Jump To Section:

Identification Taxonomy Ontology Physical properties Spectra Biological properties Concentrations Links References XML

Record Information

Version

5.0

Status

Detected but not Quantified

Creation Date

2021-09-11 15:56:52 UTC

Update Date

2021-09-26 23:11:12 UTC

HMDB ID

HMDB0255937

Secondary Accession Numbers

None

Metabolite Identification

Common Name

Oleanilide

Description

N-phenyloctadec-9-enimidic acid belongs to the class of organic compounds known as anilides. These are organic heterocyclic compounds derived from oxoacids RkE(=O)l(OH)m (l not 0) by replacing an OH group by the NHPh group or derivative formed by ring substitution. Based on a literature review very few articles have been published on N-phenyloctadec-9-enimidic acid. This compound has been identified in human blood as reported by (PMID: 31557052 ). Oleanilide is not a naturally occurring metabolite and is only found in those individuals exposed to this compound or its derivatives. Technically Oleanilide is part of the human exposome. The exposome can be defined as the collection of all the exposures of an individual in a lifetime and how those exposures relate to health. An individual's exposure begins before birth and includes insults from environmental and occupational sources.

Structure

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


  Mrv1652309112117572D          

 26 26  0  0  0  0            999 V2000
   -3.5724   -6.1875    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8579   -6.6000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1434   -6.1875    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4289   -6.6000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7145   -6.1875    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0000   -6.6000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7145   -6.1875    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4289   -6.6000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1434   -6.1875    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8579   -6.6000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5724   -6.1875    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2868   -6.6000    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
    5.7158   -6.6000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.4302   -6.1875    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.1447   -6.6000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.8592   -6.1875    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.5737   -6.6000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.5737   -7.4250    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    9.2881   -6.1875    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
   10.0026   -6.6000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   10.7171   -6.1875    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   11.4315   -6.6000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   11.4315   -7.4250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   10.7171   -7.8375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   10.0026   -7.4250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0  0  0  0
  2  3  1  0  0  0  0
  3  4  1  0  0  0  0
  4  5  1  0  0  0  0
  5  6  1  0  0  0  0
  6  7  1  0  0  0  0
  7  8  1  0  0  0  0
  9  8  1  4  0  0  0
  9 10  2  0  0  0  0
 10 11  1  0  0  0  0
 11 12  1  0  0  0  0
 12 13  1  0  0  0  0
 13 14  1  0  0  0  0
 14 15  1  0  0  0  0
 15 16  1  0  0  0  0
 16 17  1  0  0  0  0
 17 18  1  0  0  0  0
 18 19  2  0  0  0  0
 18 20  1  0  0  0  0
 20 21  1  0  0  0  0
 21 22  2  0  0  0  0
 22 23  1  0  0  0  0
 23 24  2  0  0  0  0
 24 25  1  0  0  0  0
 25 26  2  0  0  0  0
 21 26  1  0  0  0  0
M  END

