MiMeDB: Showing metabocard for toralactone (MMDBc0054678)

Record Information

Version

1.0

Status

Detected and Quantified

Creation Date

2022-06-05 23:23:56 UTC

Update Date

2025-01-16 05:33:37 UTC

Metabolite ID

MMDBc0054678

Metabolite Identification

Common Name

toralactone

Description

Toralactone is found in coffee and coffee products. Toralactone is isolated from seeds of Cassia tora (charota).

Structure

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

HMDB0038549
     RDKit          3D
Toralactone
 32 34  0  0  0  0  0  0  0  0999 V2000
    4.7116    1.8387   -0.0632 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.5446    0.4313    0.0452 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.2411   -0.0631    0.0833 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.0816   -1.4162    0.1875 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.7877   -1.9495    0.2287 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.6468   -3.3301    0.3350 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.6652   -1.1591    0.1679 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6033   -1.7033    0.2099 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9030   -3.0227    0.3115 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6831   -0.8010    0.1405 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9681   -1.2896    0.1782 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1450   -2.5220    0.2731 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9673   -0.4453    0.1133 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8411    0.8351    0.0147 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.0441    1.7112   -0.0526 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5924    1.3990   -0.0288 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4843    0.5449    0.0369 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2175    1.0737   -0.0039 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.8675    0.2125    0.0623 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1461    0.7588    0.0201 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.1830    2.2061   -0.9659 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.7638    2.1372   -0.0690 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.2313    2.2834    0.8393 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.9132   -2.1193    0.2416 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.4075   -3.9681    0.3841 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3981   -3.8344    0.3740 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.7761    2.7712   -0.0632 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.7245    1.5232    0.8206 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.5903    1.4825   -0.9958 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4201    2.4477   -0.1096 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0973    2.1424   -0.0862 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.2644    1.8249   -0.0620 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
  5  7  2  0
  7  8  1  0
  8  9  1  0
  8 10  2  0
 10 11  1  0
 11 12  2  0
 11 13  1  0
 13 14  1  0
 14 15  1  0
 14 16  2  0
 16 17  1  0
 17 18  2  0
 18 19  1  0
 19 20  2  0
 20  3  1  0
 19  7  1  0
 17 10  1  0
  1 21  1  0
  1 22  1  0
  1 23  1  0
  4 24  1  0
  6 25  1  0
  9 26  1  0
 15 27  1  0
 15 28  1  0
 15 29  1  0
 16 30  1  0
 18 31  1  0
 20 32  1  0
M  END


  Mrv0541 05061310312D          

 20 22  0  0  0  0            999 V2000
    0.7145   -1.2375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.4302   -0.4125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1434   -1.2375    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
    5.0013   -1.2375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.7158   -2.4750    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
    2.8579   -1.6500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2868   -1.6500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.7158   -1.6500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0013   -2.8875    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2868   -2.4750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8579   -2.4750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5724   -2.8875    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1434   -2.8875    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0013   -3.7125    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.5724   -3.7125    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.1434   -3.7125    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.4302   -1.2375    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.4289   -2.4750    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
  7  1  1  0  0  0  0
  7  3  2  0  0  0  0
  8  3  1  0  0  0  0
  8  4  2  0  0  0  0
  9  4  1  0  0  0  0
  9  5  2  0  0  0  0
 10  5  1  0  0  0  0
 10  6  2  0  0  0  0
 11  6  1  0  0  0  0
 12  9  1  0  0  0  0
 12 11  2  0  0  0  0
 13  8  1  0  0  0  0
 14 12  1  0  0  0  0
 14 13  2  0  0  0  0
 15 13  1  0  0  0  0
 16 11  1  0  0  0  0
 17 14  1  0  0  0  0
 18 15  2  0  0  0  0
 19  2  1  0  0  0  0
 19 10  1  0  0  0  0
 20  7  1  0  0  0  0
 20 15  1  0  0  0  0
M  END
> <DATABASE_ID>
MMDBc0054678

