| Weight | 229.305 g/mol |
|---|---|
| Formula | C9H15N3O2S |
| Hydrogen Acceptors | 3 |
| Hydrogen Donors | 2 |
| Aromatic Rings | 1 |
| Rotatable Bonds | 4 |
L-Ergothioneine (497-30-3)
Ergothioneine · Thioneine · 2 Thiol L histidine betaine
Score:
#1850 in Biochemistry
,
#3996 in Biology
,
#5035 in Chemistry
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LabBot
- Discovery of the ergothioneine transporter. (Proceedings of the National Academy of Sciences of the United States of America, 2005)
- Quantification of polyphenols and ergothioneine in cultivated mushrooms and correlation to total antioxidant capacity (Food Chemistry, 2007)
- The antioxidant action of ergothioneine. (Archives of Biochemistry and Biophysics, 1991)
- Ergothioneine; antioxidant potential, physiological function and role in disease. (Biochimica et Biophysica Acta, 2012)
- [32] Ergothioneine as antioxidant (Methods in Enzymology, 1990)
- Dietary sources and antioxidant effects of ergothioneine. (Journal of Agricultural and Food Chemistry, 2007)
-
Predict GHS Hazards for Any Chemical in silico.
Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. - Ergothioneine
- Thioneine
- 2 Thiol L histidine betaine
- 2-Thiol-L-histidine-betaine
-
SMILESC[N+](C)(C)C(CC1=CNC(=S)N1)C(=O)[O-]
-
InChIKeySSISHJJTAXXQAX-UHFFFAOYSA-N
- Pubchem - L-Ergothioneine
- Wikipedia - ergothioneine
Ergothioneine is a naturally occurring amino acid and is a thiourea derivative of histidine, containing a sulfur atom on the imidazole ring. This compound is made in relatively few organisms, notably Actinobacteria, Cyanobacteria, and certain fungi. Ergothioneine was discovered in 1909 and named after the ergot fungus from which it was first purified, with its structure being determined in 1911.
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