Please use this identifier to cite or link to this item: http://nopr.niscpr.res.in/handle/123456789/61382
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dc.contributor.authorDesai, Siddharth-
dc.contributor.authorSastry, Girija-
dc.contributor.authorSingh Chatrapati, Kishore-
dc.date.accessioned2023-02-09T11:18:59Z-
dc.date.available2023-02-09T11:18:59Z-
dc.date.issued2023-01-
dc.identifier.issn2583-1321 (Online); 0019-5103 (Print)-
dc.identifier.urihttp://nopr.niscpr.res.in/handle/123456789/61382-
dc.description11-15en_US
dc.description.abstractPyrimidine heterocycles are proven to be biologically active heterocycles, found in many biological systems, displaying a broad spectrum of biological activities including anticancer, anxiolytic, antioxidant, antiviral, antifungal, anticonvulsant, antidepressant and antibacterial activities. New substituted 2-oxopyrimidines have been synthesized from the chalcones linked via indane-1,3-dione moity by the methods discussed in experimental section. We have synthesized some new 2-[6- (substituted phenyl)-2-oxo-1,2,5,6-tetrahydropyrimidin-4-yl]-indane-1,3-dione by reacting chalcones (step-1 compounds have been reported by us) with urea.en_US
dc.language.isoenen_US
dc.publisherNIScPR-CSIR, Indiaen_US
dc.sourceIJC Vol.62(01) [Jan 2023]en_US
dc.subjectChalconesen_US
dc.subjectPyrimidinesen_US
dc.subjectAntimicribial activityen_US
dc.subjectAntitubercular activityen_US
dc.subjectMicroplate Alamar Blue Assayen_US
dc.titleSynthesis, characterization, antimicrobial and antitubercular activity of some new pyrimidine derivativesen_US
dc.typeArticleen_US
dc.identifier.doihttps://doi.org/10.56042/ijc.v62i1.70345en_US
Appears in Collections:IJC Vol.62(01) [Jan 2023]

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