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
Classification
Category
Main Class
Sub Class
Reactions
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Reactions are shown if the E.C. number of the enzyme catalysing it is annotated in the UniProt database for a species belonging to the selected taxonomic class.
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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
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
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
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Updated at
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