Al-Rashida M - Search Results

1

Synthesis, carbonic anhydrase inhibition and in silico insights of 4-formyl-2-nitrophenyl naphthalene-2-sulfonate hybrid thiosemicarbazones.

Abbas K, Islam M, Tayyab M, Al-Rashida M, Taslimi P, Islam T, Sadeghian N, Şenol H, Alanazi AK, Schenone S, Shafiq Z. Abbas K, et al. Among authors: al rashida m. Bioorg Chem. 2025 Dec;167:109243. doi: 10.1016/j.bioorg.2025.109243. Epub 2025 Nov 15. Bioorg Chem. 2025. PMID: 41260070 Free article.

2

3-(6-Fluoro-4-oxo-4H-chromen-3-yl)-3,4-dihydro-2H-1,2,4-benzothia-diazine-1,1-dione.

Al-Rashida M, Nagra SA, Khan IU, Kostakis G, Abbas G. Al-Rashida M, et al. Acta Crystallogr Sect E Struct Rep Online. 2010 Oct 2;66(Pt 11):o2707. doi: 10.1107/S1600536810038274. Acta Crystallogr Sect E Struct Rep Online. 2010. PMID: 21588921 Free PMC article.

3

Discovery of new chromone containing sulfonamides as potent inhibitors of bovine cytosolic carbonic anhydrase.

al-Rashida M, Ashraf M, Hussain B, Nagra SA, Abbas G. al-Rashida M, et al. Bioorg Med Chem. 2011 Jun 1;19(11):3367-71. doi: 10.1016/j.bmc.2011.04.040. Epub 2011 Apr 22. Bioorg Med Chem. 2011. PMID: 21555223

4

Diarylsulfonamides and their bioisosteres as dual inhibitors of alkaline phosphatase and carbonic anhydrase: Structure activity relationship and molecular modelling studies.

Al-Rashida M, Ejaz SA, Ali S, Shaukat A, Hamayoun M, Ahmed M, Iqbal J. Al-Rashida M, et al. Bioorg Med Chem. 2015 May 15;23(10):2435-44. doi: 10.1016/j.bmc.2015.03.054. Epub 2015 Mar 27. Bioorg Med Chem. 2015. PMID: 25865133

5

Facile dimethyl amino group triggered cyclic sulfonamides synthesis and evaluation as alkaline phosphatase inhibitors.

Bhatti HA, Khatoon M, Al-Rashida M, Bano H, Iqbal N, Zaib-Un-Nisa, Yousuf S, Khan KM, Hameed A, Iqbal J. Bhatti HA, et al. Bioorg Chem. 2017 Apr;71:10-18. doi: 10.1016/j.bioorg.2017.01.008. Epub 2017 Jan 18. Bioorg Chem. 2017. PMID: 28139246

6

In search of new α-glucosidase inhibitors: Imidazolylpyrazole derivatives.

Chaudhry F, Naureen S, Huma R, Shaukat A, Al-Rashida M, Asif N, Ashraf M, Munawar MA, Khan MA. Chaudhry F, et al. Bioorg Chem. 2017 Apr;71:102-109. doi: 10.1016/j.bioorg.2017.01.017. Epub 2017 Jan 23. Bioorg Chem. 2017. PMID: 28160945

7

Green synthesis, inhibition studies of yeast α-glucosidase and molecular docking of pyrazolylpyridazine amines.

Chaudhry F, Ather AQ, Akhtar MJ, Shaukat A, Ashraf M, Al-Rashida M, Munawar MA, Khan MA. Chaudhry F, et al. Bioorg Chem. 2017 Apr;71:170-180. doi: 10.1016/j.bioorg.2017.02.003. Epub 2017 Feb 9. Bioorg Chem. 2017. PMID: 28259376

8

Hetarylcoumarins: Synthesis and biological evaluation as potent α-glucosidase inhibitors.

Chaudhry F, Choudhry S, Huma R, Ashraf M, Al-Rashida M, Munir R, Sohail R, Jahan B, Munawar MA, Khan MA. Chaudhry F, et al. Bioorg Chem. 2017 Aug;73:1-9. doi: 10.1016/j.bioorg.2017.05.009. Epub 2017 May 10. Bioorg Chem. 2017. PMID: 28521172

9

Sulfonyl hydrazones derived from 3-formylchromone as non-selective inhibitors of MAO-A and MAO-B: Synthesis, molecular modelling and in-silico ADME evaluation.

Abid SMA, Younus HA, Al-Rashida M, Arshad Z, Maryum T, Gilani MA, Alharthi AI, Iqbal J. Abid SMA, et al. Bioorg Chem. 2017 Dec;75:291-302. doi: 10.1016/j.bioorg.2017.10.001. Epub 2017 Oct 4. Bioorg Chem. 2017. PMID: 29065322

10

Evaluation of α-glucosidase inhibiting potentials with docking calculations of synthesized arylidene-pyrazolones.

Chaudhry F, Naureen S, Choudhry S, Huma R, Ashraf M, Al-Rashida M, Jahan B, Hyder Khan M, Iqbal F, Ali Munawar M, Ain Khan M. Chaudhry F, et al. Bioorg Chem. 2018 Apr;77:507-514. doi: 10.1016/j.bioorg.2018.02.002. Epub 2018 Feb 10. Bioorg Chem. 2018. PMID: 29454828

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