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Record Information

Version

5.0

Status

Detected but not Quantified

Creation Date

2012-09-11 19:06:11 UTC

Update Date

2022-03-07 02:54:03 UTC

HMDB ID

HMDB0034297

Secondary Accession Numbers

HMDB34297

Metabolite Identification

Common Name

Ricinoleic acid

Description

Ricinoleic acid is found in corn. Ricinoleic acid occurs in castor oil and other oils e.g. grape and ergot (Claviceps purpurea) Ricinoleic acid (12-hydroxy-9-cis-octadecenoic acid) is an unsaturated omega-9 fatty acid that naturally occurs in mature Castor plant (Ricinus communis L., Euphorbiaceae) seeds or in sclerotium of ergot (Claviceps purpurea Tul., Clavicipitaceae). About 90% of the fatty acid content in castor oil is the triglyceride formed from ricinoleic acid. Ricinoleic acid is manufactured for industries by saponification or fractional distillation of hydrolyzed castor oil. The zinc salt is used in personal care products, such as deodorants

Structure

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

HMDB0034297
     RDKit          3D
Ricinoleic acid
 55 54  0  0  0  0  0  0  0  0999 V2000
   -7.5887    0.8820    0.5315 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.1234    0.3081    0.5949 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.8339   -0.0321    1.9970 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.6053   -0.6884    2.4211 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2874   -0.0837    2.1781 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9171   -0.0093    0.7469 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5401    0.5958    0.5312 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6028   -0.2012    1.1703 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2776    0.6464   -0.9525 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3141   -0.7040   -1.5255 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2796   -1.2365   -2.1143 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.0041   -0.5834   -2.2749 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1431   -1.3440   -1.6028 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.4035   -0.5456   -1.8555 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.6085   -1.2107   -1.2275 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.8466   -0.4004   -1.4911 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.7382    0.9914   -0.9233 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.5285    1.0357    0.5510 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.6176    0.4149    1.3367 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.6553   -0.1007    0.8624 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.5044    0.3879    2.7293 O   0  0  0  0  0  0  0  0  0  0  0  0
   -7.6046    1.8517    1.0344 H   0  0  0  0  0  0  0  0  0  0  0  0
   -8.1806    0.1419    1.0881 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.8405    0.9294   -0.5469 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.0869   -0.4556   -0.1586 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.5642    1.2148    0.1956 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.7337   -0.6616    2.3658 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.0384    0.9254    2.6155 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.6899   -1.0692    3.5020 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.5748   -1.6883    1.8253 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2582    0.9480    2.6487 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5139   -0.6996    2.7490 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6045    0.5371    0.1523 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7877   -1.0906    0.4156 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4690    1.6084    0.9952 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9456   -1.1183    1.3530 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3874    1.2440   -1.1672 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1322    1.2663   -1.4127 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2618   -1.2566   -1.4533 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3839   -2.2678   -2.5260 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.2496   -0.6398   -3.3885 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.1207    0.4533   -2.0212 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.2113   -2.3794   -1.9869 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.9568   -1.3762   -0.5174 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.5156   -0.3989   -2.9356 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.2717    0.4312   -1.3334 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.7289   -2.1985   -1.7136 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.4391   -1.3750   -0.1570 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.7310   -0.9107   -1.0907 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.9113   -0.3145   -2.6137 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.7095    1.5338   -1.1232 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.9498    1.5860   -1.4230 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.4244    2.0769    0.9170 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.5887    0.5052    0.8639 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.5698   -0.5220    3.1644 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
  7  9  1  0
  9 10  1  0
 10 11  2  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  1  0
 19 20  2  0
 19 21  1  0
  1 22  1  0
  1 23  1  0
  1 24  1  0
  2 25  1  0
  2 26  1  0
  3 27  1  0
  3 28  1  0
  4 29  1  0
  4 30  1  0
  5 31  1  0
  5 32  1  0
  6 33  1  0
  6 34  1  0
  7 35  1  0
  8 36  1  0
  9 37  1  0
  9 38  1  0
 10 39  1  0
 11 40  1  0
 12 41  1  0
 12 42  1  0
 13 43  1  0
 13 44  1  0
 14 45  1  0
 14 46  1  0
 15 47  1  0
 15 48  1  0
 16 49  1  0
 16 50  1  0
 17 51  1  0
 17 52  1  0
 18 53  1  0
 18 54  1  0
 21 55  1  0
M  END


