SCOPUS 정보 검색 플랫폼

Volumn 9, Issue 12, 2003, Pages 2717-2725

Multimeric cyclic RGD peptides as potential tools for tumor targeting: Solid-phase peptide synthesis and chemoselective oxime ligation

(4) Thumshirn, Georgette a Hersel, Ulrich a Goodman, Simon L b Kessler, Horst a

a TECHNICAL UNIVERSITY OF MUNICH (Germany)

b MERCK KGAA (Germany)

Author keywords

Chemoselective ligation; Integrin; Multimer; Peptides; Tumor targeting

Indexed keywords

MEDICAL IMAGING; SYNTHESIS (CHEMICAL); TUMORS;

PEPTIDES;

PROTEINS;

4 TRIMETHYLSTANNYLBENZALDEHYDE; ALPHA5 INTEGRIN; ANGIOGENESIS INHIBITOR; ARGINYLGLYCYLASPARTIC ACID; BENZALDEHYDE DERIVATIVE; BETA3 INTEGRIN; CILENGITIDE; CYCLOPEPTIDE; INTEGRIN RECEPTOR; OXIME; PEPTIDE; UNCLASSIFIED DRUG;

AMINO ACID SEQUENCE; ANGIOGENESIS; ARTICLE; CANCER THERAPY; CELL PROTECTION; CHEMICAL REACTION; CONJUGATION; DRUG SELECTIVITY; DRUG SPECIFICITY; HUMAN; HUMAN CELL; LIGATION; METASTASIS; PEPTIDE ANALYSIS; PEPTIDE SYNTHESIS; PRODUCT RECOVERY; PROTEIN EXPRESSION; RADIOIODINATION; RADIOIODODESTANNYLATION; RECEPTOR BINDING; RECEPTOR SENSITIVITY; SOLID; TREATMENT PLANNING; TUMOR CELL;

ANIMALS; INTEGRIN ALPHAVBETA3; MICE; MICE, NUDE; NEOPLASMS, EXPERIMENTAL; OLIGOPEPTIDES; OXIMES; PEPTIDES, CYCLIC; VITRONECTIN;

EID: 0037775714 PISSN: 09476539 EISSN: None Source Type: Journal
DOI: 10.1002/chem.200204304 Document Type: Article

Times cited : (256)

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