Structure of the Ergothioneine-Biosynthesis Amidohydrolase EgtCIn vitro reconstitution of Mycobacterial ergothioneine biosynthesisClinical and biochemical correlates of serum L-ergothioneine concentrations in community-dwelling middle-aged and older adultsConsensus rank orderings of molecular fingerprints illustrate the most genuine similarities between marketed drugs and small endogenous human metabolites [...]Functional characterization of ergothioneine transport by rat organic cation/carnitine transporter Octn1 (slc22a4).The unusual amino acid L-ergothioneine is a physiologic cytoprotectantDietary sources and antioxidant effects of ergothioneine.Antioxidative activity and antidiscoloration efficacy of ergothioneine in mushroom (Flammulina velutipes) extract added to beef and fish meats.Plasma L-ergothioneine measurement by high-performance liquid chromatography and capillary electrophoresis after a pre-column derivatization with 5-iodoacetamidofluorescein (5-IAF) and fluorescence detection.Mechanistic studies of a novel C-S lyase in ergothioneine biosynthesis: the involvement of a sulfenic acid intermediateRegulation of Ergothioneine Biosynthesis and Its Effect on Mycobacterium tuberculosis Growth and InfectivityWide tolerance to amino acids substitutions in the OCTN1 ergothioneine transporter.Food-derived hydrophilic antioxidant ergothioneine is distributed to the brain and exerts antidepressant effect in mice.Ergothioneine, an adaptive antioxidant for the protection of injured tissues? A hypothesis.Ergothioneine Maintains Redox and Bioenergetic Homeostasis Essential for Drug Susceptibility and Virulence of Mycobacterium tuberculosis.Ergothioneine oxidation in the protection against high-glucose induced endothelial senescence: Involvement of SIRT1 and SIRT6.Oxidative-stress detoxification and signalling in cyanobacteria: the crucial glutathione synthesis pathway supports the production of ergothioneine and ophthalmate.Liver ergothioneine accumulation in a guinea pig model of non-alcoholic fatty liver disease. A possible mechanism of defence?Amniotic fluid l-ergothioneine concentrations in pregnant sheep after natural mating and transfer of vitrified/thawed in-vitro produced embryos.The role of dietary ergothioneine in the development of diabetes mellitus.Production of ergothioneine by Methylobacterium species.Mushroom intolerance: a novel diet-gene interaction in Crohn's disease.Ultra-performance liquid chromatographic determination of L-ergothioneine in commercially available classes of cow milk.L-ergothioneine modulates oxidative damage in the kidney and liver of rats in vivo: studies upon the profile of polyunsaturated fatty acids.A Safety Evaluation of a Nature-Identical l-Ergothioneine in Sprague Dawley Rats.L-Ergothioneine scavenges superoxide and singlet oxygen and suppresses TNF-alpha and MMP-1 expression in UV-irradiated human dermal fibroblasts.L-ergothioneine supplementation during culture improves quality of bovine in vitro-produced embryos.Validation of a HILIC Method for the Analysis of Ergothioneine in Fermentation Broth.A mushroom-derived amino acid, ergothioneine, is a potential inhibitor of