2922-56-7
2922-56-7
Chemical Structure
S-Methylglutathione
- CAS No.: 2922-56-7
- Formula:C11H19N3O6S
- Molecular Weight:321.35
IUPAC Name: N5-((R)-1-((carboxymethyl)amino)-3-(methylthio)-1-oxopropan-2-yl)-L-glutamine
InChIKey: QTQDDTSVRVWHMO-BQBZGAKWSA-N
SMILES: O=C(O)CNC([C@H](CSC)NC(CC[C@@H](C(O)=O)N)=O)=O
Biological Activity: S-Methylglutathione is an S-substitued glutathione and a stronger nucleophile than GSH[1]. S-Methylglutathione has inhibitory effect on glyoxalase 1[2].
| Cat. No. | Product Name | Purity | Description | Pricing | |||||||||||||||||||
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S-Methylglutathione | 99.40% | S-Methylglutathione is an S-substitued glutathione and a stronger nucleophile than GSH. S-Methylglutathione has inhibitory effect on glyoxalase 1. | ||||||||||||||||||||
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Structural Analogs
-
Similarity Score 0.91
HY-131390S-Ethylglutathione -
Similarity Score 0.89
HY-131944S-Acetylglutathione -
Similarity Score 0.88
HY-D0187RL-Glutathione reduced (Standard) -
Similarity Score 0.88
HY-D0187SL-Glutathione reduced-13C2,15N -
Similarity Score 0.87
HY-126752Ophthalmic acid -
Similarity Score 0.86
HY-D0845Nitrosoglutathione -
Similarity Score 0.86
HY-14943Darinaparsin -
Similarity Score 0.81
HY-P4450Homoglutathione -
Similarity Score 0.81
HY-W614632γ-Glu-Val-Gly -
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References
- [1]. Foye WO, et al. Synthesis and evaluation of N-alkanoyl-S-benzyl-L-cysteinylglutamic acid esters as glyoxalase I inhibitors and anticancer agents. J Pharm Sci. 1984 Apr;73(4):559-61. [Content Brief]
- [2]. Milos I. Djuran,et al. Reactivity of chloro- and aqua(diethylenetriamine)platinum(II) ions with glutathione, S-methylglutathione, and guanosine 5'-monophosphate in relation to the antitumor activity and toxicity of platinum complexes. Inorg. Chem. 1991, 30, 12, 2648–2652
