Mohamed A. Al-Omar

Prof. Dr. Mohamed A. Al-Omar

Professor and Chair
orcid

Research Focus & Metrics

Academic Career Length

23Years (2004-Present)

(Calculated once Scilit publication data is synced: current year − year of first publication + 1)

Representative Publications

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1 October 2004 in Bioorganic & Medicinal Chemistry
Verified
Journal Article
Closed access
AEAli A. El-Emam
Ali A. El-Emam
OAOmar A. Al-Deeb
Omar A. Al-Deeb
Mohamed A. Al-OmarMohamed A. Al-Omar
Mohamed A. Al-Omar
JLJochen Lehmann
Jochen Lehmann

1 September 2010 in European Journal of Medicinal Chemistry
Verified
Journal Article
Closed access
AAAdel Azab
Adel Azab
Mohamed A. Al-OmarMohamed A. Al-Omar
Mohamed A. Al-Omar
AAAlaa Abdel-Aziz
Alaa Abdel-Aziz
NANaglaa I. Abdel-Aziz
Naglaa I. Abdel-Aziz
MEMagda Abd Elaziz Elsayed
Magda Abd Elaziz Elsayed
SASami G. Abdel-Hamide
Sami G. Abdel-Hamide

1 April 2010 in Bioorganic & Medicinal Chemistry
Verified
Journal Article
Closed access
FAFatmah A.M. Al-Omary
Fatmah A.M. Al-Omary
LALaila Abouzeid
Laila Abouzeid
MNMahmoud N. Nagi
Mahmoud N. Nagi
EHEl-Sayed E. Habib
El-Sayed E. Habib
AAAlaa Abdel-Aziz
Alaa Abdel-Aziz
HEHussein El-Subbagh
Hussein El-Subbagh

28 August 2019 in Molecules
Verified
Journal Article
Open access
PDF file
AHAshraf S. Hassan
Ashraf S. Hassan
AAAhmed Askar
Ahmed Askar
ENEman Nossier
Eman Nossier
ANAhmed Mohamed Naglah
Ahmed Mohamed Naglah
GMGaber Moustafa
Gaber Moustafa
Mohamed A. Al-OmarMohamed A. Al-Omar
Mohamed A. Al-Omar
A series of Schiff bases 14–25 were designed and synthesized for evaluation of their antibacterial properties against multi-drug resistant bacteria (MDRB). The antibacterial activities of Schiff bases 14–25 showed that most of the synthesized compounds displayed a significant antibacterial activity. Assessment of in silico ADMET properties (absorption, distribution, metabolism, excretion and toxicity) of Schiff bases illustrates that all derivatives showed agreement to the Lipinski’s rule of five. Further enzymatic assay aided by molecular docking study demonstrated that compound 18 is a potent inhibitor of staphylococcus aureus DNA gyrase and dihydrofolate reductase kinases. This study could be valuable in the discovery of new potent antimicrobial agents.

1 October 2013 in European Journal of Medicinal Chemistry
Verified
Journal Article
Closed access
AEAli El-Emam
Ali El-Emam
AAAbdul-Malek S. Al-Tamimi
Abdul-Malek S. Al-Tamimi
Mohamed A. Al-OmarMohamed A. Al-Omar
Mohamed A. Al-Omar
KAKhalid A. Alrashood
Khalid A. Alrashood
EHElsayed E. Habib
Elsayed E. Habib

9 April 2010 in Molecules
Verified
Journal Article
Open access
PDF file
Mohamed A. Al-OmarMohamed A. Al-Omar
Mohamed A. Al-Omar
EAEbtehal S. Al-Abdullah
Ebtehal S. Al-Abdullah
ISIhsan A. Shehata
Ihsan A. Shehata
EHElsayed E. Habib
Elsayed E. Habib
TITarek M. Ibrahim
Tarek M. Ibrahim
AEAli El-Emam
Ali El-Emam
The reaction of 5-(1-adamantyl)-4-amino-3-mercapto-1,2,4-triazole (5) with various aromatic aldehydes in ethanol or acetic acid yielded the corresponding 4-arylideneamino derivatives 6a–v. Treatment of the 4-(2,6-difluoro- and dichlorobenzylideneamino) derivatives 6o and 6q with 1-substituted piperazines, and formaldehyde solution in ethanol afforded good yields of the corresponding 5-(1-adamantyl)-4-(2,6-dihalobenzylideneamino-2-(4-substituted-1-piperazinylmethyl)-1,2,4-triazoline-3-thiones 7a–p. 5-(1-Adamantyl)-4-arylideneamino-2-(4-ethoxycarbonyl-1-piperidylmethyl)-1,2,4-triazoline-3-thiones 8a–n, were similarly prepared via the reaction of the corresponding arylideneamino derivative with ethyl 4-piperidinecarboxylate and formaldehyde solution in ethanol. Compounds 6a–v, 7a–p and 8a–n were tested for in vitro activities against a panel of Gram-positive and Gram-negative bacteria and the yeast-like pathogenic fungus Candida albicans. Several derivatives showed good or moderate activities, particularly against the tested Gram-positive bacteria. In addition, the in vivo anti-inflammatory activity of 21 compounds was determined using the carrageenan-induced paw oedema method in rats. Compounds 7d, 7g, 7i, 7j, 7l, 8c, 8e and 8l showed good or moderate dose-dependent activity in this area.