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Design, Synthesis, Anti-Proliferative and Molecular Docking Studies of Combretastatin A4 Analogues with 2-Azetidinone Moiety
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Culture of Animal Cells: A Manual of Basic Technique
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Development of combretastatins as potent tubulin polymerization inhibitors
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Microtubule associated proteins as targets for anticancer drug development
inferredcites →https://doi.org/10.1016/j.chempr.2016.12.005openalex-extracted
Structural Basis of cis- and trans-Combretastatin Binding to Tubulin
inferredcites →https://doi.org/10.1016/j.compbiolchem.2020.107268openalex-extracted
Computational study of 3-thiophene acetic acid: Molecular docking, electronic and intermolecular interactions investigations
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Novel amino-β-lactam derivatives as potent cholesterol absorption inhibitors
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Design, synthesis and characterization of dual inhibitors against new targets FabG4 and HtdX of Mycobacterium tuberculosis
inferredcites →https://doi.org/10.1016/j.ejmech.2016.08.041openalex-extracted
2-Azetidinones: Synthesis and biological evaluation as potential anti-breast cancer agents
inferredcites →https://doi.org/10.1016/j.ejmech.2017.02.049openalex-extracted
β-Lactam analogues of combretastatin A-4 prevent metabolic inactivation by glucuronidation in chemoresistant HT-29 colon cancer cells
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iLOGP: A Simple, Robust, and Efficient Description of n -Octanol/Water Partition Coefficient for Drug Design Using the GB/SA Approach
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Medicinal Chemistry of Combretastatin A4: Present and Future Directions
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Regioselective Suzuki Coupling of Dihaloheteroaromatic Compounds as a Rapid Strategy To Synthesize Potent Rigid Combretastatin Analogues
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inferredcites →https://doi.org/10.1039/b306797copenalex-extracted
Combretastatins: from natural products to drug discovery
inferredcites →https://doi.org/10.1046/j.1365-2613.2002.00211.xopenalex-extracted
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PubChem Substance and Compound databases
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Relaxation Estimation of RMSD in Molecular Dynamics Immunosimulations
inferredcites →https://doi.org/10.2174/092986711796391642openalex-extracted
Biological Potential and Structure-Activity Relationships of Most Recently Developed Vascular Disrupting Agents: An Overview of New Derivatives of Natural Combretastatin A-4
inferredcites →https://doi.org/10.2174/1871526522666220105114437openalex-extracted
Recent Advances in Combretastatin A-4 Inspired Inhibitors of Tubulin Polymerization: An Update
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Regulation of Cell Death by Mitochondrial Transport Systems of Calcium and Bcl-2 Proteins
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Pharmacoinformatics and Breed-Based De Novo Hybridization Studies to Develop New Neuraminidase Inhibitors as Potential Anti-Influenza Agents
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