John A. Wos

Preparation of 1-(2,3-dideoxy-.beta.-D-glycero-pent-2-enofuranosyl)thymine (d4T) and 2',3'-dideoxyadenosine (ddA): general methods for the synthesis of 2',3'-olefinic and 2',3'-dideoxy nucleoside analogs active against HIV

Muzammil M. Mansuri, John E. Starrett, John A. Wos et al. · The Journal of Organic Chemistry · 1989 · 92 citations

2',3'-Dideoxy Nucleoside Analogs, Bioorganic Chemistry, Altmetric Attention Score +17

Design and synthesis of substituted quinolines as novel and selective melanin concentrating hormone antagonists as anti-obesity agents

Namal C. Warshakoon, Justin Sheville, Ritu Tiku Bhatt et al. · Bioorganic & Medicinal Chemistry Letters · 2006 · 61 citations · Full text

Selective Melanin, Biochemistry, Medicine +6

Effects of β3-Adrenergic Receptor Activation on Rat Urinary Bladder Hyperactivity Induced by Ovariectomy

F. Aura Kullmann, Brian J. Limberg, Debra E. Artim et al. · Journal of Pharmacology and Experimental Therapeutics · 2009 · 42 citations · Full text

Targeting protein tyrosine phosphatase to enhance insulin action for the potential treatment of diabetes.

K. Bhavani, John A. Wos, Kevin G. Peters · PubMed · 2007 · 36 citations

Metabolic Syndrome, Protein Tyrosine Phosphatase, Insulin Signaling +15

The Synthesis and Human FP Receptor Binding Affinity of 13,14-Dihydro Prostaglandin F1.ALPHA. Sulfonamides. Potential Treatments for Osteoporosis.

Yili Wang, David L. Soper, Michelle J. Dirr et al. · Chemical and Pharmaceutical Bulletin · 2000 · 32 citations · Full text

Sclerostin, Pharmacotherapy, Pharmaceutical Chemistry +17