The chemical class identified as UGT2B28 Inhibitors constitutes a group of compounds intricately designed to selectively target the molecular entity UGT2B28. UGT2B28, or UDP-glucuronosyltransferase 2B28, belongs to the UDP-glucuronosyltransferase superfamily, which plays a pivotal role in phase II metabolism by catalyzing the glucuronidation of diverse endogenous and exogenous compounds. This enzymatic process involves the addition of a glucuronic acid moiety to substrates, facilitating their elimination from the body. While the broader UDP-glucuronosyltransferase family is well-recognized for its involvement in xenobiotic metabolism, the specific substrate preferences and regulatory mechanisms associated with UGT2B28 are subjects of ongoing research within the fields of pharmacology and biochemistry. Inhibitors within the UGT2B28 Inhibitors class are meticulously engineered molecules with the primary goal of modulating the activity or function of UGT2B28, thereby inducing an inhibitory effect. Researchers in this field utilize a multifaceted approach, integrating insights from structural biology, medicinal chemistry, and computational modeling to unravel the complex molecular interactions between the inhibitors and the target UGT2B28.
Structurally, UGT2B28 Inhibitors are characterized by specific molecular features designed to facilitate selective binding to UGT2B28. This selectivity is crucial to minimize unintended effects on other UGT isoforms or cellular components, ensuring a focused impact on the intended molecular target. The development of inhibitors within this chemical class involves a comprehensive exploration of structure-activity relationships, optimization of pharmacokinetic properties, and a deep understanding of the molecular mechanisms associated with UGT2B28. As researchers delve deeper into the functional aspects of UGT2B28 Inhibitors, the knowledge generated contributes not only to deciphering the specific roles of UDP-glucuronosyltransferase 2B28 but also to advancing our broader comprehension of drug metabolism, xenobiotic detoxification, and the intricate regulatory networks involved in cellular processes. The exploration of UGT2B28 Inhibitors stands as a significant avenue for expanding fundamental knowledge in pharmacology and biochemistry.
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Product Name | CAS # | Catalog # | QUANTITY | Price | Citations | RATING |
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Sodium Butyrate | 156-54-7 | sc-202341 sc-202341B sc-202341A sc-202341C | 250 mg 5 g 25 g 500 g | $30.00 $46.00 $82.00 $218.00 | 19 | |
Sodium butyrate acts as a histone deacetylase inhibitor, which might lead to alterations in UGT2B28 gene expression. | ||||||
Rifampicin | 13292-46-1 | sc-200910 sc-200910A sc-200910B sc-200910C | 1 g 5 g 100 g 250 g | $95.00 $322.00 $663.00 $1438.00 | 6 | |
Although rifampicin is known to induce certain UGT enzymes, it could have inhibitory effects on others, possibly including UGT2B28. |