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Bioorganic & Medicinal Chemistry Letters|December 11, 2013
Asymmetric synthesis and receptor activity of chiral simplified resiniferatoxin (sRTX) analogues as transient receptor potential vanilloid 1 (TRPV1) ligandsMyeong Seop Kim, Yooran Ki, Song Yeon Ahn, et al.Journal of Medicinal Chemistry|April 6, 2017
N6-Substituted 5'-N-Methylcarbamoyl-4'-selenoadenosines as Potent and Selective A3 Adenosine Receptor Agonists with Unusual Sugar Puckering and Nucleobase OrientationJinha Yu, Long Xuan Zhao, Jongmi Park, et al.Bioorganic & Medicinal Chemistry|September 17, 2013
TRPV1 antagonist with high analgesic efficacy: 2-Thio pyridine C-region analogues of 2-(3-fluoro-4-methylsulfonylaminophenyl)propanamidesTae-Hwan Ha, Hyungchul Ryu, Sung-Eun Kim, et al.Bioorganic & Medicinal Chemistry Letters|May 5, 2015
α-Substituted 2-(3-fluoro-4-methylsulfonamidophenyl)acetamides as potent TRPV1 antagonistsPhuong-Thao Tran, Ho Shin Kim, Jihyae Ann, et al.Journal of Medicinal Chemistry|January 25, 2014
Synthesis and anti-renal fibrosis activity of conformationally locked truncated 2-hexynyl-N(6)-substituted-(N)-methanocarba-nucleosides as A3 adenosine receptor antagonists and partial agonistsAkshata Nayak, Girish Chandra, Inah Hwang, 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.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.The Journal of Biological Chemistry|August 26, 2015
The Cell Shape-determining Csd6 Protein from Helicobacter pylori Constitutes a New Family of L,D-CarboxypeptidaseHyoun Sook Kim, Ha Na Im, Doo Ri An, et al.Pageof 4