4-(咪唑并[1,2-a]吡啶-3-基):作为抗癌剂的嘧啶衍生物。

IF 1.8 Q3 PHARMACOLOGY & PHARMACY
Pharmaceutical patent analyst Pub Date : 2023-01-01 Epub Date: 2022-11-10 DOI:10.4155/ppa-2022-0033
Rami A Al-Horani
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引用次数: 0

摘要

一系列 4-(咪唑并[1,2-a]吡啶-3-基)嘧啶衍生物被认为是 c-KIT 的抑制剂和潜在的癌症治疗药物。这些衍生物的化学制备方法和针对伊马替尼耐药肿瘤细胞的生物学评价已经得到描述。一些声称的分子具有极佳的 IC50 值,在纳摩尔范围内。一些分子还对多种激酶具有选择性。研究发现,少数特异性抑制剂具有良好的口服生物利用度,对 hERG 通道的抑制作用也达到了可接受甚至优异的水平。这类药物代表了一种新的平台,可用于开发针对胃肠道间质瘤患者可能出现的各种 c-KIT 突变和继发性突变的新型抗癌疗法。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
4-(Imidazo[1,2-a]pyridin-3-yl): pyrimidine derivatives as anticancer agents.

A series of 4-(imidazo[1,2-a]pyridin-3-yl)-pyrimidine derivatives are claimed as inhibitors of c-KIT and as potential treatments for cancer. Their chemical preparation and biological evaluation against imatinib-resistant tumor cells have been described. Several claimed molecules have excellent IC50 values in the nanomolar range. Several molecules were also selective against a wide panel of kinases. Few specific inhibitors have been found to have promising oral bioavailability and acceptable to excellent values regarding the inhibition of hERG channel. This class represents a new platform for developing new anticancer treatment against a wide range of c-KIT mutations and secondary mutations that may arise in gastrointestinal stromal tumor patients.

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来源期刊
Pharmaceutical patent analyst
Pharmaceutical patent analyst PHARMACOLOGY & PHARMACY-
CiteScore
1.80
自引率
0.00%
发文量
22
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