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

[Image: see text] Pyrazole and sulfonamide constitute an important class of drugs, with several types of pharmacological agents. Facile synthesis of two new series of 3,5-dimethyl-1H-pyrazole-4-sulfonamide and 1,3,5-trimethyl-1H-pyrazole-4-sulfonamide derivatives was designed and synthesized. These...

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Detalles Bibliográficos
Autores principales: Mahesh, Panasa, Akshinthala, Parameswari, Katari, Naresh Kumar, Gupta, Lavleen Kumar, Panwar, Dikshita, Sharma, Manoj Kumar, Jonnalagadda, Sreekantha Babu, Gundla, Rambabu
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Chemical Society 2023
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10373183/
https://www.ncbi.nlm.nih.gov/pubmed/37521676
http://dx.doi.org/10.1021/acsomega.2c07539
Descripción
Sumario:[Image: see text] Pyrazole and sulfonamide constitute an important class of drugs, with several types of pharmacological agents. Facile synthesis of two new series of 3,5-dimethyl-1H-pyrazole-4-sulfonamide and 1,3,5-trimethyl-1H-pyrazole-4-sulfonamide derivatives was designed and synthesized. These pyrazole-4-sulfonamide derivatives are characterized by Fourier transform infrared (FT-IR), (1)H NMR, (13)C NMR, and elemental analysis, and their biological evolution data are presented. This paved way for the development of new pyrazole-4-sulfonamide derivatives. These compounds are tested for their in vitro antiproliferative activity against U937 cells by the CellTiter-Glo Luminescent cell viability assay using Mitomycin C. Cytotoxicity detection is based on the measurement of LDH activity, while these compounds did not exhibit cytotoxic activity on these cells. Half maximal inhibitory concentration (IC(50)) was calculated by Graph Pad Prism software for each dose. Their structure–activity relationships were obtained and discussed.