MiMeDB: Showing metabocard for Pestaloficiol U (MMDBc0012149)

Record Information

Version

1.0

Status

Detected and Quantified

Creation Date

2021-05-15 03:46:32 UTC

Update Date

2022-08-31 06:34:07 UTC

Metabolite ID

MMDBc0012149

Metabolite Identification

Common Name

Pestaloficiol U

Description

Pestaloficiol U belongs to the class of organic compounds known as prenylated neoflavonoids. These are neoflavonoids that features a C5-isoprenoid substituent at any position of the A, B, or C ring. Neoflavonoids are compounds with a structure based on the 4-phenylchromene backbone. Based on a literature review very few articles have been published on Pestaloficiol U.

Structure

MOL SDF PDB SMILES InChI


  Mrv1652305152105462D          

 43 46  0  0  0  0            999 V2000
    2.1434   -2.8875    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7145   -2.8875    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1434    2.0625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0993    0.1433    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.5690   -0.7752    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.7158    7.4250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.1447    3.3000    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
    2.1434   -1.2375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8579    3.3000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4289    0.0000    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
    5.7158    5.7750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2868    0.8250    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
    2.8579    2.4750    0.0000 C   0  0  0  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
    1.4289    0.8250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8579    0.8250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.7158    4.9500    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
    3.5724    3.7125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0013    6.1875    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5724    2.0625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0013    4.5375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2868    3.3000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2868    5.7750    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
    5.0013    3.7125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2868    4.9500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8579    0.0000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.4302    4.5375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2868    0.0000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5724    6.1875    0.0000 Cl  0  0  0  0  0  0  0  0  0  0  0  0
    0.7145    1.2375    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.5724    4.5375    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.0013    2.0625    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.7158    3.3000    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.4663    5.0362    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    7.1447    4.9500    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.0013    7.0125    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.4302    3.7125    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.5724   -0.4125    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
  9  8  1  0  0  0  0
 15  1  1  0  0  0  0
 15  2  1  0  0  0  0
 15  8  2  0  0  0  0
 16  3  1  0  0  0  0
 16 10  2  0  0  0  0
 17  9  1  0  0  0  0
 17 11  2  0  0  0  0
 18 11  1  0  0  0  0
 18 12  2  0  0  0  0
 19 12  1  0  0  0  0
 20 13  2  0  0  0  0
 21 14  2  0  0  0  0
 21 19  1  0  0  0  0
 22 10  1  0  0  0  0
 23 13  1  0  0  0  0
 24 16  1  0  0  0  0
 24 21  1  0  0  0  0
 25 20  1  0  0  0  0
 26 22  2  0  0  0  0
 27 23  2  0  0  0  0
 28 24  2  0  0  0  0
 28 26  1  0  0  0  0
 29 25  1  0  0  0  0
 29 26  1  0  0  0  0
 30 25  2  0  0  0  0
 30 27  1  0  0  0  0
 31 17  1  0  0  0  0
 31 19  2  0  0  0  0
 32 20  1  0  0  0  0
 33  4  1  0  0  0  0
 33  5  1  0  0  0  0
 33 14  1  0  0  0  0
 34 27  1  0  0  0  0
 35 18  1  0  0  0  0
 36 22  1  0  0  0  0
 37 28  1  0  0  0  0
 38 29  2  0  0  0  0
 39 30  1  0  0  0  0
 40 32  2  0  0  0  0
 41  6  1  0  0  0  0
 41 23  1  0  0  0  0
 42  7  1  0  0  0  0
 42 32  1  0  0  0  0
 43 31  1  0  0  0  0
 43 33  1  0  0  0  0
M  END


