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(±)-Phenoxybenzamine-[d5] HCl (benzyl-[2,3,4,5,6-d5])

General Information
Catalog: BLP-013893
CAS: 1398065-71-8
Molecular Formula: C18H18D5Cl2NO
Molecular Weight: 345.32
Chemical Structure
(±)-Phenoxybenzamine-[d5] HCl (benzyl-[2,3,4,5,6-d5])
Description One of the isotopic labelled form of (±)-Phenoxybenzamine HCl, which is an α-antagonist and could be used as an ahypertensive agent.
Synonyms N-(2-Chloroethyl)-N-(1-methyl-2-phenoxyethyl)benzylamine HCl
Related CAS 63-92-3 (unlabelled)
1309283-11-1 (base)
1329838-45-0 (Phenoxy-d5)
Purity 95% by HPLC; 98% atom D

(±)-Phenoxybenzamine-[d5] HCl (benzyl-[2,3,4,5,6-d5]) serves as a crucial tool in research and pharmaceutical realms due to its deuterated composition. Here are the key applications of (±)-Phenoxybenzamine-[d5] HCl:

Pharmacokinetic Studies: Delving into drug behavior at a molecular level, (±)-Phenoxybenzamine-[d5] HCl is a cornerstone of pharmacokinetic investigations. Its deuterated nature furnishes a stable isotope label, enabling meticulous tracking within intricate biological systems. This comprehensive understanding of drug absorption, distribution, metabolism, and excretion (ADME) aids in fine-tuning dosing regimens for optimal efficacy.

Receptor Binding Studies: Unveiling the mysteries of α-adrenergic receptor binding, (±)-Phenoxybenzamine-[d5] HCl plays a pivotal role in receptor pharmacology investigations. By leveraging this compound, researchers unearth binding characteristics, scrutinizing receptor affinity and activity with precision. These studies are imperative for the design of innovative therapeutic agents targeting these vital receptors, shaping the future of pharmacological interventions.

Metabolite Identification: In the intricate realm of drug metabolism, (±)-Phenoxybenzamine-[d5] HCl emerges as a reference standard for identifying and quantifying drug metabolites. Its deuterated label brings clarity, distinguishing the parent compound from its metabolites amidst complex biological matrices. This distinction enhances the accuracy of metabolite profiling and facilitates in-depth analysis of biotransformation pathways, shedding light on drug metabolism intricacies.

Mechanistic Studies: Delving into the depths of pharmacological mechanisms, researchers turn to (±)-Phenoxybenzamine-[d5] HCl to unravel the pathways behind its pharmacological effects. By probing its interactions with biological targets, scientists untangle the molecular intricacies at play. This profound insight into molecular pathways underpins our comprehension of drug efficacy and safety, paving the way for improved pharmaceutical outcomes.

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