4°C, sealed storage, away from moistur 该产品在溶液状态不稳定,建议您现用现配,即刻使用。
产品详情
MMAF-d8 (hydrochloride)e是MMAF hydrochloride的氘代形式。
生物活性
MMAF-d 8 (hydrochloride)e is a deuterated form of MMAF hydrochloride, which is a microtubule disrupting agent.
性状
Solid
IC50 & Target[1][2]
Auristatin
体外研究(In Vitro)
MMAF shows in vitro cytotoxicity against a panel of cell lines. The IC50 values for Karpas 299, H3396, 786-O and Caki-1 are 119, 105, 257, and 200 nM, respectively. Targeted MMAF is much more potent than the free drug, and that cAC10 conjugates of MMAF display pronounced activities. On a molar basis, the cAC10-L1-MMAF4 is an average of over 2200-fold more potent than free MMAF and is active on all the CD30-positive cell lines tested. has not independently confirmed the accuracy of these methods. They are for reference only.
体内研究(In Vivo)
The maximum tolerated dose in mice of MMAF (>16 mg/kg) is much higher than MMAE (1 mg/kg). cAC10-L1-MMAF 4 has an MTD of 50 mg/kg in mice and 15 mg/kg in rats. The corresponding cAC10-L4-MMAF 4 ADC was much less toxic, having MTDs in mice and rats of >150 mg/ kg and 90 mg/kg in rats, respectively. has not independently confirmed the accuracy of these methods. They are for reference only.
运输条件
Room temperature in continental US; may vary elsewhere.
储存方式
4°C, sealed storage, away from moistur 该产品在溶液状态不稳定,建议您现用现配,即刻使用。
参考文献
[1]. Doronina SO, et al. Enhanced activity of monomethylauristatin F through monoclonal antibody delivery: effects of linker technology on efficacy and toxicity. Bioconjug Chem. 2006 Jan-Feb;17(1):114-24.
溶解度数据
In Vitro: DMSO : 100 mg/mL (128.79 mM; Need ultrasonic)配制储备液