  Mrv1652305152105462D          

 43 46  0  0  0  0            999 V2000
    2.1434   -2.8875    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7145   -2.8875    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1434    2.0625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0993    0.1433    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.5690   -0.7752    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.7158    7.4250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.1447    3.3000    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
    2.1434   -1.2375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8579    3.3000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4289    0.0000    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
    5.7158    5.7750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2868    0.8250    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
    2.8579    2.4750    0.0000 C   0  0  0  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
    1.4289    0.8250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8579    0.8250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.7158    4.9500    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
    3.5724    3.7125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0013    6.1875    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5724    2.0625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0013    4.5375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2868    3.3000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2868    5.7750    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
    5.0013    3.7125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2868    4.9500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8579    0.0000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.4302    4.5375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2868    0.0000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5724    6.1875    0.0000 Cl  0  0  0  0  0  0  0  0  0  0  0  0
    0.7145    1.2375    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.5724    4.5375    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.0013    2.0625    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.7158    3.3000    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.4663    5.0362    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    7.1447    4.9500    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.0013    7.0125    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.4302    3.7125    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.5724   -0.4125    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
  9  8  1  0  0  0  0
 15  1  1  0  0  0  0
 15  2  1  0  0  0  0
 15  8  2  0  0  0  0
 16  3  1  0  0  0  0
 16 10  2  0  0  0  0
 17  9  1  0  0  0  0
 17 11  2  0  0  0  0
 18 11  1  0  0  0  0
 18 12  2  0  0  0  0
 19 12  1  0  0  0  0
 20 13  2  0  0  0  0
 21 14  2  0  0  0  0
 21 19  1  0  0  0  0
 22 10  1  0  0  0  0
 23 13  1  0  0  0  0
 24 16  1  0  0  0  0
 24 21  1  0  0  0  0
 25 20  1  0  0  0  0
 26 22  2  0  0  0  0
 27 23  2  0  0  0  0
 28 24  2  0  0  0  0
 28 26  1  0  0  0  0
 29 25  1  0  0  0  0
 29 26  1  0  0  0  0
 30 25  2  0  0  0  0
 30 27  1  0  0  0  0
 31 17  1  0  0  0  0
 31 19  2  0  0  0  0
 32 20  1  0  0  0  0
 33  4  1  0  0  0  0
 33  5  1  0  0  0  0
 33 14  1  0  0  0  0
 34 27  1  0  0  0  0
 35 18  1  0  0  0  0
 36 22  1  0  0  0  0
 37 28  1  0  0  0  0
 38 29  2  0  0  0  0
 39 30  1  0  0  0  0
 40 32  2  0  0  0  0
 41  6  1  0  0  0  0
 41 23  1  0  0  0  0
 42  7  1  0  0  0  0
 42 32  1  0  0  0  0
 43 31  1  0  0  0  0
 43 33  1  0  0  0  0
M  END
> <DATABASE_ID>
MMDBc0012149

> <DATABASE_NAME>
MIME

> <SMILES>
COC(=O)C1=CC(OC)=C(Cl)C(O)=C1C(=O)C1=C(O)C=C(C)C(=C1O)C1=CC(C)(C)OC2=C1C=C(O)C=C2CC=C(C)C

> <INCHI_IDENTIFIER>
InChI=1S/C33H33ClO9/c1-15(2)8-9-17-11-18(35)12-19-21(14-33(4,5)43-31(17)19)24-16(3)10-22(36)26(28(24)37)29(38)25-20(32(40)42-7)13-23(41-6)27(34)30(25)39/h8,10-14,35-37,39H,9H2,1-7H3

> <INCHI_KEY>
YZQIHIQIUVBGNF-UHFFFAOYSA-N

> <FORMULA>
C33H33ClO9

> <MOLECULAR_WEIGHT>
609.07

> <EXACT_MASS>
608.1813103

> <JCHEM_ACCEPTOR_COUNT>
8

> <JCHEM_ATOM_COUNT>
76

> <JCHEM_AVERAGE_POLARIZABILITY>
63.249659946298195

> <JCHEM_BIOAVAILABILITY>
0

> <JCHEM_DONOR_COUNT>
4

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
methyl 4-chloro-2-{2,6-dihydroxy-3-[6-hydroxy-2,2-dimethyl-8-(3-methylbut-2-en-1-yl)-2H-chromen-4-yl]-4-methylbenzoyl}-3-hydroxy-5-methoxybenzoate

> <ALOGPS_LOGP>
5.92

> <JCHEM_LOGP>
9.193998309666666

> <ALOGPS_LOGS>
-5.55

> <JCHEM_MDDR_LIKE_RULE>
1

> <JCHEM_NUMBER_OF_RINGS>
4

> <JCHEM_PHYSIOLOGICAL_CHARGE>
-2

> <JCHEM_PKA>
6.816131994767897

> <JCHEM_PKA_STRONGEST_ACIDIC>
5.475463243481027

> <JCHEM_PKA_STRONGEST_BASIC>
-4.605528406119741

> <JCHEM_POLAR_SURFACE_AREA>
142.75

> <JCHEM_REFRACTIVITY>
175.0805

> <JCHEM_ROTATABLE_BOND_COUNT>
8

> <JCHEM_RULE_OF_FIVE>
0

> <ALOGPS_SOLUBILITY>
1.73e-03 g/l

> <JCHEM_TRADITIONAL_IUPAC>
methyl 4-chloro-2-{2,6-dihydroxy-3-[6-hydroxy-2,2-dimethyl-8-(3-methylbut-2-en-1-yl)chromen-4-yl]-4-methylbenzoyl}-3-hydroxy-5-methoxybenzoate

