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

被引:74
作者
Choi, Won-Kyoung [1 ]
El-Gamal, Mohammed I. [1 ,2 ]
Choi, Hong Seok [3 ]
Baek, Daejin [4 ]
Oh, Chang-Hyun [1 ,2 ]
机构
[1] Korea Inst Sci & Technol, Ctr Biomat, Seoul 130650, South Korea
[2] Univ Sci & Technol, Dept Biomol Sci, Taejon 305333, South Korea
[3] Chosun Univ, Coll Pharm, Kwangju 501759, South Korea
[4] Hanseo Univ, Dept Chem, Season 356706, South Korea
关键词
1,3,4-Triarylpyrazole; Melanoma; Diarylurea; Diarylamide; B-RAF kinase; ERK kinase; DERIVATIVES; DIAGNOSIS; TARGETS; THERAPY; RAF;
D O I
10.1016/j.ejmech.2011.08.013
中图分类号
R914 [药物化学];
学科分类号
100701 ;
摘要
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 NCl 8 tested melanoma cell-lines panel. The IC50 values for compound 23 were 0.36 mu M and 0.84 mu M 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. (C) 2011 Elsevier Masson SAS. All rights reserved.
引用
收藏
页码:5754 / 5762
页数:9
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