Synthesis and Antitumor Activities of 3-Substituted 1-(5-formylfurfuryl)indolin-2-one Derivatives
Authors: Zhou, Fusheng; Zheng, Jianbin; Dong, Xiaochun; Zhang, Zhiwen; Zhao, Lingling; Sha, Xianyi; Li, Lin; Wen, Ren
Source: Letters in Organic Chemistry, Volume 4, Number 8, December 2007 , pp. 601-605(5)
Publisher: Bentham Science Publishers
Abstract:
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 = 0.78-25 μg/mL) and human intestinal Caco-2 cells (IC50 = 0.19-9.42 μM). Eight compounds selected for further screening also showed inhibitory activities (IC50 = 1.84-10.32 μM) against human lung adenocarcinoma cells (SPC-A1).Keywords: 3-Substituted 1-(5-formylfurfuryl)indolin-2-ones; antitumor activity; antifungal activity; Pyricoraria oryzae; Caco-2 cells; SPC-A1
Document Type: Research article
DOI: http://dx.doi.org/10.2174/157017807782795484
Publication date: 2007-12-01
- Letters in Organic Chemistry publishes original letters on all areas of organic chemistry including synthesis, bioorganic, medicinal, natural products, organometallic, supramolecular, molecular recognition and physical organic chemistry. The emphasis is placed on publishing quality papers very rapidly. Letters are processed rapidly and take full advantage of the Internet technology both for the submission and the review of the manuscripts.
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- By this author: Zhou, Fusheng ; Zheng, Jianbin ; Dong, Xiaochun ; Zhang, Zhiwen ; Zhao, Lingling ; Sha, Xianyi ; Li, Lin ; Wen, Ren

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