PeptideDB

Citalopram-d3 hydrochloride

CAS: F: C20H19D3ClFN2O W: 363.87

Citalopram-d3 hydrochloride is deuterated labeled Citalopram (HY-121203). Citalopram is a racemate mixture of the active
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This product is for research use only, not for human use. We do not sell to patients.

Bioactivity Citalopram-d3 hydrochloride is deuterated labeled Citalopram (HY-121203). Citalopram is a racemate mixture of the active S(+)-enantiomer (Escitalopram; HY-14258) and R(-)-enantiomer. Citalopram is an orally active selective serotonin reuptake inhibitor (SSRI). Citalopram is an antidepressant and enhances serotoninergic neurotransmission[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]。Citalopram (25-175 μM;24 小时) 显示出浓度依赖性细胞毒性[4]。 Citalopram (100 μM;24 小时) 强烈下调 B104 细胞中的 MYBL2、BIRC5、BARD1、AURKA、CCNA2 和 CCNE1[4]。 MCE has not independently confirmed the accuracy of these methods. They are for reference only. 0 --> Citalopram-d3 hydrochloride 相关抗体:
In Vivo Citalopram (5-40mg/kg;腹腔注射) 可减少 DBA/2J 小鼠的不动时间,但不会减少 C57BL/6J 小鼠[5]。 MCE has not independently confirmed the accuracy of these methods. They are for reference only.
Formula C20H19D3ClFN2O
Molar Mass 363.87
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]. Carlsson B, et al. Enantioselective analysis of citalopram and escitalopram in postmortem blood together with genotyping for CYP2D6 and CYP2C19. J Anal Toxicol. 2009;33(2):65-76. [3]. Laurent Sakka, et al. Assessment of citalopram and escitalopram on neuroblastoma cell lines. Cell toxicity and gene modulation. Oncotarget. 2017 Jun 27;8(26):42789-42807. [4]. Milne RJ, et al. Citalopram. A review of its pharmacodynamic and pharmacokinetic properties, and therapeutic potential in depressive illness. Drugs. 1991;41(3):450-477. [5]. Zeng-Liang Jin, et al. Mouse strain differences in SSRI sensitivity correlate with serotonin transporter binding and function. Sci Rep. 2017 Aug 17;7(1):8631.