Full metadata record

DC Field Value Language
dc.contributor.authorEl-Gamal, Mohammed I.-
dc.contributor.authorPark, Yi Seul-
dc.contributor.authorChi, Dae Yoon-
dc.contributor.authorYoo, Kyung Ho-
dc.contributor.authorOh, Chang-Hyun-
dc.date.accessioned2024-01-20T12:02:30Z-
dc.date.available2024-01-20T12:02:30Z-
dc.date.created2022-01-10-
dc.date.issued2013-07-
dc.identifier.issn0223-5234-
dc.identifier.urihttps://pubs.kist.re.kr/handle/201004/127897-
dc.description.abstractA new series of diarylureas and diarylamides possessing 1,3,4-triarylpyrazole scaffold was designed and synthesized. Their in vitro antiproliferative activities against NCI-60 cell line panel were tested. Most of the compounds showed strong and broad-spectrum antiproliferative activities. Compound 18 exerted sub-micromolar IC50 values over all the subpanels of nine different cancer types. Its IC50 value over MDA-MB-435 melanoma cell line was 27 nM. Compounds 10-13, 22, and 23 possessing urea spacer exerted lethal effect over the NCI-60 panel with mean %inhibitions more than 100% in single-dose testing. Compounds 13 and 23 with urea linker and 3',5'-bis(trifluoromethyl)phenyl terminal ring showed the highest mean %inhibition over the NCI-60 panel in single-dose testing, and showed high potencies and broad-spectrum anticancer activities in five-dose testing. (C) 2013 Elsevier Masson SAS. All rights reserved.-
dc.languageEnglish-
dc.publisherELSEVIER FRANCE-EDITIONS SCIENTIFIQUES MEDICALES ELSEVIER-
dc.subjectMELANOMA-CELL LINE-
dc.subjectANTIPROLIFERATIVE ACTIVITY-
dc.subject1,3,4-TRIARYLPYRAZOLE SCAFFOLD-
dc.subjectDERIVATIVES-
dc.subjectDIARYLAMIDES-
dc.subjectDIARYLUREAS-
dc.subjectDISCOVERY-
dc.titleNew triarylpyrazoles as broad-spectrum anticancer agents: Design, synthesis, and biological evaluation-
dc.typeArticle-
dc.identifier.doi10.1016/j.ejmech.2013.04.067-
dc.description.journalClass1-
dc.identifier.bibliographicCitationEUROPEAN JOURNAL OF MEDICINAL CHEMISTRY, v.65, pp.315 - 322-
dc.citation.titleEUROPEAN JOURNAL OF MEDICINAL CHEMISTRY-
dc.citation.volume65-
dc.citation.startPage315-
dc.citation.endPage322-
dc.description.journalRegisteredClassscie-
dc.description.journalRegisteredClassscopus-
dc.identifier.wosid000322850100031-
dc.identifier.scopusid2-s2.0-84878411252-
dc.relation.journalWebOfScienceCategoryChemistry, Medicinal-
dc.relation.journalResearchAreaPharmacology & Pharmacy-
dc.type.docTypeArticle-
dc.subject.keywordPlusMELANOMA-CELL LINE-
dc.subject.keywordPlusANTIPROLIFERATIVE ACTIVITY-
dc.subject.keywordPlus1,3,4-TRIARYLPYRAZOLE SCAFFOLD-
dc.subject.keywordPlusDERIVATIVES-
dc.subject.keywordPlusDIARYLAMIDES-
dc.subject.keywordPlusDIARYLUREAS-
dc.subject.keywordPlusDISCOVERY-
dc.subject.keywordAuthorAnticancer-
dc.subject.keywordAuthorCytotoxicity-
dc.subject.keywordAuthorDiarylurea-
dc.subject.keywordAuthorDiarylamide-
dc.subject.keywordAuthor1,3,4-Triarylpyrazole-
Appears in Collections:
KIST Article > 2013
Files in This Item:
There are no files associated with this item.
Export
RIS (EndNote)
XLS (Excel)
XML

qrcode

Items in DSpace are protected by copyright, with all rights reserved, unless otherwise indicated.

BROWSE