Wei Sun

发表

Design, synthesis and biological evaluation of photoaffinity probes of antiangiogenic homoisoflavonoids.

Wei Sun, T. Corson, Seung‐Yong Seo, 2016, Bioorganic & medicinal chemistry letters.

[Progress in the study of heat shock protein 90 inhibitors].

Haoming Luo, Wei Sun, Xiao-hong Yang, 2010, Yao xue xue bao = Acta pharmaceutica Sinica.

Synthesis and glycosidase inhibition evaluation of (3S,4S)-3-((R)-1,2-dihydroxyethyl)pyrrolidine-3,4-diol.

Hong-min Liu, Peng Bai, E. Zhang, 2016, Carbohydrate research.

Design, Synthesis, and In Vitro Evaluation of the Photoactivatable Prodrug of the PARP Inhibitor Talazoparib

Wei Li, Xiaohong Yang, Xinbo Zhou, 2020, Molecules.

Design, synthesis and biological activities of sorafenib derivatives as antitumor agents.

J. Chen, H. Fang, Wenfang Xu, 2012, Bioorganic & medicinal chemistry letters.

Design, Synthesis and Antiproliferative Activities of Diaryl Thiourea Derivatives as Anticancer Agents

Wenfang Xu, J. Chen, Jianwen Yao, 2012 .

Design, synthesis and biological activities of thiourea containing sorafenib analogs as antitumor agents.

J. Chen, Wenfang Xu, Jianwen Yao, 2012, Bioorganic & Medicinal Chemistry.

Thiourea and thioether derivatives of sorafenib: synthesis, crystal structure, and antiproliferative activity

J. Chen, H. Fang, Wenfang Xu, 2013, Medicinal Chemistry Research.

Design, synthesis, and evaluation of potent, nonpeptidic mimetics of second mitochondria-derived activator of caspases.

Shaomeng Wang, Chao-yie Yang, Z. Nikolovska-Coleska, 2009, Journal of medicinal chemistry.

Design and Synthesis of Tri‐substituted Chiral Pyrrolidin‐2‐one Derivatives as CCR4 Antagonists

Linjie Tian, Jun-hai Xiao, Song Li, 2013 .

Design, synthesis, and screen of cathepsin K inhibitors

Jun-hai Xiao, Song Li, Xiaohong Yang, 2013 .

Tuina therapy for temporomandibular joint disorder syndrome

J. Chen, Wei Sun, Yongchao Li, 2021, Medicine.

6,6-Fused heterocyclic ureas as highly potent TRPV1 antagonists.

K. Schiene, Sun Choi, Jeewoo Lee, 2015, Bioorganic & medicinal chemistry letters.

Short Synthesis of the Antidiabetic Octaketide Ethyl 2-(2,3,4-Trimethoxy-6-octanoylphenyl)acetate

H. Jun, Seung‐Yong Seo, Dongyun Shin, 2017 .

Discovery of 2-(3,5-difluoro-4-methylsulfonaminophenyl)propanamides as potent TRPV1 antagonists.

G. Bahrenberg, P. Blumberg, Changhoon Kim, 2018, Bioorganic & medicinal chemistry letters.

Discovery of N-(3-fluoro-4-methylsulfonamidomethylphenyl)urea as a potent TRPV1 antagonistic template.

Sun Choi, P. Blumberg, Changhoon Kim, 2016, Bioorganic & medicinal chemistry letters.

Structures of new triterpenoids and cytotoxicity activities of the isolated major compounds from the fruit of Momordica charantia L.

Jia-qing Cao, Yuqing Zhao, Xiuli Bi, 2012, Journal of agricultural and food chemistry.

On the interpretation of tyrosinase inhibition kinetics

G. Klebe, M. Wendt, K. Röhm, 2014, Journal of enzyme inhibition and medicinal chemistry.

Design, Synthesis and Biological Evaluation of 1-Phenyl-2-(phenylamino) Ethanone Derivatives as Novel MCR-1 Inhibitors

Jun-hai Xiao, Song Li, F. Lin, 2019, Molecules.

Expression in non-melanogenic systems and purification of soluble variants of human tyrosinase

G. Klebe, P. Cordes, K. Röhm, 2013, Biological chemistry.

Studies of Interaction Mechanism between Pyrido [3,4-d] Pyrimidine Inhibitors and Mps1

Cheng Xing, Wei Sun, Qingchuan Zheng, 2021, Molecules.

Molecular design and anticancer activities of small-molecule monopolar spindle 1 inhibitors: A Medicinal chemistry perspective.

Shutao Wang, Mu-xin Zhang, Chaozai Zhang, 2019, European journal of medicinal chemistry.

Chemical Proteomics Reveals Soluble Epoxide Hydrolase as a Therapeutic Target for Ocular Neovascularization.

T. Corson, S. Mitter, M. Boulton, 2017, ACS chemical biology.

Design, synthesis and biological evaluation of acridone analogues as novel STING receptor agonists.

Jun-hai Xiao, Song Li, Wei Li, 2019, Bioorganic chemistry.

2-(4-Methylsulfonylaminophenyl) propanamide TRPV1 antagonists: Structure-activity relationships in the B and C-regions.

Vladimir A. Pavlyukovets, P. Blumberg, Keliang Liu, 2012, Bioorganic & medicinal chemistry.

The carbonate analogues of 5'-halogenated resiniferatoxin as TRPV1 ligands.

Sun Choi, P. Blumberg, L. Pearce, 2013, European journal of medicinal chemistry.

Design, synthesis, and in-vivo evaluation of 4,5-diaryloxazole as novel nonsteroidal anti-inflammatory drug.

Xiaofeng Yu, S. Qu, D. Sui, 2009, Biological & pharmaceutical bulletin.

[Progress in the studies on neuronal nitric oxide synthase inhibitors].

Chaozai Zhang, Wei Sun, Xiao-hong Yang, 2014, Yao xue xue bao = Acta pharmaceutica Sinica.

Thiourea and thioether derivatives of sorafenib: synthesis, crystal structure, and antiproliferative activity

H. Fang, Wenfang Xu, Jianwen Yao, 2013, Medicinal Chemistry Research.

Synthesis of 5-substituted benzyl-2,4-diamino pyrimidine derivatives as c-Fms kinase inhibitors

Jun-hai Xiao, Xiaohong Yang, Li-li Wang, 2010 .

Novel antibody-drug conjugate with UV-controlled cleavage mechanism for cytotoxin release.

Wei Li, Xiaohong Yang, Lei Zhao, 2020, Bioorganic chemistry.

Design, Synthesis, and In Vitro Evaluation of the Photoactivatable Prodrug of the PARP Inhibitor Talazoparib

Wei Li, Xiaohong Yang, Xinbo Zhou, 2020, Molecules.