Please use this identifier to cite or link to this item: http://nopr.niscair.res.in/handle/123456789/14508
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dc.contributor.authorBalakumar, C-
dc.contributor.authorKishore, D Pran-
dc.contributor.authorRao, K Venkat-
dc.contributor.authorNarayana, B Lakshmi-
dc.contributor.authorRajwinder, K-
dc.contributor.authorRajkumar, V-
dc.contributor.authorRao, A Raghuram-
dc.date.accessioned2012-08-06T07:28:58Z-
dc.date.available2012-08-06T07:28:58Z-
dc.date.issued2012-08-
dc.identifier.issn0975-0983(Online); 0376-4699(Print)-
dc.identifier.urihttp://hdl.handle.net/123456789/14508-
dc.description1105-1113en_US
dc.description.abstractA series of new 4H-pyrimido[2,1-b]benzothiazole-2-arylamino-3-cyano-4-ones 6a-g have been designed and synthesized by the application of microwave-assisted organic synthesis (MAOS) technique. In silico docking studies have been carried out to gain an insight into the hypothetical binding motif of the title compounds using a homology model of A2B adenosine receptor employing GOLD (CCDC, 4.0.1 version) software. The binding modes are proposed on the basis of molecular docking studies. en_US
dc.language.isoen_USen_US
dc.publisherNISCAIR-CSIR, Indiaen_US
dc.rights CC Attribution-Noncommercial-No Derivative Works 2.5 Indiaen_US
dc.sourceIJC-B Vol.51B(08) [August 2012]en_US
dc.subject4H-pyrimido[2,1-b]benzothiazole-4-oneen_US
dc.subjectAdenosine receptor antagonistsen_US
dc.subjectdocking studiesen_US
dc.subjectMicrowave-assisted organic synthesisen_US
dc.subjectGOLDen_US
dc.titleDesign, microwave-assisted synthesis and in silico docking studies of new 4H-pyrimido[2,1-b]benzothiazole-2-arylamino-3-cyano-4-ones as possible adenosine A2B receptor antagonistsen_US
dc.typeArticleen_US
Appears in Collections:IJC-B Vol.51B(08) [August 2012]

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