Efficient Synthesis of Alamethicin using a Newly Developed Coupling Reagent, CIP
スポンサーリンク
概要
- 論文の詳細を見る
- 1995-10-01
著者
-
Kiso Y
Kyoto Pharmaceutical Univ. Kyoto Jpn
-
Akaji K
Kyoto Pharmaceutical Univ. Kyoto Jpn
-
Kiso Yoshiaki
Department Of Medicinal Chemistry Center For Frontier Research In Medicinal Science 21st Century Coe
-
Akaji Kenichi
Department Of Chemistry Graduate School Of Medical Science Kyoto Prefectural University Of Medicine
-
TAMAI Yasunori
Department of Medicinal Chemistry, Kyoto Pharmaceutical University
-
Tamai Yasunori
Department Of Medicinal Chemistry Kyoto Pharmaceutical University
-
KISO Yoshiaki
Department of Ecological Engineering, Toyohashi University of Technology, JAPAN.
関連論文
- Development of New Photoresponsive Paclitaxel Prodrug
- Phototaxel : Development of First Photoresponsive Prodrug of Paclitaxel via Modification of Phenylisoserine Moiety
- "Click Peptide" : the "O-Acyl Isopeptide Method" for Peptide Synthesis and Development of Chemical Biology-Oriented Aβ Analogues
- "Click Peptide" Based on the "O-Acyl Isopeptide Method" : Development of Chemical Biology-Oriented Alzheimer's Disease-Related Aβ1-42 Analogues
- Design and Synthesis of Dipeptide-type HIV-1 Protease Inhibitors with High Antiviral Activity
- Controlled Drug Release : Design and Application of New Water-soluble Prodrugs
- Spontaneously Regenerable Prodrug : Design and Synthesis of Water-soluble Prodrugs of HIV Protease Inhibitors
- Design of Double-Drug-Type Anti-HIV Agents
- New Type Prodrugs of Anti-HIV Agents Consisting of the HIV Protease Inhibitor and Reverse Transcriptase Inhibitor
- 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
- Racemization-Free Segment Condensation Based on Isopeptide Method : An Efficient Preparation of Peptides on Solid Support
- The Synthesis of Bioactive Peptides Based on O-Acyl Isopeptide Method : Application of O-Acyl Isodipeptide Units
- Development of Racemization-Free "O-Acyl Isopeptide Method" Utilizing the "O-Acyl Isodipeptide Unit"
- P-262 "O-ACYL ISOPEPTIDE METHOD" FOR THE EFFICIENT SYNTHESIS OF DIFFICULT SEQUENSE-CONTAINING PEPTIDES : UTILIZATION OF "O-ACYL ISODIPEPTIDE UNIT"
- Conversion of Polymer-Bound Dipeptide to Evans-Type Chiral Auxiliary : A New Tool for Efficient Solid-Phase Asymmetric Reactions
- Development of Spontaneously Regenerable Water-Soluble Prodrugs Based on the Peptide Chemistry : Importance of Drug Release Time for the Improvement of Gastrointestinal Absorption
- Structure-Activity Relationship of Orally Potent Tripeptide-Based HIV Protease Inhibitors Containing Hydroxymethylcarbonyl Isostere
- 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
- Solution NMR Studies of the HIV-1 Protease/Inhibitor Complex : The HIV-1 Protease Catalytic Aspartyl Side-Chain Carboxyl Groups Have Distinct Protonation States in the Complex Formed with the Asymmetric Inhibitor KNI-272
- Synthesis of Transmembrane Protein, F_1F_0 ATP Synthase Subunit c, by Thioester Method
- Novel BACE1 Inhibitors : Design Approach Focused on Inhibitor's Conformer
- Structure-Activity Relationship Study of BACE1 Inhibitors Containing Chelidonamide
- Synthesis of HIV Protease Dipeptide Inhibitors and Prodrugs
- Oligoarginine-Based Prodrugs with Self-Cleavable Spacers for Caco-2 Cell Permeation
