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Guanfacine-[α,α-d2] HCl

General Information
Catalog: BLP-013903
CAS: 1398065-88-7
Molecular Formula: C9H8D2Cl3N3O
Molecular Weight: 284.57
Chemical Structure
Guanfacine-[α,α-d2] HCl
Description Guanfacine-α,α-[d2] HCl is an isotope labelled derivative of Guanfacine. Guanfacine is a selective α2A receptor agonist. It is used for the treatment of hypertension and attention deficit hyperactivity disorder.
Synonyms N-Amidino-2-(2,6-dichlorophenyl)acetamide; [(2,6-Dichlorophenyl)acetyl]guanidine
Related CAS 29110-48-3 (unlabelled)
Purity 95% by HPLC; 92% atom D

Guanfacine-[α,α-d2] HCl, a deuterated derivative of guanfacine, exhibits significant potential in diverse scientific and medical contexts. Here are the key applications of Guanfacine-[α,α-d2] HCl:

Pharmacokinetic Studies: Employing Guanfacine-[α,α-d2] HCl in pharmacokinetic investigations enables a comprehensive examination of the drug's metabolism and bioavailability. By leveraging the deuterated variant, researchers can differentiate it from endogenous compounds in mass spectrometry analyses, delivering precise insights into the drug's absorption, distribution, metabolism, and excretion processes. This approach yields enhanced understanding of Guanfacine-[α,α-d2] HCl's pharmacokinetic profile, facilitating informed decisions in drug development and administration.

Attention Deficit Hyperactivity Disorder (ADHD) Research: In the realm of ADHD research, Guanfacine-[α,α-d2] HCl plays a pivotal role in preclinical studies exploring novel therapeutic strategies. Acting as a tool for elucidating the mechanisms of guanfacine's actions and its impact on neurotransmitter systems, this deuterated compound contributes valuable knowledge to the quest for enhanced ADHD treatments. By unraveling the intricate workings of Guanfacine-[α,α-d2] HCl, researchers pave the way for innovative approaches in managing ADHD and improving patient outcomes.

Hypertension Studies: Guanfacine-[α,α-d2] HCl emerges as a valuable asset in hypertension research, shedding light on the efficacy and safety profile of guanfacine formulations. Through clinical investigations utilizing the deuterated form, scientists can conduct comparative assessments to discern the pharmacological benefits of the deuterated compound. This exploration holds the potential to optimize guanfacine formulations, enhancing therapeutic outcomes, and refining treatment strategies for hypertension management.

Drug Interaction Analysis: In the realm of drug safety evaluations, Guanfacine-[α,α-d2] HCl serves as a crucial tool for probing potential drug interactions. By co-administering this deuterated compound with other medications, researchers observe shifts in pharmacokinetic profiles and evaluate the risk of adverse interactions. This in-depth analysis of drug interactions is essential for ensuring the safe coadministration of guanfacine with other pharmaceutical agents, safeguarding patient well-being and optimizing treatment regimens.

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