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Bioorganic & Medicinal Chemistry Letters|March 21, 2017
Identification and structure activity relationships of quinoline tertiary alcohol modulators of RORγtDavid A Kummer, Maxwell D Cummings, Marta Abad, et al.Bioorganic & Medicinal Chemistry Letters|October 29, 2017
6-Substituted quinolines as RORγt inverse agonistsJ Kent Barbay, Maxwell D Cummings, Marta Abad, et al.Bioorganic & Medicinal Chemistry Letters|February 5, 2008
Biphenylsulfonyl-thiophene-carboxamidine inhibitors of the complement component C1sJeremy M Travins, Farah Ali, Hui Huang, et al.Bioorganic & Medicinal Chemistry Letters|July 17, 2012
Design and synthesis of polyethylene glycol-modified biphenylsulfonyl-thiophene-carboxamidine inhibitors of the complement component C1sNalin L Subasinghe, Ehab Khalil, Jeremy M Travins, et al.The Journal of Biological Chemistry|September 2, 2017
Discovery of a highly selective chemical inhibitor of matrix metalloproteinase-9 (MMP-9) that allosterically inhibits zymogen activationRobert H Scannevin, Richard Alexander, Tara Mezzasalma Haarlander, et al.Journal of Medicinal Chemistry|January 14, 2012
Design and characterization of optimized adenosine A₂A/A₁ receptor antagonists for the treatment of Parkinson's diseaseBrian C Shook, Stefanie Rassnick, Nathaniel Wallace, et al.Bioorganic & Medicinal Chemistry Letters|March 27, 2010
Optimization of arylindenopyrimidines as potent adenosine A(2A)/A(1) antagonistsBrian C Shook, Stefanie Rassnick, Devraj Chakravarty, et al.Pageof 2