Abstract
Three new DOTA-conjugated GnRH peptides with various hydrocarbon linkers were synthesized to evaluate the influences of the linkers on their receptor binding affinities. The hydrocarbon linker displayed a profound impact on the receptor binding affinities of DOTA-conjugated GnRH peptides. The Aun linker was better than Gaba, Ahx and Aoc linkers in retaining strong receptor binding affinity of the GnRH peptide. DOTA-Aun-(d-Lys6-GnRH) displayed 22.8 nM GnRH receptor binding affinity. 111In-DOTA-Aun-(d-Lys 6-GnRH) exhibited fast tumor uptake and urinary clearance in MDA-MB-231 human breast cancer-xenografted nude mice. The cellular and biological results provided an insight into the design of new GnRH peptides in the future.
| Original language | English |
|---|---|
| Pages (from-to) | 5484-5487 |
| Number of pages | 4 |
| Journal | Bioorganic and Medicinal Chemistry Letters |
| Volume | 23 |
| Issue number | 20 |
| DOIs | |
| State | Published - Oct 15 2013 |
Keywords
- GnRH receptor binding affinity
- Gonadotropin-releasing hormone peptide
- Hydrocarbon linker
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