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新型含 1,3,4-三芳基吡唑骨架的二芳基脲和二芳基酰胺:合成、对黑素瘤细胞系的抗增殖评价、ERK 激酶抑制和分子对接研究。

New diarylureas and diarylamides containing 1,3,4-triarylpyrazole scaffold: Synthesis, antiproliferative evaluation against melanoma cell lines, ERK kinase inhibition, and molecular docking studies.

机构信息

Center for Biomaterials, Korea Institute of Science and Technology, PO Box 131,Cheongryang, Seoul 130-650, Republic of Korea.

出版信息

Eur J Med Chem. 2011 Dec;46(12):5754-62. doi: 10.1016/j.ejmech.2011.08.013. Epub 2011 Aug 12.

Abstract

Synthesis of a new series of diarylureas and diarylamides possessing 1,3,4-triarylpyrazole scaffold is described. Their in vitro antiproliferative activities against 9 human melanoma cell lines were tested. Compounds 12, 13, 15, and 21-23 showed the highest potency against A375P melanoma cell line. In addition, compounds 10-15 and 19-24 showed high potency over the NCI 8 tested melanoma cell-lines panel. The IC(50) values for compound 23 were 0.36 μM and 0.84 μM over LOX IMVI and M14 cell lines, respectively. Compounds 21 and 23 showed high, dose-dependent inhibition of ERK kinase. Virtual screening was carried out through docking of compound 21 into the domain of V600E-B-RAF and the binding mode was studied.

摘要

描述了一系列具有 1,3,4-三芳基吡唑骨架的新型二芳基脲和二芳基酰胺的合成。测试了它们对 9 个人黑色素瘤细胞系的体外增殖活性。化合物 12、13、15 和 21-23 对 A375P 黑色素瘤细胞系表现出最高的活性。此外,化合物 10-15 和 19-24 对 NCI 8 种测试的黑色素瘤细胞系面板表现出高活性。化合物 23 在 LOX IMVI 和 M14 细胞系中的 IC(50)值分别为 0.36 μM 和 0.84 μM。化合物 21 和 23 对 ERK 激酶表现出高剂量依赖性抑制作用。通过将化合物 21 对接进入 V600E-B-RAF 的结构域进行虚拟筛选,并研究了结合模式。

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