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Volumn 2, Issue 10, 2004, Pages 1511-1517
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Conformationally tailored N-(2-methy-3-oxo-3,4-dihydro-2H-1,4-benzoxazin-2- yl)carbonylproline templates as molecular tools for the design of peptidomimetics. Design and synthesis of fibrinogen receptor antagonists
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Author keywords
[No Author keywords available]
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Indexed keywords
BINDING ENERGY;
BIOMIMETIC MATERIALS;
CARBOXYLIC ACIDS;
CHEMICAL BONDS;
COMPUTER SIMULATION;
CONFORMATIONS;
ISOMERIZATION;
SOLUTIONS;
STEREOCHEMISTRY;
SYNTHESIS (CHEMICAL);
AROMATIC RINGS;
FIBRINOGEN RECEPTORS;
INTEGRIN RECEPTORS;
PROLINE BONDS;
POLYPEPTIDES;
ARGINYL GLYCYL ASPARTYL SERINE;
ARGINYL-GLYCYL-ASPARTYL-SERINE;
DRUG DERIVATIVE;
FIBRINOGEN RECEPTOR;
INTEGRIN;
OLIGOPEPTIDE;
PEPTIDE;
PROLINE;
VITRONECTIN RECEPTOR;
ARTICLE;
BINDING COMPETITION;
CHEMICAL STRUCTURE;
CHEMISTRY;
CHEMOLUMINESCENCE;
CONFORMATION;
DRUG ANTAGONISM;
NUCLEAR MAGNETIC RESONANCE SPECTROSCOPY;
STEREOISOMERISM;
STRUCTURE ACTIVITY RELATION;
SYNTHESIS;
BINDING, COMPETITIVE;
CHEMILUMINESCENT MEASUREMENTS;
INTEGRINS;
MAGNETIC RESONANCE SPECTROSCOPY;
MOLECULAR CONFORMATION;
MOLECULAR STRUCTURE;
OLIGOPEPTIDES;
PEPTIDES;
PROLINE;
RECEPTORS, FIBRINOGEN;
RECEPTORS, VITRONECTIN;
STEREOISOMERISM;
STRUCTURE-ACTIVITY RELATIONSHIP;
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EID: 3342955796
PISSN: 14770520
EISSN: None
Source Type: Journal
DOI: 10.1039/b400490f Document Type: Article |
Times cited : (10)
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References (27)
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