Synthesis and biological evaluation of some N4-substituted 5-nitroisatin-3-thiosemicarbazones

被引:11
作者
Pervez, Humayun [1 ]
Manzoor, Nazia [1 ]
Yaqub, Muhammad [1 ]
Nasim, Faiz-ul-Hassan [2 ]
Khan, Khalid M. [3 ]
机构
[1] Bahauddin Zakariya Univ, Dept Chem, Multan 60800, Pakistan
[2] Islamia Univ Bahawalpur, Dept Chem, Bahawalpur, Pakistan
[3] Univ Karachi, HEJ Res Inst Chem, Int Ctr Chem & Biol Sci, Karachi 75270, Pakistan
关键词
5-Nitroisatin; Thiosemicarbazones; Antifungal; Cytotoxicity; Phytotoxicity; Urease inhibition; PRIMARY CYTOTOXICITY EVALUATION; ISATIN-BETA-THIOSEMICARBAZONES; BACILLUS-PASTEURII UREASE; JACK BEAN UREASE; X-RAY DATA; IN-VITRO; ANTITUBERCULOSIS ACTIVITY; HELICOBACTER-PYLORI; INHIBITION; DERIVATIVES;
D O I
10.1007/s00044-011-9745-7
中图分类号
R914 [药物化学];
学科分类号
100701 ;
摘要
A series of 5-nitroisatin-3-thiosemicarbazones 2a-2l was synthesised and evaluated for selected biological activities. The brine shrimp lethality bioassay was carried out to study their in vitro cytotoxicity potential and besides, their antifungal, phytotoxic and urease inhibitory effects were also investigated. Only compound 2j proved to be active in the brine shrimp assay exhibiting LD50 value 1.16 x 10(-3) M. Compounds 2a and 2d displayed moderate antifungal activity (50 and 40%, respectively) against M. canis. Similarly, compound 2l exhibited moderate activity (40%) against the fungal strain, A. flavus. In phytotoxicity assay, all the synthesised compounds including the reference point 2m showed weak to moderate (20-60%) activity at the highest tested concentrations (1,000 mu g and 500 mu g/ml, respectively). In urease inhibition assay, compounds 2a, 2i and 2k proved to be potent inhibitors demonstrating pronounced inhibition with IC50 values 0.440, 0.901 and 27.880 mu M, respectively. These compounds may act as leads for further studies.
引用
收藏
页码:2251 / 2262
页数:12
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