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• W3151323193 endingPage "127988" @default.
• W3151323193 startingPage "127988" @default.
• W3151323193 abstract "Skin cancer is the most common type of cancer in Brazil, representing 30% of all cases. Among these, melanoma represents only 3% of malignant neoplasms; however, it is the most serious and has a high capacity for metastasis. For this reason, it is extremely important to identify more efficient compounds and treatments that stop or decrease the proliferation of melanoma, even in its more advanced stages. This work reports the synthesis and biological evaluation of two homologous series of pyrazoline fatty chain derivatives as potent antitumoral agents in the melanoma B16F10 cell line. Cells were treated with pyrazoline fatty chain compounds (3, 30, 300, and 3000 μM) for 0, 24, 48, and 72 h. Decreased cell viability was observed when using most compounds at different concentrations and times. The structure–activity relationship (SAR) between antitumoral activity and the number of carbons and lipophilicity, as well as the oxygen–sulfur bioisosteric exchange, was evaluated. Among the tested derivatives, the lipophilic compounds 5-hydroxy-5-(trifluoromethyl)-3-undecyl-4,5-dihydro-1H-pyrazole-1-carboxamide (2d) and 5-hydroxy-5-(trifluoromethyl)-3-undecyl-4,5-dihydro-1H-pyrazole-1-thiocarboxamide (3d) showed the best results in the B16F10 cell line, as they produced the best cell viability decrease effects. The presence of fatty unbranched undecyl chain in the molecular structure appears to be important for its antimelanoma properties." @default.
• W3151323193 created "2021-04-13" @default.
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• W3151323193 date "2021-06-01" @default.
• W3151323193 modified "2023-09-30" @default.
• W3151323193 title "Synthesis of pyrazoline fatty chain derivatives and its effects on melanoma cells" @default.
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• W3151323193 doi "https://doi.org/10.1016/j.bmcl.2021.127988" @default.
• W3151323193 hasPubMedId "https://pubmed.ncbi.nlm.nih.gov/33775838" @default.
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