14,15-LEUKOTRIENE A4 METHYL ESTER
14,15-LEUKOTRIENE A4 METHYL ESTER Basic information
- Product Name:
- 14,15-LEUKOTRIENE A4 METHYL ESTER
- Synonyms:
-
- 14,15-LEUKOTRIENE A4 METHYL ESTER
- 5,8,10,12-Tridecatetraenoic acid, 13-[(2S,3S)-3-pentyloxiranyl]-, methyl ester, (5Z,8Z,10E,12E)- (9CI)
- CAS:
- 75290-58-3
- MF:
- C21H32O3
- MW:
- 332.48
- Mol File:
- 75290-58-3.mol
14,15-LEUKOTRIENE A4 METHYL ESTER Chemical Properties
- Boiling point:
- 442.5±45.0 °C(Predicted)
- Density
- 0.997±0.06 g/cm3(Predicted)
- solubility
- Acetone: 30 mg/ml; DMF: 30 mg/ml; DMSO: 30 mg/ml; Ethanol: 30 mg/ml
14,15-LEUKOTRIENE A4 METHYL ESTER Usage And Synthesis
Description
14,15-Leukotriene A4 (14,15-LTA4) methyl ester is an esterified form of 14,15-LTA4, a leukotriene isomer formed from arachidonic acid (Item Nos. 90010 | 90010.1 | 10006607) by 15-lipoxygenase (15-LO) that inhibits LTA4 hydrolase.
Uses
14,15-Leukotriene A4 methyl ester (14,15-LTA4 methyl ester) is the methyl esterified form of Leukotriene A4, which can be used for the study of biological effects of leukotrienes[1][2].
References
[1] Wetterholm A, et al. 14,15-Dihydroxy-5,8,10,12-eicosatetraenoic acid. Enzymatic formation from 14,15-leukotriene A4. Eur J Biochem. 1988 May 2;173(3):531-6. DOI:10.1111/j.1432-1033.1988.tb14031.x
[2] Rao A V R, et al. Enantiospecific synthesis of 14S, 15S leukotriene A4 methyl ester[J]. Bioorganic & Medicinal Chemistry Letters, 1991, 1(4): 201-204.
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