AI Article Synopsis
- * Compound A7 emerged as the most effective derivative, outperforming both ursolic acid and the antibiotic Spiramycin in inhibiting tachyzoites in infected GES-1 cells.
- * Further experiments on mice demonstrated that A7 not only inhibited tachyzoites but also impacted liver biochemical markers, highlighting its potential as a new anti-Toxoplasma gondii treatment.
Article Abstract
A series of derivatives of ursolic acid (UA) were synthesised, the anti- activity was tested, and the selectivity index (SI) of these compounds was calculated to determine the derivative with the best anti- activity. Compound A7 showed the best activity against the (IC in infected GES-1 cells: 9.1 ± 7.2 μM), better than the lead compound UA and the positive control drug Spiramycin. Compound A7 was selected for further in vivo research: A7 was tested for its effect on the inhibition rate of tachyzoites in mice and its biochemical parameters, such as alanine aminotransferase, aspartate aminotransferase, glutathione, and malondialdehyde were determined. Compound A7 was evaluated for its anti-Toxoplasma activity and partial damage to the liver. Therefore, the results show that compound A7 could be a potential lead compound for developing a novel anti-Toxoplasma gondii molecule.
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| http://dx.doi.org/10.1080/14786419.2022.2098497 | DOI Listing |
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