Date published: 2025-10-10

1-800-457-3801

SCBT Portrait Logo
Seach Input

EML4 Inhibitors

EML4 inhibitors belong to a distinct chemical class characterized by their ability to selectively target and modulate the activity of echinoderm microtubule-associated protein-like 4 (EML4). EML4 is a key protein involved in microtubule dynamics, which play an essential role in cell division, intracellular transport, and maintaining cell shape. These inhibitors are designed to interact with specific binding sites on EML4, leading to alterations in its function and subsequently influencing cellular processes that rely on microtubule function. By perturbing EML4 activity, these inhibitors have impact cell proliferation, migration, and other processes that are associated with microtubule-dependent functions. The development of EML4 inhibitors represents a significant advancement in the field of molecular targeted research, as they offer a unique approach to modulating cellular activities that are crucial for normal cell physiology. Their specific mechanism of action and the intricate interplay between EML4 and microtubules make these inhibitors an intriguing subject of study in the realm of molecular pharmacology and cell biology.
Product NameCAS #Catalog #QUANTITYPriceCitationsRATING

CH5424802

1256580-46-7sc-364461
sc-364461A
5 mg
50 mg
$191.00
$902.00
(0)

Alectinib is a tyrosine kinase inhibitor targeting ALK and ROS1 receptors. It blocks the ATP-binding site, inhibiting receptor autophosphorylation and downstream signaling pathways, ultimately inhibiting cell proliferation and survival in ALK-positive and ROS1-positive cancer cells.

Lorlatinib

1454846-35-5sc-507437
5 mg
$135.00
(0)

Lorlatinib inhibits ALK, ROS1, and other kinases. It can cross the blood-brain barrier, making it effective against brain metastases. It binds to the ATP-binding pocket of the targeted kinases, disrupting their signaling cascades.

5-Chloro-N2-(2-isopropoxy-5-methyl-4-(piperidin-4-yl)phenyl)-N4-(2-(isopropylsulfonyl)phenyl)pyrimidine-2,4-diamine

1032900-25-6sc-505041
1 mg
$230.00
(0)

Ceritinib targets ALK by competing with ATP for binding to the kinase domain. It inhibits ALK-mediated signaling, resulting in decreased cell proliferation and increased apoptosis in ALK-positive cancer cells.

TAE684

761439-42-3sc-364626
sc-364626A
5 mg
50 mg
$184.00
$969.00
2
(1)

TAE-684 selectively targets ALK by blocking its kinase activity. It interferes with ATP binding to ALK's kinase domain, preventing downstream signaling and inhibiting tumor cell growth.