A. Hijikata

发表

Selective inhibition of thrombin by (2R,4R)-4-methyl-1-[N2-[(3-methyl-1,2,3,4-tetrahydro-8-quinolinyl++ +) sulfonyl]-l-arginyl)]-2-piperidinecarboxylic acid.

R. Kikumoto, Y. Tamao, T. Tezuka, 1984, Biochemistry.

In vitro and in vivo studies of a new series of synthetic thrombin-inhibitors (OM-inhibitors).

R. Kikumoto, A. Hijikata, S. Okamoto, 1976, Thrombosis research.

THROMBIN INHIBITORS. 1. ESTER DERIVATIVES OF Nα-(ARYLSULFONYL)-L-ARGININE

R. Kikumoto, Y. Tamao, S. Tonomura, 1981 .

Thrombin inhibitors. 1. Ester derivatives of N alpha-(arylsulfonyl)-L-arginine.

R. Kikumoto, Y. Tamao, S. Tonomura, 1980, Journal of medicinal chemistry.

Thrombin inhibitors. 2. Amide derivatives of N alpha-substituted L-arginine.

T. Tezuka, R. Kikumoto, Y. Tamao, 1980, Journal of medicinal chemistry.

Rational Approach to Proteinase Inhibitors

A. Hijikata, S. Okamoto, 1975 .

Effect of proteases on plasminogen activator release from isolated perfused dog leg.

A. Hijikata, H. Kitaguchi, M. Hirata, 1980, Thrombosis research.

Some properties of the tissue plasminogen activator from the pig heart.

A. Hijikata, S. Okamoto, H. Kitaguchi, 1974, Thrombosis research.

The characteristics of stereogeometry at the active center of plasmin

Y. Tsuda, Y. Okada, A. Hijikata, 1985 .

Potent inhibition of thrombin by the newly synthesized arginine derivative No. 805. The importance of stereo-structure of its hydrophobic carboxamide portion.

R. Kikumoto, Y. Tamao, S. Tonomura, 1981, Biochemical and biophysical research communications.

Plasminogen activator release from the perfused isolated dog leg by thrombin

A. Hijikata, M. Hirata, H. Kitaguchi, 1980 .

Thrombin inhibitors. 3. Carboxyl-containing amide derivatives of N alpha-substituted L-arginine.

T. Tezuka, R. Kikumoto, Y. Tamao, 1980, Journal of medicinal chemistry.

Effect of thrombin on plasminogen activator release from isolated perfused dog leg.

A. Hijikata, H. Kitaguchi, M. Hirata, 1979, Thrombosis research.

A novel series of synthetic thrombin-inhibitors having extremely potent and highly selective action.

R. Kikumoto, A. Hijikata, S. Okamoto, 1975, The Kobe journal of medical sciences.

A Synthetic Thrombin Inhibitor Taking Extremely Active Stereo-Structure

R. Kikumoto, Y. Tamao, A. Hijikata, 1979, Thrombosis and Haemostasis.

Effect of some proteases on plasminogen activator release from perfused isolated dog leg

A. Hijikata, H. Kitaguchi, M. Hirata, 1980 .

THROMBIN INHIBITORS. 2. AMIDE DERIVATIVES OF Nα-SUBSTITUTED L-ARGININE

T. Tezuka, R. Kikumoto, Y. Tamao, 1981 .

A new series of synthetic thrombin-inhibitors (OM-inhibitors) having extremely potent and selective action.

R. Kikumoto, A. Hijikata, S. Okamoto, 1976, Thrombosis research.

Effects of a potent thrombin inhibitor, No. 407, on DIC models.

R. Kikumoto, Y. Tamao, A. Hijikata, 1980, The Kobe journal of medical sciences.

Synthesis of plasmin substrates and relationship between their structure and plasmin activity.

Y. Tsuda, Y. Okada, A. Hijikata, 2009, International journal of peptide and protein research.

Fluorescence Studies On The Mode Of Action Of Two Synthetic Thrombin Inhibitors, No. 205 And No. 805

Y. Tamao, A. Hijikata, S. Okamoto, 1981, Thrombosis and Haemostasis.

Structure-activity relationship in a series of synthetic thrombin inhibitors: No. 205, No. 407 and No. 700

T. Tezuka, R. Kikumoto, Y. Tamao, 1980 .