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Design, synthesis and biological evaluation of certain 4-(Piperazin-1-yl)quinoline derivatives / Mohamed Farouk Ali Hamissa ; Supervised Mohamed Nabil Youssef Aboulenein , Fatma Abdelfattah Ragab

By: Contributor(s): Material type: TextTextLanguage: English Publication details: Cairo : Mohamed Farouk Ali Hamissa , 2015Description: 133 P. : charts ; 25cmOther title:
  • تصميم وتشييد و تقييم بيولوجي لمشتقات 4 (بيبرازين 1 يل)كينولين [Added title page title]
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Dissertation note: Thesis (M.Sc.) - Cairo University - Faculty of Pharmacy - Department of Chemistry Summary: The search for antitumour compounds with selective activity and less toxicity continue to be an area of intensive research in medicinal chemistry. Thus, this work deals with the synthesis of certain 4-(piperazin-1-yl)quinoline derivatives IVa-t with the aim to evaluate their anticancer properties. The thesis consists of the following sections: Introduction: This part includes a review on the different biological activities of 7-chloro-4-(piperazin-1-yl)quinoline derivatives. Basis of the present investigations: This section discusses the rationale on which the design of synthesized compounds was based in addition to the schemes followed in their synthesis. Theoretical discussion: This section addresses the reactions followed in the synthesis of the new target compounds IVa-t in addition to the needed intermediates III, VIp-t, VIIp-t and VIIIo-t and their preparation. Scheme 1 described the strategies followed for the synthesis of the designed compounds, as well as starting materials and intermediates. Biological evaluation: The above mentioned synthesized compounds III and IVa-t were tested for their cytotoxic effect against breast (MCF-7) and prostate (PC3) cancer cell lines. The achieved biological results and structure activity relationship of the studied compounds were discussed
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Item type Current library Home library Call number Copy number Status Date due Barcode
Thesis Thesis قاعة الرسائل الجامعية - الدور الاول المكتبة المركزبة الجديدة - جامعة القاهرة Cai01.08.02.M.Sc.2015.Mo.D (Browse shelf(Opens below)) Not for loan 01010110068477000
CD - Rom CD - Rom مخـــزن الرســائل الجـــامعية - البدروم المكتبة المركزبة الجديدة - جامعة القاهرة Cai01.08.02.M.Sc.2015.Mo.D (Browse shelf(Opens below)) 68477.CD Not for loan 01020110068477000

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

The search for antitumour compounds with selective activity and less toxicity continue to be an area of intensive research in medicinal chemistry. Thus, this work deals with the synthesis of certain 4-(piperazin-1-yl)quinoline derivatives IVa-t with the aim to evaluate their anticancer properties. The thesis consists of the following sections: Introduction: This part includes a review on the different biological activities of 7-chloro-4-(piperazin-1-yl)quinoline derivatives. Basis of the present investigations: This section discusses the rationale on which the design of synthesized compounds was based in addition to the schemes followed in their synthesis. Theoretical discussion: This section addresses the reactions followed in the synthesis of the new target compounds IVa-t in addition to the needed intermediates III, VIp-t, VIIp-t and VIIIo-t and their preparation. Scheme 1 described the strategies followed for the synthesis of the designed compounds, as well as starting materials and intermediates. Biological evaluation: The above mentioned synthesized compounds III and IVa-t were tested for their cytotoxic effect against breast (MCF-7) and prostate (PC3) cancer cell lines. The achieved biological results and structure activity relationship of the studied compounds were discussed

Issued also as CD

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