Cat. No. 5168
Chemical Name: 4,5,6,7-Tetrachloro-3',6'-dihydroxy-2
Biological ActivityPotent VGlut and vesicular monoamine transporter (VMAT) inhibitor (Ki values are 19 and 64 nM, respectively). Inhibits ATP dependent vesicular glutamate uptake (IC50 = 37 nM) and diminishes the amount of exocytotically released glutamate in synaptosomes. Decreases synaptic transmission in the dentate gyrus. Also stains exposed epithelium in the eye. Cell permeable.
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Certificate of Analysis / Product Datasheet / Safety Datasheet
Neale et al (2013) Modulation of hippocampal synaptic transmission by the kynurenine pathway member xanthurenic acid and other VGLUT inhibitors. Neuropsychopharmacology. Neuropsychopharmacology 38 1060. PMID: 23303071.
Pietrancosta et al (2010) Rose Bengal analogs and vesicular glutamate transporters (VGLUTs). Bioorg.Med.Chem. 18 6922. PMID: 20708942.
Ogita et al (2001) Inhibition of vesicular glutamate storage and exocytotic release by Rose Bengal. J Neurochem. 77 34. PMID: 11279259.
Feenstra et al (1992) What is actually stained by rose bengal? Arch.Ophthalmol. 110 984. PMID: 1637285.
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Keywords: Rose Bengal, supplier, potent, non, competitive, inhibitors, inhibits, membrane, permeable, glutamate, vesicular, glutamate, transporters, VGLUT, excitatory, amino, acid, neuroprotective, Rose, Bengal, Tocris Bioscience, Vesicular Monoamine Transporter Inhibitor products
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