| Name | 2-[(2-amino-4-methylsulfanylbutanoyl)amino]-4-methylpentanoic acid |
|---|---|
| Synonyms |
H-MET-LEU-OH
L-Met-L-Leu L-METHIONYL-L-LEUCINE L-MET-LEU MET-LEU MET-LEU CRYSTALLINE L-Leucine, L-Methionyl (S)-2-((S)-2-Amino-4-(methylthio)butanamido)-4-methylpentanoic acid Protein (human clone US2003/0049618-SEQID-546 secreted protein sequence homolog) |
| Description | (S)-2-((S)-2-Amino-4-(methylthio)butanamido)-4-methylpentanoic acid is a leucine derivative[1]. |
|---|---|
| Related Catalog | |
| In Vitro | Amino acids and amino acid derivatives have been commercially used as ergogenic supplements. They influence the secretion of anabolic hormones, supply of fuel during exercise, mental performance during stress related tasks and prevent exercise induced muscle damage. They are recognized to be beneficial as ergogenic dietary substances[1]. |
| References |
| Molecular Formula | C11H22N2O3S |
|---|---|
| Molecular Weight | 262.36900 |
| Exact Mass | 262.13500 |
| PSA | 117.72000 |
| LogP | 1.77350 |
| RIDADR | NONH for all modes of transport |
|---|---|
| WGK Germany | 3 |
|
~%
14486-16-9 |
| Literature: Organic and Biomolecular Chemistry, , vol. 9, # 7 p. 2327 - 2335 |
|
~%
14486-16-9 |
| Literature: Organic and Biomolecular Chemistry, , vol. 9, # 7 p. 2327 - 2335 |
|
~%
14486-16-9 |
| Literature: Bioorganic Chemistry, , vol. 29, # 4 p. 211 - 222 |
| Precursor 4 | |
|---|---|
| DownStream 2 | |