Abstract
Condensation of 7-hydroxy-1,2,2,4-tetramethylhydroquinoline-6-carbaldehydes with various hetaryl-substituted 3-oxo esters afforded a series of hybrid hydro-6,8,8,9-tetramethyl-2H-pyrano[3,2-g]quinolin-2-ones. A number of these compounds exhibited relatively high inhibitory activity against blood coagulation factors Xa and XIa.
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This work was financially supported by the Russian Science Foundation (Project No. 18-74-10097).
This work does not involve human participants and animal subjects.
The authors declare no competing interests.
Published in Russian in Izvestiya Akademii Nauk. Seriya Khimicheskaya, No. 3, pp. 492–497, March, 2021.
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Potapov, A.Y., Paponov, B.V., Podoplelova, N.A. et al. Synthesis and study of new 2H-pyranoquinolin-2-one-based inhibitors of blood coagulation factors Xa and XIa. Russ Chem Bull 70, 492–497 (2021). https://doi.org/10.1007/s11172-021-3114-6
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DOI: https://doi.org/10.1007/s11172-021-3114-6