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PF-06380101

产品编号 T16490Cas号 1436391-86-4
别名 Auristatin-0101, Aur0101

PF-06380101 is an auristatin microtubule inhibitor and is a cytotoxic Dolastatin 10 analogue. When compared to other synthetic auristatin analogues that are used in the preparation of ADCs, PF-06380101 displays excellent potencies in tumor cell proliferation assays and differential ADME properties.

PF-06380101

PF-06380101

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产品编号 T16490 别名 Auristatin-0101, Aur0101Cas号 1436391-86-4

PF-06380101 is an auristatin microtubule inhibitor and is a cytotoxic Dolastatin 10 analogue. When compared to other synthetic auristatin analogues that are used in the preparation of ADCs, PF-06380101 displays excellent potencies in tumor cell proliferation assays and differential ADME properties.

规格价格库存数量
25 mg¥ 10,50010-14周
50 mg¥ 13,70010-14周
100 mg¥ 18,70010-14周
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产品介绍

生物活性
产品描述
PF-06380101 is an auristatin microtubule inhibitor and is a cytotoxic Dolastatin 10 analogue. When compared to other synthetic auristatin analogues that are used in the preparation of ADCs, PF-06380101 displays excellent potencies in tumor cell proliferation assays and differential ADME properties.
体内活性
PF-06380101 is anticipated to be of low risk to perpetrate pharmacokinetic drug interactions with compounds for which CYP1A2, CYP2B6, CYP2C8, CYP2C9, CYP2C19, CYP2D6, and/or CYP3A4/5-mediated metabolism constitutes the primary mechanism of clearance. PF-06380101 preferentially distributes into human plasma relative to whole blood and that PF-06380101 is a P-glycoprotein (P-gp) substrate. PF-06380101 exhibited a mean systemic clearance (Cl) of 70 mL/min/kg and a volume of distribution (Vss) of 14.70 L/kg after an IV dose of 20a at 20 μg/kg to Wistar Han rats, resulting in a terminal elimination half-life (t1/2) of approximately 6 h. The utility of the new auristatin analogues as ADC payloads including the development of the lead analogue 20a (PF-06380101) will be reported in due course.
别名Auristatin-0101, Aur0101
化学信息
分子量743.01
分子式C39H62N6O6S
CAS No.1436391-86-4
储存&溶解度
存储Powder: -20°C for 3 years | In solvent: -80°C for 1 year | Shipping with blue ice.
溶解度信息
DMSO: 65 mg/mL (87.48 mM)
溶液配制表
DMSO
1mg5mg10mg50mg
1 mM1.3459 mL6.7294 mL13.4588 mL67.2938 mL
5 mM0.2692 mL1.3459 mL2.6918 mL13.4588 mL
10 mM0.1346 mL0.6729 mL1.3459 mL6.7294 mL
20 mM0.0673 mL0.3365 mL0.6729 mL3.3647 mL
50 mM0.0269 mL0.1346 mL0.2692 mL1.3459 mL

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TargetMol | Animal experiments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 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% ddH2O. 那么您的工作液浓度为 2 mg/mL
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体内配方的制备方法:50μLDMSOTargetMol | reagent 母液,添加 300 μLPEG300TargetMol | reagent 混匀澄清,再加 50μLTween 80, 混匀澄清,再加 600μLddH2OTargetMol | 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。

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