53616-16-3Relevant articles and documents
Curcumin-inspired cytotoxic 3,5-bis(arylmethylene)-1-(N-(ortho-substituted aryl)maleamoyl)-4-piperidones: A novel group of topoisomerase II alpha inhibitors
Jha, Amitabh,Duffield, Katherine M.,Ness, Matthew R.,Ravoori, Sujatha,Andrews, Gabrielle,Bhullar, Khushwant S.,Rupasinghe, H.P. Vasantha,Balzarini, Jan
, p. 6404 - 6417 (2015/10/05)
Three series of novel 3,5-bis(arylmethylene)-1-(N-(ortho-substituted aryl)maleamoyl)-4-piperidones, designed as simplified analogs of curcumin with maleic diamide tether, were synthesized and bioevaluated. These compounds displayed potent cytotoxicity tow
Synthesis and antifungal activity of N-(alkyl/aryl)-2-(3-oxo-1,4- benzothiazin-2-yl)acetamide
Gupta,Wagh
, p. 697 - 702 (2007/10/03)
A series of N-(alkyl/aryl)-2-(3-oxo-1,4-benzothiazin-2-yl)acetamide have been synthesized by condensation of substituted amines with maleic anhydride (MA) followed by cyclization with o-aminothiophenol (o-ATP). All the compounds have been screened for their antifungal activity against Tricophyton rubrum, Epidermophyton floccosum and Malassazia furfur. In the primary screening, some of the compounds exhibited appreciable activity. The structures of the synthesized compounds 7a-z have been established on the basis of elemental analysis and spectral data.
Synthesis and Isomerization of the N,N-Dimethylamides of the 2'-Chloromaleanilic Acids.
Canoira, Laureano,Rodriguez, J. Gonzalo
, p. 2836 - 2855 (2007/10/02)
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