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Synthesis and biological studies of new heterocyclic compounds containing pyrazole, thiazole and/or thiadiazole moieties / Eman Kamal Mousa Dewidar ; Supervised Sobhy Mohamed Gomaa

By: Contributor(s): Material type: TextLanguage: English Publication details: Cairo : Eman Kamal Mousa Dewidar , 2016Description: 197 P. : facsimiles ; 25cmOther title:
  • {uFE97}{uFEA4}{uFEC0}{uFBFF}{uFEAE} و درا{uئإآ٣}{uئإ٩٤} ا{uئإؤئ}{uئإإ٨}{uئإآ٨}{uئإ٨إ}ط ا{uئإؤئ}{uئإ٩٢}{uئآئئ}{uئإإإ}{uئإؤئ}{uئإإإ}{uئإ٩ئ}{uئإئ٠} {uئإؤئ}{uئإإ٤}{uئإءإ}{uئإؤآ}{uئإ٩٢}{uئإ٨إ}ت {uئإأئ}{uئآئئ}{uئإءإ} {uئإإ٣}{uئإ٩٨}{uئإء٠}{uئإ٨إ}{uئإإ٧}{uئإآ٤}{uئإ٩٤} ا{uئإؤئ}{uئإء٤}{uئإإ٠}{uئإؤ٨}{uئإ٩٤} ا{uئإؤئ}{uئإ٩٨}{uئإئ٠} {uئإ٩٧}{uئإء٤}{uئإ٩٨}{uئإإإ}ى {uئإأآ}{uئإإ٠}{uئإئ٠} {uئإإ٣}{uئإآ٨}{uئإ٩٨}{uئإؤ٨}{uئإ٨إ}ت {uئإء٣}{uئإإ٠}{uئإؤ٨}{uئإ٨إ}ت {uئإ٩١}{uئآئئ}{uئإءإ}ازول: {uئإ٩آ}{uئآئئ}{uئإ٨إ}زول و/ او-{uئإ٩آ}{uئآئئ}{uئإ٨إ}دا{uئآئإ}{uئإ٨إ}زول [Added title page title]
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Dissertation note: Thesis (M.Sc.) - Cairo University - Faculty of Science - Department of Organic Chemistry Summary: The original work of the submitted thesis consists of two research projects: In the first part: A new series of 7-arylazopyrazolo[5,1-c][1,2,4] triazoles was synthesized via reaction of 3-amino-4-(arylhydrazono)-4,5-dihydropyrazol-5-one with hydrazonoyl halides using triethylamine as a basic catalyst. The structure of all the synthesized compounds was confirmed on the basis of elemental and spectral analyses data. Moreover, the antimicrobial and antitumor activities of these compounds were evaluated and the results obtained indicate the weak efficacy of some of them as antibacterial agents. But, the results of antitumor activity against HepG-2 liver cancer and HCT-116 colon cancer of some derivatives showed good activity in comparison with the reference drugs. In the second part: A novel series of 5-arylazothiazoles was prepared from 2-(-1-morpholino-1-(2-arylhydrazono)propan-2-ylidene)-hydrazinecarbothioamide by different methods. The structures of the newly synthesized compounds were established on the basis of spectroscopic evidences and their synthesis by alternative methods. Moreover, the newly synthesized products were evaluated for their anti-cancer activities and the results show that some derivatives have good to mild utility as antitumor operators. Moreover, the computational studies using MOE 2014.09 software are confirming the results of biological activity
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Thesis قاعة الرسائل الجامعية - الدور الاول المكتبة المركزبة الجديدة - جامعة القاهرة Cai01.12.10.M.Sc.2016.Em.S (Browse shelf(Opens below)) Not for loan 01010110073038000
CD - Rom مخـــزن الرســائل الجـــامعية - البدروم المكتبة المركزبة الجديدة - جامعة القاهرة Cai01.12.10.M.Sc.2016.Em.S (Browse shelf(Opens below)) 73038.CD Not for loan 01020110073038000

Thesis (M.Sc.) - Cairo University - Faculty of Science - Department of Organic Chemistry

The original work of the submitted thesis consists of two research projects: In the first part: A new series of 7-arylazopyrazolo[5,1-c][1,2,4] triazoles was synthesized via reaction of 3-amino-4-(arylhydrazono)-4,5-dihydropyrazol-5-one with hydrazonoyl halides using triethylamine as a basic catalyst. The structure of all the synthesized compounds was confirmed on the basis of elemental and spectral analyses data. Moreover, the antimicrobial and antitumor activities of these compounds were evaluated and the results obtained indicate the weak efficacy of some of them as antibacterial agents. But, the results of antitumor activity against HepG-2 liver cancer and HCT-116 colon cancer of some derivatives showed good activity in comparison with the reference drugs. In the second part: A novel series of 5-arylazothiazoles was prepared from 2-(-1-morpholino-1-(2-arylhydrazono)propan-2-ylidene)-hydrazinecarbothioamide by different methods. The structures of the newly synthesized compounds were established on the basis of spectroscopic evidences and their synthesis by alternative methods. Moreover, the newly synthesized products were evaluated for their anti-cancer activities and the results show that some derivatives have good to mild utility as antitumor operators. Moreover, the computational studies using MOE 2014.09 software are confirming the results of biological activity

Issued also as CD

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