PLP-E inhibitors are a class of chemical compounds that specifically target pyridoxal phosphate-dependent enzyme E (PLP-E), a member of the PLP-dependent family of enzymes that rely on pyridoxal 5'-phosphate (PLP), the active form of vitamin B6, as a crucial cofactor. PLP-E is involved in catalyzing important biochemical reactions, particularly those associated with amino acid metabolism, such as transamination, decarboxylation, and racemization. These enzymatic processes are essential for the transformation and synthesis of amino acids, which are the building blocks of proteins and play key roles in metabolic regulation, signaling pathways, and energy production. Inhibiting PLP-E disrupts these reactions, leading to alterations in amino acid homeostasis and the various cellular processes that depend on proper amino acid metabolism.
The action of PLP-E inhibitors works by binding to the active site of the enzyme or interfering with its interaction with pyridoxal phosphate, thus preventing the enzyme from carrying out its catalytic functions. This inhibition affects a variety of cellular pathways, particularly those that require the precise modification and utilization of amino acids, such as protein synthesis, nitrogen balance, and neurotransmitter production. PLP-E inhibitors serve as valuable tools in biochemical research, allowing scientists to study the specific role of PLP-E in amino acid metabolism and to investigate how disruptions in this process affect overall cellular function. By blocking PLP-E activity, researchers gain insights into the broader role of PLP-dependent enzymes in maintaining cellular homeostasis, uncovering their contributions to metabolic regulation, signaling cascades, and the intricate processes that govern cell growth and function.
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| Product Name | CAS # | Catalog # | QUANTITY | Price | Citations | RATING |
|---|---|---|---|---|---|---|
Actinomycin D | 50-76-0 | sc-200906 sc-200906A sc-200906B sc-200906C sc-200906D | 5 mg 25 mg 100 mg 1 g 10 g | $73.00 $238.00 $717.00 $2522.00 $21420.00 | 53 | |
Actinomycin D inhibits RNA synthesis, potentially impacting the expression of PRL7A1 at the transcriptional level. | ||||||
Triptolide | 38748-32-2 | sc-200122 sc-200122A | 1 mg 5 mg | $88.00 $200.00 | 13 | |
Triptolide inhibits RNA polymerase and NF-κB, potentially affecting the transcription of PRL7A1 and its regulatory pathways. | ||||||
Flavopiridol | 146426-40-6 | sc-202157 sc-202157A | 5 mg 25 mg | $78.00 $254.00 | 41 | |
Flavopiridol inhibits cyclin-dependent kinases, potentially affecting the transcriptional regulation of PRL7A1 and its associated pathways. | ||||||
Triamcinolone acetonide | 76-25-5 | sc-205872 sc-205872A | 50 mg 250 mg | $56.00 $149.00 | ||
Triamcinolone acetonide is a glucocorticoid receptor agonist, and its modulation of transcriptional activity may impact the expression of PRL7A1. | ||||||
α-Amanitin | 23109-05-9 | sc-202440 sc-202440A | 1 mg 5 mg | $260.00 $1029.00 | 26 | |
α-Amanitin inhibits RNA polymerase II, potentially impacting the transcription of PRL7A1 and its downstream targets. | ||||||
Trichostatin A | 58880-19-6 | sc-3511 sc-3511A sc-3511B sc-3511C sc-3511D | 1 mg 5 mg 10 mg 25 mg 50 mg | $149.00 $470.00 $620.00 $1199.00 $2090.00 | 33 | |
Trichostatin A is a histone deacetylase inhibitor, potentially impacting the epigenetic regulation of PRL7A1 expression. | ||||||
Ellipticine | 519-23-3 | sc-200878 sc-200878A | 10 mg 50 mg | $142.00 $558.00 | 4 | |
Ellipticine is a DNA-intercalating agent, potentially impacting the transcriptional regulation of PRL7A1 and its associated pathways. | ||||||