Synthesis of oxadiazole-coupled-thiadiazole derivatives as a potent β-glucuronidase inhibitors and their molecular docking study-Reference-Cited by-同舟云学术

Synthesis of oxadiazole-coupled-thiadiazole derivatives as a potent β-glucuronidase inhibitors and their molecular docking study

Published:2019-07 Issue:14 Volume:27 Page:3145-3155
ISSN:0968-0896
Container-title:Bioorganic & Medicinal Chemistry
language:en
Short-container-title:Bioorganic & Medicinal Chemistry

Author:

Taha Muhammad,Imran Syahrul,Alomari Munther,Rahim Fazal,Wadood Abdul,Mosaddik Ashik,Uddin Nizam,Gollapalli Mohammed,Alqahtani Mohammed A.,Bamarouf Yasser A.

Funder

Imama Abdulrahman bin Faisal Univervisty

Publisher

Elsevier BV

Subject

Organic Chemistry,Clinical Biochemistry,Drug Discovery,Pharmaceutical Science,Molecular Biology,Molecular Medicine,Biochemistry

Reference56 articles.

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3. Urinary beta-glucuronidase activity in patients with urinary-tract infection;Bank;N Eng J Med,1965

4. Estimation of beta-glucuronidase activity in urinary-tract infection;Roberts;N Eng J Med,1967

5. Failure of urinary beta-glucuronidase activity to localize the site of urinary tract infection;Ronald;Appl Environ Microbiol,1971

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