Synthesis and Biological Evaluation of CXCL14 and Its Derivatives
スポンサーリンク
概要
- 論文の詳細を見る
- 2011-03-01
著者
-
大高 章
Graduate School Of Pharmaceutical Sciences The University Of Tokushima
-
Otaka Akira
Institute Of Health Biosciences And Graduate School Of Pharmaceutical Sciences The University Of Tok
-
Otaka Akira
Institute Of Health Biosciences Graduate School Of Pharmaceutical Sciences The University Of Tokushi
-
Omagari Akane
Graduate School Of Pharmaceutical Sciences Kyoto University
-
Shigenaga Akira
Institute Of Health Biosciences And Graduate School Of Pharmaceutical Sciences The University Of Tok
-
SUMIKAWA Yoshitake
Institute of Health Biosciences and Graduate School of Pharmaceutical Sciences, The University of To
-
HARA Takahiko
Stem Cell Project Group, The Tokyo Metropolitan Institute of Medical Science
-
Otaka Akira
Univ. Tokushima Tokushima Jpn
-
Shigenaga Akira
Institute Of Health Biosciences And Graduate School Of Pharmaceutical Sciences The University Of Tok
-
Shigenaga Akira
Univ. Tokushima Tokushima Jpn
-
Shigenaga Akira
Institute Of Health Biosciences And Graduate School Of Pharmaceutical Sciences The University Of Tok
-
TSUJI Kohei
Institute of Health Biosciences and Graduate School of Pharmaceutical Sciences, The University of To
-
TANEGASHIMA Kosuke
Stem Cell Project Group, The Tokyo Metropolitan Institute of Medical Science, Tokyo Metropolitan Org
-
Tsuji Kohei
Institute Of Health Biosciences And Graduate School Of Pharmaceutical Sciences The University Of Tok
-
Hara Takahiko
Stem Cell Project Group The Tokyo Metropolitan Institute Of Medical Science Tokyo Metropolitan Organ
-
Sumikawa Yoshitake
Institute Of Health Biosciences And Graduate School Of Pharmaceutical Sciences The University Of Tok
-
Tanegashima Kosuke
Stem Cell Project Group The Tokyo Metropolitan Institute Of Medical Science Tokyo Metropolitan Organ
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
- Synthesis of fluoroalkene dipeptide isosteres utilizing intramolecular redox reaction
- 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
- Involvement of Stathmin in Proliferation and Differentiation of Immortalized Human Endometrial Stromal Cells
- Development of Stimulus Responsive Thiol Releasing System for Controlling Activity of Cysteine Protease
- Development of Photo-Responsive Self-Processing Peptides
- P-202 DEVELOPMENT OF PHOTO-TRIGGERED SELF-PROCESSING PEPTIDES
- 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
- Development of Amide Bond Cleavage Device with Application to Chemical Biology Use
- 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
- Caged Ceramide Which Releases Parent Ceramide After UV-Induced Amide Bond Cleavage Followed by Intramolecular O-N Acyl Transfer
- Muscle injury-induced thymosin β4 acts as a chemoattractant for myoblasts
- Double-Kinetically Controlled Proline Ligation
- N-Sulfanylethylanilide Peptide : A Peptide Thioester Equivalent Which Can Directly Participate in Native Chemical Ligation
- Development of Efficient Synthetic Protocol for Fmoc Amino Acid-Incorporated N-Sulfanylethyl-Aniline Linker as Peptide Thioester Precursor
- Design and Synthesis of Hypoxia-responsive Amino Acid Which Causes Peptide Bond Cleavage in Hypoxic Cells
- Synthesis of Antagonistic Peptide for Putative CXCL14 Receptor Proteins and Their Identification
- Convergent Chemical Synthesis of Human GM2 Activator Protein Analog Using SEAlide Chemistry
- Development of Stimulus-responsive Amino Acids and Their Application to Peptide Based Chemical Biology