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Dicyclomine hydrochloride

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纯度: 99.81%

货号 T1460Cas号 67-92-5

别名 盐酸双环维林

Dicyclomine hydrochloride 是口服活性毒蕈碱胆碱能受体拮抗剂。它是一种抗痉挛试剂,在体内可缓解胃肠道平滑肌痉挛。它对 M1 受体亚型和 M2 受体亚型,Ki 分别为5.1和54.6nM,在刷状缘膜和基底质膜中均表现出较高的亲和力。

Dicyclomine hydrochloride
其他形式的 “Dicyclomine hydrochloride”:

Dicyclomine hydrochloride

一键复制产品信息
Rating icon 很棒

纯度: 99.81%

货号 T1460 别名 盐酸双环维林Cas号 67-92-5

Dicyclomine hydrochloride 是口服活性毒蕈碱胆碱能受体拮抗剂。它是一种抗痉挛试剂,在体内可缓解胃肠道平滑肌痉挛。它对 M1 受体亚型和 M2 受体亚型,Ki 分别为5.1和54.6nM,在刷状缘膜和基底质膜中均表现出较高的亲和力。

规格价格库存数量
50 mg
¥ 148
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500 mg
¥ 282
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1 mL x 10 mM (in DMSO)
¥ 221
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产品介绍


Dicyclomine hydrochloride AI Summary
Dicyclomine hydrochloride exhibits a wide range of bioactivities. It shows antiplasmodial activity against various strains of Plasmodium falciparum, with IC50 values ranging from 5011.87 nM to 15848.93 nM as determined by the SYBR green assay over 72 hours. Additionally, it inhibits the proliferation of various Plasmodium falciparum lines, displaying potency in various biological processes including the ERK signaling pathway, Neuropeptide S receptor, and entry or binding of Lassa and Marburg Viruses. The compound also demonstrates potent inhibition of sodium fluorescein uptake in OATP1B3- and OATP1B1-transfected CHO cells, with inhibition percentages over 100% at 10 µM. Moreover, Dicyclomine hydrochloride shows antibiofilm activity against Candida albicans with an MBIC50 value of 60.0 µM. It has limited inhibition of SARS-CoV-2 in Vero E6 cells and Caco-2 cells, displaying low percentages of viral cytotoxicity inhibition and weak inhibition of the SARS-CoV-2 3CL-Pro protease. The compound also displays various degrees of antifungal and antibacterial activities, including: - Candida albicans ATCC 90028: 3.82% inhibition - Cryptococcus neoformans H99 ATCC 208821: -0.13% inhibition - Escherichia coli ATCC 25922: 0.37% inhibition - Klebsiella pneumoniae MDR ATCC 70063: 5.74% inhibition - Pseudomonas aeruginosa ATCC 27853: 3.37% inhibition - Acinetobacter baumannii ATCC 19606: 27.79% inhibition - Staphylococcus aureus MRSA ATCC 43300: 8.61% inhibition Overall, Dicyclomine hydrochloride demonstrates a multifaceted bioactivity profile with noteworthy antiparasitic, antiviral, and antibacterial properties..
Note: Summary generated by AI. Data source: ChEMBL
生物活性
产品描述
Dicyclomine hydrochloride is a muscarinic antagonist used as an antispasmodic and in urinary incontinence.
靶点活性
M1 mAChR (brush-border membrane):5.1 nM (Ki)
别名盐酸双环维林
化学信息
分子量345.95
分子式C19H36ClNO2
CAS No.67-92-5
SmilesCl.CCN(CC)CCOC(=O)C1(CCCCC1)C1CCCCC1
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
H2O: 199.5 mM, Sonication is recommended.
DMSO: 60 mg/mL (173.44 mM), Sonication is recommended.
体内实验配方
10% DMSO+40% PEG300+5% Tween 80+45% Saline: 2 mg/mL (5.78 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
DMSO/H2O
1mg5mg10mg50mg
1 mM2.8906 mL14.4530 mL28.9059 mL144.5296 mL
5 mM0.5781 mL2.8906 mL5.7812 mL28.9059 mL
10 mM0.2891 mL1.4453 mL2.8906 mL14.4530 mL
20 mM0.1445 mL0.7226 mL1.4453 mL7.2265 mL
50 mM0.0578 mL0.2891 mL0.5781 mL2.8906 mL
100 mM0.0289 mL0.1445 mL0.2891 mL1.4453 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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