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Effective enmein-type mimics of clinical candidate HAO472: Design, synthesis and biological evaluation.
- Source :
-
European Journal of Medicinal Chemistry . Jun2019, Vol. 171, p169-179. 11p. - Publication Year :
- 2019
-
Abstract
- A series of enmein-type diterpenoid amino acid ester derivatives (14 – 22) were designed and synthesized according to l -alanine-(14-oridonin) ester trifluoroacetate (clinical candidate HAO472). Their antiproliferative activities were tested against SGC-7901, Bel-7402, HL-60, PC-3, A549 and K562 cancer cell lines and L-02 normal liver cells. The results showed that compound 19 possessed the most potent cytotoxicity with IC 50 s at sub-micromolar level against human hepatoma Bel-7402 and chronic myelogenous leukemia K562 cells and more potent than l -alanine-(14-oridonin) ester (23). More importantly, 19 displayed 70-fold less cytotoxicity than parent 3 (IC 50 = 25.47 μM) against L-02 cells, which exhibited certain selectivity. Further mechanism study in Bel-7402 cells revealed that 19 could induce apoptosis, G 1 phase cell cycle arrest and mitochondrial dysfunction. Western blot results of caspase-3, Bax and cytochrome c upregulation and pro-caspase-3, Bcl-2 and Bcl-xL downregulation confirmed the intrinsic pathways. Overall, these data collectively demonstrated the high efficiency and selectivity of 19 , l -phenylalanine-enmein-type diterpenoid ester, which inspires further and effective application as a potential antitumor candidate. Image 1 • Enmein-type diterpenoid amino acid ester derivatives were synthesized. • All target derivatives showed antiproliferative activities to some extent. • 19 showed potent activities and good selectivity between normal and tumor cells. • 19 could induce apoptosis and arrest cell cycle at G 1 phase in Bel-7402 cells. • 19 induced Bel-7402 cells apoptosis via the mitochondria-related pathway. [ABSTRACT FROM AUTHOR]
Details
- Language :
- English
- ISSN :
- 02235234
- Volume :
- 171
- Database :
- Academic Search Index
- Journal :
- European Journal of Medicinal Chemistry
- Publication Type :
- Academic Journal
- Accession number :
- 136352831
- Full Text :
- https://doi.org/10.1016/j.ejmech.2019.03.046