M. Cui

发表

Transmembrane 4 L Six Family Member 5 Senses Arginine for mTORC1 Signaling.

J. Jung, S. J. Y. Macalino, M. Cui, 2019, Cell metabolism.

Transient receptor potential vanilloid type 1 antagonists: a patent review (2011 – 2014)

M. Cui, Sun Choi, P. K. Sharma, 2015, Expert opinion on therapeutic patents.

Synthesis and Anti-Renal Fibrosis Activity of Conformationally Locked Truncated 2-Hexynyl-N6-Substituted-(N)-Methanocarba-nucleosides as A3 Adenosine Receptor Antagonists and Partial Agonists

Steven M. Moss, K. Jacobson, M. Cui, 2014, Journal of medicinal chemistry.

Synthesis and evaluation of peptidyl α,β-unsaturated carbonyl derivatives as anti-malarial calpain inhibitors

Da Yu Li, Shyam Kumar Mallik, M. Cui, 2012, Archives of Pharmacal Research.

Polymodal Transient Receptor Potential Vanilloid Type 1 Nocisensor: Structure, Modulators, and Therapeutic Applications.

M. Cui, Sun Choi, S. Basith, 2016, Advances in protein chemistry and structural biology.

5-Lipoxygenase inhibitors suppress RANKL-induced osteoclast formation via NFATc1 expression.

M. Cui, Sun Choi, H. Chang, 2015, Bioorganic & medicinal chemistry.

Discovery of Conformationally Restricted Human Glutaminyl Cyclase Inhibitors as Potent Anti-Alzheimer's Agents by Structure-Based Design.

S. J. Y. Macalino, M. Cui, Sun Choi, 2019, Journal of medicinal chemistry.

Potent human glutaminyl cyclase inhibitors as potential anti-Alzheimer's agents: Structure-activity relationship study of Arg-mimetic region.

M. Cui, Sun Choi, Jiyoun Lee, 2018, Bioorganic & medicinal chemistry.

Synthesis and biological evaluation of 3-substituted 5-benzylidene-1-methyl-2-thiohydantoins as potent NADPH oxidase (NOX) inhibitors.

M. Cui, Sun Choi, Y. Bae, 2016, Bioorganic & medicinal chemistry.

Structure activity relationships of benzyl C-region analogs of 2-(3-fluoro-4-methylsulfonamidophenyl)propanamides as potent TRPV1 antagonists.

M. Cui, Sun Choi, G. Bahrenberg, 2015, Bioorganic & medicinal chemistry.

α-Substituted 2-(3-fluoro-4-methylsulfonamidophenyl)acetamides as potent TRPV1 antagonists.

M. Cui, Sun Choi, G. Bahrenberg, 2015, Bioorganic & medicinal chemistry letters.

Harnessing the Therapeutic Potential of Capsaicin and Its Analogues in Pain and Other Diseases

M. Cui, Sun Choi, S. Basith, 2016, Molecules.

N6-Substituted 5'-N-Methylcarbamoyl-4'-selenoadenosines as Potent and Selective A3 Adenosine Receptor Agonists with Unusual Sugar Puckering and Nucleobase Orientation.

Steven M. Moss, K. Jacobson, M. Cui, 2017, Journal of medicinal chemistry.

The Cell Shape-determining Csd6 Protein from Helicobacter pylori Constitutes a New Family of l,d-Carboxypeptidase

Nam Ki Lee, M. Cui, Sun Choi, 2015, The Journal of Biological Chemistry.

Exploring G Protein-Coupled Receptors (GPCRs) Ligand Space via Cheminformatics Approaches: Impact on Rational Drug Design

Sun Choi, Shaherin Basith, Soosung Kang, 2018, Front. Pharmacol..

Inhibitory effect of tartrate against phosphate-induced DJ-1 aggregation.

M. Cui, Sun Choi, P. Suh, 2018, International journal of biological macromolecules.

Structure-activity relationship investigation of Phe-Arg mimetic region of human glutaminyl cyclase inhibitors.

M. Cui, Sun Choi, Heejin Ha, 2018, Bioorganic & medicinal chemistry.

Discovery of Potent Human Glutaminyl Cyclase Inhibitors as Anti-Alzheimer's Agents Based on Rational Design.

M. Cui, Sun Choi, Jiyoun Lee, 2017, Journal of medicinal chemistry.

Anti-malarial activity of new N-acetyl-L-leucyl-L-leucyl-L-norleucinal (ALLN) derivatives against Plasmodium falciparum.

M. Cui, Hyun Park, Hyun-Ok Song, 2013, Bioorganic & medicinal chemistry letters.

2-Aryl substituted pyridine C-region analogues of 2-(3-fluoro-4-methylsulfonylaminophenyl)propanamides as highly potent TRPV1 antagonists.

M. Cui, Sun Choi, P. K. Sharma, 2014, Bioorganic & medicinal chemistry letters.

TRPV1 antagonist with high analgesic efficacy: 2-Thio pyridine C-region analogues of 2-(3-fluoro-4-methylsulfonylaminophenyl)propanamides.

Sun Choi, HyungChul Ryu, Peter M. Blumberg, 2013, Bioorganic & medicinal chemistry.

2-Alkyl/alkenyl substituted pyridine C-region analogues of 2-(3-fluoro-4-methylsulfonylaminophenyl)propanamides as highly potent TRPV1 antagonists.

K. Schiene, M. Cui, Sun Choi, 2014, Bioorganic & medicinal chemistry letters.

Anti‐angiogenic activity of thienopyridine derivative LCB03‐0110 by targeting VEGFR‐2 and JAK/STAT3 Signalling

M. Cui, Sun Choi, Yoonji Lee, 2015, Experimental dermatology.

In silico prediction of multiple-category classification model for cytochrome P450 inhibitors and non-inhibitors using machine-learning method$

M. Cui, S. Basith, J. H. Lee, 2017, SAR and QSAR in environmental research.

Synthesis and Anti-Renal Fibrosis Activity of Conformationally Locked Truncated 2-Hexynyl-N6-Substituted-(N)-Methanocarba-nucleosides as A3 Adenosine Receptor Antagonists and Partial Agonists

Steven M. Moss, M. Cui, Sun Choi, 2014, Journal of Medicinal Chemistry.