DONG Yong-Ming, MA Jian-Zhou , ZHEN Run-Fen, . SYNTHESIS OF 3-ALKYL-4-(ALKYLAMINO) ALKOXYPHENYL N, N-DIMETHYLCARBAMATES AS REVERSIBLE CHOLINESTERASE INHIBITORSJ. Acta Pharmaceutica Sinica, 1984, 19(7): 538-540.
Citation: DONG Yong-Ming, MA Jian-Zhou , ZHEN Run-Fen, . SYNTHESIS OF 3-ALKYL-4-(ALKYLAMINO) ALKOXYPHENYL N, N-DIMETHYLCARBAMATES AS REVERSIBLE CHOLINESTERASE INHIBITORSJ. Acta Pharmaceutica Sinica, 1984, 19(7): 538-540.

SYNTHESIS OF 3-ALKYL-4-(ALKYLAMINO) ALKOXYPHENYL N, N-DIMETHYLCARBAMATES AS REVERSIBLE CHOLINESTERASE INHIBITORS

  • In order to determine the effect of nuclear substituents in the para isomer of CUI XING AN (m-(2-dimethylamino) ethoxyphenyl N, N-dimethylcarbamate) on their anticholinesterase activity, a series of 3-alk-yl-4-(alkylamino) alkoxyphenyl N, N-dimethylcarbamates was prepared. Preliminary screening tests indicated that the introduction of an alkyl group increased the anticholinesterase activity but also increased toxicity.
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