Lipocalin-5 inhibitors are a specialized class of chemical compounds formulated to target and inhibit Lipocalin-5, a member of the broader lipocalin protein family. Lipocalins are recognized for their ability to bind and transport small hydrophobic molecules, playing pivotal roles in various biological processes such as cellular signaling, immune responses, and the transportation of essential biomolecules like vitamins and hormones. Lipocalin-5 distinguishes itself within this family through its unique structural and functional attributes, participating in specific biological pathways through its interactions with particular hydrophobic molecules. The development of inhibitors aimed at Lipocalin-5 requires a profound understanding of the protein's molecular structure and its interaction mechanisms with other molecules. This foundational knowledge is crucial for the design of inhibitors that can selectively and efficaciously bind to Lipocalin-5, thereby disrupting its normal biological functions. The primary goal in crafting these inhibitors is to obstruct Lipocalin-5's ability to bind to its natural ligands, a task that demands significant precision and specificity in the molecular design of the inhibitors.
The process of creating Lipocalin-5 inhibitors involves a comprehensive and interdisciplinary approach, drawing from the fields of biochemistry, molecular biology, and medicinal chemistry. Researchers focus on elucidating the detailed three-dimensional structure of Lipocalin-5, which is essential in guiding the design of effective inhibitors. This entails a thorough understanding of the protein's binding sites and its molecular interaction mechanisms to develop compounds that specifically target these areas, thus impeding Lipocalin-5's natural function. The interaction between Lipocalin-5 and its inhibitors is a critical factor in their effectiveness. The inhibitors must bind to the protein in a way that effectively negates its ability to interact with its natural ligands. This often involves the formation of a complex between the inhibitor and specific sites on Lipocalin-5, requiring a precise match in molecular structure. Additionally, the development of Lipocalin-5 inhibitors includes considerations of the compound's stability, solubility, and its ability to effectively reach and interact with the target site within biological systems. This includes balancing the hydrophobic and hydrophilic properties of the compound and considering its molecular size and shape to optimize delivery and interaction. The development of Lipocalin-5 inhibitors highlights the intricate processes involved in the design and synthesis of specific protein inhibitors, demonstrating the advanced level of current research in molecular targeting within biological systems.
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Product Name | CAS # | Catalog # | QUANTITY | Price | Citations | RATING |
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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 | |
A compound that can inhibit DNA-dependent RNA polymerase in prokaryotes and may affect gene expression indirectly in eukaryotic cells. | ||||||
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 I inhibitor that can lead to DNA damage and potentially affect transcription processes. | ||||||
Mitomycin C | 50-07-7 | sc-3514A sc-3514 sc-3514B | 2 mg 5 mg 10 mg | $65.00 $99.00 $140.00 | 85 | |
An alkylating agent that can crosslink DNA and potentially inhibit DNA synthesis and transcription. | ||||||
Etoposide (VP-16) | 33419-42-0 | sc-3512B sc-3512 sc-3512A | 10 mg 100 mg 500 mg | $32.00 $170.00 $385.00 | 63 | |
A topoisomerase II inhibitor that induces DNA strand breaks and could influence transcription regulation. | ||||||
Actinonin | 13434-13-4 | sc-201289 sc-201289B | 5 mg 10 mg | $160.00 $319.00 | 3 | |
A naturally occurring compound that can inhibit peptidyl transferase and affect protein synthesis. | ||||||
α-Amanitin | 23109-05-9 | sc-202440 sc-202440A | 1 mg 5 mg | $260.00 $1029.00 | 26 | |
A potent inhibitor of RNA polymerase II in eukaryotes, leading to inhibition of mRNA synthesis. | ||||||
Cordycepin | 73-03-0 | sc-203902 | 10 mg | $99.00 | 5 | |
An adenosine analog that can terminate RNA chain elongation due to its incorporation into RNA. | ||||||
Novobiocin | 303-81-1 | sc-362034 sc-362034A | 5 mg 25 mg | $96.00 $355.00 | ||
A coumarin compound that inhibits DNA gyrase and can indirectly affect DNA transcription. | ||||||
Aphidicolin | 38966-21-1 | sc-201535 sc-201535A sc-201535B | 1 mg 5 mg 25 mg | $82.00 $300.00 $1082.00 | 30 | |
A tetracyclic diterpene that specifically inhibits DNA polymerase α and δ, affecting DNA replication and thus gene expression. | ||||||
Staurosporine | 62996-74-1 | sc-3510 sc-3510A sc-3510B | 100 µg 1 mg 5 mg | $82.00 $150.00 $388.00 | 113 | |
A potent inhibitor of protein kinases that may affect various signal transduction pathways involved in gene expression. |