6-Hydroxy-N-methyl-4-oxo-1,2-dihydro-4H-pyrrolo[3,2,1-ij]quinoline-5-carboxamide

95%

Reagent Code: #215650
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CAS Number 384365-15-5

science Other reagents with same CAS 384365-15-5

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 244.25 g/mol
Formula C₁₃H₁₂N₂O₃
inventory_2 Storage & Handling
Storage 2-8°C, sealed, dry

description Product Description

Used in research as a fluorescent probe due to its strong emission properties in the visible range. Its structure allows for good cell membrane permeability, making it suitable for imaging intracellular components in live-cell assays. Commonly applied in neuroscience studies to label and track neuronal activity. Also investigated for use in photodynamic therapy owing to its ability to generate reactive oxygen species under light exposure. Shows potential as a scaffold in developing enzyme inhibitors, particularly for kinases involved in inflammatory pathways.

Available Sizes & Pricing

Size Availability Unit Price Quantity
50mg
10-20 days ฿7,790.00
100mg
10-20 days ฿14,010.00
250mg
10-20 days ฿29,410.00
6-Hydroxy-N-methyl-4-oxo-1,2-dihydro-4H-pyrrolo[3,2,1-ij]quinoline-5-carboxamide
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Used in research as a fluorescent probe due to its strong emission properties in the visible range. Its structure allows for good cell membrane permeability, making it suitable for imaging intracellular components in live-cell assays. Commonly applied in neuroscience studies to label and track neuronal activity. Also investigated for use in photodynamic therapy owing to its ability to generate reactive oxygen species under light exposure. Shows potential as a scaffold in developing enzyme inhibitors, par

Used in research as a fluorescent probe due to its strong emission properties in the visible range. Its structure allows for good cell membrane permeability, making it suitable for imaging intracellular components in live-cell assays. Commonly applied in neuroscience studies to label and track neuronal activity. Also investigated for use in photodynamic therapy owing to its ability to generate reactive oxygen species under light exposure. Shows potential as a scaffold in developing enzyme inhibitors, particularly for kinases involved in inflammatory pathways.

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