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Category: 7TM ReceptorsarrowAdrenergic ReceptorsarrowAlpha-1 ReceptorsarrowAntagonists
Cat.No. Product Name
0623 Prazosin hydrochloride  
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Prazosin hydrochloride
Chemical Name: 1-(4-Amino-6,7-dimethoxy-2-quinazolinyl)-4-(2-furanylca rbonyl)piperazine hydrochloride

Biological Activity:

α1 and α2B-adrenoceptor antagonist. Also a potent antagonist at the melatonin MT3 receptor (Ki = 10.2 nM).

Technical Data:

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M.Wt: 419.87
Formula: C19H21N5O4.HCl
Storage: Store at RT
Solubility: Soluble to 25 mM in DMSO and to 5 mM in Ethanol
Purity: >99%
CAS No: [19237-84-4]

Resources:

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    References:

    Merck Index 12 7897. Pickering and Niles (1990) Pharmacological characterization of melatonin binding sites in Syrian hamster hypothalamus. Eur.J.Pharmacol. 175 71. Mathe et al (1996) Prazosin inhibits MK-801-induced hyperlocomotion and dopamine release in the nucleus accumbens. Eur.J.Pharmacol. 309 1. Paul et al (1999) Characterisation of 2-[125I]iodomelatonin binding sites in syrian hamster peripheral organs. J.Pharmacol.Exp.Ther. 290 334.
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    Keywords: Prazosin Hydrochloride, Adrenergic Receptors, A1 Antagonist. MT3 Antagonist, Tocris Bioscience

    Literature in this Area
    Scientific Reviews
    Adrenoceptor Pharmacology
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