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首页-小分子抑制剂&激动剂-Tyrosine Kinase-EGFR-DBPR112
DBPR112

Chemical Structure : DBPR112

CAS No.: 1226549-49-0

DBPR112 (Gozanertinib, DBPR 112)

货号: PC-73088Not For Human Use, Lab Use Only.

Gozanertinib (DBPR112) is a highly potent, selective inhibitor of EGFR mutant L858R/T790M (IC50=48 nM) and exon 20 insertion mutations.

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纯度 & COA & 质检文件 纯度: >98% (HPLC) Select Batch:

生物&药学活性

Gozanertinib (DBPR112) is a highly potent, selective inhibitor of EGFR mutant L858R/T790M (IC50=48 nM) and exon 20 insertion mutations.
DBPR112 inhibited HCC827 cell growth with IC50 of 25 nM, exhibited tenfold potency better than the third-generation inhibitor, osimertinib, against EGFR and HER2 exon 20 insertion mutations.
DBPR112 demonstrated significant antitumor efficacy in in vivo xenograft models.

物理化学性质&存储条件

分子量 533.632
分子式 C32H31N5O3
外观性状 Solid
CAS No.
储存条件
固体粉末
-20°C 12 个月; 4°C 6 个月
配置液
-80°C 6 个月; -20°C 6 个月
Shipping
Solubility

10 mM in DMSO

Chemical Name/SMILES

(S,E)-4-(dimethylamino)-N-(3-(4-((2-hydroxy-1-phenylethyl)amino)-6-phenylfuro[2,3-d]pyrimidin-5-yl)phenyl)but-2-enamide

参考文献

1. Shu-Yu Lin, et al. J Med Chem. 2019 Nov 27;62(22):10108-10123.

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