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FEBS Letters|May 13, 2014
Targeting Nrf2 by dihydro-CDDO-trifluoroethyl amide enhances autophagic clearance and viability of β-cells in a setting of oxidative stressWenjuan Li, Weiwei Wu, Haibo Song, et al.American Journal of Nephrology|June 7, 2014
Mechanisms contributing to adverse cardiovascular events in patients with type 2 diabetes mellitus and stage 4 chronic kidney disease treated with bardoxolone methylMelanie P Chin, Scott A Reisman, George L Bakris, et al.Bioorganic & Medicinal Chemistry Letters|September 11, 2004
Discovery of potent and orally bioavailable N,N'-diarylurea antagonists for the CXCR2 chemokine receptorQi Jin, Hong Nie, Brent W McCleland, et al.Journal of Medicinal Chemistry|October 14, 2009
Antagonists of the calcium receptor. 2. Amino alcohol-based parathyroid hormone secretagoguesRobert W Marquis, Amparo M Lago, James F Callahan, et al.Journal of Medicinal Chemistry|June 5, 2009
Antagonists of the calcium receptor I. Amino alcohol-based parathyroid hormone secretagoguesRobert W Marquis, Amparo M Lago, James F Callahan, et al.Bioorganic & Medicinal Chemistry Letters|January 24, 2007
Comparison of N,N'-diarylsquaramides and N,N'-diarylureas as antagonists of the CXCR2 chemokine receptorBrent W McCleland, Roderick S Davis, Michael R Palovich, et al.Journal of Medicinal Chemistry|September 2, 2005
4-Aryl-1,2,3-triazole: a novel template for a reversible methionine aminopeptidase 2 inhibitor, optimized to inhibit angiogenesis in vivoLara S Kallander, Qing Lu, Wenfang Chen, et al.Bioorganic & Medicinal Chemistry Letters|April 2, 2003
Phenylbutyrates as potent, orally bioavailable vitronectin receptor (integrin alphavbeta3) antagonistsWilliam H Miller, Peter J Manley, Russell D Cousins, et al.Journal of Medicinal Chemistry|March 3, 2006
Structure activity relationships of 5-, 6-, and 7-methyl-substituted azepan-3-one cathepsin K inhibitorsDennis S Yamashita, Robert W Marquis, Ren Xie, et al.Pageof 7