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Triflupromazine hydrochloride

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纯度: 99.82%

货号 T0302Cas号 1098-60-8

别名 盐酸三氟丙嗪, Neoprin, Fluorofen, Fluopromazine hydrochloride, Flumazin

Triflupromazine hydrochloride (Fluopromazine hydrochloride) 是一种抗精神病药物,是多巴胺 D1/D2 受体拮抗剂。

Triflupromazine hydrochloride
其他形式的 “Triflupromazine hydrochloride”:

Triflupromazine hydrochloride

一键复制产品信息
Rating icon 很棒

纯度: 99.82%

货号 T0302 别名 盐酸三氟丙嗪, Neoprin, Fluorofen, Fluopromazine hydrochloride, FlumazinCas号 1098-60-8

Triflupromazine hydrochloride (Fluopromazine hydrochloride) 是一种抗精神病药物,是多巴胺 D1/D2 受体拮抗剂。

规格价格库存数量
50 mg
¥ 152
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100 mg
¥ 273
现货
200 mg
¥ 491
现货
500 mg
¥ 818
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1 g
¥ 1,190
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产品介绍


Triflupromazine hydrochloride AI Summary
Triflupromazine hydrochloride exhibits antiplasmodial activity against various strains of Plasmodium falciparum with IC50 values ranging from 6309.57 nM to 12589.25 nM after 72 hours of testing using the SYBR green assay, indicating moderate to potent inhibition of the parasite's growth. Additionally, the compound demonstrates significant inhibitory activity on OATP1B1 and OATP1B3 transporters in CHO cells, showing inhibition rates of 185.58% and 83.79% respectively at a 10 uM concentration using the sodium fluorescein uptake assay. Triflupromazine hydrochloride also shows antiviral activity, as evidenced by a 44.25% inhibition of SARS-CoV-2 induced cytotoxicity in Caco-2 cells at a 10 uM concentration after 48 hours. However, in Vero E6 cells infected with SARS-CoV-2 (strain BavPat1), it displayed a low inhibition of cell viability with an inhibition index of -0.1177 and a similar low inhibition of -0.07% in VERO-6 cells at the same concentration and exposure conditions. The compound's inhibition of SARS-CoV-2 3CL-Pro protease was determined to be -5.673% at a 20 µM concentration..
Note: Summary generated by AI. Data source: ChEMBL
生物活性
产品描述
Triflupromazine hydrochloride (Fluopromazine hydrochloride), an antipsychotic medication, is Dopamine D1/D2 receptor antagonists.
别名盐酸三氟丙嗪, Neoprin, Fluorofen, Fluopromazine hydrochloride, Flumazin
化学信息
分子量388.88
分子式C18H20ClF3N2S
CAS No.1098-60-8
SmilesCl.CN(C)CCCN1c2ccccc2Sc2ccc(cc12)C(F)(F)F
密度no data available
储存&溶解度
存储Powder: -20°C for 3 years | In solvent: -80°C for 1 year | Shipping with blue ice/Shipping at ambient temperature.
溶解度信息
DMSO: 50 mg/mL (128.57 mM), Sonication is recommended.
溶液配制表
DMSO
1mg5mg10mg50mg
1 mM2.5715 mL12.8574 mL25.7149 mL128.5744 mL
5 mM0.5143 mL2.5715 mL5.1430 mL25.7149 mL
10 mM0.2571 mL1.2857 mL2.5715 mL12.8574 mL
20 mM0.1286 mL0.6429 mL1.2857 mL6.4287 mL
50 mM0.0514 mL0.2571 mL0.5143 mL2.5715 mL
100 mM0.0257 mL0.1286 mL0.2571 mL1.2857 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:
TargetMol | Animal experiments 比如您的给药剂量是10 mg/kg,每只动物体重20g,给药体积100 μLTargetMol | Animal experiments 一共给药动物10只,您使用的配方为5%TargetMol | reagent DMSO + 30%PEG300 + 5%Tween 80 + 60%Saline/PBS/ddH2O, 那么您的工作液浓度为2mg/mL
母液配置方法: 2 mg 药物溶于 50 μLDMSOTargetMol | reagent ( 母液浓度为 40 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:50μLDMSOTargetMol | reagent 母液,添加 300 μLPEG300TargetMol | reagent 混匀澄清,再加 50μLTween80, 混匀澄清,再加 600μLSaline/PBS/ddH2OTargetMol | reagent 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: DMSOPEG300 / PEG400Tween 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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