About: Semiquinone anion radicals formed by the reaction of quinones with glutathione or amino acids

Facets (new session)
Description
Metadata
Settings
- owl:sameAs
- Inference Rule:

About: Semiquinone anion radicals formed by the reaction of quinones with glutathione or amino acids Goto Sponge NotDistinct Permalink

An Entity of Type : wikibase:Item, within Data Space : wikidata.demo.openlinksw.com associated with source document(s)

scientific article published on 01 June 1986

Attributes	Values
rdf:type	Item
description	wetenschappelijk artikel (nl) наукова стаття, опублікована в червні 1986 (uk) article scientifique publié en 1986 (fr) im Juni 1986 veröffentlichter wissenschaftlicher Artikel (de) artículu científicu espublizáu en xunu de 1986 (ast) scientific article published on 01 June 1986 (en)
publication date	wds:Q70140039-CF23D6F7-C9AB-4585-8EFA-6FC2D1D8BDB6
publication date	1986-06-01 00:00:00Z (xsd:dateTime)
language of work or name	wds:Q70140039-535D8CCF-D6CE-4A93-B01D-B430B07FEDD6
language of work or name	English
cites work	wds:Q70140039-2D839BA4-0218-4B4F-A5E1-1F9C6E07F6C8 wds:Q70140039-2E670AD5-E5E6-4BFE-9BE7-8C5184367456 wds:Q70140039-2EC82C63-B827-4ED9-8037-77BEBB2C6F93 wds:Q70140039-5B44C48F-9828-440B-B510-EC8BE7C9AB83 wds:Q70140039-641A0BA7-82D8-4C5C-AEA7-C59FA901D3E4 wds:Q70140039-892D5440-D920-4C21-BC21-04D3BD13B397 wds:Q70140039-89B00458-3591-4E4E-ADE3-5FCC07E10174 wds:Q70140039-A88CBA83-AFB5-4D6E-B6DD-9E54A6632449 wds:Q70140039-BB49A2EF-C984-469F-9775-92BB670A085B wds:Q70140039-BB4CF7D9-BC15-4650-9E9A-B30F05C5172B wds:Q70140039-CB237764-C650-4EB7-A287-E1A6311A1248 wds:Q70140039-D807656D-FFF9-42F6-8682-67A925D6091C wds:Q70140039-E3C2DC46-090E-43E0-B282-6BD1D30D9E45 wds:Q70140039-E6FC56DD-67A7-44F2-8828-11F7031EDEF8
cites work	Adriamycin. A new anticancer drug with significant clinical activity Glutathione Effects of modifying structure on electrophilic reactions with biological nucleophiles The reaction of benzoquinone with amines and proteins Interaction of menadione (2-methyl-1,4-naphthoquinone) with glutathione Toxic drug effects associated with oxygen metabolism: redox cycling and lipid peroxidation One-electron-transfer reactions in biochemical systems. V. Difference in the mechanism of quinone reduction by the NADH dehydrogenase and the NAD(P)H dehydrogenase (DT-diaphorase) Overview of enzyme systems involved in bio-reduction of drugs and in redox cycling A proposed mechanism of benzene toxicity: formation of reactive intermediates from polyphenol metabolites. STUDIES ON QUINONE-THIOETHERS. I. MECHANISM OF FORMATION AND PROPERTIES OF THIODIONE Free radical formation from anthracycline antitumour agents and model systems--I. Model naphthoquinones and anthraquinones Relationship of the single-electron reduction potential of quinones to their reduction by flavoproteins The addition of sulfhydryl derivatives to 2-methyl-1,4-naphthoquinone The interaction of thiols and quinones
author name string	wds:Q70140039-01CE0812-AA12-4A35-8637-73CD8CFE1E33 wds:Q70140039-491B3686-A66F-4307-B085-312FA7A6D2AA wds:Q70140039-58EB3138-A774-4532-9C81-9DAEEC6AF717 wds:Q70140039-B877CB27-DE07-4FEE-9E87-01B7AA77336D wds:Q70140039-E94150CF-0B5E-43B6-8C61-8D7B211C9E13
author name string	G M Cohen M D Doherty D Odowole K D Sales T W Grant
rdfs:label	Semiquinone anion radicals formed by the reaction of quinones with glutathione or amino acids (en) Semiquinone anion radicals formed by the reaction of quinones with glutathione or amino acids (nl)
