927812-47-3

Upstream product

• 603-35-0 triphenylphosphine 
• 927812-49-5 4-(1,3-diacetoxypropan-2-yloxy)indoline 
• 927812-42-8 4-(1,3-diacetoxypropan-2-yloxy)indole 
• 927812-45-1 1-(4-azidobutanoyl)-4-(1,3-dihydroxypropan-2-yloxy)-7-nitroindoline 
• 927812-44-0 1-(4-azidobutanoyl)-4-(1,3-diacetoxypropan-2-yloxy)-7-nitroindoline 
• 927812-50-8 2-(1H-indol-4-yloxy)propane-1,3-diol 
• 927812-43-9 1-(4-azidobutanoyl)-4-(1,3-diacetoxypropan-2-yloxy)indoline 
• 868947-76-6 diethyl 2-(indol-4-yloxy)malonate 
• 927866-59-9 1-(4-azidobutanoyl)-4-(1,3-bis(dihydroxyphosohoryloxy)propan-2-yloxy)-7-nitroindoline 

Relevant academic research and scientific papers

Synthesis of an anionically substituted nitroindoline-caged GABA reagent that has reduced affinity for GABA receptors

A 7-nitroindolin-1-yl amide of the neuroactive amino acid γ-aminobutryate (GABA) has been synthesised with two phosphate groups attached to the indoline nucleus at 4-alkoxy substituent. The compound is designed to release GABA on a sub-microsecond time sc

Anionically substituted 7-Nitroindoline derivatives and their uses

Anionically substituted 7-nitroindoline derivatives are disclosed and their uses as caged compounds from which effector species such as neurotransmitters and amino acids are releasable on irradiation with light.