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首页> 外文期刊>Heterocycles: An International Journal for Reviews and Communications in Heterocyclic Chemistry >DESIGN, SYNTHESIS AND BIOLOGICAL ACTIVITY EVALUATION OF 2-MERCAPTO-4(3H)-QUINAZOLINONE DERIVATIVES AS NOVEL INHIBITORS OF PROTEIN TYROSINE PHOSPHATASE 1B
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DESIGN, SYNTHESIS AND BIOLOGICAL ACTIVITY EVALUATION OF 2-MERCAPTO-4(3H)-QUINAZOLINONE DERIVATIVES AS NOVEL INHIBITORS OF PROTEIN TYROSINE PHOSPHATASE 1B

机译:作为蛋白质酪氨酸磷酸酶1B的新型抑制剂的2-巯基-4(3H)-喹唑啉酮衍生物的设计,合成和生物活性评估

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摘要

A series of novel 2-mercapto-4(3H)-quinazolinone derivatives have been synthesized and their inhibitory effects on PTP1B and TCPTP are evaluated for the first time. Most of these derivatives showed good inhibitory activity on PTP1B and reasonable selectivity for PTP1B over TCPTP, among them 32 was the most potent PTP1B inhibitor (IC_(50) = 1.50 μg/mL), and 27 possessed the best selectivity of 3.0-fold.
机译:合成了一系列新颖的2-巯基-4(3H)-喹唑啉酮衍生物,并首次评估了它们对PTP1B和TCPTP的抑制作用。这些衍生物中的大多数对PTP1B表现出良好的抑制活性,并且对PTP1B的选择性优于TCPTP,其中32种是最有效的PTP1B抑制剂(IC_(50)= 1.50μg/ mL),而27种具有3.0倍的最佳选择性。

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