LBF20207HP02

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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	DFA8091
LipidMaps	-
CAS
KEGG	{{{KEGG}}}
KNApSAcK	{{{KNApSAcK}}}
mol	LBF20207HP02

7- [3,5-Epidioxy-2- (3-hydroperoxy-1-octenyl) cycropentyl] -5-heptenoic acid
Structural Information
Systematic Name	7- [3,5-Epidioxy-2- (3-hydroperoxy-1-octenyl) cycropentyl] -5-heptenoic acid
Common Name	7- [3,5-Epidioxy-2- (3-hydroperoxy-1-octenyl) cycropentyl] -5-heptenoic acid
Symbol
Formula	C20H32O6
Exact Mass	368.219888756
Average Mass	368.46448
SMILES	C(CCC(OO)C=CC(C21)C(CC=CCCCC(O)=O)C(OO2)C1)CC
Physicochemical Information
Melting Point
Boiling Point
Density
Optical Rotation
Refractive Index
Solubility
Source	Oxidation of arachidonic acid in the presence of hemoglobin, mioglobin Terao_J et al.or Fe(III)- ascorbic acid Yamagata_S et al.. It is produced from arachidonic acid by cyclooxygenase in vivo(PGG2).
Chemical Synthesis
Metabolism
Biological Activity
Genetic Information
Note
Spectral Information
Mass Spectra	GC-EI-MS(Me-ester; after reduction and TMS) TeraoJet al.: m/e=569[M-CH3]; 513[M-(CH2)4CH3]; 494[M-HOTMS]; 404[M-2xHOTMS]; 378[494-SMTO=CHCH2]; 367[M-SMTOCH=CHCH=OTMS]; 191[SMTO=CHOTMS]; 173[SMTO=CH(CH2)4CH3]; GC-EI-MS(Me-ester; after reduction, hydrogenation and TMS)
UV Spectra
IR Spectra
NMR Spectra
Other Spectra
Chromatograms

Reported Metabolites, References
Biospecies ID Compound Name Reference Comment n.a. LBF20207HP02 See above. Terao_J et al. 1981 n.a. LBF20207HP02 See above. Yamagata_S et al. 1983