Amberlite IR-120H catalyzed MCR: Design, synthesis and crystal structure analysis of 1,8-dioxodecahydroacridines as potential inhibitors of sirtuins

A rapid, inexpensive and high yielding method has been developed for the synthesis of 1,8-dioxodecahydroacridines using Amberlite IR-120H as a reusable catalyst under open air. These compounds were designed as potential inhibitors of sirtuins and prepared via the MCR of 5,5-dimethyl-1,3-cyclohexaned...

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Veröffentlicht in:Bioorganic & medicinal chemistry letters 2013-03, Vol.23 (6), p.1828-1833
Hauptverfasser: Nakhi, Ali, Srinivas, P.T.V.A., Rahman, Md. Shafiqur, Kishore, Ravada, Seerapu, G.P.K., Lalith Kumar, K., Haldar, Devyani, Rao, M.V. Basaveswara, Pal, Manojit
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Sprache:eng
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Zusammenfassung:A rapid, inexpensive and high yielding method has been developed for the synthesis of 1,8-dioxodecahydroacridines using Amberlite IR-120H as a reusable catalyst under open air. These compounds were designed as potential inhibitors of sirtuins and prepared via the MCR of 5,5-dimethyl-1,3-cyclohexanedione, (hetero)aryl aldehydes and (hetero)aromatic amines under mild conditions. Further structure elaboration of a representative compound was performed via Pd catalyzed C–C bond forming reactions. The crystal structure analysis and H-bonding patterns along with in vitro inhibitory activity against yeast Sir2 of the same compound is presented. Docking studies indicated that the compound interacts well with the yeast Sir2.
ISSN:0960-894X
1464-3405
DOI:10.1016/j.bmcl.2013.01.026