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dc.contributor.authorTatar, Esra
dc.contributor.authorŞenkardeş, Sevil
dc.contributor.authorSellitepe, Hasan Erdinç
dc.contributor.authorKüçükgüzel, Şükriye Güniz
dc.contributor.authorKaraoğlu, Şengül Alpay
dc.contributor.authorBozdeveci, Arif
dc.contributor.authorKüçükgüzel, İlkay
dc.date.accessioned2020-12-19T20:22:55Z
dc.date.available2020-12-19T20:22:55Z
dc.date.issued2016
dc.identifier.issn1300-0527
dc.identifier.issn1303-6130
dc.identifier.urihttps://app.trdizin.gov.tr/makale/TWpVMk1EZzNOdz09
dc.identifier.urihttps://hdl.handle.net/11436/4586
dc.description.abstractA series of 38 new acylhydrazones [3{40], derived from (2S)-4-(methylsulfanyl)-2-[[(4-methylphenyl)sulfonyl]amino]butanoic acid hydrazide [2], were synthesized and evaluated for their anti-HIV and antimicrobial activity withthe further aim to develop acylhydrazones carrying an amino acid side chain. All tested compounds possess strongeractivity against gram (+) bacteria. Compound23was found active against methicillin-resistantStaphylococcus aureus(MRSA) with a MIC value of 3.9?g/mL. The MIC value of compound30againstEnterococcus faecalis,Listeriamonocytogenes, andBacillus cereuswas 8?g/mL. A computational study for prediction of ADME and drug-likeproperties (solubility, drug-likeness, and drug score) as well as potential toxicity pro les of compounds2{40wasperformed using the Molinspiration online property calculation toolkit and Osiris Property Explorer. As most of ourcompounds meet Lipinski\'s rule of ve, they promise good solubility and permeability. According to Osiris calculations,the majority of our compounds are supposed to be nonmutagenic and nonirritating.en_US
dc.language.isoengen_US
dc.rightsinfo:eu-repo/semantics/closedAccessen_US
dc.subjectMühendislik, Kimyaen_US
dc.titleSynthesis, and prediction of molecular properties and antimicrobial activity ofsome acylhydrazones derived fromN-(arylsulfonyl)methionineen_US
dc.typearticleen_US
dc.contributor.departmentRTEÜen_US
dc.identifier.volume40en_US
dc.identifier.issue3en_US
dc.identifier.startpage510en_US
dc.identifier.endpage534en_US
dc.ri.editoaen_US
dc.relation.journalTurkish Journal of Chemistryen_US
dc.relation.publicationcategoryMakale - Ulusal Hakemli Dergi - Kurum Öğretim Elemanen_US


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