Synthesis and cytotoxicity of new 4-aza-2,3-didehydropodophyllotoxins

Nguyen Thi Thuy Hang, Tran Thi Yen, Vu Dinh Hoang, Ngo Quoc Anh
Author affiliations

Authors

  • Nguyen Thi Thuy Hang Institute of Chemistry, Vietnam Academy of Science and Technology (VAST), 18 Hoang Quoc Viet, Cau Giay, Ha Noi, Viet Nam
  • Tran Thi Yen Institute of Chemistry, Vietnam Academy of Science and Technology (VAST), 18 Hoang Quoc Viet, Cau Giay, Ha Noi, Viet Nam
  • Vu Dinh Hoang Department of Pharmaceutical Chemistry, Hanoi University of Science and Technology, 1 Dai Co Viet, Bach Khoa, Hai Ba Trung, Ha Noi, Viet Nam
  • Ngo Quoc Anh Institute of Chemistry, Vietnam Academy of Science and Technology (VAST), 18 Hoang Quoc Viet, Cau Giay, Ha Noi, Viet Nam

DOI:

https://doi.org/10.15625/2525-2518/15577

Keywords:

quinolin, podophyllotoxin, one-pot, cytotoxiccity

Abstract

Five new 4-aza-2,3-didehydropodophyllotoxins were synthesized by a straightforward multi-component reaction in the hope of finding new structures with interesting anticancer activity. The “one-pot” synthesis process is developed to increase performance as well as minimize the steps involved. The obtained compounds with podophyllotoxin frame have the corresponding yields of 60-83%. Five new 4-aza-2,3-didehydropodophyllotoxins demonstrated comparable cytotoxicity against the Hep-G2, MCF7cell lines with an IC50 value of 52.2 - 261.2 µM with ellipsitine as the positive control.

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Published

23-03-2022

How to Cite

[1]
N. T. T. Hang, T. T. Yen, V. D. Hoang, and N. Quoc Anh, “Synthesis and cytotoxicity of new 4-aza-2,3-didehydropodophyllotoxins”, Vietnam J. Sci. Technol., vol. 60, no. 2, pp. 183–190, Mar. 2022.

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Section

Natural Products

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