BLVRB Activators comprise a specific array of chemical entities that function to enhance the activity of Biliverdin Reductase B (BLVRB), a pivotal enzyme in the heme catabolism pathway. These activators, through their distinct biochemical mechanisms, selectively upregulate the catalytic efficiency of BLVRB, which is responsible for the conversion of biliverdin to bilirubin. This conversion is critical for the antioxidant defense system of the body, as bilirubin exerts a powerful antioxidant effect. One key class of BLVRB activators includes molecules that stabilize the protein's conformation, ensuring that its active site remains accessible for substrate interaction. These stabilizers often function by binding to allosteric sites on BLVRB, inducing a conformational change that results in an enhanced affinity for biliverdin. Moreover, there are activators that function by facilitating the electron transfer process necessary for the catalytic action of BLVRB. These compounds can donate electrons more efficiently to the enzyme, streamlining the reduction of biliverdin.
In addition to conformational stabilizers and electron donors, BLVRB activation is positively influenced by compounds that modulate the levels of its substrates and cofactors. Some activators work by increasing the intracellular concentration of biliverdin, supplying more substrate for the enzyme to act upon. Others enhance the availability or recycling of NADPH, the cofactor required in the enzymatic reduction process, thereby boosting the overall reaction rate. Another set of activators includes signaling molecules that indirectly upregulate BLVRB activity through the induction of cellular stress responses. These molecules typically initiate a cascade of intracellular events leading to the upregulation of antioxidant proteins, including BLVRB, to counteract the increased oxidative stress. Such a stratagem ensures that the cell's redox balance is maintained, with BLVRB activators playing a critical role in the orchestrated response to oxidative challenges. Collectively, these BLVRB Activators work synergistically to prop up the functional activity of BLVRB, contributing to the maintenance of cellular redox homeostasis.
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Product Name | CAS # | Catalog # | QUANTITY | Price | Citations | RATING |
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β-Nicotinamide adenine dinucleotide phosphate | 53-59-8 | sc-215560 sc-215560A | 100 mg 250 mg | $114.00 $198.00 | ||
As a reducing agent, NADPH is essential for BLVRB activity. By donating electrons through its oxidation to NADP+, NADPH directly enhances the reducing power of BLVRB, enabling the catalysis of the conversion of biliverdin to bilirubin. | ||||||
Zinc | 7440-66-6 | sc-213177 | 100 g | $47.00 | ||
Zinc ions can act as a cofactor for BLVRB, potentially enhancing its structural stability and, consequently, its enzymatic activity. Zinc may interact with specific residues in BLVRB, leading to a conformation optimal for substrate interaction. | ||||||
Magnesium chloride | 7786-30-3 | sc-255260C sc-255260B sc-255260 sc-255260A | 10 g 25 g 100 g 500 g | $27.00 $34.00 $47.00 $123.00 | 2 | |
Magnesium ions may provide structural support to BLVRB or influence its interaction with coenzymes like NADPH, thus indirectly enhancing its enzymatic activity. | ||||||
Palmitic Acid | 57-10-3 | sc-203175 sc-203175A | 25 g 100 g | $112.00 $280.00 | 2 | |
As a common fatty acid, palmitic acid can integrate into cellular membranes and may affect the membrane-associated enzymes' activities, potentially influencing the function of BLVRB by altering its microenvironment. | ||||||
Uridine 5′-diphosphoglucose disodium salt from Saccharomyces cerevisiae | 28053-08-9 | sc-222402 sc-222402A | 10 mg 25 mg | $26.00 $33.00 | ||
UDP-glucuronic acid is involved in glucuronidation, a process that can work in tandem with BLVRB's reduction of biliverdin, facilitating the subsequent clearance of bilirubin. By increasing the demand for bilirubin, it can indirectly enhance the functional activity of BLVRB. | ||||||
Retinoic Acid, all trans | 302-79-4 | sc-200898 sc-200898A sc-200898B sc-200898C | 500 mg 5 g 10 g 100 g | $65.00 $319.00 $575.00 $998.00 | 28 | |
Retinoic acid can influence gene expression and might indirectly enhance BLVRB activity by upregulating mechanisms or proteins that are part of the same metabolic pathways, such as those involved in heme metabolism. | ||||||
Glutathione, reduced | 70-18-8 | sc-29094 sc-29094A | 10 g 1 kg | $76.00 $2050.00 | 8 | |
Glutathione in its reduced form can maintain the cellular redox state, which is necessary for the proper function of redox-sensitive enzymes like BLVRB. By maintaining a reducing environment, glutathione indirectly supports BLVRB activity. | ||||||
α-Ketoglutaric Acid | 328-50-7 | sc-208504 sc-208504A sc-208504B sc-208504C sc-208504D sc-208504E sc-208504F | 25 g 100 g 250 g 500 g 1 kg 5 kg 16 kg | $32.00 $42.00 $62.00 $108.00 $184.00 $724.00 $2050.00 | 2 | |
Alpha-ketoglutaric acid is a key molecule in the Krebs cycle and can influence cellular energy levels. Adequate energy levels and metabolite availability can indirectly affect BLVRB activity by ensuring sufficient cellular resources for its function. | ||||||
Nicotinamide | 98-92-0 | sc-208096 sc-208096A sc-208096B sc-208096C | 100 g 250 g 1 kg 5 kg | $43.00 $65.00 $200.00 $815.00 | 6 | |
Nicotinamide can be a precursor for NAD+, which is convertible to NADPH via cellular metabolic pathways. Enhancing NADPH levels indirectly supports BLVRB activity. | ||||||
Riboflavin | 83-88-5 | sc-205906 sc-205906A sc-205906B | 25 g 100 g 1 kg | $40.00 $110.00 $515.00 | 3 | |
As a precursor for FAD and FMN, cofactors for various redox reactions, riboflavin supplementation can support the overall redox balance and indirectly enhance BLVRB activity within the context of cellular metabolism. |