618095-50-4

Upstream product

• 165811-64-3 4,5-dimethoxy-2-nitrobenzyl 2-aminoacetate hydrochloride 
• 53413-67-5 6-nitroveratrylbromide 
• 24277-39-2 N-tert-butoxycarbonyl glutamic acid tert-butyl ester 
• 1016-58-6 6-nitroveratryl alcohol 

Downstream Products

• 1353745-55-7 (S)-2-amino-5-(4,5-dimethoxy-2-nitrobenzyloxy)-5-oxopentanoic acid hydrochloride 
• 618095-48-0 γ-(4,5-dimethoxy-2-nitrobenzyl)-L-glutamate 
• 618095-52-6 N^α-(tert-butoxycarbonyl)-γ-(6-nitroveratryl)glutamic acid cyanomethyl ester 
• 618095-51-5 N^α-(tert-butoxycarbonyl)-γ-(6-nitroveratryl)glutamic acid 

Relevant academic research and scientific papers

STIMULI-SWITCHABLE MOIETIES, MONOMERS AND POLYMERS INCORPORATING STIMULI-SWITCHABLE MOIETIES, AND METHODS OF MAKING AND USING SAME

Stimuli-switchable moieties, monomers incorporating stimuli-switchable moieties, and polymers incorporating such stimuli-switchable moieties are provided. The stimuli-switchable moiety can be a pyrano aryl chromenone-derivative. The stimuli-switchable monomer can be a lactone monomer. The stimuli-switchable monomer can be an amino acid, which can be incorporated into a specific peptide sequence by peptide synthesis.

Wavelength-orthogonal photolysis of neurotransmitters in vitro

Irradiation of a mixture of 4-methoxyphenacyl-caged (S)-glutamate and 4,5-dimethoxy-2-nitrobenzyl-caged γ-amino butyric acid (GABA) on neurons, at ～260 nm, evokes selective photorelease of (S)-glutamate (Glu) whereas photolysis at 405 nm causes selective photorelease of GABA.

Design and synthesis of photochemically controllable restriction endonuclease BamHI by manipulating the salt-bridge network in the dimer interface

The strategy for the design of photochemically controllable enzymes by manipulating the dimer interface is described. Employing a restriction endonuclease BamHI, the selective incorporation of amino acids having a photoremovable 6-nitroveratryl group into