34136-53-3Relevant academic research and scientific papers
Inhibitory activity of corn-derived bisamide compounds against α-glucosidase
Niwa, Toshio,Doi, Umeyuki,Osawa, Toshihiko
, p. 90 - 94 (2003)
Bioassay guided fractionation from corn gluten meal, a byproduct of a starch manufacturing plant, gave N-p-coumaroyl-N′-feruloylputrescine (1) and N,N′-diferuloylputrescine (2) as α-glucosidase inhibitors. Some structure-activity relationships were studied by comparing the inhibitory activity by preparing some related compounds, and it was revealed that the hydroxyl group was important for the inhibitory activity of bisamide alkaloids, but not the redox potential.
Solid-phase synthesis and antibacterial activity of hydroxycinnamic acid amides and analogues against methicillin-resistant Staphylococcus aureus and vancomycin-resistant S. aureus
Yingyongnarongkul, Boon-ek,Apiratikul, Nuttapon,Aroonrerk, Nuntana,Suksamrarn, Apichart
, p. 5870 - 5873 (2007/10/03)
A library of hydroxycinnamic acid amides (HCAAs) and analogues were synthesized using solid-phase synthesis technique. These compounds were screened for antibacterial against methicillin-resistant Staphylococcus aureus (MRSA) (11 strains) and vancomycin-r
AN EFFICIENT SYNTHESIS OF SOME BIOLOGICALLY IMPORTANT MONOACYLATED DIAMINES
Kunesch, Gerhard
, p. 5211 - 5214 (2007/10/02)
Some biologically important monoacylated diamines were synthesyzed via azide intermediates in good yield.
