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Bioorganic & Medicinal Chemistry Letters|February 26, 2004
Synthesis and structure-activity relationship studies on a novel series of naphthylidinoylureas as inhibitors of acyl-CoA:cholesterol O-acyltransferase (ACAT)Satoshi Ohnuma, Masami Muraoka, Katsuhisa Ioriya, et al.Bioorganic & Medicinal Chemistry Letters|February 26, 2004
Orally active PDE4 inhibitors with therapeutic potentialHiroshi Ochiai, Tazumi Ohtani, Akiharu Ishida, et al.Bioorganic & Medicinal Chemistry Letters|September 20, 2005
Design, synthesis, and enzymatic property of a sulfur-substituted analogue of trigalacturonic acidKazunori Yamamoto, Naoki Watanabe, Hiroko Matsuda, et al.Bioorganic & Medicinal Chemistry Letters|September 27, 2005
Angiogenesis inhibitors derived from thalidomideTomomi Noguchi, Haruka Fujimoto, Hiroko Sano, et al.Bioorganic & Medicinal Chemistry Letters|September 27, 2005
New series of potent delta-opioid antagonists containing the H-Dmt-Tic-NH-hexyl-NH-R motifTingyou Li, Kimitaka Shiotani, Anna Miyazaki, et al.Bioorganic & Medicinal Chemistry Letters|December 8, 2004
Modulators of the human CCR5 receptor. Part 1: Discovery and initial SAR of 1-(3,3-diphenylpropyl)-piperidinyl amides and ureasJeremy N Burrows, John G Cumming, Shaun M Fillery, et al.Bioorganic & Medicinal Chemistry Letters|December 8, 2004
2,3-Ethylene- and 2,3-trimethylene-bridged analogues of the group III metabotropic glutamate receptor ligand 2-amino-4-phosphonobutanoic acidRodney L Johnson, Kolluri S S P RaoBioorganic & Medicinal Chemistry Letters|December 8, 2004
Design, synthesis and evaluation of 5-substituted amino-2,4-diamino-8-chloropyrimido-[4,5-b]quinolines as novel antimalarialsAdvait A Joshi, Sachin S Narkhede, C L ViswanathanBioorganic & Medicinal Chemistry Letters|December 8, 2004
N-hydroxy-2-(naphthalene-2-ylsulfanyl)-acetamide, a novel hydroxamic acid-based inhibitor of aminopeptidase N and its anti-angiogenic activityJiyong Lee, Joong Sup Shim, Sun-Ah Jung, et al.Bioorganic & Medicinal Chemistry Letters|December 8, 2004
Amino-substituted heterocycles as isosteres of trans-cinnamides: design and synthesis of heterocyclic biaryl sulfides as potent antagonists of LFA-1/ICAM-1 bindingGary T Wang, Sheldon Wang, Robert Gentles, et al.Pageof 2,632