALOGPS_LOGS>
-3.56

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
3

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
15.816314133038201

> <JCHEM_PKA_STRONGEST_ACIDIC>
8.397204320523224

> <JCHEM_PKA_STRONGEST_BASIC>
-4.492396726526867

> <JCHEM_POLAR_SURFACE_AREA>
64.99000000000001

> <JCHEM_REFRACTIVITY>
78.46470000000001

> <JCHEM_ROTATABLE_BOND_COUNT>
2

> <JCHEM_RULE_OF_FIVE>
1

> <ALOGPS_SOLUBILITY>
7.89e-02 g/l

> <JCHEM_TRADITIONAL_IUPAC>
5-hydroxy-8,10-dimethoxy-2-methylbenzo[h]chromen-4-one

> <JCHEM_VEBER_RULE>
0

$$$$

HMDB0030852
     RDKit          3D
Asperxanthone
 35 37  0  0  0  0  0  0  0  0999 V2000
    5.2115    0.4613    0.0332 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.3016   -0.6146    0.1233 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.9523   -0.3651    0.1603 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0727   -1.4119    0.2478 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.6923   -1.2006    0.2879 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2320   -2.2265    0.3760 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.1519   -3.5867    0.4328 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.2423    0.1088    0.2360 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1100    1.1711    0.1482 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.4989    0.9241    0.1096 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.6934    2.4544    0.0964 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6785    2.7685    0.1309 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0985    4.0492    0.0794 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5758    1.7146    0.2194 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9414    1.8698    0.2620 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4405    2.9959    0.2215 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8175    0.7811    0.3515 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2396   -0.4669    0.3954 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1159   -1.6667    0.4907 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9405   -0.6242    0.3554 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1135    0.4032    0.2709 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.1992    0.0273   -0.2387 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.9426    1.1707   -0.7885 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.2562    1.0610    0.9680 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.3897   -2.4438    0.2902 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.5124   -3.8617    1.4449 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.9700   -3.7715   -0.3213 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6954   -4.2671    0.2098 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.1771    1.7798    0.0396 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.3609    3.2995    0.0274 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9456    4.4897    0.0878 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.8727    0.8671    0.3861 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.1693   -1.3869    0.6127 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.0493   -2.2789   -0.4432 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8094   -2.2239    1.3885 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  2  3  1  0
  3  4  2  0
  4  5  1  0
  5  6  1  0
  6  7  1  0
  5  8  2  0
  8  9  1  0
  9 10  2  0
  9 11  1  0
 11 12  2  0
 12 13  1  0
 12 14  1  0
 14 15  1  0
 15 16  2  0
 15 17  1  0
 17 18  2  0
 18 19  1  0
 18 20  1  0
 20 21  1  0
 10  3  1  0
 21 14  2  0
 21  8  1  0
  1 22  1  0
  1 23  1  0
  1 24  1  0
  4 25  1  0
  7 26  1  0
  7 27  1  0
  7 28  1  0
 10 29  1  0
 11 30  1  0
 13 31  1  0
 17 32  1  0
 19 33  1  0
 19 34  1  0
 19 35  1  0
M  END

