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Jatrorrhizine hydrochloride

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纯度: 99.22%

货号 T2986Cas号 960383-96-4

Jatrorrhizine hydrochloride 是从小檗的根中提取的化合物,具有具有神经保护、抗菌、抗疟原虫和抗氧化活性。Jatrorrhizine hydrochloride 是一种具有口服活性和选择性的乙酰胆碱酯酶 (AChE)抑制剂,抑制去甲肾上腺素 (NE) 的摄取。

Jatrorrhizine hydrochloride

Jatrorrhizine hydrochloride

一键复制产品信息
Rating icon 很棒

纯度: 99.22%

货号 T2986Cas号 960383-96-4

Jatrorrhizine hydrochloride 是从小檗的根中提取的化合物,具有具有神经保护、抗菌、抗疟原虫和抗氧化活性。Jatrorrhizine hydrochloride 是一种具有口服活性和选择性的乙酰胆碱酯酶 (AChE)抑制剂,抑制去甲肾上腺素 (NE) 的摄取。

规格价格库存数量
20 mg
¥ 290
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产品介绍


Jatrorrhizine hydrochloride AI Summary
Jatrorrhizine hydrochloride exhibits a broad spectrum of bioactivities, most notably antimalarial and anti-HIV activities. It shows significant in vitro antimalarial activity against Plasmodium falciparum strains D6 and W2 with IC50 values of 0.422 ug/mL and 1.607 ug/mL, respectively. Additionally, it demonstrates antiplasmodial activity against the multi-drug-resistant Plasmodium falciparum K1 strain with an IC50 of 3150.0 nM and against the drug-susceptible 3D7 strain with an EC50 of 939.0 nM. In terms of HIV inhibition, Jatrorrhizine hydrochloride inhibits HIV1 reverse transcriptase activity with an IC50 of 71.0 ug/mL. The compound also displays antiamnesic activity against Entamoeba histolytica NIH 200 and some cytotoxicity towards human KB cells and Huh7 hepatocellular carcinoma cells, with IC50 values of 82700.0 nM and 8940.0 nM, respectively. Furthermore, it exhibits estrogenic activity at ERalpha in human MVLN cells, with activities of 71.19% at 100 ug/mL and 52.2% at 20 ug/mL. In terms of physicochemical properties, Jatrorrhizine hydrochloride has varying solubility levels in different pH conditions (1300000.0 nM to 1500000.0 nM), log P values ranging from 0.1 to -1.5, log D values from -1.5 to 0.6, a binding affinity to bovine serum albumin with a Kb value of 1.73 x 10^-3 L/mol, and a dissociation constant pKa of 9.6..
Note: Summary generated by AI. Data source: ChEMBL
生物活性
产品描述
Jatrorrhizine hydrochloride is a compound extracted from the roots of Berberis vulgaris with neuroprotective, antimicrobial, antiplasmodial, and antioxidant activities.Jatrorrhizine hydrochloride is an orally active and selective inhibitor of acetylcholinesterase (AChE), which inhibits norepinephrine (NE) uptake. It inhibits the uptake of norepinephrine (NE).
化学信息
分子量373.83
分子式C20H20ClNO4
CAS No.960383-96-4
Smilesc12c(c(c(cc1)OC)OC)c[n+]1c(c2)c2c(CC1)cc(c(c2)OC)O.[Cl-]
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: 3.33 mg/mL (8.91 mM), Sonication is recommended.
溶液配制表
DMSO
1mg5mg10mg50mg
1 mM2.6750 mL13.3751 mL26.7501 mL133.7506 mL
5 mM0.5350 mL2.6750 mL5.3500 mL26.7501 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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