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CAS No. : | 20595-30-6 | MDL No. : | MFCD00004383 |
Formula : | C9H7FO2 | Boiling Point : | - |
Linear Structure Formula : | - | InChI Key : | RTSIUKMGSDOSTI-SNAWJCMRSA-N |
M.W : | 166.15 | Pubchem ID : | 1551219 |
Synonyms : |
|
Signal Word: | Danger | Class: | 6.1 |
Precautionary Statements: | P261-P301+P310-P305+P351+P338 | UN#: | 2811 |
Hazard Statements: | H301-H315-H319-H335 | Packing Group: | Ⅲ |
GHS Pictogram: |
* All experimental methods are cited from the reference, please refer to the original source for details. We do not guarantee the accuracy of the content in the reference.
Yield | Reaction Conditions | Operation in experiment |
---|---|---|
With phenylalanine ammonia lyase from Rhodotorula graminis; ammonium carbamate; In aq. buffer; at 30℃;pH 9.0;Kinetics; | General procedure: Solutions of the substrates under investigation were made up in 0.5M ammonium carbamate/1M Tris, pH 9.0 and dilutions were made with the following concentrations: 3, 2, 1, 0.5, 0.2, 0.02, 0.002 and 0mM of cinnamic acid. Scopoletin solution - 288.25mg of scopoletin was dissolved in 50mL dH2O to make a stock solution. This stock solution was then diluted 1/5 to create a working solution that had a fluorescence of approximately 30,000 RFU. The screening was set up in a 96-well plate and each well contained the following: 100muL substrate solution, 10muL HRP (1mg/mL in dH2O), 10muL l-AAO (1 in 10 dilution of stock in dH2O), 40muL scopoletin solution, 40muL purified PAL. Kinetic data was measured on a plate reader at 30C. Excitation wavelength 360nm; emission wavelength 480nm; 15s interval. |
Yield | Reaction Conditions | Operation in experiment |
---|---|---|
With phenylalanine ammonia lyase from Rhodotorula graminis; In aq. buffer; for 1h;pH 8.8;Enzymatic reaction; | General procedure: Substrate solutions of 4-bromo, 3-bromo, 4-fluoro, 3-fluoro and 3-nitro phenylalanine were made, 20mM substrate in 100mM Tris buffer pH 8.8. The screening was set up in a UV-Star Microplates (96 well, F-bottom, Greiner Bio-one) and each well contained the following: 140muL Tris buffer 100mM, pH 8.8, 10muL of purified enzyme, 50muL phenylalanine solution. Absorbance was measured using a plate reader at 290nm for 1h with intervals of 43s and hits were identified by an increase in the absorbance. |
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