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Volumn 12, Issue 17, 2002, Pages 2463-2465
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Non-peptide αvβ3 antagonists. Part 4: Potent and orally bioavailable chain-shortened RGD mimetics
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Author keywords
[No Author keywords available]
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Indexed keywords
AMIDE;
ARGINYLGLYCYLASPARTIC ACID DERIVATIVE;
INTEGRIN;
PEPTIDE;
PROTEIN INHIBITOR;
UNCLASSIFIED DRUG;
ARGINYL-GLYCYL-ASPARTIC ACID;
ARGINYLGLYCYLASPARTIC ACID;
OLIGOPEPTIDE;
VITRONECTIN RECEPTOR;
ANIMAL CELL;
ANIMAL EXPERIMENT;
ARTICLE;
CHEMICAL BOND;
CONTROLLED STUDY;
DOG;
DRUG BIOAVAILABILITY;
DRUG CLEARANCE;
DRUG HALF LIFE;
DRUG STRUCTURE;
LIPOPHILICITY;
NONHUMAN;
PEPTIDE SYNTHESIS;
PLASMA CLEARANCE;
STRUCTURE ACTIVITY RELATION;
ANIMAL;
BIOAVAILABILITY;
DRUG ANTAGONISM;
HALF LIFE TIME;
IC 50;
METABOLIC CLEARANCE RATE;
MOLECULAR MIMICRY;
ORAL DRUG ADMINISTRATION;
ADMINISTRATION, ORAL;
ANIMALS;
BIOLOGICAL AVAILABILITY;
DOGS;
HALF-LIFE;
INHIBITORY CONCENTRATION 50;
INTEGRIN ALPHAVBETA3;
METABOLIC CLEARANCE RATE;
MOLECULAR MIMICRY;
OLIGOPEPTIDES;
STRUCTURE-ACTIVITY RELATIONSHIP;
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EID: 4243299683
PISSN: 0960894X
EISSN: None
Source Type: Journal
DOI: 10.1016/S0960-894X(02)00396-7 Document Type: Article |
Times cited : (36)
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References (18)
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