Design and synthesis of isatin/triazole conjugates that induce apoptosis and inhibit migration of MGC-803 cells
European Journal of Medicinal Chemistry, ISSN: 0223-5234, Vol: 124, Page: 350-360
2016
- 38Citations
- 35Captures
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Example: if you select the 1-year option for an article published in 2019 and a metric category shows 90%, that means that the article or review is performing better than 90% of the other articles/reviews published in that journal in 2019. If you select the 3-year option for the same article published in 2019 and the metric category shows 90%, that means that the article or review is performing better than 90% of the other articles/reviews published in that journal in 2019, 2018 and 2017.
Citation Benchmarking is provided by Scopus and SciVal and is different from the metrics context provided by PlumX Metrics.
Metrics Details
- Citations38
- Citation Indexes38
- 38
- CrossRef27
- Captures35
- Readers35
- 35
Article Description
A series of new isatin/triazole conjugates were designed based on the hypothesis that the ester-linked compounds could be enzymatically hydrolyzed by cellular esterases inside the cells. These compounds showed moderate to good growth inhibition toward the tested cancer cells, exerted selective inhibition toward MGC-803 cells and were less toxic to normal cells HL-7702 and GES-1. Of these compounds, compound 5a showed the best inhibitory activity against MGC-803 cells (IC 50 = 9.78 μM), induced apoptosis through multiple mechanisms, as well as inhibited migration of MGC-803 cells.
Bibliographic Details
http://www.sciencedirect.com/science/article/pii/S022352341630722X; http://dx.doi.org/10.1016/j.ejmech.2016.08.065; http://www.scopus.com/inward/record.url?partnerID=HzOxMe3b&scp=84984691760&origin=inward; http://www.ncbi.nlm.nih.gov/pubmed/27597411; https://linkinghub.elsevier.com/retrieve/pii/S022352341630722X; https://dx.doi.org/10.1016/j.ejmech.2016.08.065
Elsevier BV
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