HMDB0255937
     RDKit          3D
Oleanilide
 65 65  0  0  0  0  0  0  0  0999 V2000
   -6.8453    1.2181    3.0317 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.7686    0.4759    2.2627 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.4191   -0.6347    1.4727 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.4449   -1.4308    0.6767 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.6550   -0.5741   -0.3436 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.6473    0.0136   -1.2590 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.2348    0.9637   -2.2933 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2364    0.5415   -3.3007 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9120    0.3212   -2.7479 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8914    1.0800   -3.2163 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5164    0.9197   -2.7084 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4186   -0.1574   -1.6473 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.0212   -0.2523   -1.1842 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.0737   -1.3332   -0.1328 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.4789   -1.5176    0.4090 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.4182   -1.9008   -0.6947 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.8170   -2.1026   -0.1992 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.4198   -0.8765    0.3774 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.8069    0.1956    0.3092 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.6823   -0.9621    0.9923 N   0  0  0  0  0  0  0  0  0  0  0  0
    7.3356    0.1505    1.5614 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.3873   -0.1253    2.4451 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.0874    0.8881    3.0290 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.7781    2.1932    2.7646 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.7601    2.5143    1.9087 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.0556    1.4659    1.3208 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.5313    2.2707    3.1943 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.7550    1.2008    2.3876 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.0701    0.6821    3.9591 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.3183    1.2178    1.5439 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.9778    0.1243    2.9259 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.8476   -1.3560    2.2448 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.2922   -0.2609    0.9422 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.9624   -2.1864    0.0507 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.7364   -1.9844    1.3102 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.0522   -1.4082   -0.8529 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9427    0.0893    0.1217 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.4755    0.5435   -0.6642 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.2408   -0.8627   -1.6908 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.7400    1.8641   -1.7606 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.1434    1.4348   -2.7965 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.5732   -0.4368   -3.7999 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1717    1.3017   -4.1377 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6517   -0.3801   -2.0196 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0452    1.8347   -3.9829 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0591    1.8528   -2.3599 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.1081    0.5632   -3.5720 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0835    0.0724   -0.7903 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6613   -1.1483   -2.1066 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.4059    0.7194   -0.8193 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.5992   -0.6115   -2.0835 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.7312   -2.2753   -0.6373 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.3511   -1.1411    0.6779 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.7798   -0.5574    0.8355 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.4790   -2.3452    1.1546 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.0575   -2.8441   -1.1858 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.4868   -1.0872   -1.4755 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.8410   -2.9314    0.5693 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.4796   -2.5078   -1.0224 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.1926   -1.9048    1.0367 H   0  0  0  0  0  0  0  0  0  0  0  0
    8.6458   -1.1574    2.6672 H   0  0  0  0  0  0  0  0  0  0  0  0
    9.9066    0.6810    3.7175 H   0  0  0  0  0  0  0  0  0  0  0  0
    9.3373    3.0053    3.2315 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.5294    3.5489    1.7112 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.2682    1.7465    0.6420 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  2  3  1  0
  3  4  1  0
  4  5  1  0
  5  6  1  0
  6  7  1  0
  7  8  1  0
  8  9  1  0
  9 10  2  3
 10 11  1  0
 11 12  1  0
 12 13  1  0
 13 14  1  0
 14 15  1  0
 15 16  1  0
 16 17  1  0
 17 18  1  0
 18 19  2  0
 18 20  1  0
 20 21  1  0
 21 22  2  0
 22 23  1  0
 23 24  2  0
 24 25  1  0
 25 26  2  0
 26 21  1  0
  1 27  1  0
  1 28  1  0
  1 29  1  0
  2 30  1  0
  2 31  1  0
  3 32  1  0
  3 33  1  0
  4 34  1  0
  4 35  1  0
  5 36  1  0
  5 37  1  0
  6 38  1  0
  6 39  1  0
  7 40  1  0
  7 41  1  0
  8 42  1  0
  8 43  1  0
  9 44  1  0
 10 45  1  0
 11 46  1  0
 11 47  1  0
 12 48  1  0
 12 49  1  0
 13 50  1  0
 13 51  1  0
 14 52  1  0
 14 53  1  0
 15 54  1  0
 15 55  1  0
 16 56  1  0
 16 57  1  0
 17 58  1  0
 17 59  1  0
 20 60  1  0
 22 61  1  0
 23 62  1  0
 24 63  1  0
 25 64  1  0
 26 65  1  0
M  END


  Mrv1652309112117572D          

 26 26  0  0  0  0            999 V2000
   -3.5724   -6.1875    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8579   -6.6000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1434   -6.1875    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4289   -6.6000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7145   -6.1875    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0000   -6.6000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7145   -6.1875    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4289   -6.6000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1434   -6.1875    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8579   -6.6000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5724   -6.1875    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2868   -6.6000    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
    5.7158   -6.6000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.4302   -6.1875    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.1447   -6.6000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.8592   -6.1875    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.5737   -6.6000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.5737   -7.4250    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    9.2881   -6.1875    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
   10.0026   -6.6000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   10.7171   -6.1875    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   11.4315   -6.6000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   11.4315   -7.4250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   10.7171   -7.8375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   10.0026   -7.4250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0  0  0  0
  2  3  1  0  0  0  0
  3  4  1  0  0  0  0
  4  5  1  0  0  0  0
  5  6  1  0  0  0  0
  6  7  1  0  0  0  0
  7  8  1  0  0  0  0
  9  8  1  4  0  0  0
  9 10  2  0  0  0  0
 10 11  1  0  0  0  0
 11 12  1  0  0  0  0
 12 13  1  0  0  0  0
 13 14  1  0  0  0  0
 14 15  1  0  0  0  0
 15 16  1  0  0  0  0
 16 17  1  0  0  0  0
 17 18  1  0  0  0  0
 18 19  2  0  0  0  0
 18 20  1  0  0  0  0
 20 21  1  0  0  0  0
 21 22  2  0  0  0  0
 22 23  1  0  0  0  0
 23 24  2  0  0  0  0
 24 25  1  0  0  0  0
 25 26  2  0  0  0  0
 21 26  1  0  0  0  0
M  END
> <DATABASE_ID>
HMDB0255937

