20-CARBOXY-LEUKOTRIENE B4
20-CARBOXY-LEUKOTRIENE B4 Basic information
- Product Name:
- 20-CARBOXY-LEUKOTRIENE B4
- Synonyms:
-
- 20-CARBOXY-LEUKOTRIENE B4
- 20-COOH-LTB4
- 5S,12R-DIHYDROXY-6Z,8E,10E,14Z-EICOSATETRAENE-1,20-DIOIC ACID
- (5S,6Z,8E,10E,12R,14Z)-5,12-dihydroxyicosa-6,8,10,14-tetraenedioic acid
- 20-hydroxy-20-oxoleukotriene B4
- 6,8,10,14-Eicosatetraenedioic acid, 5,12-dihydroxy-, (5S,6Z,8E,10E,12R,14Z)-
- 20-carboxy Leukotriene B4 (20-carboxy LTB4)
- CAS:
- 80434-82-8
- MF:
- C20H30O6
- MW:
- 366.45
- Product Categories:
-
- Fatty Acids
- Leukotrienes
- Lipids
- Mol File:
- 80434-82-8.mol
20-CARBOXY-LEUKOTRIENE B4 Chemical Properties
- Boiling point:
- 588.3±50.0 °C(Predicted)
- Density
- 1.151±0.06 g/cm3(Predicted)
- Flash point:
- 14℃
- storage temp.
- −20°C
- solubility
- DMF: 50 mg/ml; DMSO: 50 mg/ml; Ethanol: 50 mg/ml; PBS pH 7.2: 1 mg/ml
- form
- Liquid
- pka
- 4.66±0.10(Predicted)
- color
- Colorless to light yellow
Safety Information
- Hazard Codes
- F,Xi
- Risk Statements
- 11-36/37/38
- Safety Statements
- 16-26-36
- RIDADR
- UN 1170 3/PG 2
- WGK Germany
- 3
20-CARBOXY-LEUKOTRIENE B4 Usage And Synthesis
Description
20-
Uses
20-COOH-LTB4 is a leukotriene B4 metabolite and substrate for β-oxidation pathways.
Definition
ChEBI: A member of the class of leukotrienes that is leukotriene B4 in which the terminal methyl group has undergone formal oxidation to the corresponding carboxylic acid.
IC 50
Human Endogenous Metabolite; BLT1
References
[1] G?RAN HANSSON . Identification and biological activity of novel ω-oxidized metabolites of leukotriene B4 from human leukocytes[J]. FEBS Letters, 1981, 130 1: Pages 107-112. DOI: 10.1016/0014-5793(81)80676-x
[2] T. HARPER R M M Garrity. Metabolism of leukotriene B4 in isolated rat hepatocytes. Identification of a novel 18-carboxy-19,20-dinor leukotriene B4 metabolite.[J]. The Journal of Biological Chemistry, 1986, 140 1: 5414-5418. DOI: 10.1016/s0021-9258(19)57231-3
[3] STEVEN J. FEINMARK. Stimulation of human leukocyte degranulation by leukotriene B4 and its ω-oxidized metabolites[J]. FEBS Letters, 1981, 136 1: Pages 141-144. DOI: 10.1016/0014-5793(81)81233-1
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