Palmdelphin inhibitors are a class of chemical compounds that specifically target and modulate the activity of the palmdelphin protein. Palmdelphin is a member of the paralemmin family, a group of proteins that are involved in cellular processes, particularly those related to cytoskeletal dynamics, membrane organization, and vesicle trafficking. Palmdelphin, characterized by its palmitoylation, has a significant role in shaping the morphology of cells by interacting with the plasma membrane and the actin cytoskeleton. By inhibiting palmdelphin, these compounds are able to interfere with its function, potentially affecting cellular architecture, membrane dynamics, and intracellular transport mechanisms. Such inhibitors can offer insights into how palmdelphin contributes to cellular processes, which can help in understanding the broader role of palmdelphin-related pathways in cellular biology.
These inhibitors work through various mechanisms, such as binding to palmdelphin directly or interfering with the post-translational modifications, like palmitoylation, that are crucial for its membrane association and function. This disruption can lead to changes in cellular processes such as endocytosis, exocytosis, and cytoskeletal reorganization. Palmdelphin inhibitors, therefore, provide valuable tools for researchers studying the molecular mechanisms that govern cell shape, motility, and intracellular communication. By manipulating palmdelphin activity, these compounds can shed light on the regulation of membrane-bound signaling complexes and vesicular trafficking, offering deeper insights into how cells maintain their structure and respond to external stimuli.
SEE ALSO...
Items 1 to 10 of 11 total
Display:
| Product Name | CAS # | Catalog # | QUANTITY | Price | Citations | RATING |
|---|---|---|---|---|---|---|
PD 98059 | 167869-21-8 | sc-3532 sc-3532A | 1 mg 5 mg | $39.00 $90.00 | 212 | |
Palmdelphin can be linked to ERK/MAPK signaling. PD98059 inhibits MEK, an upstream regulator of ERK, potentially affecting Palmdelphin activity. | ||||||
LY 294002 | 154447-36-6 | sc-201426 sc-201426A | 5 mg 25 mg | $121.00 $392.00 | 148 | |
Palmdelphin might be influenced by PI3K/Akt signaling. LY294002 inhibits PI3K, thus can affect processes where Palmdelphin plays a role. | ||||||
Wortmannin | 19545-26-7 | sc-3505 sc-3505A sc-3505B | 1 mg 5 mg 20 mg | $66.00 $219.00 $417.00 | 97 | |
Another PI3K inhibitor, Wortmannin can modulate the PI3K/Akt pathway, indirectly affecting Palmdelphin-associated activities. | ||||||
SP600125 | 129-56-6 | sc-200635 sc-200635A | 10 mg 50 mg | $40.00 $150.00 | 257 | |
Targets JNK signaling. If Palmdelphin is associated with JNK-mediated processes, this inhibitor can influence its function. | ||||||
SB202190 hydrochloride | 350228-36-3 | sc-222294 sc-222294A | 1 mg 5 mg | $128.00 $495.00 | 13 | |
Inhibits p38 MAPK. Given the potential interplay between Palmdelphin and MAPK pathways, SB202190 might impact Palmdelphin's role. | ||||||
BAY 11-7082 | 19542-67-7 | sc-200615B sc-200615 sc-200615A | 5 mg 10 mg 50 mg | $61.00 $83.00 $349.00 | 155 | |
Inhibits NF-κB activation. If Palmdelphin interacts with or is regulated by NF-κB, this inhibitor can modulate its function. | ||||||
Rapamycin | 53123-88-9 | sc-3504 sc-3504A sc-3504B | 1 mg 5 mg 25 mg | $62.00 $155.00 $320.00 | 233 | |
Targets mTOR signaling. If Palmdelphin's function is linked to mTOR pathways, Rapamycin can have an inhibitory effect. | ||||||
2-APB | 524-95-8 | sc-201487 sc-201487A | 20 mg 100 mg | $27.00 $52.00 | 37 | |
Influences IP3 receptor-mediated calcium signaling. If Palmdelphin is linked to this, 2-APB can indirectly inhibit its activity. | ||||||
KN-93 | 139298-40-1 | sc-202199 | 1 mg | $178.00 | 25 | |
Targets Ca2+/calmodulin-dependent protein kinases. Can modulate Palmdelphin's role if associated with these kinases. | ||||||
Ro 31-8220 | 138489-18-6 | sc-200619 sc-200619A | 1 mg 5 mg | $90.00 $240.00 | 17 | |
Inhibits protein kinase C. If Palmdelphin's function is influenced by PKC-mediated signaling, Ro-31-8220 can inhibit this interaction. | ||||||