  Mrv0541 05061307422D          

 21 20  0  0  0  0            999 V2000
    9.4875    2.1434    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.6625    2.1434    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.2500    1.4289    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.4250    1.4289    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.7125    0.7145    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3000    1.4289    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3000    0.0000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.4750    1.4289    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.7125   -0.7145    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0625    0.7145    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.0125    0.7145    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.5375   -0.7145    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.2375    0.7145    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.1875    0.7145    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.9500    0.0000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.8250    0.0000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.7750    0.0000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0000    0.0000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.1875   -0.7145    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4125   -0.7145    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4125    0.7145    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
  2  1  1  0  0  0  0
  3  2  1  0  0  0  0
  4  3  1  0  0  0  0
  6  5  1  0  0  0  0
  7  5  1  0  0  0  0
  8  6  1  0  0  0  0
  9  7  1  0  0  0  0
 10  8  1  0  0  0  0
 11  4  1  0  0  0  0
 12  9  2  0  0  0  0
 13 10  1  0  0  0  0
 14 11  1  0  0  0  0
 15 12  1  0  0  0  0
 16 13  1  0  0  0  0
 17 14  1  0  0  0  0
 17 15  1  0  0  0  0
 18 16  1  0  0  0  0
 19 17  1  0  0  0  0
 20 18  2  0  0  0  0
 21 18  1  0  0  0  0
M  END
> <DATABASE_ID>
HMDB0034297

> <DATABASE_NAME>
hmdb

> <SMILES>
CCCCCCC(O)C\C=C/CCCCCCCC(O)=O

> <INCHI_IDENTIFIER>
InChI=1S/C18H34O3/c1-2-3-4-11-14-17(19)15-12-9-7-5-6-8-10-13-16-18(20)21/h9,12,17,19H,2-8,10-11,13-16H2,1H3,(H,20,21)/b12-9-

> <INCHI_KEY>
WBHHMMIMDMUBKC-XFXZXTDPSA-N

> <FORMULA>
C18H34O3

> <MOLECULAR_WEIGHT>
298.4608

> <EXACT_MASS>
298.250794954

> <JCHEM_ACCEPTOR_COUNT>
3

> <JCHEM_AVERAGE_POLARIZABILITY>
37.85424145779921

> <JCHEM_BIOAVAILABILITY>
0

> <JCHEM_DONOR_COUNT>
2

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
(9Z)-12-hydroxyoctadec-9-enoic acid

> <ALOGPS_LOGP>
6.14

> <JCHEM_LOGP>
5.397079924

> <ALOGPS_LOGS>
-5.07

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
0

> <JCHEM_PHYSIOLOGICAL_CHARGE>
-1

> <JCHEM_PKA>
18.401256348683585

> <JCHEM_PKA_STRONGEST_ACIDIC>
4.988167501938923

> <JCHEM_PKA_STRONGEST_BASIC>
-1.3110906911209161

> <JCHEM_POLAR_SURFACE_AREA>
57.53

> <JCHEM_REFRACTIVITY>
89.07169999999999

> <JCHEM_ROTATABLE_BOND_COUNT>
15

> <JCHEM_RULE_OF_FIVE>
0

> <ALOGPS_SOLUBILITY>
2.54e-03 g/l

> <JCHEM_TRADITIONAL_IUPAC>
12-hydroxy-oleic acid

> <JCHEM_VEBER_RULE>
0

$$$$

HMDB0034297
     RDKit          3D
Ricinoleic acid
 55 54  0  0  0  0  0  0  0  0999 V2000
   -7.5887    0.8820    0.5315 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.1234    0.3081    0.5949 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.8339   -0.0321    1.9970 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.6053   -0.6884    2.4211 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2874   -0.0837    2.1781 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9171   -0.0093    0.7469 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5401    0.5958    0.5312 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6028   -0.2012    1.1703 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2776    0.6464   -0.9525 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3141   -0.7040   -1.5255 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2796   -1.2365   -2.1143 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.0041   -0.5834   -2.2749 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1431   -1.3440   -1.6028 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.4035   -0.5456   -1.8555 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.6085   -1.2107   -1.2275 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.8466   -0.4004   -1.4911 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.7382    0.9914   -0.9233 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.5285    1.0357    0.5510 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.6176    0.4149    1.3367 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.6553   -0.1007    0.8624 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.5044    0.3879    2.7293 O   0  0  0  0  0  0  0  0  0  0  0  0
   -7.6046    1.8517    1.0344 H   0  0  0  0  0  0  0  0  0  0  0  0
   -8.1806    0.1419    1.0881 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.8405    0.9294   -0.5469 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.0869   -0.4556   -0.1586 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.5642    1.2148    0.1956 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.7337   -0.6616    2.3658 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.0384    0.9254    2.6155 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.6899   -1.0692    3.5020 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.5748   -1.6883    1.8253 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2582    0.9480    2.6487 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5139   -0.6996    2.7490 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6045    0.5371    0.1523 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7877   -1.0906    0.4156 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4690    1.6084    0.9952 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9456   -1.1183    1.3530 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3874    1.2440   -1.1672 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1322    1.2663   -1.4127 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2618   -1.2566   -1.4533 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3839   -2.2678   -2.5260 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.2496   -0.6398   -3.3885 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.1207    0.4533   -2.0212 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.2113   -2.3794   -1.9869 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.9568   -1.3762   -0.5174 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.5156   -0.3989   -2.9356 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.2717    0.4312   -1.3334 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.7289   -2.1985   -1.7136 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.4391   -1.3750   -0.1570 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.7310   -0.9107   -1.0907 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.9113   -0.3145   -2.6137 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.7095    1.5338   -1.1232 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.9498    1.5860   -1.4230 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.4244    2.0769    0.9170 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.5887    0.5052    0.8639 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.5698   -0.5220    3.1644 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
  7  9  1  0
  9 10  1  0
 10 11  2  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  1  0
 19 20  2  0
 19 21  1  0
  1 22  1  0
  1 23  1  0
  1 24  1  0
  2 25  1  0
  2 26  1  0
  3 27  1  0
  3 28  1  0
  4 29  1  0
  4 30  1  0
  5 31  1  0
  5 32  1  0
  6 33  1  0
  6 34  1  0
  7 35  1  0
  8 36  1  0
  9 37  1  0
  9 38  1  0
 10 39  1  0
 11 40  1  0
 12 41  1  0
 12 42  1  0
 13 43  1  0
 13 44  1  0
 14 45  1  0
 14 46  1  0
 15 47  1  0
 15 48  1  0
 16 49  1  0
 16 50  1  0
 17 51  1  0
 17 52  1  0
 18 53  1  0
 18 54  1  0
 21 55  1  0
M  END

