Al-Rashida M - Search Results

1

Synthesis of benzimidazole based hydrazones as non-sugar based α-glucosidase inhibitors: Structure activity relation and molecular docking.

Ahmad MU, Rafiq M, Zahra B, Islam M, Ashraf M, Al-Rashida M, Khan A, Hussain J, Shafiq Z, Al-Harrasi A. Ahmad MU, et al. Drug Dev Res. 2021 Nov;82(7):1033-1043. doi: 10.1002/ddr.21807. Epub 2021 Mar 5. Drug Dev Res. 2021. PMID: 33665884

2

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

3

Identification of novel chromone based sulfonamides as highly potent and selective inhibitors of alkaline phosphatases.

al-Rashida M, Raza R, Abbas G, Shah MS, Kostakis GE, Lecka J, Sévigny J, Muddassar M, Papatriantafyllopoulou C, Iqbal J. al-Rashida M, et al. Eur J Med Chem. 2013 Aug;66:438-49. doi: 10.1016/j.ejmech.2013.06.015. Epub 2013 Jun 19. Eur J Med Chem. 2013. PMID: 23831808

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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