The store will not work correctly in the case when cookies are disabled.
JavaScript seems to be disabled in your browser. For the best experience on our site, be sure to turn on Javascript in your browser.
Biological Data Biological description α1 and α2 adrenoceptor antagonist (Ki values are 0.32, 0.19 and 0.27 nM respectively). Also shows selective activity at MT3 melatonin receptor. Shows variety of biological actions.
Solubility & Handling Storage instructions Room temperature
Solubility overview Soluble in DMSO (25mM)
Important This product is for RESEARCH USE ONLY and is not intended for therapeutic or diagnostic use. Not for human or veterinary use.
Chemical Data Chemical name 1-(4-Amino-6,7-dimethoxy-2-quinazol inyl)-4-(2-furanylcarbonyl)piperazine hydrochloride
Chemical structure
Molecular Formula C19 H21 N5 O4 .HCl
SMILES COC1=C(C=C2C(=C1)C(=NC(=N2)N3CCN(CC3)C(=O)C4=CC=CO4)N)OC.Cl
InChi InChI=1S/C19H21N5O4.ClH/c1-26-15-10-12-13(11-16(15)27-2)21-19(22-17(12)20)24-7-5-23(6-8-24)18(25)14-4-3-9-28-14;/h3-4,9-11H,5-8H2,1-2H3,(H2,20,21,22);1H
InChiKey WFXFYZULCQKPIP-UHFFFAOYSA-N
References for Prazosin hydrochloride References are publications that support the biological activity of the product
Prazosin Inhibits MK-801-induced Hyperlocomotion and Dopamine Release in the Nucleus Accumbens Mathe et al (1996) Eur J Pharmacol 309(1) : 1-11 Pharmacological Characterization of Melatonin Binding Sites in Syrian Hamster Hypothalamus Pickering and Niles (1990) Eur J Pharmacol 175(1) : 71-7 The Pharmacology of Prazosin, a Novel Antihypertensive Agent Cavero (1980) Life Sci 27(17) : 1525-40
Tell us about your publication! What Hello Bio product(s) have you cited?
Captcha Please type the letters and numbers below Submit
α1 and α2 adrenoceptor antagonist