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ECB-ART-43201
Eur J Med Chem 2014 Feb 12;73:112-25. doi: 10.1016/j.ejmech.2013.12.006.
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3-(5-)-Amino-o-diarylisoxazoles: regioselective synthesis and antitubulin activity.

Tsyganov DV , Khrustalev VN , Konyushkin LD , Raihstat MM , Firgang SI , Semenov RV , Kiselyov AS , Semenova MN , Semenov VV .


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A regioselective synthesis of both 5-amino- and 3-aminodiarylisoxazoles substituted with polyalkoxyaryl pharmacophores has been validated. Starting materials for the synthetic scheme were easily available from plant extracts. The targeted molecules were further tested in the phenotypic sea urchin embryo assay to identify compounds with antimitotic microtubule destabilizing activity. Structure-activity relationship studies suggested that the structural features essential for potent antiproliferative activity include: 1) 5-aminoisoxazole bridge linking biaryl substituents (rings A and B); 2) unsubstituted 5-amino group; 3) 3,4,5-methoxy substituted benzene and 4-methoxy benzene pharmacophores as rings A and B, respectively. The most potent compounds also showed strong in vitro cytotoxicity in NCI60 anticancer drug screen against a panel of 60 human cancer cell lines, including multi-drug resistant cells.

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Genes referenced: LOC100887844 LOC100893907 LOC115919910