Cys | |
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Salts [] | |
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Cysteine monohydrate | |
Cysteine hydrochloride | |
Esters [] | |
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Cysteine acetate | |
Molecular structure via molpic | |
Conformer structure via 3Dmol.js | |
Molecular formula | C3H7NO2S |
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Molecular mass | 121.16 g/mol |
Predicted LogP | -2.5 |
Chirality | racemic |
Identifiers [] | |
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IUPAC name | 2-amino-3-sulfanylpropanoic acid |
SMILES | C(C(C(=O)O)N)S |
InChI | InChI=1S/C3H7NO2S/c4-2(1-7)3(5)6/h2,7H,1,4H2,(H,5,6) |
InChIKey | XUJNEKJLAYXESH-UHFFFAOYSA-N |
Dosing |
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Cysteine
(Redirected from L-Cysteine)
Cysteine (also known as DL-Cysteine, 2-Amino-3-mercaptopropanoic acid, DL-Cystein, Cysteine, dl-, (+/-)-2-Amino-3-mercaptopropionic acid, 150146-94-4, L-hsch2ch(nh2)cooh, H-Cys-OH HCl HO, Ncgc00160365-01 or (+-)-Cysteine) is a substance of the amino acid class.
Chemistry
Cysteine is typically found in the form of its monohydrate and hydrochloride salts or its acetate ester.
Stereochemistry
DL-Cysteine is a racemic mixture of the logical stereoisomers:Stereoisomers [] | ||
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D-Cysteine | L-Cysteine | DL-Cysteine |
See also
External links
- Cysteine (Wikipedia)
- Cysteine / D-Cysteine / L-Cysteine (Wikidata)
- Cysteine / D-Cysteine / L-Cysteine (PubChem)
- Cysteine / D-Cysteine / L-Cysteine (ChEMBL)
- Cysteine / D-Cysteine / L-Cysteine (ChEBI)
- Cysteine / D-Cysteine / L-Cysteine (Common Chemistry)
- Cysteine / D-Cysteine / L-Cysteine (HMDB)
- Cysteine / D-Cysteine / L-Cysteine (KEGG)
- Cysteine / D-Cysteine / L-Cysteine (UNII)
- Cysteine / D-Cysteine / L-Cysteine (EPA DSSTox)