Evaluation of Peptide-Based Inhibitors using R188I Mutant of SARS 3CL Protease as a Proteolysis-Resistant Mutant
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概要
- 論文の詳細を見る
- 2008-03-01
著者
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Konno Hiroyuki
Graduate School Of Medical Science Kyoto Prefectural University Of Medicine
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Akaji Kenichi
Graduate School Of Medical Science Kyoto Prefectural University Of Medicine
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ONOZUKA Mari
Graduate School of Medical Science, Kyoto Prefectural University of Medicine
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SAITO Hiroyuki
Kobe Pharmaceutical University
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MAKINO Ayumi
Kobe Pharmaceutical University
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NOSAKA Kazuto
Graduate School of Medical Science, Kyoto Prefectural University of Medicine
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Onozuka Mari
Graduate School Of Medical Science Kyoto Prefectural University Of Medicine
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Nosaka Kazuto
Graduate School Of Medical Science Kyoto Prefectural University Of Medicine
関連論文
- Synthesis and Structure Activity Relationship Studies of Miraziridine A, a Cysteine Protease Inhibitor
- Evaluation of Peptide-Based Inhibitors using R188I Mutant of SARS 3CL Protease as a Proteolysis-Resistant Mutant
- Synthetic Studies on Miraziridine A, a Cysteine Protease Inhibitor Isolated from Theonella aff. mirabilis
- P-61 SYNTHESES OF TOKARAMIDE A AND MIRAZIRIDINE A CYSTEINE PROTEASE INHIBITORS FROM THEONELLA AFF. MIRABILIS
- Synthetic Studies of Tokaramide A and Miraziridine A Isolated from Marine Sponge Theonella aff. mirabilis
- Molecular Cloning and Analysis of the 5'-Flanking Region of the Human Thiamin Pyrophosphokinase Gene
- Syntheses and Evaluations of Peptide-Based Inhibitors Using R188I Mutant of SARS 3CL Protease
- Synthetic Studies on Callipeltins B and E Isolated from Marine Sponge
- Synthetic study of callipeltin A, an anti-HIV cyclic depsipeptide isolated from marine sponge
- Synthesis and Evaluation of Small Peptide Inhibitors for SARS 3CL Protease
- Evaluation of modified proteins for targeting exogenously prepared proteins on the cell surface
- Synthesis of Cyclic Lipopeptide Derivatives of Burkholdines and Its Antifungal Activity
- Synthetic Study of the Depsipeptides Analogues of Callipeltin B and Its Cytotoxicity
- Synthesis of Hydroxyethyl-type Inhibitor Containing Superior BACE1 Cleavage Sequence
- Synthesis and Evaluation of Serine Derivatives for SARS 3CL protease