LBF20406HO12

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Fatty acid (脂肪酸)

Glycerolipid (グリセロ脂質)

Sphingolipid (スフィンゴ脂質)

Journals (雑誌一覧)

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Upper classes: LB LBF

IDs and Links
LipidBank	DFA8130
LipidMaps	LMFA03060021
CAS
KEGG	{{{KEGG}}}
KNApSAcK	{{{KNApSAcK}}}
mol	LBF20406HO12

8R-Hydroxy- (5Z,9E,11Z,14Z) -eicosatetraenoic acid
Structural Information
Systematic Name	8R-Hydroxy- (cis-5,trans-9,cis-11,cis-14) -eicosatetraenoic acid
Common Name	8R-Hydroxy- (5Z,9E,11Z,14Z) -eicosatetraenoic acid
Symbol	8(R)-HETE
Formula	C20H32O3
Exact Mass	320.23514489
Average Mass	320.46628
SMILES	C(CC=CCC=CC=C[C@@H](CC=CCCCC(O)=O)O)CCC
Physicochemical Information
Melting Point
Boiling Point
Density
Optical Rotation
Refractive Index
Solubility
Source	8(R)-HETE is a metabolite of arachidonic acid by the 8-lipoxygenase pathway in marine organisms Meijer_L et al. Brash_AR et al..
Chemical Synthesis
Metabolism	The precursor of 8(R)-HETE, 8(R)-HpETE, is the putative intermediate in the biosynthesis of marine prostaglandins via the allene oxide synthase pathway. Brash_AR et al..
Biological Activity	8(R)-HETE induces maturation of starfish oocytes at a concentration of 0.071 μ M Meijer_L et al.. This activity if neglible in the 8(S)-enantiomer Meijer_L et al..
Genetic Information
Note
Spectral Information
Mass Spectra
UV Spectra	λ max: 237nm ε : 27,000
IR Spectra
NMR Spectra
Other Spectra
Chromatograms

Reported Metabolites, References
Biospecies ID Compound Name Reference Comment n.a. LBF20406HO12 See above. Brash_AR et al. 1987 n.a. LBF20406HO12 See above. Meijer_L et al. 1986