HEADER    PROTEIN                                 06-MAY-13   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   06-MAY-13         0                                  
HETATM    1  C   UNK     0      17.710   4.001   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0      16.170   4.001   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0      15.400   2.667   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0      13.860   2.667   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0       6.930   1.334   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0       6.160   2.667   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0       6.160   0.000   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0       4.620   2.667   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0       6.930  -1.334   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0       3.850   1.334   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0      13.090   1.334   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0       8.470  -1.334   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0       2.310   1.334   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0      11.550   1.334   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0       9.240   0.000   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0       1.540   0.000   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0      10.780   0.000   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0       0.000   0.000   0.000  0.00  0.00           C+0
HETATM   19  O   UNK     0      11.550  -1.334   0.000  0.00  0.00           O+0
HETATM   20  O   UNK     0      -0.770  -1.334   0.000  0.00  0.00           O+0
HETATM   21  O   UNK     0      -0.770   1.334   0.000  0.00  0.00           O+0
CONECT    1    2                                                            
CONECT    2    1    3                                                       
CONECT    3    2    4                                                       
CONECT    4    3   11                                                       
CONECT    5    6    7                                                       
CONECT    6    5    8                                                       
CONECT    7    5    9                                                       
CONECT    8    6   10                                                       
CONECT    9    7   12                                                       
CONECT   10    8   13                                                       
CONECT   11    4   14                                                       
CONECT   12    9   15                                                       
CONECT   13   10   16                                                       
CONECT   14   11   17                                                       
CONECT   15   12   17                                                       
CONECT   16   13   18                                                       
CONECT   17   14   15   19                                                  
CONECT   18   16   20   21                                                  
CONECT   19   17                                                            
CONECT   20   18                                                            
CONECT   21   18                                                            
MASTER        0    0    0    0    0    0    0    0   21    0   40    0
END

