MiMeDB: Showing metabocard for Hericenone E (MMDBc0003514)

Record Information

Version

1.0

Status

Detected and Quantified

Creation Date

2021-05-14 21:31:51 UTC

Update Date

2022-12-15 22:51:43 UTC

Metabolite ID

MMDBc0003514

Metabolite Identification

Common Name

Hericenone E

Description

Hericenone E belongs to the class of organic compounds known as lineolic acids and derivatives. These are derivatives of lineolic acid. Lineolic acid is a polyunsaturated omega-6 18 carbon long fatty acid, with two CC double bonds at the 9- and 12-positions. Based on a literature review very few articles have been published on Hericenone E.

Structure

MOL SDF PDB SMILES InChI


  Mrv1652305142123312D          

 48 48  0  0  0  0            999 V2000
    1.3144   -2.0898    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   16.7708   -8.0390    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   15.7800   -9.0686    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   13.0058   -8.3822    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   12.8076   -6.2085    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1163   -2.8907    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.7108   -3.4627    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5126   -4.2636    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1071   -4.8356    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9089   -5.6364    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5034   -6.2085    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.2960   -5.9797    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.8905   -6.5517    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.6831   -6.3229    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.8813   -5.5220    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
    4.4850   -4.1492    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.2776   -3.9203    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.8721   -4.4924    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.6647   -4.2636    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.2592   -4.8356    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   12.6095   -7.0093    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   11.8169   -7.2381    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   15.3837   -7.6958    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   13.9966   -7.3525    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   10.8261   -5.2932    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.0426   -6.5517    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.4389   -4.9500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   15.9782   -8.2678    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   13.2040   -7.5814    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   10.0334   -5.5220    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   14.5911   -7.9246    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   11.2224   -6.6661    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.8353   -6.3229    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   11.4205   -5.8653    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.0518   -4.6068    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   10.4297   -6.8949    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.8445   -7.3525    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   14.3929   -8.7254    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    8.2500   -3.8059    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   10.2316   -7.6958    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   12.2132   -5.6364    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    8.6463   -5.1788    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.1163   -5.8653    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.3052   -7.0093    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.6923   -7.3525    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.2776   -6.8949    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
   12.0150   -6.4373    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
  6  1  1  0  0  0  0
  7  6  1  0  0  0  0
  8  7  1  0  0  0  0
  9  8  1  0  0  0  0
 10  9  1  0  0  0  0
 11 10  2  0  0  0  0
 12 11  1  0  0  0  0
 13 12  1  0  0  0  0
 14 13  2  0  0  0  0
 15 14  1  0  0  0  0
 16 15  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 19  1  0  0  0  0
 21 20  1  0  0  0  0
 23 22  1  0  0  0  0
 29  2  1  0  0  0  0
 29  3  1  0  0  0  0
 29 24  2  0  0  0  0
 30  4  1  0  0  0  0
 30 22  2  0  0  0  0
 30 25  1  0  0  0  0
 31 26  2  0  0  0  0
 31 28  1  0  0  0  0
 32 24  1  0  0  0  0
 32 25  1  0  0  0  0
 33 23  1  0  0  0  0
 34 27  1  0  0  0  0
 34 31  1  0  0  0  0
 35 26  1  0  0  0  0
 35 33  2  0  0  0  0
 36 21  1  0  0  0  0
 37 33  1  0  0  0  0
 37 34  2  0  0  0  0
 38 27  2  0  0  0  0
 39 32  2  0  0  0  0
 40 36  2  0  0  0  0
 41 37  1  0  0  0  0
 42  5  1  0  0  0  0
 42 35  1  0  0  0  0
 43 28  1  0  0  0  0
 43 36  1  0  0  0  0
 44 10  1  0  0  0  0
 45 11  1  0  0  0  0
 46 13  1  0  0  0  0
 47 14  1  0  0  0  0
 48 22  1  0  0  0  0
M  END


