Synthesis of novel pyrimidine nucleoside analogues owning multiple bases/sugars and their glycosidase inhibitory activity
IR@CDRI: CSIR-Central Drug Research Institute, Lucknow
View Archive Info| Field | Value | |
| Creator |
Thakur, R K
Mishra, Akansha Ramakrishna, K K G Mahar, Rohit Shukla, S K Srivastava, A K Tripathi, R P |
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| Date |
2015-05-13T06:30:44Z
2015-05-13T06:30:44Z 2014 |
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| Identifier |
Tetrahedron, 2014, 70(45), 8462–8473
http://hdl.handle.net/123456789/1450 |
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| 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%).
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| Format |
567596 bytes
application/pdf |
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| Language |
en
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| Relation |
CSIR-CDRI communication No. 8805
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| Subject |
Pyrimidine Nucleosides
Triazoles Azido Sugars α-glucosidase |
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| Title |
Synthesis of novel pyrimidine nucleoside analogues owning multiple bases/sugars and their glycosidase inhibitory activity
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| Type |
Article
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