Lofexidine-d4 hydrochloride(Synonyms: 盐酸洛非西定 d4 (盐酸盐))

上海金畔生物科技有限公司为生命科学和医药研发人员提供生物活性分子抑制剂、激动剂、特异性抑制剂、化合物库、重组蛋白、同位素标记物，专注于信号通路和疾病研究领域。
Lofexidine-d4 hydrochloride (Synonyms: 盐酸洛非西定 d4 (盐酸盐))

Lofexidine-d4 hydrochloride 是 Lofexidine hydrochloride 的氘代物。Lofexidine (hydrochloride) 是选择性的、 α2 受体 激动剂，常用于缓解海洛因和其他阿片类戒断的躯体症状。

Lofexidine-d4 hydrochloride Chemical Structure

CAS No. : 1206845-57-9

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生物活性	Lofexidine-d4 hydrochloride (Baq-168-d4) is the deuterium labeled Lofexidine hydrochloride. Lofexidine hydrochloride is a selective α2-receptor agonist, commonly used to alleviate the physical symptoms of heroin and other types of opioid withdrawal^[1]^[2].
体外研究 (In Vitro)	Stable heavy isotopes of hydrogen, carbon, and other elements have been incorporated into drug molecules, largely as tracers for quantitation during the drug development process. Deuteration has gained attention because of its potential to affect the pharmacokinetic and metabolic profiles of drugs^[1]. Shanghai Jinpan Biotech Co Ltd has not independently confirmed the accuracy of these methods. They are for reference only.
分子量	299.62
Formula	C₁₁H₉D₄Cl₃N₂O
CAS 号	1206845-57-9
中文名称	盐酸洛非西定 d4 (盐酸盐)
运输条件	Room temperature in continental US; may vary elsewhere.
储存方式	Please store the product under the recommended conditions in the Certificate of Analysis.
参考文献	[1]. Russak EM, et al. Impact of Deuterium Substitution on the Pharmacokinetics of Pharmaceuticals. Ann Pharmacother. 2019;53(2):211-216. [2]. Vartak AP, et al. The preclinical discovery of lofexidine for the treatment of opiate addiction. Expert Opin Drug Discov. 2014 Nov;9(11):1371-7. [3]. Gish EC, et al. Lofexidine, an {alpha}2-receptor agonist for opioid detoxification. Ann Pharmacother. 2010 Feb;44(2):343-51.

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