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Chemistry of Natural Compounds

, Volume 55, Issue 4, pp 622–625 | Cite as

Synthesis of Monosubstituted Purpurins and Their Biological Activity

  • T. V. KharlamovaEmail author
  • R. B. Seidakhmetova
  • K. D. Praliev
Article
  • 32 Downloads

Products were obtained from acylation of 1,2,4-trihydroxy-9,10-anthraquinone (purpurin) by saturated cyclic carboxylic acid chlorides. The compositions and structures of the monosubstituted compounds were confirmed by elemental analysis and IR and PMR spectroscopy. The cytotoxicities of the derivatives were evaluated in an Artemia salina Leach brine shrimp test.

Keywords

purpurin saturated cyclic carboxylic acid chlorides Artemia salina Leach brine shrimp cytotoxicity 

Notes

Acknowledgment

The work was financially supported by the Science Committee, Ministry of Education and Science of the Republic of Kazakhstan, under contract No. 83 (Appendix 1.7) dated March 2, 2018, in the framework of the project on “Search for new drugs based on available synthetic analogs of natural anthraquinone derivatives” (IRN AR05131788).

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Copyright information

© Springer Science+Business Media, LLC, part of Springer Nature 2019

Authors and Affiliations

  • T. V. Kharlamova
    • 1
    Email author
  • R. B. Seidakhmetova
    • 1
  • K. D. Praliev
    • 1
  1. 1.JSC “A. B. Bekturov Institute of Chemical Sciences”AlmatyRepublic of Kazakhstan

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