Al-Rashida M - Search Results

1

N-hexylsulfonyl indole based thiosemicarbazones as potent and selective ecto-5'-nucleotidase and NTPDase inhibitors.

Batool Z, Dutt SM, Al-Rashida M, Gelsleichter NE, Pelletier J, Sévigny J, Islam T, Aftab H, Almutairi TM, Çakır F, Shafiq Z, Iqbal J. Batool Z, et al. Among authors: al rashida m. Bioorg Chem. 2025 Aug;163:108717. doi: 10.1016/j.bioorg.2025.108717. Epub 2025 Jul 1. Bioorg Chem. 2025. PMID: 40644817

2

Chromone containing sulfonamides as potent carbonic anhydrase inhibitors.

Ekinci D, Al-Rashida M, Abbas G, Şentürk M, Supuran CT. Ekinci D, et al. J Enzyme Inhib Med Chem. 2012 Oct;27(5):744-7. doi: 10.3109/14756366.2011.614607. Epub 2011 Oct 10. J Enzyme Inhib Med Chem. 2012. PMID: 21985426 Free article.

3

In-silico analysis of chromone containing sulfonamide derivatives as human carbonic anhydrase inhibitors.

Ul-Haq Z, Usmani S, Mahmood U, Al-Rashida M, Abbas G. Ul-Haq Z, et al. Med Chem. 2013 Jun 1;9(4):608-16. doi: 10.2174/1573406411309040015. Med Chem. 2013. PMID: 23151266

4

3-(6-Bromo-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 Nov 6;66(Pt 12):o3081-2. doi: 10.1107/S1600536810044648. Acta Crystallogr Sect E Struct Rep Online. 2010. PMID: 21589389 Free PMC article.

5

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

6

Therapeutic potentials of ecto-nucleoside triphosphate diphosphohydrolase, ecto-nucleotide pyrophosphatase/phosphodiesterase, ecto-5'-nucleotidase, and alkaline phosphatase inhibitors.

al-Rashida M, Iqbal J. al-Rashida M, et al. Med Res Rev. 2014 Jul;34(4):703-43. doi: 10.1002/med.21302. Epub 2013 Sep 23. Med Res Rev. 2014. PMID: 24115166 Review.

7

Carbonic anhydrase inhibition by 1-aroyl-3-(4-aminosulfonylphenyl)thioureas.

Saeed A, Al-Rashida M, Hamayoun M, Mumtaz A, Iqbal J. Saeed A, et al. J Enzyme Inhib Med Chem. 2014 Dec;29(6):901-5. doi: 10.3109/14756366.2013.866660. Epub 2014 Mar 25. J Enzyme Inhib Med Chem. 2014. PMID: 24666305 Free article.

8

Cholinesterase Inhibitory Activities of N-Phenylthiazol-2-Amine Derivatives and their Molecular Docking Studies.

Iqbal J, al-Rashida M, Babar A, Hameed A, Khan MS, Munawar MA, Khan AF. Iqbal J, et al. Med Chem. 2015;11(5):489-96. doi: 10.2174/1573406411666141230104536. Med Chem. 2015. PMID: 25537128

9

Sulfa drugs as inhibitors of carbonic anhydrase: new targets for the old drugs.

al-Rashida M, Hussain S, Hamayoun M, Altaf A, Iqbal J. al-Rashida M, et al. Biomed Res Int. 2014;2014:162928. doi: 10.1155/2014/162928. Epub 2014 Sep 8. Biomed Res Int. 2014. PMID: 25538942 Free PMC article.

10

Quinolinyl-thienyl chalcones as monoamine oxidase inhibitors and their in silico modeling studies.

Zaib S, Rizvi SU, Aslam S, Ahmad M, Ali Abid SM, Al-Rashida M, Iqbal J. Zaib S, et al. Med Chem. 2015;11(6):580-9. doi: 10.2174/1573406410666141226131252. Med Chem. 2015. PMID: 25541744

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