Kouji Sato

TAS-108, a novel oral steroidal antiestrogenic agent, is a pure antagonist on estrogen receptor alpha and a partial agonist on estrogen receptor beta with low uterotrophic effect.

A. Buzdar, Y. Aoyagi, K. Wierzba, 2005, Clinical cancer research : an official journal of the American Association for Cancer Research.

Application of the GA-PLS method for Aromatic nucleophilic substitution reaction on Quinolone derivatives using result of molcular orbital calculation for transition states

K. Funatsu, K. Hori, K. Okano, 2001 .

Domino Michael–O-alkylation reaction: one-pot synthesis of 2,4-diacylhydrofuran derivatives and its application to antitumor naphthofuran synthesis

Toshio Suzuki, M. Ando, H. Hagiwara, 2001 .

Tandem Nucleophilic Reaction Leading to Hydrofurans: Application to One-Pot Synthesis of Antitumor Naphthofuran Natural Product

Toshio Suzuki, M. Ando, H. Hagiwara, 1999 .

Tandem nucleophilic reaction of 1,3-dicarbonyl compounds to methyl α-bromoacrylate: [3+2]heteroannulation leading to hydrofuran derivatives

Toshio Suzuki, M. Ando, H. Hagiwara, 1997 .

TAS-108, a Novel Oral Steroidal Antiestrogenic Agent, Is a Pure Antagonist on Estrogen Receptor α and a Partial Agonist on Estrogen Receptor β with Low Uterotrophic Effect

A. Buzdar, Y. Aoyagi, K. Wierzba, 2005 .

Tandem Nucleophilic Reaction Leading to Hydrofurans: Application to the One‐Pot Synthesis of an Antitumor Naphthofuran Natural Product.

Toshio Suzuki, M. Ando, H. Hagiwara, 1999 .

Estrogen agonistic/antagonistic effects of miproxifene phosphate (TAT-59)

A. Fujioka, H. Saito, K. Wierzba, 2000, Cancer Chemotherapy and Pharmacology.

Steroidal versus Non-steroidal Forms. II. Conformations of 4, 6α(H), 5β(H)-Tetrahydro-α-santonin and 4, 6α(H), 5β(H)-Tetrahydro-β-santonin

H. Ogura, Kouji Sato, R. Kawaoka, 1992 .