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SR 2640

Known as: SR-2640, SR2640 
National Institutes of Health

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1 relation

Broader (1)

Quinolines

Papers overview

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2020
2020
MK-571, a Cysteinyl Leukotriene Receptor 1 Antagonist, Inhibits Hepatitis C Virus Replication
The quinoline MK-571 is the most commonly used inhibitor of multidrug resistance protein-1 (MRP-1) but was originally developed… 
2017
2017
Involvements of cysteinyl leukotrienes in antigen-induced venodilatation of sensitized rats in vivo and nitric oxide nasal mucosa in
To determine an in vivo venodilatation of nasal mucosa, which is thought to be one of the causes of nasal obstruction in allergic… 
2007
2007
Involvements of cysteinyl leukotrienes and nitric oxide in antigen-induced venodilatation of nasal mucosa in sensitized rats in vivo.
To determine an in vivo venodilatation of nasal mucosa, which is thought to be one of the causes of nasal obstruction in allergic… 
2005
2005
The leukotriene D4/E4 antagonist SR2640: Recent results with smooth muscle preparations
SR2640 is a competitive LTD4/E 4 antagonist with a pA 2 value of 8.7 (slope 0.97) in guinea-pig tracheal strips [1]. The compound… 
2005
2005
SR2640 (2-[3-(2-quinolylmethoxy) phenylamino]benzoic acid): A novel leukotriene antagonist
ConclusionSR2640 is a new specific and competitive LTD4/LTE4 receptor antagonist. It does not antagonize histamine effects, thus… 
1990
1990
LTD4 increases cytosolic free calcium and inositol phosphates in human neutrophils: inhibition by the novel LTD4 receptor antagonist, SR2640, and possible relation to modulation of chemotaxis
LTD4 increased the level of free intracellular calcium ([Ca++]i) and stimulated the production of inositol phosphates (IP) in… 
1989
1989
Inhibition by the LTD4 antagonist, SR2640, of effects of LTD4 on canine polymorphonuclear leukocyte functions.
1988
1988
A novel leukotriene D4/E4 antagonist, SR2640 (2-[3-(2-quinolylmethoxy)phenylamino]benzoic acid).
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