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- W2080784297 abstract "Eleven analogues of the laminin pentapeptide amide fragment Tyr-Ile-Gly-Ser-Arg-NH2 (YIGSR-NH2) corresponding to a B1 chain fragment of the glycoprotein laminin have been synthesized by the solid phase method, and their biological activity has been studied in vitro by a cell adhesion assay: all of them inhibited the adhesion of LLC tumor cells to laminin. The analogues were found to be more resistant to enzymatic degradation in human serum than YIGSR-NH2 itself. Analogue DatIGSHar-NH2 was selected for an experimental pulmonary metastasis assay in vivo: it had higher antimetastatic activity than YIGSR-NH2. Copyright © 2003 European Peptide Society and John Wiley & Sons, Ltd." @default.
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- W2080784297 date "2004-04-26" @default.
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- W2080784297 title "New analogues of laminin active fragment YIGSR: synthesis and biological activityin vitro andin vivo" @default.
- W2080784297 doi "https://doi.org/10.1002/psc.537" @default.
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