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Temoporfin

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纯度: 99.71%

货号 T17035Cas号 122341-38-2

别名 替莫卟吩, 替莫泊芬

Temoporfin 能够用于头颈部鳞状细胞癌的光动力学研究。

Temoporfin
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Temoporfin

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Rating icon 很棒

纯度: 99.71%

货号 T17035 别名 替莫卟吩, 替莫泊芬Cas号 122341-38-2

Temoporfin 能够用于头颈部鳞状细胞癌的光动力学研究。

规格价格库存数量
1 mg
¥ 816
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2 mg
¥ 1,180
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5 mg
¥ 1,830
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10 mg
¥ 3,160
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25 mg
¥ 5,200
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50 mg
¥ 7,350
现货
100 mg
¥ 9,890
待询
1 mL x 10 mM (in DMSO)
¥ 2,730
现货
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产品介绍


Temoporfin AI Summary
Temoporfin demonstrates various bioactivities and physicochemical properties. It has a drug level ratio of 3.0 in tumor to skin in iv dosed BDXI rats implanted with rat LSBD1 cells after 24 hours. The compound is soluble in 25% aqueous ethanolic medium at 25°C with a solubility of 600000.0 nM. It exhibits significant antiviral activity against SARS-CoV-2, inhibiting cytotoxicity in Caco-2 cells by 85.92% at 10 µM, and has a 30.74% inhibition of SARS-CoV-2 3CL-Pro protease at 20 µM. In VERO-6 cells, it shows a 2.08% inhibition rate at 10 µM after 48 hours against SARS-CoV-2. Additionally, Temoporfin has photodynamic antibacterial activity against Enterococcus faecalis at 10 µM and 30 µM concentrations under light irradiation, with log(activity) values of 5.8 and 6.7, respectively. It displays both photodynamic cytotoxicity and dark toxicity against human A549 cells and Enterococcus faecalis. In human QBC939 cells, it shows dark toxicity with a TC50 of 6.08 µM and phototoxic effects upon 650 nm laser irradiation in QBC939 cell xenografts in mice, reducing tumor weight by 35%. The compound also demonstrates phototoxic effects against human HT-29 cells, human MDA-MB-231, mouse 4T1, and HUVEC cells, with varying IC50 values. It is a potent HDAC6 inhibitor, with inhibition percentages of 36.91% and 2.63% using different substrates. Moreover, it shows antiviral activity against West Nile virus, Zika virus, and DENV2, with EC50 values of 10.0 nM, 22.0 nM, and 20.0 nM, respectively. Additionally, it exhibits cytotoxicity against human A549 cells with a CC50 of 40700.0 nM..
Note: Summary generated by AI. Data source: ChEMBL
生物活性
产品描述
Temoporfin used in photodynamic therapy for the treatment of squamous cell carcinoma of the head and neck.
别名替莫卟吩, 替莫泊芬
化学信息
分子量680.75
分子式C44H32N4O4
CAS No.122341-38-2
SmilesOc1cccc(c1)-c1c2CCc(n2)c(-c2cccc(O)c2)c2ccc([nH]2)c(-c2cccc(O)c2)c2ccc(n2)c(-c2cccc(O)c2)c2ccc1[nH]2
密度1.386 g/cm3 (Predicted)
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: 27 mg/mL (39.66 mM), Sonication is recommended.
体内实验配方
10% DMSO+40% PEG300+5% Tween 80+45% Saline: 1 mg/mL (1.47 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
1mg5mg10mg50mg
1 mM1.4690 mL7.3448 mL14.6897 mL73.4484 mL
5 mM0.2938 mL1.4690 mL2.9379 mL14.6897 mL
10 mM0.1469 mL0.7345 mL1.4690 mL7.3448 mL
20 mM0.0734 mL0.3672 mL0.7345 mL3.6724 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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