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

Authors
Choi, Won-KyoungEl-Gamal, Mohammed I.Choi, Hong SeokBaek, DaejinOh, Chang-Hyun
Issue Date
2011-12
Publisher
ELSEVIER FRANCE-EDITIONS SCIENTIFIQUES MEDICALES ELSEVIER
Citation
EUROPEAN JOURNAL OF MEDICINAL CHEMISTRY, v.46, no.12, pp.5754 - 5762
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 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.
Keywords
DERIVATIVES; DIAGNOSIS; TARGETS; THERAPY; RAF; DERIVATIVES; DIAGNOSIS; TARGETS; THERAPY; RAF; 1,3,4-Triarylpyrazole; Melanoma; Diarylurea; Diarylamide; B-RAF kinase; ERK kinase
ISSN
0223-5234
URI
https://pubs.kist.re.kr/handle/201004/129738
DOI
10.1016/j.ejmech.2011.08.013
Appears in Collections:
KIST Article > 2011
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