Molecular design of multitarget neuroprotectors 2. Synthesis and bioactivity of carbazole—γ-carboline conjugates

Earlier unknown conjugates of carbazoles and γ-carbolines were obtained by the reaction of 3,6-substituted 9-oxiranylmethylcarbazoles and 2,8-substituted 2,3,4,5-tetrahydro-1 H -pyrido-[4,3]indoles. The effects of synthesized 1-(9 H -carbazol-9-yl)-3-(1,2,3,4-tetrahydro-5 H -pyrido-[4,3- b ]indol-5-...

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Veröffentlicht in:Russian chemical bulletin 2016-05, Vol.65 (5), p.1346-1353
Hauptverfasser: Sokolov, V. B., Aksinenko, A. Yu, Goreva, T. V., Epishina, T. A., Grigor´ev, V. V., Gabrel´yan, A. V., Vinogradova, D. V., Dubova, L. G., Shevtsov, P. N., Shevtsova, E. F., Bachurin, S. O.
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Sprache:eng
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Zusammenfassung:Earlier unknown conjugates of carbazoles and γ-carbolines were obtained by the reaction of 3,6-substituted 9-oxiranylmethylcarbazoles and 2,8-substituted 2,3,4,5-tetrahydro-1 H -pyrido-[4,3]indoles. The effects of synthesized 1-(9 H -carbazol-9-yl)-3-(1,2,3,4-tetrahydro-5 H -pyrido-[4,3- b ]indol-5-yl)propan-2-ones and their hydrochlorides on neuronal NMDA receptors, polymerization of tubulin to form microtubules, and functional characteristics of rat liver mitochondria were studied.
ISSN:1066-5285
1573-9171
DOI:10.1007/s11172-016-1460-6