CAS 57836-11-0

(2S)-4-amino-2-[methyl(N-methylglycyl)amino]-3-oxobutanoic acid

Description:

(2S)-4-amino-2-[methyl(N-methylglycyl)amino]-3-oxobutanoic acid, also known by its CAS number 57836-11-0, is an amino acid derivative characterized by its complex structure that includes an amino group, a ketone functional group, and a side chain containing a methylated glycine moiety. This compound is a chiral molecule, with the (2S) designation indicating its specific stereochemistry. It is soluble in water due to the presence of polar functional groups, which enhances its interaction with biological systems. The presence of both amino and carboxylic acid groups allows it to participate in various biochemical reactions, making it relevant in the study of metabolic pathways and protein synthesis. Its unique structure may also contribute to its potential role as a biochemical marker or therapeutic agent. Overall, this compound exemplifies the complexity and diversity of amino acid derivatives in biochemistry.

Formula: C₈H₁₅N₃O₄

InChI: InChI=1/C8H15N3O4/c1-10-4-6(13)11(2)7(8(14)15)5(12)3-9/h7,10H,3-4,9H2,1-2H3,(H,14,15)/t7-/m0/s1

SMILES: CNCC(=O)N(C)[C@@H](C(=O)CN)C(=O)O

H-Gly-Sar-Sar-OH

CAS: 57836-11-0

Bachem ID: 4013914.

Formula: C₈H₁₅N₃O₄

Purity: > 99%

Color and Shape: White Powder

Molecular weight: 217.22

Ref: 01-4013914

H-Gly-Sar-Sar-OH

CAS: 57836-11-0

H-Gly-Sar-Sar-OH is an amide that is a prodrug for the antibiotic Glycylcycline. This drug has been shown to inhibit peptidases and transport in caco-2 cells, as well as to have affinity for intestinal peptidases. H-Gly-Sar-Sar-OH has also been shown to be able to penetrate the cell membrane and inhibit peptidase activity in extracellular space. The bond cleavage of this drug has been rationalized by comparing it with other bioisosteres.

Formula: C₈H₁₅N₃O₄

Purity: Min. 95%

Molecular weight: 217.22 g/mol

Ref: 3D-FG109917