New imidazo[2,1-b]thiazole derivatives: Synthesis, in vitro anticancer evaluation, and in silico studies

Authors
Park, Jin-HunEl-Gamal, Mohammed I.Lee, Yong SupOh, Chang-Hyun
Issue Date
2011-12
Publisher
ELSEVIER FRANCE-EDITIONS SCIENTIFIQUES MEDICALES ELSEVIER
Citation
EUROPEAN JOURNAL OF MEDICINAL CHEMISTRY, v.46, no.12, pp.5769 - 5777
Abstract
A series of 18 new imidazo[2,1-b]thiazole derivatives was synthesized. Their in vitro antiproliferative activities against A375P human melanoma cell line and NCI-60 cell line panel were tested. Compounds 15, 16, 18, 22, 26-28, and 31 showed superior potency against A375P to sorafenib. In addition, compounds 26 and 27 showed selectivity toward melanoma cell lines than for other cancer types. Both compounds exerted sub-micromolar IC50 values over 7 (including A375P) and 6 melanoma cell lines, respectively. in silico studies are also reported. ADME profiling, in silico toxicity, drug-likeness, and drug-score data of compounds 26 and 27 are promising. (C) 2011 Elsevier Masson SAS. All rights reserved.
Keywords
POTENTIAL ANTITUMOR AGENTS; MELANOMA; GUANYLHYDRAZONES; INHIBITORS; CHEMISTRY; THERAPY; POTENTIAL ANTITUMOR AGENTS; MELANOMA; GUANYLHYDRAZONES; INHIBITORS; CHEMISTRY; THERAPY; Anticancer; Antiproliferative activity; Imidazo[2,1-b]thiazole; A375P; Melanoma
ISSN
0223-5234
URI
https://pubs.kist.re.kr/handle/201004/129739
DOI
10.1016/j.ejmech.2011.08.024
Appears in Collections:
KIST Article > 2011
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