Synthesis of chromen-4-one-oxadiazole substituted analogs as potent β-glucuronidase inhibitors
Chromen-4-one substituted oxadiazole analogs 1–19 have been synthesized, characterized and evaluated for β-glucuronidase inhibition. All analogs exhibited a variable degree of β-glucuronidase inhibitory activity with IC50 values ranging in between 0.8 ± 0.1–42.3 ± 0.8 µM when compared with the st...
Similar Items
-
Synthesis of new isoquinoline-base-oxadiazole derivatives as potent inhibitors of thymidine phosphorylase and molecular docking study
by: Zaman, Khalid, et al.
Published: (2019) -
In silico designing of thermostabe β-Glucuronidase (GUS)
by: Noorbatcha, Ibrahim Ali, et al.
Published: (2010) -
Molecular dynamics studies of human β-glucuronidase
by: Salleh, Hamzah Mohd., et al.
Published: (2009) -
Molecular dynamics studies of human β-Glucuronidase
by: Noorbatcha, Ibrahim Ali, et al.
Published: (2010) -
Homology Modeling Of β-Glucuronidases From E. Coli and T. Maritima
by: Noorbatcha, Ibrahim Ali, et al.
Published: (2009)