Structural Analysis of SARS 3CL Protease Complexed with Peptide-Mimetic Inhibitors
スポンサーリンク
概要
- 論文の詳細を見る
- 2013-03-01
著者
-
Akaji Kenichi
Department Of Chemistry Graduate School Of Medical Science Kyoto Prefectural University Of Medicine
-
Hattori Yasunao
Department Of Chemistry Graduate School Of Medicinal Science Kyoto Prefectural University Of Medicin
-
Teruya Kenta
Graduate School Of Medical Science Kyoto Prefectural University Of Medicine
-
HATTORI Yasunao
Department of Medicinal Chemistry, Kyoto Pharmaceutical University
-
KONNO Hiroyuki
Yamagata University
-
OZAKI Takeshi
Institute for Protein Research, Osaka University
-
KUSUNOKI Masami
University of Yamanashi
-
SANJOH Akira
R&D Center, Protein Wave Co.
関連論文
- Effect of Multimerization of a Linear Arg-Gly-Asp Peptide on Integrin Binding Affinity and Specificity
- Synthesis and Activity of a New Type of Anti-HIV Agents, Conjugate of HIV Protease Inhibitor with Reverse Transcriptase Inhibitor
- Synthesis of an HIV-1 Protease Analogue by the Chemoselective Ligation Method Using a New Disulfide Type Linker
- A CONCISE SYNTHESIS OF SOLAMIN AND CIS-SOLAMIN, MONO-THF ACETOGENINS FROM ANNONA MURICATA
- P-364 Total Synthesis of Murisolin, Murisolin A, and 16,19-cis-Murisolin
- 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
- 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
- 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
- AROUND THE NAGATA'S METRICS
- SYNTHESES AND BIOLOGICAL ACTIVITIES OF SEVERAL NEWLY ISOLATED NATRIURETIC PEPTIDES
- Synthetic study of callipeltin A, an anti-HIV cyclic depsipeptide isolated from marine sponge
- Synthesis of Annonacin Isolated from Annona densicoma
- 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
- Transfinite large inductive dimensions modulo absolute Borel classes
- The behaviour of dimension functions on unions of closed subsets
- Evaluation of modified proteins for targeting exogenously prepared proteins on the cell surface
- Evaluation of Substrate Specificities for BACE1 using Synthetic Peptide Libraries
- Estimations of small transfinite dimension in separable metrizable spaces
- 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
- Targeting Exogenous Proteins to Cell Surface by C-terminal Modification with Cholesterol via a Hydrophilic Linker
- Design, Synthesis and Evalution of Tripeptidomimetics with Arylketone as Inhibitors of SARS-CoV 3CL Protease
- 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
- Evaluation of a tooth bleaching system incorporating titanium dioxide : Influence of the concentrations of hydrogen peroxide and titanium dioxide on bleaching effect
- 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