Yasser H. Zaki - Search Results

Year	Number of Results
2015	1
2016	1
2017	2
2018	1
2019	2
2020	1
2022	2
2023	1
2024	1

1

Utility of 5-(furan-2-yl)-3-(p-tolyl)-4,5-dihydro-1H-pyrazole-1-carbothioamide in the synthesis of heterocyclic compounds with antimicrobial activity.

Abdelhamid AO, El Sayed IE, Zaki YH, Hussein AM, Mangoud MM, Hosny MA. Abdelhamid AO, et al. Among authors: zaki yh. BMC Chem. 2019 Apr 1;13(1):48. doi: 10.1186/s13065-019-0566-y. eCollection 2019 Dec. BMC Chem. 2019. PMID: 31384796 Free PMC article.

2

Investigation of the Anticancer Effect of α-Aminophosphonates and Arylidine Derivatives of 3-Acetyl-1-aminoquinolin-2(1H)-one on the DMBA Model of Breast Cancer in Albino Rats with In Silico Prediction of Their Thymidylate Synthase Inhibitory Effect.

Nassan MA, Aldhahrani A, Amer HH, Elhenawy A, Swelum AA, Ali OM, Zaki YH. Nassan MA, et al. Among authors: zaki yh. Molecules. 2022 Jan 24;27(3):756. doi: 10.3390/molecules27030756. Molecules. 2022. PMID: 35164019 Free PMC article.

3

Synthesis, Molecular Docking, and Dynamic Simulation Targeting Main Protease (Mpro) of New, Thiazole Clubbed Pyridine Scaffolds as Potential COVID-19 Inhibitors.

Alghamdi A, Abouzied AS, Alamri A, Anwar S, Ansari M, Khadra I, Zaki YH, Gomha SM. Alghamdi A, et al. Among authors: zaki yh. Curr Issues Mol Biol. 2023 Feb 7;45(2):1422-1442. doi: 10.3390/cimb45020093. Curr Issues Mol Biol. 2023. PMID: 36826038 Free PMC article.

4

Design, Synthesis, and Spectroscopic Studies of Some New α-Aminophosphonate Analogues Derived from 4-Hydroxybenzaldehyde with Special Reference to Anticancer Activity.

Ali OM, Alotaibi MT, Zaki YH, Amer HH. Ali OM, et al. Among authors: zaki yh. Drug Des Devel Ther. 2022 Aug 5;16:2589-2599. doi: 10.2147/DDDT.S357998. eCollection 2022. Drug Des Devel Ther. 2022. PMID: 35965965 Free PMC article.

5

Synthesis, Characterization, Antimicrobial Activity and Anticancer of Some New Pyrazolo[1,5-a]pyrimidines and Pyrazolo[5,1-c]1,2,4-triazines.

Hosny MA, Zaki YH, Mokbel WA, Abdelhamid AO. Hosny MA, et al. Among authors: zaki yh. Med Chem. 2020;16(6):750-760. doi: 10.2174/1573406415666190620144404. Med Chem. 2020. PMID: 31218963

6

Green Biocatalyst for Ultrasound-Assisted Thiazole Derivatives: Synthesis, Antibacterial Evaluation, and Docking Analysis.

Hussein AM, Gomha SM, El-Ghany NAA, Zaki MEA, Farag B, Al-Hussain SA, Sayed AR, Zaki YH, Mohamed NA. Hussein AM, et al. Among authors: zaki yh. ACS Omega. 2024 Mar 12;9(12):13666-13679. doi: 10.1021/acsomega.3c07785. eCollection 2024 Mar 26. ACS Omega. 2024. PMID: 38559991 Free PMC article.

7

Synthesis of novel thiazole, pyranothiazole, thiazolo[4,5-b]pyridines and thiazolo[5',4':5,6]pyrano[2,3-d]pyrimidine derivatives and incorporating isoindoline-1,3-dione group.

Hosny MA, Zaki YH, Mokbel WA, Abdelhamid AO. Hosny MA, et al. Among authors: zaki yh. BMC Chem. 2019 Mar 26;13(1):37. doi: 10.1186/s13065-019-0559-x. eCollection 2019 Dec. BMC Chem. 2019. PMID: 31384785 Free PMC article.

8

A facile synthesis, and antimicrobial and anticancer activities of some pyridines, thioamides, thiazole, urea, quinazoline, β-naphthyl carbamate, and pyrano[2,3-d]thiazole derivatives.

Zaki YH, Al-Gendey MS, Abdelhamid AO. Zaki YH, et al. Chem Cent J. 2018 Jun 20;12(1):70. doi: 10.1186/s13065-018-0439-9. Chem Cent J. 2018. PMID: 29926299 Free PMC article.

9

Synthesis of some new pyrazolo[1,5-a]pyrimidine, pyrazolo[5,1-c]triazine, 1,3,4-thiadiazole and pyridine derivatives containing 1,2,3-triazole moiety.

Abdelriheem NA, Zaki YH, Abdelhamid AO. Abdelriheem NA, et al. Among authors: zaki yh. Chem Cent J. 2017 Jun 12;11(1):53. doi: 10.1186/s13065-017-0282-4. Chem Cent J. 2017. PMID: 29086836 Free PMC article.

10

Regioselectivity of 1,3-dipolar cycloadditions and antimicrobial activity of isoxazoline, pyrrolo[3,4-d]isoxazole-4,6-diones, pyrazolo[3,4-d]pyridazines and pyrazolo[1,5-a]pyrimidines.

Zaki YH, Sayed AR, Elroby SA. Zaki YH, et al. Chem Cent J. 2016 Apr 1;10:17. doi: 10.1186/s13065-016-0163-2. eCollection 2016. Chem Cent J. 2016. PMID: 27042207 Free PMC article.

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