| 000 | 01927cam a2200349 a 4500 | ||
|---|---|---|---|
| 003 | EG-GiCUC | ||
| 005 | 20250223030741.0 | ||
| 008 | 130120s2012 ua dh f m 000 0 eng d | ||
| 040 |
_aEG-GiCUC _beng _cEG-GiCUC |
||
| 041 | 0 | _aeng | |
| 049 | _aDeposite | ||
| 097 | _aM.Sc | ||
| 099 | _aCai01.08.04.M.Sc.2012.Sa.S | ||
| 100 | 0 | _aSara Shaban Ibrahim Mohamed | |
| 245 | 1 | 0 |
_aSynthesis of new thiazole derivatives bearing a sulfonamide moiety of expected anticancer and radiosensitizing activities / _cSara Shaban Ibrahim Mohamed ; Supervised Mohamed Abdelrahman Shaaban , Helmy Imail Heiba , Hanan Mohamed Refaat |
| 246 | 1 | 5 | _aتحضير مشتقات الثيازول الجديدة والتى تحتوى على مجموعة السلفوناميد والمتوقع لها نشاطا كمضادات للسرطان وكمحفزات للاشعاع |
| 260 |
_aCairo : _bSara Shaban Ibrahim Mohamed , _c2012 |
||
| 300 |
_a123P. : _bcharts , facsimiles ; _c25cm |
||
| 502 | _aThesis (M.Sc.) - Cairo University - Faculty of Pharmacy - Department of Organic Chemistry | ||
| 520 | _aIn a search for new cytotoxic agents with improved antitumor activity and selectivity , some new pyranothiazole and thiazolopyranopyimidine derivatives bearing sulfonamide moiety were synthesized . The newly synthesized compounds were evaluated for their antitumor activity alone and in combination with y - irradiation . These new compounds were docked inside the active site of carbonic anhydrase II to predict their mechanism of action | ||
| 530 | _aIssued also as CD | ||
| 653 | 4 | _aAnticancer | |
| 653 | 4 | _aSulfonamide | |
| 653 | 4 | _aThiazole | |
| 700 | 0 |
_aHanan Mohamed Refaat , _eSupervisor |
|
| 700 | 0 |
_aHelmy Imail Heiba , _eSupervisor |
|
| 700 | 0 |
_aMohamed Abdelrahman Shaaban , _eSupervisor |
|
| 856 | _uhttp://172.23.153.220/th.pdf | ||
| 905 |
_aFatma _eCataloger |
||
| 905 |
_aNazla _eRevisor |
||
| 942 |
_2ddc _cTH |
||
| 999 |
_c41174 _d41174 |
||