Threo-Pentaric acid, 3-carboxy-2,3-dideoxy-4-C-methyl- is a chemical compound characterized by its unique structure, which includes multiple functional groups that contribute to its reactivity and properties. This compound features a carboxylic acid group, which typically imparts acidic characteristics, allowing it to participate in various chemical reactions, such as esterification and neutralization. The presence of dideoxy and C-methyl groups suggests that it may exhibit specific stereochemical configurations, influencing its biological activity and interactions with enzymes or receptors. Additionally, the compound's molecular structure may affect its solubility in different solvents, stability under various conditions, and potential applications in pharmaceuticals or biochemistry. As a compound with a specific CAS number, it is cataloged in chemical databases, facilitating research and development in related fields. Overall, threo-Pentaric acid, 3-carboxy-2,3-dideoxy-4-C-methyl- is of interest for its potential applications and the insights it may provide into the chemistry of similar compounds.

threo-Pentaric acid, 3-carboxy-2,3-dideoxy-4-C-methyl-

71183-66-9: DL-threo-Pentaric acid, 3-carboxy-2,3-dideoxy-4-C-methyl-, threo-Pentaric acid, 3-carboxy-2,3-dideoxy-4-C-methyl-

dl-threo-2-methylisocitrate, substrate for ICL1, has Km of ~752µM, kcat of 1.25s^-1; higher Km and lower kcat than ICA.

DL-threo-2-methylisocitrate

DL-threo-2-methylisocitrate sodium salt is an enzyme substrate for isocitrate lyase 1 (ICL1), an enzyme involved in the glyoxylate cycle, a metabolic pathway that allows organisms to convert acetate into glucose. It is also a substrate for bovine heart aconitase and acts as inhibitor of TPN-linked isocitrate dehydrogenase.

CAS 71183-66-9: threo-Pentaric acid, 3-carboxy-2,3-dideoxy-4-C-methyl-

DL-threo-2-methylisocitrate

Ref: TM-T19292

DL-threo-2-methylisocitrate sodium salt

Ref: 3D-WCA18366