Antiproliferative Activity of New Pyrazole-4-sulfonamide Derivatives: Synthesis and Biological Evaluation

被引:9
作者
Mahesh, Panasa [1 ]
Akshinthala, Parameswari [2 ]
Katari, Naresh Kumar [1 ,4 ]
Gupta, Lavleen Kumar [3 ]
Panwar, Dikshita [3 ]
Sharma, Manoj Kumar [3 ]
Jonnalagadda, Sreekantha Babu [4 ]
Gundla, Rambabu [1 ]
机构
[1] GITAM Deemed Univ, Dept Chem, Hyderabad 502329, Telangana, India
[2] MLR Inst Technol, Dept Sci & Humanities, Hyderabad 500043, Telangana, India
[3] IgY Immunologix India Pvt Ltd, Drug Discovery Div, Hyderabad 500089, Telangana, India
[4] Univ KwaZulu Natal, Coll Agr Engn & Sci, Sch Chem & Phys, ZA-4000 Durban, South Africa
来源
ACS OMEGA | 2023年 / 8卷 / 29期
关键词
LACTATE-DEHYDROGENASE; PYRAZOLE;
D O I
10.1021/acsomega.2c07539
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Pyrazole and sulfonamideconstitute an important class of drugs,with several types of pharmacological agents. Facile synthesis oftwo new series of 3,5-dimethyl-1H-pyrazole-4-sulfonamideand 1,3,5-trimethyl-1H-pyrazole-4-sulfonamide derivativeswas designed and synthesized. These pyrazole-4-sulfonamide derivativesare characterized by Fourier transform infrared (FT-IR), H-1 NMR, C-13 NMR, and elemental analysis, and their biologicalevolution data are presented. This paved way for the development ofnew pyrazole-4-sulfonamide derivatives. These compounds are testedfor their in vitro antiproliferative activity against U937 cells bythe CellTiter-Glo Luminescent cell viability assay using MitomycinC. Cytotoxicity detection is based on the measurement of LDH activity,while these compounds did not exhibit cytotoxic activity on thesecells. Half maximal inhibitory concentration (IC50) wascalculated by Graph Pad Prism software for each dose. Their structure-activityrelationships were obtained and discussed.
引用
收藏
页码:25698 / 25709
页数:12
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