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003 | EG-GiCUC | ||
005 | 20250223031143.0 | ||
008 | 150221s2014 ua o f m 000 0 eng d | ||
040 |
_aEG-GiCUC _beng _cEG-GiCUC |
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041 | 0 | _aeng | |
049 | _aDeposite | ||
097 | _aM.Sc | ||
099 | _aCai01.08.05.M.Sc.2014.Ba.S | ||
100 | 0 | _aBasma Serag Eldin Alsayed Habib | |
245 | 1 | 0 |
_aSynthesis and biological evaluation of some novel phthalimide derivatives incorporated into other heterocycles as anticancer and antimicrobial agents / _cBasma Serag Eldin Alsayed Habib ; Supervised Kamelia Mahmoud Amin , Afaf Hussein Elmasry |
246 | 1 | 5 | _aالتشييد و التقييم البيولوجى لبعض مشتقات الفثاليميدات المرتبطة مع حلقات غير متجانسة كمضادات للسرطانات و الميكروبات |
260 |
_aCairo : _bBasma Serag Eldin Alsayed Habib , _c2014 |
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300 |
_a186 P. : _bphotographs ; _c25cm |
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502 | _aThesis (M.Sc.) - Cairo University - Faculty of Pharmacy - Department of Pharmaceutical Chemistry | ||
520 | _aThe phthalimide moiety has been utilized extensively in medicinal chemistry and is considered to be a privileged structure that shows various pharmacological activities including anti inflammatory, hypoglycemic, hypolipidemic, anticonvulsant, anxiolytic, antiviral, antitumor and antimicrobial activity. Therefore, we are considered with the synthesis of novel series of substituted (4- substituted phenylamino) methyl phthalimides with the objective of discovering novel antitumor antimicrobial agents. Moreover docking of the some biologically tested compounds into the active site of GyrB enzyme was performed to correlate the docking results with the biological results | ||
530 | _aIssued also as CD | ||
653 | 4 | _aPhthalimides | |
653 | 4 | _aRing closure reactions | |
653 | 4 | _aThiazoles and other heterocycles | |
700 | 0 |
_aAfaf Hussein Elmasry , _eSupervisor |
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700 | 0 |
_aKamelia Mahmoud Amin , _eSupervisor |
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856 | _uhttp://172.23.153.220/th.pdf | ||
905 |
_aNazla _eRevisor |
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905 |
_aSamia _eCataloger |
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942 |
_2ddc _cTH |
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999 |
_c49490 _d49490 |