| dc.contributor.author | Kushwaha, R N | |
| dc.contributor.author | Haq, W | |
| dc.contributor.author | Katti, S B | |
| dc.date.accessioned | 2014-09-19T07:57:09Z | |
| dc.date.available | 2014-09-19T07:57:09Z | |
| dc.date.issued | 2014 | |
| dc.identifier.citation | Chemistry & Biology Interface, 2014, 4(3), 137-162 | en |
| dc.identifier.uri | http://hdl.handle.net/123456789/1409 | |
| dc.description.abstract | Gliptins, commonly known as clinical DPP-IV inhibitors have become a new class of potential drug candidate and are being hoped as a permanent eraser for type 2 diabetes. Therefore, gliptins have been a centre of research and development. As a result of the efforts made towards developing effective gliptins, the first clinical proof of concept for efficacy was confirmed in 1998 when NVP-DPP728 came into focus. Thus, from 1998 to 2014, these 17-years of the heightened research towards drug discovery has resulted in seventeen gliptins. Among these, eight gliptins are currently approved and in clinical usages for type 2 diabetes therapies, while others are in different stages of clinical trials. This review covers the various approaches and methodologies used in the syntheses of only those DPP-IV inhibitors in clinical uses having suffix gliptin. In addition, it also encompasses their biological activity and their binding interactions in the active site of DPP-IV that are responsible for their drug candidacy. | en |
| dc.format.extent | 724148 bytes | |
| dc.format.mimetype | application/pdf | |
| dc.language.iso | en | en |
| dc.relation.ispartofseries | CSIR-CDRI Communication No. 8713 | en |
| dc.subject | Discovery | en |
| dc.subject | Gliptins | en |
| dc.subject | 17-Years of Research for the Treatment | en |
| dc.subject | Type 2 Diabetes | en |
| dc.subject | Ynthetic Overview | en |
| dc.title | Discovery of 17 Gliptins in 17-Years of Research for the Treatment of Type 2 Diabetes: A Synthetic Overview | en |
| dc.type | Article | en |