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期刊论文
Synthesis
Letters in Organic Chemistry, 2007, 4, ???-???,-0001,():
Forty-two 3-substituted 1-(5-formylfurfuryl)indolin-2-ones were synthesized and most of these compounds exhibited potent inhibitory activities against P. oryzae (MIC=0.78-25μg/mL) and human intestinal Caco-2 cells (IC50=0.19-9.42μM). Eight compounds selected for further screening also showed inhibitory activities (IC50=1.84-10.32μM) against human lung adenocarcinoma cells (SPC-A1).
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