1189508-34-6

Prazosin-d<sub>8</sub> hydrochloride Chemical Structure
1189508-34-6

Chemical Structure

Prazosin-d8 hydrochloride

  • CAS No.: 1189508-34-6
  • Formula:C19H14D8ClN5O4
  • Molecular Weight:427.91

IUPAC Name: (4-(4-amino-6,7-dimethoxyquinazolin-2-yl)piperazin-1-yl-2,2,3,3,5,5,6,6-d8)(furan-2-yl)methanone hydrochloride

InChIKey: WFXFYZULCQKPIP-CADLHFACSA-N

SMILES: NC1=NC(N2C([2H])([2H])C([2H])([2H])N(C([2H])([2H])C2([2H])[2H])C(C3=CC=CO3)=O)=NC4=C1C=C(OC)C(OC)=C4.Cl

Biological Activity: Prazosin-d8 hydrochloride is the deuterium labeled Prazosin hydrochloride. Prazosin hydrochloride is an alpha-adrenergic blocker[1].

Cat. No. Product Name Purity Description Pricing
HY-B0193AS
Prazosin-d8 hydrochloride 99.78% Prazosin-d8 hydrochloride is the deuterium labeled Prazosin hydrochloride. Prazosin hydrochloride is an alpha-adrenergic blocker.
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HY-B0193AR
Prazosin hydrochloride (Standard) ≥98% Prazosin (hydrochloride) (Standard) is the analytical standard of Prazosin (hydrochloride). This product is intended for research and analytical applications. Prazosin hydrochloride is a well-tolerated, CNS-active α1-adrenergic receptor antagonist for the research of high blood pressure and alcohol use disorders. Prazosin hydrochloride potently inhibits Norepinephrine (NE)-stimulated 45Ca efflux with an IC50 of 0.15 nM.Prazosin hydrochloride inhibits organic cation transporters OCT-1 and OCT-3 with IC50s of 1.8, and 13 μM, respectively.
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HY-B0193A
Prazosin hydrochloride 99.89% Prazosin hydrochloride is a well-tolerated, CNS-active α1-adrenergic receptor antagonist for the research of high blood pressure and alcohol use disorders. Prazosin hydrochloride potently inhibits Norepinephrine (NE)-stimulated 45Ca efflux with an IC50 of 0.15 nM.Prazosin hydrochloride inhibits organic cation transporters OCT-1 and OCT-3 with IC50s of 1.8, and 13 μM, respectively.
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