Studies on the impact of modifications at the Gln-Trp site in RM2-based GRPR ligands
Abstract Background One of the most studied, and preclinically as well as clinically applied gastrin-releasing peptide receptor (GRPR) ligands represents the antagonist RM2 (DOTA-Pip5-D-Phe6-Gln7-Trp8-Ala9-Val10-Gly11-His12-Sta13-Leu14-NH2). As an improved in vivo stability was observed for a RM2 an...
Wedi'i Gadw mewn:
| Prif Awduron: | , , , , , |
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| Fformat: | Artigo |
| Iaith: | Inglês |
| Cyhoeddwyd: |
SpringerOpen
2025-09-01
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| Cyfres: | EJNMMI Research |
| Pynciau: | |
| Mynediad Ar-lein: | https://doi.org/10.1186/s13550-025-01241-7 |
| Tagiau: |
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