You are using an unsupported browser. Please upgrade your browser to a newer version to get the best experience on Bovine Metabolome Database.
Showing metabocard for S-Methyl glutathione (BMDB0109752)
| Record Information | |||||||||||||||||
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| Version | 1.0 | ||||||||||||||||
| Creation Date | 2020-05-06 19:45:34 UTC | ||||||||||||||||
| Update Date | 2020-05-07 14:45:02 UTC | ||||||||||||||||
| BMDB ID | BMDB0109752 | ||||||||||||||||
| Secondary Accession Numbers | None | ||||||||||||||||
| Metabolite Identification | |||||||||||||||||
| Common Name | S-Methyl glutathione | ||||||||||||||||
| Description | S-(methyl)glutathione, also known as S-methyl GSH, belongs to the class of organic compounds known as oligopeptides. These are organic compounds containing a sequence of between three and ten alpha-amino acids joined by peptide bonds. S-(methyl)glutathione is a very strong basic compound (based on its pKa). Within cattle, S-(methyl)glutathione participates in a number of enzymatic reactions. In particular, hydrogen bromide and S-(methyl)glutathione can be biosynthesized from bromomethane and glutathione; which is catalyzed by the enzyme glutathione S-transferase omega-2. In addition, S-(methyl)glutathione can be converted into L-glutamic acid and methyl-S-cysteinylglycine; which is catalyzed by the enzyme Gamma-glutamyltransferase 6. In cattle, S-(methyl)glutathione is involved in the metabolic pathway called the glutathione metabolism pathway. | ||||||||||||||||
| Structure |  | ||||||||||||||||
| Synonyms |
| ||||||||||||||||
| Chemical Formula | C11H19N3O6S | ||||||||||||||||
| Average Molecular Weight | 321.35 | ||||||||||||||||
| Monoisotopic Molecular Weight | 321.099456045 | ||||||||||||||||
| IUPAC Name | Not Available | ||||||||||||||||
| Traditional Name | Not Available | ||||||||||||||||
| CAS Registry Number | Not Available | ||||||||||||||||
| SMILES | Not Available | ||||||||||||||||
| InChI Identifier | InChI=1S/C11H19N3O6S/c1-21-5-7(10(18)13-4-9(16)17)14-8(15)3-2-6(12)11(19)20/h6-7H,2-5,12H2,1H3,(H,13,18)(H,14,15)(H,16,17)(H,19,20)/t6-,7-/m0/s1 | ||||||||||||||||
| InChI Key | QTQDDTSVRVWHMO-BQBZGAKWSA-N | ||||||||||||||||
| Chemical Taxonomy | |||||||||||||||||
| Description | belongs to the class of organic compounds known as oligopeptides. These are organic compounds containing a sequence of between three and ten alpha-amino acids joined by peptide bonds. | ||||||||||||||||
| Kingdom | Organic compounds | ||||||||||||||||
| Super Class | Organic acids and derivatives | ||||||||||||||||
| Class | Carboxylic acids and derivatives | ||||||||||||||||
| Sub Class | Amino acids, peptides, and analogues | ||||||||||||||||
| Direct Parent | Oligopeptides | ||||||||||||||||
| Alternative Parents |
| ||||||||||||||||
| Substituents |
| ||||||||||||||||
| Molecular Framework | Aliphatic acyclic compounds | ||||||||||||||||
| External Descriptors |
| ||||||||||||||||
| Ontology | |||||||||||||||||
| Status | Detected but not Quantified | ||||||||||||||||
| Origin | Not Available | ||||||||||||||||
| Biofunction | Not Available | ||||||||||||||||
| Application | Not Available | ||||||||||||||||
| Cellular locations | Not Available | ||||||||||||||||
| Physical Properties | |||||||||||||||||
| State | Not Available | ||||||||||||||||
| Experimental Properties |
| ||||||||||||||||
| Predicted Properties | Not Available | ||||||||||||||||
| Spectra | |||||||||||||||||
| Spectra |
| ||||||||||||||||
| Biological Properties | |||||||||||||||||
| Cellular Locations | Not Available | ||||||||||||||||
| Biospecimen Locations |
| ||||||||||||||||
| Pathways |
| ||||||||||||||||
| Normal Concentrations | |||||||||||||||||
| |||||||||||||||||
| Abnormal Concentrations | |||||||||||||||||
| Not Available | |||||||||||||||||
| External Links | |||||||||||||||||
| HMDB ID | HMDB0061366 | ||||||||||||||||
| DrugBank ID | DB04701 | ||||||||||||||||
| Phenol Explorer Compound ID | Not Available | ||||||||||||||||
| FooDB ID | Not Available | ||||||||||||||||
| KNApSAcK ID | Not Available | ||||||||||||||||
| Chemspider ID | Not Available | ||||||||||||||||
| KEGG Compound ID | C11347 | ||||||||||||||||
| BioCyc ID | S-METHYLGLUTATHIONE | ||||||||||||||||
| BiGG ID | Not Available | ||||||||||||||||
| Wikipedia Link | Not Available | ||||||||||||||||
| METLIN ID | Not Available | ||||||||||||||||
| PubChem Compound | 115260 | ||||||||||||||||
| PDB ID | Not Available | ||||||||||||||||
| ChEBI ID | 141472 | ||||||||||||||||
| References | |||||||||||||||||
| Synthesis Reference | Not Available | ||||||||||||||||
| Material Safety Data Sheet (MSDS) | Not Available | ||||||||||||||||
| General References | Not Available | ||||||||||||||||
