HSPC159 inhibitors are a class of chemical compounds designed to modulate the activity of the HSPC159 protein, which is known to play a role in various cellular processes. HSPC159, often studied in the context of its involvement in cellular signaling pathways, is part of the larger family of proteins associated with intracellular regulation and communication. Inhibitors of HSPC159 function by binding to this protein and altering its native conformation or activity, potentially disrupting its role in cellular pathways. The design of these inhibitors typically focuses on targeting key structural domains or functional motifs within the HSPC159 protein, such as binding pockets or active sites critical for its normal function. The chemical structures of HSPC159 inhibitors can vary widely, but they are often characterized by the presence of specific functional groups that facilitate binding affinity and specificity to the HSPC159 protein.
These inhibitors are of interest in biochemical research because of their ability to modulate protein-protein interactions or enzyme activity within cells. Structurally, HSPC159 inhibitors may encompass diverse scaffolds, including small molecules, peptides, or peptidomimetics, each designed to achieve optimal interactions with the protein target. Often, these inhibitors are developed using structure-based design approaches, utilizing computational modeling and structural biology to predict and enhance their binding capabilities. The physico-chemical properties of HSPC159 inhibitors, such as hydrophobicity, charge distribution, and molecular weight, are finely tuned to improve their interaction with the HSPC159 protein and to achieve selectivity, thereby minimizing off-target effects. Understanding and characterizing the binding kinetics, structural features, and molecular interactions of these inhibitors provide valuable insights into the biological role of HSPC159 and the mechanisms underlying its function in cellular processes.
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| Product Name | CAS # | Catalog # | QUANTITY | Price | Citations | RATING |
|---|---|---|---|---|---|---|
17-AAG | 75747-14-7 | sc-200641 sc-200641A | 1 mg 5 mg | $66.00 $153.00 | 16 | |
HSP90 inhibitor that can disrupt the function of client proteins, potentially including HSPC159-associated proteins. | ||||||
Geldanamycin | 30562-34-6 | sc-200617B sc-200617C sc-200617 sc-200617A | 100 µg 500 µg 1 mg 5 mg | $38.00 $58.00 $102.00 $202.00 | 8 | |
HSP90 inhibitor that can destabilize proteins associated with HSPC159, potentially affecting its activity. | ||||||
Quercetin | 117-39-5 | sc-206089 sc-206089A sc-206089E sc-206089C sc-206089D sc-206089B | 100 mg 500 mg 100 g 250 g 1 kg 25 g | $11.00 $17.00 $108.00 $245.00 $918.00 $49.00 | 33 | |
A flavonoid that can inhibit heat shock protein function, potentially affecting HSPC159 through stress response pathways. | ||||||
Heat Shock Protein Inhibitor I | 218924-25-5 | sc-221709 | 5 mg | $95.00 | 5 | |
A heat shock protein inhibitor that can suppress the heat shock response, potentially affecting HSPC159 activity. | ||||||
Triptolide | 38748-32-2 | sc-200122 sc-200122A | 1 mg 5 mg | $88.00 $200.00 | 13 | |
A diterpene triepoxide that can inhibit heat shock protein expression, potentially impacting HSPC159 function. | ||||||
Zerumbone | 471-05-6 | sc-364148 sc-364148A | 10 mg 50 mg | $110.00 $400.00 | ||
Compound that can modify heat shock protein expression, potentially affecting HSPC159. | ||||||
Pifithrin-μ | 64984-31-2 | sc-203195 sc-203195A | 10 mg 50 mg | $127.00 $372.00 | 4 | |
An inhibitor of HSP70 that can alter its chaperone activity, potentially impacting HSPC159. | ||||||
VER 155008 | 1134156-31-2 | sc-358808 sc-358808A | 10 mg 50 mg | $199.00 $825.00 | 9 | |
An HSP70 inhibitor that can affect client protein stability, potentially impacting the function of HSPC159. | ||||||
JG-98 | 1456551-16-8 | sc-507517 | 5 mg | $220.00 | ||
An allosteric inhibitor of HSP70 that can affect its association with client proteins, potentially including HSPC159. | ||||||