> <DATABASE_NAME>
hmdb

> <SMILES>
CCCCCCCCC=CCCCCCCCC(=O)NC1=CC=CC=C1

> <INCHI_IDENTIFIER>
InChI=1S/C24H39NO/c1-2-3-4-5-6-7-8-9-10-11-12-13-14-15-19-22-24(26)25-23-20-17-16-18-21-23/h9-10,16-18,20-21H,2-8,11-15,19,22H2,1H3,(H,25,26)

> <INCHI_KEY>
YPUOCYKJOLQYQS-UHFFFAOYSA-N

> <FORMULA>
C24H39NO

> <MOLECULAR_WEIGHT>
357.582

> <EXACT_MASS>
357.30316488

> <JCHEM_ACCEPTOR_COUNT>
1

> <JCHEM_ATOM_COUNT>
65

> <JCHEM_AVERAGE_POLARIZABILITY>
47.05000488599016

> <JCHEM_BIOAVAILABILITY>
0

> <JCHEM_DONOR_COUNT>
1

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
N-phenyloctadec-9-enamide

> <ALOGPS_LOGP>
8.07

> <JCHEM_LOGP>
8.218100348666667

> <ALOGPS_LOGS>
-7.14

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
1

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA_STRONGEST_ACIDIC>
14.204334967041536

> <JCHEM_PKA_STRONGEST_BASIC>
-3.521437080888037

> <JCHEM_POLAR_SURFACE_AREA>
29.1

> <JCHEM_REFRACTIVITY>
115.6795

> <JCHEM_ROTATABLE_BOND_COUNT>
16

> <JCHEM_RULE_OF_FIVE>
0

> <ALOGPS_SOLUBILITY>
2.58e-05 g/l

> <JCHEM_TRADITIONAL_IUPAC>
N-phenyloctadec-9-enamide

> <JCHEM_VEBER_RULE>
0

$$$$

HMDB0255937
     RDKit          3D
Oleanilide
 65 65  0  0  0  0  0  0  0  0999 V2000
   -6.8453    1.2181    3.0317 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.7686    0.4759    2.2627 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.4191   -0.6347    1.4727 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.4449   -1.4308    0.6767 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.6550   -0.5741   -0.3436 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.6473    0.0136   -1.2590 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.2348    0.9637   -2.2933 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2364    0.5415   -3.3007 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9120    0.3212   -2.7479 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8914    1.0800   -3.2163 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5164    0.9197   -2.7084 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4186   -0.1574   -1.6473 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.0212   -0.2523   -1.1842 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.0737   -1.3332   -0.1328 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.4789   -1.5176    0.4090 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.4182   -1.9008   -0.6947 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.8170   -2.1026   -0.1992 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.4198   -0.8765    0.3774 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.8069    0.1956    0.3092 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.6823   -0.9621    0.9923 N   0  0  0  0  0  0  0  0  0  0  0  0
    7.3356    0.1505    1.5614 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.3873   -0.1253    2.4451 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.0874    0.8881    3.0290 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.7781    2.1932    2.7646 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.7601    2.5143    1.9087 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.0556    1.4659    1.3208 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.5313    2.2707    3.1943 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.7550    1.2008    2.3876 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.0701    0.6821    3.9591 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.3183    1.2178    1.5439 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.9778    0.1243    2.9259 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.8476   -1.3560    2.2448 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.2922   -0.2609    0.9422 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.9624   -2.1864    0.0507 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.7364   -1.9844    1.3102 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.0522   -1.4082   -0.8529 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9427    0.0893    0.1217 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.4755    0.5435   -0.6642 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.2408   -0.8627   -1.6908 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.7400    1.8641   -1.7606 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.1434    1.4348   -2.7965 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.5732   -0.4368   -3.7999 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1717    1.3017   -4.1377 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6517   -0.3801   -2.0196 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0452    1.8347   -3.9829 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0591    1.8528   -2.3599 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.1081    0.5632   -3.5720 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0835    0.0724   -0.7903 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6613   -1.1483   -2.1066 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.4059    0.7194   -0.8193 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.5992   -0.6115   -2.0835 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.7312   -2.2753   -0.6373 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.3511   -1.1411    0.6779 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.7798   -0.5574    0.8355 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.4790   -2.3452    1.1546 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.0575   -2.8441   -1.1858 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.4868   -1.0872   -1.4755 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.8410   -2.9314    0.5693 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.4796   -2.5078   -1.0224 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.1926   -1.9048    1.0367 H   0  0  0  0  0  0  0  0  0  0  0  0
    8.6458   -1.1574    2.6672 H   0  0  0  0  0  0  0  0  0  0  0  0
    9.9066    0.6810    3.7175 H   0  0  0  0  0  0  0  0  0  0  0  0
    9.3373    3.0053    3.2315 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.5294    3.5489    1.7112 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.2682    1.7465    0.6420 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  2  3  1  0
  3  4  1  0
  4  5  1  0
  5  6  1  0
  6  7  1  0
  7  8  1  0
  8  9  1  0
  9 10  2  3
 10 11  1  0
 11 12  1  0
 12 13  1  0
 13 14  1  0
 14 15  1  0
 15 16  1  0
 16 17  1  0
 17 18  1  0
 18 19  2  0
 18 20  1  0
 20 21  1  0
 21 22  2  0
 22 23  1  0
 23 24  2  0
 24 25  1  0
 25 26  2  0
 26 21  1  0
  1 27  1  0
  1 28  1  0
  1 29  1  0
  2 30  1  0
  2 31  1  0
  3 32  1  0
  3 33  1  0
  4 34  1  0
  4 35  1  0
  5 36  1  0
  5 37  1  0
  6 38  1  0
  6 39  1  0
  7 40  1  0
  7 41  1  0
  8 42  1  0
  8 43  1  0
  9 44  1  0
 10 45  1  0
 11 46  1  0
 11 47  1  0
 12 48  1  0
 12 49  1  0
 13 50  1  0
 13 51  1  0
 14 52  1  0
 14 53  1  0
 15 54  1  0
 15 55  1  0
 16 56  1  0
 16 57  1  0
 17 58  1  0
 17 59  1  0
 20 60  1  0
 22 61  1  0
 23 62  1  0
 24 63  1  0
 25 64  1  0
 26 65  1  0
M  END

