L-(+)-Ergothioneine
CAS No. 497-30-3
L-(+)-Ergothioneine( Ergothioneine )
Catalog No. M21510 CAS No. 497-30-3
Ergothioneine is synthesized by certain bacteria and fungi. It is generally considered an antioxidant.
Purity : >98% (HPLC)
COA
Datasheet
HNMR
HPLC
MSDS
Handing Instructions
| Size | Price / USD | Stock | Quantity |
| 10MG | 70 | Get Quote |
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| 25MG | 141 | Get Quote |
|
| 50MG | 267 | Get Quote |
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| 100MG | Get Quote | Get Quote |
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| 200MG | Get Quote | Get Quote |
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| 500MG | Get Quote | Get Quote |
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| 1G | Get Quote | Get Quote |
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Biological Information
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Product NameL-(+)-Ergothioneine
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NoteResearch use only, not for human use.
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Brief DescriptionErgothioneine is synthesized by certain bacteria and fungi. It is generally considered an antioxidant.
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DescriptionErgothioneine is synthesized by certain bacteria and fungi. It is generally considered an antioxidant.
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In VitroCell Viability Assay Cell Line:PC12 Concentration:0.25, 1 mM Incubation Time:23 h Result:Increased cell viability by approximately 13% and 34%, respectively.Western Blot Analysis Cell Line:PC12 Concentration:0.25, 1 mM Incubation Time:23 h Result:Counteracted the p38 phosphorylation induced by 1 h incubation with H2O2.
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In VivoAnimal Model:Cisplatin-treated ratsDosage:70 mg/kg Administration:p.o.Result:Decreased serum creatinine and BUN.Increased GFR at two-fold.Suppressed cisplatin-induced oxidative stress and GCT.Up-regulated the levels of Nrf2, NQO1, and HO-1. Suppresses NF-κB signaling and the pro-inflammatory cytokines.
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SynonymsErgothioneine
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PathwayOthers
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TargetAntioxidant
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RecptorAntioxidant
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Research Area——
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Indication——
Chemical Information
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CAS Number497-30-3
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Formula Weight229.3
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Molecular FormulaC9H15N3O2S
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Purity>98% (HPLC)
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SolubilityH2O:125 mg/mL (545.14 mM; Need ultrasonic)
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SMILESC[N+](C)(C)[C@@H](Cc1c[nH]c(=S)[nH]1)C([O-])=O
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Chemical Name(S)-3-(2-thioxo-23-dihydro-1H-imidazol-4-yl)-2-(trimethylammonio)propanoate
Shipping & Storage Information
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Storage(-20℃)
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ShippingWith Ice Pack
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Stability≥ 2 years
Reference
1.Oumari M et al. Regeneration of ergothioneine after reaction with singlet oxygen. Free Radic Biol Med. 2019 Apr;134:498-504.
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