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dc.creatorSrećo Zelenović, Bojana
dc.creatorKekezović, Slađana
dc.creatorKojić, Vesna V.
dc.creatorBenedeković, Goran
dc.creatorJadranin, Milka
dc.creatorPopsavin, Mirjana
dc.creatorPopsavin, Velimir
dc.date.accessioned2024-01-04T15:03:09Z
dc.date.available2024-01-04T15:03:09Z
dc.date.issued2019
dc.identifier.urihttps://cer.ihtm.bg.ac.rs/handle/123456789/7275
dc.description.abstract(-)-Goniofufurone (1) is a synthetic styryl lactone that exhibits significant antitumor activity. In the search for new and more potent antitumor agents the synthesis of lactones 5 and 6 was planned from D-glucose. Compounds 5 and 6 are designed as dephenylated analogues of 1 (Figure 1). The results of the evaluation of antiproliferative activity of 5 and 6 against a number of human tumor cell lines, as well as the structure-activity relationship (SAR), will be presented and discussed in details.sr
dc.language.isoensr
dc.publisherValahia University of Targovistesr
dc.publisherUniversity Politehnica of Bucharestsr
dc.relationinfo:eu-repo/grantAgreement/MESTD/Basic Research (BR or ON)/172006/RS//sr
dc.rightsopenAccesssr
dc.rights.urihttps://creativecommons.org/licenses/by/4.0/
dc.sourceBook of Abstracts - 9th International Conferences of the Chemical Societies of the South-Eastern European Countries, ICOSECS9, "Chemistry a Nature Challenger", Targoviste, Romaniasr
dc.subject(-)-Goniofufuronesr
dc.subjectsynthesissr
dc.subjectD-glucosesr
dc.subjectantiproliferative activitysr
dc.subjectstructure-activity relationshipsr
dc.titleSynthesis and antitumour activity of two dephenilated (-)-goniofufurone analoguessr
dc.typeconferenceObjectsr
dc.rights.licenseBYsr
dc.citation.spageS3_P16
dc.citation.epageS3_P16
dc.identifier.rcubhttps://hdl.handle.net/21.15107/rcub_cer_7275
dc.identifier.fulltexthttp://cer.ihtm.bg.ac.rs/bitstream/id/29163/M34_27.pdf
dc.type.versionpublishedVersionsr


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