MiMeDB: Showing metabocard for Hesseltin A photoisomer C (MMDBc0015101)

Record Information

Version

2.0

Status

Detected and Quantified

Creation Date

2021-05-15 05:59:48 UTC

Update Date

2025-10-07 16:06:22 UTC

Metabolite ID

MMDBc0015101

Metabolite Identification

Common Name

Hesseltin A photoisomer C

Description

Hesseltin A photoisomer C is a flavonoid derivative. There is little literature available on this metabolite, indicating that further research may be needed to fully understand its properties and biological significance.

Structure

MOL SDF PDB SMILES InChI


  Mrv1652305152107592D          

 38 42  0  0  1  0            999 V2000
    8.4840   -0.8475    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.2935   -1.4509    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.6256   -0.6782    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2303   -2.1737    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.9205   -0.1474    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.5325    0.5806    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.7080    0.6087    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.2715   -0.0914    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3307   -2.0101    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3040    0.5898    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5088   -1.8336    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5468    0.9427    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.0590    0.6648    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8913    0.4745    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.4470   -0.0633    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.2345    0.6928    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.7979   -0.0072    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.9734    0.0208    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    3.5368   -0.6792    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    5.1859   -0.7353    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4497   -0.6408    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.9248   -1.4073    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.7430   -0.2751    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.2476   -1.0034    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.2140    0.1752    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    4.8465    1.4209    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.5854    0.7489    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.6299   -1.5502    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.3907    0.2279    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.0572    0.0708    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.0104   -0.7634    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.7493   -1.4354    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    9.7450   -0.1755    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
    8.9691    1.2807    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.3200    1.3368    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.6595   -0.8194    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.1489    0.0488    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.9590   -1.2680    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
  5  1  1  0  0  0  0
  6  5  2  0  0  0  0
  7  6  1  0  0  0  0
  8  7  2  0  0  0  0
 11  9  1  0  0  0  0
 12 10  1  0  0  0  0
 15  8  1  0  0  0  0
 15 13  2  0  0  0  0
 16 13  1  0  0  0  0
 17 16  1  0  0  0  0
 18 17  1  0  0  0  0
 19 18  1  0  0  0  0
 20 17  2  0  0  0  0
 21  2  1  0  0  0  0
 21  3  1  0  0  0  0
 22  4  1  1  0  0  0
 22  9  1  0  0  0  0
 22 19  1  0  0  0  0
 23 10  1  6  0  0  0
 23 14  1  0  0  0  0
 23 19  1  0  0  0  0
 24 11  1  0  0  0  0
 24 21  1  0  0  0  0
 24 23  1  0  0  0  0
 25 12  1  0  0  0  0
 25 21  1  0  0  0  0
 26 16  2  0  0  0  0
 18 27  1  1  0  0  0
 24 28  1  6  0  0  0
 25 29  1  1  0  0  0
 30 14  1  0  0  0  0
 30 25  1  0  0  0  0
 31 15  1  0  0  0  0
 31 20  1  0  0  0  0
 32 20  1  0  0  0  0
 32 22  1  0  0  0  0
 33  5  1  0  0  0  0
 34  6  1  0  0  0  0
 35  7  1  0  0  0  0
 36  8  1  0  0  0  0
 18 37  1  6  0  0  0
 19 38  1  6  0  0  0
M  END


