Abstract
Unknown conjugates of carbazoles and tetrahydrocarbazoles were obtained by the alkylation of carbazoles and tetrahydrocarbazoles with 3,6-substituted 9-oxiranylmethylcarbazoles. The influence of synthesized 1-(9Н-carbazol-9-yl)-3-(1,2,3,4-tetrahydro-5Н-pyrido[4,3-b]-indol-5-yl)propan-2-ones on functional characteristics of brain mitochondria has been studied. The potential neuroprotective activity of a several representatives of conjugates has been demonstrated using glutamate toxicity model.
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For Part 3 see Ref. 1
Based on materials of the IV all-Russian Conference on Organic Chemistry and the XVIII Youth School-Conference on Organic Chemistry (November 22—27, 2015, Moscow, Russia).
Published in Russian in Izvestiya Akademii Nauk. Seriya Khimicheskaya, No. 9, pp. 2306—2311, September, 2016.
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Sokolov, V.B., Aksinenko, A.Y., Goreva, T.V. et al. Molecular construction of multitarget neuroprotectors 4.* Synthesis and biological activity of conjugates of carbazoles and tetrahydrocarbazoles. Russ Chem Bull 65, 2306–2311 (2016). https://doi.org/10.1007/s11172-016-1582-x
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DOI: https://doi.org/10.1007/s11172-016-1582-x
Key words
- carbazoles
- tetrahydrocarbazoles
- 3,6-substituted 9-oxiranylmethylcarbazoles
- 2,8-substituted 2,3,4,5-tetrahydro-1H-pyrido[4,3-b]indoles
- 1-(9Н-carbazol-9-yl)-3-(1,2,3,4-tetrahydro-5Н-pyrido[4,3-b]indol-5-yl)propan-2-ones
- catalytic alkylation
- mitochondria
- neuroprotection
- mitochondrial permeability transition
- tubulin
- glutamate toxicity