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Nucleosides, Nucleotides & Nucleic Acids|December 11, 2007
Stereoselective synthesis of homo-apioneplanocin A as potential inhibitor of S-adenosylhomocysteine hydrolaseMoon Woo Chun, Hyuk Woo Lee, Jin-Hee Kim, et al.Nucleosides, Nucleotides & Nucleic Acids|December 11, 2007
Synthesis and antitumor activity of fluorocyclopentenyl-pyrimidinesLak Shin Jeong, Long Xuan Zhao, Won Jun Choi, et al.Bioorganic & Medicinal Chemistry Letters|June 22, 2007
Design, synthesis, and molecular modeling studies of 5'-deoxy-5'-ureidoadenosine: 5'-ureido group as multiple hydrogen bonding donor in the active site of S-adenosylhomocysteine hydrolaseTing Wang, Hyun Joo Lee, Dilip K Tosh, et al.Bioorganic & Medicinal Chemistry|April 21, 2009
Structure-activity relationships of truncated adenosine derivatives as highly potent and selective human A3 adenosine receptor antagonistsShantanu Pal, Won Jun Choi, Seung Ah Choe, et al.Bioorganic & Medicinal Chemistry Letters|February 8, 2008
Structure-activity relationships of 2-chloro-N6-substituted-4'-thioadenosine-5'-N,N-dialkyluronamides as human A3 adenosine receptor antagonistsLak Shin Jeong, Hyuk Woo Lee, Hea Ok Kim, et al.Journal of Medicinal Chemistry|September 25, 2008
Structure-activity relationships of truncated D- and l-4'-thioadenosine derivatives as species-independent A3 adenosine receptor antagonistsLak Shin Jeong, Shantanu Pal, Seung Ah Choe, et al.Pageof 4