4.7 Article

Synthesis and Biological Evaluation of 4-Phenylquinazoline-2-carboxamides Designed as a Novel Class of Potent Ligands of the Translocator Protein

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JOURNAL OF MEDICINAL CHEMISTRY
卷 55, 期 9, 页码 4506-4510

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AMER CHEMICAL SOC
DOI: 10.1021/jm201703k

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  1. Istituto Toscano Tumori [2007]
  2. MIUR
  3. Universita di Salerno
  4. Universita di Trieste

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A series of novel 4-phenylquinazoline-2-carboxamides (1-58) were designed as aza-isosters of PK11195, the wellknown 18 kDa translocator protein (TSPO) reference ligand, and synthesized by means of a very simple and efficient procedure. A number of these derivatives bind to the TSPO with K-i values in the nanomolar/subnanomolar range, show selectivity toward the central benzodiazepine receptor (BzR) and exhibit structure-affinity relationships consistent with a previously published pharmacophore/topological model of ligand-TSPO interaction.

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