Identification of 3,4-dihydro-2 H -thiochromene 1,1-dioxide derivatives with a phenoxyethylamine group as highly potent and selective α 1D adrenoceptor antagonists

Author:

Sakauchi Nobuki,Furukawa Hideki,Shirai Junya,Sato Ayumu,Kuno Haruhiko,Saikawa Reiko,Yoshida Masato

Publisher

Elsevier BV

Subject

Organic Chemistry,Drug Discovery,Pharmacology,General Medicine

Reference31 articles.

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2. Cloning, expression and characterization of human α adrenergic receptors α1A, α1B and α1D;Weinberg;Biochem. Biophys. Res. Commun.,1994

3. Pharmacological characterization of alpha 1-adrenoceptor subtypes in the human prostate: functional and binding studies;Muramatsu;Br. J. Urol.,1994

4. International union of pharmacology. X. recommendation for nomenclature of alpha 1-adrenoceptors: consensus update;Hieble;Pharmacol. Rev.,1995

5. The α1-adrenergic receptor that mediates smooth muscle contraction in human prostate has the pharmacological properties of the cloned human α1c subtype;Forray;Mol. Pharmacol.,1994

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