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dc.creatorDimopoulou A., Manta S., Parmenopoulou V., Kollatos N., Christidou O., Triantakonstanti V.V., Schols D., Komiotis D.en
dc.date.accessioned2023-01-31T07:56:35Z
dc.date.available2023-01-31T07:56:35Z
dc.date.issued2015
dc.identifier10.3389/fchem.2015.00021
dc.identifier.issn22962646
dc.identifier.urihttp://hdl.handle.net/11615/73350
dc.description.abstractWe describe the synthesis of C8-alkynyl adenine pyranonucleosides 4, 5, and 8-phenylethynyl-adenine (II), via Sonogashira cross-coupling reaction under microwave irradiation. Compounds 4e and II were less cytostatic than 5-fluorouracil (almost an order of magnitude) against murine leukemia (L1210) and human cervix carcinoma (HeLa) cells, while the same compounds proved to be more active than 5-fluorouracil against human lymphocyte (CEM) cells. © 2015 Dimopoulou, Manta, Parmenopoulou, Kollatos, Christidou, Triantakonstanti, Schols and Komiotis.en
dc.language.isoenen
dc.sourceFrontiers in Chemistryen
dc.source.urihttps://www.scopus.com/inward/record.uri?eid=2-s2.0-84969174858&doi=10.3389%2ffchem.2015.00021&partnerID=40&md5=a885c0364d64b79089de76e787c8f69f
dc.subjectFrontiers Media S. Aen
dc.titleAn easy microwave-assisted synthesis of C8-alkynyl adenine pyranonucleosides as novel cytotoxic antitumor agentsen
dc.typejournalArticleen


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