PHLDA3 Inhibitors represent a specialized category of chemical compounds designed to modulate the activity of the PHLDA3 protein. PHLDA3, or Pleckstrin Homology-Like Domain, Family A, Member 3, is known to play a crucial role in various cellular processes, including cell proliferation, apoptosis, and signal transduction pathways. The inhibitors of PHLDA3 are primarily focused on altering its interaction with key signaling molecules, thereby influencing its functional role in the cell. These chemical inhibitors are characterized by their ability to bind selectively to PHLDA3, leading to the modulation of its activity. This binding is typically achieved through the interaction with the pleckstrin homology domain of PHLDA3, which is pivotal in its function and interaction with other cellular components.
The chemical structure of PHLDA3 inhibitors is diverse, encompassing a range of small molecules with specific affinities and binding capabilities. These compounds are designed to achieve high specificity and potency, ensuring minimal off-target effects. The mode of action of these inhibitors can vary; some may inhibit PHLDA3 by directly binding to its active or allosteric sites, thereby preventing its interaction with other proteins or cellular components. Others may act indirectly by modulating signaling pathways upstream or downstream of PHLDA3, thereby influencing its activity or expression levels. The development of PHLDA3 inhibitors involves extensive research into the protein's structure, the dynamics of its interaction with other cellular components, and the pathways it influences. This understanding is crucial in designing molecules that can effectively modulate PHLDA3 activity for specific cellular outcomes. The precise mechanism of inhibition often dictates the chemical structure and properties of these inhibitors, which are tailored for optimal interaction with the target protein.
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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 | |
Rapamycin is a specific inhibitor of mTOR (mammalian target of rapamycin). It binds to FKBP12 and the resultant complex inhibits mTORC1, leading to decreased protein synthesis and cell proliferation. | ||||||
LY 294002 | 154447-36-6 | sc-201426 sc-201426A | 5 mg 25 mg | $123.00 $400.00 | 148 | |
LY294002 is a potent inhibitor of PI3K (phosphoinositide 3-kinases). It blocks AKT phosphorylation and activation, thereby inhibiting the PI3K/AKT/mTOR pathway. | ||||||
Wortmannin | 19545-26-7 | sc-3505 sc-3505A sc-3505B | 1 mg 5 mg 20 mg | $67.00 $223.00 $425.00 | 97 | |
Wortmannin is a steroidal metabolite and a potent, irreversible inhibitor of PI3K. It inhibits the AKT signaling pathway by preventing PI3K-mediated phosphorylation of AKT. | ||||||
AZD8055 | 1009298-09-2 | sc-364424 sc-364424A | 10 mg 50 mg | $163.00 $352.00 | 12 | |
AZD8055 is a potent, selective mTOR inhibitor that targets both mTORC1 and mTORC2 complexes, leading to a comprehensive blockade of the mTOR pathway. | ||||||
Torin 1 | 1222998-36-8 | sc-396760 | 10 mg | $245.00 | 7 | |
Torin 1 is an ATP-competitive inhibitor of mTOR that targets both mTORC1 and mTORC2 complexes. It has a higher selectivity for mTOR compared to PI3K. | ||||||
MK-2206 dihydrochloride | 1032350-13-2 | sc-364537 sc-364537A | 5 mg 10 mg | $182.00 $332.00 | 67 | |
MK-2206 is an allosteric inhibitor of AKT. It inhibits all isoforms of AKT (AKT1, AKT2, AKT3) by modifying the kinase domain, leading to reduced cell proliferation. | ||||||
Perifosine | 157716-52-4 | sc-364571 sc-364571A | 5 mg 10 mg | $188.00 $327.00 | 1 | |
Perifosine is an alkylphospholipid that inhibits AKT activation in the plasma membrane, thereby disrupting the AKT signaling pathway. | ||||||
BEZ235 | 915019-65-7 | sc-364429 | 50 mg | $211.00 | 8 | |
BEZ235, also known as Dactolisib, is a dual inhibitor of both PI3K and mTOR. It inhibits the activation of PI3K and the downstream AKT/mTOR signaling pathway. | ||||||
GSK 690693 | 937174-76-0 | sc-363280 sc-363280A | 10 mg 50 mg | $255.00 $1071.00 | 4 | |
GSK690693 is a pan-AKT inhibitor that binds competitively to the ATP binding pocket of AKT, inhibiting its kinase activity. | ||||||
Palomid 529 | 914913-88-5 | sc-364563 sc-364563A | 10 mg 50 mg | $300.00 $1000.00 | ||
Palomid 529 is a novel PI3K/AKT/mTOR inhibitor. It disrupts the AKT/mTOR signaling pathway, leading to reduced cellular growth and proliferation. | ||||||