rBAT inhibitors are a class of chemical compounds that specifically target and inhibit the function of the rBAT (related to b0,+ amino acid transporter) protein, which plays a crucial role in amino acid transport across cellular membranes. rBAT, also known as SLC3A1, is part of a heterodimeric transporter complex that works in conjunction with another protein, b0,+AT, to mediate the exchange of neutral and basic amino acids in the kidney and intestine. This transporter is involved in the reabsorption and uptake of essential amino acids such as cystine, lysine, and arginine. By facilitating the transport of these molecules across the epithelial cells of the kidney and intestine, rBAT ensures the proper balance of amino acids in the body and supports crucial metabolic functions. Inhibitors of rBAT interfere with its ability to transport amino acids by binding to specific regions of the protein, thereby disrupting its normal transport activity.
The inhibition of rBAT leads to a disruption in the transport and reabsorption of certain amino acids, particularly those that are essential for various physiological processes. By blocking rBAT's function, these inhibitors prevent the proper exchange and balance of amino acids in cells, potentially causing changes in cellular metabolism. Researchers use rBAT inhibitors to study the specific role of this protein in amino acid homeostasis and to explore how defects in amino acid transport can affect metabolic and physiological pathways. These inhibitors are valuable tools for understanding the intricate mechanisms of membrane transporters and the regulation of amino acid levels in tissues such as the kidneys and intestines. Additionally, rBAT inhibitors provide insights into the broader family of solute carrier proteins, revealing how amino acid transport is coordinated across different organs and how this process impacts overall metabolic balance. Through studying rBAT inhibitors, scientists gain a deeper understanding of the molecular mechanisms governing amino acid transport and its significance in maintaining cellular and organismal homeostasis.
| Product Name | CAS # | Catalog # | QUANTITY | Price | Citations | RATING |
|---|---|---|---|---|---|---|
N-Ethylmaleimide | 128-53-0 | sc-202719A sc-202719 sc-202719B sc-202719C sc-202719D | 1 g 5 g 25 g 100 g 250 g | $22.00 $69.00 $214.00 $796.00 $1918.00 | 19 | |
An alkylating agent that can modify cysteine residues on proteins, potentially affecting transporter function. | ||||||
Phloretin | 60-82-2 | sc-3548 sc-3548A | 200 mg 1 g | $64.00 $255.00 | 13 | |
A dihydrochalcone that is known to inhibit various glucose transporters, which could affect amino acid transport indirectly. | ||||||
Probenecid | 57-66-9 | sc-202773 sc-202773A sc-202773B sc-202773C | 1 g 5 g 25 g 100 g | $28.00 $39.00 $100.00 $277.00 | 28 | |
An inhibitor of anion transporters that could non-specifically affect other transporter systems. | ||||||
Quercetin | 117-39-5 | sc-206089 sc-206089A sc-206089E sc-206089C sc-206089D sc-206089B | 100 mg 500 mg 100 g 250 g 1 kg 25 g | $11.00 $17.00 $110.00 $250.00 $936.00 $50.00 | 33 | |
A flavonoid that has been shown to inhibit a wide range of transporters and ion channels. | ||||||
Amiloride • HCl | 2016-88-8 | sc-3578 sc-3578A | 25 mg 100 mg | $22.00 $57.00 | 6 | |
A diuretic that inhibits sodium transport and may indirectly affect sodium-dependent amino acid transporters. | ||||||
2,3-Dichlorobenzoyl chloride | 2905-60-4 | sc-265962 | 5 g | $77.00 | ||
A serine analog that could compete with natural amino acids for transport, thereby inhibiting the system. | ||||||