Cinalukast
Discontinued Product
Chemical Name: 4-[[3-[(1E)-2-(4-Cyclobutyl-2-thiazolyl)ethenyl]phenyl]amino]-2,2-diethyl-4-oxobutanoic acid
Purity: ≥98%
Biological Activity
Potent, selective CysLT1 (LTD4) leukotriene receptor antagonist (IC50 = 6.4 nM). Inhibits LTD4-induced bronchoconstriction in guinea pigs when administered intravenously, orally or by aerosol.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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Ro 24-5913: a potent, specific, orally active LTD4 antagonist.
O'Donnell
Ann.N.Y.Acad.Sci., 1991;629:413 -
Pharmacologic actions of Ro 24-5913, a novel antagonist of leukotriene D4.
O'Donnell et al.
J.Pharmacol.Exp.Ther., 1991;259:751
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Citation for Cinalukast
The citations listed below are publications that use Tocris products. Selected citations for Cinalukast 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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