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Volumn 63, Issue 2, 2002, Pages 141-149
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An optimized solid phase synthesis strategy - Including on-resin lactamization - Of astressin, its retro-, inverso-, and retro-inverso isomers as corticotropin releasing factor antagonists
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Author keywords
Antagonists; CD; Cyclic peptides; Mimetics; Peptide synthesis; Retro inverso peptides
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Indexed keywords
AROMATIC HYDROCARBONS;
BIOSYNTHESIS;
DERIVATIVES;
ISOMERS;
ORGANIC ACIDS;
SOLUTIONS;
SECONDRY STRUCTURES;
BIOPOLYMERS;
ASTRESSIN;
CORTICOTROPIN RELEASING FACTOR ANTAGONIST;
PEPTIDE HORMONE;
RESIN;
SYNTHETIC PEPTIDE;
ARTICLE;
CHEMICAL REACTION;
CHEMICAL STRUCTURE;
CIRCULAR DICHROISM;
HIGH PERFORMANCE LIQUID CHROMATOGRAPHY;
HORMONE RECEPTOR INTERACTION;
ISOMERISM;
PEPTIDE SYNTHESIS;
SOLID;
SYNTHESIS;
AMINO ACID SEQUENCE;
ANIMALS;
BETA-GALACTOSIDASE;
CELLS, CULTURED;
CIRCULAR DICHROISM;
CORTICOTROPIN-RELEASING HORMONE;
GENES, REPORTER;
GLUTAMIC ACID;
HUMANS;
LACTAMS;
LYSINE;
MICE;
MOLECULAR SEQUENCE DATA;
PEPTIDE FRAGMENTS;
PEPTIDES;
PROTEIN CONFORMATION;
PROTEIN STRUCTURE, SECONDARY;
RECEPTORS, CORTICOTROPIN-RELEASING HORMONE;
RESINS, PLANT;
STEREOISOMERISM;
WATER;
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EID: 0036160502
PISSN: 00063525
EISSN: None
Source Type: Journal
DOI: 10.1002/bip.10052 Document Type: Article |
Times cited : (10)
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References (35)
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