| Literature DB >> 29172528 |
Emanuele Amata1, Maria Dichiara1, Emanuela Arena1, Valeria Pittalà1, Venerando Pistarà2, Venera Cardile3, Adriana Carol Eleonora Graziano3, Aurore Fraix4, Agostino Marrazzo1, Salvatore Sortino4, Orazio Prezzavento1.
Abstract
This contribution reports the synthesis and evaluation of novel hybrid compounds that conjugate a sigma (σ) receptor pharmacophore and a nitric oxide (NO) photodonor. All compounds preserve their capability to generate NO under visible light and possess overall σ receptor nanomolar affinity, with one of them (8b) exhibiting remarkable σ2 receptor selectivity. Compounds 8b, 11a, and 11b were tested on tumorigenic MCF-7 and A2058 cells expressing high levels of σ2 and σ1 receptor, respectively. Considerable loss of cell viability was detected under light excitation, while negligible effects in the dark were detected. Moreover, they did not show any significant cytotoxicity in the dark or under irradiation on nontumorigenic NCTC-2544 keratinocytes. NO-induced reduction of cellular viability was demonstrated by in-cell NO detection and total nitrite estimation. For the first time, a combination of σ receptor moieties and a NO photodonor is reported, providing distinctive ligands potentially useful for cancer management.Entities:
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Year: 2017 PMID: 29172528 DOI: 10.1021/acs.jmedchem.7b00791
Source DB: PubMed Journal: J Med Chem ISSN: 0022-2623 Impact factor: 7.446