Jun Shibata

Structure-based drug design of a highly potent CDK1,2,4,6 inhibitor with novel macrocyclic quinoxalin-2-one structure

Nobuhiko Kawanishi, T Sugimoto, Jun Shibata et al. · Bioorganic & Medicinal Chemistry Letters · 2006 · 101 citations · Full text

Medicinal Chemistry, Medicine, Natural Sciences +10

An enantioselective synthesis of the A-ring synthon for vitamin D3 metabolites by chemicoenzymatic approach

Susumu Kobayashi, Jun Shibata, Mitsuyuki Shimada et al. · Tetrahedron Letters · 1990 · 35 citations

A-ring Synthon, Biochemistry, Natural Sciences +8

An Effective Method for the Preparation of Chiral Polyoxy 8-Membered Ring Enone Corresponding to the B Ring of Taxol

Isamu Shiina, Jun Shibata, Ryoutarou Ibuka et al. · Bulletin of the Chemical Society of Japan · 2001 · 32 citations

Engineering, Aldehyde 3, Active Trioxy Aldehyde +11

Spectral Tuning in Sensory Rhodopsin I from Salinibacter ruber

Yuki Sudo, Yasufumi Yuasa, Jun Shibata et al. · Journal of Biological Chemistry · 2011 · 29 citations · Full text

Identification of potent 5-pyrimidinyl-2-aminothiazole CDK4, 6 inhibitors with significant selectivity over CDK1, 2, 5, 7, and 9

Tadashi Shimamura, Jun Shibata, Hideki Kurihara et al. · Bioorganic & Medicinal Chemistry Letters · 2006 · 29 citations · Full text

Medicinal Chemistry, Drug Target, Biochemistry +11