HEADER    PROTEIN                                 06-MAY-13   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   06-MAY-13         0                                  
HETATM    1  C   UNK     0       1.127   5.747   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0      11.137   4.414   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0       4.207   5.747   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0       1.127   3.080   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0       8.057   1.746   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0       5.747   0.413   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0       8.057   4.414   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0       1.897   4.414   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0       6.517   1.746   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0       8.827   3.080   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0       1.897   1.746   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0       4.207   0.413   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0       6.517   4.414   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0       5.747   3.080   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0       3.437   1.746   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0       4.207   3.080   0.000  0.00  0.00           C+0
HETATM   17  O   UNK     0       1.127   0.413   0.000  0.00  0.00           O+0
HETATM   18  O   UNK     0       3.437  -0.921   0.000  0.00  0.00           O+0
HETATM   19  O   UNK     0      10.367   3.080   0.000  0.00  0.00           O+0
HETATM   20  O   UNK     0       5.747   5.747   0.000  0.00  0.00           O+0
HETATM   21  O   UNK     0       3.437   4.414   0.000  0.00  0.00           O+0
CONECT    1    8                                                            
CONECT    2   19                                                            
CONECT    3   20                                                            
CONECT    4    8   11                                                       
CONECT    5    9   10                                                       
CONECT    6    9   12                                                       
CONECT    7   10   13                                                       
CONECT    8    1    4   21                                                  
CONECT    9    5    6   14                                                  
CONECT   10    5    7   19                                                  
CONECT   11    4   15   17                                                  
CONECT   12    6   15   18                                                  
CONECT   13    7   14   20                                                  
CONECT   14    9   13   16                                                  
CONECT   15   11   12   16                                                  
CONECT   16   14   15   21                                                  
CONECT   17   11                                                            
CONECT   18   12                                                            
CONECT   19    2   10                                                       
CONECT   20    3   13                                                       
CONECT   21    8   16                                                       
MASTER        0    0    0    0    0    0    0    0   21    0   46    0
END

COMPND    HMDB0030852
HETATM    1  C1  UNL     1       5.212   0.461   0.033  1.00  0.00           C  
HETATM    2  O1  UNL     1       4.302  -0.615   0.123  1.00  0.00           O  
HETATM    3  C2  UNL     1       2.952  -0.365   0.160  1.00  0.00           C  
HETATM    4  C3  UNL     1       2.073  -1.412   0.248  1.00  0.00           C  
HETATM    5  C4  UNL     1       0.692  -1.201   0.288  1.00  0.00           C  
HETATM    6  O2  UNL     1      -0.232  -2.226   0.376  1.00  0.00           O  
HETATM    7  C5  UNL     1       0.152  -3.587   0.433  1.00  0.00           C  
HETATM    8  C6  UNL     1       0.242   0.109   0.236  1.00  0.00           C  
HETATM    9  C7  UNL     1       1.110   1.171   0.148  1.00  0.00           C  
HETATM   10  C8  UNL     1       2.499   0.924   0.110  1.00  0.00           C  
HETATM   11  C9  UNL     1       0.693   2.454   0.096  1.00  0.00           C  
HETATM   12  C10 UNL     1      -0.678   2.768   0.131  1.00  0.00           C  
HETATM   13  O3  UNL     1      -1.099   4.049   0.079  1.00  0.00           O  
HETATM   14  C11 UNL     1      -1.576   1.715   0.219  1.00  0.00           C  
HETATM   15  C12 UNL     1      -2.941   1.870   0.262  1.00  0.00           C  
HETATM   16  O4  UNL     1      -3.440   2.996   0.222  1.00  0.00           O  
HETATM   17  C13 UNL     1      -3.817   0.781   0.351  1.00  0.00           C  
HETATM   18  C14 UNL     1      -3.240  -0.467   0.395  1.00  0.00           C  
HETATM   19  C15 UNL     1      -4.116  -1.667   0.491  1.00  0.00           C  
HETATM   20  O5  UNL     1      -1.941  -0.624   0.355  1.00  0.00           O  
HETATM   21  C16 UNL     1      -1.113   0.403   0.271  1.00  0.00           C  
HETATM   22  H1  UNL     1       6.199   0.027  -0.239  1.00  0.00           H  
HETATM   23  H2  UNL     1       4.943   1.171  -0.788  1.00  0.00           H  
HETATM   24  H3  UNL     1       5.256   1.061   0.968  1.00  0.00           H  
HETATM   25  H4  UNL     1       2.390  -2.444   0.290  1.00  0.00           H  
HETATM   26  H5  UNL     1       0.512  -3.862   1.445  1.00  0.00           H  
HETATM   27  H6  UNL     1       0.970  -3.772  -0.321  1.00  0.00           H  
HETATM   28  H7  UNL     1      -0.695  -4.267   0.210  1.00  0.00           H  
HETATM   29  H8  UNL     1       3.177   1.780   0.040  1.00  0.00           H  
HETATM   30  H9  UNL     1       1.361   3.299   0.027  1.00  0.00           H  
HETATM   31  H10 UNL     1      -1.946   4.490   0.088  1.00  0.00           H  
HETATM   32  H11 UNL     1      -4.873   0.867   0.386  1.00  0.00           H  
HETATM   33  H12 UNL     1      -5.169  -1.387   0.613  1.00  0.00           H  
HETATM   34  H13 UNL     1      -4.049  -2.279  -0.443  1.00  0.00           H  
HETATM   35  H14 UNL     1      -3.809  -2.224   1.389  1.00  0.00           H  
CONECT    1    2   22   23   24
CONECT    2    3
CONECT    3    4    4   10
CONECT    4    5   25
CONECT    5    6    8    8
CONECT    6    7
CONECT    7   26   27   28
CONECT    8    9   21
CONECT    9   10   10   11
CONECT   10   29
CONECT   11   12   12   30
CONECT   12   13   14
CONECT   13   31
CONECT   14   15   21   21
CONECT   15   16   16   17
CONECT   17   18   18   32
CONECT   18   19   20
CONECT   19   33   34   35
CONECT   20   21
END

