TY  - BOOK
AU  - Mai Saeed Mohamed Nour
AU  - Nehad Abulmagd Elsayed , 
AU  - Reem Khidr Arafa , 
TI  - New oxadiazole based molecules : : Design, synthesis, molecular modeling and biological screening / 
PY  - 2020///
CY  - Cairo : 
PB  - Mai Saeed Mohamed Nour , 
KW  - Adenosine triphosphate (ATP)
KW  - Angstrom (Å)
KW  - Protein kinase B (Akt)
N1  - Thesis  (Ph.D.) - Cairo University - Faculty of Pharmacy - Department of Pharmaceutical Chemistry; Issued also as CD
N2  - Novel heterocyclic oxadiazoles viz. 2-subsituted-5-(4-pyridyl)-1,3,4-oxadiazoles, 2-subsituted-5-(3-pyridyl)-1,3,4-oxadiazoles and 2-subsituted-5-(phenyl/4-chlorophenyl-1,3,4-oxadiazoles) were designed and synthesized as potential anticancer agents. In this investigation, all compounds were evaluated for their COX-1 and COX-2 inhibitory activity in vitro as new therapeutic approaches highlighted observations of cytotoxic effects associated with selective COX-2 inhibition. Results showed that most of the derivatives demonstrated inhibition towards both isoforms of COX with higher selectivity towards COX-2. Some derivatives were more potent than the standard reference drugs indomethacin, diclofenac sodium and celecoxib. Then, nine selected compounds (IIId, VIb, VIIc, IX, XI, XIIa, XIVa, XVIb and XVIIIb) were subjected to cytotoxic screening against UO-31 renal cancer cell line using MTT assay. Compounds IIId, IX and XIIa displayed promising behavior by showing good anticancer activity. Moreover, kinase inhibitory assay against the tyrosine kinase EGFR was performed for the three compounds showing the highest cytotoxic activity. The tested compounds were potent against EGFR with the highest activity being observed for compound IX showing nearly double the potency of the reference drug Erlotinib
UR  - http://172.23.153.220/th.pdf
ER  -