Ul-Haq Z - Search Results

1

Synthesis of Highly Potent Anti-Inflammatory Compounds (ROS Inhibitors) from Isonicotinic Acid.

Yaqoob S, Nasim N, Khanam R, Wang Y, Jabeen A, Qureshi U, Ul-Haq Z, El-Seedi HR, Jiang ZH, Khan FA. Yaqoob S, et al. Molecules. 2021 Feb 26;26(5):1272. doi: 10.3390/molecules26051272. Molecules. 2021. PMID: 33652837 Free PMC article.

2

Identification of potent urease inhibitors via ligand- and structure-based virtual screening and in vitro assays.

Khan KM, Wadood A, Ali M, Zia-Ullah, Ul-Haq Z, Lodhi MA, Khan M, Perveen S, Choudhary MI. Khan KM, et al. J Mol Graph Model. 2010 Jun;28(8):792-8. doi: 10.1016/j.jmgm.2010.02.004. Epub 2010 Feb 17. J Mol Graph Model. 2010. PMID: 20338793

3

A novel pharmacophore model to identify leads for simultaneous inhibition of anti-coagulation and anti-inflammatory activities of snake venom phospholipase A(2).

Wadood A, Ali SA, Sattar R, Lodhi MA, Ul-Haq Z. Wadood A, et al. Chem Biol Drug Des. 2012 Apr;79(4):431-41. doi: 10.1111/j.1747-0285.2011.01281.x. Epub 2012 Jan 30. Chem Biol Drug Des. 2012. PMID: 22136624

4

In silico and in vitro immunomodulatory studies on compounds of Lindelofia stylosa.

Mesaik MA, Jabeen A, Halim SA, Begum A, Khalid AS, Asif M, Fatima B, Ul-Haq Z, Choudhary MI. Mesaik MA, et al. Chem Biol Drug Des. 2012 Mar;79(3):290-9. doi: 10.1111/j.1747-0285.2011.01310.x. Chem Biol Drug Des. 2012. PMID: 22181857

5

Synthesis, biological evaluation, and molecular docking studies of benzyl, alkyl and glycosyl [2-(arylamino)-4,4-dimethyl-6-oxo-cyclohex-1-ene]carbodithioates, as potential immunomodulatory and immunosuppressive agents.

El Ashry el SH, Amer MR, Abdalla OM, Aly AA, Soomro S, Jabeen A, Halim SA, Ahmed Mesaik M, Ul-Haq Z. El Ashry el SH, et al. Bioorg Med Chem. 2012 May 1;20(9):3000-8. doi: 10.1016/j.bmc.2012.03.003. Epub 2012 Mar 15. Bioorg Med Chem. 2012. PMID: 22480848

6

In-vitro immunomodulatory and anti-cancerous activities of biotransformed products of Dianabol through Azadirachta indica and its molecular docking studies.

Saifullah, Khan S, Azizuddin, Halim SA, Kashif M, Jabeen A, Asif M, Mesaik MA, Ul-Haq Z, Dar A, Choudhary MI. Saifullah, et al. Chem Cent J. 2013 Oct 7;7:163. doi: 10.1186/1752-153X-7-163. eCollection 2013. Chem Cent J. 2013. PMID: 24764465 Free PMC article.

7

Synthesis, anti-microbial and molecular docking studies of quinazolin-4(3H)-one derivatives.

Mabkhot YN, Al-Har MS, Barakat A, Aldawsari FD, Aldalbahi A, Ul-Haq Z. Mabkhot YN, et al. Molecules. 2014 Jun 25;19(7):8725-39. doi: 10.3390/molecules19078725. Molecules. 2014. PMID: 24968329 Free PMC article.

8

Synthesis, bioactivity, molecular docking and POM analyses of novel substituted thieno[2,3-b]thiophenes and related congeners.

Mabkhot YN, Aldawsari FD, Al-Showiman SS, Barakat A, Hadda TB, Mubarak MS, Naz S, Ul-Haq Z, Rauf A. Mabkhot YN, et al. Molecules. 2015 Jan 23;20(2):1824-41. doi: 10.3390/molecules20021824. Molecules. 2015. PMID: 25621424 Free PMC article.

9

Synthesis of pyrimidine-2,4,6-trione derivatives: Anti-oxidant, anti-cancer, α-glucosidase, β-glucuronidase inhibition and their molecular docking studies.

Barakat A, Islam MS, Al-Majid AM, Ghabbour HA, Yousuf S, Ashraf M, Shaikh NN, Iqbal Choudhary M, Khalil R, Ul-Haq Z. Barakat A, et al. Bioorg Chem. 2016 Oct;68:72-9. doi: 10.1016/j.bioorg.2016.07.009. Epub 2016 Jul 19. Bioorg Chem. 2016. PMID: 27454620

10

5-Acetyl-6-methyl-4-aryl-3,4-dihydropyrimidin-2(1H)-ones: As potent urease inhibitors; synthesis, in vitro screening, and molecular modeling study.

Shamim S, Khan KM, Salar U, Ali F, Lodhi MA, Taha M, Khan FA, Ashraf S, Ul-Haq Z, Ali M, Perveen S. Shamim S, et al. Bioorg Chem. 2018 Feb;76:37-52. doi: 10.1016/j.bioorg.2017.10.021. Epub 2017 Nov 2. Bioorg Chem. 2018. PMID: 29125971

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