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ACS Medicinal Chemistry Letters|March 28, 2015
Design, Synthesis, and Evaluation of Tetrasubstituted Pyridines as Potent 5-HT2C Receptor AgonistsGuy Rouquet, Dianna E Moore, Malcolm Spain, et al.
Chemistry & Biology|November 12, 2013
Design, synthesis, and biological evaluation of an allosteric inhibitor of HSET that targets cancer cells with supernumerary centrosomesCiorsdaidh A Watts, Frances M Richards, Andreas Bender, et al.
Chemistry (Weinheim an Der Bergstrasse, Germany)|March 18, 2011
Total synthesis of chloptosin: a dimeric cyclohexapeptideAlexander J Oelke, Francesca Antonietti, Leonardo Bertone, et al.
ACS Medicinal Chemistry Letters|June 6, 2014
A-ring dihalogenation increases the cellular activity of combretastatin-templated tetrazolesThomas M Beale, Daniel M Allwood, Andreas Bender, et al.
Drug Discovery Today|August 3, 2013
Fragment-based hit identification: thinking in 3DAndrew D Morley, Angelo Pugliese, Kristian Birchall, et al.
The Journal of Organic Chemistry|November 27, 2018
Highly Diastereoselective Synthesis of a HCV NS5B Nucleoside Polymerase InhibitorYong-Li Zhong, Ed Cleator, Zhijian Liu, et al.
Chemistry (Weinheim an Der Bergstrasse, Germany)|September 30, 2008
The synthesis of azadirachtin: a potent insect antifeedantSteven V Ley, Antonio Abad-Somovilla, James C Anderson, et al.
Science Advances|October 21, 2016
Promiscuous targeting of bromodomains by bromosporine identifies BET proteins as master regulators of primary transcription response in leukemiaSarah Picaud, Katharina Leonards, Jean-Philippe Lambert, et al.
Proceedings of the National Academy of Sciences of the United States of America|November 10, 2010
Trapping of palindromic ligands within native transthyretin prevents amyloid formationSimon E Kolstoe, Palma P Mangione, Vittorio Bellotti, et al.
ACS Medicinal Chemistry Letters|March 16, 2018
Identification and Structure-Guided Development of Pyrimidinone Based USP7 InhibitorsColin R O'Dowd, Matthew D Helm, J S Shane Rountree, et al.
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