Atpenins, potent and specific inhibitors of mitochondrial complex II (succinate-ubiquinone oxidoreductase).
about
Physiological consequences of complex II inhibition for aging, disease, and the mKATP channelThiabendazole inhibits ubiquinone reduction activity of mitochondrial respiratory complex II via a water molecule mediated binding featureStructural and computational analysis of the quinone-binding site of complex II (succinate-ubiquinone oxidoreductase): a mechanism of electron transfer and proton conduction during ubiquinone reductionUbiquinone-binding site mutagenesis reveals the role of mitochondrial complex II in cell death initiationAcute inhibition of selected membrane-proximal mouse T cell receptor signaling by mitochondrial antagonistsAlterations in cellular energy metabolism associated with the antiproliferative effects of the ATM inhibitor KU-55933 and with metforminThe Open Form Inducer Approach for Structure-Based Drug Design.The mitochondrial complex II and ATP-sensitive potassium channel interaction: quantitation of the channel in heart mitochondria.Mutation of the heme axial ligand of Escherichia coli succinate-quinone reductase: implications for heme ligation in mitochondrial complex II from yeastAn analysis of the effects of Mn2+ on oxidative phosphorylation in liver, brain, and heart mitochondria using state 3 oxidation rate assaysMitochondrial ROS Metabolism: 10 Years Later.Anti-apoptotic MCL-1 localizes to the mitochondrial matrix and couples mitochondrial fusion to respiration.Mitochondrial complex II can generate reactive oxygen species at high rates in both the forward and reverse reactionsInhibition of Mitochondrial Complex II by the Anticancer Agent Lonidamine.Co-regulation of mitochondrial respiration by proline dehydrogenase/oxidase and succinate.Disruption of glycolytic flux is a signal for inflammasome signaling and pyroptotic cell deathDeletion of MCL-1 causes lethal cardiac failure and mitochondrial dysfunction.Sulfonylurea receptor-dependent and -independent pathways mediate vasodilation induced by ATP-sensitive K+ channel openersA spectrophotometric coupled enzyme assay to measure the activity of succinate dehydrogenaseSites of superoxide and hydrogen peroxide production during fatty acid oxidation in rat skeletal muscle mitochondria.The complex II inhibitor atpenin A5 protects against cardiac ischemia-reperfusion injury via activation of mitochondrial KATP channelsMitochondrial diaphorases as NAD⁺ donors to segments of the citric acid cycle that support substrate-level phosphorylation yielding ATP during respiratory inhibition.Electron-transfer pathways in the heme and quinone-binding domain of complex II (succinate dehydrogenase).Mitochondrial respiratory chain complexes: apoptosis sensors mutated in cancer?Inhibitors of succinate: quinone reductase/Complex II regulate production of mitochondrial reactive oxygen species and protect normal cells from ischemic damage but induce specific cancer cell death.Mitochondria as a pharmacological target: magnum overview.Fungal natural products in research and development.Ecological functions of Trichoderma spp. and their secondary metabolites in the rhizosphere: interactions with plants.The Assembly Factor SDHAF2 Is Dispensable for Flavination of the Catalytic Subunit of Mitochondrial Complex II in Breast Cancer Cells.The Slo(w) path to identifying the mitochondrial channels responsible for ischemic protection.Inhibitory effects of respiration inhibitors on aflatoxin production.Affinity of vitamin E analogues for the ubiquinone complex II site correlates with their toxicity to cancer cells.Differential metabolic responses to pluronic in MDR and non-MDR cells: a novel pathway for chemosensitization of drug resistant cancers.Bioisosteric Exchange of Csp3 -Chloro and Methyl Substituents: Synthesis and Initial Biological Studies of Atpenin A5 Analogues.Pleiotropic Effects of Biguanides on Mitochondrial Reactive Oxygen Species Production.Sartorypyrone D: a new NADH-fumarate reductase inhibitor produced by Neosartorya fischeri FO-5897.Structural Insights into the Molecular Design of Flutolanil Derivatives Targeted for Fumarate Respiration of Parasite Mitochondria.Expression of Saccharomyces cerevisiae Sdh3p and Sdh4p paralogs results in catalytically active succinate dehydrogenase isoenzymes.Crystallization of mitochondrial rhodoquinol-fumarate reductase from the parasitic nematode Ascaris suum with the specific inhibitor flutolanilRespiratory Complex I in Bos taurus and Paracoccus denitrificans Pumps Four Protons across the Membrane for Every NADH Oxidized.
