Date published: 2025-11-24

00800 4573 8000

SCBT Portrait Logo
Seach Input

Inhibiteurs MerTK

MerTK inhibitors represent a specialized category of chemical compounds designed to specifically target and impede the activity of the MerTK receptor tyrosine kinase. MerTK, an abbreviation for Mer Tyrosine Kinase, is a prominent member of the TAM (Tyro3, Axl, and Mer) family of receptor kinases, which exert pivotal control over numerous cellular processes. Predominantly expressed on the surfaces of phagocytic cells, such as macrophages and dendritic cells, MerTK activation plays a central role in recognizing and engulfing apoptotic cells and cellular debris, a fundamental aspect of the body's immune response and tissue equilibrium. However, when MerTK becomes dysregulated or experiences overexpression, it has been linked to various diseases, including cancer, autoimmune disorders, and chronic inflammation.

Consequently, MerTK inhibitors have been meticulously engineered to selectively disrupt MerTK's signaling pathways. These inhibitors primarily function by binding to the catalytic site of MerTK, effectively obstructing the receptor's ability to phosphorylate downstream signaling molecules. Consequently, they interrupt its cellular functions, exerting influence over vital processes such as phagocytosis, cytokine production, and interactions between immune cells. The ramifications of MerTK inhibition extend to diseases characterized by irregular cell clearance, immune evasion, or tissue remodeling. Researchers are continually refining MerTK inhibitors, exploring their capacity to address health challenges associated with MerTK-related cellular pathways.

VOIR ÉGALEMENT...

Items  11  to  13  of  13 total

Afficher:

Nom du produitCAS #Ref. CatalogueQuantitéPrix HTCITATIONS Classement

Bortezomib

179324-69-7sc-217785
sc-217785A
2.5 mg
25 mg
$132.00
$1064.00
115
(2)

Inhibe le protéasome, entraînant l'accumulation de protéines mal repliées et l'apoptose dans le myélome multiple.

Palbociclib

571190-30-2sc-507366
50 mg
$315.00
(0)

Inhibe sélectivement CDK4 et CDK6, arrêtant la progression du cycle cellulaire dans le cancer du sein.

ABT-199

1257044-40-8sc-472284
sc-472284A
sc-472284B
sc-472284C
sc-472284D
1 mg
5 mg
10 mg
100 mg
3 g
$116.00
$330.00
$510.00
$816.00
$1632.00
10
(0)

Cible BCL-2, favorisant l'apoptose dans les cellules de leucémie lymphoïde chronique.