Tetrahydroindolocarbazoles (THICZs) as new class of urokinase (uPA) inhibitors: Synthesis, anticancer evaluation, DNA-damage determination, and molecular modelling study

Author:

El-Sharief Marwa A.M.Sh.,El-Naggar Mohamed H.,Ahmed Entesar M.,El-Messery Shahenda M.,Mahmoud Abeer E.,Ali Mamdouh M.,Salem Lamiaa M.,Mahrous Karima F.,El Sayed Mardia T.

Publisher

Elsevier BV

Subject

Organic Chemistry,Drug Discovery,Molecular Biology,Biochemistry

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3. M. El Sayed, A. Voronkov, I. Ogungbe, S. El-Hallouty, K. Ahmed, B. Vladimir, K. Balakin, Anti-cancer, Molecular docking and structure activity relationship studies of some Novel Synthetic spiroindolo[3,2-b]carbazoles as predicted HER2 and BrK Kinase Inhibitors (2017). doi: https://doi.org/10.2174/1573407213666170213154357.

4. Plasminogen activator secretion of human tumors in short-term organ culture, including a comparison of primary and metastatic colon tumors;Markus;Cancer Res.,1983

5. In vitro degradation of radiolabelled, intact basement membrane mediated by cellular plasminogen activator;Siicela;Carcinogenesis (Lond.),1982

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