1018075-50-7Relevant academic research and scientific papers
An efficient preparation of new homoallylamines and α-aminonitriles bearing furyl and thienyl rings
Mendez, Leonor Y. Vargas,Kouznetsov, Vladimir V.
, p. 927 - 930 (2008)
(Chemical Equation Presented) New diverse N-aryl-N-[1-furyl(thienyl)but-3- enyl]amines (homoallylamines) or 2-(N-arylmethylamino)-2-furyl(thienyl) acetonitriles (α-aminonitriles) were easily prepared in good to excellent yields by an indium-mediated Barbi
Antifungal and cytotoxic activities of some N-substituted aniline derivatives bearing a hetaryl fragment
Kouznetsov, Vladímir V.,Vargas Méndez, Leonor Y.,Sortino, Maximiliano,Vásquez, Yelkaira,Gupta, Mahabir P.,Freile, Mónica,Enriz, Ricardo D.,Zacchino, Susana A.
, p. 794 - 809 (2008/09/17)
Diverse N-substituted anilines bearing hetaryl fragments were easily prepared from corresponding aldimines derived from commercially available aromatic aldehydes and anilines. 2-Furyl substituted anilines showed very good antifungal activities against dermatophytes, particularly against Trichophyton rubrum (MIC = 3.12-6.25 μg/mL). In addition, all active compounds, 45-47, 73, and 74, were tested for cytotoxic activities against breast (MCF-7), lung (H-460), and central nervous system (SF-268) human cancer cell lines with the NCI-anticancer-drug screen. The activity of amines described in this paper, along with the low toxicity of most of them, shows promise for the future development of non-toxic new antimycotic agents.
