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Record Information |
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| Version |
1.0 |
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| Update Date |
1/22/2018 12:54:54 PM |
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Metabolite ID | PAMDB120099 |
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Identification |
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| Name: |
glutathioselenol |
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| Description: | A glutathione derivative that is glutathione in which the hydrogen attached to the sulfur is replaced by a selenol group. |
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Structure |
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| Synonyms: | - GSSeH
- selenoglutathione persulfide
- selenoglutathione
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Chemical Formula: |
C10H16N3O6SSE |
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| Average Molecular Weight: |
384.265 |
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| Monoisotopic Molecular
Weight: |
388.00815 |
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| InChI Key: |
UUYVRXVWXDDDGX-UHFFFAOYSA-M |
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| InChI: | InChI=1S/C10H17N3O6SSe/c11-5(10(18)19)1-2-7(14)13-6(4-20-21)9(17)12-3-8(15)16/h5-6,21H,1-4,11H2,(H,12,17)(H,13,14)(H,15,16)(H,18,19)/p-1 |
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| CAS
number: |
Not Available |
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| IUPAC Name: | L-γ-glutamyl-S-selanyl-L-cysteinylglycine |
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Traditional IUPAC Name: |
Not Available |
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| SMILES: | C(S[Se])C(NC(=O)CCC([N+])C(=O)[O-])C(=O)NCC(=O)[O-] |
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Chemical Taxonomy |
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Taxonomy Description | This compound 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. |
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Kingdom |
Organic compounds |
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| Super Class | Organic acids and derivatives |
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Class |
Carboxylic acids and derivatives |
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| Sub Class | Amino acids, peptides, and analogues |
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Direct Parent |
Oligopeptides |
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| Alternative Parents |
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| Substituents |
- Alpha-oligopeptide
- Gamma-glutamyl alpha peptide
- Glutamine or derivatives
- N-acyl-alpha amino acid or derivatives
- N-acyl-alpha-amino acid
- Alpha-amino acid amide
- Cysteine or derivatives
- N-substituted-alpha-amino acid
- Alpha-amino acid or derivatives
- N-acyl-amine
- Fatty acyl
- Fatty amide
- Fatty acid
- Dicarboxylic acid or derivatives
- Carboxamide group
- Secondary carboxylic acid amide
- Carboxylic acid salt
- Carboxylic acid
- Sulfenyl compound
- Organosulfur compound
- Organic nitrogen compound
- Organic salt
- Hydrocarbon derivative
- Organic oxide
- Carbonyl group
- Organopnictogen compound
- Organic oxygen compound
- Organooxygen compound
- Organonitrogen compound
- Organic anion
- Aliphatic acyclic compound
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| Molecular Framework |
Aliphatic acyclic compounds |
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| External Descriptors |
Not Available |
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Physical Properties |
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| State: |
Not Available |
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| Charge: | 0 |
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Melting point: |
Not Available |
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| Experimental Properties: |
Not Available |
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| Predicted Properties |
Not Available |
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Biological Properties |
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| Cellular Locations: |
Not Available |
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| Reactions: | |
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Pathways: |
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Spectra |
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| Spectra: |
Not Available |
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References |
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| References: |
- Turner RJ, Weiner JH, Taylor DE (1998)Selenium metabolism in Escherichia coli. Biometals : an international journal on the role of metal ions in biology, biochemistry, and medicine 11, Pubmed: 9850565
- Hsieh HS, Ganther HE (1975)Acid-volatile selenium formation catalyzed by glutathione reductase. Biochemistry 14, Pubmed: 235962
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| Synthesis Reference: |
Not Available |
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| Material Safety Data Sheet (MSDS) |
Not Available |
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Links |
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| External Links: |
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