MSE
SELENOMETHIONINE
Find entries where: MSE
is present as a standalone ligand in 20 entries
is present in a polymer sequence 10,166 entries
Chemical Component Summary | |
|---|---|
| Name | SELENOMETHIONINE |
| Identifiers | (2S)-2-amino-4-methylselanyl-butanoic acid |
| Formula | C5 H11 N O2 Se |
| Molecular Weight | 196.106 |
| Type | L-PEPTIDE LINKING |
| Isomeric SMILES | C[Se]CC[C@@H](C(=O)O)N |
| InChI | InChI=1S/C5H11NO2Se/c1-9-3-2-4(6)5(7)8/h4H,2-3,6H2,1H3,(H,7,8)/t4-/m0/s1 |
| InChIKey | RJFAYQIBOAGBLC-BYPYZUCNSA-N |
Chemical Details | |
|---|---|
| Formal Charge | 0 |
| Atom Count | 20 |
| Chiral Atom Count | 1 |
| Bond Count | 19 |
| Aromatic Bond Count | 0 |
Drug Info: DrugBank
| DrugBank ID | DB11142 |
|---|---|
| Name | Selenomethionine |
| Groups |
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| Description | Selenomethionine is a naturally occuring amino acid in some plant materials such as cereal grains, soybeans and enriched yeast but it cannot be synthesized from animals or humans. It can be produced from post-structural modifications. *In vivo*, selenomethionine plays an essential role in acting as an antioxidant, where it depletes reactive oxygen species (ROS) and aids in the formation and recycling of glutathione, another important antioxidant. In comparison to selenite, which is the inorganic form of selenium, the organic form of selenomethionine is more readily absorbed in the human body. Selenomethionin is used in biochemical laboratories where its incorporation into proteins that need to be visualized enhances the performance of X-ray crystallography. |
| Synonyms | Selenomethionine |
| Brand Names |
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| Categories |
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| CAS number | 3211-76-5 |
Related Resource References
| Resource Name | Reference |
|---|---|
| PubChem | 53262363, 105024 |
| ChEMBL | CHEMBL113178 |
| ChEBI | CHEBI:62621, CHEBI:30021 |
| CCDC/CSD | MAJTAT |