COMPND    HMDB0034297
HETATM    1  C1  UNL     1      -7.589   0.882   0.531  1.00  0.00           C  
HETATM    2  C2  UNL     1      -6.123   0.308   0.595  1.00  0.00           C  
HETATM    3  C3  UNL     1      -5.834  -0.032   1.997  1.00  0.00           C  
HETATM    4  C4  UNL     1      -4.605  -0.688   2.421  1.00  0.00           C  
HETATM    5  C5  UNL     1      -3.287  -0.084   2.178  1.00  0.00           C  
HETATM    6  C6  UNL     1      -2.917  -0.009   0.747  1.00  0.00           C  
HETATM    7  C7  UNL     1      -1.540   0.596   0.531  1.00  0.00           C  
HETATM    8  O1  UNL     1      -0.603  -0.201   1.170  1.00  0.00           O  
HETATM    9  C8  UNL     1      -1.278   0.646  -0.953  1.00  0.00           C  
HETATM   10  C9  UNL     1      -1.314  -0.704  -1.525  1.00  0.00           C  
HETATM   11  C10 UNL     1      -0.280  -1.237  -2.114  1.00  0.00           C  
HETATM   12  C11 UNL     1       1.004  -0.583  -2.275  1.00  0.00           C  
HETATM   13  C12 UNL     1       2.143  -1.344  -1.603  1.00  0.00           C  
HETATM   14  C13 UNL     1       3.404  -0.546  -1.856  1.00  0.00           C  
HETATM   15  C14 UNL     1       4.608  -1.211  -1.227  1.00  0.00           C  
HETATM   16  C15 UNL     1       5.847  -0.400  -1.491  1.00  0.00           C  
HETATM   17  C16 UNL     1       5.738   0.991  -0.923  1.00  0.00           C  
HETATM   18  C17 UNL     1       5.528   1.036   0.551  1.00  0.00           C  
HETATM   19  C18 UNL     1       6.618   0.415   1.337  1.00  0.00           C  
HETATM   20  O2  UNL     1       7.655  -0.101   0.862  1.00  0.00           O  
HETATM   21  O3  UNL     1       6.504   0.388   2.729  1.00  0.00           O  
HETATM   22  H1  UNL     1      -7.605   1.852   1.034  1.00  0.00           H  
HETATM   23  H2  UNL     1      -8.181   0.142   1.088  1.00  0.00           H  
HETATM   24  H3  UNL     1      -7.841   0.929  -0.547  1.00  0.00           H  
HETATM   25  H4  UNL     1      -6.087  -0.456  -0.159  1.00  0.00           H  
HETATM   26  H5  UNL     1      -5.564   1.215   0.196  1.00  0.00           H  
HETATM   27  H6  UNL     1      -6.734  -0.662   2.366  1.00  0.00           H  
HETATM   28  H7  UNL     1      -6.038   0.925   2.615  1.00  0.00           H  
HETATM   29  H8  UNL     1      -4.690  -1.069   3.502  1.00  0.00           H  
HETATM   30  H9  UNL     1      -4.575  -1.688   1.825  1.00  0.00           H  
HETATM   31  H10 UNL     1      -3.258   0.948   2.649  1.00  0.00           H  
HETATM   32  H11 UNL     1      -2.514  -0.700   2.749  1.00  0.00           H  
HETATM   33  H12 UNL     1      -3.604   0.537   0.152  1.00  0.00           H  
HETATM   34  H13 UNL     1      -2.788  -1.091   0.416  1.00  0.00           H  
HETATM   35  H14 UNL     1      -1.469   1.608   0.995  1.00  0.00           H  
HETATM   36  H15 UNL     1      -0.946  -1.118   1.353  1.00  0.00           H  
HETATM   37  H16 UNL     1      -0.387   1.244  -1.167  1.00  0.00           H  
HETATM   38  H17 UNL     1      -2.132   1.266  -1.413  1.00  0.00           H  
HETATM   39  H18 UNL     1      -2.262  -1.257  -1.453  1.00  0.00           H  
HETATM   40  H19 UNL     1      -0.384  -2.268  -2.526  1.00  0.00           H  
HETATM   41  H20 UNL     1       1.250  -0.640  -3.388  1.00  0.00           H  
HETATM   42  H21 UNL     1       1.121   0.453  -2.021  1.00  0.00           H  
HETATM   43  H22 UNL     1       2.211  -2.379  -1.987  1.00  0.00           H  
HETATM   44  H23 UNL     1       1.957  -1.376  -0.517  1.00  0.00           H  
HETATM   45  H24 UNL     1       3.516  -0.399  -2.936  1.00  0.00           H  
HETATM   46  H25 UNL     1       3.272   0.431  -1.333  1.00  0.00           H  
HETATM   47  H26 UNL     1       4.729  -2.198  -1.714  1.00  0.00           H  
HETATM   48  H27 UNL     1       4.439  -1.375  -0.157  1.00  0.00           H  
HETATM   49  H28 UNL     1       6.731  -0.911  -1.091  1.00  0.00           H  
HETATM   50  H29 UNL     1       5.911  -0.314  -2.614  1.00  0.00           H  
HETATM   51  H30 UNL     1       6.709   1.534  -1.123  1.00  0.00           H  
HETATM   52  H31 UNL     1       4.950   1.586  -1.423  1.00  0.00           H  
HETATM   53  H32 UNL     1       5.424   2.077   0.917  1.00  0.00           H  
HETATM   54  H33 UNL     1       4.589   0.505   0.864  1.00  0.00           H  
HETATM   55  H34 UNL     1       6.570  -0.522   3.164  1.00  0.00           H  
CONECT    1    2   22   23   24
CONECT    2    3   25   26
CONECT    3    4   27   28
CONECT    4    5   29   30
CONECT    5    6   31   32
CONECT    6    7   33   34
CONECT    7    8    9   35
CONECT    8   36
CONECT    9   10   37   38
CONECT   10   11   11   39
CONECT   11   12   40
CONECT   12   13   41   42
CONECT   13   14   43   44
CONECT   14   15   45   46
CONECT   15   16   47   48
CONECT   16   17   49   50
CONECT   17   18   51   52
CONECT   18   19   53   54
CONECT   19   20   20   21
CONECT   21   55
END