  Mrv1652305142123312D          

 48 48  0  0  0  0            999 V2000
    1.3144   -2.0898    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   16.7708   -8.0390    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   15.7800   -9.0686    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   13.0058   -8.3822    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   12.8076   -6.2085    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1163   -2.8907    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.7108   -3.4627    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5126   -4.2636    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1071   -4.8356    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9089   -5.6364    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5034   -6.2085    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.2960   -5.9797    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.8905   -6.5517    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.6831   -6.3229    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.8813   -5.5220    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
    4.4850   -4.1492    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.2776   -3.9203    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.8721   -4.4924    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.6647   -4.2636    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.2592   -4.8356    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   12.6095   -7.0093    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   11.8169   -7.2381    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   15.3837   -7.6958    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   13.9966   -7.3525    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   10.8261   -5.2932    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.0426   -6.5517    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.4389   -4.9500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   15.9782   -8.2678    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   13.2040   -7.5814    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   10.0334   -5.5220    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   14.5911   -7.9246    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   11.2224   -6.6661    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.8353   -6.3229    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   11.4205   -5.8653    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.0518   -4.6068    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   10.4297   -6.8949    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.8445   -7.3525    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   14.3929   -8.7254    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    8.2500   -3.8059    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   10.2316   -7.6958    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   12.2132   -5.6364    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    8.6463   -5.1788    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.1163   -5.8653    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.3052   -7.0093    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.6923   -7.3525    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.2776   -6.8949    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
   12.0150   -6.4373    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
  6  1  1  0  0  0  0
  7  6  1  0  0  0  0
  8  7  1  0  0  0  0
  9  8  1  0  0  0  0
 10  9  1  0  0  0  0
 11 10  2  0  0  0  0
 12 11  1  0  0  0  0
 13 12  1  0  0  0  0
 14 13  2  0  0  0  0
 15 14  1  0  0  0  0
 16 15  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 19  1  0  0  0  0
 21 20  1  0  0  0  0
 23 22  1  0  0  0  0
 29  2  1  0  0  0  0
 29  3  1  0  0  0  0
 29 24  2  0  0  0  0
 30  4  1  0  0  0  0
 30 22  2  0  0  0  0
 30 25  1  0  0  0  0
 31 26  2  0  0  0  0
 31 28  1  0  0  0  0
 32 24  1  0  0  0  0
 32 25  1  0  0  0  0
 33 23  1  0  0  0  0
 34 27  1  0  0  0  0
 34 31  1  0  0  0  0
 35 26  1  0  0  0  0
 35 33  2  0  0  0  0
 36 21  1  0  0  0  0
 37 33  1  0  0  0  0
 37 34  2  0  0  0  0
 38 27  2  0  0  0  0
 39 32  2  0  0  0  0
 40 36  2  0  0  0  0
 41 37  1  0  0  0  0
 42  5  1  0  0  0  0
 42 35  1  0  0  0  0
 43 28  1  0  0  0  0
 43 36  1  0  0  0  0
 44 10  1  0  0  0  0
 45 11  1  0  0  0  0
 46 13  1  0  0  0  0
 47 14  1  0  0  0  0
 48 22  1  0  0  0  0
M  END
> <DATABASE_ID>
MMDBc0003514

> <DATABASE_NAME>
MIME

> <SMILES>
[H]\C(CCCCC)=C(/[H])C\C([H])=C(\[H])CCCCCCCC(=O)OCC1=CC(OC)=C(CC([H])=C(C)CC(=O)C=C(C)C)C(O)=C1C=O

> <INCHI_IDENTIFIER>
InChI=1S/C37H54O6/c1-6-7-8-9-10-11-12-13-14-15-16-17-18-19-20-21-36(40)43-28-31-26-35(42-5)33(37(41)34(31)27-38)23-22-30(4)25-32(39)24-29(2)3/h10-11,13-14,22,24,26-27,41H,6-9,12,15-21,23,25,28H2,1-5H3/b11-10-,14-13-,30-22+