- Synthesis and Activity of Tetrapeptidic Human T-cell Leukemia Virus Type I Protease Inhibitors Possessing Different P_1'- and P_3-cap Moieties
- Design of BACE1 Inhibitors : Replacing the P_1' Residue with Non-Acidic Moiety
- Design and Synthesis of Conformationally Constrained Dimerization Inhibitors of HIV-1 Protease
- The N-Terminal Helical Segments Modulate Structure and Lipid Interaction of Human Apolipoprotein A-I
- Studies on Structure-Activity Relationship of HTLV-1 Protease Inhibitors
- Solid-Phase Syntheses of Olefin-Containing Protease Inhibitors Using Horner-Emmons Reaction
- Synthesis of Olefin-Containing Cyclic Peptide Library Using the Solid-Phase Horner-Emmons Reaction
- Solid-Phase Peptide Synthesis Using N^α-Fmoc(2-F)-Amino Acid and Its Application to the Synthesis of Phosphorylated Peptide Thioesters
- Total Synthesis of Human T-cell Leukemia Virus Type-1 Protease via the Thioester Method
- Synthesis of a Molt-Inhibiting Hormone of the American Crayfish, Procambarus clarkii and Determination of Its Disulfide Linkage
- Synthesis of Phosphorylated Polypeptide Using an Expressed Peptide as a Building Block
- Synthesis of a Molt-Inhibiting Hormone of the American Crayfish, Procambarus clarkii, and Determination of the Location of Its Disulfide Linkages^1
- Use of an Expressed Peptide Segment as a Building Block for the Preparation of Phosphorylated Polypeptide via the Thioester Method
- Synthesis of Negamycin and Its Derivatives as Potential Therapeutic Agents for Duchenne Muscular Dystrophy
- Phenylthionorstatine as a Transition-State Mimic in BACE1 Inhibitors
- Tripeptide Mimetics with Potent Inhibitory Activity against Malarial Aspartic Protease Plasmepsin II
- P-296 DEVELOPMENT OF RESIN SUPPORTED EVANS-TYPE CHIRAL AUXILIARY FOR SOLID-PHASE ASYMMETRIC REACTION
- Modification of P4 Position in β-secretase (BACE1) Inhibitors Containing Phenylnorstatine
- Design of β-Secretase (BACE1) Inhibitors with Carboxylic Acid Bioisosteres
- Evaluation of Peptidomimetic HTLV-I Protease Inhibitors Containing Hydroxymethylcarbonyl as a Transition-State Isostere
- O-N Intramolecular Acyloxy Migration Reaction : from the Prodrug Strategy to the Migration of Protective Groups in Amino Acids
- "Click Peptide" Based on the "O-Acyl Isopeptide Method" : an Efficient Preparation of Amyloid β Peptide 1-42 Mutants
- Design and Synthesis of β-Secretase Inhibitors Containing Hydroxymethylcarbonyl Isostere as a Transition State Mimic
- SYNTHESES AND STRUCTURE-ACTIVITY RELATIONSHIPS OF ATRIAL NATRIURETIC PEPTIDE (ANP) DERIVATIVES
- High-throughput Screening Method for Ligand Peptides Using Capillary Electrophoresis-Mass Spectrometry (CE-MS)
- A Novel S-Acyl Isopeptide Method for the Synthesis of Difficult Sequence-Containing Peptide
- Isopeptide Method : A Racemization-Free Peptide Synthesis by Segment Condensation
- Synthesis and Biological Activities of Phenylahistin Derivatives
- Design and Synthesis of Inhibitory Peptides against EGF Receptor Dimerization
- SAR study of BACE1 inhibitors containing pyridine derivatives
- Significance of interaction of BACE1-Arg235 with its ligands and design of BACE1 inhibitors
- Chemical Synthesis of 71-meric Neuregulin 1-β1
- Click Peptide by Use of the O-Acyl Isopeptide Method : Production of Amyloid β Peptide from Water-Soluble Analogue
