CAS: 1089283-49-7; N-(2,6-Difluorophenyl)-5-(3-(2-((5-Ethyl-2-Methoxy-4-(4-(4-(Methylsulfonyl)Piperazin-1-yl)Piperidin-1-yl)Phenyl)Amino)Pyrimidin-4-yl)Imidazo[1,2-A]Pyridin-2-yl)-2-Methoxybenzamide

该化合物是一个小分子,主要因其潜在的治疗应用,特别是在肿瘤学和免疫学领域,受到调查,主要受到调查,它有选择地抑制某些种类的酶,这些酶在细胞生长,扩散和存活等各种细胞过程中起着关键作用.该化合物的行动机制通常包括调控经常在癌症细胞中受到约束的信号路径.在临床前的研究中,GSK 1904529A表明,它有希望抑制肿瘤的生长,提高其他治疗剂的功效.其药理基因特性,如吸收,分布,新陈代谢和排泄,对于确定其是否适合临床使用至关重要.此外,安全和毒性特征是研究人员在药物开发过程中评估的关键因素.

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上下游产品

5-ethyl-2-(methyloxy)-4-{4-[4-(methylsulfonyl)-1-piperazinyl]-1-piperidinyl}aniline 5-[3-(2-chloro-4-pyrimidinyl)imidazo[1,2-a]pyridin-2-yl]-N-(2,6-difluorophenyl)-2-(methyloxy)benzamide

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    专利信息


    专利号:US-2017107577-A1
    优先权日:2014-03-11
    标题:Determining Cancer Aggressiveness, Prognosis and Responsiveness to Treatment
    发明人:AL-EJEH FARES
    权利人:THE COUNCIL OF THE QUEENSLAND INST OF MEDICAL RES
    摘要:The invention provides methods of determining the aggressiveness, prognosis and response to therapy for particular cancers, which include comparing the expression levels of one or a plurality of differentially expressed genes from one or more 5 functional metagenes, including a Carbohydrate/Lipid Metabolism metagene, a Cell Signalling metagene, a Cellular Development metagene, a Cellular Growth metagene, a Chromosome Segregation metagene, a DNA Replication/Recombination metagene, an Immune system metagene, a Metabolic Disease metagene, a Nucleic Acid Metabolism metagene, a Post-Translational Modification metagene, a Protein 10 Synthesis/Modification metagene and a Multiple Networks metagene. The method disclosed herein may be particularly suitable as a companion diagnostic for cancer therapies.

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    主要参考文献


    1: Sabbatini P, Rowand JL, Groy A, Korenchuk S, Liu Q, Atkins C, Dumble M, Yang J, Anderson K, Wilson BJ, Emmitte KA, Rabindran SK, Kumar R. Antitumor activity of GSK1904529A, a small-molecule inhibitor of the insulin-like growth factor-I eceptor tyrosine kinase. Clin Cancer Res. 2009 May 1;15(9):3058-67. Epub 2009 Apr 21.

    合成参考文献


    参考文献:10.1124/mol.119.115964
    摘要:Lee TD, Lee OW, Brimacombe KR, Chen L, Guha R, Lusvarghi S, Tebase BG, Klumpp-Thomas C, Robey RW, Ambudkar SV, Shen M, Gottesman MM, Hall MD. A High-Throughput Screen of a Library of Therapeutics Identifies Cytotoxic Substrates of P-glycoprotein. Molecular Pharmacology. 2019 Nov;96(5):629–40. doi: 10.1124/mol.119.115964.
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