Powder: -20°C for 3 years | In solvent: -80°C for 1 year
Tiafenacil is a novel herbicide that inhibits protoporphyrinogen IX oxidase (PPO), exhibiting IC50 values ranging from 22 to 28 nM across different plant species such as amaranth (Amaranthus tuberculatus), soybean (Glycine max), arabidopsis (Arabidopsis thaliana), and rapeseed (Brassica napus)[1].
产品描述 | Tiafenacil is a novel herbicide that inhibits protoporphyrinogen IX oxidase (PPO), exhibiting IC50 values ranging from 22 to 28 nM across different plant species such as amaranth (Amaranthus tuberculatus), soybean (Glycine max), arabidopsis (Arabidopsis thaliana), and rapeseed (Brassica napus)[1]. |
体外活性 | Tiafenacil has low oral and dermal acute toxicity[1].In velvetleaf, Tiafenacil causes severe growth inhibition at 1 μM and results in desiccation and death at 5 μM[1]. |
分子量 | 511.87 |
分子式 | C19H18ClF4N3O5S |
CAS No. | 1220411-29-9 |
Powder: -20°C for 3 years | In solvent: -80°C for 1 year
DMSO: 100 mg/mL (195.36 mM), Sonication is recommended.
可选溶剂 | 浓度 体积 质量 | 1 mg | 5 mg | 10 mg | 25 mg |
DMSO | 1 mM | 1.9536 mL | 9.7681 mL | 19.5362 mL | 48.8405 mL |
5 mM | 0.3907 mL | 1.9536 mL | 3.9072 mL | 9.7681 mL | |
10 mM | 0.1954 mL | 0.9768 mL | 1.9536 mL | 4.8841 mL | |
20 mM | 0.0977 mL | 0.4884 mL | 0.9768 mL | 2.442 mL | |
50 mM | 0.0391 mL | 0.1954 mL | 0.3907 mL | 0.9768 mL | |
100 mM | 0.0195 mL | 0.0977 mL | 0.1954 mL | 0.4884 mL |
对于不同动物的给药剂量换算,您也可以参考 更多...
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5% DMSO+30% PEG300+5% Tween 80+60% 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 50 μL DMSO (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:取 50 μL DMSO 主液,加入 300 μL PEG300, 混匀澄清,再加 50 μL Tween 80,混匀澄清,再加 600 μL ddH2O, 混匀澄清。
您可能有的问题的答案可以在抑制剂处理说明中找到,包括如何准备库存溶液,如何存储产品,以及基于细胞的分析和动物实验需要特别注意的问题。
Tiafenacil 1220411-29-9 Inhibitor inhibitor inhibit