TMEM156 inhibitors are a specialized category of chemical agents designed to interact with and modulate the function of the transmembrane protein 156 (TMEM156). This protein is embedded in the cellular membrane and is implicated in a variety of biological processes due to its transmembrane nature, which allows it to participate in signaling and transport activities across the cell membrane. The inhibition of TMEM156 involves the binding of these compounds to specific sites on the protein, which may interfere with its normal conformation, block its interaction with other cellular molecules or substrates, or otherwise impede its function. By targeting TMEM156, these inhibitors can alter the protein's contribution to the maintenance of cellular homeostasis, membrane dynamics, and intracellular communication. The development of TMEM156 inhibitors requires an in-depth understanding of the protein's structure, the cellular context in which it operates, and the molecular interactions it typically engages in within the lipid bilayer of cells.
Creating effective TMEM156 inhibitors involves a multi-faceted approach that encompasses both discovery and optimization. Initial steps often include high-throughput screening to identify lead compounds with potential inhibitory effects on TMEM156. These leads are further investigated using a range of analytical techniques to elucidate their binding mechanisms. Techniques such as molecular docking and structure-activity relationship (SAR) studies play a critical role in this process, helping to refine the chemical structure of the inhibitors for increased potency and specificity. Understanding the 3D structure of TMEM156 through methods like cryo-electron microscopy or X-ray crystallography can provide detailed insights into potential binding sites and inform the design of molecules that can interact with these sites effectively. The chemical profiles of TMEM156 inhibitors are diverse, ranging from small organic molecules to larger, more complex structures, all tailored to interface with TMEM156's unique features.
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| Product Name | CAS # | Catalog # | QUANTITY | Price | Citations | RATING |
|---|---|---|---|---|---|---|
Cholesterol | 57-88-5 | sc-202539C sc-202539E sc-202539A sc-202539B sc-202539D sc-202539 | 5 g 5 kg 100 g 250 g 1 kg 25 g | $27.00 $2809.00 $129.00 $210.00 $583.00 $88.00 | 11 | |
Known to modulate the fluidity and function of cell membranes. Alterations in membrane fluidity can influence the activity of transmembrane proteins, including potentially TMEM156. | ||||||
β-Cyclodextrin | 7585-39-9 | sc-204430 sc-204430A | 25 g 500 g | $60.00 $538.00 | 3 | |
Can extract cholesterol from membranes, leading to alterations in membrane structure and function which may indirectly affect TMEM156 activity. | ||||||
L-α-Phosphatidylinositol sodium salt | 383907-36-6 | sc-221821 | 10 mg | $408.00 | 1 | |
A lipid involved in various signaling pathways. Changes in its levels can alter membrane-associated signal transduction processes, potentially impacting TMEM156's function if it's involved in such pathways. | ||||||
Amiloride | 2609-46-3 | sc-337527 | 1 g | $296.00 | 7 | |
Inhibitor of certain ion channels. If TMEM156 functions as, or is modulated by, ion flow, amiloride can impact its activity. | ||||||
Verapamil | 52-53-9 | sc-507373 | 1 g | $374.00 | ||
Calcium channel blocker. If TMEM156's activity is associated with calcium flow, verapamil can affect its function. | ||||||
Genistein | 446-72-0 | sc-3515 sc-3515A sc-3515B sc-3515C sc-3515D sc-3515E sc-3515F | 100 mg 500 mg 1 g 5 g 10 g 25 g 100 g | $45.00 $164.00 $200.00 $402.00 $575.00 $981.00 $2031.00 | 46 | |
Tyrosine kinase inhibitor. If TMEM156 is phosphorylated by or interacts with tyrosine kinases, genistein can modulate its activity. | ||||||
Progesterone | 57-83-0 | sc-296138A sc-296138 sc-296138B | 1 g 5 g 50 g | $20.00 $52.00 $298.00 | 3 | |
Can modulate the function of some transmembrane proteins. If TMEM156's function or activity is influenced by steroid hormones, progesterone can play a role in its modulation. | ||||||
Ouabain-d3 (Major) | sc-478417 | 1 mg | $516.00 | |||
Inhibitor of the Na+/K+-ATPase pump. If TMEM156's function is linked to sodium or potassium levels, ouabain can influence its activity. | ||||||
Brefeldin A | 20350-15-6 | sc-200861C sc-200861 sc-200861A sc-200861B | 1 mg 5 mg 25 mg 100 mg | $31.00 $53.00 $124.00 $374.00 | 25 | |
Disrupts protein trafficking from the endoplasmic reticulum to the Golgi. If TMEM156 relies on specific post-translational modifications occurring in the Golgi or proper trafficking for its function, Brefeldin A can impact its activity. | ||||||
Filipin III | 480-49-9 | sc-205323 sc-205323A | 500 µg 1 mg | $118.00 $148.00 | 26 | |
Binds sterols in membranes, disrupting lipid raft domains. If TMEM156's function or localization is associated with lipid rafts, filipin can influence its activity. | ||||||