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Nature Communications|July 12, 2019
Quantitative characterization of 3D bioprinted structural elements under cell generated forcesCameron D Morley, S Tori Ellison, Tapomoy Bhattacharjee, et al.Bioorganic & Medicinal Chemistry Letters|August 4, 2012
Isosteric replacements for benzothiazoles and optimisation to potent Cathepsin K inhibitors free from hERG channel inhibitionAlexander G Dossetter, Jonathan Bowyer, Calum R Cook, et al.Bioorganic & Medicinal Chemistry Letters|June 12, 2009
Dipeptidyl nitrile inhibitors of Cathepsin LNabil Asaad, Paul A Bethel, Michelle D Coulson, et al.Bioorganic & Medicinal Chemistry Letters|September 2, 2006
Novel thienopyrrole glycogen phosphorylase inhibitors: synthesis, in vitro SAR and crystallographic studiesPaul R O Whittamore, Matthew S Addie, Stuart N L Bennett, et al.Journal of Medicinal Chemistry|September 19, 2012
Pharmacokinetic benefits of 3,4-dimethoxy substitution of a phenyl ring and design of isosteres yielding orally available cathepsin K inhibitorsJames J Crawford, Peter W Kenny, Jonathan Bowyer, et al.Nature Materials|March 11, 2026
Stress-relaxing granular bioprinting materials enable complex and uniform organoid self-organizationAustin J Graham, Michelle W L Khoo, Vasudha Srivastava, et al.Journal of Medicinal Chemistry|June 30, 2012
(1R,2R)-N-(1-cyanocyclopropyl)-2-(6-methoxy-1,3,4,5-tetrahydropyrido[4,3-b]indole-2-carbonyl)cyclohexanecarboxamide (AZD4996): a potent and highly selective cathepsin K inhibitor for the treatment of osteoarthritisAlexander G Dossetter, Howard Beeley, Jonathan Bowyer, et al.Pageof 16