> <INCHI_KEY>
SUAXEWQRYKSWIW-OFVWHMROSA-N

> <FORMULA>
C37H54O6

> <MOLECULAR_WEIGHT>
594.833

> <EXACT_MASS>
594.392039459

> <JCHEM_ACCEPTOR_COUNT>
5

> <JCHEM_ATOM_COUNT>
97

> <JCHEM_AVERAGE_POLARIZABILITY>
71.05440163644482

> <JCHEM_BIOAVAILABILITY>
0

> <JCHEM_DONOR_COUNT>
1

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
{4-[(2E)-3,7-dimethyl-5-oxoocta-2,6-dien-1-yl]-2-formyl-3-hydroxy-5-methoxyphenyl}methyl (9Z,12Z)-octadeca-9,12-dienoate

> <ALOGPS_LOGP>
8.14

> <JCHEM_LOGP>
10.762318420333337

> <ALOGPS_LOGS>
-6.57

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
1

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
16.89287980765651

> <JCHEM_PKA_STRONGEST_ACIDIC>
7.996502421198149

> <JCHEM_PKA_STRONGEST_BASIC>
-4.308583547017478

> <JCHEM_POLAR_SURFACE_AREA>
89.9

> <JCHEM_REFRACTIVITY>
181.59210000000004

> <JCHEM_ROTATABLE_BOND_COUNT>
24

> <JCHEM_RULE_OF_FIVE>
0

> <ALOGPS_SOLUBILITY>
1.61e-04 g/l

> <JCHEM_TRADITIONAL_IUPAC>
{4-[(2E)-3,7-dimethyl-5-oxoocta-2,6-dien-1-yl]-2-formyl-3-hydroxy-5-methoxyphenyl}methyl (9Z,12Z)-octadeca-9,12-dienoate

