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Discovery of Novel Tricyclic Heterocycles as Potent and Selective DPP-4 Inhibitors for the Treatment of Type 2 Diabetes
[Image: see text] In our efforts to develop second generation DPP-4 inhibitors, we endeavored to identify distinct structures with long-acting (once weekly) potential. Taking advantage of X-ray cocrystal structures of sitagliptin and other DPP-4 inhibitors, such as alogliptin and linagliptin bound t...
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Опубликовано в: : | ACS Med Chem Lett |
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Главные авторы: | , , , , , , , , , , , , , , , |
Формат: | Artigo |
Язык: | Inglês |
Опубликовано: |
American Chemical
Society
2016
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Online-ссылка: | https://ncbi.nlm.nih.gov/pmc/articles/PMC4867478/ https://ncbi.nlm.nih.gov/pubmed/27190600 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1021/acsmedchemlett.6b00027 |
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