Abstract
New derivatives of 2-oxo-1-azetidinylacetamide have been synthesized by the four-component condensation of β-amino acids with aldehydes and isonitriles. Study of their cytotoxic activity in vitro revealed a cytotoxic effect of individual compounds in relation to cancer cells of human fibrosarcoma, mouse hepatoma, and mouse neuroblastoma.
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Translated from Khimiya Geterotsiklicheskikh Soedinenii, No. 1, pp. 107–112, January, 2005.
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Veinberg, G., Dikovskaya, K., Vorona, M. et al. Synthesis of cytotoxic derivatives of 2-oxo-1-azetidinylacetamide. Chem Heterocycl Compd 41, 93–97 (2005). https://doi.org/10.1007/s10593-005-0113-8
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DOI: https://doi.org/10.1007/s10593-005-0113-8
Keywords
- N-cyclohexyl-α-(4-benzyloxycarbonyl-2-oxo-1-azetidinyl)-α-(aryl)acetamides
- N-cyclohexyl-α-(2-oxo-4-phenyl-1-azetidinyl)-α-(aryl)acetamides
- N-cyclohexyl-α-(3-benzyloxycarbonylamino-2-oxo-1-azetidinyl)-α-(4-cyanophenyl)acetamide
- N-cyclohexyl-α-(3-tert-butoxycarbonylamino-2-oxo-1-azetidinyl)-α-(aryl)acetamides
- N-tolylsulfonyl-α-(2-chloro-4-nitrophenyl)-α-(2-oxo-1-azetidinyl)-acetamide
- cytotoxic activity