"目录号: HY-14291
Vildagliptin (LAF-237; NVP-LAF 237)能抑制DPP-4,IC50为2.3 nM。
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Description
Vildagliptin (LAF-237; NVP-LAF 237) inhibits DPP-4 with IC50 of 2.3 nM.IC50 Value: 2.3 nM[1]Target: DPP-4in vitro: Vildagliptin is an N-substituted glycyl-2-cyanopyrrolidine (figure 2). It is a potent competitive and reversible inhibitor of human and rodent DPP-4 in vitro, with a median inhibitory concentration (IC50) ~2-3 nmol/L. Importantly, vildagliptin inhibits DPP-4 with high specificity relative to other similar peptidases where its IC50 exceeds 200 mol/L [1].in vivo: Compared to age-, gender-, BMI-matched subjects with normal renal function, the mean AUC of vildagliptin after 14 days in patients with mild, moderate, and severe RI increased by 40%, 71%, and 100%, respectively [2]. The treatment was effective in modulating stress in pancreatic tissue, both by reducing levels of stress markers as well as by increasing activity of SOD and catalase. After analyzing the pancreatic histology, we found that vildagliptin was also able to preserve islets and pancreatic β-cells, especially at the concentration of 5 mg/kg [3].Clinical trial: FDA approved drug.
Clinical Trial
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Pusan National University Hospital
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Lund University
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Medical University of Vienna
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Rio de Janeiro State University-Laboratory for Clinical and Experimental Research on Vascular Biology
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Dr. José Fernando Vilela-Martin MD PhD-Novartis-Hospital de Base
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Lund University
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Johann Wolfgang Goethe University Hospital
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Novartis Pharmaceuticals-Novartis
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Novartis
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Novartis Pharmaceuticals-Novartis
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Seoul National University Bundang Hospital
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Federal University of S?o Paulo-Novartis
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Genuine Research Center, Egypt-EVA pharma, Egypt
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February 2014
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Novartis
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July 2007
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Radboud University
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January 2010
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Novartis
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Novartis
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Novartis
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Novartis Pharmaceuticals-Novartis
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Novartis Pharmaceuticals-Novartis
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Azienda Ospedaliero-Universitaria di Parma
Type 2