Synthesis, 18F-labelling and radiopharmacological characterisation of the C-terminal 30mer of Clostridium perfringens enterotoxin as a potential claudin-targeting peptide
Author:
Publisher
Springer Science and Business Media LLC
Subject
Organic Chemistry,Clinical Biochemistry,Biochemistry
Link
http://link.springer.com/article/10.1007/s00726-018-2657-9/fulltext.html
Reference81 articles.
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2. Bollhagen R, Schmiedberger M, Barlos K, Grell E (1994) A new reagent for the cleavage of fully protected peptides synthesized on 2-chlorotrityl chloride resin. J Chem Soc Chem Commun. https://doi.org/10.1039/c39940002559
3. Cocco E, Casagrande F, Bellone S, Richter CE, Bellone M, Todeschini P, Holmberg JC, Fu HH, Montagna MK, Mor G, Schwartz PE, Arin-Silasi D, Azoudi M, Rutherford TJ, Abu-Khalaf M, Pecorelli S, Santin AD (2010) Clostridium perfringens enterotoxin carboxy-terminal fragment is a novel tumor-homing peptide for human ovarian cancer. BMC Cancer 10:349. https://doi.org/10.1186/1471-2407-10-349
4. de Mol NJ, Dekker FJ, Broutin I, Fischer MJE, Liskamp RMJ (2005) Surface plasmon resonance thermodynamic and kinetic analysis as a strategic tool in drug design. Distinct ways for phosphopeptides to plug into Src- and Grb2 SH2 domains. J Med Chem 48:753–763. https://doi.org/10.1021/jm049359e
5. Ding L, Lu Z, Lu Q, Chen YH (2013) The claudin family of proteins in human malignancy: a clinical perspective. Cancer Manag Res 5:367–375. https://doi.org/10.2147/CMAR.S38294
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