Incorporation of Thioether Building Blocks into an α vβ3-Specific RGD Peptide: Synthesis and Biological Activity

Biopolymers - Peptide Science Section

Volumn 71, Issue 6, 2003, Pages 686-695

  Kelleman, Audrey ^a   Mattern, Ralph Heiko ^b   Pierschbacher, Michael D ^b   Goodman, Murray ^a  

^a UNIVERSITY OF CALIFORNIA   (United States)

^b Integra LifeSciences Corporation   (United States)

Author keywords

5 1 integrin antagonist; v 3 integrin antagonist; RGD peptide; Thioether

Indexed keywords

DATA REDUCTION; ETHERS; SULFUR COMPOUNDS; SYNTHESIS (CHEMICAL);

CYCLIZATION; THIOETHERS;

PROTEINS;

ARGINYLGLYCYLASPARTIC ACID; CYCLO[(MERCAPTOPROPIONIC ACID)ARGINYLGLYCYLASPARTIC ACID CYCLO(TERT BUTYLGLYCINE)] AMIDE; S ACETYLCYSTEINE DERIVATIVE; S ACETYLHOMOCYSTEINE DERIVATIVE; S PROPIONYLCYSTEINE DERIVATIVE; S PROPIONYLHOMOCYSTEINE DERIVATIVE; SULFIDE; UNCLASSIFIED DRUG; VERY LATE ACTIVATION ANTIGEN 5; VITRONECTIN RECEPTOR;

ARTICLE; BINDING AFFINITY; CYCLIZATION; DRUG ACTIVITY; DRUG BINDING; DRUG DESIGN; DRUG SYNTHESIS; PEPTIDE SYNTHESIS;

AMINO ACID SEQUENCE; INTEGRIN ALPHAVBETA3; OLIGOPEPTIDES; SULFIDES;

EID: 1542284161     PISSN: 00063525     EISSN: None     Source Type: Journal    
DOI: 10.1002/bip.10586     Document Type: Article

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