HEADER    PROTEIN                                 11-SEP-21   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   11-SEP-21         0                                  
HETATM    1  C   UNK     0      -6.668 -11.550   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0      -5.335 -12.320   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0      -4.001 -11.550   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0      -2.667 -12.320   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0      -1.334 -11.550   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0       0.000 -12.320   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0       1.334 -11.550   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0       2.667 -12.320   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0       4.001 -11.550   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0       5.335 -12.320   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0       6.668 -11.550   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0       8.002 -12.320   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0       9.336 -11.550   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0      10.669 -12.320   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0      12.003 -11.550   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0      13.337 -12.320   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0      14.670 -11.550   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0      16.004 -12.320   0.000  0.00  0.00           C+0
HETATM   19  O   UNK     0      16.004 -13.860   0.000  0.00  0.00           O+0
HETATM   20  N   UNK     0      17.338 -11.550   0.000  0.00  0.00           N+0
HETATM   21  C   UNK     0      18.672 -12.320   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0      20.005 -11.550   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0      21.339 -12.320   0.000  0.00  0.00           C+0
HETATM   24  C   UNK     0      21.339 -13.860   0.000  0.00  0.00           C+0
HETATM   25  C   UNK     0      20.005 -14.630   0.000  0.00  0.00           C+0
HETATM   26  C   UNK     0      18.672 -13.860   0.000  0.00  0.00           C+0
CONECT    1    2                                                            
CONECT    2    1    3                                                       
CONECT    3    2    4                                                       
CONECT    4    3    5                                                       
CONECT    5    4    6                                                       
CONECT    6    5    7                                                       
CONECT    7    6    8                                                       
CONECT    8    7    9                                                       
CONECT    9    8   10                                                       
CONECT   10    9   11                                                       
CONECT   11   10   12                                                       
CONECT   12   11   13                                                       
CONECT   13   12   14                                                       
CONECT   14   13   15                                                       
CONECT   15   14   16                                                       
CONECT   16   15   17                                                       
CONECT   17   16   18                                                       
CONECT   18   17   19   20                                                  
CONECT   19   18                                                            
CONECT   20   18   21                                                       
CONECT   21   20   22   26                                                  
CONECT   22   21   23                                                       
CONECT   23   22   24                                                       
CONECT   24   23   25                                                       
CONECT   25   24   26                                                       
CONECT   26   25   21                                                       
MASTER        0    0    0    0    0    0    0    0   26    0   52    0
END