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 14-MAY-21   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   14-MAY-21         0                                  
HETATM    1  C   UNK     0       2.454  -3.901   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0      31.306 -15.006   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0      29.456 -16.928   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0      24.278 -15.647   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0      23.908 -11.589   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0       2.084  -5.396   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0       3.193  -6.464   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0       2.824  -7.959   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0       3.933  -9.026   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0       3.563 -10.521   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0       4.673 -11.589   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0       6.153 -11.162   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0       7.262 -12.230   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0       8.742 -11.803   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0       9.112 -10.308   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0       8.002  -9.240   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0       8.372  -7.745   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0       9.852  -7.318   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0      10.961  -8.386   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0      12.441  -7.959   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0      13.551  -9.026   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0      23.538 -13.084   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0      22.058 -13.511   0.000  0.00  0.00           C+0
HETATM   24  C   UNK     0      28.716 -14.365   0.000  0.00  0.00           C+0
HETATM   25  C   UNK     0      26.127 -13.725   0.000  0.00  0.00           C+0
HETATM   26  C   UNK     0      20.209  -9.881   0.000  0.00  0.00           C+0
HETATM   27  C   UNK     0      16.880 -12.230   0.000  0.00  0.00           C+0
HETATM   28  C   UNK     0      17.619  -9.240   0.000  0.00  0.00           C+0
HETATM   29  C   UNK     0      29.826 -15.433   0.000  0.00  0.00           C+0
HETATM   30  C   UNK     0      24.647 -14.152   0.000  0.00  0.00           C+0
HETATM   31  C   UNK     0      18.729 -10.308   0.000  0.00  0.00           C+0
HETATM   32  C   UNK     0      27.237 -14.793   0.000  0.00  0.00           C+0
HETATM   33  C   UNK     0      20.948 -12.443   0.000  0.00  0.00           C+0
HETATM   34  C   UNK     0      18.359 -11.803   0.000  0.00  0.00           C+0
HETATM   35  C   UNK     0      21.318 -10.948   0.000  0.00  0.00           C+0
HETATM   36  C   UNK     0      15.030  -8.599   0.000  0.00  0.00           C+0
HETATM   37  C   UNK     0      19.469 -12.871   0.000  0.00  0.00           C+0
HETATM   38  O   UNK     0      16.510 -13.725   0.000  0.00  0.00           O+0
HETATM   39  O   UNK     0      26.867 -16.287   0.000  0.00  0.00           O+0
HETATM   40  O   UNK     0      15.400  -7.104   0.000  0.00  0.00           O+0
HETATM   41  O   UNK     0      19.099 -14.365   0.000  0.00  0.00           O+0
HETATM   42  O   UNK     0      22.798 -10.521   0.000  0.00  0.00           O+0
HETATM   43  O   UNK     0      16.140  -9.667   0.000  0.00  0.00           O+0
HETATM   44  H   UNK     0       2.084 -10.948   0.000  0.00  0.00           H+0
HETATM   45  H   UNK     0       4.303 -13.084   0.000  0.00  0.00           H+0
HETATM   46  H   UNK     0       6.892 -13.725   0.000  0.00  0.00           H+0
HETATM   47  H   UNK     0       9.852 -12.871   0.000  0.00  0.00           H+0
HETATM   48  H   UNK     0      22.428 -12.016   0.000  0.00  0.00           H+0
CONECT    1    6                                                            
CONECT    2   29                                                            
CONECT    3   29                                                            
CONECT    4   30                                                            
CONECT    5   42                                                            
CONECT    6    1    7                                                       
CONECT    7    6    8                                                       
CONECT    8    7    9                                                       
CONECT    9    8   10                                                       
CONECT   10    9   11   44                                                  
CONECT   11   10   12   45                                                  
CONECT   12   11   13                                                       
CONECT   13   12   14   46                                                  
CONECT   14   13   15   47                                                  
CONECT   15   14   16                                                       
CONECT   16   15   17                                                       
CONECT   17   16   18                                                       
CONECT   18   17   19                                                       
CONECT   19   18   20                                                       
CONECT   20   19   21                                                       
CONECT   21   20   36                                                       
CONECT   22   23   30   48                                                  
CONECT   23   22   33                                                       
CONECT   24   29   32                                                       
CONECT   25   30   32                                                       
CONECT   26   31   35                                                       
CONECT   27   34   38                                                       
CONECT   28   31   43                                                       
CONECT   29    2    3   24                                                  
CONECT   30    4   22   25                                                  
CONECT   31   26   28   34                                                  
CONECT   32   24   25   39                                                  
CONECT   33   23   35   37                                                  
CONECT   34   27   31   37                                                  
CONECT   35   26   33   42                                                  
CONECT   36   21   40   43                                                  
CONECT   37   33   34   41                                                  
CONECT   38   27                                                            
CONECT   39   32                                                            
CONECT   40   36                                                            
CONECT   41   37                                                            
CONECT   42    5   35                                                       
CONECT   43   28   36                                                       
CONECT   44   10                                                            
CONECT   45   11                                                            
CONECT   46   13                                                            
CONECT   47   14                                                            
CONECT   48   22                                                            
MASTER        0    0    0    0    0    0    0    0   48    0   96    0
END

Synonyms

Not Available

Molecular Formula

C₃₇H₅₄O₆

Average Mass

594.833

Monoisotopic Mass

594.392039459

IUPAC Name

{4-[(2E)-3,7-dimethyl-5-oxoocta-2,6-dien-1-yl]-2-formyl-3-hydroxy-5-methoxyphenyl}methyl (9Z,12Z)-octadeca-9,12-dienoate

Traditional Name

{4-[(2E)-3,7-dimethyl-5-oxoocta-2,6-dien-1-yl]-2-formyl-3-hydroxy-5-methoxyphenyl}methyl (9Z,12Z)-octadeca-9,12-dienoate

