Shibata S, Inoue H, Iwata S, Ma R D, Yu L J, Ueyama H, Takayasu J, Hasegawa T, Tokuda H, Nishino A
Shibata Laboratory of Natural Medicinal Materials, Minophagen Pharmaceutical Co., Tokyo, Japan.
Planta Med. 1991 Jun;57(3):221-4. doi: 10.1055/s-2006-960078.
Licochalcone A, 3-a,a-dimethylallyl-4,4'-dihydroxy-6-methoxychalcone, from the root of Glycyrrhiza inflata Beta (Leguminosae) (Xin-jiang liquorice) showed anti-inflammatory action towards mouse ear edema induced by arachidonic acid (AA) and 12-O-tetradecanoylphorbol 13-acetate (TPA) by topical application. Anti-tumour promoting action of licochalcone A was also observed in vivo for mouse skin papilloma initiated by dimethylbenz[a]anthracene (DMBA) and promoted by TPA. It inhibited in vitro 32Pi-incorporation to phospholipids in HeLa cells promoted by TPA. A competitive interaction of licochalcone A with the TPA-receptors in the cell membrane has been suggested.