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DC Field | Value | Language |
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dc.contributor.author | Patel, Bhumika | - |
dc.date.accessioned | 2015-01-24T05:17:43Z | - |
dc.date.available | 2015-01-24T05:17:43Z | - |
dc.date.issued | 2014 | - |
dc.identifier.uri | http://hdl.handle.net/123456789/5330 | - |
dc.description | European Journal of Medicinal Chemistry 74 (2014) 574e605 | en_US |
dc.description.abstract | Dipeptidyl peptidase-4 (DPP-4) is one of the widely explored novel targets for Type 2 diabetes mellitus (T2DM) currently. Research has been focused on the strategy to preserve the endogenous glucagon like peptide (GLP)-1 activity by inhibiting the DPP-4 action. The DPP-4 inhibitors are weight neutral, well tolerated and give better glycaemic control over a longer duration of time compared to existing conventional therapies. The journey of DPP-4 inhibitors in the market started from the launch of sitagliptin in 2006 to latest drug teneligliptin in 2012. This review is mainly focusing on the recent medicinal aspects and advancements in the designing of DPP-4 inhibitors with the therapeutic potential of DPP-4 as a target to convey more clarity in the diffused data. Peptidomimetics | en_US |
dc.publisher | Elsevier | en_US |
dc.relation.ispartofseries | IPFP0138; | - |
dc.subject | Dipeptidyl peptidase-4 | en_US |
dc.subject | Glucagon like peptide (GLP)-1 | en_US |
dc.subject | Non-peptidomimetics | en_US |
dc.subject | Diabetes | en_US |
dc.title | Recent approaches to medicinal chemistry and therapeutic potential of dipeptidyl peptidase-4 (DPP-4) inhibitors | en_US |
dc.type | Faculty Papers | en_US |
Appears in Collections: | Faculty Papers |
Files in This Item:
File | Description | Size | Format | |
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IPFP0138.pdf | IPFP0138 | 4.45 MB | Adobe PDF | ![]() View/Open |
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