γ-Glu-Cys
Substrate used for the biosynthesis of L-glutathione by glutathione synthetase(s)
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| CAT# | CP27730 |
| Chemical Structure |  |
| CAS | 636-58-8 |
| Synonyms/Alias | Gamma-L-glutamyl-L-cysteine; gamma-Glu-Cys; gamma-Glutamylcysteine |
| Chemical Name | (2S)-2-amino-5-[[(1R)-1-carboxy-2-sulfanylethyl]amino]-5-oxopentanoic acid |
| M.F/Formula | C8H14N2O5S |
| M.W/Mr. | 250.27 |
| Sequence | H-γ-Glu-Cys-OH |
| Application | Di- and Tripeptides |
| Biological Activity | γ-Glu-Cys is produced by cleaving the Cys-Gly peptide bond of glutathione. It is also necessary for the formation of phytochelins, which are cysteine-rich thiol-reactive peptides. |
| Storage | Store at -20°C |
Solubility | ≥25mg/mL in H2O, ≥52 mg/mL in DMSO, ≥54.8 mg/mL in EtOH |
Shipping Condition | Evaluation sample solution: ship with blue ice. All other available sizes: ship with RT, or blue ice upon request. |
InChI | InChI=1S/C8H14N2O5S/c9-4(7(12)13)1-2-6(11)10-5(3-16)8(14)15/h4-5,16H,1-3,9H2,(H,10,11)(H,12,13)(H,14,15)/t4-,5-/m0/s1 |
InChI Key | RITKHVBHSGLULN-WHFBIAKZSA-N |
Canonical SMILES | C(CC(=O)NC(CS)C(=O)O)C(C(=O)O)N |
Isomeric SMILES | C(CC(=O)N[C@@H](CS)C(=O)O)[C@@H](C(=O)O)N |
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