Difference between revisions of "Acetaminophen Radicals"
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Web MO/Gaussian is a software containing various basis sets that allow for various levels of computational chemistry. | Web MO/Gaussian is a software containing various basis sets that allow for various levels of computational chemistry. | ||
===B3YLP/6-311+G(2d,p)=== | ===B3YLP/6-311+G(2d,p)=== | ||
| − | [[File:Pchem_APAP_WINSIM.png|400px | + | [[File:Pchem_APAP_WINSIM.png|400px\WINSIM ESR Simulation|thumb|center|WINSIM ESR Simulation]] |
| − | [[File:APAP_Rad.png|400px]] | + | [[File:WEBMO_electronDensity.png|400px|Electron Density|thumb|center|Electron Density]] |
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| + | [[File:APAP_Rad.png|400px|Acetaminophen Radical|thumb|center|Acetaminophen Radical]] | ||
Revision as of 20:18, 15 April 2021
The Ab-initio computation of the acetaminophen radical. The goal of this project is to elucidate where electrons are located on the molecule when a radicalization occurs.
Background
Acetaminophen(APAP) is an active ingredient in many over-the-counter and prescription painkillers, such as Tylenol and Oxycodone. APAP is also responsible for approximately 50% of the cases of acute liver-failure in the United States and Great Britain. Treatments for acetaminophen-induced liver injury(AILI) are limited. The current mechanism for AILI is the production of hepatotoxic NAPQI as a metabolite in an enzymatic, two-electron oxidation(1). However, evidence also supports a one electron oxidation.
Web MO/Gaussian
Web MO/Gaussian is a software containing various basis sets that allow for various levels of computational chemistry.
