Keywords
arylnitromethanes
combretastatin
Knoevenagel condensation
microtubule
sea urchin embryo
tubulin
α-nitrostilbenes
Abstract
A series of nitro analogues of potent antimitotic combretastatin A-4 (diaryl α-nitrostilbenes, DNSs) was synthesized by the Knoevenagel condensation of arylnitromethanes with methylamine Schiff bases of benzaldehydes. The obtained stilbenes featured only cis-diaryl topology irrespective of substitution pattern in the aryl fragments. The evaluation on a sea urchin embryo model suggested that DNSs exhibited both antitubulin and tubulin-unrelated effects similar to those of corresponding monoaryl nitrostyrenes.
Funders
Ministry of Education and Science of the Russian Federation
0088-2024-0015
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