HMDB0030852
     RDKit          3D
Asperxanthone
 35 37  0  0  0  0  0  0  0  0999 V2000
    5.2115    0.4613    0.0332 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.3016   -0.6146    0.1233 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.9523   -0.3651    0.1603 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0727   -1.4119    0.2478 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.6923   -1.2006    0.2879 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2320   -2.2265    0.3760 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.1519   -3.5867    0.4328 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.2423    0.1088    0.2360 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1100    1.1711    0.1482 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.4989    0.9241    0.1096 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.6934    2.4544    0.0964 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6785    2.7685    0.1309 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0985    4.0492    0.0794 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5758    1.7146    0.2194 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9414    1.8698    0.2620 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4405    2.9959    0.2215 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8175    0.7811    0.3515 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2396   -0.4669    0.3954 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1159   -1.6667    0.4907 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9405   -0.6242    0.3554 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1135    0.4032    0.2709 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.1992    0.0273   -0.2387 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.9426    1.1707   -0.7885 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.2562    1.0610    0.9680 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.3897   -2.4438    0.2902 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.5124   -3.8617    1.4449 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.9700   -3.7715   -0.3213 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6954   -4.2671    0.2098 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.1771    1.7798    0.0396 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.3609    3.2995    0.0274 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9456    4.4897    0.0878 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.8727    0.8671    0.3861 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.1693   -1.3869    0.6127 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.0493   -2.2789   -0.4432 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8094   -2.2239    1.3885 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  2  3  1  0
  3  4  2  0
  4  5  1  0
  5  6  1  0
  6  7  1  0
  5  8  2  0
  8  9  1  0
  9 10  2  0
  9 11  1  0
 11 12  2  0
 12 13  1  0
 12 14  1  0
 14 15  1  0
 15 16  2  0
 15 17  1  0
 17 18  2  0
 18 19  1  0
 18 20  1  0
 20 21  1  0
 10  3  1  0
 21 14  2  0
 21  8  1  0
  1 22  1  0
  1 23  1  0
  1 24  1  0
  4 25  1  0
  7 26  1  0
  7 27  1  0
  7 28  1  0
 10 29  1  0
 11 30  1  0
 13 31  1  0
 17 32  1  0
 19 33  1  0
 19 34  1  0
 19 35  1  0
M  END

Synonyms

Value	Source
Antibiotic TMC 256c2	ChEBI
Asperxanthon	ChEBI
TMC 256c2	ChEBI
5-Hydroxy-8,10-dimethoxy-2-methyl-4H-naphtho[1,2-b]pyran-4-one, 9ci	HMDB
Flavasperone	HMDB
Asperxanthone	ChEBI

