78701-22-1

Upstream product

• 1198-84-1 4-hydroxymandelic acid 
• 75-36-5 acetyl chloride 
• 108-24-7 acetic anhydride 

Downstream Products

• 1450726-90-5 C₁₉H₂₆N₂O₇ 
• 1450726-91-6 C₁₅H₂₂N₂O₅ 
• 919350-83-7 Acetic acid (2S,3R,4S,5S,6R)-4,5-diacetoxy-6-acetoxymethyl-2-(4-{2-[4-(7-acetoxy-2-oxo-2H-chromene-3-carbonyl)-piperazin-1-yl]-1-fluoro-2-oxo-ethyl}-phenoxy)-tetrahydro-pyran-3-yl ester 
• 919350-78-0 4-{2-hydroxy-2-[4-(3,4,5-triacetoxy-6-acetoxymethyltetrahydropyran-2-yloxy)phenyl]acetyl}piperazine-1-carboxylic acid benzyl ester 
• 919350-79-1 acetic acid 3,5-diacetoxy-2-acetoxymethyl-6-[4-(1-hydroxy-2-oxo-2-piperazin-1-ylethyl)phenoxy]tetrahydropyran-4-yl ester 
• 919350-77-9 4-[2-hydroxy-2-(4-hydroxyphenyl)acetyl]piperazine-1-carboxylic acid benzyl ester 
• 919350-76-8 4-[2-acetoxy-2-(4-acetoxyphenyl)acetyl]piperazine-1-carboxylic acid benzyl ester 

Relevant academic research and scientific papers

Fluorescent probe for covalently connecting labeled cells and method for tracking labeled cells

The invention discloses a fluorescence probe for covalently connecting labeled cells and a method for tracking labeled cells, and relates to a cell fluorescence probe, wherein the fluorescent probe for covalently connecting labeled cells consists of a cov

A covalent reporter of β-lactamase activity for fluorescent imaging and rapid screening of antibiotic-resistant bacteria

Bacterial resistance to antibiotics poses a great clinical challenge in fighting serious infectious diseases due to complicated resistant mechanisms and time-consuming testing methods. Chemical reaction-directed covalent labeling of resistance-associated

Nucleic-acid triggered release of molecules

It is an object of the present invention to provide a method for highly selectively releasing a molecule of interest such as an agent at a desired site while suppressing the influence of catabolic enzymes existing in vivo. The present invention provides a

Design and synthesis of an enzyme activity-based labeling molecule with fluorescence spectral change

Methods of covalent labeling of a specific tag protein with small-molecular dyes play an important role in studying dynamic behaviors of proteins in living cells. On the basis of quinone methide chemistry, we designed and synthesized a β-galactosidase labeling probe, CMFβ-gal, which shows a fluorescence wavelength change accompanying the labeling reaction, owing to fluorescence resonance energy transfer (FRET). Since the FRET efficiency changes accompanying the labeling reaction, fluorescence of labeled protein can be observed separately from that of the unreacted probe, so immediate detection of the target protein is possible. This is the first report of a protein labeling probe which features a change of fluorescence wavelength upon reaction, allowing the labeled protein to be detected even in the presence of unreacted probe. Copyright

Phenyl alpha acyloxyalkanoic acids, derivatives and their therapeutic use

Therapeutic as well as preventative measures to improve the cosmetic conditions or to alleviate the symptoms of dermatologic disorders with phenyl alpha acyloxyalkanoic acids and derivatives is disclosed. The cosmetic conditions and dermatologic disorders