Motohashi N, Sakagami H, Kurihara T, Ferenczy L, Csuri K, Molnar J
Department of Medicinal Chemistry, Meiji College of Pharmacy, Tokyo, Japan.
Anticancer Res. 1992 Jul-Aug;12(4):1207-10.
The abilities of 14 phenothiazines, 8 benzo[a]phenothiazines and 12 benz[c]acridines to induce an antibacterial effect against Escherichia coli K12 were compared. Several phenothiazines, which showed antiplasmid activity, displayed the most potent antibacterial activity. All benz[c]acridine derivatives were moderately antibacterial, whereas benzo[a]phenothiazines were inactive. The active phenothiazine derivatives had more potent inhibitory activity against fungi, including phytopathogen filamentous, human pathogen filamentous fungi and yeasts, than against gram-positive and -negative bacteria. Taken together with previously reported data, the induction mechanism of antimicrobial and antiplasmid activity by these compounds seems to be different from that of antitumor, differentiation-inducing and carcinogenic activity.
比较了14种吩噻嗪、8种苯并[a]吩噻嗪和12种苯并[c]吖啶对大肠杆菌K12的抗菌作用。几种表现出抗质粒活性的吩噻嗪具有最强的抗菌活性。所有苯并[c]吖啶衍生物具有中等抗菌活性,而苯并[a]吩噻嗪无活性。活性吩噻嗪衍生物对真菌,包括植物病原丝状真菌、人类病原丝状真菌和酵母的抑制活性比对革兰氏阳性和阴性细菌更强。结合先前报道的数据,这些化合物抗菌和抗质粒活性的诱导机制似乎与抗肿瘤、诱导分化和致癌活性的机制不同。