Rune Ringom

Substituted benzylamino-6-(trifluoromethyl)pyrimidin-4(1H)-ones: a novel class of selective human A-FABP inhibitors

Rune Ringom, Eva Axén, J. Uppenberg et al. · Bioorganic & Medicinal Chemistry Letters · 2004 · 65 citations · Full text

Medicinal Chemistry, Drug Target, Biochemistry +9

Design and synthesis of potent, orally active, inhibitors of carboxypeptidase U (TAFIa)

Magnus Polla, Louise Tottie, Carita Nordén et al. · Bioorganic & Medicinal Chemistry · 2004 · 56 citations

Medicinal Chemistry, Biochemistry, Natural Sciences +6

Synthesis and Nucleophilic Substitution Reactions of Mono alpha-Fluoro Ethers.

Rune Ringom, Tore Benneche, Marcello Colapietro et al. · Acta chemica Scandinavica/Acta chemica Scandinavica. B, Organic chemistry and biochemistry/Acta chemica Scandinavica. A, Physical and inorganic chemistry/Acta chemica Scandinavica. Series B. Organic chemistry and biochemistry/Acta chemica Scandinavica. Series A, Physical and inorganic chemistry · 1999 · 29 citations · Full text

Fluorous Synthesis, Mono Alpha-fluoro Ethers, Organic Chemistry +3

The Oncolytic Efficacy and in Vivo Pharmacokinetics of [2-(4-Chlorophenyl)quinolin-4-yl](piperidine-2-yl)methanol (Vacquinol-1) Are Governed by Distinct Stereochemical Features

Lars G.J. Hammarström, Robert K. Harmel, Mikael Granath et al. · Journal of Medicinal Chemistry · 2016 · 17 citations · Full text

Pharmaceutical Science, Active Isomers, Oncolytic Efficacy +19