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|Title:||Synthesis of novel pyrimidine nucleoside analogues owning multiple bases/sugars and their glycosidase inhibitory activity|
|Authors:||Thakur, R K;Mishra, Akansha;Ramakrishna, K K G;Mahar, Rohit;Shukla, S K;Srivastava, A K;Tripathi, R P|
|Keywords:||Pyrimidine Nucleosides;Triazoles;Azido Sugars;α-glucosidase|
|Description:||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%).|
|URI:||Tetrahedron, 2014, 70(45), 8462–8473|
|Appears in Collections:||Medicinal and Process Chemistry|
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