Powder: -20°C for 3 years | In solvent: -80°C for 1 year
Pyribencarb (), a benzylcarbamate-type fungicide, exhibits broad-spectrum activity against various plant pathogenic fungi. Acting as a potent Qo inhibitor of cytochrome b, Pyribencarb demonstrates particular efficacy against Botrytis cinerea and Sclerotinia sclerotiorum.
规格 | 价格/CNY | 货期 | 数量 | |
---|---|---|---|---|
1 mg | ¥ 413 | 现货 | ||
5 mg | ¥ 945 | 现货 | ||
10 mg | ¥ 1,660 | 现货 | ||
25 mg | ¥ 3,230 | 现货 | ||
50 mg | ¥ 4,790 | 现货 | ||
100 mg | ¥ 6,850 | 现货 | ||
500 mg | ¥ 13,700 | 现货 | ||
1 mL * 10 mM (in DMSO) | ¥ 996 | 现货 |
产品描述 | Pyribencarb (), a benzylcarbamate-type fungicide, exhibits broad-spectrum activity against various plant pathogenic fungi. Acting as a potent Qo inhibitor of cytochrome b, Pyribencarb demonstrates particular efficacy against Botrytis cinerea and Sclerotinia sclerotiorum. |
体外活性 | Pyribencarb potently inhibits succinate-cytochrome c reductase (SCR) activities of Botrytis cinerea (cucumber gray mold), Corynespora cassiicola (leaf spot) and decylubiquinol-cytochrome c reductase (UCR) activity of B. cinerea. Pyribencarb inhibits the UCR of B. cinerea in an uncompetitive manner, and the substrate-dependent inhibition constant is found from calculation to be 13 nM[1]. The target site of Pyribencarb is cytochrome b of complex III in the electron transport system of the respiratory chain. The inhibitory potency of pyribencarb on SCR activities of plants, rats and carp is relatively weak compared with that of strobilurin fungicides[1]. |
别名 | 吡菌苯威, ZINC43065336 |
分子量 | 361.82 |
分子式 | C18H20ClN3O3 |
CAS No. | 799247-52-2 |
Powder: -20°C for 3 years | In solvent: -80°C for 1 year
DMSO: 90 mg/mL (248.7 mM)
可选溶剂 | 浓度 体积 质量 | 1 mg | 5 mg | 10 mg | 25 mg |
DMSO | 1 mM | 2.7638 mL | 13.819 mL | 27.6381 mL | 69.0951 mL |
5 mM | 0.5528 mL | 2.7638 mL | 5.5276 mL | 13.819 mL | |
10 mM | 0.2764 mL | 1.3819 mL | 2.7638 mL | 6.9095 mL | |
20 mM | 0.1382 mL | 0.691 mL | 1.3819 mL | 3.4548 mL | |
50 mM | 0.0553 mL | 0.2764 mL | 0.5528 mL | 1.3819 mL | |
100 mM | 0.0276 mL | 0.1382 mL | 0.2764 mL | 0.691 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。
Pyribencarb 799247-52-2 Microbiology/Virology Antifungal 吡菌苯威 ZINC43065336 ZINC 43065336 ZINC-43065336 Inhibitor inhibitor inhibit