Publication | Closed Access
Potential Antitumor Agents. 37. Synthesis and Antitumor Activity of Guanylhydrazones from Imidazo[2,1-<i>b</i>]thiazoles and from the New Heterocyclic System Thiazolo[2‘,3‘:2,3]imidazo[4,5-<i>c</i>]quinoline
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Citations
13
References
2005
Year
Mitochondrial Respiratory ChainNational Cancer InstituteMedicinal ChemistryBioorganic ChemistryAntitumor ActivityBiochemistryHeterocyclicNatural SciencesMedicineAnti-cancer AgentPotential Antitumor AgentsHeterocycle ChemistryPharmacologyComplex IiiPharmaceutical ChemistryDrug DiscoveryNatural Product Synthesis
This paper reports synthesis and antitumor activity of new guanylhydrazones from imidazo[2,1-b]thiazoles and from the new heterocyclic system thiazolo[2',3':2,3]imidazo[4,5-c]quinoline. The compounds were tested as potential antitumor agents at the National Cancer Institute. The effect of the guanylhydrazone of 2-chloro-6-(2,5-dimethoxy-4-nitrophenyl)imidazo[2,1-b]thiazole-5-carbaldehyde (41) was investigated, and it was found to be an inhibitor of Complex III of the mitochondrial respiratory chain and is able to induce apoptosis in the cell lines HT29 and HL60.
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