H. Xiang

发表

Structure-based design of potent and selective 3-phosphoinositide-dependent kinase-1 (PDK1) inhibitors.

S. Rabindran, N. Campobasso, V. Sudakin, 2011, Journal of medicinal chemistry.

Discovery of a new series of Aurora inhibitors through truncation of GSK1070916.

Ramona N Plant, M. A. Hardwicke, J. Axten, 2010, Bioorganic & medicinal chemistry letters.

Novel cyclohexyl-amides as potent antibacterials targeting bacterial type IIA topoisomerases.

S. Dabbs, D. Davies, Susanne Eyrisch, 2011, Bioorganic & medicinal chemistry letters.

Discovery of GSK1070916, a potent and selective inhibitor of Aurora B/C kinase.

Nicholas D. Adams, Ramona N Plant, J. Adams, 2010, Journal of medicinal chemistry.

Total enzymatic synthesis of cholecystokinin CCK-5

H. Xiang, H. Eckstein, L. Guo, 2004, Amino Acids.

Identification, Substrate Specificity, and Inhibition of theStreptococcus pneumoniae β-Ketoacyl-Acyl Carrier Protein Synthase III (FabH)*

M. Doyle, C. Silverman, S. Khandekar, 2001, The Journal of Biological Chemistry.

Highly efficient transparent air filter prepared by collecting-electrode-free bipolar electrospinning apparatus.

Yunze Long, Chao Song, H. Xiang, 2019, Journal of hazardous materials.

Dual Antimelanogenic Effect of Nicotinamide-Stabilized Phloretin Nanocrystals in Larval Zebrafish

H. Xiang, Xiaoqing Miao, Zhiyuan He, 2022, Pharmaceutics.

Bis-pyridyl-bis-amide-modulated a series of metal-organic frameworks: Formation, transformation and selectivity for the efficient detection of multiple analytes

Jian Luan, Yu Liu, Wenze Li, 2022, CrystEngComm.

Identification of peroxiredoxin II and its related molecules as potential biomarkers of dermal mesenchymal stem cell homing using network analysis

Taeho Kwon, Ying-Hao Han, H. Xiang, 2022, Applied Biological Chemistry.

Two new compounds from an endophytic fungus Alternaria solani

H. Xiang, Yong Shen, Da-Ke Zhao, 2012, Journal of Asian natural products research.

Structure of 4-chlorobenzoyl coenzyme A dehalogenase determined to 1.8 A resolution: an enzyme catalyst generated via adaptive mutation.

D. Dunaway-Mariano, H. Holden, M. Benning, 1996, Biochemistry.

Acyl-adenylate motif of the acyl-adenylate/thioester-forming enzyme superfamily: a site-directed mutagenesis study with the Pseudomonas sp. strain CBS3 4-chlorobenzoate:coenzyme A ligase.

D. Dunaway-Mariano, K. H. Chang, H. Xiang, 1997, Biochemistry.