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Merck
CN

T1692

Sigma-Aldrich

噻奈普汀 钠盐 水合物

≥98% (HPLC), powder

别名:

7-[(3-氯-6,11-二氢-6-甲基-二苯并[c,f] [1,2]硫氮平-11-基)氨基]庚酸S,S二氧化物 钠盐 水合物

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About This Item

经验公式(希尔记法):
C21H24ClN2NaO4S · xH2O
CAS号:
分子量:
458.93 (anhydrous basis)
UNSPSC代码:
12352200
PubChem化学物质编号:
NACRES:
NA.77

质量水平

方案

≥98% (HPLC)

表单

powder

储存条件

desiccated

颜色

white to tan

溶解性

DMSO: ≥20 mg/mL

创始人

Servier

储存温度

room temp

SMILES字符串

O.[Na+].CN1c2ccccc2C(NCCCCCCC([O-])=O)c3ccc(Cl)cc3S1(=O)=O

InChI

1S/C21H25ClN2O4S.Na.H2O/c1-24-18-9-6-5-8-16(18)21(23-13-7-3-2-4-10-20(25)26)17-12-11-15(22)14-19(17)29(24,27)28;;/h5-6,8-9,11-12,14,21,23H,2-4,7,10,13H2,1H3,(H,25,26);;1H2/q;+1;/p-1

InChI key

HNTRDGDHBBFLPG-UHFFFAOYSA-M

一般描述

噻奈普汀是一种μ-阿片受体(MOR)和δ-阿片受体(DOR)激动剂。

应用

水合噻奈普汀钠盐已被用于在人胚肾293细胞系中进行的5-羟色胺转运体(SERT)测定中作为5-羟色胺再摄取增强剂(SSRE)阳性对照。

生化/生理作用

噻奈普汀是一种可增强5-羟色胺再摄取的三环类抗抑郁药。这种药物会影响到神经保护、神经兴奋性、记忆和焦虑。然而,噻奈普汀与不良的精神运动、认知、心血管、睡眠和体重影响无关。该药物具有较低的滥用倾向性,以及正向的药代动力学曲线
噻奈普汀是最少参与到药物相互作用的,因为它并不会被肝脏中的细胞色素P450系统所代谢。在海马体和杏仁核中,噻奈普汀可参与到谷氨酸能传递过程并引起神经可塑性。

特点和优势

该化合物由Servier开发。要浏览其他药物开发化合物和批准的药物/候选药物列表,单击此处

制备说明

噻奈普汀钠盐水合物可溶于 DMSO,浓度大于或等于 20 mg/ml。

储存分类代码

11 - Combustible Solids

WGK

WGK 3

闪点(°F)

Not applicable

闪点(°C)

Not applicable

个人防护装备

Eyeshields, Gloves, type N95 (US)


历史批次信息供参考:

分析证书(COA)

Lot/Batch Number

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