Abstract
Background: Ester and amide derivatives of shikonin were synthesized to improve the chemical stability of shikonin.
Methods: All synthesized compounds were evaluated for their antiproliferative activity against A549 cell line by SRB assay, and five of them demonstrated comparable cytotoxicity to shikonin.
Results and Conclusion: The most potent compound, 22d, was more stable and potent than shikonin.
Keywords: Amidation, chemical stability, cytotoxicity, esterification, shikonin derivatives, synthesis, SRB assay, cell lines.
Letters in Drug Design & Discovery
Title:Synthesis and Bioevaluation of Shikonin Derivatives
Volume: 15 Issue: 9
Author(s): Sufen Cao, Jiangang Zhang and Wenhu Duan*
Affiliation:
- Department of Pharmaceutical Sciences, School of Pharmacy, East China University of Science and Technology, Shanghai,China
Keywords: Amidation, chemical stability, cytotoxicity, esterification, shikonin derivatives, synthesis, SRB assay, cell lines.
Abstract: Background: Ester and amide derivatives of shikonin were synthesized to improve the chemical stability of shikonin.
Methods: All synthesized compounds were evaluated for their antiproliferative activity against A549 cell line by SRB assay, and five of them demonstrated comparable cytotoxicity to shikonin.
Results and Conclusion: The most potent compound, 22d, was more stable and potent than shikonin.
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Cite this article as:
Cao Sufen , Zhang Jiangang and Duan Wenhu *, Synthesis and Bioevaluation of Shikonin Derivatives, Letters in Drug Design & Discovery 2018; 15 (9) . https://dx.doi.org/10.2174/1570180815666171229152139
DOI https://dx.doi.org/10.2174/1570180815666171229152139 |
Print ISSN 1570-1808 |
Publisher Name Bentham Science Publisher |
Online ISSN 1875-628X |
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