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MK-4827 (Niraparib)1038915-60-4

更新時(shí)間:2024-11-17

訪問(wèn)量:844

廠商性質(zhì):經(jīng)銷商

生產(chǎn)地址:上海一基

簡(jiǎn)要描述:
MK-4827 (Niraparib)1038915-60-4
上海一基實(shí)業(yè)有限公司是主要從事配套試劑的生產(chǎn)和銷售的企業(yè),產(chǎn)品用途:科研實(shí)驗(yàn),標(biāo)準(zhǔn)對(duì)照品研究中心代理的作為一種衡量標(biāo)準(zhǔn)

MK-4827 (Niraparib)1038915-60-4

MK4827 (Niraparib)
分子式:C19H20N4O    分子量:320.39
 
 
產(chǎn)品描述
MK-4827是選擇性PARP1/2抑制劑,IC50為3.8 nM/2.1 nM, 作用于攜帶突變型BRCA-1和BRCA-2的癌細(xì)胞,具有強(qiáng)的作用活性。比作用于PARP3, V-PARP 和Tank1選擇性高330倍以上。
靶點(diǎn)
PARP1
PARP2
       
IC50
3.8 nM
2.1 nM
       
體外研究
MK-4827 displays excellent PARP 1 and 2 inhibition with IC(50) = 3.8 and 2.1 nM, respectively, and in a whole cell assay, it inhibits PARP activity with EC(50) = 4 nM and inhibits proliferation of cancer cells with mutant BRCA-1 and BRCA-2 with CC(50) in the 10-100 nM range.
體內(nèi)研究
MK-4827 is well tolerated in vivo and demonstrates efficacy as a single agent in a xenograft model of BRCA-1 deficient cancer.In addition, MK-4827 strongly enhances the effect of radiation on a variety of human tumor xenografts, both p53 wild type and p53 mutant. The enhancement of radiation response is observed in clinically relevant radiation-dose fractionation schedules. The therapeutic window during which time MK-4827 interacts with radiation lasts for several hours. These biological attributes make translation of this therapeutic combination treatment feasible for translation to the treatment of a variety of human cancers.
溶解性
可溶于DMSO
穩(wěn)定性
2年 -20°C粉狀,6月-80°C溶于DMSO

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