File:N-Acetyl-p-benzochinonimin.svg - Wikimedia Commons
Transformation of Acetaminophen by Chlorination Produces the Toxicants 1 , 4 -Benzoquinone and N-Acetyl-p-benzoquinone Imine | Semantic Scholar
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In-source formation of N-acetyl-p-benzoquinone imine (NAPQI), the putatively toxic acetaminophen (paracetamol) metabolite, after derivatization with pentafluorobenzyl bromide and GC–ECNICI-MS analysis - ScienceDirect
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N-acetyl-p-benzoquinone imine - Wikipedia
NAPQI - N-acetyl-p-benzoquinone imine
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3,5-Dimethyl-NAPQI - CAS-Number 74827-85-3 - Order from Chemodex
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LC-MS analyses of N-acetyl-p-benzoquinone imine-adducts of glutathione, cysteine, N-acetylcysteine, and albumin in a plasma sample: A case study from a patient with a rare acetaminophen-induced acute swelling rash. | Semantic Scholar
Reduction of toxic metabolite formation of acetaminophen
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BHR 5282002 Acetaminophen Hepatotoxicity Barry H Rumack M
NAPQI - N-acetyl-p-benzoquinone imine
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The biochemistry of acetaminophen hepatotoxicity and rescue: a mathematical model | Theoretical Biology and Medical Modelling | Full Text
Acetaminophen metabolism. NAPQI, N-acetyl-p-benzoquinone imine; CYP450,... | Download Scientific Diagram
NABQI - "N-acetyl-p-benzoquinone imine" by AcronymsAndSlang.com
A) The CID pathways of N-acetyl-p-benzoquinone imine-glutathione... | Download Scientific Diagram
Scheme 1. Transformation of acetaminophen to... | Download Scientific Diagram
Observation of the generation of peroxynitrite in mouse liver after acetaminophen overdose with a boronate-based ratiometric fluorescence probe - RSC Advances (RSC Publishing) DOI:10.1039/C8RA10053E
