Basic information Safety Supplier Related

20-CARBOXY-LEUKOTRIENE B4

Basic information Safety Supplier Related

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
More
Less

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
More
Less

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
More
Less

20-CARBOXY-LEUKOTRIENE B4 Usage And Synthesis

Description

20-carboxy LTB4 is a metabolite of LTB4 in human neutrophils. In human leukocytes, LTB4 is inactivated by the enzyme LTB4 20-hydroxylase. The resulting 20-hydroxy LTB4 is further oxidized to 20-carboxy LTB4. LTB4 metabolism in isolated rat hepatocytes also results in production of 20-carboxy LTB4 along with other ω-oxidation products. The biological activity of 20-carboxy LTB4 is only about 2.6% compared to that of LTB4 in causing PMNL degranulation.

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

20-CARBOXY-LEUKOTRIENE B4Supplier

Shanghai EFE Biological Technology Co., Ltd.
Tel
021-65675885 18964387627
Email
info@efebio.com
Shanghai Hongye Biotechnology Co. Ltd
Tel
400-9205774
Email
sales@glpbio.cn
ChemeGen(Shanghai) Biotechnology Co.,Ltd.
Tel
18818260767
Email
sales@chemegen.com
amyjetsci
Tel
027-59626688 18771149750
Email
sales@amyjet.com
TargetMol Chemicals Inc.
Tel
4008200310
Email
marketing@tsbiochem.com
More
Less