COMPND    HMDB0255937
HETATM    1  C1  UNL     1      -6.845   1.218   3.032  1.00  0.00           C  
HETATM    2  C2  UNL     1      -5.769   0.476   2.263  1.00  0.00           C  
HETATM    3  C3  UNL     1      -6.419  -0.635   1.473  1.00  0.00           C  
HETATM    4  C4  UNL     1      -5.445  -1.431   0.677  1.00  0.00           C  
HETATM    5  C5  UNL     1      -4.655  -0.574  -0.344  1.00  0.00           C  
HETATM    6  C6  UNL     1      -5.647   0.014  -1.259  1.00  0.00           C  
HETATM    7  C7  UNL     1      -5.235   0.964  -2.293  1.00  0.00           C  
HETATM    8  C8  UNL     1      -4.236   0.542  -3.301  1.00  0.00           C  
HETATM    9  C9  UNL     1      -2.912   0.321  -2.748  1.00  0.00           C  
HETATM   10  C10 UNL     1      -1.891   1.080  -3.216  1.00  0.00           C  
HETATM   11  C11 UNL     1      -0.516   0.920  -2.708  1.00  0.00           C  
HETATM   12  C12 UNL     1      -0.419  -0.157  -1.647  1.00  0.00           C  
HETATM   13  C13 UNL     1       1.021  -0.252  -1.184  1.00  0.00           C  
HETATM   14  C14 UNL     1       1.074  -1.333  -0.133  1.00  0.00           C  
HETATM   15  C15 UNL     1       2.479  -1.518   0.409  1.00  0.00           C  
HETATM   16  C16 UNL     1       3.418  -1.901  -0.695  1.00  0.00           C  
HETATM   17  C17 UNL     1       4.817  -2.103  -0.199  1.00  0.00           C  
HETATM   18  C18 UNL     1       5.420  -0.877   0.377  1.00  0.00           C  
HETATM   19  O1  UNL     1       4.807   0.196   0.309  1.00  0.00           O  
HETATM   20  N1  UNL     1       6.682  -0.962   0.992  1.00  0.00           N  
HETATM   21  C19 UNL     1       7.336   0.150   1.561  1.00  0.00           C  
HETATM   22  C20 UNL     1       8.387  -0.125   2.445  1.00  0.00           C  
HETATM   23  C21 UNL     1       9.087   0.888   3.029  1.00  0.00           C  
HETATM   24  C22 UNL     1       8.778   2.193   2.765  1.00  0.00           C  
HETATM   25  C23 UNL     1       7.760   2.514   1.909  1.00  0.00           C  
HETATM   26  C24 UNL     1       7.056   1.466   1.321  1.00  0.00           C  
HETATM   27  H1  UNL     1      -6.531   2.271   3.194  1.00  0.00           H  
HETATM   28  H2  UNL     1      -7.755   1.201   2.388  1.00  0.00           H  
HETATM   29  H3  UNL     1      -7.070   0.682   3.959  1.00  0.00           H  
HETATM   30  H4  UNL     1      -5.318   1.218   1.544  1.00  0.00           H  
HETATM   31  H5  UNL     1      -4.978   0.124   2.926  1.00  0.00           H  
HETATM   32  H6  UNL     1      -6.848  -1.356   2.245  1.00  0.00           H  
HETATM   33  H7  UNL     1      -7.292  -0.261   0.942  1.00  0.00           H  
HETATM   34  H8  UNL     1      -5.962  -2.186   0.051  1.00  0.00           H  
HETATM   35  H9  UNL     1      -4.736  -1.984   1.310  1.00  0.00           H  
HETATM   36  H10 UNL     1      -4.052  -1.408  -0.853  1.00  0.00           H  
HETATM   37  H11 UNL     1      -3.943   0.089   0.122  1.00  0.00           H  
HETATM   38  H12 UNL     1      -6.475   0.543  -0.664  1.00  0.00           H  
HETATM   39  H13 UNL     1      -6.241  -0.863  -1.691  1.00  0.00           H  
HETATM   40  H14 UNL     1      -4.740   1.864  -1.761  1.00  0.00           H  
HETATM   41  H15 UNL     1      -6.143   1.435  -2.797  1.00  0.00           H  
HETATM   42  H16 UNL     1      -4.573  -0.437  -3.800  1.00  0.00           H  
HETATM   43  H17 UNL     1      -4.172   1.302  -4.138  1.00  0.00           H  
HETATM   44  H18 UNL     1      -2.652  -0.380  -2.020  1.00  0.00           H  
HETATM   45  H19 UNL     1      -2.045   1.835  -3.983  1.00  0.00           H  
HETATM   46  H20 UNL     1      -0.059   1.853  -2.360  1.00  0.00           H  
HETATM   47  H21 UNL     1       0.108   0.563  -3.572  1.00  0.00           H  
HETATM   48  H22 UNL     1      -1.084   0.072  -0.790  1.00  0.00           H  
HETATM   49  H23 UNL     1      -0.661  -1.148  -2.107  1.00  0.00           H  
HETATM   50  H24 UNL     1       1.406   0.719  -0.819  1.00  0.00           H  
HETATM   51  H25 UNL     1       1.599  -0.612  -2.083  1.00  0.00           H  
HETATM   52  H26 UNL     1       0.731  -2.275  -0.637  1.00  0.00           H  
HETATM   53  H27 UNL     1       0.351  -1.141   0.678  1.00  0.00           H  
HETATM   54  H28 UNL     1       2.780  -0.557   0.835  1.00  0.00           H  
HETATM   55  H29 UNL     1       2.479  -2.345   1.155  1.00  0.00           H  
HETATM   56  H30 UNL     1       3.057  -2.844  -1.186  1.00  0.00           H  
HETATM   57  H31 UNL     1       3.487  -1.087  -1.475  1.00  0.00           H  
HETATM   58  H32 UNL     1       4.841  -2.931   0.569  1.00  0.00           H  
HETATM   59  H33 UNL     1       5.480  -2.508  -1.022  1.00  0.00           H  
HETATM   60  H34 UNL     1       7.193  -1.905   1.037  1.00  0.00           H  
HETATM   61  H35 UNL     1       8.646  -1.157   2.667  1.00  0.00           H  
HETATM   62  H36 UNL     1       9.907   0.681   3.717  1.00  0.00           H  
HETATM   63  H37 UNL     1       9.337   3.005   3.231  1.00  0.00           H  
HETATM   64  H38 UNL     1       7.529   3.549   1.711  1.00  0.00           H  
HETATM   65  H39 UNL     1       6.268   1.747   0.642  1.00  0.00           H  
CONECT    1    2   27   28   29
CONECT    2    3   30   31
CONECT    3    4   32   33
CONECT    4    5   34   35
CONECT    5    6   36   37
CONECT    6    7   38   39
CONECT    7    8   40   41
CONECT    8    9   42   43
CONECT    9   10   10   44
CONECT   10   11   45
CONECT   11   12   46   47
CONECT   12   13   48   49
CONECT   13   14   50   51
CONECT   14   15   52   53
CONECT   15   16   54   55
CONECT   16   17   56   57
CONECT   17   18   58   59
CONECT   18   19   19   20
CONECT   20   21   60
CONECT   21   22   22   26
CONECT   22   23   61
CONECT   23   24   24   62
CONECT   24   25   63
CONECT   25   26   26   64
CONECT   26   65
END