inflammation-related DNA halogenation.Quantification of L-ergothioneine in whole blood by hydrophilic interaction ultra-performance liquid chromatography and UV-detectionErgothioneine levels in an elderly population decrease with age and incidence of cognitive decline; a risk factor for neurodegeneration?Serum Metabolomics Identifies Altered Bioenergetics, Signaling Cascades in Parallel with Exposome Markers in Crohn's DiseaseQuantification of L-ergothioneine in human plasma and erythrocytes by liquid chromatography-tandem mass spectrometryReproductive safety evaluation of L-Ergothioneine
P921
Q27701026-AF722F29-1244-448F-B773-B1F57B44A4DEQ28501829-4CEDB3E6-2244-4B76-8B73-ABC7D1F651DFQ28538290-265296B8-F537-4534-BC6C-DDD6A395567CQ33957481-7928a810-4065-8cb9-6b71-d526c1f8b287Q34594964-F44F37DD-981C-4308-85E4-901E9C786BA1Q34613774-B50E0DD6-960C-45A1-86FE-2E3ED1703679Q34646899-7478340C-A9D1-444A-A441-ED41280D41C5Q34848103-02CAB9ED-85CA-4EBA-A67C-4F94134DC5DCQ34906980-7256DE7B-E6E2-4663-997F-81EFB45A1CFDQ35824616-DA43E6CC-ECDE-45A0-9040-0411E7500100Q36281665-9B918ADF-8B7D-4B7C-8189-74C58AF1AF16Q36817792-1ED1F481-AAB7-41E0-8461-8068EDABFA9CQ36830164-1226A744-3E55-4CD2-9839-54D582F1EC2AQ38698212-9560982B-0E42-4162-9AB5-DA7B21E9E778Q38802915-25A89A27-7B87-4877-B25E-A58A56B810F5Q39833061-005FCB3D-A0EB-4778-8BD3-89329312763DQ40162381-02CF8431-7648-44F3-B6E5-3017177865CDQ40244113-3F76EA5D-BD5B-4906-B44C-6EE67AFED878Q41600221-BB5E5F87-6954-4F62-BA89-B710BCCFCD27Q41626709-ECE56442-E907-4DAB-A415-FADF749E1863Q41896390-1D6D9F91-DEF0-4280-A1D9-31C34A99BF80Q43297582-244D2CA2-E42F-4FC5-8618-7B56188F8BBCQ43322149-119F10BF-3406-4257-8428-0212AE17D3F3Q44805379-025689DB-A25F-4524-A492-A9589009F3AEQ45036126-3F5B0483-ABEC-4259-AD96-282E9F1CADC9Q45296520-63681F4C-93D8-4437-95F9-FB5BC53F923DQ48565007-1759E9C7-CFD0-4A49-9464-629EAD468DBFQ51487878-D2F6BBFA-D8EB-4880-B882-C4929F038239Q53357013-B6F71C82-9AE8-46BD-9AF4-7C76845C1ABBQ58294574-5DB01C08-0D3A-414E-B50C-D66370A19F9DQ59273889-812FE977-270D-434A-B42B-9BF5ECCA91D8Q64270070-7428D3A0-238E-4551-B554-05B2714AE657Q86392272-4BC54B1D-3FF7-4914-8D66-514C09761CCDQ86863210-565DC30E-4623-4FF9-9755-A79374F35F9A
P921
description
amino acid
@en
chemesch Verbindung
@lb
chemical compound
@en-ca
chemical compound
@en-gb
chemická sloučenina
@cs
chemická zlúčenina
@sk
chemiese verbinding
@af
chemische Verbindung
@de
chemische Verbindung
@de-ch
chemische verbinding
@nl
name
Ergothioneine
@nl
Ergothionéine
@fr
Ergotionein
@sh
Ergotionein
@sr
Ergotioneina
@es
ergothioneine
@en
ergotioneina
@it
ارقوتیونین
@azb
ارگوتیونین
@fa
type
label
Ergothioneine
@nl
Ergothionéine
@fr
Ergotionein
@sh
Ergotionein
@sr
Ergotioneina
@es
ergothioneine
@en
ergotioneina
@it
ارقوتیونین
@azb
ارگوتیونین
@fa
prefLabel
Ergothioneine
@nl
Ergothionéine
@fr
Ergotionein
@sh
Ergotionein
@sr
Ergotioneina
@es
ergothioneine
@en
ergotioneina
@it
ارقوتیونین
@azb
ارگوتیونین
@fa
P361
P486
P6366
P646
P661
P662
P665
P683
P1417
science/ergothioneine
P1579
P2017
C[N+](C)(C)[C@@H](CC1=CNC(=S)N1)C(=O)[O-]
P2057
HMDB0003045
P2067
229.088498
P231
P232
P233
C[N+](C)(C)C(CC1=CNC(=S)N1)C(=O)[O-]
P234
1S/C9H15N3O2S/c1-12(2,3)7(8(13 ...... (H2-,10,11,13,14,15)/t7-/m0/s1