HMDB0034297
     RDKit          3D
Ricinoleic acid
 55 54  0  0  0  0  0  0  0  0999 V2000
   -7.5887    0.8820    0.5315 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.1234    0.3081    0.5949 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.8339   -0.0321    1.9970 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.6053   -0.6884    2.4211 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2874   -0.0837    2.1781 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9171   -0.0093    0.7469 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5401    0.5958    0.5312 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6028   -0.2012    1.1703 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2776    0.6464   -0.9525 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3141   -0.7040   -1.5255 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2796   -1.2365   -2.1143 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.0041   -0.5834   -2.2749 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1431   -1.3440   -1.6028 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.4035   -0.5456   -1.8555 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.6085   -1.2107   -1.2275 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.8466   -0.4004   -1.4911 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.7382    0.9914   -0.9233 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.5285    1.0357    0.5510 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.6176    0.4149    1.3367 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.6553   -0.1007    0.8624 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.5044    0.3879    2.7293 O   0  0  0  0  0  0  0  0  0  0  0  0
   -7.6046    1.8517    1.0344 H   0  0  0  0  0  0  0  0  0  0  0  0
   -8.1806    0.1419    1.0881 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.8405    0.9294   -0.5469 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.0869   -0.4556   -0.1586 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.5642    1.2148    0.1956 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.7337   -0.6616    2.3658 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.0384    0.9254    2.6155 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.6899   -1.0692    3.5020 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.5748   -1.6883    1.8253 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2582    0.9480    2.6487 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5139   -0.6996    2.7490 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6045    0.5371    0.1523 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7877   -1.0906    0.4156 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4690    1.6084    0.9952 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9456   -1.1183    1.3530 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3874    1.2440   -1.1672 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1322    1.2663   -1.4127 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2618   -1.2566   -1.4533 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3839   -2.2678   -2.5260 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.2496   -0.6398   -3.3885 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.1207    0.4533   -2.0212 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.2113   -2.3794   -1.9869 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.9568   -1.3762   -0.5174 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.5156   -0.3989   -2.9356 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.2717    0.4312   -1.3334 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.7289   -2.1985   -1.7136 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.4391   -1.3750   -0.1570 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.7310   -0.9107   -1.0907 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.9113   -0.3145   -2.6137 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.7095    1.5338   -1.1232 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.9498    1.5860   -1.4230 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.4244    2.0769    0.9170 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.5887    0.5052    0.8639 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.5698   -0.5220    3.1644 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
  7  9  1  0
  9 10  1  0
 10 11  2  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  1  0
 19 20  2  0
 19 21  1  0
  1 22  1  0
  1 23  1  0
  1 24  1  0
  2 25  1  0
  2 26  1  0
  3 27  1  0
  3 28  1  0
  4 29  1  0
  4 30  1  0
  5 31  1  0
  5 32  1  0
  6 33  1  0
  6 34  1  0
  7 35  1  0
  8 36  1  0
  9 37  1  0
  9 38  1  0
 10 39  1  0
 11 40  1  0
 12 41  1  0
 12 42  1  0
 13 43  1  0
 13 44  1  0
 14 45  1  0
 14 46  1  0
 15 47  1  0
 15 48  1  0
 16 49  1  0
 16 50  1  0
 17 51  1  0
 17 52  1  0
 18 53  1  0
 18 54  1  0
 21 55  1  0
M  END

View in JSmol View Stereo Labels

Synonyms

Value	Source
12-Hydroxyoleic acid	ChEBI
12-Hydroxyoleate	Generator
Ricinoleate	Generator
(9Z)-(12S)-Hydroxyoctadecenoic acid	HMDB
(9Z)-12-Hydroxy-9-octadecenoic acid	HMDB
(9Z)-12-Hydroxyoctadec-9-enoic acid	HMDB
(9Z,12R)-12-Hydroxyoctadec-9-enoic acid	HMDB
(R)-12-Hydroxy-cis-9-octadecenoic acid	HMDB
12-Hydroxy-(9Z,12R)-9-octadecenoic acid	HMDB
12-Hydroxy-9-octadecenoic acid	HMDB, MeSH
12-Hydroxy-cis-9-octadecenoic acid	HMDB
12-Hydroxy-oleic acid	HMDB
12-Hydroxy-[R-(Z)]-9-octadecenoic acid	HMDB
D-12-Hydroxyoleic acid	HMDB
Flexricin 100	HMDB
L'acide ricinoleique	HMDB
P -10 acid	HMDB
RCL	HMDB
Ricinelaidic acid	HMDB, MeSH
Ricinic acid	HMDB
Ricinolic acid	HMDB
Ricinusoleic acid	HMDB
Riconoleic acid	HMDB
12-Hydroxy-9-octadecenic acid	MeSH, HMDB
12-Hydroxyoctadec-cis-9-enoic acid	MeSH, HMDB
Ricinoleic acid, (R-(e))-isomer	MeSH, HMDB
(9Z)-12-Hydroxyoctadec-9-enoate	Generator
12-D-Hydroxy-9-trans-octadecenoic acid	MeSH
Ricinoleic acid	MeSH

