Target intelligence / Profile preview

Oxalate production

Molecular classification
Other
01

Overview

Oxalate production" refers to the **metabolic process** by which the body synthesizes **oxalic acid (oxalate)**, primarily in the liver. The terminal steps involve conversion of glyoxylate to oxalate, catalyzed mainly by lactate dehydrogenase (LDH) rather than glycolate oxidase under physiological conditions. This process is modulated by factors such as NADH, lactate, alanine, and the overall metabolic state of hepatocytes. While not itself a molecular target like an enzyme or receptor, dysregulation of this pathway contributes to pathological conditions such as kidney stone formation and primary hyperoxaluria[1]. Thus, therapeutic strategies often focus on inhibiting enzymes involved in this pathway rather than targeting "oxalate production" per se.

02

Biological functions

Metabolic byproduct formationEnd product of glyoxylate metabolismInvolved in hepatic metabolic regulation[1]
03

Disease associations

Other (not a direct target, but oxalate accumulation is implicated in kidney stone disease and primary hyperoxaluria)
04

Safety considerations

Excessive inhibition of oxalate production could disrupt normal metabolism; accumulation leads to nephrolithiasis and systemic oxalosis in certain diseases.
05

Biomarkers

Urinary oxalate concentration (used for monitoring risk of kidney stones and primary hyperoxaluria)

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