LOC727909 Inhibitors
LOC727909 Inhibitors belongs to a group of compounds characterized by their ability to modulate the activity of the LOC727909 protein. The term "LOC727909" is a placeholder for a specific gene or protein whose detailed molecular identity might be proprietary or under ongoing research. Inhibitors targeting LOC727909 are designed to selectively hinder or block the functional capabilities of this protein, thus exerting a regulatory effect on the biochemical processes in which LOC727909 participates. The development and study of LOC727909 inhibitors often involve a comprehensive understanding of the protein's structure, function, and the molecular pathways in which it is implicated.
Researchers in the field of biochemistry focus on designing molecules with the capacity to interact specifically with LOC727909, inhibiting its normal physiological function. This targeted inhibition is crucial for investigating the role of LOC727909 in cellular processes and understanding its potential implications in various biological contexts. The ongoing exploration of LOC727909 inhibitors contributes to the broader field offering insights into the intricate web of molecular interactions that govern cellular functions. The specificity of LOC727909 inhibitors provides a valuable tool for researchers aiming to elucidate the intricate mechanisms underlying cellular processes linked to the LOC727909 protein.
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| Product Name | CAS # | Catalog # | QUANTITY | Price | Citations | RATING |
|---|---|---|---|---|---|---|
Wortmannin | 19545-26-7 | sc-3505 sc-3505A sc-3505B | 1 mg 5 mg 20 mg | $66.00 $219.00 $417.00 | 97 | |
Wortmannin is a covalent inhibitor of phosphoinositide 3-kinases (PI3K), which are involved in numerous signaling pathways including those that regulate cell growth and vesicular trafficking. If protein name’s function is associated with these pathways, inhibition of PI3K by Wortmannin could lead to a reduction in protein name’s activity by disrupting its regulatory or signaling mechanisms. | ||||||
LY 294002 | 154447-36-6 | sc-201426 sc-201426A | 5 mg 25 mg | $121.00 $392.00 | 148 | |
LY294002 is a synthetic molecule that inhibits PI3K, leading to the blockade of Akt/PKB signaling pathway. This inhibition can result in the suppression of downstream processes that might involve protein name, thereby reducing its activity if it is part of the PI3K/Akt signaling axis. | ||||||
Brefeldin A | 20350-15-6 | sc-200861C sc-200861 sc-200861A sc-200861B | 1 mg 5 mg 25 mg 100 mg | $30.00 $52.00 $122.00 $367.00 | 25 | |
Brefeldin A is an inhibitor of ADP-ribosylation factor (ARF), which plays a crucial role in vesicle formation in the Golgi apparatus. If protein name is implicated in Golgi-mediated processes, Brefeldin A could impede its functional activity by disrupting vesicle trafficking and Golgi dynamics. | ||||||
Monensin A | 17090-79-8 | sc-362032 sc-362032A | 5 mg 25 mg | $152.00 $515.00 | ||
Monensin is an ionophore that disrupts intracellular ion gradients, particularly in the Golgi apparatus. Its action impacts protein sorting and trafficking. If protein name is involved in these Golgi processes, Monensin could indirectly decrease protein name’s functional activity by altering the ion homeostasis required for its proper function. | ||||||
Dynamin Inhibitor I, Dynasore | 304448-55-3 | sc-202592 | 10 mg | $87.00 | 44 | |
Dynasore is a small molecule that inhibits the GTPase activity of dynamin, a protein involved in endocytosis. If protein name functions in a pathway that relies on endocytic processes, Dynasore could inhibit protein name indirectly by blocking the recycling of components necessary for its activity. | ||||||
Nocodazole | 31430-18-9 | sc-3518B sc-3518 sc-3518C sc-3518A | 5 mg 10 mg 25 mg 50 mg | $58.00 $83.00 $140.00 $242.00 | 38 | |
Nocodazole is a microtubule depolymerizing agent that interferes with microtubule dynamics. If protein name relies on microtubule-based transport for its localization or function, Nocodazole could inhibit protein name by disrupting essential transport mechanisms. | ||||||
Cytochalasin D | 22144-77-0 | sc-201442 sc-201442A | 1 mg 5 mg | $145.00 $442.00 | 64 | |
Cytochalasin D is an inhibitor of actin polymerization, affecting cell shape and motility. If protein name's activity is dependent on the actin cytoskeleton, for example in cell signaling or motility, its inhibition by Cytochalasin D could lead to reduced protein name activity through impaired cytoskeletal dynamics. | ||||||
Golgicide A | 1005036-73-6 | sc-215103 sc-215103A | 5 mg 25 mg | $187.00 $670.00 | 11 | |
Golgicide A is an inhibitor of the Golgi BFA resistance factor 1 (GBF1), a key regulator of Golgi structure and function. If protein name is involved in Golgi apparatus function or maintenance, Golgicide A could indirectly lead to decreased protein name activity by disrupting Golgi integrity. | ||||||
Tunicamycin | 11089-65-9 | sc-3506A sc-3506 | 5 mg 10 mg | $169.00 $299.00 | 66 | |
Tunicamycin inhibits N-linked glycosylation, an essential process for protein folding and stability. If protein name is a glycoprotein or interacts with glycoproteins, Tunicamycin could lead to protein misfolding or degradation, hence decreasing protein name’s activity. | ||||||
Chloroquine | 54-05-7 | sc-507304 | 250 mg | $68.00 | 2 | |
Chloroquine raises the pH in lysosomes, affecting their function. If protein name is involved in lysosomal degradation, autophagy, or any process dependent on the acidic lysosomal environment, Chloroquine could decrease protein name’s activity by impairing lysosomal function. | ||||||