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dc.creatorTratrat, Christophe
dc.creatorHaroun, Michelyne
dc.creatorPaparisva, Aliki
dc.creatorGeronikaki, Athina
dc.creatorCamoutsis, Charalabos
dc.creatorĆirić, Ana
dc.creatorGlamočlija, Jasmina
dc.creatorSoković, Marina
dc.creatorFotakis, Charalmpos
dc.creatorZoumpoulakis, Panagiotis
dc.creatorBhunia, Shome
dc.creatorSaxena, Anil
dc.date.accessioned2021-09-02T13:31:27Z
dc.date.available2021-09-02T13:31:27Z
dc.date.issued2018
dc.identifier.issn1878-5352
dc.identifier.urihttps://radar.ibiss.bg.ac.rs/handle/123456789/4306
dc.description.abstractAs a part of our ongoing studies in developing new derivatives as antimicrobial agents we describe the synthesis of novel substituted 5-benzylideno-2-adamantylthiazol[3,2-b][1,2,4]triazol-6 (5H)ones.The twenty-five newly synthesized compounds were tested for their antimicrobial and antifungal activity. All compounds have shown antibacterial properties with compounds 1–9 showing the lowest activity, followed by compounds 10–14 while compounds 15–25 the highest antibacterial activity. Specific compounds appeared to be more active than ampicillin in most studied strains and in some cases more active than streptomycin. Antifungal activity in most cases also was better than that of reference drugs ketoconazole and bifonazole. Elucidating the relation of molecular properties to antimicrobial activity as well as generation of pharmacophore model for antifungal activity of two fungal species Aspergillus fumigatus and Candida albicans were performed.sr
dc.language.isoensr
dc.publisherElsevier B.V. on behalf of King Saud Universitysr
dc.rightsopenAccesssr
dc.rights.urihttps://creativecommons.org/licenses/by/4.0/
dc.sourceArabian Journal of Chemistrysr
dc.subjectAdamantlythiazolessr
dc.subjectAnti-inflammatorysr
dc.subjectAntibacterialsr
dc.subjectAntifungalsr
dc.subjectPharmacophoresr
dc.subjectSARsr
dc.titleDesign, synthesis and biological evaluation of new substituted 5-benzylideno-2-adamantylthiazol[3,2- b][1,2,4]triazol-6(5H)ones. Pharmacophore models for antifungal activitysr
dc.typearticlesr
dc.rights.licenseBY-NC-NDsr
dcterms.abstractПапарисва, Aлики; Хароун, Мицхелyне; Ћирић, Aна; Саxена, Aнил; Тратрат, Цхристопхе; Героникаки, Aтхина; Цамоутсис, Цхаралабос; Бхуниа, Схоме; Зоумпоулакис, Панагиотис; Фотакис, Цхаралмпос; Соковић, Марина; Гламочлија, Јасмина;
dc.rights.holder© 2016 The Authors. Production and hosting by Elsevier B.V. on behalf of King Saudsr
dc.citation.issue4
dc.citation.volume11
dc.identifier.doi10.1016/j.arabjc.2016.06.007
dc.identifier.scopus2-s2.0-84978525382
dc.identifier.wos000438122800013
dc.citation.spage573
dc.citation.epage590
dc.type.versionpublishedVersionsr
dc.identifier.fulltexthttps://radar.ibiss.bg.ac.rs/bitstream/id/8666/bitstream_8666.pdf
dc.citation.rankM21


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