HMDB0255937
     RDKit          3D
Oleanilide
 65 65  0  0  0  0  0  0  0  0999 V2000
   -6.8453    1.2181    3.0317 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.7686    0.4759    2.2627 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.4191   -0.6347    1.4727 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.4449   -1.4308    0.6767 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.6550   -0.5741   -0.3436 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.6473    0.0136   -1.2590 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.2348    0.9637   -2.2933 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2364    0.5415   -3.3007 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9120    0.3212   -2.7479 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8914    1.0800   -3.2163 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5164    0.9197   -2.7084 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4186   -0.1574   -1.6473 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.0212   -0.2523   -1.1842 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.0737   -1.3332   -0.1328 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.4789   -1.5176    0.4090 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.4182   -1.9008   -0.6947 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.8170   -2.1026   -0.1992 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.4198   -0.8765    0.3774 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.8069    0.1956    0.3092 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.6823   -0.9621    0.9923 N   0  0  0  0  0  0  0  0  0  0  0  0
    7.3356    0.1505    1.5614 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.3873   -0.1253    2.4451 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.0874    0.8881    3.0290 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.7781    2.1932    2.7646 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.7601    2.5143    1.9087 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.0556    1.4659    1.3208 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.5313    2.2707    3.1943 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.7550    1.2008    2.3876 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.0701    0.6821    3.9591 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.3183    1.2178    1.5439 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.9778    0.1243    2.9259 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.8476   -1.3560    2.2448 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.2922   -0.2609    0.9422 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.9624   -2.1864    0.0507 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.7364   -1.9844    1.3102 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.0522   -1.4082   -0.8529 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9427    0.0893    0.1217 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.4755    0.5435   -0.6642 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.2408   -0.8627   -1.6908 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.7400    1.8641   -1.7606 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.1434    1.4348   -2.7965 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.5732   -0.4368   -3.7999 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1717    1.3017   -4.1377 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6517   -0.3801   -2.0196 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0452    1.8347   -3.9829 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0591    1.8528   -2.3599 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.1081    0.5632   -3.5720 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0835    0.0724   -0.7903 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6613   -1.1483   -2.1066 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.4059    0.7194   -0.8193 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.5992   -0.6115   -2.0835 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.7312   -2.2753   -0.6373 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.3511   -1.1411    0.6779 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.7798   -0.5574    0.8355 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.4790   -2.3452    1.1546 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.0575   -2.8441   -1.1858 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.4868   -1.0872   -1.4755 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.8410   -2.9314    0.5693 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.4796   -2.5078   -1.0224 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.1926   -1.9048    1.0367 H   0  0  0  0  0  0  0  0  0  0  0  0
    8.6458   -1.1574    2.6672 H   0  0  0  0  0  0  0  0  0  0  0  0
    9.9066    0.6810    3.7175 H   0  0  0  0  0  0  0  0  0  0  0  0
    9.3373    3.0053    3.2315 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.5294    3.5489    1.7112 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.2682    1.7465    0.6420 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  2  3  1  0
  3  4  1  0
  4  5  1  0
  5  6  1  0
  6  7  1  0
  7  8  1  0
  8  9  1  0
  9 10  2  3
 10 11  1  0
 11 12  1  0
 12 13  1  0
 13 14  1  0
 14 15  1  0
 15 16  1  0
 16 17  1  0
 17 18  1  0
 18 19  2  0
 18 20  1  0
 20 21  1  0
 21 22  2  0
 22 23  1  0
 23 24  2  0
 24 25  1  0
 25 26  2  0
 26 21  1  0
  1 27  1  0
  1 28  1  0
  1 29  1  0
  2 30  1  0
  2 31  1  0
  3 32  1  0
  3 33  1  0
  4 34  1  0
  4 35  1  0
  5 36  1  0
  5 37  1  0
  6 38  1  0
  6 39  1  0
  7 40  1  0
  7 41  1  0
  8 42  1  0
  8 43  1  0
  9 44  1  0
 10 45  1  0
 11 46  1  0
 11 47  1  0
 12 48  1  0
 12 49  1  0
 13 50  1  0
 13 51  1  0
 14 52  1  0
 14 53  1  0
 15 54  1  0
 15 55  1  0
 16 56  1  0
 16 57  1  0
 17 58  1  0
 17 59  1  0
 20 60  1  0
 22 61  1  0
 23 62  1  0
 24 63  1  0
 25 64  1  0
 26 65  1  0
M  END