> <DATABASE_NAME>
MIME

> <SMILES>
COC1=CC(O)=C2C(O)=C3C(=O)OC(C)=CC3=CC2=C1

> <INCHI_IDENTIFIER>
InChI=1S/C15H12O5/c1-7-3-8-4-9-5-10(19-2)6-11(16)12(9)14(17)13(8)15(18)20-7/h3-6,16-17H,1-2H3

> <INCHI_KEY>
WEHXAEGTVPWKDY-UHFFFAOYSA-N

> <FORMULA>
C15H12O5

> <MOLECULAR_WEIGHT>
272.2528

> <EXACT_MASS>
272.068473494

> <JCHEM_ACCEPTOR_COUNT>
4

> <JCHEM_AVERAGE_POLARIZABILITY>
27.479918076704386

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
2

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
9,10-dihydroxy-7-methoxy-3-methyl-1H-benzo[g]isochromen-1-one

> <ALOGPS_LOGP>
2.68

> <JCHEM_LOGP>
3.1301378890000002

> <ALOGPS_LOGS>
-3.32

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
3

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
9.656418012712935

> <JCHEM_PKA_STRONGEST_ACIDIC>
8.448629138871892

> <JCHEM_PKA_STRONGEST_BASIC>
-4.4827965879874165

> <JCHEM_POLAR_SURFACE_AREA>
75.99000000000001

> <JCHEM_REFRACTIVITY>
74.1803

> <JCHEM_ROTATABLE_BOND_COUNT>
1

> <JCHEM_RULE_OF_FIVE>
1

> <ALOGPS_SOLUBILITY>
1.31e-01 g/l

> <JCHEM_TRADITIONAL_IUPAC>
9,10-dihydroxy-7-methoxy-3-methylbenzo[g]isochromen-1-one

> <JCHEM_VEBER_RULE>
0

$$$$

HMDB0038549
     RDKit          3D
Toralactone
 32 34  0  0  0  0  0  0  0  0999 V2000
    4.7116    1.8387   -0.0632 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.5446    0.4313    0.0452 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.2411   -0.0631    0.0833 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.0816   -1.4162    0.1875 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.7877   -1.9495    0.2287 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.6468   -3.3301    0.3350 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.6652   -1.1591    0.1679 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6033   -1.7033    0.2099 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9030   -3.0227    0.3115 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6831   -0.8010    0.1405 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9681   -1.2896    0.1782 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1450   -2.5220    0.2731 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9673   -0.4453    0.1133 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8411    0.8351    0.0147 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.0441    1.7112   -0.0526 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5924    1.3990   -0.0288 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4843    0.5449    0.0369 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2175    1.0737   -0.0039 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.8675    0.2125    0.0623 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1461    0.7588    0.0201 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.1830    2.2061   -0.9659 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.7638    2.1372   -0.0690 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.2313    2.2834    0.8393 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.9132   -2.1193    0.2416 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.4075   -3.9681    0.3841 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3981   -3.8344    0.3740 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.7761    2.7712   -0.0632 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.7245    1.5232    0.8206 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.5903    1.4825   -0.9958 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4201    2.4477   -0.1096 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0973    2.1424   -0.0862 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.2644    1.8249   -0.0620 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
  5  7  2  0
  7  8  1  0
  8  9  1  0
  8 10  2  0
 10 11  1  0
 11 12  2  0
 11 13  1  0
 13 14  1  0
 14 15  1  0
 14 16  2  0
 16 17  1  0
 17 18  2  0
 18 19  1  0
 19 20  2  0
 20  3  1  0
 19  7  1  0
 17 10  1  0
  1 21  1  0
  1 22  1  0
  1 23  1  0
  4 24  1  0
  6 25  1  0
  9 26  1  0
 15 27  1  0
 15 28  1  0
 15 29  1  0
 16 30  1  0
 18 31  1  0
 20 32  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       1.334  -2.310   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0      12.003  -0.770   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0       4.001  -2.310   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0       6.668  -2.310   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0       9.336  -2.310   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0      10.669  -4.620   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0       2.667  -3.080   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0       5.335  -3.080   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0       8.002  -3.080   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0      10.669  -3.080   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0       9.336  -5.390   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0       8.002  -4.620   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0       5.335  -4.620   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0       6.668  -5.390   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0       4.001  -5.390   0.000  0.00  0.00           C+0
HETATM   16  O   UNK     0       9.336  -6.930   0.000  0.00  0.00           O+0
HETATM   17  O   UNK     0       6.668  -6.930   0.000  0.00  0.00           O+0
HETATM   18  O   UNK     0       4.001  -6.930   0.000  0.00  0.00           O+0
HETATM   19  O   UNK     0      12.003  -2.310   0.000  0.00  0.00           O+0
HETATM   20  O   UNK     0       2.667  -4.620   0.000  0.00  0.00           O+0
CONECT    1    7                                                            
CONECT    2   19                                                            
CONECT    3    7    8                                                       
CONECT    4    8    9                                                       
CONECT    5    9   10                                                       
CONECT    6   10   11                                                       
CONECT    7    1    3   20                                                  
CONECT    8    3    4   13                                                  
CONECT    9    4    5   12                                                  
CONECT   10    5    6   19                                                  
CONECT   11    6   12   16                                                  
CONECT   12    9   11   14                                                  
CONECT   13    8   14   15                                                  
CONECT   14   12   13   17                                                  
CONECT   15   13   18   20                                                  
CONECT   16   11                                                            
CONECT   17   14                                                            
CONECT   18   15                                                            
CONECT   19    2   10                                                       
CONECT   20    7   15                                                       
MASTER        0    0    0    0    0    0    0    0   20    0   44    0
END

