董永明, 高企秀, 甄润芬. 可逆性胆碱酯酶抑制剂 Ⅱ.二甲氨基甲酸间-(烷氨基)烷硫基苯酯的合成J. 药学学报, 1984, 19(5): 394-396.
引用本文: 董永明, 高企秀, 甄润芬. 可逆性胆碱酯酶抑制剂 Ⅱ.二甲氨基甲酸间-(烷氨基)烷硫基苯酯的合成J. 药学学报, 1984, 19(5): 394-396.
DONG Yong-ming, GAO qi-xiu , ZHEN Run-fen, . STUDIES ON REVERSTBLE CHOLINESTERASE INHIBITORS.Ⅱ.SYNTHESIS OF m-(ALKYLAMINO) ALKYLTHIOPHENYL N,N-DIMETHYLCARBAMATESJ. Acta Pharmaceutica Sinica, 1984, 19(5): 394-396.
Citation: DONG Yong-ming, GAO qi-xiu , ZHEN Run-fen, . STUDIES ON REVERSTBLE CHOLINESTERASE INHIBITORS.Ⅱ.SYNTHESIS OF m-(ALKYLAMINO) ALKYLTHIOPHENYL N,N-DIMETHYLCARBAMATESJ. Acta Pharmaceutica Sinica, 1984, 19(5): 394-396.

可逆性胆碱酯酶抑制剂 Ⅱ.二甲氨基甲酸间-(烷氨基)烷硫基苯酯的合成

STUDIES ON REVERSTBLE CHOLINESTERASE INHIBITORS.Ⅱ.SYNTHESIS OF m-(ALKYLAMINO) ALKYLTHIOPHENYL N,N-DIMETHYLCARBAMATES

  • Abstract: In a previous paper we have described the synthesis and biological evaluation of some m-(alkylamino) alkoxyphenyl N, N-dimethylcarbamates. One of these compounds, CUI XING AN, is now used as an analeptic for Chinese traditional herbal anesthesia. In order to search for further anticholinesterases with higher activity on the CNS, a number of thio-analogues of the above series were synthesized. Several of these compounds were found to have much higher anticholinesterase activity than the corresponding oxygen analogues, among which m-(2-diethylamino)-ethylthiophenyl-N, N-dimethylcarbamate (Ⅱ2) was shown to be the most active. Compound Ⅱ2 exhibited a longer duration of action in animal experiments than CUI XING AN.

     

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