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Orally active anti-proliferation agents: novel diphenylamine derivatives as FGF-R2 autophosphorylation inhibitors.

Toshiyuki Shimizu, K. Kimura, T. Sakai, 2004, Bioorganic & medicinal chemistry letters.

Pharmacologic profile of (R)-5-[(1-methyl-3-indolyl)carbonyl]-4,5,6,7-tetrahydro-1H- benzimidazole hydrochloride (YM060), a potent and selective 5-hydroxytryptamine3 receptor antagonist, and its enantiomer in the isolated tissue.

A. Nishida, K. Miyata, R. Tsutsumi, 1991, The Journal of pharmacology and experimental therapeutics.

Novel potent orally active selective VEGFR-2 tyrosine kinase inhibitors: synthesis, structure-activity relationships, and antitumor activities of N-phenyl-N'-{4-(4-quinolyloxy)phenyl}ureas.

Toshiyuki Shimizu, N. Takahashi, Yoshiko Kobayashi, 2005, Journal of medicinal chemistry.

Synthesis and structure-activity relationship of Quinazoline-Urea derivatives as novel orally active VEGF receptor tyrosine kinase selective inhibitors

M. Shibuya, N. Takahashi, Yoshiko Kobayashi, 2002 .