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Volumn 56, Issue 1, 2000, Pages 20-26
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A three-residue cyclic scaffold of non-RGD containing peptide analogues as platelet aggregation inhibitors: Design, synthesis, and structure-function relationships
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Author keywords
Cyclic non RGD containing analogues; Cyclization on solid support; Cystine non RGD analogues; Disulfide bond formation; Platelet aggregation inhibitors
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Indexed keywords
MOLECULES;
STRUCTURE (COMPOSITION);
SYNTHESIS (CHEMICAL);
CONFORMATIONAL CONSTRAINTS;
PROTEINS;
ANTITHROMBOCYTIC AGENT;
ARGINYLGLYCYLASPARTIC ACID;
FIBRINOGEN RECEPTOR ANTAGONIST;
PEPTIDE DERIVATIVE;
ARTICLE;
CYCLIZATION;
DISULFIDE BOND;
DRUG DESIGN;
DRUG STRUCTURE;
DRUG SYNTHESIS;
IC 50;
PEPTIDE SYNTHESIS;
STRUCTURE ACTIVITY RELATION;
STRUCTURE ANALYSIS;
THROMBOCYTE AGGREGATION INHIBITION;
AMINO ACID SEQUENCE;
DRUG DESIGN;
ELECTROCHEMISTRY;
HUMANS;
OLIGOPEPTIDES;
PEPTIDES, CYCLIC;
PLATELET AGGREGATION INHIBITORS;
PLATELET GLYCOPROTEIN GPIIB-IIIA COMPLEX;
PROTEIN CONFORMATION;
STRUCTURE-ACTIVITY RELATIONSHIP;
THERMODYNAMICS;
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EID: 0034425097
PISSN: 00063525
EISSN: None
Source Type: Journal
DOI: 10.1002/1097-0282(2000)56:1<20::AID-BIP1039>3.0.CO;2-K Document Type: Article |
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Times cited : (15)
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References (39)
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