An‐Hu Li

Synthesis, CoMFA Analysis, and Receptor Docking of 3,5-Diacyl-2,4-Dialkylpyridine Derivatives as Selective A₃ Adenosine Receptor Antagonists

An‐Hu Li, Stefano Moro, Nancy E. Forsyth et al. · Journal of Medicinal Chemistry · 1999 · 179 citations · Full text

Methanocarba Analogues of Purine Nucleosides as Potent and Selective Adenosine Receptor Agonists

Kenneth A. Jacobson, Xiao‐duo Ji, An‐Hu Li et al. · Journal of Medicinal Chemistry · 2000 · 122 citations · Full text

Structure−Activity Relationships and Molecular Modeling of 3,5-Diacyl-2,4-dialkylpyridine Derivatives as Selective A₃ Adenosine Receptor Antagonists

An‐Hu Li, Stefano Moro, Neli Melman et al. · Journal of Medicinal Chemistry · 1998 · 121 citations · Full text

Adenosine Receptors, Heterocycle Chemistry, Experimental Pharmacology +18

A highly effective one-pot synthesis of quinolines from o-nitroarylcarbaldehydes

An‐Hu Li, Eilaf Ahmed, Xin Chen et al. · Organic & Biomolecular Chemistry · 2006 · 81 citations

Effective One-pot Synthesis, Engineering, Di-substituted Quinolines +7

OSI-930: A Novel Selective Inhibitor of Kit and Kinase Insert Domain Receptor Tyrosine Kinases with Antitumor Activity in Mouse Xenograft Models

Andrew J. Garton, Andrew P. Crew, Maryland Franklin et al. · Cancer Research · 2006 · 80 citations · Full text

Mouse Xenograft Models, Antitumor Activity, Chemoprevention Strategy +18