Wenfeng Liu

发表

Fragment-Based Discovery of a Selective and Cell-Active Benzodiazepinone CBP/EP300 Bromodomain Inhibitor (CPI-637).

Y. Leblanc, H. Jayaram, R. Sims, 2016, ACS medicinal chemistry letters.

A Unique Approach to Design Potent and Selective Cyclic Adenosine Monophosphate Response Element Binding Protein, Binding Protein (CBP) Inhibitors.

Fei Wang, H. Jayaram, F. A. Romero, 2017, Journal of medicinal chemistry.

Synthesis and Biological Evaluation of Novel Homocamptothecins Conjugating with Dihydropyrimidine Derivatives as Potent Topoisomerase I Inhibitors

Shengzhang Wang, Wei Guo, Wenfeng Liu, 2011, Archiv der Pharmazie.

Design and synthesis of a biaryl series as inhibitors for the bromodomains of CBP/P300.

Fei Wang, F. A. Romero, E. Choo, 2018, Bioorganic & medicinal chemistry letters.

Discovery of a Potent and Selective in Vivo Probe (GNE-272) for the Bromodomains of CBP/EP300.

Karen E Gascoigne, Fei Wang, S. Kharbanda, 2016, Journal of medicinal chemistry.

Trifluoromethyl-promoted homocamptothecins: synthesis and biological activity.

Wei Guo, Wenfeng Liu, Zhenyuan Miao, 2010, European journal of medicinal chemistry.

Synthesis and Pharmacological Evaluation of Novel Homocamptothecin-Dihydropyridine Derivative Conjugates as Potent Topoisomerase I Inhibitors

W. Guo, Wenfeng Liu, Zhenyuan Miao, 2011 .

Synthesis of novel benzoxanthone analogues as non-Camptothecin topoisomerase I inhibitors

Wei Guo, Wenfeng Liu, Yongqiang Zhang, 2012, Journal of enzyme inhibition and medicinal chemistry.

Synthesis and evaluation of 9-benzylideneamino derivatives of homocamptothecin as potent inhibitors of DNA topoisomerase I.

Wei Guo, Wenfeng Liu, Zhenyuan Miao, 2010, European journal of medicinal chemistry.

Cell Active Hydroxylactam Inhibitors of Human Lactate Dehydrogenase with Oral Bioavailability in Mice.

Marie Evangelista, BinQing Wei, M. Ultsch, 2016, ACS medicinal chemistry letters.

Structure- and Ligand-Based Discovery of Chromane Arylsulfonamide Nav1.7 Inhibitors for the Treatment of Chronic Pain.

D. Sutherlin, Jun Chen, D. Hackos, 2019, Journal of medicinal chemistry.

Synthesis and Biological Assays of 9‐(Acylamino)homocamptothecins as DNA Topoisomerase I Inhibitors

Wei Guo, Wenfeng Liu, Guoqiang Dong, 2013, Chemistry & biodiversity.

Synthesis of 9‐(Heteroarylmethylidene)amino Derivatives of Homocamptothecin with Biological Activities

Wei Guo, Wenfeng Liu, Yongqiang Zhang, 2011, Chemistry & biodiversity.

Synthesis and Biological Evaluation of 7‐Alkenyl Homocamptothecins as Potent Topoisomerase I Inhibitors

Wei Guo, Wenfeng Liu, Guoqiang Dong, 2012, Chemistry & biodiversity.

Topoisomerase I‐Mediated Antiproliferative Activity of 10‐Substituted and 12‐Substituted Homocamptothecins

W. Guo, Wenfeng Liu, Yongqiang Zhang, 2011 .

Synthesis and biological evaluation of novel 7-acyl homocamptothecins as Topoisomerase I inhibitors.

Shengzheng Wang, Wei Guo, Wenfeng Liu, 2011, European journal of medicinal chemistry.

Phosphate ester derivatives of homocamptothecin: synthesis, solution stabilities and antitumor activities.

Juan Wang, Wei Guo, Wenfeng Liu, 2010, Bioorganic & medicinal chemistry.

GNE-781, A Highly Advanced Potent and Selective Bromodomain Inhibitor of Cyclic Adenosine Monophosphate Response Element Binding Protein, Binding Protein (CBP).

Karen E Gascoigne, Y. Ran, G. Hatzivassiliou, 2017, Journal of medicinal chemistry.

Discovery of 7‐Methyl‐10‐Hydroxyhomocamptothecins with 1,2,3‐Triazole Moiety as Potent Topoisomerase I Inhibitors

Wenfeng Liu, Guoqiang Dong, Zhenyuan Miao, 2016, Chemical biology & drug design.

Structure-based Optimization of Hydroxylactam as Potent, Cell-Active Inhibitors of Lactate Dehydrogenase.

BinQing Wei, M. Ultsch, C. Eigenbrot, 2022, Bioorganic & medicinal chemistry letters.

Synthesis and evaluation of 9-benzylideneamino derivatives of homocamptothecin as potent inhibitors of DNA topoisomerase I.

Wei Guo, Wenfeng Liu, Zhenyuan Miao, 2010, European journal of medicinal chemistry.