13 articles for thisTarget
The following articles (labelled with PubMed ID or TBD) are for your review
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Article Title
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Biology-oriented drug synthesis (BIODS): In vitroß-glucuronidase inhibitory and in silico studies on 2-(2-methyl-5-nitro-1H-imidazol-1-yl)ethyl aryl carboxylate derivatives.
University Of Karachi
Thiadiazole derivatives as New Class ofß-glucuronidase inhibitors.
University Of Karachi
Synthesis of novel benzohydrazone-oxadiazole hybrids asß-glucuronidase inhibitors and molecular modeling studies.
Universiti Teknologi Mara (Uitm)
Evaluation of bisindole as potentß-glucuronidase inhibitors: synthesis and in silico based studies.
University Of Karachi
Substituent Position of Iminocyclitols Determines the Potency and Selectivity for Gut Microbial Xenobiotic-Reactivating Enzymes.
Academia Sinica
Synthesis of novel inhibitors of ?-glucuronidase based on benzothiazole skeleton and study of their binding affinity by molecular docking.
University Of Karachi
Scoparic acid A, a beta-glucuronidase inhibitor from Scoparia dulcis.
Toyama Medical And Pharmaceutical University
Synthesis, in vitro ?-glucuronidase inhibitory potential and molecular docking studies of quinolines.
University Of Karachi
Synthesis, in vitro ß-glucuronidase inhibitory activity and in silico studies of novel (E)-4-Aryl-2-(2-(pyren-1-ylmethylene)hydrazinyl)thiazoles.
University Of Karachi
Synthesis of novel disulfide and sulfone hybrid scaffolds as potent ß-glucuronidase inhibitor.
Universiti Teknologi Mara
Synthesis of 6-chloro-2-Aryl-1H-imidazo[4,5-b]pyridine derivatives: Antidiabetic, antioxidant, ß-glucuronidase inhibiton and their molecular docking studies.
Universiti Teknologi Mara (Uitm), Puncak Alam Campus