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Journal of Natural Products|January 24, 2009
Development of synthetic methodology suitable for the radiosynthesis of combretastatin A-1 (CA1) and its corresponding prodrug CA1PAnupama Shirali, Madhavi Sriram, John J Hall, et al.Journal of Natural Products|March 21, 2020
Bioreductively Activatable Prodrug Conjugates of Combretastatin A-1 and Combretastatin A-4 as Anticancer Agents Targeted toward Tumor-Associated HypoxiaBlake A Winn, Laxman Devkota, Bunnarack Kuch, et al.Cancer Research|September 10, 2009
Contribution of granulocyte colony-stimulating factor to the acute mobilization of endothelial precursor cells by vascular disrupting agentsYuval Shaked, Terence Tang, Jill Woloszynek, et al.Cancer Letters|September 2, 2015
The vascular disrupting activity of OXi8006 in endothelial cells and its phosphate prodrug OXi8007 in breast tumor xenograftsTracy E Strecker, Samuel O Odutola, Ramona Lopez, et al.Bioorganic & Medicinal Chemistry|October 14, 2015
Synthesis and biochemical evaluation of benzoylbenzophenone thiosemicarbazone analogues as potent and selective inhibitors of cathepsin LErica N Parker, Jiangli Song, G D Kishore Kumar, et al.Journal of Natural Products|September 11, 2013
Synthesis of a 2-aryl-3-aroyl indole salt (OXi8007) resembling combretastatin A-4 with application as a vascular disrupting agentMallinath B Hadimani, Matthew T Macdonough, Anjan Ghatak, et al.Pageof 5