Structure Database (LMSD)
Common Name
2R-hydroxypalmitic acid
Systematic Name
2R-hydroxyhexadecanoic acid
Synonyms
- (R)-2OH PA
3D model of 2R-hydroxypalmitic acid
Please note: Where there are chiral atoms but the stereochemistry is undefined, the 3D model takes an arbitrary conformation
Main
Classification
Category
Main Class
Sub Class
String Representations
InChiKey (Click to copy)
JGHSBPIZNUXPLA-OAHLLOKOSA-N
InChi (Click to copy)
InChI=1S/C16H32O3/c1-2-3-4-5-6-7-8-9-10-11-12-13-14-15(17)16(18)19/h15,17H,2-14H2,1H3,(H,18,19)/t15-/m1/s1
SMILES (Click to copy)
C(CCCCCCCCCCCCC)[C@@H](O)C(=O)O
References
Reference
Stereospecificity of fatty acid 2-hydroxylase and differential functions of 2-hydroxy fatty acid enantiomers
Lin Guo, Xu Zhang, Dequan Zhou, Adewole L. Okunade, and Xiong Su
J. Lipid Res. 2012 53:(7) 1327-1335
Lin Guo, Xu Zhang, Dequan Zhou, Adewole L. Okunade, and Xiong Su
J. Lipid Res. 2012 53:(7) 1327-1335
Taxonomy Information
Curated from
NCBI taxonomy class
Reference
Homo sapiens
(#9606)
Mammalia
(#40674)
Stereospecificity of fatty acid 2-hydroxylase and differential functions of 2-hydroxy fatty acid enantiomers.,
J Lipid Res, 2012
J Lipid Res, 2012
Pubmed ID:
22517924
Other Databases
Calculated Physicochemical Properties
Heavy Atoms
19
Rings
0
Aromatic Rings
0
Rotatable Bonds
14
Van der Waals Molecular Volume
309.09
Topological Polar Surface Area
57.53
Hydrogen Bond Donors
2
Hydrogen Bond Acceptors
3
logP
4.81
Molar Refractivity
79.85
Reactions
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