Synthesis and Evaluation of Serine Derivatives for SARS 3CL protease
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概要
- 論文の詳細を見る
- 2013-03-01
著者
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Konno Hiroyuki
Graduate School Of Medical Science Kyoto Prefectural University Of Medicine
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Akaji Kenichi
Department Of Chemistry Graduate School Of Medical Science Kyoto Prefectural University Of Medicine
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KONNO Hiroyuki
Graduate School of Science and Technology, Yamagata University
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TAKANUMA Daiki
Graduate School of Science and Technology, Yamagata University
関連論文
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- Synthesis of an HIV-1 Protease Analogue by the Chemoselective Ligation Method Using a New Disulfide Type Linker
- Small-sized HIV Protease Inhibitors Containing Allophenylnorstatine as a Substrate Transition-state Mimic
- Design of HIV Protease Inhibitors Based on the Transition State Analogue Concept
- 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
- Synthesis of HIV Protease Dipeptide Inhibitors and Prodrugs
- Studies on N^〈in〉-Protecting Groups during the Synthesis of Trp : Containing Cystine Peptide by Silyl Chloride Sulfoxide Method
- A Reductive Acidolysis Final Deprotection Strategy in Solid Phase Peptide Synthesis Based on Safety-Catch Protection
- 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
- Synthesis of Human C-Type Natriuretic Peptide 22 Using Chlorotrityl Resin and Tetrafluoroboric Acid Deprotection
- SYNTHESES AND STRUCTURE-ACTIVITIES RELATIONSHIPS OF SMALLSIZED ATRIAL NATRIURETIC PEPTIDE (ANP) DERIVATIVES WITH POTENT ACTIVITY
- SYNTHESES AND STRUCTURE-ACTIVITY RELATIONSHIPS OF SMALL-SIZED ATRIAL NATRIURETIC PEPTIDE (ANP) DERIVATIVES
- Solid Phase Synthesis of a Mercaptoamide Peptide Using New Linkers
- SYNTHESES OF CYSTINE-PEPTIDES BY A NEW DISULPHIDE BOND FORMING REACTION
- SYNTHESES AND BIOLOGICAL ACTIVITIES OF SEVERAL NEWLY ISOLATED NATRIURETIC PEPTIDES
- Synthetic study of callipeltin A, an anti-HIV cyclic depsipeptide isolated from marine sponge
- Structure Activity Relationship Study of SARS Coronavirus 3CL Protease Inhibitors with an Electrophilic Aryl Ketone Structure
- Development of Stimulus Responsive Thiol Releasing System for Controlling Activity of Cysteine Protease
- Synthesis and Evaluation of Small Peptide Inhibitors for SARS 3CL Protease
- Evaluation of Substrate Specificities for BACE1 using Synthetic Peptide Libraries
- Convergent Synthesis of Dolastatin 15 by Solid Phase Coupling of N-methylamino Acid
- Total Synthesis of (-)-Mirabazole B Using a Chloroimidazolidium Reagent, CIP
- Efficient Synthesis of Alamethicin using a Newly Developed Coupling Reagent, CIP
- Efficient Coupling of Dialky Amino Acid Using a Chloro Imidazolidium Reagent, CIP
- Design, Synthesis and Evalution of Tripeptidomimetics with Arylketone as Inhibitors of SARS-CoV 3CL Protease
- Synthesis of Cyclic Lipopeptide Derivatives of Burkholdines and Its Antifungal Activity
- Synthetic Study of the Depsipeptides Analogues of Callipeltin B and Its Cytotoxicity
- Evaluation of Inhibitory Activities of Curcumin Derivatives Using BACE1 and Amyloid Beta Peptide
- Synthesis of O-Acyl Isopeptide by Use of Native Chemical Ligation to Efficiently Construct Hydrophobic Polypeptide
- Selective Liposome Binding of Protein Modified with Hydrophobic Compounds at the C-Terminal
- Synthesis of Hydroxyethyl-type Inhibitor Containing Superior BACE1 Cleavage Sequence
- Structural Analysis of SARS 3CL Protease Complexed with Peptide-Mimetic Inhibitors
- Synthesis and Evaluation of Serine Derivatives for SARS 3CL protease