Bayomi SM - Search Results

1

Synthesis, biological evaluation, and molecular modeling simulations of new heterocyclic hybrids as multi-targeted anti-Alzheimer's agents.

Waly OM, Saad KM, El-Subbagh HI, Bayomi SM, Ghaly MA. Waly OM, et al. Among authors: bayomi sm. Eur J Med Chem. 2022 Mar 5;231:114152. doi: 10.1016/j.ejmech.2022.114152. Epub 2022 Jan 22. Eur J Med Chem. 2022. PMID: 35101650

2

Synthesis and anti-inflammatory activity of novel (substituted)benzylidene acetone oxime ether derivatives: molecular modeling study.

El-Gamal MI, Bayomi SM, El-Ashry SM, Said SA, Abdel-Aziz AA, Abdel-Aziz NI. El-Gamal MI, et al. Among authors: bayomi sm. Eur J Med Chem. 2010 Apr;45(4):1403-14. doi: 10.1016/j.ejmech.2009.12.041. Epub 2009 Dec 28. Eur J Med Chem. 2010. PMID: 20079558

3

Synthesis and biological evaluation of new curcumin analogues as antioxidant and antitumor agents: molecular modeling study.

Bayomi SM, El-Kashef HA, El-Ashmawy MB, Nasr MN, El-Sherbeny MA, Abdel-Aziz NI, El-Sayed MA, Suddek GM, El-Messery SM, Ghaly MA. Bayomi SM, et al. Eur J Med Chem. 2015 Aug 28;101:584-94. doi: 10.1016/j.ejmech.2015.07.014. Epub 2015 Jul 14. Eur J Med Chem. 2015. PMID: 26197162

4

Synthesis, anti-inflammatory, analgesic, COX-1/2 inhibition activities and molecular docking study of pyrazoline derivatives.

Abdel-Sayed MA, Bayomi SM, El-Sherbeny MA, Abdel-Aziz NI, ElTahir KE, Shehatou GS, Abdel-Aziz AA. Abdel-Sayed MA, et al. Among authors: bayomi sm. Bioorg Med Chem. 2016 May 1;24(9):2032-42. doi: 10.1016/j.bmc.2016.03.032. Epub 2016 Mar 18. Bioorg Med Chem. 2016. PMID: 27025563

5

Synthesis, in vivo anti-inflammatory, COX-1/COX-2 and 5-LOX inhibitory activities of new 2,3,4-trisubstituted thiophene derivatives.

Qandeel NA, El-Damasy AK, Sharawy MH, Bayomi SM, El-Gohary NS. Qandeel NA, et al. Among authors: bayomi sm. Bioorg Chem. 2020 Sep;102:103890. doi: 10.1016/j.bioorg.2020.103890. Epub 2020 May 4. Bioorg Chem. 2020. PMID: 32801081

6

Synthesis and biological screening of new thiazolo[4,5-d]pyrimidine and dithiazolo[3,2-a:5',4'-e]pyrimidinone derivatives as antimicrobial, antiquorum-sensing and antitumor agents.

Abd Elhameed AA, El-Gohary NS, El-Bendary ER, Shaaban MI, Bayomi SM. Abd Elhameed AA, et al. Among authors: bayomi sm. Bioorg Chem. 2018 Dec;81:299-310. doi: 10.1016/j.bioorg.2018.08.013. Epub 2018 Aug 12. Bioorg Chem. 2018. PMID: 30172111

7

Synthesis and Molecular Docking Study of New Thiazole Derivatives as Potential Tubulin Polymerization Inhibitors.

El-Abd AO, Bayomi SM, El-Damasy AK, Mansour B, Abdel-Aziz NI, El-Sherbeny MA. El-Abd AO, et al. Among authors: bayomi sm. ACS Omega. 2022 Sep 7;7(37):33599-33613. doi: 10.1021/acsomega.2c05077. eCollection 2022 Sep 20. ACS Omega. 2022. PMID: 36157722 Free PMC article.

8

Design, synthesis, and antitumor screening of new thiazole, thiazolopyrimidine, and thiazolotriazine derivatives as potent inhibitors of VEGFR-2.

Abd Elhameed AA, Ali AR, Ghabbour HA, Bayomi SM, El-Gohary NS. Abd Elhameed AA, et al. Among authors: bayomi sm. Drug Dev Res. 2023 Dec;84(8):1664-1698. doi: 10.1002/ddr.22109. Epub 2023 Sep 3. Drug Dev Res. 2023. PMID: 37661648

9

Synthesis of certain new 2,4,5(6) trisubstituted-1,2,4-triazolo[1,5-alpha]pyrimidines as potential antihypertensive agents.

Bayomi SM, Abdelal AM, el-Ashry SM, Ghoneim OA. Bayomi SM, et al. Boll Chim Farm. 1999 May;138(5):227-32. Boll Chim Farm. 1999. PMID: 10450124

10

Cardiovascular effects of some 2-substituted triazolo[1,5-a]pyrimidin-7(4H)one-6-carboxylic acid ethyl esters.

El-Tahir KE, Al-Khamees HA, Bayomi SM. El-Tahir KE, et al. Among authors: bayomi sm. Boll Chim Farm. 1995 Dec;134(11):604-8. Boll Chim Farm. 1995. PMID: 8820975

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