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Bioorganic & Medicinal Chemistry|May 6, 2014
Synthesis, biological, and biophysical studies of DAG-indololactones designed as selective activators of RasGRPLia C Garcia, Lucia Gandolfi Donadío, Ella Mann, et al.
Bioorganic & Medicinal Chemistry Letters|June 21, 2014
2-Alkyl/alkenyl substituted pyridine C-region analogues of 2-(3-fluoro-4-methylsulfonylaminophenyl)propanamides as highly potent TRPV1 antagonistsHyungChul Ryu, Sejin Seo, Seong-Hee Cho, et al.
Journal of Medicinal Chemistry|March 17, 2006
Branched diacylglycerol-lactones as potent protein kinase C ligands and alpha-secretase activatorsJeewoo Lee, Ji-Hye Kang, Kee-Chung Han, et al.
Bioorganic & Medicinal Chemistry Letters|July 12, 2014
2-Aryl substituted pyridine C-region analogues of 2-(3-fluoro-4-methylsulfonylaminophenyl)propanamides as highly potent TRPV1 antagonistsHyungChul Ryu, Sejin Seo, Myeong Seop Kim, et al.
Bioorganic & Medicinal Chemistry|January 10, 2012
2-(4-Methylsulfonylaminophenyl) propanamide TRPV1 antagonists: Structure-activity relationships in the B and C-regionsWei Sun, Keliang Liu, HyungChul Ryu, et al.
Bioorganic & Medicinal Chemistry|December 16, 2011
N-4-t-Butylbenzyl 2-(4-methylsulfonylaminophenyl) propanamide TRPV1 antagonists: Structure-activity relationships in the A-regionYong Soo Kim, Min-Jung Kil, Sang-Uk Kang, et al.
Bioorganic & Medicinal Chemistry|February 11, 2016
2-Sulfonamidopyridine C-region analogs of 2-(3-fluoro-4-methylsulfonamidophenyl)propanamides as potent TRPV1 antagonistsJihyae Ann, Yooran Ki, Suyoung Yoon, et al.
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