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2000
Volume 7, Issue 3
  • ISSN: 1389-5575
  • E-ISSN: 1875-5607

Abstract

Several classes of compounds (thioureas, ureas, β-glucosides, sulfonamides, and cyclic peptides) show enhanced binding affinity and selectivity at somatostatin subtype 4 receptors (sst4). Pharmacophore models have recently been proposed to explain receptor subtype selectivity. The chemistry and therapeutic potential of sst4 ligands will be the subject of this review.

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/content/journals/mrmc/10.2174/138955707780059880
2007-03-01
2025-06-26
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