Prazosin-d8 hydrochloride

For research use only. Not for therapeutic Use.

  • CAT Number: I040123
  • CAS Number: 1189508-34-6
  • Molecular Formula: C19H14D8ClN5O4
  • Molecular Weight: 427.91
  • Purity: ≥95%
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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.
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[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.
[Content Brief]

[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.
[Content Brief]

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