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Amitriptyline-d3 hydrochloride
本产品不向个人销售,仅用作科学研究,不用于任何人体实验及非科研性质的动物实验。
Amitriptyline-d3 hydrochloride图片
CAS NO:342611-00-1
包装与价格:
包装价格(元)
2.5mg电议
1mg电议
5mg电议
10mg电议

产品介绍
Amitriptyline-d3 hydrochloride 是 Amitriptyline (hydrochloride) 的氘代物。Amitriptyline hydrochloride 是一种血清素再摄取转运体 (SERT) 和去甲肾上腺素再摄取转运体 (NET) 抑制剂,对人的 SERT 和 NET 作用的Ki值分别为 3.45 nM 和 13.3 nM。Amitriptyline hydrochloride 还与多巴胺再摄取转运体 (DAT) 结合,其Ki为 2.58 μM。Amitriptyline hydrochloride 也抑制肾上腺素能受体 (adrenergic receptor)、毒蕈碱受体 (muscarinic receptor)、组胺受体 (histamine receptor)、5-羟色胺受体 (5-HT receptor)。Amitriptyline hydrochloride 是一种具有强神经营养活性的TrkATrkA受体激动剂。Amitriptyline hydrochloride 具有抗抑郁作用。
生物活性

Amitriptyline-d3 hydrochloride is the deuterium labeled Amitriptyline (hydrochloride). Amitriptyline hydrochloride is an inhibitor ofserotonin reuptake transporter (SERT)andnoradrenaline reuptake transporter (NET), withKis of 3.45 nM and 13.3 nM for human SERT and NET, respectively. Amitriptyline hydrochloride also weakly binds todopamine reuptake transporter (DAT)with aKiof 2.58 μM. Amitriptyline hydrochloride also inhibitsadrenergic,muscarinic,histamineand5-HT receptors. Amitriptyline hydrochloride is aTrkAandTrkBreceptors agonist with potent neurotrophic activity. Amitriptyline hydrochloride has antidepressant activity[1][2][3].

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].

分子量

316.88

Formula

C20H21D3ClN

CAS 号

342611-00-1

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.