Riaz M - Search Results

1

Hybrid benzothiazole analogs as antiurease agent: Synthesis and molecular docking studies.

Taha M, Ismail NH, Imran S, Wadood A, Rahim F, Khan KM, Riaz M. Taha M, et al. Among authors: riaz m. Bioorg Chem. 2016 Jun;66:80-7. doi: 10.1016/j.bioorg.2016.03.010. Epub 2016 Mar 24. Bioorg Chem. 2016. PMID: 27038849

2

Synthesis of potent urease inhibitors based on disulfide scaffold and their molecular docking studies.

Taha M, Ismail NH, Imran S, Wadood A, Rahim F, Riaz M. Taha M, et al. Among authors: riaz m. Bioorg Med Chem. 2015 Nov 15;23(22):7211-8. doi: 10.1016/j.bmc.2015.10.017. Epub 2015 Oct 22. Bioorg Med Chem. 2015. PMID: 26507431

3

Thiadiazole derivatives as New Class of β-glucuronidase inhibitors.

Salar U, Taha M, Ismail NH, Khan KM, Imran S, Perveen S, Wadood A, Riaz M. Salar U, et al. Among authors: riaz m. Bioorg Med Chem. 2016 Apr 15;24(8):1909-18. doi: 10.1016/j.bmc.2016.03.020. Epub 2016 Mar 10. Bioorg Med Chem. 2016. PMID: 26994638

4

Synthesis, in vitro α-glucosidase inhibitory activity and molecular docking studies of new thiazole derivatives.

Khan KM, Qurban S, Salar U, Taha M, Hussain S, Perveen S, Hameed A, Ismail NH, Riaz M, Wadood A. Khan KM, et al. Among authors: riaz m. Bioorg Chem. 2016 Oct;68:245-58. doi: 10.1016/j.bioorg.2016.08.010. Epub 2016 Aug 24. Bioorg Chem. 2016. PMID: 27592296

5

5-Bromo-2-aryl benzimidazole derivatives as non-cytotoxic potential dual inhibitors of α-glucosidase and urease enzymes.

Arshad T, Khan KM, Rasool N, Salar U, Hussain S, Asghar H, Ashraf M, Wadood A, Riaz M, Perveen S, Taha M, Ismail NH. Arshad T, et al. Among authors: riaz m. Bioorg Chem. 2017 Jun;72:21-31. doi: 10.1016/j.bioorg.2017.03.007. Epub 2017 Mar 20. Bioorg Chem. 2017. PMID: 28346872

6

Hydrazinyl arylthiazole based pyridine scaffolds: Synthesis, structural characterization, in vitro α-glucosidase inhibitory activity, and in silico studies.

Ali F, Khan KM, Salar U, Taha M, Ismail NH, Wadood A, Riaz M, Perveen S. Ali F, et al. Among authors: riaz m. Eur J Med Chem. 2017 Sep 29;138:255-272. doi: 10.1016/j.ejmech.2017.06.041. Epub 2017 Jun 26. Eur J Med Chem. 2017. PMID: 28672278

7

New α-Glucosidase inhibitors from the resins of Boswellia species with structure-glucosidase activity and molecular docking studies.

Ur Rehman N, Khan A, Al-Harrasi A, Hussain H, Wadood A, Riaz M, Al-Abri Z. Ur Rehman N, et al. Among authors: riaz m. Bioorg Chem. 2018 Sep;79:27-33. doi: 10.1016/j.bioorg.2018.04.020. Epub 2018 Apr 25. Bioorg Chem. 2018. PMID: 29715636

8

Synthetic nicotinic/isonicotinic thiosemicarbazides: In vitro urease inhibitory activities and molecular docking studies.

Ali B, Mohammed Khan K, Arshia, Kanwal, Hussain S, Hussain S, Ashraf M, Riaz M, Wadood A, Perveen S. Ali B, et al. Among authors: riaz m. Bioorg Chem. 2018 Sep;79:34-45. doi: 10.1016/j.bioorg.2018.04.004. Epub 2018 Apr 16. Bioorg Chem. 2018. PMID: 29723741

9

1-[(4'-Chlorophenyl) carbonyl-4-(aryl) thiosemicarbazide derivatives as potent urease inhibitors: Synthesis, in vitro and in silico studies.

Ali B, Khan KM, Salar U, Kanwal, Hussain S, Ashraf M, Riaz M, Wadood A, Taha M, Perveen S. Ali B, et al. Among authors: riaz m. Bioorg Chem. 2018 Sep;79:363-371. doi: 10.1016/j.bioorg.2018.05.017. Epub 2018 May 23. Bioorg Chem. 2018. PMID: 29859384

10

Synthesis of 1H-1,2,3-triazole derivatives as new α-glucosidase inhibitors and their molecular docking studies.

Avula SK, Khan A, Rehman NU, Anwar MU, Al-Abri Z, Wadood A, Riaz M, Csuk R, Al-Harrasi A. Avula SK, et al. Among authors: riaz m. Bioorg Chem. 2018 Dec;81:98-106. doi: 10.1016/j.bioorg.2018.08.008. Epub 2018 Aug 7. Bioorg Chem. 2018. PMID: 30118991

Save citations to file

Email citations

Send citations to clipboard

Add to Collections

Add to My Bibliography

Create a file for external citation management software

Your saved search

Your RSS Feed

My Custom Filters

Publication date

Text availability

Article attribute

Article type

Article Language

Species

Sex

Age

Other

1,209 results

Search Page

Filters