  Mrv1652305152107592D          

 38 42  0  0  1  0            999 V2000
    8.4840   -0.8475    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.2935   -1.4509    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.6256   -0.6782    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2303   -2.1737    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.9205   -0.1474    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.5325    0.5806    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.7080    0.6087    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.2715   -0.0914    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3307   -2.0101    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3040    0.5898    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5088   -1.8336    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5468    0.9427    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.0590    0.6648    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8913    0.4745    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.4470   -0.0633    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.2345    0.6928    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.7979   -0.0072    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.9734    0.0208    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    3.5368   -0.6792    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    5.1859   -0.7353    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4497   -0.6408    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.9248   -1.4073    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.7430   -0.2751    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.2476   -1.0034    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.2140    0.1752    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    4.8465    1.4209    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.5854    0.7489    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.6299   -1.5502    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.3907    0.2279    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.0572    0.0708    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.0104   -0.7634    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.7493   -1.4354    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    9.7450   -0.1755    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
    8.9691    1.2807    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.3200    1.3368    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.6595   -0.8194    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.1489    0.0488    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.9590   -1.2680    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
  5  1  1  0  0  0  0
  6  5  2  0  0  0  0
  7  6  1  0  0  0  0
  8  7  2  0  0  0  0
 11  9  1  0  0  0  0
 12 10  1  0  0  0  0
 15  8  1  0  0  0  0
 15 13  2  0  0  0  0
 16 13  1  0  0  0  0
 17 16  1  0  0  0  0
 18 17  1  0  0  0  0
 19 18  1  0  0  0  0
 20 17  2  0  0  0  0
 21  2  1  0  0  0  0
 21  3  1  0  0  0  0
 22  4  1  1  0  0  0
 22  9  1  0  0  0  0
 22 19  1  0  0  0  0
 23 10  1  6  0  0  0
 23 14  1  0  0  0  0
 23 19  1  0  0  0  0
 24 11  1  0  0  0  0
 24 21  1  0  0  0  0
 24 23  1  0  0  0  0
 25 12  1  0  0  0  0
 25 21  1  0  0  0  0
 26 16  2  0  0  0  0
 18 27  1  1  0  0  0
 24 28  1  6  0  0  0
 25 29  1  1  0  0  0
 30 14  1  0  0  0  0
 30 25  1  0  0  0  0
 31 15  1  0  0  0  0
 31 20  1  0  0  0  0
 32 20  1  0  0  0  0
 32 22  1  0  0  0  0
 33  5  1  0  0  0  0
 34  6  1  0  0  0  0
 35  7  1  0  0  0  0
 36  8  1  0  0  0  0
 18 37  1  6  0  0  0
 19 38  1  6  0  0  0
M  END
> <DATABASE_ID>
MMDBc0015101

> <DATABASE_NAME>
MIME

> <SMILES>
[H]\C(C)=C(/[H])\C(\[H])=C(/[H])C1=CC(=O)C2=C(O1)O[C@]1(C)CC[C@@]3(O)C(C)(C)[C@]4(O)CC[C@]3(CO4)[C@@]1([H])[C@@]2([H])O

> <INCHI_IDENTIFIER>
InChI=1S/C25H32O7/c1-5-6-7-8-15-13-16(26)17-18(27)19-22(4,32-20(17)31-15)9-11-24(28)21(2,3)25(29)12-10-23(19,24)14-30-25/h5-8,13,18-19,27-29H,9-12,14H2,1-4H3/b6-5-,8-7+/t18-,19-,22+,23-,24+,25-/m0/s1

> <INCHI_KEY>
LFPBILWIIIPSMS-OUEPJCAYSA-N

> <FORMULA>
C25H32O7

> <MOLECULAR_WEIGHT>
444.524

> <EXACT_MASS>
444.21480337

> <JCHEM_ACCEPTOR_COUNT>
7

> <JCHEM_ATOM_COUNT>
64

> <JCHEM_AVERAGE_POLARIZABILITY>
47.89370775427949

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
3

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
(1R,2S,3R,11R,14S,16S)-3,14,16-trihydroxy-11,15,15-trimethyl-7-[(1E,3Z)-penta-1,3-dien-1-yl]-8,10,17-trioxapentacyclo[14.2.2.0^{1,14}.0^{2,11}.0^{4,9}]icosa-4(9),6-dien-5-one

