Lipocalin-11 inhibitors are a group of chemical compounds specifically formulated to interact with and inhibit the activity of Lipocalin-11, a protein belonging to the larger family of lipocalins. Lipocalins are a diverse and widespread group of proteins known for their ability to bind small hydrophobic molecules. They play a variety of roles in different biological processes, primarily involving the transport and storage of these molecules. Lipocalin-11, in particular, is distinguished by its unique structure and function within this family. The specific role of Lipocalin-11 in biological processes is characterized by its interaction with certain molecules, which it binds and transports. The development of inhibitors targeting Lipocalin-11 requires a detailed understanding of the protein's structure and its interaction mechanisms with other molecules. This knowledge is crucial for designing inhibitors that can effectively bind to Lipocalin-11 and impede its normal function, thereby inhibiting its activity within the biological system.
The process of creating Lipocalin-11 inhibitors involves advanced research in biochemistry and molecular biology. Scientists focus on elucidating the three-dimensional structure of Lipocalin-11, which is essential for the precise design of effective inhibitors. Understanding the binding sites and the mechanism by which Lipocalin-11 interacts with other molecules allows for the development of inhibitors that can specifically target these sites. The interaction between Lipocalin-11 inhibitors and the protein is a critical aspect of their design, as the inhibitors must bind in a way that effectively disrupts the protein's normal function. This typically involves the formation of a complex between the inhibitor and specific sites on Lipocalin-11, requiring a highly precise alignment of molecular structures. In addition to binding affinity, the design of Lipocalin-11 inhibitors also takes into account the compound's stability, solubility, and its ability to reach the target site within biological systems. These factors include a balance between hydrophobic and hydrophilic properties, as well as considerations of the compound's molecular size and shape. The development of Lipocalin-11 inhibitors is a testament to the sophistication of current research in molecular targeting and the intricate processes involved in the design and synthesis of specific protein inhibitors.
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| Product Name | CAS # | Catalog # | QUANTITY | Price | Citations | RATING |
|---|---|---|---|---|---|---|
Mithramycin A | 18378-89-7 | sc-200909 | 1 mg | $54.00 | 6 | |
A compound that binds to GC-rich sequences in DNA, inhibiting transcription factors from binding and initiating transcription. | ||||||
Mitomycin C | 50-07-7 | sc-3514A sc-3514 sc-3514B | 2 mg 5 mg 10 mg | $65.00 $99.00 $140.00 | 85 | |
A compound that can crosslink DNA, thereby potentially inhibiting DNA transcription and subsequent protein expression. | ||||||
Camptothecin | 7689-03-4 | sc-200871 sc-200871A sc-200871B | 50 mg 250 mg 100 mg | $57.00 $182.00 $92.00 | 21 | |
A topoisomerase inhibitor that prevents DNA relegation and can lead to decreased gene transcription and protein expression. | ||||||
Fostriecin | 87860-39-7 | sc-202160 | 50 µg | $260.00 | 9 | |
A phosphate ester that selectively inhibits protein phosphatases, which can influence a number of cellular processes including gene expression. | ||||||
Quinomycin A | 512-64-1 | sc-202306 | 1 mg | $163.00 | 4 | |
A bisintercalator that selectively binds to DNA at the CpG motifs, potentially repressing transcription of various genes. | ||||||
PMA | 16561-29-8 | sc-3576 sc-3576A sc-3576B sc-3576C sc-3576D | 1 mg 5 mg 10 mg 25 mg 100 mg | $40.00 $129.00 $210.00 $490.00 $929.00 | 119 | |
A diester of phorbol that activates protein kinase C, which may regulate gene expression by modulating transcription factor activity. | ||||||
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 | |
A short-chain fatty acid that acts as a histone deacetylase inhibitor, changing the chromatin structure and potentially affecting gene expression. | ||||||
RG 108 | 48208-26-0 | sc-204235 sc-204235A | 10 mg 50 mg | $128.00 $505.00 | 2 | |
A non-nucleoside inhibitor of DNA methyltransferase, which could lead to demethylation and activation of some genes while repressing others. | ||||||
Scriptaid | 287383-59-9 | sc-202807 sc-202807A | 1 mg 5 mg | $63.00 $179.00 | 11 | |
A histone deacetylase inhibitor that alters chromatin structure and can change gene expression profiles. | ||||||
MS-275 | 209783-80-2 | sc-279455 sc-279455A sc-279455B | 1 mg 5 mg 25 mg | $24.00 $88.00 $208.00 | 24 | |
A benzamide histone deacetylase inhibitor that can alter gene expression patterns in cells. | ||||||