Abdu-Allah HHM - Search Results

1

Further insight into the dual COX-2 and 15-LOX anti-inflammatory activity of 1,3,4-thiadiazole-thiazolidinone hybrids: The contribution of the substituents at 5th positions is size dependent.

Omar YM, Abdel-Moty SG, Abdu-Allah HHM. Omar YM, et al. Bioorg Chem. 2020 Apr;97:103657. doi: 10.1016/j.bioorg.2020.103657. Epub 2020 Feb 11. Bioorg Chem. 2020. PMID: 32086052

2

Design and synthesis of novel 5-aminosalicylate (5-ASA)-4-thiazolinone hybrid derivatives with promising antiproliferative activity.

Abdu-Allah HH, Abdel-Moty SG, El-Awady R, El-Shorbagi AN. Abdu-Allah HH, et al. Bioorg Med Chem Lett. 2016 Apr 1;26(7):1647-50. doi: 10.1016/j.bmcl.2016.02.073. Epub 2016 Feb 26. Bioorg Med Chem Lett. 2016. PMID: 26947606

3

Novel N-substituted 5-aminosalicylamides as dual inhibitors of cyclooxygenase and 5-lipoxygenase enzymes: Synthesis, biological evaluation and docking study.

El-Nagar MKS, Abdu-Allah HHM, Salem OIA, Kafafy AN, Farghaly HSM. El-Nagar MKS, et al. Bioorg Chem. 2018 Aug;78:80-93. doi: 10.1016/j.bioorg.2018.02.023. Epub 2018 Mar 6. Bioorg Chem. 2018. PMID: 29550533

4

Synthesis, biological evaluation and docking study of 1,3,4-thiadiazole-thiazolidinone hybrids as anti-inflammatory agents with dual inhibition of COX-2 and 15-LOX.

Omar YM, Abdu-Allah HHM, Abdel-Moty SG. Omar YM, et al. Bioorg Chem. 2018 Oct;80:461-471. doi: 10.1016/j.bioorg.2018.06.036. Epub 2018 Jul 3. Bioorg Chem. 2018. PMID: 29986191

5

Conjugation of 4-aminosalicylate with thiazolinones afforded non-cytotoxic potent in vitro and in vivo anti-inflammatory hybrids.

Abdu-Allah HHM, Abdelmoez AAB, Tarazi H, El-Shorbagi AA, El-Awady R. Abdu-Allah HHM, et al. Bioorg Chem. 2020 Jan;94:103378. doi: 10.1016/j.bioorg.2019.103378. Epub 2019 Oct 24. Bioorg Chem. 2020. PMID: 31677858

6

Click chemistry synthesis, biological evaluation and docking study of some novel 2'-hydroxychalcone-triazole hybrids as potent anti-inflammatory agents.

Boshra AN, Abdu-Allah HHM, Mohammed AF, Hayallah AM. Boshra AN, et al. Bioorg Chem. 2020 Jan;95:103505. doi: 10.1016/j.bioorg.2019.103505. Epub 2019 Dec 17. Bioorg Chem. 2020. PMID: 31901755

7

Design and synthesis of novel 2,3-dihydropyrazino[1,2-a]indole-1,4-dione derivatives as antiproliferative EGFR and BRAF^V600E dual inhibitors.

Al-Wahaibi LH, Gouda AM, Abou-Ghadir OF, Salem OIA, Ali AT, Farghaly HS, Abdelrahman MH, Trembleau L, Abdu-Allah HHM, Youssif BGM. Al-Wahaibi LH, et al. Bioorg Chem. 2020 Nov;104:104260. doi: 10.1016/j.bioorg.2020.104260. Epub 2020 Sep 3. Bioorg Chem. 2020. PMID: 32920363

8

Synthesis, biological evaluation and molecular docking study of some new 4-aminosalicylic acid derivatives as anti-inflammatory and antimycobacterial agents.

Qahtan MQM, Bakhite EA, Kumari J, M Sayed A, Kandeel M, Sriram D, Abdu-Allah HHM. Qahtan MQM, et al. Among authors: abdu allah hhm. Bioorg Chem. 2023 Mar;132:106344. doi: 10.1016/j.bioorg.2023.106344. Epub 2023 Jan 12. Bioorg Chem. 2023. PMID: 36669356

9

Design, synthesis, biological evaluation and docking study of some new aryl and heteroaryl thiomannosides as FimH antagonists.

Mohammed AF, Othman SA, Abou-Ghadir OF, Kotb AA, Mostafa YA, El-Mokhtar MA, Abdu-Allah HHM. Mohammed AF, et al. Among authors: abdu allah hhm. Bioorg Chem. 2024 Apr;145:107258. doi: 10.1016/j.bioorg.2024.107258. Epub 2024 Mar 2. Bioorg Chem. 2024. PMID: 38447463

10

CD22-antagonists with nanomolar potency: the synergistic effect of hydrophobic groups at C-2 and C-9 of sialic acid scaffold.

Abdu-Allah HH, Watanabe K, Completo GC, Sadagopan M, Hayashizaki K, Takaku C, Tamanaka T, Takematsu H, Kozutsumi Y, Paulson JC, Tsubata T, Ando H, Ishida H, Kiso M. Abdu-Allah HH, et al. Bioorg Med Chem. 2011 Mar 15;19(6):1966-71. doi: 10.1016/j.bmc.2011.01.060. Epub 2011 Feb 2. Bioorg Med Chem. 2011. PMID: 21349726 Free PMC article.

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