MUP6 inhibitors are a class of chemicals that can specifically target and inhibit the activity of the major urinary protein 6 (MUP6). MUP6 is a protein primarily found in the urine of rodents and plays a role in chemical communication and territorial marking. It is involved inthe binding and transport of pheromones, as well as in the regulation of social behaviors. The inhibitors listed above can directly or indirectly inhibit the function of MUP6 by targeting different aspects of its activity. For example, chemicals like 2-Phenylethanol and Sodium azide can directly bind to the active site of MUP6, either by disrupting its structure or interfering with ligand binding. This prevents MUP6 from carrying out its enzymatic activity. Other inhibitors, such as 2,4-Dinitrophenol and Sodium fluoride, target cellular processes that are essential for MUP6 function. They disrupt energy production or phosphorylation, which are crucial for the enzymatic activity of MUP6. Additionally, inhibitors like N-Ethylmaleimide and 3-Bromopyruvate covalently modify key residues or enzymes involved in MUP6's pathway, leading to inhibition of its function. These modifications disrupt the structure or activity of MUP6, impairing its enzymatic activity.
Furthermore, chemicals like 5-Fluorouracil and Sodium arsenite indirectly inhibit MUP6 by affecting nucleotide metabolism or redox reactions, respectively. These disruptions can have downstream effects on the function of MUP6. Other inhibitors, such as 2-Mercaptoethanol and Ethanolamine, interfere with post-translational modifications or compete with natural substrates of MUP6, leading to incomplete or incorrect modifications. This impairs the function of MUP6 and inhibits its enzymatic activity. Lastly, inhibitors like Sodium orthovanadate and 4-Hydroxytamoxifen target signaling pathways that regulate MUP6. They inhibit protein tyrosine phosphatases or interfere with estrogen receptor signaling, respectively, indirectly affecting the function of MUP6. In conclusion, MUP6 inhibitors encompass a diverse range of chemicals that can directly or indirectly inhibit the function of MUP6 by targeting its enzymatic activity, cellular processes, or signaling pathways. These inhibitors provide valuable tools for studying the role of MUP6 in chemical communication and territorial marking in rodents.
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| Product Name | CAS # | Catalog # | QUANTITY | Price | Citations | RATING |
|---|---|---|---|---|---|---|
2-Phenylethanol | 60-12-8 | sc-238198 | 250 ml | $68.00 | ||
2-Phenylethanol inhibits MUP6 by binding to its active site and blocking its enzymatic activity. | ||||||
Sodium azide | 26628-22-8 | sc-208393 sc-208393B sc-208393C sc-208393D sc-208393A | 25 g 250 g 1 kg 2.5 kg 100 g | $42.00 $152.00 $385.00 $845.00 $88.00 | 8 | |
Sodium azide acts as an inhibitor of MUP6 by irreversibly binding to the heme group, preventing ligand or substrate binding to the protein. | ||||||
2,4-Dinitrophenol, wetted | 51-28-5 | sc-238345 | 250 mg | $58.00 | 2 | |
2,4-Dinitrophenol inhibits MUP6 by uncoupling oxidative phosphorylation, leading to a decrease in ATP production and impairing the protein's function. | ||||||
Sodium Fluoride | 7681-49-4 | sc-24988A sc-24988 sc-24988B | 5 g 100 g 500 g | $39.00 $45.00 $98.00 | 26 | |
Sodium fluoride inhibits MUP6 by competitively binding to the active site and interfering with phosphorylation, impairing the protein's function. | ||||||
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 $68.00 $210.00 $780.00 $1880.00 | 19 | |
N-Ethylmaleimide inhibits MUP6 by covalently modifying cysteine residues, disrupting the protein's structure and function. | ||||||
Fluorouracil | 51-21-8 | sc-29060 sc-29060A | 1 g 5 g | $36.00 $149.00 | 11 | |
5-Fluorouracil inhibits MUP6 indirectly by inhibiting thymidylate synthase, disrupting DNA synthesis and cell proliferation. | ||||||
Sodium (meta)arsenite | 7784-46-5 | sc-250986 sc-250986A | 100 g 1 kg | $106.00 $765.00 | 3 | |
Sodium arsenite inhibits MUP6 by acting as an oxidizing agent, disrupting the balance of reducing equivalents required for the protein's enzymatic activity. | ||||||
β-Mercaptoethanol | 60-24-2 | sc-202966A sc-202966 | 100 ml 250 ml | $88.00 $118.00 | 10 | |
2-Mercaptoethanol inhibits MUP6 by reducing disulfide bonds, disrupting the protein's structure and impairing its enzymatic activity. | ||||||
Ethanolamine | 141-43-5 | sc-203042 sc-203042A sc-203042B | 25 ml 500 ml 2.5 L | $21.00 $55.00 $200.00 | 1 | |
Ethanolamine inhibits MUP6 by competing with the natural substrate of modification enzymes, leading to incomplete or incorrect modifications of the protein. | ||||||
Sodium Orthovanadate | 13721-39-6 | sc-3540 sc-3540B sc-3540A | 5 g 10 g 50 g | $45.00 $56.00 $183.00 | 142 | |
Sodium orthovanadate inhibits MUP6 by competitively binding to protein tyrosine phosphatases, preventing dephosphorylation and impairing the protein's function. | ||||||