Abstract
Synthesis of coumarin 3-(N-aryl) sulfonamides was accomplished either by Knoevenagel condensation of anilinosulfonylacetic acids with suitable salicylaldehydes or by the reaction of methyl anilinosulfonylacetates with substituted salicylaldehydes in presence of a catalytic amount of a base. All the compounds tested for antiproliferative activity in different cancer cell lines have shown GI(50) values less than 100 microM.
Publication types
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Research Support, Non-U.S. Gov't
MeSH terms
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Antineoplastic Agents / chemical synthesis*
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Antineoplastic Agents / chemistry
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Antineoplastic Agents / toxicity
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Cell Line, Tumor
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Cell Survival / drug effects*
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Coumarins / chemical synthesis
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Coumarins / toxicity
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Humans
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K562 Cells
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Molecular Conformation
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Molecular Structure
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Sulfonamides / chemical synthesis*
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Sulfonamides / chemistry
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Sulfonamides / toxicity*
Substances
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Antineoplastic Agents
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Coumarins
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Sulfonamides