Synthesis of oxadiazole-coupled-thiadiazole derivatives as a potent β-glucuronidase inhibitors and their molecular docking study
A new series of oxadiazole with thiadiazole moiety (6–27) were synthesized, characterized by different spectroscopic techniques and evaluated for β-glucuronidase inhibitory potential. Sixteen analogs such as 6, 7, 8, 9, 10, 12, 13, 14, 17, 18, 20, 23, 24, 25, 26 and 27 showed IC50 values in the rang...
الحاوية / القاعدة: | Bioorganic and Medicinal Chemistry |
---|---|
المؤلف الرئيسي: | Taha M.; Imran S.; Alomari M.; Rahim F.; Wadood A.; Mosaddik A.; Uddin N.; Gollapalli M.; Alqahtani M.A.; Bamarouf Y.A. |
التنسيق: | مقال |
اللغة: | English |
منشور في: |
Elsevier Ltd
2019
|
الوصول للمادة أونلاين: | https://www.scopus.com/inward/record.uri?eid=2-s2.0-85066996057&doi=10.1016%2fj.bmc.2019.05.049&partnerID=40&md5=ecd950b1a53d346832bbb97fc0a2db8b |
مواد مشابهة
-
Thiadiazole derivatives as New Class of β-glucuronidase inhibitors
بواسطة: 2-s2.0-84961126449
منشور في: (2016) -
Synthesis of chromen-4-one-oxadiazole substituted analogs as potent β-glucuronidase inhibitors
بواسطة: 2-s2.0-85064857181
منشور في: (2019) -
Synthesis of diindolylmethane (DIM) bearing thiadiazole derivatives as a potent urease inhibitor
بواسطة: 2-s2.0-85084696332
منشور في: (2020) -
Synthesis and β-glucuronidase inhibitory activity of 2-arylquinazolin-4(3H)-ones
بواسطة: 2-s2.0-84901927895
منشور في: (2014) -
Synthesis, β-glucuronidase inhibition and molecular docking studies of cyano-substituted bisindole hydrazone hybrids
بواسطة: 2-s2.0-85083494465
منشور في: (2021)