COMPND    HMDB0038549
HETATM    1  C1  UNL     1       4.712   1.839  -0.063  1.00  0.00           C  
HETATM    2  O1  UNL     1       4.545   0.431   0.045  1.00  0.00           O  
HETATM    3  C2  UNL     1       3.241  -0.063   0.083  1.00  0.00           C  
HETATM    4  C3  UNL     1       3.082  -1.416   0.188  1.00  0.00           C  
HETATM    5  C4  UNL     1       1.788  -1.950   0.229  1.00  0.00           C  
HETATM    6  O2  UNL     1       1.647  -3.330   0.335  1.00  0.00           O  
HETATM    7  C5  UNL     1       0.665  -1.159   0.168  1.00  0.00           C  
HETATM    8  C6  UNL     1      -0.603  -1.703   0.210  1.00  0.00           C  
HETATM    9  O3  UNL     1      -0.903  -3.023   0.312  1.00  0.00           O  
HETATM   10  C7  UNL     1      -1.683  -0.801   0.141  1.00  0.00           C  
HETATM   11  C8  UNL     1      -2.968  -1.290   0.178  1.00  0.00           C  
HETATM   12  O4  UNL     1      -3.145  -2.522   0.273  1.00  0.00           O  
HETATM   13  O5  UNL     1      -3.967  -0.445   0.113  1.00  0.00           O  
HETATM   14  C9  UNL     1      -3.841   0.835   0.015  1.00  0.00           C  
HETATM   15  C10 UNL     1      -5.044   1.711  -0.053  1.00  0.00           C  
HETATM   16  C11 UNL     1      -2.592   1.399  -0.029  1.00  0.00           C  
HETATM   17  C12 UNL     1      -1.484   0.545   0.037  1.00  0.00           C  
HETATM   18  C13 UNL     1      -0.218   1.074  -0.004  1.00  0.00           C  
HETATM   19  C14 UNL     1       0.868   0.213   0.062  1.00  0.00           C  
HETATM   20  C15 UNL     1       2.146   0.759   0.020  1.00  0.00           C  
HETATM   21  H1  UNL     1       4.183   2.206  -0.966  1.00  0.00           H  
HETATM   22  H2  UNL     1       5.764   2.137  -0.069  1.00  0.00           H  
HETATM   23  H3  UNL     1       4.231   2.283   0.839  1.00  0.00           H  
HETATM   24  H4  UNL     1       3.913  -2.119   0.242  1.00  0.00           H  
HETATM   25  H5  UNL     1       2.407  -3.968   0.384  1.00  0.00           H  
HETATM   26  H6  UNL     1      -0.398  -3.834   0.374  1.00  0.00           H  
HETATM   27  H7  UNL     1      -4.776   2.771  -0.063  1.00  0.00           H  
HETATM   28  H8  UNL     1      -5.724   1.523   0.821  1.00  0.00           H  
HETATM   29  H9  UNL     1      -5.590   1.483  -0.996  1.00  0.00           H  
HETATM   30  H10 UNL     1      -2.420   2.448  -0.110  1.00  0.00           H  
HETATM   31  H11 UNL     1      -0.097   2.142  -0.086  1.00  0.00           H  
HETATM   32  H12 UNL     1       2.264   1.825  -0.062  1.00  0.00           H  
CONECT    1    2   21   22   23
CONECT    2    3
CONECT    3    4    4   20
CONECT    4    5   24
CONECT    5    6    7    7
CONECT    6   25
CONECT    7    8   19
CONECT    8    9   10   10
CONECT    9   26
CONECT   10   11   17
CONECT   11   12   12   13
CONECT   13   14
CONECT   14   15   16   16
CONECT   15   27   28   29
CONECT   16   17   30
CONECT   17   18   18
CONECT   18   19   31
CONECT   19   20   20
CONECT   20   32
END

