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Tizanidine hydrochloride

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纯度: 99.96%

货号 T0290Cas号 64461-82-1

别名 盐酸替扎尼定, Tizanidine HCl, DS 103-282

Tizanidine hydrochloride (Tizanidine HCl) 是一种 α2-肾上腺素受体激动剂,可抑制神经递质从 CNS 去甲肾上腺素激活的神经元中释放。

Tizanidine hydrochloride
其他形式的 “Tizanidine hydrochloride”:

Tizanidine hydrochloride

一键复制产品信息
Rating icon 很棒

纯度: 99.96%

货号 T0290 别名 盐酸替扎尼定, Tizanidine HCl, DS 103-282Cas号 64461-82-1

Tizanidine hydrochloride (Tizanidine HCl) 是一种 α2-肾上腺素受体激动剂,可抑制神经递质从 CNS 去甲肾上腺素激活的神经元中释放。

规格价格库存数量
10 mg
¥ 288
现货
25 mg
¥ 457
现货
50 mg
¥ 672
现货
100 mg
¥ 913
现货
200 mg
¥ 1,350
现货
500 mg
¥ 2,280
现货
1 mL x 10 mM (in DMSO)
¥ 191
现货
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纯度: 99.96%
颜色: 白色
性状: Solid
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产品介绍


Tizanidine hydrochloride AI Summary
Tizanidine hydrochloride is a multifaceted bioactive agent displaying diverse pharmacological effects across various biological targets. It acts as an inhibitor of several enzymes, with notable potencies: AmpC Beta-Lactamase (5623.4 nM), BAZ2B (707.9 nM), delayed death in the malarial parasite plastid (11689.1 nM), and Polymerase Iota (31622.8 nM). Additionally, Tizanidine hydrochloride induces DNA re-replication in MCF 10a normal breast cells (4.1 nM) and SW480 colon adenocarcinoma cells (259.3 nM). The compound’s antiviral activity against SARS-CoV-2 is limited, showing minimal inhibition effects on viral-induced cytotoxicity in various cell lines, including Caco-2 and VERO-6 cells, with slight inhibition percentages at 10-20 μM concentrations. It exhibits low efficacy in SARS-CoV-2 3CL-Pro protease inhibition and an overall lack of positive impact on cell viability against SARS-CoV-2. In terms of antimicrobial properties, Tizanidine hydrochloride exhibits mild antibacterial activity, inhibiting the growth of Escherichia coli (6.6%), Klebsiella pneumoniae (10.36%), Pseudomonas aeruginosa (18.39%), and Acinetobacter baumannii (4.87%), while showing negligible or negative effects on Candida albicans, Cryptococcus neoformans, and Staphylococcus aureus MRSA. The compound's effects on cell viability are cell type-dependent, influencing growth rates in assays involving U2OS, human fibroblasts, and HEK293T cells variably. It also affects the thermal stability of different protein domains, suggesting a modulatory effect on protein conformation and stability, with observed changes ranging from -1.91°C to +1.21°C. Furthermore, Tizanidine hydrochloride demonstrates diverse interactions with GPCR targets, affecting beta-arrestin recruitment. It inhibits receptors such as GPR119, GLP1R, and FPR2 while activating others like ADRA2A and AGTR1, indicating its broad and variable receptor modulatory capabilities..
Note: Summary generated by AI. Data source: ChEMBL
生物活性
产品描述
Tizanidine hydrochloride (Tizanidine HCl), an α2-adrenergic receptor agonist, inhibits neurotransmitter release from CNS noradrenergic neurons.
别名盐酸替扎尼定, Tizanidine HCl, DS 103-282
化学信息
分子量290.17
分子式C9H9Cl2N5S
CAS No.64461-82-1
SmilesCl.Clc1c(NC2=NCCN2)c2nsnc2cc1
密度no data available
储存&溶解度
存储In solvent: -80°C for 1 year | Shipping with blue ice/Shipping at ambient temperature.
溶解度信息
DMSO: 45 mg/mL (155.08 mM), Sonication is recommended.
H2O: 29 mg/mL (99.94 mM), Sonication is recommended.
体内实验配方
10% DMSO+40% PEG300+5% Tween 80+45% Saline: 5 mg/mL (17.23 mM), Sonication is recommended.
请按顺序添加溶剂,在添加下一种溶剂之前,尽可能使溶液澄清。如有必要,可通过加热、超声、涡旋处理进行溶解。工作液建议现配现用。以上配方仅供参考,体内配方并不是绝对的,请根据不同情况进行调整。
溶液配制表
H2O/DMSO
1mg5mg10mg50mg
1 mM3.4463 mL17.2313 mL34.4626 mL172.3128 mL
5 mM0.6893 mL3.4463 mL6.8925 mL34.4626 mL
10 mM0.3446 mL1.7231 mL3.4463 mL17.2313 mL
20 mM0.1723 mL0.8616 mL1.7231 mL8.6156 mL
50 mM0.0689 mL0.3446 mL0.6893 mL3.4463 mL
DMSO
1mg5mg10mg50mg
100 mM0.0345 mL0.1723 mL0.3446 mL1.7231 mL

计算器

  • 摩尔浓度 计算器
  • 稀释 计算器
  • 配液 计算器
  • 分子量 计算器

体内实验配液计算器

请在以下方框中输入您的动物实验信息后点击计算,可以得到母液配置方法和体内配方的制备方法:
比如您的给药剂量是10 mg/kg,每只动物体重20 g,给药体积100 μL, 一共给药动物10只,您使用的配方为 10% DMSO + 40% PEG300 + 5% Tween 80 + 45% Saline / PBS / ddH2O, 那么您的工作液浓度为2 mg/mL
母液配置方法:2 mg 药物溶于 100 μL DMSO ( 母液浓度为 20 mg/mL ), 如您需要配置的浓度超过该产品的溶解度,请先与我们联系。
体内配方的制备方法:100 μL DMSO 母液, 添加 400 μL PEG300 混匀澄清, 再加 50 μL Tween 80, 混匀澄清, 再加 450 μL Saline / PBS / ddH2O 混匀澄清
以上为“体内实验配液计算器”的使用方法举例,并不是具体某个化合物的推荐配制方式,请根据您的实验动物和给药方式选择适当的溶解方案。
方案所需的各类助溶剂如: DMSOPEG300PEG400Tween 80SBE-β-CD玉米油等, 均可在TargetMol网站点击购买。
1 请输入动物实验的基本信息
mg/kg
g
μL
2 请输入动物体内配方组成,不同的产品配方组成不同,如有配方需求,可先联系我们提供正确的体内配方。
% DMSO
%
% Tween 80
% Saline/PBS/ddH2O

剂量转换

对于不同动物的给药剂量换算,您也可以参考 更多

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