| 000 | 01789cam a2200337 a 4500 | ||
|---|---|---|---|
| 003 | EG-GiCUC | ||
| 005 | 20250223030749.0 | ||
| 008 | 130211s2012 ua d 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.2012.Ah.S | ||
| 100 | 0 | _aAhmed Abdelhamid Bayomi | |
| 245 | 1 | 0 |
_aSynthesis of some novel quinazolone derivatives and studying their combined anticancer effect with Þ - radiation / _cAhmed Abdelhamid Bayomi ; Supervised Fatma Abdelfattah Ragab , Mostafa Mohamed Ghorab |
| 246 | 1 | 5 | _aتحضير بعض مشتقات الكينازولون الجديدة ودراسة التأثير التداخلى مع أشعة جاما كمضادات الأورام السرطانية |
| 260 |
_aCairo : _bAhmed Abdelhamid Bayomi , _c2012 |
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| 300 |
_a137P. : _bcharts ; _c25cm |
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| 502 | _aThesis (M.Sc.) - Cairo University - Faculty of Pharmacy - Department of Pharmaceutical Chemistry | ||
| 520 | _a24 New quinazolone and triazoloquinazolone derivatives bearing sulfapyridine moiety were synthesized . The structure of the newly synthesized compounds were confirmed by elemental analyses and spectral data (IR, ¹H - NMR and mass spectroscopy) . The newly synthesized compounds were subjected to in vitro anticancer screening against human liver cancer cell line (HEPG2) and showed anticancer activity | ||
| 530 | _aIssued also as CD | ||
| 653 | 4 | _aDerivatives and studying | |
| 653 | 4 | _aNovel quinazolone | |
| 653 | 4 | _aÞ - radiation | |
| 700 | 0 |
_aFatma Abdelfattah Ragab , _eSupervisor |
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| 700 | 0 |
_aMostafa Mohamed Ghorab , _eSupervisor |
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| 856 | _uhttp://172.23.153.220/th.pdf | ||
| 905 |
_aFatma _eCataloger |
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| 905 |
_aNazla _eRevisor |
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| 942 |
_2ddc _cTH |
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| 999 |
_c41424 _d41424 |
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