Synthesis of novel pyrimidine nucleoside analogues owning multiple bases/sugars and their glycosidase inhibitory activity

Show simple item record

dc.contributor.author Thakur, R K
dc.contributor.author Mishra, Akansha
dc.contributor.author Ramakrishna, K K G
dc.contributor.author Mahar, Rohit
dc.contributor.author Shukla, S K
dc.contributor.author Srivastava, A K
dc.contributor.author Tripathi, R P
dc.date.accessioned 2015-05-13T06:30:44Z
dc.date.available 2015-05-13T06:30:44Z
dc.date.issued 2014
dc.identifier.citation Tetrahedron, 2014, 70(45), 8462–8473 en
dc.identifier.uri http://hdl.handle.net/123456789/1450
dc.description.abstract A series of novel nucleoside analogues having dual bases (pyrimidine and triazole) and sugars have been synthesized by CuAAC reaction of azido sugars with propynylated pyrimidines. These compounds were evaluated for their in vitro α-glucosidase inhibitory activity. In this series, compounds 4b, 4d, 8a, 8b, 8c, 8e, 8g, 8h and 8i exhibited very good inhibition of α-glucosidase enzyme. Nucleoside analogues 8a, 4b, 8h and 8c displayed 47.4%, 41.8%, 39.4% and 34.6% inhibition respectively, comparable to the standard drug acarbose (53.4%). en
dc.format.extent 567596 bytes
dc.format.mimetype application/pdf
dc.language.iso en en
dc.relation.ispartofseries CSIR-CDRI communication No. 8805 en
dc.subject Pyrimidine Nucleosides en
dc.subject Triazoles en
dc.subject Azido Sugars en
dc.subject α-glucosidase en
dc.title Synthesis of novel pyrimidine nucleoside analogues owning multiple bases/sugars and their glycosidase inhibitory activity en
dc.type Article en


Files in this item

This item appears in the following Collection(s)

Show simple item record

Search DSpace


Advanced Search

Browse

My Account