Joan B. Schmidt

Biphenylsulfonamide Endothelin Antagonists:  Structure−Activity Relationships of a Series of Mono- and Disubstituted Analogues and Pharmacology of the Orally Active Endothelin Antagonist 2‘-Amino-<i>N</i>- (3,4-dimethyl-5-isoxazolyl)-4‘-(2-methylpropyl)[1,1‘-biphenyl]-2-sulfonamide (BMS-187308)

Natesan Murugesan, Zhengxiang Gu, Philip D. Stein et al. · Journal of Medicinal Chemistry · 1998 · 40 citations · Full text

Molecular Pharmacology, Medicinal Chemistry, Pharmaceutical Science +15

Benzopyran sulfonamides as KV1.5 potassium channel blockers

John Lloyd, Karnail S. Atwal, Heather J. Finlay et al. · Bioorganic & Medicinal Chemistry Letters · 2007 · 32 citations · Full text

Heterocyclic, Medicine, Ion Channels +4

Solid phase synthesis of phosphinic acid endothelin converting enzyme inhibitors

John Lloyd, Joan B. Schmidt, John T. Hunt et al. · Bioorganic & Medicinal Chemistry Letters · 1996 · 26 citations

Medicinal Chemistry, Biochemistry, Medicine +7

Design and Synthesis of 4-Substituted Benzamides as Potent, Selective, and Orally Bioavailable <i>I</i>_Ks Blockers

John Lloyd, Joan B. Schmidt, George C. Rovnyak et al. · Journal of Medicinal Chemistry · 2001 · 18 citations · Full text

Heart Failure, Cardiovascular Pharmacology, Organic Chemistry +18

N-[1-Aryl-2-(1-imidazolo)ethyl]-guanidine derivatives as potent inhibitors of the bovine mitochondrial F1F0 ATP hydrolase

Karnail S. Atwal, Saleem Ahmad, Charles Z. Ding et al. · Bioorganic & Medicinal Chemistry Letters · 2004 · 18 citations · Full text