Chemical Formula

C₁₈H₃₄O₃

Average Molecular Weight

298.4608

Monoisotopic Molecular Weight

298.250794954

IUPAC Name

(9Z)-12-hydroxyoctadec-9-enoic acid

Traditional Name

12-hydroxy-oleic acid

CAS Registry Number

141-22-0

SMILES

CCCCCCC(O)C\C=C/CCCCCCCC(O)=O

InChI Identifier

InChI=1S/C18H34O3/c1-2-3-4-11-14-17(19)15-12-9-7-5-6-8-10-13-16-18(20)21/h9,12,17,19H,2-8,10-11,13-16H2,1H3,(H,20,21)/b12-9-

InChI Key

WBHHMMIMDMUBKC-XFXZXTDPSA-N

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as long-chain fatty acids. These are fatty acids with an aliphatic tail that contains between 13 and 21 carbon atoms.

Kingdom

Organic compounds

Super Class

Lipids and lipid-like molecules

Class

Fatty Acyls

Sub Class

Fatty acids and conjugates

Direct Parent

Long-chain fatty acids

Alternative Parents

Substituents

Long-chain fatty acid
Hydroxy fatty acid
Unsaturated fatty acid
Secondary alcohol
Monocarboxylic acid or derivatives
Carboxylic acid
Carboxylic acid derivative
Organic oxygen compound
Organic oxide
Hydrocarbon derivative
Organooxygen compound
Carbonyl group
Alcohol
Aliphatic acyclic compound

Molecular Framework

Aliphatic acyclic compounds

External Descriptors

long-chain fatty acid (CHEBI:85639 )
monounsaturated fatty acid (CHEBI:85639 )
hydroxy fatty acid (CHEBI:85639 )

Ontology

Physiological effect

Not Available

Disposition

Biological location

Cellular substructure

Organelle

Adiposome (HMDB: HMDB0034297)

Non-excretory biofluid

Biofluid or Excreta

Saliva (PMID: 24421258)

Excreta

Biofluid or Excreta

Feces (PMID: 27543620)
Urine (HMDB: HMDB0034297)

Route of exposure

Enteral

Ingestion (HMDB: HMDB0034297)

Source

Exogenous

Exogenous (HMDB: HMDB0034297)

Food

Food (HMDB: HMDB0034297)

Cereal and cereal product

Cereal

Corn (FooDB: FOOD00205)

Fruit

Fruits (FooDB: FOOD00871)

Fat and oil

Fats and oils (FooDB: FOOD00864)

Synthetic

Personal care products

Soap (HMDB: HMDB0034297)

Endogenous

Endogenous (HMDB: HMDB0034297)

Plant

Plant (HMDB: HMDB0034297)
Poaceae (HMDB: HMDB0034297)

Animal

Animal (HMDB: HMDB0034297)

Process

Naturally occurring process

Biological process

Chemical reaction

Lipid Peroxidation (HMDB: HMDB0034297)

Biochemical pathway

Metabolic pathway

Fatty Acid Metabolism (HMDB: HMDB0034297)

Lipid metabolism pathway (HMDB: HMDB0034297)

Cellular process

Cell signaling (HMDB: HMDB0034297)

Biochemical process

Lipid transport (HMDB: HMDB0034297)

Role

Physical Properties

State

Liquid

Experimental Molecular Properties

Property	Value	Reference
Melting Point	5.5 °C	Not Available
Boiling Point	314.00 to 315.00 °C. @ 760.00 mm Hg (est)	The Good Scents Company Information System
Water Solubility	3.46 mg/mL at 25 °C	Not Available
LogP	4.565 (est)	The Good Scents Company Information System

Experimental Chromatographic Properties

Not Available

Predicted Molecular Properties

Property	Value	Source
Water Solubility	0.0025 g/L	ALOGPS
logP	6.14	ALOGPS
logP	5.4	ChemAxon
logS	-5.1	ALOGPS
pKa (Strongest Acidic)	4.99	ChemAxon
pKa (Strongest Basic)	-1.3	ChemAxon
Physiological Charge	-1	ChemAxon
Hydrogen Acceptor Count	3	ChemAxon
Hydrogen Donor Count	2	ChemAxon
Polar Surface Area	57.53 Å²	ChemAxon
Rotatable Bond Count	15	ChemAxon
Refractivity	89.07 m³·mol⁻¹	ChemAxon
Polarizability	37.85 Å³	ChemAxon
Number of Rings	0	ChemAxon
Bioavailability	No	ChemAxon
Rule of Five	No	ChemAxon
Ghose Filter	Yes	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
DarkChem	[M+H]+	179.628	31661259
DarkChem	[M-H]-	176.958	31661259
DeepCCS	[M+H]+	184.008	30932474
DeepCCS	[M-H]-	180.014	30932474
DeepCCS	[M-2H]-	216.533	30932474
DeepCCS	[M+Na]+	192.823	30932474
AllCCS	[M+H]+	183.2	32859911
AllCCS	[M+H-H2O]+	180.3	32859911
AllCCS	[M+NH4]+	185.9	32859911
AllCCS	[M+Na]+	186.6	32859911
AllCCS	[M-H]-	181.3	32859911
AllCCS	[M+Na-2H]-	182.9	32859911
AllCCS	[M+HCOO]-	184.7	32859911

