木曽良明 | 京都薬大

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著作論文

A Synthetic Method Suitable for the Rapid Preparation of ^N-Labeled Dermorphin Analogue, H-Try-D-Met(O)-Phe-Gly-NH_2 (SD-62)
P-26 キラルアミン反応剤を用いる不斉Michael付加反応の開発と(+)-negamycinへの応用(ポスター発表の部)
SOLUTION STRUCTURE OF HIV-1 PROTEASE-ALLOPHENYLNORSTATINE DERIVATIVE INHIBITOR COMPLEX OBTAINED FROM MOLECULAR DYNAMICS SIMULATION
RATIONAL DESIGN AND SYNTHESIS OF A NOVEL CLASS OF ACTIVE SITE-TARGETED HIV PROTEASE INHIBITORS CONTAINING A HYDROXYMETHYLCARBONYL ISOSTERE. USE OF PHENYLNORSTATINE OR ALLOPHENYLNORSTATINE AS A TRANSITION-STATE MIMIC
HIVプロテアーゼ阻害剤・KNI-272のProdrugの体内動態に関する研究
NEW HYDROXYL PROTECTING GROUPS OF A SAFETY-CATCH TYPE REMOVABLE BY TEDUCTIVE ACIDOLYSIS
KYNOSTATIN (KNI)-227 AND -272,HIGHLY POTENT ANTI-HIV AGENTS : CONFORMATIONALLY CONSTRAINED TRIPEPTIDE INHIBITORS OF HIV PROTEASE CONTAINING ALLOPHENYLNORSTATINE
KNI-102,A NOVEL TRIPEPTIDE HIV PROTEASE INHIBITOR CONTAINING ALLOPHENYLNORSTATINE AS A TRANSITION-STATE MIMIC
Protease Inhibitor (PI) 耐性 HIV-1 に対抗ウイルス活性を有する新規 PI の開発

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