View in JSmol View Stereo Labels

Synonyms

Value	Source
N-Phenyloctadec-9-enimidate	Generator

Chemical Formula

C₂₄H₃₉NO

Average Molecular Weight

357.582

Monoisotopic Molecular Weight

357.30316488

IUPAC Name

N-phenyloctadec-9-enamide

Traditional Name

N-phenyloctadec-9-enamide

CAS Registry Number

Not Available

SMILES

CCCCCCCCC=CCCCCCCCC(=O)NC1=CC=CC=C1

InChI Identifier

InChI=1S/C24H39NO/c1-2-3-4-5-6-7-8-9-10-11-12-13-14-15-19-22-24(26)25-23-20-17-16-18-21-23/h9-10,16-18,20-21H,2-8,11-15,19,22H2,1H3,(H,25,26)

InChI Key

YPUOCYKJOLQYQS-UHFFFAOYSA-N

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as anilides. These are organic heterocyclic compounds derived from oxoacids RkE(=O)l(OH)m (l not 0) by replacing an OH group by the NHPh group or derivative formed by ring substitution.

Kingdom

Organic compounds

Super Class

Benzenoids

Class

Benzene and substituted derivatives

Sub Class

Anilides

Direct Parent

Anilides

Alternative Parents

Substituents

Anilide
N-arylamide
Fatty acyl
Fatty amide
Secondary carboxylic acid amide
Carboxamide group
Carboxylic acid derivative
Organic nitrogen compound
Organic oxygen compound
Organic oxide
Hydrocarbon derivative
Organooxygen compound
Organonitrogen compound
Carbonyl group
Aromatic homomonocyclic compound

Molecular Framework

Aromatic homomonocyclic compounds

External Descriptors

Not Available

Ontology

Physiological effect

Not Available

Disposition

Biological location

Non-excretory biofluid

Biofluid or Excreta

Blood (PMID: 31557052)

Process

Not Available

Role

Not Available

Physical Properties

State

Not Available

Experimental Molecular Properties

Property	Value	Reference
Melting Point	Not Available	Not Available
Boiling Point	Not Available	Not Available
Water Solubility	Not Available	Not Available
LogP	Not Available	Not Available

Experimental Chromatographic Properties

Not Available

Predicted Molecular Properties

Property	Value	Source
logP	8.07	ALOGPS
logP	8.22	ChemAxon
logS	-7.1	ALOGPS
pKa (Strongest Acidic)	14.2	ChemAxon
pKa (Strongest Basic)	-3.5	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	1	ChemAxon
Hydrogen Donor Count	1	ChemAxon
Polar Surface Area	29.1 Å²	ChemAxon
Rotatable Bond Count	16	ChemAxon
Refractivity	115.68 m³·mol⁻¹	ChemAxon
Polarizability	47.05 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

Predicted Chromatographic Properties

Predicted Collision Cross Sections

Predictor	Adduct Type	CCS Value (Å²)	Reference
DeepCCS	[M+H]+	198.997	30932474
DeepCCS	[M-H]-	196.447	30932474
DeepCCS	[M-2H]-	229.649	30932474
DeepCCS	[M+Na]+	205.34	30932474