Predicted Retention Times

Underivatized

Chromatographic Method	Retention Time	Reference
Measured using a Waters Acquity ultraperformance liquid chromatography (UPLC) ethylene-bridged hybrid (BEH) C18 column (100 mm × 2.1 mm; 1.7 μmparticle diameter)). Predicted by Afia on May 17, 2022.	9.96 minutes	32390414
Predicted by Siyang on May 30, 2022	18.5988 minutes	33406817
Predicted by Siyang using ReTip algorithm on June 8, 2022	0.99 minutes	32390414
AjsUoB = Accucore 150 Amide HILIC with 10mM Ammonium Formate, 0.1% Formic Acid	37.4 seconds	40023050
Fem_Long = Waters ACQUITY UPLC HSS T3 C18 with Water:MeOH and 0.1% Formic Acid	2831.8 seconds	40023050
Fem_Lipids = Ascentis Express C18 with (60:40 water:ACN):(90:10 IPA:ACN) and 10mM NH4COOH + 0.1% Formic Acid	393.2 seconds	40023050
Life_Old = Waters ACQUITY UPLC BEH C18 with Water:(20:80 acetone:ACN) and 0.1% Formic Acid	205.9 seconds	40023050
Life_New = RP Waters ACQUITY UPLC HSS T3 C18 with Water:(30:70 MeOH:ACN) and 0.1% Formic Acid	207.5 seconds	40023050
RIKEN = Waters ACQUITY UPLC BEH C18 with Water:ACN and 0.1% Formic Acid	531.3 seconds	40023050
Eawag_XBridgeC18 = XBridge C18 3.5u 2.1x50 mm with Water:MeOH and 0.1% Formic Acid	863.2 seconds	40023050
BfG_NTS_RP1 =Agilent Zorbax Eclipse Plus C18 (2.1 mm x 150 mm, 3.5 um) with Water:ACN and 0.1% Formic Acid	647.0 seconds	40023050
HILIC_BDD_2 = Merck SeQuant ZIC-HILIC with ACN(0.1% formic acid):water(16 mM ammonium formate)	119.2 seconds	40023050
UniToyama_Atlantis = RP Waters Atlantis T3 (2.1 x 150 mm, 5 um) with ACN:Water and 0.1% Formic Acid	1748.8 seconds	40023050
BDD_C18 = Hypersil Gold 1.9µm C18 with Water:ACN and 0.1% Formic Acid	568.0 seconds	40023050
UFZ_Phenomenex = Kinetex Core-Shell C18 2.6 um, 3.0 x 100 mm, Phenomenex with Water:MeOH and 0.1% Formic Acid	1709.5 seconds	40023050
SNU_RIKEN_POS = Waters ACQUITY UPLC BEH C18 with Water:ACN and 0.1% Formic Acid	586.1 seconds	40023050
RPMMFDA = Waters ACQUITY UPLC BEH C18 with Water:ACN and 0.1% Formic Acid	436.7 seconds	40023050
MTBLS87 = Merck SeQuant ZIC-pHILIC column with ACN:Water and :ammonium carbonate	396.2 seconds	40023050
KI_GIAR_zic_HILIC_pH2_7 = Merck SeQuant ZIC-HILIC with ACN:Water and 0.1% FA	421.1 seconds	40023050
Meister zic-pHILIC pH9.3 = Merck SeQuant ZIC-pHILIC column with ACN:Water 5mM NH4Ac pH9.3 and 5mM ammonium acetate in water	8.2 seconds	40023050

Predicted Kovats Retention Indices

Underivatized

Metabolite	SMILES	Kovats RI Value	Column Type	Reference
Ricinoleic acid	CCCCCCC(O)C\C=C/CCCCCCCC(O)=O	3517.9	Standard polar	33892256
Ricinoleic acid	CCCCCCC(O)C\C=C/CCCCCCCC(O)=O	2165.6	Standard non polar	33892256
Ricinoleic acid	CCCCCCC(O)C\C=C/CCCCCCCC(O)=O	2332.9	Semi standard non polar	33892256

