Synthesis of New Hispolon Derived Pyrazole Sulfonamides for Possible Antitubercular and Antimicrobial Agents

被引:9
|
作者
Raju, Pericherla V. S. Narasimha [1 ]
Saketi, Jagan Mohana Rao [2 ]
Balaji, Neduri, V [1 ,2 ]
Kurmarayuni, Chandra Mohan [2 ]
Subbaraju, Gottumukkala, V [1 ]
Bollikolla, Hari Babu [2 ]
机构
[1] Natsol Labs Private Ltd, 2 Floor,Res & Dev Bldg, Visakhapatnam 531019, AP, India
[2] Acharya Nagarjuna Univ, Dept Chem, Guntur 522510, AP, India
关键词
Hispolon; sulfonamides; hispolon pyrazole; antimicrobial activity; pyrazole sulfonamides; anti TB; PHELLINUS-LINTEUS; APOPTOSIS; CELLS; INHIBITION; ANALOGS; ERK1/2; BREAST; ACID;
D O I
10.29356/jmcs.v65i2.1458
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
A series of 10 new hispolonpyrazole sulfonamides were designed and synthesized using hispolons and 4-sulfonamide phenylhydrazine hydrochloride with better yields. The synthesized pyrazole sulfonamides were screened for anti-TB, anti-bacterial, and anti-fungal activities to compare the role sulfonamide moiety. Among them, 3a and 3b showed selective potent anti-tubercular nature (MIC 6.25 mu g/mL). Further, the antimicrobial studies of the compounds showed only compound 3b with a good inhibition zone on Staphylococcus aureus among other bacteria and fungi studied.
引用
收藏
页码:237 / 246
页数:10
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