Oxaloacetic acid

Oxaloacetic acid, also known as oxosuccinic acid or oxalacetic acid, is a four-carbon dicarboxylic acid appearing as an intermediate of the citric acid cycle. In vivo, oxaloacetate (the ionized form of oxaloacetic acid) is formed by the oxidation of L-mal

Oxaloacetic acid-13C4 is the 13C labeled form of oxaloacetic acid. Oxaloacetic acid (2-Oxosuccinic acid) serves as a metabolic intermediate involved in various pathways, including the citric acid cycle, gluconeogenesis, the urea cycle, the glyoxylate cycle, amino acid synthesis, and fatty acid synthesis.

Oxaloacetic acid (Standard) is a reference standard for research and analysis in studies involving Oxaloacetic acid. Oxaloacetic acid, also known as oxosuccinic acid or oxalacetic acid, is a four-carbon dicarboxylic acid appearing as an intermediate of the citric acid cycle. In vivo, oxaloacetate (the ionized form of oxaloacetic acid) is formed by the oxidation of L-malate, catalyzed by malate dehydrogenase, and reacts with Acetyl-CoA to form citrate, catalyzed by citrate synthase.(wikipedia) A class of ketodicarboxylic acids derived from oxalic acid. Oxaloacetic acid is an intermediate in the citric acid cycle and is converted to aspartic acidD by a transamination reaction.

DL-4-Hydroxy-2-ketoglutarate (DL-4KG) is a gamma-keto acid as well as a structural analogue of glutamic acid that functions as a biochemical substrate for enzymes such as 4-hydroxy-2-oxoglutarate aldolase (HOGA1) and glutamic-oxaloacetic transaminase (GOT),DL-4-Hydroxy-2-ketoglutarate also serves as a lysine analogue used in mechanistic studies of enzyme inhibition and metabolic pathways.