- "O-Acyl Isopeptide Method" for the Synthesis of Difficult Sequence-Containing Peptides : Application to the Synthesis of Amyloid β Peptide (Aβ) 1-42
- Development of Biotin-Tagged Tubulin Photoaffinity Probes Derivatized from Diketopiperazine Based Anti-Microtubule Agents
- Effect of the Phenyl Ring Modification on the Antitumor Activity of Anti-Microtubule Agent Dehydrophenylahistin
- Uptake Mechanisms of FITC-Oligoarginine Conjugates in HeLa Cells
- Design and Synthesis of Oligoarginine-Fluorescein Conjugates Possessing Novel Self-Cleavable Spacers as a Model for Effective Intestinal Absorption
- Efficient Total Synthesis of (+)-Negamycin and Its Derivatives
- Small Peptide-based Medicinal Chemistry for Intractable Disease
- A Synthetic Method for Monodehydro-Cyclic-Dipeptides toward Natural Product Synthesis
- New Aspects of Potent Anti-Microtubule Agents Phenylahistin and Tubulin Photoaffinity Labeling
- P-518 DEVELOPMENT OF POTENT ANTI-MICROTUBULE AGENTS BASED ON NATURAL DIKETOPIPERAZINE PHENYLAHISTIN AND TUBULIN PHOTOAFFINITY LABELING
- Development of a New Synthetic Method for Monodehydro-2,5-diketopiperazines
- Synthetic Study of Anti-microtubule Diketopiperazines : Phenylahistin and Aurantiamine
- 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
- Effect of Dipeptidomimetics on Malaria Parasite Proliferation Inhibition Targeting Plasmepsin
- Design and Synthesis of Highly Active β-Secretase (BACE1) inhibitors, KMI-420 and KMI-429, with Enhanced Chemical Stability
- Evaluation of Peptidomimetic Inhibitors against Malarial Protease Plasmepsin
- Dipeptide-Type Inhibitors Targeting Plasmepsins from Plasmodium Falciparum
- Analysis of Side Reaction in the Amide Bond Formation with an α-Hydroxy-β-amino Acid as an Acyl Componemt
- Substrate Transition-State Analogue Inhibitors of Plasmepsin II as Antimalarial Drugs
- An Approach for Peptidic Aspartic Protease Inhibitors Using Ala-containing Oligopeptides Independent of the Substrate Sequence
- Development of a New Synthetic Method for L-Tetrahydrofuranylglycine and Its Application for Substrate-based HIV-1 Protease Inhibitors
- Synthesis of Human C-Type Natriuretic Peptide 22 Using Chlorotrityl Resin and Tetrafluoroboric Acid Deprotection
- O-N Intramolecular Acyl and Acyloxy Migration Reaction in the Development of Water-Soluble Prodrugs of Taxoids
- A Novel Method for the Synthesis of Difficult Sequence-Containing Peptides via O-Acyl Isopeptides : The Use of O-N Intramolecular Acyl Migration Reaction
- Development of New Water-Soluble Prodrugs Based on Intramolecular Nucleophilic Reactions in Peptide Chemistry
- 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
- Click Peptide : Application to E22Δ-type Mutant of Amyloid β Peptide
- Click Peptide : In Situ Production of pyroGlu-Abeta from the O-Acyl Isopeptide
- Use of O-Acyl Isopeptides to Identify New Functions of Amyloid β Peptides
- SYNTHESES AND OPIOID ACTIVITIES OF ENKEPHALIN-AND DERMORPHIN-RELATED PEPTIDES
- NMR Studies on Reorientation Process of the Inhibitor Tightly Bound to HIV Protease
- Design and Synthesis of a Covalently Linked HIV-1 Protease Dimer Analog and Peptidomimetic Inhibitors
- 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