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Structure-based design and synthesis of novel Ý-carboline derivatives and their biological evaluation as phosphodiesterase 5 inhibitors and anticancer agents / Amal Hassan Ali Hassan ; Supervised Ashraf H. Abadi , Nermin Salah Ahmed

By: Contributor(s): Material type: TextTextLanguage: English Publication details: Cairo : Amal Hassan Ali Hassan , 2011Description: 98 Leaves : facsimiles ; 30cmOther title:
  • التصميم القائم على الهيكل و تشييد مشتقات جديدة من البيتا كاربولين و تقييمهم الأحياني كمثبطات لإنزيم فوسفوداي إستريز ٥ و كعوامل مضادة للسرطان [Added title page title]
Online resources: Dissertation note: Thesis (M.Sc.) - German University - Faculty of Postgraduate Studies and Scientific Research - Department of Pharmaceutical Chemistry Summary: Tadalafil, a Ý-carboline derivatives that has been introduced to the market for treatment of Male Erectile Dysfunction, acts through inhibition of Phosphodiesterase 5, leading to elevation of cGMP, vascular relaxation in the corpora cavernosa and penile erection during sexual stimulation. The safety, tolerability of PDE5 inhibition as well as the involvement of cGMP as a key component in itracellular signaling may provide new therapeutic applications for this class of drugs
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Thesis Thesis قاعة الثقاقات الاجنبية - الدور الثالث المكتبة المركزبة الجديدة - جامعة القاهرة Cai01.34.M.Sc.2011.Am.S (Browse shelf(Opens below)) Not for loan 01010110060172000

Thesis (M.Sc.) - German University - Faculty of Postgraduate Studies and Scientific Research - Department of Pharmaceutical Chemistry

Tadalafil, a Ý-carboline derivatives that has been introduced to the market for treatment of Male Erectile Dysfunction, acts through inhibition of Phosphodiesterase 5, leading to elevation of cGMP, vascular relaxation in the corpora cavernosa and penile erection during sexual stimulation. The safety, tolerability of PDE5 inhibition as well as the involvement of cGMP as a key component in itracellular signaling may provide new therapeutic applications for this class of drugs

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