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العنوان
Ligational and pharmacological applications of some nonsteroidal anti­inflammatory drugs and their derivatives /
المؤلف
Sherif, Yousery El-­Said Abd El-­Bary.
هيئة الاعداد
باحث / يسرى السيد عبدالباري شريف
مشرف / احمد فوزى عبدالحميد العاصمي
مشرف / جمال محمد مأمون دهب
مشرف / محمد عبدالغنى قابيل
مشرف / محمد عهدى عطية سعد.
الموضوع
Rheumatoid. Oxicam nucleus. Chemical Characterization. Pharmacological techniques. Copper and Zinc.
تاريخ النشر
2005.
عدد الصفحات
213 p. :
اللغة
الإنجليزية
الدرجة
الدكتوراه
التخصص
الكيمياء
تاريخ الإجازة
1/1/2005
مكان الإجازة
جامعة المنصورة - كلية العلوم - Department of Chemistry
الفهرس
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Abstract

The thesis comprises three main chapters : The first chapter is concerned with an introduction which deals with literature survey for the pathophysiology, etiology and current lines of treatment for rheumatoid arthritis. This survey includes the chemistry of prostaglandin hydrogen synthase (PGHS), The second chapter is related to the experimental part which describes the preparation of oxicam nucleus, piroxicam, copper piroxicam complex, zinc piroxicam complex and EX14u. Pharmacological techniques which have been used to study the biological activity of the studied compounds . The third chapter is concerned with the results and discussion. It is divided into two parts: Part one ­Comparison between market and the synthesized piroxicam by both Chemical characterization and Pharmacological tools. The two piroxicams are similar. ­Chemical characterization and Pharmacological evaluation were used for the synthesized piroxicam copper(II) and zinc(II) complexes . Part two This part is divided into three sections : Section 1 It is concerned with quantitative structure activity relationship (QSAR) to predicate a more selective compound against COX­2 from different proposed compounds. Among them is EX14u Second section It is concerned with :­ a) Chemical Characterization of EX14u. b) Chemical Characterization of EX14u­Copper(II) complex. The pharmacological COX­2 selectivity of EX14u is in accordance with the estimated chemical COX­2 selectivity obtained from QSAR.