Synthesis, molecular modelling and biological evaluation of novel phthalazine and its bioisostere derivatives as potential anticancer agents / Wagdy Mohamed Mohamed Eldehna ; Supervised Dalal Abdelrahman Abouelella , Sahar Mahmoud Abouseri
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TextLanguage: English Publication details: Cairo : Wagdy Mohamed Mohamed Eldehna , 2015Description: 186 Leaves : charts , facsimiles ; 25cmOther title: - التشييد والنمذجة الجزيئية وتقييم الفاعلية البيولوجية لمشتقات الفيثالازين ومتماثلاتها البيولوجية الجديدة ذات تأثير محتمل كمضادات للسرطان [Added title page title]
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Thesis
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قاعة الرسائل الجامعية - الدور الاول | المكتبة المركزبة الجديدة - جامعة القاهرة | Cai01.08.02.Ph.D.2015.Wa.S (Browse shelf(Opens below)) | Not for loan | 01010110068412000 | ||
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مخـــزن الرســائل الجـــامعية - البدروم | المكتبة المركزبة الجديدة - جامعة القاهرة | Cai01.08.02.Ph.D.2015.Wa.S (Browse shelf(Opens below)) | 68412.CD | Not for loan | 01020110068412000 |
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Thesis (Ph.D.) - Cairo University - Faculty of Pharmacy - Department of Chemistry
The discovery of efficacious new human therapeutic agents is one of humanity{u2019}s most vital tasks. It is an enormously demanding activity that requires creativity, a vast range of scientific knowledge, and great persistence. Cancer is one of the most difficult diseases to treat and it is a major disease responsible for deaths worldwide, it can be considered as one of the foremost health problems. Yet there is no cancer treatment that is 100% effective against disseminated cancer. Therefore, there is an urgent need to give much attention to update and modify drug leads to develop more potent and safe therapies. Encouraged by the marked anticancer activity exhibited by phthalazines and indolin-2-ones and the apparent role of VEGFR-2 inhibitors in the treatment of several tumors, it deemed of interest to design and synthesize novel series of 4- phenyl-1-(piperazin-1-yl)phthalazines, 4-(4-methoxybenzyl)phthalazines and 1-(4- ((2-oxoindolin-3-ylidene)amino)phenyl)-3-phenylureas as novel VEGFR-2 inhibitors and anticancer agents. The newly synthesized compounds were screened for their inhibitory activity against VEGFR-2 and their anticancer activity against different cell lines
Issued also as CD
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