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005 | 20250223030816.0 | ||
008 | 130401s2010 ua dh f m 000 0 eng d | ||
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_aEG-GiCUC _beng _cEG-GiCUC |
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041 | 0 | _aeng | |
049 | _aGift | ||
097 | _aM.Sc | ||
099 | _aCai01.34.M.Sc.2010.Am.S | ||
100 | 0 | _aAmal Mahmoud Yassin Mohsen | |
245 | 1 | 0 |
_aSynthesis and pharmacological evaluation of 1-Benzyl and 1-Benzoyl melatonin analogs as ligands for melatonin receptors / _cAmal Mahmoud Yassin Mohsen ; Supervised Darius P. Zlotos |
246 | 1 | 5 | _aتشييد وتقييم بيولوجى ل ن 1 بنزايل و ن 1 بنزويل من مشتقات الميلاتونين كلجائن لمستقبلات الميلاتونين |
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_aCairo : _bAmal Mahmoud Yassin Mohsen , _c2010 |
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_a84Leaves : _bcharts , facsimiles ; _c30cm |
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502 | _aThesis (M.Sc.) - German University - Faculty of Postgraduate Studies and Scientific Research - Department of Pharmaceutical Chemistry | ||
520 | _aThe neurohormone melatonin (MLT) exerts its diverse physiological actions mostly through activation of the two G-protein-coupled MT₁ and MT₂ receptors . An accurate characterization of MLT receptor-mediated functions requires MT₁ and MT₂ selective ligands . One of the most selective MT₂ antagonists up to date is the p - chlorobenzl substituted indole derivative UCM 454 | ||
700 | 0 |
_aDarius Pawel Zlotos , _eSupervisor |
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856 | _uhttp://172.23.153.220/th.pdf | ||
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_aFatma _eCataloger |
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_aNazla _eRevisor |
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_2ddc _cTH |
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_c42379 _d42379 |