リン酸化ペプチドの化学合成 (構造生物学のフロンティア--シグナル伝達とDNAトランスアクション) -- (構造生物学の方法論の新しい展開)
スポンサーリンク
概要
著者
-
Omagari Akane
Graduate School Of Pharmaceutical Sciences Kyoto University
-
Otaka Akira
Univ. Tokushima Tokushima Jpn
関連論文
- Synthesis of a CC Chemokine, vMIP-II, Encoded by Kaposi's Sarcoma-Associated Herpesvirus and Its Biological Activity
- Synthesis and Biological Evaluation of Peptidomimetic Analogs of the CXCR4 Antagonist FC131
- The Chemokine Receptor CXCR4 as a Therapeutic Target for Several Diseases Including AIDS, Cancer and Rheumatoid Arthritis
- New Leads of Low Molecular Weight CXCR4 Antagonists Based on Enhancement of the T140-based Pharmacophores
- A New Strategy for Molecular-size Reduction of Bioactive Peptide, Using Two Orthogonal Libraries of Cyclic peptides
- CXCR4 Antagonists Identified as Anti-Cancer-Metastatic Agents
- Synthesis of Novel Anti-HIV Peptides Based on a CXCR4 Antagonist, T140, and Their SAR Study
- Development of Specific CXCR4 Inhibitors Based on an Anti-HIV Peptide, T140, and Their Structure-Activity Relationships Study
- HIV-cell Fusion Inhibitors Targeted to the HIV Second Receptor : T22 and Its Downsized Analogs with High Activity
- リン酸化ペプチドの化学合成 (構造生物学のフロンティア--シグナル伝達とDNAトランスアクション) -- (構造生物学の方法論の新しい展開)
- Synthesis and Biological Activity of Bombesin Analogues Containing (E)-Alkene Dipeptide Isosteres
- Development of Stimulus-Responsive Amino Acid with Peptide Bond-Cleavage Ability and Its Application to a Nucleocytoplasmic Shuttle Peptide
- Efficient Synthesis of Cyclic RGD Pseudopeptide with (E)-Alkene Dipeptide Isostere and Its Biological Activity
- Identification of a Polyphemusin Analog(T22)-Zn(II) Complex by Mass Spectrometric Analysis and Its Anti-HIV Activity
- Identification of Binding Proteins of an Anti-HIV Peptide, T22
- Design and Synthesis of Highly Active Anti-HIV Peptide Based on Gp41-C34 Peptide
- Synthesis of Alkene Type Dipeptide Isosteres and Their Use to Probe the Structural Requirements of Peptide Transporter (PEPT1)
- Structure-Activity Relationship Study on hOT7T175 Agonist with RW-Amide
- Synthesis of (Z)-Alkene cis-Ala-Pro Mimetics Using Organocopper Reagents
- Endeavors for Highly Stereoselective Synthesis of Functionalized Fluoroalkene Dipeptide Isosteres
- Stereoselective Synthesis of Diketopiperazine Mimetics as Promising Scaffolds for Drug Discovery Utilizing Organocopper-Mediated anti-S_N2' Reaction
- Synthesis of ψ[(E)-CH=CMe]- and ψ[(Z)-CH=CMe]-type Dipeptide Isosteres and their Application to a Cyclic RGD Peptide
- Synthesis of ψ[(E)-CMe=CMe]- and ψ[(E)-CMe=CH]-type Alkene Dipeptide Isosteres from a Chiral Amino Acid
- A New Practical Strategy for the Synthesis of Long-Chain Phosphopeptide
- Synthesis of Nonhydrolyzable Phosphothreonine Derivatives and Their Practical Application to Peptide Synthesis
- Practical Phosphoeptides Synthesis Using Dimenthylphosphono Amino Acids (No.2)
- Development of Low Molecular Weight CXCR4 Antagonists by Exploratory Structural Tuning of Cyclic Tetrapeptide-scaffolds
- Synthesis of (Z)-Alkene cis-Xaa-Pro Type Dipeptide Isosteres Using Organocopper-Mediated Anti-S_N2' Reactions
- 4-(Dimethylamino)phenacyl Group : New Photoremovable Protecting Group for Amines and Carboxylic Acids
- Application of Ring Closing Olefin Metathesis to the Conformational Restriction of Biologically Active Peptide. Part 1
- Stereoselective Synthesis of CF_2 or CHF-Substituted Phosphoamino Acids and Their Incorporation into Peptides
- Synthesis of β-Secretase Inhibitors Containing a Hydroxyethylamine Dipeptide Isostere and their Structure-activity Relationship Studies
- Synthesis of Peptide Thioesters using N-Substituted Aniline Derivatives
- Translocation of Basic Peptides through Human Cell Membranes
- New Strategy for The Synthesis of Aspartyl Protease Inhibitor Based on "Aza-Payne Rearrangement"
- Synthetic Studies on 7TM-GPCR (I) : Lipid Bilayer Assisted Membrane Peptide Ligation
- Influence of an Amino Acid Sequence on Kinetics of Peptide Bond Cleavage Reaction Induced by a Stimulus-responsive Amino Acid
- Application of Peptide Thioacids to NCL-type Sequential Condensation of Peptide Fragments
- Development of Potent β-Secretase Inhibitors Containing a Hydroxyethylamine Dipeptide Isostere
- Development of Stimulus Responsive Thiol Releasing System for Controlling Activity of Cysteine Protease
- Synthesis of Nonhydrolyzable AMPylated Amino Acid Analogues for Uncovering the Physiological Role of AMPylation
- Development of Recapturable Cleavable Linker for Efficient Enrichment and Specific Labeling of Target Proteins
- Native Chemical Ligation Using N-peptidyl Anilide as Crypto-thioester
- Enantioselective Synthesis of Stimulus-responsive Amino Acid via Pyrrolidinyl Tetrazole Catalyzed Asymmetric α-Amination of Aldehyde
- Synthesis and Biological Evaluation of CXCL14 and Its Derivatives
- Synthesis of Fluoroalkene Dipeptide Isosteres Utilizing Organocopper or SmI_2 Reagents
- 高付加価値ペプチド合成のための最終脱保護法の開発と細胞内情報伝達機構解明への展開研究