Difference between revisions of "User:Mary Mendoza/Notebook/CHEM572 Exp. Biological Chemistry II/2013/03/27"

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(Continuation of Histogram runs)
(Continuation of Histogram runs)
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==Continuation of Histogram runs==
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* The final trial for 4-acetoxybenzoic acid was completed. This compound showed inhibition.
 
* A stock solution of 5-hydroxy-2-methylbenzoic acid was prepared in DMSO.
 
* A 500 μM stock solution of 3-methylacetylsalicylic acid was prepared in 0.05 M phosphate buffer.
 
* Assay for each of the mentioned compounds showed inhibition which can be seen on the data below. The data is provided by [[User:Dhea Patel/Notebook/CHEM 572: ADA&Inhibitor Kinetics/2013/03/27|Dhea Patel]].
 
  
 
==Preparing 500uM [Inhibitor] Solutions==
 
==Preparing 500uM [Inhibitor] Solutions==

Revision as of 14:28, 8 May 2013

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Preparing 500uM [Inhibitor] Solutions

  • 500uM [5-Hydroxy-2-methylbenzoic acid] (Aldrich 696366-1G) [ZINC01668680] made in DMSO:

Screen Shot 2013-03-27 at 1.57.40 PM.png

  • 500uM [3-Methylacetylsalicylic acid] (Aldrich S376647-1G) [ZINC00001221] made in Phosphate Buffer:

Screen Shot 2013-03-27 at 2.49.54 PM.png

Data Table

File:20130327 Data Table.tiff

  • The table above shows the concentrations and volumes of the substrate and other chemical constituents present in the cuvette during data collection.
  • The kinetics was performed by the UVProbe of UV 2500 Shimadzu spectrophotometer at 25°C.

Data

File:20130327 data.tiff

  • The histogram above shows that the 4-acetoxybenzoic acid shows the greatest inhibition as an aspirin analog.