Structure Database (LMSD)

Common Name
2R-hydroxypalmitic acid
Systematic Name
2R-hydroxyhexadecanoic acid
Synonyms
  • (R)-2OH PA
LM ID
LMFA01050423
Formula
Exact Mass
Calculate m/z
272.235145
Sum Composition
Status
Active

Classification

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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Reactions graph legend

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

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
Pubmed ID: 22517924

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

HMDB ID
CHEBI ID
PubChem CID
SwissLipids ID

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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