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Pharmacology & Therapeutics|August 31, 2014
Small molecule Mcl-1 inhibitors for the treatment of cancerJohannes Belmar, Stephen W FesikTetrahedron Letters|February 7, 2012
Total synthesis of (±)-isophellibilineRaymond L Funk, Johannes BelmarJournal of the American Chemical Society|September 18, 2012
Total synthesis of (±)-communesin F via a cycloaddition with indol-2-oneJohannes Belmar, Raymond L FunkBioorganic & Medicinal Chemistry|April 22, 2017
Structure of a Myeloid cell leukemia-1 (Mcl-1) inhibitor bound to drug site 3 of Human Serum AlbuminBin Zhao, John Sensintaffar, Zhiguo Bian, et al.Journal of Medicinal Chemistry|April 7, 2015
Discovery of tricyclic indoles that potently inhibit Mcl-1 using fragment-based methods and structure-based designJason P Burke, Zhiguo Bian, Subrata Shaw, et al.Journal of Medicinal Chemistry|January 12, 2018
Optimization of Potent and Selective Tricyclic Indole Diazepinone Myeloid Cell Leukemia-1 Inhibitors Using Structure-Based DesignSubrata Shaw, Zhiguo Bian, Bin Zhao, et al.Journal of Medicinal Chemistry|February 16, 2016
Discovery of 2-Indole-acylsulfonamide Myeloid Cell Leukemia 1 (Mcl-1) Inhibitors Using Fragment-Based MethodsNicholas F Pelz, Zhiguo Bian, Bin Zhao, et al.FEBS Letters|November 24, 2016
Discovery and biological characterization of potent myeloid cell leukemia-1 inhibitorsTaekyu Lee, Zhiguo Bian, Bin Zhao, et al.Pageof 1