Hog1 inhibitors represent a class of chemical compounds designed to selectively target and inhibit the activity of the Hog1 kinase, a pivotal component of the stress response signaling pathway in yeast, particularly Saccharomyces cerevisiae. These inhibitors are primarily employed as research tools to elucidate the intricate mechanisms underlying cellular responses to various environmental stressors, such as high osmolarity, oxidative stress, and heat shock. Researchers have harnessed Hog1 inhibitors to explore the specific roles of Hog1 in stress adaptation, gene expression regulation, and cell cycle control within yeast cells.
Chemically, Hog1 inhibitors encompass a range of small molecules, including synthetic chemicals and natural products. Some well-known Hog1 inhibitors fall into the category of protein kinase inhibitors, as they exhibit the ability to interfere with the phosphorylation activity of Hog1, preventing its downstream signaling cascade. These inhibitors often feature pyridinyl imidazole cores, which have been shown to inhibit Hog1 and other related kinases like p38 MAPK. Additionally, certain Hog1 inhibitors are peptide-based, designed to mimic specific regions of the Hog1 protein, which competes with the native substrate for binding to the active site of Hog1. Other compounds within this class may have entirely distinct chemical structures but still achieve their inhibitory effects on Hog1 through various mechanisms, such as disrupting protein-protein interactions or altering the kinase's conformation. The study of Hog1 inhibitors has greatly contributed to our understanding of stress response mechanisms in yeast and has facilitated the dissection of signaling pathways regulated by this kinase. By selectively inhibiting Hog1, researchers can dissect its precise functions and the downstream events that occur upon its activation. This knowledge is valuable not only for fundamental research into cell biology but also for applications in biotechnology and the development of novel strategies for stress tolerance in yeast and related microorganisms.
| Product Name | CAS # | Catalog # | QUANTITY | Price | Citations | RATING |
|---|---|---|---|---|---|---|
SB 203580 | 152121-47-6 | sc-3533 sc-3533A | 1 mg 5 mg | $88.00 $342.00 | 284 | |
SB203580 is a pyridinyl imidazole compound that acts as a potent inhibitor of Hog1. It is also known to inhibit p38 MAPK in mammalian cells. | ||||||
Staurosporine | 62996-74-1 | sc-3510 sc-3510A sc-3510B | 100 µg 1 mg 5 mg | $82.00 $150.00 $388.00 | 113 | |
Staurosporine is a product found in certain bacteria, and it inhibits Hog1 among other kinases. It has been widely used as a broad-spectrum kinase inhibitor. | ||||||
Spermidine | 124-20-9 | sc-215900 sc-215900B sc-215900A | 1 g 25 g 5 g | $56.00 $595.00 $173.00 | ||
Spermidine, a polyamine, has been shown to inhibit Hog1 activity in yeast cells under osmotic stress conditions. | ||||||
SB 202190 | 152121-30-7 | sc-202334 sc-202334A sc-202334B | 1 mg 5 mg 25 mg | $30.00 $125.00 $445.00 | 45 | |
Similar to SB203580, SB202190 is a pyridinyl imidazole compound that inhibits Hog1. It is also known to inhibit p38 MAPK. | ||||||
PD 169316 | 152121-53-4 | sc-204168 sc-204168A sc-204168B sc-204168C | 1 mg 5 mg 10 mg 25 mg | $86.00 $153.00 $275.00 $452.00 | 3 | |
PD169316 is another inhibitor primarily designed for p38 MAPK but also inhibits Hog1 to some extent. | ||||||
Nifedipine | 21829-25-4 | sc-3589 sc-3589A | 1 g 5 g | $58.00 $170.00 | 15 | |
Nifedipine is a calcium channel blocker that has been found to inhibit Hog1 signaling in yeast cells. | ||||||