HMDB0038549
     RDKit          3D
Toralactone
 32 34  0  0  0  0  0  0  0  0999 V2000
    4.7116    1.8387   -0.0632 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.5446    0.4313    0.0452 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.2411   -0.0631    0.0833 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.0816   -1.4162    0.1875 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.7877   -1.9495    0.2287 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.6468   -3.3301    0.3350 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.6652   -1.1591    0.1679 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6033   -1.7033    0.2099 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9030   -3.0227    0.3115 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6831   -0.8010    0.1405 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9681   -1.2896    0.1782 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1450   -2.5220    0.2731 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9673   -0.4453    0.1133 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8411    0.8351    0.0147 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.0441    1.7112   -0.0526 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5924    1.3990   -0.0288 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4843    0.5449    0.0369 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2175    1.0737   -0.0039 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.8675    0.2125    0.0623 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1461    0.7588    0.0201 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.1830    2.2061   -0.9659 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.7638    2.1372   -0.0690 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.2313    2.2834    0.8393 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.9132   -2.1193    0.2416 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.4075   -3.9681    0.3841 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3981   -3.8344    0.3740 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.7761    2.7712   -0.0632 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.7245    1.5232    0.8206 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.5903    1.4825   -0.9958 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4201    2.4477   -0.1096 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0973    2.1424   -0.0862 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.2644    1.8249   -0.0620 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
  5  7  2  0
  7  8  1  0
  8  9  1  0
  8 10  2  0
 10 11  1  0
 11 12  2  0
 11 13  1  0
 13 14  1  0
 14 15  1  0
 14 16  2  0
 16 17  1  0
 17 18  2  0
 18 19  1  0
 19 20  2  0
 20  3  1  0
 19  7  1  0
 17 10  1  0
  1 21  1  0
  1 22  1  0
  1 23  1  0
  4 24  1  0
  6 25  1  0
  9 26  1  0
 15 27  1  0
 15 28  1  0
 15 29  1  0
 16 30  1  0
 18 31  1  0
 20 32  1  0
M  END

Synonyms

Value	Source
9,10-Dihydroxy-7-methoxy-3-methyl-1H-naphtho(2,3-c)pyran-1-one	ChEBI
9,10-Dihydroxy-7-methoxy-3-methyl-1H-naphtho[2,3-c]pyran-1-one, 9ci	HMDB

Molecular Formula

C₁₅H₁₂O₅

Average Mass

272.2528

Monoisotopic Mass

272.068473494

IUPAC Name

9,10-dihydroxy-7-methoxy-3-methyl-1H-benzo[g]isochromen-1-one

Traditional Name

9,10-dihydroxy-7-methoxy-3-methylbenzo[g]isochromen-1-one

CAS Registry Number

Not Available

SMILES

COC1=CC(O)=C2C(O)=C3C(=O)OC(C)=CC3=CC2=C1

InChI Identifier

InChI=1S/C15H12O5/c1-7-3-8-4-9-5-10(19-2)6-11(16)12(9)14(17)13(8)15(18)20-7/h3-6,16-17H,1-2H3

