Mostafa Ghorab

Prof. Mostafa Ghorab


Research Focus & Metrics

Academic Career Length

20Years (2007-Present)

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

Representative Publications

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1 January 2010 in European Journal of Medicinal Chemistry
Verified
Journal Article
Closed access
MGMostafa Ghorab
Mostafa Ghorab
FRFatma A. Ragab
Fatma A. Ragab
SASaleh I. Alqasoumi
Saleh I. Alqasoumi
AAAhmed M. Alafeefy
Ahmed M. Alafeefy
SASarah A. Aboulmagd
Sarah A. Aboulmagd

1 October 2009 in European Journal of Medicinal Chemistry
Verified
Journal Article
Closed access
MGMostafa Ghorab
Mostafa Ghorab
FRFatma A. Ragab
Fatma A. Ragab
MHMostafa M. Hamed
Mostafa M. Hamed

1 September 2010 in European Journal of Medicinal Chemistry
Verified
Journal Article
Closed access
MGMostafa Ghorab
Mostafa Ghorab
FRFatma A. Ragab
Fatma A. Ragab
HHHelmy I. Heiba
Helmy I. Heiba
RAReem Arafa
Reem Arafa
EEEbaa M. El-Hossary
Ebaa M. El-Hossary

1 November 2016 in European Journal of Medicinal Chemistry
Verified
Journal Article
Closed access
MGMostafa Ghorab
Mostafa Ghorab
MAMansour S. Alsaid
Mansour S. Alsaid
MEMohamed S.A. El-Gaby
Mohamed S.A. El-Gaby
NSNesreen A. Safwat
Nesreen A. Safwat
MEMahmoud M. Elaasser
Mahmoud M. Elaasser
ASAiten M. Soliman
Aiten M. Soliman

1 January 2017 in Journal of Enzyme Inhibition and Medicinal Chemistry
Verified
Journal Article
Open access
MGMostafa Ghorab
Mostafa Ghorab
MAMansour S. Alsaid
Mansour S. Alsaid
ASAiten M. Soliman
Aiten M. Soliman
FRFatma A. Ragab
Fatma A. Ragab
Two series of novel 4-(2-(2-(2-(substituted) hydrazinyl)-2-oxoethylthio)-4-oxobenzo[g]quinazolin-3(4H)-yl) benzenesulfonamide 5–17 and 4-(2-(2-(substituted-1H-pyrazol-1-yl)-2-oxoethylthio)-4-oxobenzo[g]quinazolin-3(4H)-yl) benzenesulfonamide 18–24 were synthesised from the starting material 4-(2-(2-hydrazinyl-2-oxoethylthio)-4-oxobenzo[g]quinazolin-3(4H)-yl) benzenesulfonamide 5, to be evaluated for their inhibitory activity towards VEGFR-2. The target compounds 5–24, were screened for their cytotoxic activity against MCF-7 breast cancer cell line and the percentage inhibition against VEGFR-2. Compounds 9, 20, 22 and 23, showed excellent VEGFR-2 inhibitory activity with IC50 ranging from 0.64 to 1.04 µm. Being the most potent, compound 9 was evaluated for its apoptotic inducer effect by studying the effect on caspase-3, it was found to increase its level. Compound 9 boosted the level of Bax and reduced the level of BCl2, compared to the control. Cell cycle analysis was conducted, compound 9 showed cell cycle arrest at G2/M phase. Moreover, mild cytotoxic effect (IC50 = 29.41 µm, respectively) in normal breast cells MCF-12 A, was observed when treated with the same compound. Finally, a molecular docking study was performed to investigate the possible binding interaction inside the active site of the VEGFR-2 enzyme. Graphical Abstract

1 January 2019 in Journal of Enzyme Inhibition and Medicinal Chemistry
Verified
Journal Article
Open access
ASAiten M. Soliman
Aiten M. Soliman
AAAli Alqahtani
Ali Alqahtani
MGMostafa Ghorab
Mostafa Ghorab
A series of sulphonamide benzoquinazolinones 5–18 was synthesized and evaluated for cytotoxic activity against MDA-MB-231 cell line. The compounds showed IC50 ranging from 0.26 to 161.49 µM. The promising compounds were evaluated for their inhibitory profile against epidermal growth factor (EGFR) and HER2 enzymes. Compound 10 showed more potent activity on both EGFR and HER2 than erlotinib (IC50 3.90 and 5.40 µM versus 6.21 and 9.42 µM). The pro-apoptotic activity of 10 was evaluated against caspase-3, Bax, B-cell lymphoma protein 2 (Bcl-2) expression levels, and cell cycle analysis. Compound 10 increased the level of caspase-3 by 10 folds, Bax level by 9 folds, decreased the level of the Bcl-2 by 0.14 and arrested the cell cycle in the G2/M phase. The radio-sensitizing activity of 10 was measured using a single dose of 8 Gy gamma radiation (IC50 decreased from 0.31 to 0.22 µM). Molecular docking was performed on EGFR and HER2 receptors.