Sharma Rahul, Kumar Rakesh, Kodwani Rishi, Kapoor Sukriti, Khare Anukriti, Bansal Ritu, Khurana Sonali, Singh Sandhya, Thomas Jennifer, Roy Bornika, Phartyal Rajendra, Saluja Shukla, Kumar Sanjay
Sri Venkateswara College, University of Delhi, Delhi - 110021, India.
Anticancer Agents Med Chem. 2015;16(2):200-11. doi: 10.2174/1871520615666150518093144.
Chalcones comprise a characteristic framework of 1, 3-diaryl-2-propen-1-one. They have been heralded as promising anti cancer drugs and have received much attention in the field of cancer research and drug development. The cytotoxicity of these potent pharmacophores is attributable to a wide spectrum of biological activities like anti inflammatory, anti proliferative, anti fungal, etc. These anti tumor activities are effectuated through apoptosis, cell cycle arrest, anti tubulin and so forth. This review summarizes the recent developments on anti tumor activity of synthetic and natural chalcones and their detailed underlying mechanisms as reported in the past.
查耳酮包含1,3 - 二芳基 - 2 - 丙烯 - 1 - 酮的特征性骨架。它们被誉为有前景的抗癌药物,在癌症研究和药物开发领域受到了广泛关注。这些强效药效基团的细胞毒性归因于广泛的生物活性,如抗炎、抗增殖、抗真菌等。这些抗肿瘤活性是通过细胞凋亡、细胞周期阻滞、抗微管蛋白等实现的。本综述总结了过去报道的合成查耳酮和天然查耳酮抗肿瘤活性的最新进展及其详细的潜在机制。