Design and synthesis of novel anti-cancer curcumin derivatives: Investigation of anti-cancer properties against HepG2 cell line

Fatemeh Ranjbar, E. Mosaddegh, A. Hassankhani, M. Torkzadeh-Mahani
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Abstract

The new anti-cancer and water-soluble curcumin derivatives have been synthesized solvent-freely by functionalizing the phenolic group of curcumin with various NH compounds to increase water solubility and cancerous properties. The biological applications of the new drugs have been investigated against the highly potent HepG2 carcinoma cell line. The studies showed that new curcumin derivatives could be used in low concentrations (µM/l<1) to avoid the anti-apoptotic properties against the cancerous cell. Also, the designed molecules with concentrations below 1 µM/l showed a good percentage of viability of 31.5, 45.3, and 66.7% against HepG2 cells. Furthermore, FTIR and 1H, and 13CNMR spectroscopy fully characterized the new curcumin derivatives.
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新型抗癌姜黄素衍生物的设计与合成:对HepG2细胞系抗癌特性的研究
通过在姜黄素的酚基上加入不同的氢化合物,以提高姜黄素的水溶性和抗癌性,合成了新的抗肿瘤和水溶性姜黄素衍生物。研究了新药物对高效HepG2癌细胞的生物学应用。研究表明,新的姜黄素衍生物可以在低浓度(µM/l<1)下使用,以避免对癌细胞的抗凋亡特性。在浓度低于1µM/l的情况下,设计的分子对HepG2细胞的存活率分别为31.5%、45.3和66.7%。此外,FTIR、1H和13CNMR光谱对新姜黄素衍生物进行了全面表征。
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