For research use only. Not for therapeutic Use.
Prazosin-d8 hydrochloride (Cat No.: I040123) is a deuterated analog of prazosin, a selective alpha-1 adrenergic receptor antagonist. The deuteration of prazosin (replacing hydrogen atoms with deuterium) enhances its stability and can help in pharmacokinetic studies by reducing isotope effects. Prazosin is commonly used to treat hypertension and symptoms of benign prostatic hyperplasia (BPH). Prazosin-d8 hydrochloride is primarily used in research to investigate the drug’s metabolism, pharmacodynamics, and pharmacokinetics, offering insights into its therapeutic efficacy and behavior in the body.
CAS Number | 1189508-34-6 |
Synonyms | [4-(4-amino-6,7-dimethoxyquinazolin-2-yl)-2,2,3,3,5,5,6,6-octadeuteriopiperazin-1-yl]-(furan-2-yl)methanone;hydrochloride |
Molecular Formula | C19H14D8ClN5O4 |
Purity | ≥95% |
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/i5D2,6D2,7D2,8D2; |
InChIKey | WFXFYZULCQKPIP-CADLHFACSA-N |
SMILES | COC1=C(C=C2C(=C1)C(=NC(=N2)N3CCN(CC3)C(=O)C4=CC=CO4)N)OC.Cl |
Reference | [1]. Russak EM, et al. Impact of Deuterium Substitution on the Pharmacokinetics of Pharmaceuticals. Ann Pharmacother. 2019;53(2):211-216. [2]. Day HE, et al. Distribution of alpha 1a-, alpha 1b- and alpha 1d-adrenergic receptor mRNA in the rat brain and spinal cord. J Chem Neuroanat. 1997 Jul;13(2):115-39. [3]. Yu CX, et al. Selective MT(2) melatonin receptor antagonist blocks melatonin-induced antinociception in rats. Neurosci Lett. 2000 Mar 24;282(3):161-4. |
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