LBF20309HO02: Difference between revisions

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|LipidBank=DFA8142
|LipidBank=DFA8142
|LipidMaps=LMFA03050005
|LipidMaps=LMFA03050005
|SysName=5S-hydroxy-6E,8Z,11Z-eicosatrienoic acid
|SysName=5S-Hydroxy- (6-trans,8-cis,11-cis) -icosatrienoic acid
|Common Name=&&5S-hydroxy-6E,8Z,11Z-eicosatrienoic acid&&
|Common Name=&&5S-Hydroxy- (6E,8Z,11Z) -eicosatrienoic acid&&
|UV Spectra= lambda max: 235nm  epsilon : 23,000
|UV Spectra= lambda max: 235nm  epsilon : 23,000
|Source=5(S)-HETrE is produced by the action of 5-lipoxygenase when mead acid is the substrate [[Reference:Jakschik_BA:Sams_AR:Sprecher_H:Needleman_P:,Prostaglandins,1980,20,401|{{RelationTable/GetFirstAuthor|Reference:Jakschik_BA:Sams_AR:Sprecher_H:Needleman_P:,Prostaglandins,1980,20,401}}]][[Reference:Jakschik_BA:Morrison_AR:Sprecher_H:,J. Biol. Chem.,1983,258,12797|{{RelationTable/GetFirstAuthor|Reference:Jakschik_BA:Morrison_AR:Sprecher_H:,J. Biol. Chem.,1983,258,12797}}]].
|Source=5(S)-HETrE is produced by the action of 5-lipoxygenase when mead acid is the substrate [[Reference:Jakschik_BA:Sams_AR:Sprecher_H:Needleman_P:,Prostaglandins,1980,20,401|{{RelationTable/GetFirstAuthor|Reference:Jakschik_BA:Sams_AR:Sprecher_H:Needleman_P:,Prostaglandins,1980,20,401}}]][[Reference:Jakschik_BA:Morrison_AR:Sprecher_H:,J. Biol. Chem.,1983,258,12797|{{RelationTable/GetFirstAuthor|Reference:Jakschik_BA:Morrison_AR:Sprecher_H:,J. Biol. Chem.,1983,258,12797}}]].

Revision as of 06:46, 28 May 2010

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Upper classes: LB LBF



5S-Hydroxy- (6E,8Z,11Z) -eicosatrienoic acid
LBF20309HO02.png
Structural Information
5S-Hydroxy- (6-trans,8-cis,11-cis) -icosatrienoic acid
  • 5S-Hydroxy- (6E,8Z,11Z) -eicosatrienoic acid
5(S)-HETrE
Formula C20H34O3
Exact Mass 322.25079495399996
Average Mass 322.48216
SMILES C(CCCCC=CCC=CC=CC(CCCC(O)=O)O)CCC
Physicochemical Information
5(S)-HETrE is produced by the action of 5-lipoxygenase when mead acid is the substrate Jakschik_BA et al. Jakschik_BA et al..
Spectral Information
Mass Spectra
UV Spectra λ max: 235nm ε : 23,000
IR Spectra
NMR Spectra
Other Spectra
Chromatograms
Reported Metabolites, References
Biospecies ID Compound Name Reference Comment
n.a. LBF20309HO02 See above. Jakschik_BA et al. 1983
n.a. LBF20309HO02 See above. Jakschik_BA et al. 1980