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Chemical Communications (Cambridge, England)|May 25, 2013
Receptor conformational change induces fluoride binding despite competitive water bindingLaurent Trembleau, Tim A D Smith, Mostafa H Abdelrahman
Chemical Biology & Drug Design|December 27, 2016
Design, synthesis and pharmacophoric model building of new 3-alkoxymethyl/3-phenyl indole-2-carboxamides with potential antiproliferative activityMostafa H Abdelrahman, Ahmed S Aboraia, Bahaa G M Youssif, et al.
Pharmaceuticals (Basel, Switzerland)|July 29, 2023
Design, Synthesis, and Biological Evaluation of Indole-2-carboxamides as Potential Multi-Target Antiproliferative AgentsLamya H Al-Wahaibi, Anber F Mohammed, Mostafa H Abdelrahman, et al.
Pharmaceuticals (Basel, Switzerland)|August 26, 2022
Synthesis and Biological Evaluation of Indole-2-Carboxamides with Potent Apoptotic Antiproliferative Activity as EGFR/CDK2 Dual InhibitorsLamya H Al-Wahaibi, Yaser A Mostafa, Mostafa H Abdelrahman, et al.
Archiv Der Pharmazie|December 1, 2018
Novel quinoline derivatives carrying nitrones/oximes nitric oxide donors: Design, synthesis, antiproliferative and caspase-3 activation activitiesMahmoud S Abdelbaset, Mohamed Abdel-Aziz, Gamal El-Din A Abuo-Rahma, et al.
Frontiers in Chemistry|September 23, 2024
Design and synthesis new indole-based aromatase/iNOS inhibitors with apoptotic antiproliferative activityLamya H Al-Wahaibi, Hesham A Abou-Zied, Mostafa H Abdelrahman, et al.
Bioorganic & Medicinal Chemistry|September 23, 2022
New potent ciprofloxacin-uracil conjugates as DNA gyrase and topoisomerase IV inhibitors against methicillin-resistant Staphylococcus aureusMohamed Samir, Mohamed Ramadan, Mostafa H Abdelrahman, et al.
Bioorganic Chemistry|March 6, 2021
3,7-bis-benzylidene hydrazide ciprofloxacin derivatives as promising antiproliferative dual TOP I & TOP II isomerases inhibitorsMohamed Samir, Mohamed Ramadan, Mostafa H Abdelrahman, et al.
Journal of Enzyme Inhibition and Medicinal Chemistry|May 31, 2023
Design, synthesis, apoptotic, and antiproliferative effects of 5-chloro-3- (2-methoxyvinyl)-indole-2-carboxamides and pyrido[3,4-b]indol-1-ones as potent EGFRWT/EGFRT790M inhibitorsLamya H Al-Wahaibi, Anber F Mohammed, Fatema El-Zahraa S Abdel Rahman, et al.
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