InChI Key

WEHXAEGTVPWKDY-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
Isocoumarin
1-naphthol
Benzopyran
Naphthalene
2-benzopyran
Anisole
Alkyl aryl ether
1-hydroxy-4-unsubstituted benzenoid
1-hydroxy-2-unsubstituted benzenoid
Pyranone
Pyran
Benzenoid
Heteroaromatic compound
Vinylogous acid
Lactone
Ether
Oxacycle
Organooxygen compound
Hydrocarbon derivative
Organic oxide
Organic oxygen compound
Aromatic heteropolycyclic compound

Molecular Framework

Aromatic heteropolycyclic compounds

External Descriptors

aromatic ether (CHEBI:78029 )
organic heterotricyclic compound (CHEBI:78029 )
phenols (CHEBI:78029 )
polyketide (CHEBI:78029 )
lactone (CHEBI:78029 )

Functional Ontology

Not Available

Physical Properties

State

Solid

Predicted Properties

Property	Value	Source
Water Solubility	0.13 g/L	ALOGPS
logP	2.68	ALOGPS
logP	3.13	ChemAxon
logS	-3.3	ALOGPS
pKa (Strongest Acidic)	8.45	ChemAxon
pKa (Strongest Basic)	-4.5	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	4	ChemAxon
Hydrogen Donor Count	2	ChemAxon
Polar Surface Area	75.99 Å²	ChemAxon
Rotatable Bond Count	1	ChemAxon
Refractivity	74.18 m³·mol⁻¹	ChemAxon
Polarizability	27.48 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

Spectrum Type	Description	Splash Key	Deposition Date	View
Predicted GC-MS	Predicted GC-MS Spectrum - GC-MS (Non-derivatized) - 70eV, Positive	splash10-0abc-0190000000-0b6644937e0069cfba34	2017-09-01	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - GC-MS (2 TMS) - 70eV, Positive	splash10-0uk9-2009400000-28388824cb8fdaf3e748	2017-10-06	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - GC-MS (Non-derivatized) - 70eV, Positive	Not Available	2021-10-12	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 10V, Positive	splash10-00di-0090000000-af0e4aa15b772877e705	2016-06-03	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 20V, Positive	splash10-00di-0090000000-67a31feccf2de0c2d09c	2016-06-03	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 40V, Positive	splash10-002b-0890000000-b766d9ba09c1aa5c07ac	2016-06-03	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 10V, Negative	splash10-00di-0090000000-a304bd0b8e4313937885	2016-08-03	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 20V, Negative	splash10-00di-0090000000-b199e2cdf9b618446ccb	2016-08-03	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 40V, Negative	splash10-004j-1980000000-284d4a71b00b8c9cc8c5	2016-08-03	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 10V, Positive	splash10-00di-0090000000-031a5312b116bdf1aa4a	2021-09-24	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 20V, Positive	splash10-00di-0090000000-e8cad39c3f9c861b9b61	2021-09-24	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 40V, Positive	splash10-0fi9-0490000000-d32339d75f0f0ea86780	2021-09-24	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 10V, Negative	splash10-00di-0090000000-d6b6f6391b4e9f4522f4	2021-09-24	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 20V, Negative	splash10-00di-0090000000-d6b6f6391b4e9f4522f4	2021-09-24	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 40V, Negative	splash10-00dj-3970000000-0694d792101fade0dd10	2021-09-24	View Spectrum

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	3

Exposure Sources

Source Type	Activity	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

HMDB0038549

DrugBank ID

Not Available

Phenol Explorer Compound ID

Not Available

FooDB ID

KNApSAcK ID

Chemspider ID

KEGG Compound ID

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

5321980

PDB ID

Not Available

ChEBI ID

78029

Food Biomarker Ontology

Not Available

References

Synthesis Reference

Not Available

General References

Bansal P, Morgat A, Axelsen KB, Muthukrishnan V, Coudert E, Aimo L, Hyka-Nouspikel N, Gasteiger E, Kerhornou A, Neto TB, Pozzato M, Blatter MC, Ignatchenko A, Redaschi N, Bridge A: Rhea, the reaction knowledgebase in 2022. Nucleic Acids Res. 2022 Jan 7;50(D1):D693-D700. doi: 10.1093/nar/gkab1016. [PubMed:34755880 ]
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 toralactone (MMDBc0054678)

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3D Structure for #<Metabolite:0x00007f5398ca4660>