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dc.contributor.authorKazan, F.
dc.contributor.authorYagci, Z.B.
dc.contributor.authorBai, R.
dc.contributor.authorOzkirimli, E.
dc.contributor.authorHamel, E.
dc.contributor.authorOzkirimli, S.
dc.date.accessioned2021-12-21T08:40:54Z
dc.date.available2021-12-21T08:40:54Z
dc.date.issued2019
dc.identifier.issn14769271
dc.identifier.urihttps://doi.org/10.1016/j.compbiolchem.2019.05.002
dc.identifier.urihttp://dspace.yeniyuzyil.edu.tr:8080/xmlui/handle/20.500.12629/1242
dc.description.abstractA new series of N’-(substituted phenyl)-5-chloro/iodo-3-phenyl-1H-indole-2-carbohydrazide (5, 6) and N-[2-(substituted phenyl)-4-oxo-1,3-thiazolidin-3-yl]-5-iodo/chloro-3-phenyl-1H-indole-2-carboxamide (7, 8) derivatives were synthesized and evaluated for
dc.description.sponsorshipThis work was supported by the Istanbul University Scientific Research Projects Unit [project number T-721/30062005]. EO thanks Prof Amedeo Caflisch for hosting her at University of Zurich. We thank the Developmental Therapeutics Program of the National C
dc.language.isoEnglish
dc.publisherElsevier Ltd
dc.titleSynthesis and biological evaluation of indole-2-carbohydrazides and thiazolidinyl-indole-2-carboxamides as potent tubulin polymerization inhibitors
dc.typeArticle
dc.relation.journalComputational Biology and Chemistry
dc.identifier.startpage512
dc.identifier.endpage523
dc.identifier.volume80
dc.identifier.doi10.1016/j.compbiolchem.2019.05.002
dc.relation.volume80


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