P2860
Q27002338-EB0AE318-CB76-4D5B-8101-E2397426E2C7Q27671605-AC1CD951-2511-4466-811F-CB720D822382Q28291140-AE2636F1-6D14-4EEC-A348-8B5029CD7900Q28395613-E963A45E-B910-4165-A514-5E9CB906FE28Q28471810-A0B1F2DD-5683-437D-A027-53E5B9710ADBQ28485299-7BCE2D1F-4B2D-43ED-9526-1629B5BFDF0AQ28554455-BC8C272C-F1FB-4401-ABA6-4B0682B6F679Q33647869-74B18D72-6D0E-4580-96C6-245E6D96F7FBQ33926010-A423EB7D-E72C-4E40-BCC7-A76C8E6A8DFAQ34416087-D99F9154-4121-4B8A-935F-AB5571D64384Q35879792-F8E40765-A4CB-412E-A2E9-6DF6A02BF233Q36108255-E7EE62E6-ED69-47A9-8213-FE105EC4C900Q36137552-8DED6053-F3AE-469A-858D-71647373EDC6Q36419289-D80AF179-C0BB-437A-990B-E332EAFE39EFQ36578312-5A05CCBB-EE3D-4766-BEDC-351542B9C1E9Q36839612-FC023AB3-2D6E-4696-8B34-CC6C9657A060Q36981764-10D514F8-07CC-4A04-9C08-3BF7EF1F046CQ37036859-8BC90EC9-6518-42F6-AFEE-34F9F77F74ADQ37199352-DF1FA2F7-1899-4B29-B430-980E102D4536Q37412145-766451DE-4ECF-4103-8C9E-78CA7642182DQ37419750-C6DEDDF6-96DB-4232-AABD-A1DA40D0E974Q37657133-74213B67-F147-4FBA-9A03-B9E9D6ACD9B2Q37701708-72859845-9473-418D-B8E2-4A0A4C733839Q37882392-6154E18F-73F3-44BD-A6FE-2CC94A4F3C70Q37921677-3B9893A7-2715-4562-886F-49D90BBADFADQ38084631-BB9178B6-3768-4BB2-B281-B9FFD610F4B5Q38239799-3178C7BD-6AF9-4203-A50E-D39C8C0D79E3Q38746656-5308E5C0-61E3-448B-90D6-A3FBEA14D1B8Q38748591-ECA03E03-CC3F-4675-A6A2-3FDDCF6D16E3Q39363477-B3E40210-DF86-41C2-AF2F-D8FF4D2BB572Q39396806-4C45A63F-C205-4C0E-83ED-6EEC106154A8Q39527969-DAF3B39C-D957-462D-9903-646F52C52BFDQ39789933-6F99F9C4-F62B-463C-A482-8D43242F3115Q40786331-61B357F2-53A5-4C11-B6CA-291B31BAB3DAQ41509991-A67CF3CC-7D1D-4A1E-A7B6-8DFDC2C90EBAQ41546549-492AAA7A-9797-464D-BFC7-29FF45A8719FQ41763256-D45A9F96-2A7C-468D-B1EF-05367B9B8002Q41830350-D582D895-A206-4564-83C1-136C04EA80EDQ41953091-6E54EDEC-6DC3-42C6-A153-21CC4F038DB7Q42293000-10AD1CD1-F708-4579-B560-51DA142E10AD
P2860
Atpenins, potent and specific inhibitors of mitochondrial complex II (succinate-ubiquinone oxidoreductase).
description
2003 nî lūn-bûn
@nan
2003 թուականի Յունուարին հրատարակուած գիտական յօդուած
@hyw
2003 թվականի հունվարին հրատարակված գիտական հոդված
@hy
2003年の論文
@ja
2003年論文
@yue
2003年論文
@zh-hant
2003年論文
@zh-hk
2003年論文
@zh-mo
2003年論文
@zh-tw
2003年论文
@wuu
name
Atpenins, potent and specific ...... te-ubiquinone oxidoreductase).
@ast
Atpenins, potent and specific ...... te-ubiquinone oxidoreductase).
@en
Atpenins, potent and specific ...... te-ubiquinone oxidoreductase).
@nl
type
label
Atpenins, potent and specific ...... te-ubiquinone oxidoreductase).
@ast
Atpenins, potent and specific ...... te-ubiquinone oxidoreductase).
@en
Atpenins, potent and specific ...... te-ubiquinone oxidoreductase).
@nl
prefLabel
Atpenins, potent and specific ...... te-ubiquinone oxidoreductase).
@ast
Atpenins, potent and specific ...... te-ubiquinone oxidoreductase).
@en
Atpenins, potent and specific ...... te-ubiquinone oxidoreductase).
@nl
P2093
P2860
P356
P1476
Atpenins, potent and specific ...... te-ubiquinone oxidoreductase).
@en
P2093
Arihiro Osanai
Hideaki Ui
Hideto Miyoshi
Hiroko Miyadera
Hiroshi Tomoda
Kazuro Shiomi
Rokuro Masuma
Yuichi Yamaguchi
P2860
P304
P356
10.1073/PNAS.0237315100
P407
P577
2003-01-06T00:00:00Z