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Synthesis and biological evaluation of cytotoxic activity of 14-(β-D-2-deoxy-ribopyranosyl)-naphtho [2,1-a]pyrrolo[3,4-c]carbazole-5,7(6H,12H)-dione
DING Ning * #
School of Pharmacy, Fudan University
*Correspondence author
#Submitted by
Subject:
Funding: This work is supported by Research Fund for the Doctoral Program of Higher Education of China (No.RFDP, 20100071120051))
Opened online:26 January 2014
Accepted by: none
Citation: DING Ning.Synthesis and biological evaluation of cytotoxic activity of 14-(β-D-2-deoxy-ribopyranosyl)-naphtho [2,1-a]pyrrolo[3,4-c]carbazole-5,7(6H,12H)-dione[OL]. [26 January 2014] http://en.paper.edu.cn/en_releasepaper/content/4583216
 
 
Naphtho[2,1-a]pyrrolo[3,4-c]carbazole-5,7(6H,12H)-dione (NPCD) is known to be a very potent and selective cyclin D1-CDK4 inhibitors and could induce strong G1 phase arrest in breast tumor cell lines. In this work, the synthesis and biological evaluation of cytotoxic activity of a novel NPCD glycoside, 14-(α-L-rhamnopyranosyl)-naphtho[2,1-a]pyrrolo[3,4-c] carbazole-5,7 (6H,12H)- dione (1) were reported. The results showed the NPCD glycoside 1 displayed strong tumor cell growth inhibitory activities in the range of micromolar IC50 towards a broad spectrum of tumor cell lines. Analysis of cell cycle profiles revealed that NPCD glycoside 1 arrested the cells at different phases depending on the cell lines.)
Keywords:indolocarbazole; cytotoxicity; rebeccamycin; cell-cycleglycoside
 
 
 

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