Derivatized

Derivative Name / Structure	SMILES	Kovats RI Value	Column Type	Reference
Ricinoleic acid,1TMS,isomer #1	CCCCCCC(C/C=C\CCCCCCCC(=O)O)O[Si](C)(C)C	2434.4	Semi standard non polar	33892256
Ricinoleic acid,1TMS,isomer #2	CCCCCCC(O)C/C=C\CCCCCCCC(=O)O[Si](C)(C)C	2381.5	Semi standard non polar	33892256
Ricinoleic acid,2TMS,isomer #1	CCCCCCC(C/C=C\CCCCCCCC(=O)O[Si](C)(C)C)O[Si](C)(C)C	2428.6	Semi standard non polar	33892256
Ricinoleic acid,1TBDMS,isomer #1	CCCCCCC(C/C=C\CCCCCCCC(=O)O)O[Si](C)(C)C(C)(C)C	2673.1	Semi standard non polar	33892256
Ricinoleic acid,1TBDMS,isomer #2	CCCCCCC(O)C/C=C\CCCCCCCC(=O)O[Si](C)(C)C(C)(C)C	2623.8	Semi standard non polar	33892256
Ricinoleic acid,2TBDMS,isomer #1	CCCCCCC(C/C=C\CCCCCCCC(=O)O[Si](C)(C)C(C)(C)C)O[Si](C)(C)C(C)(C)C	2894.7	Semi standard non polar	33892256

Spectra

Biological Properties

Cellular Locations

Extracellular
Membrane

Biospecimen Locations

Feces
Saliva

Tissue Locations

Not Available

Pathways

Not Available

Name	SMPDB/PathBank	KEGG

Normal Concentrations

Biospecimen	Status	Value	Age	Sex	Condition	Reference	Details
Feces	Detected but not Quantified	Not Quantified	Adult (>18 years old)	Both	Normal	27543620	details
Saliva	Detected but not Quantified	Not Quantified	Adult (>18 years old)	Not Specified	Normal	24421258	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

KNApSAcK ID

Chemspider ID

KEGG Compound ID

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Ricinoleic acid

METLIN ID

Not Available

PubChem Compound

5282942

PDB ID

Not Available

ChEBI ID

85639

Food Biomarker Ontology

Not Available

VMH ID

Not Available

MarkerDB ID

Not Available

Good Scents ID

rw1473331

References

Synthesis Reference

Not Available

Material Safety Data Sheet (MSDS)

Download (PDF)

General References

Gullikson GW, Sender M, Bass P: Laxative-like effects of nonsteroidal anti-inflammatory drugs on intestinal fluid movement and membrane integrity. J Pharmacol Exp Ther. 1982 Feb;220(2):236-42. [PubMed:6948953 ]
Vieira C, Evangelista S, Cirillo R, Terracciano R, Lippi A, Maggi CA, Manzini S: Antinociceptive activity of ricinoleic acid, a capsaicin-like compound devoid of pungent properties. Eur J Pharmacol. 2000 Oct 27;407(1-2):109-16. [PubMed:11050297 ]
Simons K, Toomre D: Lipid rafts and signal transduction. Nat Rev Mol Cell Biol. 2000 Oct;1(1):31-9. [PubMed:11413487 ]
Watson AD: Thematic review series: systems biology approaches to metabolic and cardiovascular disorders. Lipidomics: a global approach to lipid analysis in biological systems. J Lipid Res. 2006 Oct;47(10):2101-11. Epub 2006 Aug 10. [PubMed:16902246 ]
Sethi JK, Vidal-Puig AJ: Thematic review series: adipocyte biology. Adipose tissue function and plasticity orchestrate nutritional adaptation. J Lipid Res. 2007 Jun;48(6):1253-62. Epub 2007 Mar 20. [PubMed:17374880 ]
Lingwood D, Simons K: Lipid rafts as a membrane-organizing principle. Science. 2010 Jan 1;327(5961):46-50. doi: 10.1126/science.1174621. [PubMed:20044567 ]
(). Yannai, Shmuel. (2004) Dictionary of food compounds with CD-ROM: Additives, flavors, and ingredients. Boca Raton: Chapman & Hall/CRC.. .
Gunstone, Frank D., John L. Harwood, and Albert J. Dijkstra (2007). The lipid handbook with CD-ROM. CRC Press.

Showing metabocard for Ricinoleic acid (HMDB0034297)

MOL for HMDB0034297 (Ricinoleic acid)

3D MOL for HMDB0034297 (Ricinoleic acid)

3D SDF for HMDB0034297 (Ricinoleic acid)

3D-SDF for HMDB0034297 (Ricinoleic acid)

PDB for HMDB0034297 (Ricinoleic acid)

3D PDB for HMDB0034297 (Ricinoleic acid)

SMILES for HMDB0034297 (Ricinoleic acid)

INCHI for HMDB0034297 (Ricinoleic acid)

Structure for HMDB0034297 (Ricinoleic acid)

3D Structure for HMDB0034297 (Ricinoleic acid)

Predicted Collision Cross Sections

Predicted Retention Times

Underivatized

Predicted Kovats Retention Indices

Underivatized

Derivatized