NHSL2 inhibitors are a class of chemical compounds that act by specifically targeting and inhibiting the activity of the protein NHSL2. This protein, often classified within the family of scaffolding proteins, plays a pivotal role in a variety of cellular processes, particularly those involving intracellular signaling and structural organization. The inhibition of NHSL2 can modulate various pathways that are dependent on its scaffolding function, altering cellular dynamics and potentially affecting processes like protein-protein interactions and cytoskeletal organization. NHSL2 inhibitors are typically characterized by their selective binding affinities, which allow them to modulate the functional state of NHSL2 by either direct or allosteric inhibition, preventing the protein from fulfilling its usual biological roles within the cell.
The design of NHSL2 inhibitors often involves structure-based drug design techniques, wherein the three-dimensional structure of the NHSL2 protein is analyzed to identify binding pockets or active sites that are key to its function. These inhibitors can have various chemical backbones, ranging from small organic molecules to more complex macrocyclic structures, depending on the specific mode of inhibition required. Researchers studying NHSL2 inhibitors are primarily interested in understanding the molecular mechanisms by which they influence intracellular signaling and how these compounds alter the dynamics of NHSL2-related complexes. Through detailed biochemical and structural analyses, NHSL2 inhibitors are investigated to explore how their interaction with NHSL2 can lead to changes in the conformation and activity of this scaffolding protein, thus affecting the broader network of cellular signaling in which NHSL2 plays a crucial role.
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| Product Name | CAS # | Catalog # | QUANTITY | Price | Citations | RATING |
|---|---|---|---|---|---|---|
Rapamycin | 53123-88-9 | sc-3504 sc-3504A sc-3504B | 1 mg 5 mg 25 mg | $63.00 $158.00 $326.00 | 233 | |
Binds to FKBP12 and inhibits mTOR (mechanistic target of rapamycin). NHSL2 is a downstream effector of mTOR signaling, thus its activity is reduced when mTOR is inhibited. | ||||||
Wortmannin | 19545-26-7 | sc-3505 sc-3505A sc-3505B | 1 mg 5 mg 20 mg | $67.00 $223.00 $425.00 | 97 | |
Inhibits PI3K, leading to a decrease in AKT phosphorylation and subsequent downregulation of mTOR activity, which in turn reduces NHSL2 function. | ||||||
LY 294002 | 154447-36-6 | sc-201426 sc-201426A | 5 mg 25 mg | $123.00 $400.00 | 148 | |
A selective inhibitor of PI3Ks, leading to impaired AKT activation and reduced mTOR signaling, consequently inhibiting NHSL2 activity. | ||||||
Triciribine | 35943-35-2 | sc-200661 sc-200661A | 1 mg 5 mg | $104.00 $141.00 | 14 | |
Specifically inhibits the phosphorylation and activation of AKT, which is upstream of mTOR signaling that regulates NHSL2 activity. | ||||||
Everolimus | 159351-69-6 | sc-218452 sc-218452A | 5 mg 50 mg | $131.00 $651.00 | 7 | |
An mTOR inhibitor that directly reduces NHSL2 activity by diminishing downstream signaling processes that are crucial for NHSL2 function. | ||||||
AZD8055 | 1009298-09-2 | sc-364424 sc-364424A | 10 mg 50 mg | $163.00 $352.00 | 12 | |
An ATP-competitive inhibitor of mTOR that suppresses downstream signaling pathways, including those involving NHSL2. | ||||||
Torin 1 | 1222998-36-8 | sc-396760 | 10 mg | $245.00 | 7 | |
A selective mTOR inhibitor that impairs downstream signaling required for NHSL2 activity. | ||||||
PP242 | 1092351-67-1 | sc-301606A sc-301606 | 1 mg 5 mg | $57.00 $172.00 | 8 | |
An mTOR kinase inhibitor that attenuates mTORC1 and mTORC2 signaling, leading to reduced NHSL2 activity. | ||||||
Apigenin | 520-36-5 | sc-3529 sc-3529A sc-3529B sc-3529C sc-3529D sc-3529E sc-3529F | 5 mg 100 mg 1 g 5 g 25 g 100 g 1 kg | $33.00 $214.00 $734.00 $1151.00 $2348.00 $3127.00 $5208.00 | 22 | |
Inhibits mTOR by reducing its phosphorylation, thereby impacting downstream effectors such as NHSL2. | ||||||
KU 0063794 | 938440-64-3 | sc-361219 | 10 mg | $209.00 | ||
A selective mTOR inhibitor, thereby decreasing the activity of downstream proteins including NHSL2. | ||||||