Hong Li

发表

Chemo-enzymatic synthesis of trimeric sialyl Lewisx pentadecasaccharide

M. Palcic, Yeuk-Chuen Liu, Hong Li, 2002 .

Development of a novel tricyclic class of potent and selective FIXa inhibitors.

J. Metzger, R. Berger, Hong Li, 2015, Bioorganic & medicinal chemistry letters.

Design, Synthesis, and Evaluation of Glycopeptides ContainingGlucosamine

Hong Li, Xiaoming Wang, P. Gao, 2014 .

Design, Synthesis, and Evaluation of Glycopeptides Containing Glucosamine

Hong Li, Xiaoming Wang, P. Gao, 2014 .

βGal(1→S-4)βGlcNAc-OR : A galactosidase-stable substrate for α(1→3)fucosyltransferase

M. Palcic, Yili Ding, Hong Li, 1998 .

Unexpected Enzymatic Fucosylation of the Hindered Tertiary Alcohol of 3-C-Methyl-N-Acetyllactosamine Produces a Novel Analogue of the LeX-Trisaccharide

M. Palcic, Hong Li, O. Hindsgaul, 1998 .

Synthesis, resolution and biological evaluation of cyclopropyl analogs of abscisic acid.

Hong Li, Xiaoqian Han, Yumei Xiao, 2015, Bioorganic & medicinal chemistry.

Synthesis and bioactivity of 2',3'-benzoabscisic acid analogs.

Hong Li, Xiaoqian Han, Yumei Xiao, 2015, Bioorganic & medicinal chemistry letters.

Frontal Affinity Chromatography Coupled to Mass Spectrometry: An Effective Method for Kd Determination and Screening of α‐Gal Derivatives Binding to Anti‐Gal Antibodies (IgG)

P. Wang, M. Palcic, Hong Li, 2003 .

Synthesis of GDP-5-thiosugars and their use as glycosyl donor substrates for glycosyltransferases.

M. Palcic, Hong Li, A. Otter, 2003, The Journal of organic chemistry.

Design, Synthesis and Evaluation of Novel Dehydroabietic Acid-Dithiocarbamate Hybrids as Potential Multi-Targeted Compounds for Tumor Cytotoxicity

Fangyao Li, Hong Li, Ya-Jun Wu, 2022, Arabian Journal of Chemistry.

Synthesis and biological activity of abscisic acid esters

Hong Li, Xiaoqian Han, Yumei Xiao, 2015 .

Design, synthesis and biological evaluation of novel trimethylpyrazine-2-carbonyloxy-cinnamic acids as potent cardiovascular agents

P. Zhan, Xinyong Liu, Hong Li, 2014 .

Synthesis and biological evaluation of a novel class of coumarin derivatives.

Hong Li, Xiaoming Wang, K. Cheng, 2014, Bioorganic & medicinal chemistry letters.

Synthesis and Bioactivities of Novel Pyrazole Oxime Derivatives Containing a 5-Trifluoromethylpyridyl Moiety

Hong Li, H. Dai, Yujun Shi, 2016, Molecules.

Biphenyl-substituted oxazolidinones as cholesteryl ester transfer protein inhibitors: modifications of the oxazolidinone ring leading to the discovery of anacetrapib.

Amjad Ali, S. Wright, Hong Li, 2011, Journal of medicinal chemistry.

Design, synthesis and evaluation of a novel class of glucosamine mimetic peptides containing 1,3-dioxane.

Hong Li, P. Gao, Meng Zhang, 2015, European journal of medicinal chemistry.

Synthesis, Antifungal Activity and QSAR of Some Novel Carboxylic Acid Amides

Hong Li, Shijie Du, Huizhe Lu, 2015, Molecules.

Sequential Interchange of Four Amino Acids from Blood Group B to Blood Group A Glycosyltransferase Boosts Catalytic Activity and Progressively Modifies Substrate Recognition in Human Recombinant Enzymes*

M. Palcic, Hong Li, S. Narang, 1997, The Journal of Biological Chemistry.

Synthesis of Ether‐ and Imino‐Linked Octyl N‐Acetyl‐5a′‐carba‐β‐lactosaminides and ‐isolactosaminides: Acceptor Substrates for α‐(1→3/4)‐Fucosyltransferase, and Enzymatic Synthesis of 5a′‐Carbatrisaccharides

M. Palcic, Hong Li, S. Ogawa, 1999 .

Pseudosugars. Part 40. Synthesis of Ether- and Imino-Linked Octyl N-Acetyl-5a′-carba-β-lactosaminides and -isolactosaminides: Acceptor Substrates for α-(1→3/4)-Fucosyltransferase, and Enzymatic Synthesis of 5a′-Carbatrisaccharides.

M. Palcic, Hong Li, S. Ogawa, 1999 .

Synthesis and initial evaluation of novel, non-peptidic antagonists of the alpha(v)-integrins alpha(v)beta(3) and alpha(v)beta(5).

M. Webb, M. Ohlmeyer, Hong Li, 2009, Bioorganic & medicinal chemistry letters.

Synthesis, Antifungal Activity and Structure-Activity Relationships of Novel 3-(Difluoromethyl)-1-methyl-1H-pyrazole-4-carboxylic Acid Amides

Hong Li, Shijie Du, Dongyan Yang, 2015, Molecules.