> <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       4.001  -5.390   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0       1.334  -5.390   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0       4.001   3.850   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0       9.519   0.267   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0       8.529  -1.447   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0      10.669  13.860   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0      13.337   6.160   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0       2.667  -3.080   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0       4.001  -2.310   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0       5.335   6.160   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0       2.667   0.000   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0       4.001   2.310   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0      10.669  10.780   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0       8.002   1.540   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0       2.667  -4.620   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0       5.335   4.620   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0       4.001  -0.770   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0       2.667   1.540   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0       5.335   1.540   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0      10.669   9.240   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0       6.668   2.310   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0       6.668   6.930   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0       9.336  11.550   0.000  0.00  0.00           C+0
HETATM   24  C   UNK     0       6.668   3.850   0.000  0.00  0.00           C+0
HETATM   25  C   UNK     0       9.336   8.470   0.000  0.00  0.00           C+0
HETATM   26  C   UNK     0       8.002   6.160   0.000  0.00  0.00           C+0
HETATM   27  C   UNK     0       8.002  10.780   0.000  0.00  0.00           C+0
HETATM   28  C   UNK     0       8.002   4.620   0.000  0.00  0.00           C+0
HETATM   29  C   UNK     0       9.336   6.930   0.000  0.00  0.00           C+0
HETATM   30  C   UNK     0       8.002   9.240   0.000  0.00  0.00           C+0
HETATM   31  C   UNK     0       5.335   0.000   0.000  0.00  0.00           C+0
HETATM   32  C   UNK     0      12.003   8.470   0.000  0.00  0.00           C+0
HETATM   33  C   UNK     0       8.002   0.000   0.000  0.00  0.00           C+0
HETATM   34 Cl   UNK     0       6.668  11.550   0.000  0.00  0.00          Cl+0
HETATM   35  O   UNK     0       1.334   2.310   0.000  0.00  0.00           O+0
HETATM   36  O   UNK     0       6.668   8.470   0.000  0.00  0.00           O+0
HETATM   37  O   UNK     0       9.336   3.850   0.000  0.00  0.00           O+0
HETATM   38  O   UNK     0      10.669   6.160   0.000  0.00  0.00           O+0
HETATM   39  O   UNK     0       6.471   9.401   0.000  0.00  0.00           O+0
HETATM   40  O   UNK     0      13.337   9.240   0.000  0.00  0.00           O+0
HETATM   41  O   UNK     0       9.336  13.090   0.000  0.00  0.00           O+0
HETATM   42  O   UNK     0      12.003   6.930   0.000  0.00  0.00           O+0
HETATM   43  O   UNK     0       6.668  -0.770   0.000  0.00  0.00           O+0
CONECT    1   15                                                            
CONECT    2   15                                                            
CONECT    3   16                                                            
CONECT    4   33                                                            
CONECT    5   33                                                            
CONECT    6   41                                                            
CONECT    7   42                                                            
CONECT    8    9   15                                                       
CONECT    9    8   17                                                       
CONECT   10   16   22                                                       
CONECT   11   17   18                                                       
CONECT   12   18   19                                                       
CONECT   13   20   23                                                       
CONECT   14   21   33                                                       
CONECT   15    1    2    8                                                  
CONECT   16    3   10   24                                                  
CONECT   17    9   11   31                                                  
CONECT   18   11   12   35                                                  
CONECT   19   12   21   31                                                  
CONECT   20   13   25   32                                                  
CONECT   21   14   19   24                                                  
CONECT   22   10   26   36                                                  
CONECT   23   13   27   41                                                  
CONECT   24   16   21   28                                                  
CONECT   25   20   29   30                                                  
CONECT   26   22   28   29                                                  
CONECT   27   23   30   34                                                  
CONECT   28   24   26   37                                                  
CONECT   29   25   26   38                                                  
CONECT   30   25   27   39                                                  
CONECT   31   17   19   43                                                  
CONECT   32   20   40   42                                                  
CONECT   33    4    5   14   43                                             
CONECT   34   27                                                            
CONECT   35   18                                                            
CONECT   36   22                                                            
CONECT   37   28                                                            
CONECT   38   29                                                            
CONECT   39   30                                                            
CONECT   40   32                                                            
CONECT   41    6   23                                                       
CONECT   42    7   32                                                       
CONECT   43   31   33                                                       
MASTER        0    0    0    0    0    0    0    0   43    0   92    0
END

Synonyms

Not Available

Molecular Formula

C₃₃H₃₃ClO₉

Average Mass

609.07

Monoisotopic Mass

608.1813103

IUPAC Name

methyl 4-chloro-2-{2,6-dihydroxy-3-[6-hydroxy-2,2-dimethyl-8-(3-methylbut-2-en-1-yl)-2H-chromen-4-yl]-4-methylbenzoyl}-3-hydroxy-5-methoxybenzoate