> <ALOGPS_LOGP>
2.22

> <JCHEM_LOGP>
2.188081860999999

> <ALOGPS_LOGS>
-3.49

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
5

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
13.56855406830977

> <JCHEM_PKA_STRONGEST_ACIDIC>
11.60071916510894

> <JCHEM_PKA_STRONGEST_BASIC>
-3.3068514029940133

> <JCHEM_POLAR_SURFACE_AREA>
105.45000000000002

> <JCHEM_REFRACTIVITY>
130.4128

> <JCHEM_ROTATABLE_BOND_COUNT>
2

> <JCHEM_RULE_OF_FIVE>
1

> <ALOGPS_SOLUBILITY>
1.42e-01 g/l

> <JCHEM_TRADITIONAL_IUPAC>
(1R,2S,3R,11R,14S,16S)-3,14,16-trihydroxy-11,15,15-trimethyl-7-[(1E,3Z)-penta-1,3-dien-1-yl]-8,10,17-trioxapentacyclo[14.2.2.0^{1,14}.0^{2,11}.0^{4,9}]icosa-4(9),6-dien-5-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      15.837  -1.582   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0       2.414  -2.708   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0       1.168  -1.266   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0       7.897  -4.058   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0      16.652  -0.275   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0      15.927   1.084   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0      14.388   1.136   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0      13.573  -0.171   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0       6.217  -3.752   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0       4.301   1.101   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0       4.683  -3.423   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0       2.887   1.760   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0      11.310   1.241   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0       5.397   0.886   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0      12.034  -0.118   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0       9.771   1.293   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0       8.956  -0.014   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0       7.417   0.039   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0       6.602  -1.268   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0       9.680  -1.373   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0       2.706  -1.196   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0       7.326  -2.627   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0       5.120  -0.514   0.000  0.00  0.00           C+0
HETATM   24  C   UNK     0       4.196  -1.873   0.000  0.00  0.00           C+0
HETATM   25  C   UNK     0       2.266   0.327   0.000  0.00  0.00           C+0
HETATM   26  O   UNK     0       9.047   2.652   0.000  0.00  0.00           O+0
HETATM   27  O   UNK     0       6.693   1.398   0.000  0.00  0.00           O+0
HETATM   28  O   UNK     0       3.042  -2.894   0.000  0.00  0.00           O+0
HETATM   29  O   UNK     0       0.729   0.425   0.000  0.00  0.00           O+0
HETATM   30  O   UNK     0       3.840   0.132   0.000  0.00  0.00           O+0
HETATM   31  O   UNK     0      11.219  -1.425   0.000  0.00  0.00           O+0
HETATM   32  O   UNK     0       8.865  -2.679   0.000  0.00  0.00           O+0
HETATM   33  H   UNK     0      18.191  -0.328   0.000  0.00  0.00           H+0
HETATM   34  H   UNK     0      16.742   2.391   0.000  0.00  0.00           H+0
HETATM   35  H   UNK     0      13.664   2.495   0.000  0.00  0.00           H+0
HETATM   36  H   UNK     0      14.298  -1.530   0.000  0.00  0.00           H+0
HETATM   37  H   UNK     0       5.878   0.091   0.000  0.00  0.00           H+0
HETATM   38  H   UNK     0       5.523  -2.367   0.000  0.00  0.00           H+0
CONECT    1    5                                                            
CONECT    2   21                                                            
CONECT    3   21                                                            
CONECT    4   22                                                            
CONECT    5    1    6   33                                                  
CONECT    6    5    7   34                                                  
CONECT    7    6    8   35                                                  
CONECT    8    7   15   36                                                  
CONECT    9   11   22                                                       
CONECT   10   12   23                                                       
CONECT   11    9   24                                                       
CONECT   12   10   25                                                       
CONECT   13   15   16                                                       
CONECT   14   23   30                                                       
CONECT   15    8   13   31                                                  
CONECT   16   13   17   26                                                  
CONECT   17   16   18   20                                                  
CONECT   18   17   19   27   37                                             
CONECT   19   18   22   23   38                                             
CONECT   20   17   31   32                                                  
CONECT   21    2    3   24   25                                             
CONECT   22    4    9   19   32                                             
CONECT   23   10   14   19   24                                             
CONECT   24   11   21   23   28                                             
CONECT   25   12   21   29   30                                             
CONECT   26   16                                                            
CONECT   27   18                                                            
CONECT   28   24                                                            
CONECT   29   25                                                            
CONECT   30   14   25                                                       
CONECT   31   15   20                                                       
CONECT   32   20   22                                                       
CONECT   33    5                                                            
CONECT   34    6                                                            
CONECT   35    7                                                            
CONECT   36    8                                                            
CONECT   37   18                                                            
CONECT   38   19                                                            
MASTER        0    0    0    0    0    0    0    0   38    0   84    0
END

Synonyms

Not Available

Molecular Formula

C₂₅H₃₂O₇

Average Mass

444.524

Monoisotopic Mass

444.21480337

IUPAC Name

(1R,2S,3R,11R,14S,16S)-3,14,16-trihydroxy-11,15,15-trimethyl-7-[(1E,3Z)-penta-1,3-dien-1-yl]-8,10,17-trioxapentacyclo[14.2.2.0^{1,14}.0^{2,11}.0^{4,9}]icosa-4(9),6-dien-5-one

Traditional Name

(1R,2S,3R,11R,14S,16S)-3,14,16-trihydroxy-11,15,15-trimethyl-7-[(1E,3Z)-penta-1,3-dien-1-yl]-8,10,17-trioxapentacyclo[14.2.2.0^{1,14}.0^{2,11}.0^{4,9}]icosa-4(9),6-dien-5-one

CAS Registry Number

Not Available

SMILES

[H]\C(C)=C(/[H])\C(\[H])=C(/[H])C1=CC(=O)C2=C(O1)O[C@]1(C)CC[C@@]3(O)C(C)(C)[C@]4(O)CC[C@]3(CO4)[C@@]1([H])[C@@]2([H])O

InChI Identifier

InChI=1S/C25H32O7/c1-5-6-7-8-15-13-16(26)17-18(27)19-22(4,32-20(17)31-15)9-11-24(28)21(2,3)25(29)12-10-23(19,24)14-30-25/h5-8,13,18-19,27-29H,9-12,14H2,1-4H3/b6-5-,8-7+/t18-,19-,22+,23-,24+,25-/m0/s1

InChI Key

LFPBILWIIIPSMS-OUEPJCAYSA-N

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as naphthopyrans. Naphthopyrans are compounds containing a pyran ring fused to a naphthalene moiety. Furan is a 6 membered-ring non-aromatic ring with five carbon and one oxygen atoms. Naphthalene is a polycyclic aromatic hydrocarbon made up of two fused benzene rings.

