E. Baader

Inhibition of prolyl 4-hydroxylase by oxalyl amino acid derivatives <i>in vitro</i>, in isolated microsomes and in embryonic chicken tissues

E. Baader, Georg Tschank, Karl‐Heinz Baringhaus et al. · Biochemical Journal · 1994 · 77 citations · Full text

Little Inhibitory Activity, Aldo-keto Reductase, Oxalyl Amino +18

Synthesis and biological activity of new HMG-CoA reductase inhibitors. 1. Lactones of pyridine- and pyrimidine-substituted 3,5-dihydroxy-6-heptenoic (-heptanoic) acids

G. Beck, E. Baader, Wilhelm Bartmann et al. · Journal of Medicinal Chemistry · 1990 · 68 citations · Full text

Stereoselective synthesis of HR 780 a new highly potent HMG-CoA reductase inhibitor

Günther Wess, E. Baader, Wilhelm Bartmann et al. · Tetrahedron Letters · 1990 · 65 citations

Medicinal Chemistry, Biochemistry, Medicine +8

Synthesis and biological activity of new HMG-CoA reductase inhibitors. 2. Derivatives of 7-(1H-pyrrol-3-yl)-substituted-3,5-dihydroxyhept-6(E)-enoic (-heptanoic) acids

Heiner Jendralla, E. Baader, Wilhelm Bartmann et al. · Journal of Medicinal Chemistry · 1990 · 64 citations · Full text

Synthesis and biological activity of new HMG-CoA reductase inhibitors. 3. Lactones of 6-phenoxy-3,5-dihydroxyhexanoic acids

Heiner Jendralla, E. Granzer, B. v. Kerékjártó et al. · Journal of Medicinal Chemistry · 1991 · 51 citations · Full text