Design and synthesis of new 7,8-dimethoxy-α-naphthoflavones as CYP1A1 inhibitors
摘要:
The flavonoids as inhibitors of CYP1A1 exhibit chemopreventive effects against certain procarcinogens and have been considered as the promising cancer preventive agents. A series of novel 7,8-dimethoxy-alpha-naphthoflavones as the substrate analogs were designed and prepared. The enzyme assay suggested that all of these new flavones were stronger inhibitors of CYP1A1 than the lead compound alpha-naphthoflavone. Among the tested ones, 3h showed the most potent inhibitory effects. (C) 2013 Shao-Shun Li. Published by Elsevier B.V. on behalf of Chinese Chemical Society. All rights reserved.
Design and synthesis of new 7,8-dimethoxy-α-naphthoflavones as CYP1A1 inhibitors
摘要:
The flavonoids as inhibitors of CYP1A1 exhibit chemopreventive effects against certain procarcinogens and have been considered as the promising cancer preventive agents. A series of novel 7,8-dimethoxy-alpha-naphthoflavones as the substrate analogs were designed and prepared. The enzyme assay suggested that all of these new flavones were stronger inhibitors of CYP1A1 than the lead compound alpha-naphthoflavone. Among the tested ones, 3h showed the most potent inhibitory effects. (C) 2013 Shao-Shun Li. Published by Elsevier B.V. on behalf of Chinese Chemical Society. All rights reserved.