33 articles for thisTarget
The following articles (labelled with PubMed ID or TBD) are for your review
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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
Synthesis and biological evaluation of novel N-arylidenequinoline-3-carbohydrazides as potentß-glucuronidase inhibitors.
Universiti Teknologi Mara (Uitm)
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)
Novel 2,5-disubtituted-1,3,4-oxadiazoles with benzimidazole backbone: a new class ofß-glucuronidase inhibitors and in silico studies.
Universiti Teknologi Mara
Substituted thieno[2,3-b]thiophenes and related congeners: Synthesis,ß-glucuronidase inhibition activity, crystal structure, and POM analyses.
King Saud University
Synthesis andß-glucuronidase inhibitory activity of 2-arylquinazolin-4(3H)-ones.
University of Karachi
Evaluation of bisindole as potentß-glucuronidase inhibitors: synthesis and in silico based studies.
University of Karachi
Anti-inflammatory flavonoids and pterocarpanoid from Crotalaria pallida and C. assamica.
Kaohsiung Medical University
Lead identification of novel tetrahydroimidazo[1,2-a]pyridine-5-carboxylic acid derivative as a potent heparanase-1 inhibitor.
Taisho Pharmaceutical Co.
Metronidazole-conjugates: A comprehensive review of recent developments towards synthesis and medicinal perspective.
North-West University
One-pot synthesis of thioxo-tetrahydropyrimidine derivatives as potent ?-glucuronidase inhibitor, biological evaluation, molecular docking and molecular dynamics studies.
Shiraz University of Medical Sciences
Therapeutic significance of ?-glucuronidase activity and its inhibitors: A review.
University of Kwazulu-Natal
Synthetic approaches and pharmaceutical applications of chloro-containing molecules for drug discovery: A critical review.
Wuhan University of Technology
Substituent Position of Iminocyclitols Determines the Potency and Selectivity for Gut Microbial Xenobiotic-Reactivating Enzymes.
Academia Sinica
Synthesis of oxadiazole-coupled-thiadiazole derivatives as a potent ?-glucuronidase inhibitors and their molecular docking study.
Imam Abdulrahman Bin Faisal University
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 of bis-indolylmethanes as new potential inhibitors of ?-glucuronidase and their molecular docking studies.
Imam Abdulrahman Bin Faisal University
Synthesis, in vitro ?-glucuronidase inhibitory potential and molecular docking studies of quinolines.
University of Karachi
Synthesis and in silico studies of novel sulfonamides having oxadiazole ring: As ß-glucuronidase inhibitors.
Universiti Teknologi Mara (Uitm)
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, ß-glucuronidase inhibition and molecular docking studies of hybrid bisindole-thiosemicarbazides analogs.
Universiti Teknologi Mara
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