Please use this identifier to cite or link to this item: http://nopr.niscpr.res.in/handle/123456789/4549
Full metadata record
DC FieldValueLanguage
dc.contributor.authorChandrika, P Mani-
dc.contributor.authorYakaiah, T-
dc.contributor.authorNarsaiah, B-
dc.contributor.authorSridhar, V-
dc.contributor.authorVenugopal, G-
dc.contributor.authorRao, J Venkateshwara-
dc.contributor.authorKumar, K Pranay-
dc.contributor.authorMurthy, U S N-
dc.contributor.authorRao, A Raghu Ram-
dc.date.accessioned2009-06-09T11:52:56Z-
dc.date.available2009-06-09T11:52:56Z-
dc.date.issued2009-06-
dc.identifier.issn0376-4699-
dc.identifier.urihttp://hdl.handle.net/123456789/4549-
dc.description840-847en_US
dc.description.abstract A series of novel 2,4,6-trisubstituted quinazoline derivatives 6 have been synthesized from anthranilic acids 1 in five steps via benzoxazinones 2, N-benzoyl benzamides 3, quinazol-4-ones 4, 4-chloroquinazolines 5. Products 6 have been screened for antibacterial and cytotoxic activity, promising compounds have been identified. en_US
dc.language.isoen_USen_US
dc.publisherCSIRen_US
dc.sourceIJC-B Vol.48B(06) [June 2009]en_US
dc.subjectBenzoylationen_US
dc.subjectacylationen_US
dc.subjectcyclisationen_US
dc.subjectquinazolonesen_US
dc.subjectquinazolinesen_US
dc.titleSynthesis leading to novel 2,4,6-trisubstituted quinazoline derivatives, their antibacterial and cytotoxic activity against THP-1, HL-60 and A375 cell linesen_US
dc.typeArticleen_US
Appears in Collections:IJC-B Vol.48B(06) [June 2009]

Files in This Item:
File Description SizeFormat 
IJCB 48B(6) 840-847.pdf203.36 kBAdobe PDFView/Open


Items in NOPR are protected by copyright, with all rights reserved, unless otherwise indicated.