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  • Research paperSynthesis and biological evaluation of Indole-2-carboxamide (cas 1670-84-4)s bearing photoactivatable functionalities as novel allosteric modulators for the cannabinoid CB1 receptor
  • Add time:10/01/2019         Source:sciencedirect.com

    5-Chloro-3-ethyl-N-(4-(piperidin-1-yl)phenethyl)-1H-indole-2-carboxamide (ORG27569, 1) is a prototypical allosteric modulator for the cannabinoid CB1 receptor. Based on this indole-2-carboxamide scaffold, we designed and synthesized novel CB1 allosteric modulators that possess photoactivatable functionalities, which include benzophenone, phenyl azide, aliphatic azide and phenyltrifluoromethyldiazrine. To assess their allosteric effects, the dissociation constant (KB) and allosteric binding cooperativity factor (α) were determined and compared to their parent compounds. Within this series, benzophenone-containing compounds 26 and 27, phenylazide-containing compound 28, and the aliphatic azide containing compound 36b showed allosteric binding parameters (KB and α) comparable to their parent compound 1, 7, 8, and 9, respectively. We further assessed these modulators for their impact on G-protein coupling activity. Interestingly, these compounds exhibited negative allosteric modulator properties in a manner similar to their parent compounds, which antagonize agonist-induced G-protein coupling. These novel CB1 allosteric modulators, possessing photoactivatable functionalities, provide valuable tools for future photo-affinity labeling and mapping the CB1 allosteric binding site(s).

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    Prev:A convenient synthesis of indoloquinolinones via 3-arylation of Indole-2-carboxamide (cas 1670-84-4)s and PIDA-mediated C–N bond formation
    Next: Structure–activity relationships of substituted 1H-Indole-2-carboxamide (cas 1670-84-4)s as CB1 receptor allosteric modulators)

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