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Novel, Potent and Radio-Iodinatable Somatostatin Receptor 1 (sst(1)) Selective Analogues
The proposed sst(1) pharmacophore1 derived from the NMR structures of a family of mono- and dicyclic undecamers was used to design octa-, hepta- and hexamers with high affinity and selectivity for the somatostatin sst(1) receptor. These compounds were tested for their in vitro binding properties to...
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| Autors principals: | , , , , , , , , |
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| Format: | Artigo |
| Idioma: | Inglês |
| Publicat: |
2009
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| Matèries: | |
| Accés en línia: | https://ncbi.nlm.nih.gov/pmc/articles/PMC2779710/ https://ncbi.nlm.nih.gov/pubmed/19351180 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1021/jm801314f |
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