Date published: 2026-4-24

1-800-457-3801

SCBT Portrait Logo
Seach Input

Mel-CAM Inhibitors

Mel-CAM inhibitors, belonging to the class of cell adhesion molecule (CAM) inhibitors, are compounds specifically designed to target and modulate the activity of Mel-CAM, also known as MUC18 or CD146. Mel-CAM is a transmembrane glycoprotein that plays a pivotal role in cell adhesion and migration processes within various physiological and pathological contexts. This class of inhibitors aims to interfere with the interactions involving Mel-CAM, which is recognized for its involvement in mediating cell-cell adhesion and promoting cellular motility. Structurally, Mel-CAM possesses five extracellular immunoglobulin-like domains that participate in adhesive interactions. Mel-CAM is prominently expressed on the surface of endothelial cells, smooth muscle cells, melanocytes, and other cell types, and its aberrant expression has been associated with several diseases, particularly in cancer progression and metastasis.

Mel-CAM inhibitors are designed to selectively hinder the binding interactions between Mel-CAM and its ligands, which include integrins, other CAMs, and extracellular matrix components. By impeding these interactions, these inhibitors aim to modulate cellular adhesion and migration processes, altering cell behavior in various physiological and pathological contexts. The structural diversity within this class of inhibitors allows for the development of compounds with distinct binding affinities and mechanisms of action, enabling researchers to investigate the precise molecular mechanisms through which Mel-CAM participates in cell adhesion and migration. As our understanding of Mel-CAM's role in disease progression continues to evolve, the development and characterization of Mel-CAM inhibitors hold promise not only for advancing our fundamental knowledge of cellular processes but also for identifying novel strategies to intervene in diseases characterized by aberrant cell adhesion and migration.

SEE ALSO...

Product NameCAS #Catalog #QUANTITYPriceCitationsRATING

Trametinib

871700-17-3sc-364639
sc-364639A
sc-364639B
5 mg
10 mg
1 g
$114.00
$166.00
$947.00
19
(1)

Trametinib inhibits MEK1 and MEK2, key components of the MAPK pathway. By blocking MEK, it prevents the activation of downstream ERK and inhibits cell proliferation in cancers with RAS/RAF mutations.

Cobimetinib

934660-93-2sc-507421
5 mg
$270.00
(0)

Cobimetinib selectively inhibits MEK1 and MEK2, disrupting the MAPK pathway.

MEK 162

606143-89-9sc-488879
10 mg
$306.00
(0)

Binimetinib inhibits MEK1 and MEK2, interfering with the MAPK pathway. It has shown efficacy in various solid tumors, particularly BRAF-mutated melanoma.

Selumetinib

606143-52-6sc-364613
sc-364613A
sc-364613B
sc-364613C
sc-364613D
5 mg
10 mg
100 mg
500 mg
1 g
$29.00
$82.00
$420.00
$1897.00
$3021.00
5
(1)

Selumetinib targets MEK1/2, impeding the MAPK pathway. It has been studied for its potential for various cancers, including KRAS-mutated lung cancer.

BAY 869766

923032-37-5sc-364427
sc-364427A
5 mg
10 mg
$245.00
$428.00
1
(1)

Refametinib blocks MEK1/2, affecting the MAPK pathway and reducing cell proliferation. It has been evaluated in reserach models for different malignancies.

AS703026

1236699-92-5sc-364412
sc-364412A
5 mg
10 mg
$80.00
$130.00
(0)

Pimasertib is a selective MEK inhibitor that hinders the MAPK pathway, potentially suppressing tumor growth in cancers with specific mutations.

TAK-733

1035555-63-5sc-364630
sc-364630A
5 mg
10 mg
$340.00
$640.00
1
(0)

TAK-733 targets MEK1/2, interfering with the MAPK pathway. It has been explored in research models for its anti-cancer properties.