Kingdom

Organic compounds

Super Class

Organoheterocyclic compounds

Class

Naphthopyrans

Sub Class

Not Available

Direct Parent

Naphthopyrans

Alternative Parents

Substituents

Naphthopyran
Naphthalene
Alkyl aryl ether
Pyranone
Oxane
Pyran
Cyclic alcohol
Heteroaromatic compound
Vinylogous ester
Tertiary alcohol
Hemiacetal
Secondary alcohol
Oxacycle
Ether
Polyol
Organooxygen compound
Hydrocarbon derivative
Alcohol
Organic oxide
Organic oxygen compound
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	0.14 g/L	ALOGPS
logP	2.22	ALOGPS
logP	2.19	ChemAxon
logS	-3.5	ALOGPS
pKa (Strongest Acidic)	11.6	ChemAxon
pKa (Strongest Basic)	-3.3	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	7	ChemAxon
Hydrogen Donor Count	3	ChemAxon
Polar Surface Area	105.45 Å²	ChemAxon
Rotatable Bond Count	2	ChemAxon
Refractivity	130.41 m³·mol⁻¹	ChemAxon
Polarizability	47.89 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

Not Available

Biological Properties

Cellular Locations

Not Available

Biospecimen Locations

Not Available

Tissue Locations

Not Available

Associated OMIM IDs

114500 (Colorectal cancer)
610247 (Eosinophilic esophagitis)

Human Proteins and Enzymes

Protein ID	Protein Name	Protein Type	Uniprot ID	Species

Human Pathways

Pathways

Name	SMPDB/PathBank

Microbial Pathways

Pathways

Not Available

Metabolic Reactions

Reactions

This table shows at most 20 reactions. For the full list of associated reactions:

See All Associated Reactions

Reaction ID	Precursor	Product	Enzyme	Reaction Type	Data Source	Reference

Health Effects and Bioactivity

Health Outcome/Bioactivity	Metabolite Response/Effect	Evidence Type	Host and Biospecimen	Data Source	Reference

Microbial Sources

Superkingdom/Kingdom	Phylum	Total species	Hosts and Body Sites	Microbial Links
Eukaryota/Fungi	Ascomycota	1	Human feces	Metabolic reconstruction

Exposure Sources

Other Exposures

Source Type	Data Source	Reference

Host Biospecimen and Location

Host and Biospecimen	Status	Mean	Std	Min	Max	Units	Age	Sex	Health Condition	Data Source	Reference

External Links

HMDB ID

Not Available

DrugBank ID

Not Available

Phenol Explorer Compound ID

Not Available

FooDB ID

Not Available

KNApSAcK ID

Not Available

Chemspider ID

Not Available

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

139587241

PDB ID

Not Available

ChEBI ID

Not Available

Food Biomarker Ontology

Not Available

CMMC Knowledgebase

Not Available

General References

van Santen JA, Poynton EF, Iskakova D, McMann E, Alsup TA, Clark TN, Fergusson CH, Fewer DP, Hughes AH, McCadden CA, Parra J, Soldatou S, Rudolf JD, Janssen EM, Duncan KR, Linington RG: The Natural Products Atlas 2.0: a database of microbially-derived natural products. Nucleic Acids Res. 2022 Jan 7;50(D1):D1317-D1323. doi: 10.1093/nar/gkab941. [PubMed:34718710 ]

Showing metabocard for Hesseltin A photoisomer C (MMDBc0015101)

MOL for #<Metabolite:0x00007f8de8b0b6c0>

3D MOL for #<Metabolite:0x00007f8de8b0b6c0>

3D SDF for #<Metabolite:0x00007f8de8b0b6c0>

3D-SDF for #<Metabolite:0x00007f8de8b0b6c0>

PDB for #<Metabolite:0x00007f8de8b0b6c0>

3D PDB for #<Metabolite:0x00007f8de8b0b6c0>

SMILES for #<Metabolite:0x00007f8de8b0b6c0>

INCHI for #<Metabolite:0x00007f8de8b0b6c0>

Structure for #<Metabolite:0x00007f8de8b0b6c0>

3D Structure for #<Metabolite:0x00007f8de8b0b6c0>