Please use this identifier to cite or link to this item: https://scidar.kg.ac.rs/handle/123456789/19481
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dc.contributor.authorBranković, Jovica-
dc.contributor.authorMilovanović, Vesna-
dc.contributor.authorPetrović, Zorica D.-
dc.contributor.authorPetrović, Vladimir P.-
dc.date.accessioned2023-11-27T19:35:08Z-
dc.date.available2023-11-27T19:35:08Z-
dc.date.issued2021-
dc.identifier.isbn978-86-82172-01-7en_US
dc.identifier.urihttps://scidar.kg.ac.rs/handle/123456789/19481-
dc.description.abstractGallic hydrazones, as gallic acid derivatives, are known as pharmacophores of numerous multipotent agents. Among them, antiproliferative activity is one of the most important. On the other hand, thioredoxin reductase (TrxR1) is a part of the thioredoxin system, one of the most important systems responsible for maintaining the redox equilibrium inside the cell. It is overexpressed in different forms of tumors. Bearing this in mind, TrxR1 is a valid target for the development of compounds with potential antiproliferative activity. For this purpose, eight gallic acid-based hydrazones are selected and examined in silico for their potential inhibitory activity towards TrxR1en_US
dc.language.isoenen_US
dc.publisherKragujevac : University, Institute for Information Technologiesen_US
dc.relationMESTD - 451-03-9/2021-14/200122en_US
dc.subjectGallic aciden_US
dc.subjecthydrazonesen_US
dc.subjectmolecular dockingen_US
dc.subjectTrxR1en_US
dc.titleGALLIC ACID HYDRAZONES: ‘IN SILICO’ INHIBITION OF THIOREDOXIN REDUCTASEen_US
dc.typeconferenceObjecten_US
dc.description.versionPublisheden_US
dc.identifier.doi10.46793/ICCBI21.320Ben_US
dc.relation.conference1st International Conference on Chemo and BioInformatics, ICCBIKGen_US
dc.type.versionPublishedVersionen_US
Appears in Collections:Faculty of Agronomy, Čačak
Faculty of Science, Kragujevac

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