Conclusions
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1.
A study was made of the reaction of acetylcholinesterase and butyrylcholinesterase with some methyl-(ω-alkoxyalkoxy)phosphoryloxylupinanes and N-[methyl-(ω-alkoxyalkoxy)phosphoryloxyethyl]anabasines, and with the corresponding methiodides and dimethiodides.
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2.
The studied compounds are reversible inhibitors, whose activity depends both on the presence and position of a hydrophilic oxygen atom in the alkoxyl group.
Literature cited
M. Kh. Bekanov, Dissertation, Moscow (1974).
N. N. Godovikov, A. A. Abduvakhabov, Kh. A. Aslanov, S. A. Auelbekov, M. I. Kabachnik, and A. S. Sadykov, Zh. Obshch. Khim.,44, 687 (1974).
J. L. Webb, Enzyme and Metabolic Inhibitors, Academic Press (1963).
I. L. Brik and V. A. Yakovlev, Biokhimiya,27, 481 (1962).
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Translated from Izvestiya Akademii Nauk SSSR, Seriya Khimicheskaya, No. 11, pp. 2606–2609, November, 1981.
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Abduvakhabov, A.A., Kholbekov, O.K., Auelbekov, S.A. et al. Anticholinesterase properties of methyl-(ω-alkoxyalkoxy)-phosphoryloxylupinanes, N-[methyl-(ω-alkoxyalkoxy)-phosphoryloxyethyl]anabasines, and their methiodides. Russ Chem Bull 30, 2164–2166 (1981). https://doi.org/10.1007/BF01094649
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DOI: https://doi.org/10.1007/BF01094649