
Journal of Medicinal Chemistry p. 2474 - 2485 (1989)
Update date:2022-08-02
Topics:
Reich
Fabio
Lee
Kuck
Testa
The preparation and biological activities of a series of pyrido[3,4-e]-1,2,4-triazines, 1,2,4-triazino[5,6-c]quinolines, and related fused triazines are described. Methyl, amino, and acylamino substituents were placed in the pyridyl ring of the former system. Other structural modifications included various alkyl, cycloalkyl, substituted phenyl, and heterocyclic groups in the 3-position of these ring systems. In agar dilution assays, actives in this series inhibited strains of Candida, Aspergillus, Mucor, and Trychophyton species at MIC's of ≤ 16 μg/mL.
View MoreTIANJIN GST CHEMICAL TECHNOLOGY CO., LTD
Contact:+86-22-25210964
Address:Room. 208, No. -12-C, No. 13, Xinbei Road, Tanggu District, New Haixin Area, Tianjin City, China
Contact:+49-9398-993127
Address:Untertorstr. 27
Nanjing Capatue Chemical Co., Ltd
Contact:+86-25-86371192 +86-025-85720158
Address:No.20 Jiangjun Avenue, Jiangning Economic & Technical Development Zone
Contact:+86-15995924277
Address:WuZhongOu suzhou new south road 89
Changsha Goomoo Chemical Technology Co.Ltd
Contact:+86-731-82197655
Address:No.649,Chezhan Rd.(N),Changsha,Hunan,China
Doi:10.1016/j.jorganchem.2019.02.014
(2019)Doi:10.1021/jo00315a014
(1981)Doi:10.1021/jo00316a014
(1981)Doi:10.1039/C1967001297a
(1967)Doi:10.1016/j.mcat.2019.110628
(2020)Doi:10.1021/ja00862a043
(1962)