Traditional Name

methyl 4-chloro-2-{2,6-dihydroxy-3-[6-hydroxy-2,2-dimethyl-8-(3-methylbut-2-en-1-yl)chromen-4-yl]-4-methylbenzoyl}-3-hydroxy-5-methoxybenzoate

CAS Registry Number

Not Available

SMILES

COC(=O)C1=CC(OC)=C(Cl)C(O)=C1C(=O)C1=C(O)C=C(C)C(=C1O)C1=CC(C)(C)OC2=C1C=C(O)C=C2CC=C(C)C

InChI Identifier

InChI=1S/C33H33ClO9/c1-15(2)8-9-17-11-18(35)12-19-21(14-33(4,5)43-31(17)19)24-16(3)10-22(36)26(28(24)37)29(38)25-20(32(40)42-7)13-23(41-6)27(34)30(25)39/h8,10-14,35-37,39H,9H2,1-7H3

InChI Key

YZQIHIQIUVBGNF-UHFFFAOYSA-N

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as prenylated neoflavonoids. These are neoflavonoids that features a C5-isoprenoid substituent at any position of the A, B, or C ring. Neoflavonoids are compounds with a structure based on the 4-phenylchromene backbone.

Kingdom

Organic compounds

Super Class

Phenylpropanoids and polyketides

Class

Neoflavonoids

Sub Class

Prenylated neoflavonoids

Direct Parent

Prenylated neoflavonoids

Alternative Parents

Substituents

Prenylated neoflavonoid
Neoflavene
Benzophenone
Aryl-phenylketone
Diphenylmethane
2,2-dimethyl-1-benzopyran
M-hydroxybenzoic acid ester
M-methoxybenzoic acid or derivatives
1-benzopyran
Halobenzoic acid or derivatives
4-halobenzoic acid or derivatives
Methoxyphenol
Benzopyran
Benzoate ester
Benzoic acid or derivatives
Phenoxy compound
Methoxybenzene
Aryl ketone
Resorcinol
Phenol ether
2-chlorophenol
M-cresol
2-halophenol
Benzoyl
Anisole
1-hydroxy-4-unsubstituted benzenoid
1-hydroxy-2-unsubstituted benzenoid
Toluene
Phenol
Halobenzene
Chlorobenzene
Alkyl aryl ether
Benzenoid
Monocyclic benzene moiety
Aryl halide
Aryl chloride
Vinylogous acid
Methyl ester
Ketone
Carboxylic acid ester
Oxacycle
Organoheterocyclic compound
Monocarboxylic acid or derivatives
Ether
Carboxylic acid derivative
Organic oxygen compound
Organic oxide
Hydrocarbon derivative
Organooxygen compound
Organochloride
Organohalogen 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	0.0017 g/L	ALOGPS
logP	5.92	ALOGPS
logP	9.19	ChemAxon
logS	-5.6	ALOGPS
pKa (Strongest Acidic)	5.48	ChemAxon
pKa (Strongest Basic)	-4.6	ChemAxon
Physiological Charge	-2	ChemAxon
Hydrogen Acceptor Count	8	ChemAxon
Hydrogen Donor Count	4	ChemAxon
Polar Surface Area	142.75 Å²	ChemAxon
Rotatable Bond Count	8	ChemAxon
Refractivity	175.08 m³·mol⁻¹	ChemAxon
Polarizability	63.25 Å³	ChemAxon
Number of Rings	4	ChemAxon
Bioavailability	No	ChemAxon
Rule of Five	No	ChemAxon
Ghose Filter	No	ChemAxon
Veber's Rule	No	ChemAxon
MDDR-like Rule	Yes	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

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

Not Available

DrugBank ID

Not Available

Phenol Explorer Compound ID

Not Available

FooDB ID

Not Available

KNApSAcK ID

Not Available

Chemspider ID

78435674

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

132969604

PDB ID

Not Available

ChEBI ID

Not Available

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 ]

Showing metabocard for Pestaloficiol U (MMDBc0012149)

MOL for #<Metabolite:0x00007f923635f348>

3D MOL for #<Metabolite:0x00007f923635f348>

3D SDF for #<Metabolite:0x00007f923635f348>

3D-SDF for #<Metabolite:0x00007f923635f348>

PDB for #<Metabolite:0x00007f923635f348>

3D PDB for #<Metabolite:0x00007f923635f348>

SMILES for #<Metabolite:0x00007f923635f348>

INCHI for #<Metabolite:0x00007f923635f348>

Structure for #<Metabolite:0x00007f923635f348>

3D Structure for #<Metabolite:0x00007f923635f348>