2位酸性アミノ酸置換Demorphinテトラペプチド同族体の合成とオピオイド受容体親和性
スポンサーリンク
概要
著者
関連論文
- [D-Arg2]Demorphin関連テトラペプチド同族体の合成とオピオイド活性
- [D-Arg^2]Dermorphinテトラペプチド同族体,Tyr-D-Arg-Phe-Xの構造活性相関
- Synthesis of Carboxyl-Terminal Extension Analogs of Dermorphin and Evaluation of Their Opioid Receptor-Binding and Opioid Activities
- Degradation of Deltorphins and Their Analogs by Rat Brain Synaptosomal Peptidases
- ダイノルフィン(1-8)のアドレス部置換同族体の合成とオピオイドレセプター親和性
- 2位酸性アミノ酸置換Demorphinテトラペプチド同族体の合成とオピオイド受容体親和性
- Solid-Phase Synthesis and Opioid Activities of [D-Ala^2]Deltorphin II Analogs
- Studies on Analgesic Oligopeptides. VII. Solid Phase Synthesis and Biological Properties of Tyr-D-Arg-Phe-βAla-NH_2 and Its Fluorinated Aromatic Amino Acid Derivatives
- Solid Phase Synthesis and Opioid Receptor Binding Properties of Presumable Dermorphin Precursor Derivatives
- Solid Phase Synthesis and Opioid Receptor Binding Activities of[D-Ala^2,D-Leu^5]Enkephalin Analogs Containing a Fluorinated Aromatic Amino Acid
- Studies on Analgesic Oligopeptides. VI. : Further Studies of Synthesis and Biological Properties of Tripeptide Alkylamides, Try-D-Arg-Phe-X
- Studies on analgesic Oligopeptides. V. : Structure-Activity Relationship of Tripeptide Alkylamides, Tyr-D-Arg-Phe-X
- Studies on Analgesic Oligopeptides. IV. Synthesis and Analgesic Activity of N-Terminal Shorter Analogs of [D-Arg^2] Dermorphin and Des-Tyr^1-Dermorphin Analogs
- Studies on Analgesic Oligopeptides. III. Synthesis and Analgesic Activity after Subcutaneous Administration of [D-Arg^2] dermorphin and Its N-Terminal Tetrapeptide Analogs
- Studies on Analgesic Oligopeptides. II. Structure-Activity Relationship among Thirty Analogs of a Cyclic Dipeptide, Cyclo (-Tyr-Arg-)
- Structure and Analgesic Activity Relationship of Cyclo-Tyrosyl-Arginyl and Its Three Stereoisomers
- 講演要旨の請求は遠慮せずに(重複発表の是非)
- Acetic Acid-Catalyzed Diketopiperazine Synthesis
- The β-p-Nitrobenzyl Ester to Minimize Side Reaction during Treatment of Aspartyl Peptides with Methanesulfonic Acid
- Selective Cleavage of tert-Butyloxycarbonyl Protecting Group with Dilute Organic Sulfonic Acid without Decomposition of Tryptophan Residue
- The γ-Phenacyl and γ-p-Nitrobenzyl Esters to Minimize Side Reactions during Treatment of Glutamyl Peptides with Hydrogen Fluoride-Anisole Mixture
- Pichia pastoris IFO 0948株マンナン : タンパク質複合体のO-結合型マンノオリゴ糖鎖の化学講造
- デルトルフィンのアドレス部置換同族体の合成と生物活性
- コルチコトロピンの合成のための最小限度に保護されたペプチドフラグメントの固相合成--〔Lys(Tfa)15,16,21〕-ACTH-(15-24)-decapeptideの合成
- 新規ダイノルフィン誘導体, Tyr-D-Ala-Phe-Leu-Arg-ψ(CH_2NH)Arg-NH_2 の抗侵害作用について
- BIOLOGICALLY ACTIVE SYNTHETIC FRAGMENTS OF BRADYKININ
- Tactics for Simplification of Purification Process in the Solid Phase Peptide Synthesis
- Studies on Encephalitogenic Fragments of Myelin Protein. I. Synthesis of Tryptophan-containing Fragments
- "Low-Molecular Kininogen"類似ペプチドのモルモット回腸収縮作用とTrypsinとの関係
- Fmoc法とMerrifield樹脂を併用したペプチドアルキルアミドの固相合成
- Tyr-D-Arg-Phe-Xペプチドにおける4位塩基性残基のオピオイド受容体親和性への影響
- 南米産カエル皮膚由来ペプチドDeltorphin:Deltorphin類および関連同族体の生物学的特性とオピオイド活性
- The β-Phenacyl and β-p-Nitrobenzyl Esters to Suppress Side Reactions during Treatment of Aspartyl Peptides with Hydrogen Fluoride
- Studies on Encephalitogenic Fragments of Myelin Protein. IV. Synthesis of Glycine Analogs of Tryptophan-containing Fragment
- Studies on Encephalitogenic Fragments of Myelin Protein. II. Solid Phase Synthesis of Tryptophan-containing Decapeptide