N-Methylleukotriene C4

N-Methylleukotriene C4 Structure
CAS No.
131391-65-6
Chemical Name:
N-Methylleukotriene C4
Synonyms
NMLTC4;N-METHYL LTC4;N-Methylleukotriene C4;FPLBRCJNODNRQZ-UYCXAPQFSA-N;N methyl Leukotriene C4,N-methyl Leukotriene C-4,Nmethyl Leukotriene C4;Glycine, N-methyl-L-γ-glutamyl-S-[(1R,2E,4E,6Z,9Z)-1-[(1S)-4-carboxy-1-hydroxybutyl]-2,4,6,9-pentadecatetraen-1-yl]-L-cysteinyl-;N-[S-[(1R,2E,4E,6Z,9Z)-1-[(1S)-4-Carboxy-1-hydroxybutyl]-2,4,6,9-pentadecatetren-1-yl]-N-(L-γ-glutamyl)-L-cysteinyl]-N-methylglycine
CBNumber:
CB12192012
Molecular Formula:
C31H49N3O9S
Molecular Weight:
639.81
MOL File:
131391-65-6.mol
Modify Date:
2023/6/8 9:03:09

N-Methylleukotriene C4 Properties

Boiling point 965.7±65.0 °C(Predicted)
Density 1.202±0.06 g/cm3(Predicted)
storage temp. Store at -20°C
solubility DMF: 50 mg/ml; DMSO: 50 mg/ml; Ethanol: 1 mg/ml; Ethanol:H20 (95:5): 2 mg/ml; PBS (pH 7.2): 100 μg/ml
pka 2.23±0.10(Predicted)

SAFETY

Risk and Safety Statements

Symbol(GHS) 
GHS02,GHS07
Signal word  Danger
Hazard statements  H225-H319
Precautionary statements  P210-P233-P240-P241-P242-P243-P264-P280-P303+P361+P353-P305+P351+P338-P337+P313-P370+P378-P403+P235-P501
NFPA 704
3
2 0

N-Methylleukotriene C4 Chemical Properties,Uses,Production

Uses

Produced by neutrophils, macrophages, mast cells, and by transcellular metabolism in platelets, leukotriene C4 (LTC4) is the parent cysteinyl leukotriene formed by the LTC4 synthase-catalyzed conjugation of glutathione to LTA4. It is one of the constituents of slow-reacting substance of anaphylaxis (SRS-A) and exhibits potent smooth muscle contracting activity. LTC4, however, is rapidly metabolized to LTD4 and LTE4, which makes the characterization of LTC4 pharmacology difficult. N-methyl Leukotriene C4 (N-methyl LTC4) is a synthetic analog of LTC4 that is not readily metabolized to LTD4 and LTE4.It acts as a potent and selective CysLT2 receptor agonist exhibiting EC50 values of 122 and > 2,000 nM at the human CysLT2 and CysLT1 receptors, respectively. It has essentially the same potency as LTC4 at both the human and murine receptors CysLT2 receptors. N-methyl LTC4 is potent and active in vivo, causing vascular leak in mice overexpressing the human CysLT2 receptor but not in CysLT2 receptor knockout mice.

N-Methylleukotriene C4 Preparation Products And Raw materials

Raw materials

Preparation Products

N-[S-[(1R,2E,4E,6Z,9Z)-1-[(1S)-4-Carboxy-1-hydroxybutyl]-2,4,6,9-pentadecatetren-1-yl]-N-(L-γ-glutamyl)-L-cysteinyl]-N-methylglycine N-Methylleukotriene C4 NMLTC4 N-METHYL LTC4 FPLBRCJNODNRQZ-UYCXAPQFSA-N Glycine, N-methyl-L-γ-glutamyl-S-[(1R,2E,4E,6Z,9Z)-1-[(1S)-4-carboxy-1-hydroxybutyl]-2,4,6,9-pentadecatetraen-1-yl]-L-cysteinyl- N methyl Leukotriene C4,N-methyl Leukotriene C-4,Nmethyl Leukotriene C4 131391-65-6 C31H49N3O9S