SR 2640 hydrochloride
Discontinued Product
Chemical Name: 2-[[3-(2-Quinolinylmethoxy)phenyl]amino]benzoic acid hydrochloride
Purity: ≥99%
Biological Activity
SR 2640 hydrochloride is a potent and selective competitive leukotriene D4 and E4 receptor antagonist. Inhibits LTD4- but not histamine-induced guinea pig ileum and trachea contraction (pA2 = 8.7). Also inhibits LTD4-attenuation of human PMN chemotaxis. Orally active in vivo.Technical Data
The technical data provided above is for guidance only.
For batch specific data refer to the Certificate of Analysis.
Tocris products are intended for laboratory research use only, unless stated otherwise.
Background References
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A novel leukotriene D4/E4 antagonist, SR2640 (2-[3-(2-quinolylmethoxy)phenylamino]benzoic acid).
Ahnfelt-Ronne et al.
Eur.J.Pharmacol., 1988;155:117 -
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.
Bouchelouche et al.
Agents Actions, 1990;29:299 -
Inhibition by the LTD4 antagonist, SR2640, of effects of LTD4 on canine polymorphonuclear leukocyte functions.
Thomsen and Ahnfelt-Ronne
Biochem.Pharmacol., 1989;38:2291
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Citation for SR 2640 hydrochloride
The citations listed below are publications that use Tocris products. Selected citations for SR 2640 hydrochloride include:
1 Citation: Showing 1 - 1
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Pranlukast is a novel small molecule activator of the two-pore domain potassium channel TREK2.
Authors: Wright Et al.
Biochem Biophys Res Commun 2019;520:35
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