KIAA1462 inhibitors are a class of chemical compounds that target the KIAA1462 gene, also known as JCAD (Junctional Cadherin 5 Associated). This gene encodes a protein involved in maintaining endothelial cell-to-cell junctions and plays a role in cardiovascular health by regulating the integrity of blood vessels. The protein encoded by KIAA1462 is located primarily at cell junctions in endothelial tissues, where it contributes to the organization and stability of the vascular barrier. Inhibition of KIAA1462 activity has been studied primarily in the context of how this protein interacts with cellular pathways that govern the architecture of endothelial cells. Such interactions are important in maintaining the structural balance of blood vessel walls, which is a key factor in processes like vascular permeability and cell migration.
The molecular mechanisms of KIAA1462 inhibitors typically involve disrupting the protein's interaction with its associated partners at endothelial junctions. By targeting this gene, inhibitors can alter the assembly and disassembly of protein complexes at these junctions, affecting the cytoskeletal arrangement of cells. The chemical composition of these inhibitors varies, but they are often designed to interfere with specific binding domains on the KIAA1462 protein, preventing it from fulfilling its role in junctional stability. Given its involvement in the maintenance of vascular barriers, inhibition of KIAA1462 can lead to changes in the tightness and flexibility of these cell junctions. This disruption has implications for studies focused on cell behavior, endothelial dynamics, and the modulation of intracellular signaling pathways related to vascular function.
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| Product Name | CAS # | Catalog # | QUANTITY | Price | Citations | RATING |
|---|---|---|---|---|---|---|
Actinomycin D | 50-76-0 | sc-200906 sc-200906A sc-200906B sc-200906C sc-200906D | 5 mg 25 mg 100 mg 1 g 10 g | $74.00 $243.00 $731.00 $2572.00 $21848.00 | 53 | |
Interferes with the transcription process by binding to DNA. | ||||||
Cycloheximide | 66-81-9 | sc-3508B sc-3508 sc-3508A | 100 mg 1 g 5 g | $41.00 $84.00 $275.00 | 127 | |
Inhibits protein synthesis by affecting ribosomal function. | ||||||
Mitoxantrone | 65271-80-9 | sc-207888 | 100 mg | $285.00 | 8 | |
An antineoplastic agent that intercalates into DNA and inhibits topoisomerase II, affecting transcription. | ||||||
Camptothecin | 7689-03-4 | sc-200871 sc-200871A sc-200871B | 50 mg 250 mg 100 mg | $58.00 $186.00 $94.00 | 21 | |
Inhibits DNA topoisomerase I, affecting DNA replication and transcription processes. | ||||||
RG 108 | 48208-26-0 | sc-204235 sc-204235A | 10 mg 50 mg | $131.00 $515.00 | 2 | |
A DNA methyltransferase inhibitor that could affect methylation status of gene promoters. | ||||||
Y-27632, free base | 146986-50-7 | sc-3536 sc-3536A | 5 mg 50 mg | $186.00 $707.00 | 88 | |
A ROCK inhibitor that may influence cytoskeleton organization and gene expression. | ||||||
Resveratrol | 501-36-0 | sc-200808 sc-200808A sc-200808B | 100 mg 500 mg 5 g | $80.00 $220.00 $460.00 | 64 | |
May modulate various signaling pathways and influence gene expression. | ||||||
Suberoylanilide Hydroxamic Acid | 149647-78-9 | sc-220139 sc-220139A | 100 mg 500 mg | $133.00 $275.00 | 37 | |
Histone deacetylase (HDAC) inhibitor affecting chromatin structure and gene expression. | ||||||
SP600125 | 129-56-6 | sc-200635 sc-200635A | 10 mg 50 mg | $40.00 $150.00 | 257 | |
JNK inhibitor that may affect various cellular signaling pathways influencing gene expression. | ||||||
Nutlin-3 | 548472-68-0 | sc-45061 sc-45061A sc-45061B | 1 mg 5 mg 25 mg | $62.00 $225.00 $779.00 | 24 | |
MDM2 inhibitor, may affect p53 pathway and influence gene expression patterns. | ||||||