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What Are the Potential Sites of Protein Arylation by N-Acetyl-p-benzoquinone Imine (NAPQI)? | Chemical Research in Toxicology
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Transformation of Acetaminophen by Chlorination Produces the Toxicants 1 , 4 -Benzoquinone and N-Acetyl-p-benzoquinone Imine | Semantic Scholar
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Transformation of Acetaminophen by Chlorination Produces the Toxicants 1 , 4 -Benzoquinone and N-Acetyl-p-benzoquinone Imine | Semantic Scholar
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Acetaminophen metabolism. NAPQI, N-acetyl-p-benzoquinone imine; CYP450,... | Download Scientific Diagram
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N-Acetyl-p-benzoquinone Imine, the Toxic Metabolite of Acetaminophen, Is a Topoisomerase II Poison | Biochemistry
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Figure 9. [1] Paracetamol, [2] p-Aminophenol and [3], N-acetyl-p-benzoquinone imine : Organic Redox-Flow Batteries Using Hair Dyes and Pharmaceuticals : Science and Education Publishing
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PDF) N-Acetyl-p-benzoquinone imine (NAPQI) induces Ca2+ release from mitochondria by stimulating pyridine nucleotide hydrolysis
![What Are the Potential Sites of Protein Arylation by N-Acetyl-p-benzoquinone Imine (NAPQI)? | Chemical Research in Toxicology What Are the Potential Sites of Protein Arylation by N-Acetyl-p-benzoquinone Imine (NAPQI)? | Chemical Research in Toxicology](https://pubs.acs.org/cms/10.1021/acs.chemrestox.5b00373/asset/images/large/tx-2015-00373z_0007.jpeg)
What Are the Potential Sites of Protein Arylation by N-Acetyl-p-benzoquinone Imine (NAPQI)? | Chemical Research in Toxicology
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What Are the Potential Sites of Protein Arylation by N-Acetyl-p-benzoquinone Imine (NAPQI)? | Chemical Research in Toxicology
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