New adamantyl chalcones: Synthesis, antimicrobial and anticancer activities

A Tabbi, D Tebbani, A Caporale… - Current Topics in …, 2017 - ingentaconnect.com
A Tabbi, D Tebbani, A Caporale, C Saturnino, SF Nabavi, P Giuseppe, C Arra, Z Canturk
Current Topics in Medicinal Chemistry, 2017ingentaconnect.com
Background: A new variety of adamantyl chalcones (2, 3a-o) were efficiently prepared by
Claisen-Schmidt reaction of 4-adamantyl acetophenone 2 with a serie of aromatic
aldehydes in good yields. Their structures were confirmed by spectroscopic data, and the
relative configuration of 3d was confirmed by X-ray crystallography. All synthesized
chalcones were tested against a panel of Grampositive and Gram-negative bacteria and
pathogenic fungus and displayed strong antibacterial activity against Enterococcus faecali …
Background: A new variety of adamantyl chalcones (2, 3a-o) were efficiently prepared by Claisen-Schmidt reaction of 4-adamantyl acetophenone 2 with a serie of aromatic aldehydes in good yields. Their structures were confirmed by spectroscopic data, and the relative configuration of 3d was confirmed by X-ray crystallography. All synthesized chalcones were tested against a panel of Grampositive and Gram-negative bacteria and pathogenic fungus and displayed strong antibacterial activity against Enterococcus faecali 29212, Pseudomonas aeruginosa ATCC27853, Escherichia coli and interesting antifungal activity against Candida glabrata ATCC 90030. Result: The effect of these compounds was also tested in vitro as antitumor on Miapaca2 cells. Compounds also showed anticancer activity against human pancreas cancer cell MiaPaca2.
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