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Department Of Medicinal Chemistry Kyoto Pharmaceutical University | 論文
- Synthesis of the Heptadecapeptide Corresponding to the Entire Amino Acid Sequence of Salmon Melanin-Concentrating Hormone (MCH)
- Synthesis of Transmembrane Protein, F_1F_0 ATP Synthase Subunit c, by Thioester Method
- NEW HYDROXYL PROTECTING GROUPS OF A SAFETY-CATCH TYPE REMOVABLE BY TEDUCTIVE ACIDOLYSIS
- Fluoren-9-ylmethyloxycarbonyl (Fmoc) Amino Acid Chloride as an Efficient Reagent for Anchoring Fmoc Amino Acid to 4-Alkoxybenzyl Alcohol Resin
- Deprotection of the S-Trimetylacetamidomethyl (Tacm) Group Using Silver Tetrafluoroborate : : Application to the Synthesis of Porcine Brain Natriuretic Peptide-32 (pBNP-32)
- Solution-Phase Synthesis of Porcine Brain Natriuretic Peptide (pBNP) Using S-Trimethylacetamido-methylcysteine
- Trimethylacetamidomethyl (Tacm) Group, a New Protecting Group for the Thiol Function of Cysteine
- SYNTHESIS OF PORCINE BRAIN NATRIURETIC PEPTIDE-32 USING SILVER TETRAFLUOROBORATE AS A NEW DEPROTECTING REAGENT OF THE S-TRIMETHYLACETAMIDOMETHYL GROUP
- EFFICIENT SOLID PHASE PEPTIDE SYNTHESIS ON A PHENACYL-RESIN BY A METHANESULFONIC ACID α-AMINO DEPROTECTING PROCEDURE
- TETRAFLUOROBORIC ACID, A USEFUL DEPROTECTING REAGENT IN PEPTIDE SYNTHESIS
- A FLUORIDE ION DEPROTECTION STRATEGY IN PEPTIDE SYNTHESIS. : COMBINATION WITH SELECTIVE DEPROTECTION USING THE DILUTE METHANESULFONIC ACID OF α-MAINO PROTECTING GROUPS
- RACEMIZATION-FREE SYNTHESIS OF C-TERMINAL CYSTEINE-PEPTIDE USING 2-CHLOROTRITYL RESIN
- Synthesis of Rat Brain Natriuretic Peptide 45 Using Tetrafluoroboric Acid Deprotection and Silyl Chloride Disulfide Formation
- KYNOSTATIN (KNI)-227 AND -272,HIGHLY POTENT ANTI-HIV AGENTS : CONFORMATIONALLY CONSTRAINED TRIPEPTIDE INHIBITORS OF HIV PROTEASE CONTAINING ALLOPHENYLNORSTATINE
- KNI-102,A NOVEL TRIPEPTIDE HIV PROTEASE INHIBITOR CONTAINING ALLOPHENYLNORSTATINE AS A TRANSITION-STATE MIMIC
- Solution-Phase Synthesis of α-Rat Atrial Natriuretic Peptide (α-rANP)
- Solution-Phase Synthesis of α-Human Atrial Natriuretic Peptide (α-hANP)
- 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