skos:prefLabel	Semiquinone anion radicals formed by the reaction of quinones with glutathione or amino acids (en) Semiquinone anion radicals formed by the reaction of quinones with glutathione or amino acids (nl)
name	Semiquinone anion radicals formed by the reaction of quinones with glutathione or amino acids (en) Semiquinone anion radicals formed by the reaction of quinones with glutathione or amino acids (nl)
title	wds:Q70140039-2E6B68A3-BE31-4F5E-B36E-225EE586BCA9
title	Semiquinone anion radicals formed by the reaction of quinones with glutathione or amino acids (en)
page(s)	wds:Q70140039-84358170-FD17-4254-A3D7-D8C45D8A50F6
page(s)	296-300
instance of	wds:Q70140039-50D652D5-FC5B-42B7-941A-B856B93DEFBF
instance of	scholarly article
main subject	wds:Q70140039-963F5CE6-6FC9-4ED0-8887-57C76656C8B9
main subject	glutathione
PubMed ID	wds:Q70140039-4A959B17-EEE4-46AF-8721-97CFAD3F6BE4
PubMed ID	http://rdf.ncbi.nlm.nih.gov/pubchem/reference/3011514
PubMed ID	3011514
published in	wds:Q70140039-DED32387-8E0B-4601-A4E4-E5433B1839BA
published in	FEBS Letters
issue	wds:Q70140039-C0A1B042-1D13-478A-BB92-A60C5F95CD70
volume	wds:Q70140039-C7723DAC-14AC-476B-9641-8C713BCA0291
issue	2
volume	201
DOI	wds:Q70140039-0CEC17BC-9F1C-492C-9A0E-2AF036F5D51C
DOI	http://dx.doi.org/10.1016/0014-5793(86)80627-5
DOI	10.1016/0014-5793(86)80627-5
is about of	https://www.wikidata.org/wiki/Special:EntityData/Q70140039
is cites work of	Nonenzymatic displacement of chlorine and formation of free radicals upon the reaction of glutathione with PCB quinones Quinone chemistry and toxicity DNA barcoding detects contamination and substitution in North American herbal products Antioxidant and prooxidant functions of DT-diaphorase in quinone metabolism Electron spin resonance investigation of semiquinone radicals formed from the reaction of ubiquinone 0 with human oxyhemoglobin The biological significance of non-enzymatic reaction of menadione with plasma thiols: enhancement of menadione-induced cytotoxicity to platelets by the presence of blood plasma DT-diaphorase-catalysed reduction of 1,4-naphthoquinone derivatives and glutathionyl-quinone conjugates. Effect of substituents on autoxidation rates Bioactivation of thiols by one-electron oxidation The pro-oxidant role of protein SH groups of hemoglobin in rat erythrocytes exposed to menadione Optimisation of cell-based assays for medium throughput screening of oxidative stress Reactions of halogen-substituted aziridinylbenzoquinones with glutathione. Formation of diglutathionyl conjugates and semiquinones Reduction of daunorubicin in the presence of sulfur-containing peptides
is cites work of	wds:Q37210829-2CA05CFC-F1AD-4077-A0B9-995B36D043A7 wds:Q62066175-00CA4A08-0469-4A4E-A64F-F90788FC6798 wds:Q21245290-EE5772CC-933D-493A-BDA7-0AE58650609C wds:Q46189527-F4E4728A-D97E-4914-A1DD-166193FECFC3 wds:Q36748286-38BD2768-63ED-4726-B327-AC9D6A954EE6 wds:Q40693454-5DDBD117-3582-4C2E-8EC3-8D8B6E5959BA wds:Q77781049-32C29650-42DA-4101-9795-2681C16D28BB wds:Q67906306-716D6763-7BAA-4D2A-A1A9-FE9DE6BC4864 wds:Q28340699-CB2EF311-A291-49A3-ACF4-2B1E51C4D6F1 wds:Q30780542-D0415131-2FD5-4746-9A04-99A5F0FE8926 wds:Q44371237-5B72CC27-7C5A-498F-8399-3C13240433B3 wds:Q40397225-73942B58-E0A9-4724-B3F8-2465F1D47CDF

Faceted Search & Find service v1.16.117 as of May 05 2024

Alternative Linked Data Documents: ODE Content Formats:

RDF

ODATA

Microdata

About

OpenLink Virtuoso version 07.20.3239 as of May 5 2024, on Linux (x86_64-centos_6-linux-gnu), Single-Server Edition (378 GB total memory, 173 GB memory in use)
Data on this page belongs to its respective rights holders.
Virtuoso Faceted Browser Copyright © 2009-2024 OpenLink Software