Abstract
The possibility of enhancing the oral bioavailability of certain 1,4-benzodiazepinones by using them as complexes with a series of calix[4]arene derivatives was examined. All the inclusion compounds prepared exhibit anticonvulsant activity by antagonism with Corazol spasmodic agent. Complexes with 25,27-bis[(hydrazinocarbonyl)methoxy]-26,28-dihydroxy-p-tert-butylcalix[4]arene exhibit higher pharmacological activity compared to the starting 7-bromo-5-(o-chloro)phenyl-and 1-hydrazinocarbonylmethyl-7-bromo-5-phenyl-1,2-dihydro-3H-1,4-benzodiazepin-2-ones.
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Original Russian Text © E.A. Alekseeva, A.P. Luk’yanenko, I.A. Kravchenko, N.A. Nevarko, 2008, published in Zhurnal Obshchei Khimii, 2008, Vol. 78, No. 5, pp. 806–810.
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Alekseeva, E.A., Luk’yanenko, A.P., Kravchenko, I.A. et al. Preparation and biological properties of inclusion compounds of calix[4]arene and 1,4-benzodiazepinone derivatives. Russ J Gen Chem 78, 949–953 (2008). https://doi.org/10.1134/S1070363208050204
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DOI: https://doi.org/10.1134/S1070363208050204