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Baclofen-d5 hydrochloride

CAS: 2012598-58-0 F: C10H8D5Cl2NO2 W: 255.15

Baclofen-d5 hydrochloride is deuterated labeled Baclofen (HY-B0007). Baclofen, a lipophilic derivative of γ-aminobutyri
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Bioactivity Baclofen-d5 hydrochloride is deuterated labeled Baclofen (HY-B0007). Baclofen, a lipophilic derivative of γ-aminobutyric acid (GABA), is an orally active, selective metabotropic GABAB receptor (GABABR) agonist. Baclofen mimics the action of GABA and produces slow presynaptic inhibition through the GABAB receptor. Baclofen has high blood brain barrier penetrance. Baclofen has the potential for muscle spasticity research[1][2][3].
Invitro 氢、碳和其他元素的稳定重同位素已被纳入药物分子中,主要作为药物开发过程中定量的示踪剂。氘化引起了人们的关注,因为它可能影响药物的药代动力学和代谢谱[1]。Baclofen (1,10 μM;24 h) 导致乳酸脱氢酶 (LDH) 活性显著降低,表明表达野生型或突变亨廷顿蛋白的纹状体细胞 (HD19 或 HD43) 的细胞活力增加。Baclofen 显著增加 HD43 细胞中的胰凝乳蛋白酶样蛋白酶体活性和细胞活力[4]。 MCE has not independently confirmed the accuracy of these methods. They are for reference only. 0 --> Baclofen-d5 hydrochloride 相关抗体:
In Vivo Baclofen (ip;10 μg/g;每天两次,连续 3 天) 改善 YAC128 HD 转基因小鼠的运动缺陷[4]。 MCE has not independently confirmed the accuracy of these methods. They are for reference only.
CAS 2012598-58-0
Formula C10H8D5Cl2NO2
Molar Mass 255.15
Transport Room temperature in continental US; may vary elsewhere.
Storage

Please store the product under the recommended conditions in the Certificate of Analysis.

Reference [1]. Russak EM, et al. Impact of Deuterium Substitution on the Pharmacokinetics of Pharmaceuticals. Ann Pharmacother. 2019 Feb;53(2):211-216. [2]. Woori Kim, et al. Baclofen, a GABAB receptor agonist, enhances ubiquitin-proteasome system functioning and neuronal survival in Huntington's disease model mice. Biochem Biophys Res Commun. 2014 Jan 10;443(2):706-11. [3]. Mehdi Farokhnia, et al. A deeper insight into how GABA-B receptor agonism via baclofen may affect alcohol seeking and consumption: lessons learned from a human laboratory investigation. Mol Psychiatry. 2018 Oct 31. [4]. Bexis, S., et al., Baclofen prevents MDMA-induced rise in core body temperature in rats. Drug Alcohol Depend, 2004. 74(1): p. 89-96.