Structure Database (LMSD)

Common Name
5S-HEPE
Systematic Name
5S-hydroxy-6E,8Z,11Z,14Z,17Z-eicosapentaenoic acid
Synonyms
LM ID
LMFA03070010
Formula
Exact Mass
Calculate m/z
318.219495
Sum Composition
Status
Curated


Classification

Biological Context

5(S)-HEPE is an active metabolite of eicosapentaenoic acid (EPA).1 It is formed from EPA by 5-lipoxygenase (5-LO). 5(S)-HEPE is an agonist of G protein-coupled receptor 119 (GPR119).2 It increases cAMP accumulation in CHO-K1 cells expressing human GPR119 when used at a concentration of 10 µM. 5(S)-HEPE increases glucose-induced insulin secretion from MING6 insulinoma pancreatic islets and glucagon-like peptide 1 (GLP-1) secretion from HuTu 80 adenocarcinoma cells when used at a concentration of 10 µM. Serum levels of 5(S)-HEPE are elevated in patients with hyperlipidemia.3

This information has been provided by Cayman Chemical

References

1. Noguchi, N., Yoshida, Y., Kaneda, H., et al. Action of ebselen as an antioxidant against lipid peroxidation. Biochem. Pharmacol. 44(1), 39-44 (1992).
2. Kogure, R., Toyama, K., Kiyamuta, S., et al. 5-Hydroxy-eicosapentaenoic acid is an endogenous GPR119 agonist and enhances glucose-dependent insulin secretion. Biochem. Biophys. Res. Commun. 416(1-2), 58-63 (2011).

String Representations

InChiKey (Click to copy)
FTAGQROYQYQRHF-GHWNLOBHSA-N
InChi (Click to copy)
InChI=1S/C20H30O3/c1-2-3-4-5-6-7-8-9-10-11-12-13-14-16-19(21)17-15-18-20(22)23/h3-4,6-7,9-10,12-14,16,19,21H,2,5,8,11,15,17-18H2,1H3,(H,22,23)/b4-3-,7-6-,10-9-,13-12-,16-14+/t19-/m1/s1
SMILES (Click to copy)
C(/C/C=C\C/C=C\C/C=C\CC)=C/C=C/[C@@H](O)CCCC(=O)O

Other Databases

HMDB ID
CHEBI ID
PubChem CID
Cayman ID

Calculated Physicochemical Properties

Heavy Atoms 23
Rings 0
Aromatic Rings 0
Rotatable Bonds 13
Van der Waals Molecular Volume 365.09
Topological Polar Surface Area 57.53
Hydrogen Bond Donors 2
Hydrogen Bond Acceptors 3
logP 5.25
Molar Refractivity 97.85

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Updated at
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