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Cited by 269

The DOI matches its Crossref record; 2 of the 2 references it cites were found in a registry or an index.

Multimeric Cyclic RGD Peptides as Potential Tools for Tumor Targeting: Solid‐Phase Peptide Synthesis and Chemoselective Oxime Ligation

Thumshirn, Georgette, Hersel, Ulrich, Goodman, Simon L., Kessler, Horst·2003·Chemistry – A European Journal

Abstract

The α v β 3 integrin receptor plays an important role in human metastasis and tumor‐induced angiogenesis. Targeting this receptor may provide information about the receptor status of the tumor and enable specific therapeutic planning. Solid‐phase peptide synthesis of multimeric cyclo(‐RGDfE‐)‐peptides is described, which offer the possibility of enhanced integrin targeting due to polyvalency effects. These peptides contain an aminooxy group for versatile chemoselective oxime ligation. Conjugation with para‐trimethylstannylbenzaldehyde results in a precursor for radioiododestannylation, which would allow them to be used as potential tools for targeting and imaging α v β 3‐expressing tumor cells. The conjugates were obtained in good yield without the need of a protection strategy and under mild conditions.

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Crossref · 10.1002/chem.200204304

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Metadata

Authors
Thumshirn, G., Hersel, U., Goodman, S. L., & Kessler, H.
Venue
Chemistry – A European Journal
Publisher
Wiley
Published
2003-05-21
Volume
9
Issue
12
Pages
2717-2725
ISSN
  • 0947-6539 (ISSN-L)
  • 1521-3765
OpenAlex
W2120172300
Cited by
269
References
2
FWCI
5.25
Type
journal article
Language
en
Open access
closed

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CoChat. (2026). Citation check: Multimeric Cyclic RGD Peptides as Potential Tools for Tumor Targeting: Solid‐Phase Peptide Synthesis and Chemoselective Oxime Ligation. https://app.cochat.ai/papers/10.1002/chem.200204304
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Thumshirn, G., Hersel, U., Goodman, S. L., & Kessler, H. (2003). Multimeric Cyclic RGD Peptides as Potential Tools for Tumor Targeting: Solid‐Phase Peptide Synthesis and Chemoselective Oxime Ligation. Chemistry – A European Journal. https://doi.org/10.1002/chem.200204304

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