H. Liu

发表

Copper-catalyzed C–N coupling of amides and nitrogen-containing heterocycles in the presence of cesium fluoride

Xiaohui He, D. Phillips, Xuefeng Zhu, 2009 .

Design and synthesis of arylaminoethyl amides as noncovalent inhibitors of cathepsin S. Part 1.

Jennifer L. Harris, R. Epple, B. Bursulaya, 2005, Bioorganic & medicinal chemistry letters.

Characterization of a novel, brain-penetrating CB1 receptor inverse agonist: metabolic profile in diet-induced obese models and aspects of central activity

P. McNamara, J. Gromada, S. Commerford, 2011, Naunyn-Schmiedeberg's Archives of Pharmacology.

Bicyclic carbamates as inhibitors of papain-like cathepsin proteases.

Jennifer L. Harris, D. Mason, R. Epple, 2007, Bioorganic & medicinal chemistry letters.

Synthesis and SAR of succinamide peptidomimetic inhibitors of cathepsin S.

Jennifer L. Harris, A. Chatterjee, R. Epple, 2007, Bioorganic & medicinal chemistry letters.

Synthesis and evaluation of arylaminoethyl amides as noncovalent inhibitors of cathepsin S. Part 3: heterocyclic P3.

Jun Li, Glen Spraggon, Tove Tuntland, 2006, Bioorganic & medicinal chemistry letters.

Synthesis and antitumor activity of heterocyclic acid ester derivatives of 20S-camptothecins

Y. Li, Jing Yang, H. Liu, 2007 .

Highly efficient synthesis of fused bicyclic 2,3-diaryl-pyrimidin-4(3H)-ones via Lewis acid assisted cyclization reaction

Kunyong Yang, H. Liu, Zhicheng Wang, 2008 .

Synthesis and cytotoxic activity of heterocycle-substituted phthalimide derivatives

H. Liu, Jian-shuang Jiang, Yanan Yang, 2010 .

Synthesis of a potential tetrasaccharide ligand for E-selectin.

H. Liu, M. Cai, Hui Li, 2002, Carbohydrate research.

Identification of Potent and Selective RIPK2 Inhibitors for the Treatment of Inflammatory Diseases.

Tao Jiang, Bo Liu, Glen Spraggon, 2017, ACS medicinal chemistry letters.

Facile synthesis and cytotoxicity of 5-C-alkylates of 20(S)-camptothecins

Song Wu, H. Liu, Xian-dao Pan, 2008 .

Discovery and profiling of a selective and efficacious Syk inhibitor.

Eric Vangrevelinghe, E. Vangrevelinghe, Christian C. Lee, 2015, Journal of medicinal chemistry.

Syk inhibitors with high potency in presence of blood.

Jianwei Che, E. Vangrevelinghe, Christian C. Lee, 2014, Bioorganic & medicinal chemistry letters.

Synthesis and SAR of arylaminoethyl amides as noncovalent inhibitors of cathepsin S: P3 cyclic ethers.

Jun Li, Glen Spraggon, Tove Tuntland, 2006, Bioorganic & medicinal chemistry letters.

Arylaminoethyl carbamates as a novel series of potent and selective cathepsin S inhibitors.

Jun Li, Tove Tuntland, Jennifer L. Harris, 2006, Bioorganic & medicinal chemistry letters.

Arylaminoethyl amides as noncovalent inhibitors of cathepsin S. Part 2: Optimization of P1 and N-aryl.

Jennifer L. Harris, A. Chatterjee, T. Hollenbeck, 2006, Bioorganic & Medicinal Chemistry Letters.