Publication | Closed Access
Redox Center Modification of Lapachones towards the Synthesis of Nitrogen Heterocycles as Selective Fluorescent Mitochondrial Imaging Probes
24
Citations
50
References
2017
Year
Combinatorial ChemistryBioorganic ChemistryMolecular BiologyOrganic ChemistryHeterocycle ChemistryRedox BiologyMedicinal ChemistryRedox ChemistryMolecular ImagingBiochemistryPhotochemistryMechanistic PhotochemistryRedox Center ModificationSynthetic StrategyMitochondrial FunctionNatural SciencesNew Fluorescent ImidazoleNitrogen HeterocyclesChemical ProbePhenazine DerivativesMedicine
We describe herein a synthetic strategy for the synthesis of new fluorescent imidazole and phenazine derivatives synthesized from lapachol, a naturally occurring naphthoquinone isolated from Tabebuia species (ipê tree). The photophysical properties and computational details of these compounds have been studied, aiming at gaining a complete understanding of the potential of these derivatives as probes capable of staining mitochondria selectively. Cell imaging experiments proved the capacity of the imidazole derivatives as selective fluorescent mitochondrial imaging probes. These heterocycles present the same staining patterns as MitoTracker Red, corroborating the potential of these compounds as new mitochondria markers permeable to the cell membrane.
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