Targeting KRAS Mutant Cancers via Combination Treatment: Discovery of a 5-Fluoro-4-(3<i>H</i>)-quinazolinone Aryl Urea pan-RAF Kinase Inhibitor.
第一作者:
Malcolm P,Huestis
第一单位:
Discovery Chemistry, Genentech, Inc., 1 DNA Way, South San Francisco, California 94080, United States.
作者:
医学主题词
动物(Animals);吖丁啶类(Azetidines);细胞系, 肿瘤(Cell Line, Tumor);细胞增殖(Cell Proliferation);结晶学, X线(Crystallography, X-Ray);狗(Dogs);复方合剂(Drug Combinations);药物协同作用(Drug Synergism);女(雌)性(Female);人类(Humans);小鼠, 裸(Mice, Nude);分子结构(Molecular Structure);突变(Mutation);肿瘤(Neoplasms);苯脲化合物(Phenylurea Compounds);哌啶类(Piperidines);蛋白质结合(Protein Binding);蛋白激酶抑制剂(Protein Kinase Inhibitors);喹唑啉酮类(Quinazolinones);构效关系(Structure-Activity Relationship);异种移植模型抗肿瘤试验(Xenograft Model Antitumor Assays);raf激酶类(raf Kinases);小鼠(Mice)
DOI
10.1021/acs.jmedchem.0c02085
PMID
33780623
发布时间
2024-02-26
- 浏览4
Journal of medicinal chemistry
3940-3955页
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