PL6 inhibitors belong to a class of small molecules designed to target and modulate the activity of Phospholipase 6 (PL6), an enzyme involved in various cellular signaling pathways. Phospholipase 6 is a critical player in intracellular signal transduction, particularly in response to extracellular stimuli such as growth factors and hormones. This enzyme acts by cleaving phospholipids in the cell membrane, generating second messengers like inositol trisphosphate (IP3) and diacylglycerol (DAG), which trigger downstream cellular responses. Inhibitors of PL6 are meticulously designed compounds aimed at interfering with the catalytic activity of this enzyme, ultimately disrupting its downstream signaling pathways. These inhibitors typically function through competitive binding to the active site of PL6, impeding its substrate interaction and subsequent hydrolysis of membrane phospholipids.
The development and study of PL6 inhibitors have been of significant interest in the field of cell biology and molecular pharmacology due to their ability to unveil the intricacies of cellular signaling cascades. Researchers employ PL6 inhibitors as valuable tools to dissect the roles of PL6-mediated pathways in various cellular processes, including cell growth, proliferation, differentiation, and migration. By selectively blocking PL6 activity, these inhibitors enable scientists to explore the specific contributions of PL6 in cellular responses to external stimuli and gain insights into the underlying molecular mechanisms. Additionally, PL6 inhibitors can serve as starting points for drug discovery and development efforts aimed at targeting aberrant signaling pathways in diseases such as cancer and inflammatory disorders. In summary, PL6 inhibitors represent a versatile class of compounds that play a pivotal role in advancing our understanding of cellular signaling processes and hold promise for future interventions.
| Product Name | CAS # | Catalog # | QUANTITY | Price | Citations | RATING |
|---|---|---|---|---|---|---|
Sunitinib, Free Base | 557795-19-4 | sc-396319 sc-396319A | 500 mg 5 g | $153.00 $938.00 | 5 | |
Inhibits PL6 by binding to its ATP-binding site, disrupting downstream signaling pathways crucial for cell proliferation and angiogenesis. | ||||||
Erlotinib Hydrochloride | 183319-69-9 | sc-202154 sc-202154A | 10 mg 25 mg | $75.00 $121.00 | 33 | |
Targets PL6 by blocking the activation of its downstream signaling, leading to the inhibition of cell growth and proliferation. | ||||||
Palbociclib | 571190-30-2 | sc-507366 | 50 mg | $321.00 | ||
Selectively inhibits PL6 by binding to CDK4/6, preventing cell cycle progression and inhibiting | ||||||
Dasatinib | 302962-49-8 | sc-358114 sc-358114A | 25 mg 1 g | $70.00 $145.00 | 51 | |
Inhibits PL6 through its action as a multi-kinase inhibitor, interfering with PL6-mediated pathways implicated. | ||||||
Everolimus | 159351-69-6 | sc-218452 sc-218452A | 5 mg 50 mg | $131.00 $651.00 | 7 | |
Acts as an mTOR inhibitor, thereby suppressing PL6 activity by disrupting mTORC1 complex and inhibiting protein synthesis. | ||||||
Ribociclib | 1211441-98-3 | sc-507367 | 10 mg | $450.00 | ||
Selective CDK4/6 inhibitor that hinders PL6 activity by blocking the cell cycle progression and suppressing | ||||||
Pazopanib | 444731-52-6 | sc-396318 sc-396318A | 25 mg 50 mg | $130.00 $182.00 | 2 | |
Targets PL6 by inhibiting angiogenesis through VEGFR and PDGFR blockade. | ||||||
BIBF1120 | 656247-17-5 | sc-364433 sc-364433A | 5 mg 10 mg | $184.00 $321.00 | 2 | |
Blocks PL6 via simultaneous inhibition of FGFR, PDGFR, and VEGFR, reducing angiogenesis and fibrosis | ||||||
Ridaforolimus | 572924-54-0 | sc-212783 | 5 mg | $248.00 | 1 | |
Inhibits PL6 through mTOR inhibition, preventing downstream signaling and protein synthesis | ||||||