CAS Registry Number

Not Available

SMILES

[H]\C(CCCCC)=C(/[H])C\C([H])=C(\[H])CCCCCCCC(=O)OCC1=CC(OC)=C(CC([H])=C(C)CC(=O)C=C(C)C)C(O)=C1C=O

InChI Identifier

InChI=1S/C37H54O6/c1-6-7-8-9-10-11-12-13-14-15-16-17-18-19-20-21-36(40)43-28-31-26-35(42-5)33(37(41)34(31)27-38)23-22-30(4)25-32(39)24-29(2)3/h10-11,13-14,22,24,26-27,41H,6-9,12,15-21,23,25,28H2,1-5H3/b11-10-,14-13-,30-22+

InChI Key

SUAXEWQRYKSWIW-OFVWHMROSA-N

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as lineolic acids and derivatives. These are derivatives of lineolic acid. Lineolic acid is a polyunsaturated omega-6 18 carbon long fatty acid, with two CC double bonds at the 9- and 12-positions.

Kingdom

Organic compounds

Super Class

Lipids and lipid-like molecules

Class

Fatty Acyls

Sub Class

Lineolic acids and derivatives

Direct Parent

Lineolic acids and derivatives

Alternative Parents

Substituents

Octadecanoid
Aromatic monoterpenoid
Benzyloxycarbonyl
Methoxyphenol
Monocyclic monoterpenoid
Monoterpenoid
Hydroxybenzaldehyde
Methoxybenzene
Benzaldehyde
Phenol ether
Benzoyl
Anisole
Phenoxy compound
1-hydroxy-4-unsubstituted benzenoid
Aryl-aldehyde
Phenol
Fatty acid ester
Alkyl aryl ether
Benzenoid
Monocyclic benzene moiety
Enone
Vinylogous acid
Acryloyl-group
Alpha,beta-unsaturated ketone
Carboxylic acid ester
Ketone
Ether
Carboxylic acid derivative
Monocarboxylic acid or derivatives
Carbonyl group
Aldehyde
Organooxygen compound
Organic oxygen compound
Hydrocarbon derivative
Organic oxide
Aromatic homomonocyclic compound

Molecular Framework

Aromatic homomonocyclic compounds

External Descriptors

Not Available

Functional Ontology

Not Available

Physical Properties

State

Expected Solid

Predicted Properties

Property	Value	Source
Water Solubility	0.00016 g/L	ALOGPS
logP	8.14	ALOGPS
logP	10.76	ChemAxon
logS	-6.6	ALOGPS
pKa (Strongest Acidic)	8	ChemAxon
pKa (Strongest Basic)	-4.3	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	5	ChemAxon
Hydrogen Donor Count	1	ChemAxon
Polar Surface Area	89.9 Å²	ChemAxon
Rotatable Bond Count	24	ChemAxon
Refractivity	181.59 m³·mol⁻¹	ChemAxon
Polarizability	71.05 Å³	ChemAxon
Number of Rings	1	ChemAxon
Bioavailability	No	ChemAxon
Rule of Five	No	ChemAxon
Ghose Filter	No	ChemAxon
Veber's Rule	No	ChemAxon
MDDR-like Rule	No	ChemAxon

Spectra

Not Available

Biological Properties

Cellular Locations

Extracellular
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

Not Available

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	Basidiomycota	3	Human feces	Metabolic reconstruction

Exposure Sources

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

C00023977

Chemspider ID

78434647

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

15658907

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 Hericenone E (MMDBc0003514)

MOL for #<Metabolite:0x00007fdb00227008>

3D MOL for #<Metabolite:0x00007fdb00227008>

3D SDF for #<Metabolite:0x00007fdb00227008>

3D-SDF for #<Metabolite:0x00007fdb00227008>

PDB for #<Metabolite:0x00007fdb00227008>

3D PDB for #<Metabolite:0x00007fdb00227008>

SMILES for #<Metabolite:0x00007fdb00227008>

INCHI for #<Metabolite:0x00007fdb00227008>

Structure for #<Metabolite:0x00007fdb00227008>

3D Structure for #<Metabolite:0x00007fdb00227008>