The Synthesis and Biological Evaluation of Anithiactin A/Thiasporine C and Analogues

AUSTRALIAN JOURNAL OF CHEMISTRY(2016)

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Abstract
The synthesis of anithiactin A has been achieved in four steps. Several closely related analogues were synthesised and their biological activity against colon and breast cancer cell lines evaluated. Anithiactin A was found not to be cytotoxic even at a high concentration (100 mu M); however, two 4-substituted phenyl thiazoles were found to be moderately cytotoxic at 10 mM. Based on these results, 4-substitution on the phenyl group appears to be critical for cytotoxicity. However, the exact electronic and structural requirements are unclear.
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peptide,reaction mechanisms,mass spectrometry,biological chemistry,ab initio calculations,nanotechnology,educational,ionic liquids,colloids,pharmaceutical chemistry,photochemistry,structure,surface chemistry,analytical chemistry,quantum chemistry,green chemistry,polymer chemistry,biosensors,physical chemistry,kinetics,medicinal chemistry,computational chemistry,organic chemistry,crystal structures,density functional theory,spectroscopy,interfaces,electrochemistry,enzymes,sensors,supramolecular chemistry,combinatorial chemistry,inorganic chemistry,amino acids,biocatalysis,combinatorial,crystallography,self assembly,catalysis,macromolecules,proteins
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