Predicted Kovats Retention Indices

Underivatized

Metabolite	SMILES	Kovats RI Value	Column Type	Reference
Oleanilide	CCCCCCCCC=CCCCCCCCC(=O)NC1=CC=CC=C1	3473.7	Standard polar	33892256
Oleanilide	CCCCCCCCC=CCCCCCCCC(=O)NC1=CC=CC=C1	2887.2	Standard non polar	33892256
Oleanilide	CCCCCCCCC=CCCCCCCCC(=O)NC1=CC=CC=C1	3001.7	Semi standard non polar	33892256

Derivatized

Derivative Name / Structure	SMILES	Kovats RI Value	Column Type	Reference
Oleanilide,1TMS,isomer #1	CCCCCCCCC=CCCCCCCCC(=O)N(C1=CC=CC=C1)[Si](C)(C)C	2837.1	Semi standard non polar	33892256
Oleanilide,1TMS,isomer #1	CCCCCCCCC=CCCCCCCCC(=O)N(C1=CC=CC=C1)[Si](C)(C)C	2637.0	Standard non polar	33892256
Oleanilide,1TMS,isomer #1	CCCCCCCCC=CCCCCCCCC(=O)N(C1=CC=CC=C1)[Si](C)(C)C	3035.3	Standard polar	33892256
Oleanilide,1TBDMS,isomer #1	CCCCCCCCC=CCCCCCCCC(=O)N(C1=CC=CC=C1)[Si](C)(C)C(C)(C)C	3069.1	Semi standard non polar	33892256
Oleanilide,1TBDMS,isomer #1	CCCCCCCCC=CCCCCCCCC(=O)N(C1=CC=CC=C1)[Si](C)(C)C(C)(C)C	2837.7	Standard non polar	33892256
Oleanilide,1TBDMS,isomer #1	CCCCCCCCC=CCCCCCCCC(=O)N(C1=CC=CC=C1)[Si](C)(C)C(C)(C)C	3117.8	Standard polar	33892256

Spectra

GC-MS Spectra

Spectrum Type	Description	Splash Key	Deposition Date	Source	View
Predicted GC-MS	Predicted GC-MS Spectrum - Oleanilide GC-MS (Non-derivatized) - 70eV, Positive	splash10-0ukc-9851000000-6830b03f573a9eabc1e2	2021-09-23	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - Oleanilide GC-MS (Non-derivatized) - 70eV, Positive	Not Available	2021-10-12	Wishart Lab	View Spectrum

Biological Properties

Cellular Locations

Not Available

Biospecimen Locations

Blood

Tissue Locations

Not Available

Pathways

Not Available

Name	SMPDB/PathBank	KEGG

Normal Concentrations

Biospecimen	Status	Value	Age	Sex	Condition	Reference	Details
Blood	Detected but not Quantified	Not Quantified	Not Specified	Not Specified	Normal	31557052	details

Abnormal Concentrations

Not Available

Associated Disorders and Diseases

Disease References

None

Associated OMIM IDs

None

External Links

DrugBank ID

Not Available

Phenol Explorer Compound ID

Not Available

FooDB ID

Not Available

KNApSAcK ID

Not Available

Chemspider ID

82660

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

Not Available

PDB ID

Not Available

ChEBI ID

Not Available

Food Biomarker Ontology

Not Available

VMH ID

Not Available

MarkerDB ID

Not Available

Good Scents ID

Not Available

References

Synthesis Reference

Not Available

Material Safety Data Sheet (MSDS)

Not Available

General References

Barupal DK, Fiehn O: Generating the Blood Exposome Database Using a Comprehensive Text Mining and Database Fusion Approach. Environ Health Perspect. 2019 Sep;127(9):97008. doi: 10.1289/EHP4713. Epub 2019 Sep 26. [PubMed:31557052 ]

Showing metabocard for Oleanilide (HMDB0255937)

MOL for HMDB0255937 (Oleanilide)

3D MOL for HMDB0255937 (Oleanilide)

3D SDF for HMDB0255937 (Oleanilide)

3D-SDF for HMDB0255937 (Oleanilide)

PDB for HMDB0255937 (Oleanilide)

3D PDB for HMDB0255937 (Oleanilide)

SMILES for HMDB0255937 (Oleanilide)

INCHI for HMDB0255937 (Oleanilide)

Structure for HMDB0255937 (Oleanilide)

3D Structure for HMDB0255937 (Oleanilide)

Predicted Collision Cross Sections

Predicted Kovats Retention Indices

Underivatized

Derivatized

GC-MS Spectra