GLUD1 inhibitors belong to a chemical class characterized by their ability to selectively target and inhibit the activity of the enzyme glutamate dehydrogenase 1 (GLUD1). Glutamate dehydrogenase is an enzyme involved in cellular metabolism, specifically in the conversion of glutamate to alpha-ketoglutarate. GLUD1 is a specific isoform of this enzyme found predominantly in the mitochondria of certain tissues, including the brain, liver, and pancreas. The primary function of GLUD1 is to regulate the interconversion of glutamate and alpha-ketoglutarate, thereby playing a crucial role in the balance of cellular energy metabolism. GLUD1 inhibitors exert their effects by binding to the active site of the enzyme and modulating its catalytic activity, leading to a reduction in the rate of glutamate conversion. This inhibition of GLUD1 activity has downstream implications for various cellular processes, such as neurotransmitter homeostasis, glucose metabolism, and nitrogen balance. By interfering with the activity of GLUD1, these inhibitors can potentially alter the cellular metabolic profile and affect the levels of key metabolites involved in energy production and neurotransmission.
The development and study of GLUD1 inhibitors provide valuable insights into the intricate mechanisms governing cellular metabolism. By selectively inhibiting GLUD1, researchers can explore the functional significance of this enzyme and its potential involvement in various physiological and pathological conditions. Moreover, GLUD1 inhibitors have the potential to serve as useful tools in the investigation of glutamate-related processes and may contribute to a better understanding of metabolic dysregulation in certain diseases. Overall, GLUD1 inhibitors constitute a chemical class of compounds that specifically target and inhibit the activity of the GLUD1 enzyme. Through their modulation of glutamate metabolism, these inhibitors have the potential to shed light on the intricate interplay between cellular energy balance and neurotransmitter regulation. Further research into GLUD1 inhibitors may unveil their broader implications and applications in the context of cellular metabolism and pathophysiology.
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Product Name | CAS # | Catalog # | QUANTITY | Price | Citations | RATING |
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Isoniazid | 54-85-3 | sc-205722 sc-205722A sc-205722B | 5 g 50 g 100 g | $25.00 $99.00 $143.00 | ||
Originally developed as an anti-tuberculosis agent in research, isoniazid has also been found to inhibit GAD1 activity. It is studied in the research of neurological disorders such as epilepsy and neuropathic pain. | ||||||
3-Mercaptopropionic acid | 107-96-0 | sc-256523 sc-256523A | 5 g 100 g | $37.00 $39.00 | ||
3-MPA is another irreversible inhibitor of GADIt acts by binding to the enzyme and disrupting its activity. | ||||||
Valproic Acid | 99-66-1 | sc-213144 | 10 g | $85.00 | 9 | |
Valproic acid is an anticonvulsant and mood stabilizer studied in the research of epilepsy and bipolar disorder. It has been shown to inhibit GAD1 activity, leading to increased GABA levels. | ||||||
Gabapentin | 60142-96-3 | sc-201481 sc-201481A sc-201481B | 20 mg 100 mg 1 g | $52.00 $92.00 $132.00 | 7 | |
Gabapentin is an anticonvulsant agent in research that is structurally related to GABA. Studies show that it modulates GABA synthesis by inhibiting GAD1. |