S. Satoh

发表

Nonpeptide mimic of bradykinin with long-acting properties at the bradykinin B2 receptor.

K. Nakahara, T. Inoue, Y. Notsu, 1997, Molecular pharmacology.

Erythropoietin mimetics derived from solution phase combinatorial libraries.

D. Boger, Y. Ambroise, J. Desharnais, 2002, Journal of the American Chemical Society.

Nonpeptide mimic of bradykinin with long-acting properties.

K. Nakahara, T. Inoue, Y. Notsu, 1999, Immunopharmacology.

Pharmacological characterization of a novel, orally active, nonpeptide bradykinin B2 receptor antagonist, FR167344.

K. Nakahara, T. Inoue, H. Kayakiri, 1997, European journal of pharmacology.

The identification of an orally active, nonpeptide bradykinin B2 receptor antagonist, FR173657

K. Nakahara, M. Okuhara, H. Kayakiri, 1997, British journal of pharmacology.

Pharmacological characterization of a nonpeptide bradykinin B2 receptor antagonist, FR165649, and agonist, FR190997

K. Nakahara, T. Inoue, H. Kayakiri, 1998, British journal of pharmacology.

Organic solid photochromism by photoreduction mechanism: Aryl viologens embedded in poly(N‐vinyl‐2‐pyrrolidone)

H. Kamogawa, S. Satoh, 1988 .

Discovery of orally active nonpeptide bradykinin B2 receptor antagonists.

K. Nakahara, H. Kayakiri, N. Inamura, 1999, Immunopharmacology.

A novel class of orally active non-peptide bradykinin B2 receptor antagonists. 3. Discovering bioisosteres of the imidazo[1,2-a] pyridine moiety.

T. Inoue, I. Aramori, H. Kayakiri, 1998, Journal of medicinal chemistry.

A novel class of orally active non-peptide bradykinin B2 receptor antagonists. 1. Construction of the basic framework.

T. Inoue, H. Kayakiri, N. Inamura, 1998, Journal of medicinal chemistry.

Selective Manipulation of Hydroxy Groups in (2S,3S)-Threitol

Y. Sekiguchi, S. Takano, K. Ogasawara, 1986 .

Stereoselective formation of a cyclopentanoid with three contiguous substituents via intramolecular cycloaddition

S. Takano, K. Ogasawara, S. Satoh, 1985 .

Silicon-mediated isoquinoline alkaloid synthesis: a new route to the dibenzopyrrocoline alkaloid (±)-cryptaustoline

S. Takano, K. Ogasawara, S. Satoh, 1987 .

Enantio-controlled route to the furofuran lignans: the total synthesis of (–)-sesamolin, (–)-sesamin, and (–)-acuminatolide

S. Takano, K. Ogasawara, S. Tamori, 1988 .

Enantioselective synthesis of (−)-kainic acid

S. Takano, K. Ogasawara, T. Sugihara, 1988 .

Racemization of (−)-Vincadifformine Using Microwave Oven

S. Takano, K. Ogasawara, T. Sugihara, 1989 .

A novel class of orally active non-peptide bradykinin B2 receptor antagonists. 4. Discovery of novel frameworks mimicking the active conformation.

T. Inoue, I. Aramori, H. Kayakiri, 1998, Journal of medicinal chemistry.

Non-Amide-Based Combinatorial Libraries Derived fromN-Boc-Iminodiacetic Acid: Solution-Phase Synthesis of Piperazinone Libraries with Activity Against LEF-1/β-Catenin-Mediated Transcription

Shigeki Satoh, Dale L. Boger, Peter K. Vogt, 2000 .

Bilirubin conjugation and biliary bilirubin excretion after intravenous bilirubin injection in dogs.

S. Satoh, H. Ise, Y. Abe, 1991, Tohoku journal of experimental medicine.