Molecular Formula

C₁₆H₁₄O₅

Average Mass

286.2794

Monoisotopic Mass

286.084123558

IUPAC Name

5-hydroxy-8,10-dimethoxy-2-methyl-4H-benzo[h]chromen-4-one

Traditional Name

5-hydroxy-8,10-dimethoxy-2-methylbenzo[h]chromen-4-one

CAS Registry Number

Not Available

SMILES

COC1=CC(OC)=C2C(C=C(O)C3=C2OC(C)=CC3=O)=C1

InChI Identifier

InChI=1S/C16H14O5/c1-8-4-11(17)15-12(18)6-9-5-10(19-2)7-13(20-3)14(9)16(15)21-8/h4-7,18H,1-3H3

InChI Key

ARXPDHLVDOYIPX-UHFFFAOYSA-N

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as naphthopyranones. Naphthopyranones are compounds containing a naphthopyran skeleton where a ring carbon bears a carboxylic acid group. Naphthtopyran is made up of the pyran ring fused to a naphthalene ring system.

Kingdom

Organic compounds

Super Class

Organoheterocyclic compounds

Class

Naphthopyrans

Sub Class

Naphthopyranones

Direct Parent

Naphthopyranones

Alternative Parents

Substituents

Naphthopyranone
Chromone
2-naphthol
Benzopyran
1-benzopyran
Naphthalene
Anisole
1-hydroxy-2-unsubstituted benzenoid
Alkyl aryl ether
Pyranone
Benzenoid
Pyran
Heteroaromatic compound
Vinylogous acid
Oxacycle
Ether
Organic oxygen compound
Hydrocarbon derivative
Organic oxide
Organooxygen compound
Aromatic heteropolycyclic compound

Molecular Framework

Aromatic heteropolycyclic compounds

External Descriptors

Not Available

Functional Ontology

Not Available

Physical Properties

State

Solid

Predicted Properties

Property	Value	Source
Water Solubility	0.079 g/L	ALOGPS
logP	2.95	ALOGPS
logP	2.89	ChemAxon
logS	-3.6	ALOGPS
pKa (Strongest Acidic)	8.4	ChemAxon
pKa (Strongest Basic)	-4.5	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	5	ChemAxon
Hydrogen Donor Count	1	ChemAxon
Polar Surface Area	64.99 Å²	ChemAxon
Rotatable Bond Count	2	ChemAxon
Refractivity	78.46 m³·mol⁻¹	ChemAxon
Polarizability	29.24 Å³	ChemAxon
Number of Rings	3	ChemAxon
Bioavailability	Yes	ChemAxon
Rule of Five	Yes	ChemAxon
Ghose Filter	Yes	ChemAxon
Veber's Rule	No	ChemAxon
MDDR-like Rule	No	ChemAxon

Spectra

Not Available

Biological Properties

Cellular Locations

Membrane

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

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

HMDB0030852

DrugBank ID

Not Available

Phenol Explorer Compound ID

Not Available

FooDB ID

FDB002811

KNApSAcK ID

C00054889

Chemspider ID

4678011

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

5748546

PDB ID

Not Available

ChEBI ID

133814

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 ]
Yannai, Shmuel (2004). Yannai, Shmuel. (2004) Dictionary of food compounds with CD-ROM: Additives, flavors, and ingredients. Boca Raton: Chapman & Hall/CRC.. Boca Raton: Chapman & Hall/CRC..

Showing metabocard for Flavasperone (MMDBc0006724)

MOL for #<Metabolite:0x00005645ca2667e8>

3D MOL for #<Metabolite:0x00005645ca2667e8>

3D SDF for #<Metabolite:0x00005645ca2667e8>

3D-SDF for #<Metabolite:0x00005645ca2667e8>

PDB for #<Metabolite:0x00005645ca2667e8>

3D PDB for #<Metabolite:0x00005645ca2667e8>

SMILES for #<Metabolite:0x00005645ca2667e8>

INCHI for #<Metabolite:0x00005645ca2667e8>

Structure for #<Metabolite:0x00005645ca2667e8>

3D Structure for #<Metabolite:0x00005645ca2667e8>