Please use this identifier to cite or link to this item: http://gukir.inflibnet.ac.in:8080/jspui/handle/123456789/4784
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dc.contributor.authorBiradar J.S
dc.contributor.authorSomappa S.B.
dc.date.accessioned2020-06-12T15:04:53Z-
dc.date.available2020-06-12T15:04:53Z-
dc.date.issued2012
dc.identifier.citationDer Pharmacia Lettre , Vol. 4 , 1 , p. 344 - 348en_US
dc.identifier.urihttp://gukir.inflibnet.ac.in:8080/jspui/handle/123456789/4784-
dc.description.abstractDue to the rapid bacterial resistance to antibacterial agents, it is vital to discover novel scaffold for the design of new antibacterial agents to help in the battle against pathogenic microorganisms. Herewith, a series of novel indolyl pyrimidine analogues were evaluated for their antimicrobial activity. The antibacterial activity was carried out against E. coli, B. subtilis and S. aureus. Compounds i, f & c have shown maximum zone of inhibition and a, g & h have shown good zone of inhibition against all the three bacteria. In antifungal activity against A. niger, A. flavus and A. oryzae, compounds i, f & c have shown excellent potency with maximum zone of inhibition and a & c have shown moderate activity against all the three fungi. Hence, compounds i, f & c with interesting results have emerged as most potent antimicrobial agents.en_US
dc.subjectAntibacterial activity
dc.subjectAntifungal activity
dc.subjectIndole
dc.subjectPyrimidines
dc.title2,5-Disubstituted novel indolyl pyrimidine analogues as potent antimicrobial agentsen_US
dc.typeArticle
Appears in Collections:1. Journal Articles

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