Abstract
N-Alkaloid acetic acid hydrazides have been obtained by the hydrazinolysis of morpholones, and the acylation reactions of these hydrazides have been carried out. Screening investigations of the synthesized derivatives in vitro and in vivo have revealed, for the first time among the ephedrine alkaloids, a promising compound (N-d-pseudoephedrinylacetic acid hydrazide) possessing pronounced antituberculosis activity comparable with that of isoniazid.
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Translated from Khimiko-Farmatsevticheskii Zhurnal, Vol. 41, No. 11, pp. 52–56, November, 2007.
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Kulakov, I.V., Nurkenov, O.A., Gazalieva, M.A. et al. Synthesis and tuberculostatic activity of N-aminoacetic acid hydrazides and acylhydrazides based on ephedrine alkaloids. Pharm Chem J 41, 620–624 (2007). https://doi.org/10.1007/s11094-008-0020-2
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DOI: https://doi.org/10.1007/s11094-008-0020-2