S. Odake

发表

Inhibition of matrix metalloproteinases by peptidyl hydroxamic acids.

N. Yoshida, H. Hori, Y. Nagai, 1994, Biochemical and biophysical research communications.

Highly water-soluble matrix metalloproteinases inhibitors and their effects in a rat adjuvant-induced arthritis model.

J. Yasuda, K. Igeta, T. Morikawa, 2002, Bioorganic & medicinal chemistry.

Inhibition of Helicobacter pylori urease activity by hydroxamic acid derivatives.

K. Kobashi, T. Morikawa, L. Imamura, 1994, Biological & pharmaceutical bulletin.

Design and synthesis of sulfur based inhibitors of matrix metalloproteinase-1.

Y. Ogawa, J. Yasuda, T. Morikawa, 2002, Chemical & pharmaceutical bulletin.

Design and synthesis of carboxylate inhibitors for matrix metalloproteinases.

J. Yasuda, I. Yasumatsu, T. Morikawa, 2001, Chemical & pharmaceutical bulletin.

Introduction of a 3-Alkoxycarbonyl-2-propenyl Group at the ortho Position of Phenol and Naphthol via α-Aryloxy-γ-butyrolactone. Application to Syntheses of (±)-Nanaomycin A and a 1-Anthracenone

Y. Takéuchi, K. Nomura, E. Yoshii, 1984 .

Proteases--structures, mechanism and inhibitors.

J. Powers, J. Oleksyszyn, C. Kam, 1993, Agents and actions. Supplements.

Synthetic dipeptide, N-stearoyl-D-Ser-L-Pro-OEt, induces release of tissue-type plasminogen activator in cultured cells and in experimental animals.

O. Matsuo, S. Ueshima, M. Nakano, 1994, Chemical & pharmaceutical bulletin.

INTRODUCTION OF A 3‐ALKOXYCARBONYL‐2‐PROPENYL GROUP AT THE ORTHO POSITION OF PHENOL AND NAPHTHOL VIA α‐ARYLOXY‐Γ‐BUTYROLACTONE. APPLICATION TO SYNTHESIS OF (.+‐.)‐NANAOMYCIN A AND A 1‐ANTHRACENONE

Y. Takéuchi, K. Nomura, E. Yoshii, 1985 .

Inhibition of urease activity by dipeptidyl hydroxamic acids.

K. Kobashi, T. Morikawa, S. Odake, 1992, Chemical & pharmaceutical bulletin.

Serine Protease Control of Lymphocyte-Mediated Cytolysis

J. Powers, C. Kam, D. Redelman, 1993 .

Human and murine cytotoxic T lymphocyte serine proteases: subsite mapping with peptide thioester substrates and inhibition of enzyme activity and cytolysis by isocoumarins.

J. Tschopp, M. Poe, J. Powers, 1991, Biochemistry.

Inhibition of thrombin by arginine-containing peptide chloromethyl ketones and bis chloromethyl ketone-albumin conjugates.

J. Powers, C. Kam, S. Odake, 1995, Journal of enzyme inhibition.

Cytotoxic T-lymphocyte serine proteases: Substrate and inhibitor studies with granzymes A and B, and human Q31 chymase

J. Tschopp, M. Poe, J. Powers, 1992 .

Inhibition of corneal ulceration by tetrapeptidyl hydroxamic acid.

Y. Nagai, K. Kigasawa, T. Morikawa, 1995, Japanese journal of ophthalmology.

Synthetic substrates and inhibitors for serine proteases from lymphocytes, mast cells, semen, and blood.

J. Powers, C. Kam, D. Hudig, 1992, Agents and actions. Supplements.