IN VITRO ANTI-TUBERCULOSIS AND ANTI-DIABETIC ACTIVITY OF O-TOSYLATES-β-AMINOPROPIOAMIDOXIMES AND CHLORIDES OF 2-(HETEROAMINO)-1,5-DIAZOSPIRO[4,5]DECANE-1-EN-5-AMMONIUMS

Authors

  • L. A. Kayukova A.B. Bekturov Institute of chemical sciences
  • K. D. Praliev A.B. Bekturov Institute of chemical sciences
  • A. B. Myrzabek A.B. Bekturov Institute of chemical sciences
  • B. T. Toksanbaeva National Scientific Center Of Phthisiopulmonology Ministry Of Health Of The Republic Of Kazakhstan
  • L. T. Chingisova National Scientific Center Of Phthisiopulmonology Ministry Of Health Of The Republic Of Kazakhstan
  • V. L. Bismilda National Science Center of Phtisiopulmonology of RK
  • A. E. Gulyaev National Center for Biotechnology
  • Z. T. Shul'gau National Center for Biotechnology
  • Sh. D. Sergazy National Center for Biotechnology

Keywords:

O-tosylates-β-aminopropioamidoximes, chlorides of 2-amino-4,5-dihydrospyropyrazolylammoniums, in vitro anti-tuberculosis and anti-diabetic activity

Abstract

O-Tosylates-β-aminopropioamidoximes and chlorides of 2-amino-4,5-dihydrospyropyrazolylammoniums have been studied in vitro for anti-tuberculosis and anti-diabetic activity. In two groups of compounds containing β-amino groups: piperidin-1-yl, morpholin-1-yl, thiomorpholin-1-yl, 4-phenylpiperazine-1-yl, benzimidazol-1-yl (with the exception of the benzimidazole derivative in the spiro derivative series), drugs with an average anti-tuberculosis activity were detected on the DS strains of M. tuberculosis (MBC 50 μg/ml) and with moderate anti-diabetic α-amylase activity (27% to 29%) in the first row, containing β-amino groups: piperidin-1-yl, morpholin-1-yl and in the second row – piperidin-1-yl.

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Published

2021-05-03