Date published: 2025-9-14

1-800-457-3801

SCBT Portrait Logo
Seach Input

MMD2 Activators

MMD2 Activators are a class of chemical compounds that specifically enhance the functional activity of MMD2, a crucial protein involved in the mitochondrial leucine degradation pathway. Several compounds that participate in or influence this process can logically serve as MMD2 activators. For instance, Pyruvate, Acetyl-CoA, and Leucine are compounds that directly participate in the metabolic pathways where MMD2 operates. Pyruvate enhances the Krebs cycle, leading to an increase in Acetyl-CoA, which is a substrate in the leucine degradation pathway, hence enhancing MMD2 activity. Acetyl-CoA directly provides the substrate for the leucine degradation pathway, thus enhancing MMD2 activity, while increased levels of Leucine, being the primary substrate, enhance MMD2 activity byincreasing the rate of the leucine degradation pathway.

Other MMD2 activators, Alpha-Ketoglutarate, Citrate, Oxaloacetate, Coenzyme A (CoA), NADH, Isocitrate, Succinate, Fumarate, and Malate, are compounds that indirectly enhance MMD2 activity by influencing metabolic pathways related to the function of MMD2. Alpha-Ketoglutarate, Citrate, Oxaloacetate, NADH, Isocitrate, Succinate, Fumarate, and Malate all enhance the Krebs cycle, leading to an increase in the production of Acetyl-CoA, which is a substrate in the leucine degradation pathway, potentially leading to enhanced MMD2 activity. CoA, as a central molecule in many metabolic pathways, including the leucine degradation pathway, increases the conversion of 3-methylglutaconyl-CoA to 3-hydroxy-3-methylglutaryl-CoA, thus enhancing MMD2 activity.

SEE ALSO...

Items 11 to 11 of 11 total

Display:

Product NameCAS #Catalog #QUANTITYPriceCitationsRATING

Malic acid

6915-15-7sc-257687
100 g
$127.00
2
(0)

Malate is a component of the Krebs cycle. By enhancing the Krebs cycle, malate can increase the production of Acetyl-CoA, a substrate in the leucine degradation pathway, potentially leading to enhanced MMD2 activity.