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- W2953052890 abstract "Abstract Developed herein is a facile and efficient methodology toward the synthesis of novel turmerone motif-fused spiropyrrolidine oxindoles via a multicomponent 1,3-dipolar cycloaddition event of dienones 2 with azomethine ylides (thermally generated in situ from isatin derivatives and sarcosine). Products bearing adjacent quaternary–tertiary centers were smoothly obtained in high yields (up to 93% yield) with good diastereoselectivity (up to >20:1). In addition, their biological activity has been preliminarily demonstrated by in vitro evaluation against human lung cancer cells A549 and human leukemia cells K562 by the MTT-based assays, using the commercially available standard drug of Cisplatin as a positive control. The results also demonstrated that most of the compounds showed considerable cytotoxicities to these two cell lines of K562 and A549, showed comparably potent or even more potent than the positive control of Cisplatin (up to 5.1 times), and indicated that novel turmerone motif-fused spiropyrrolidine oxindoles may be potential leads for further biological screenings and may generate drug-like molecules." @default.
- W2953052890 created "2019-06-27" @default.
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- W2953052890 date "2016-06-01" @default.
- W2953052890 modified "2023-09-23" @default.
- W2953052890 title "ChemInform Abstract: Construction of Turmerone Motif-Fused Spiropyrrolidine Oxindoles and Their Biological Evaluation for Anticancer Activities." @default.
- W2953052890 cites W2280592040 @default.
- W2953052890 doi "https://doi.org/10.1002/chin.201629110" @default.
- W2953052890 hasPublicationYear "2016" @default.
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