ALK and LTK ligand 1, also known as ALKAL1 (or FAM150A/AUGα), is a protein that serves as a ligand for the receptor tyrosine kinases ALK (Anaplastic Lymphoma Kinase) and LTK (Leukocyte Tyrosine Kinase). These receptor tyrosine kinases are implicated in various cellular processes, including growth, differentiation, and repair.ALKAL1 is part of the ALKAL family, which includes ALKAL2 (FAM150B/AUGβ). It is a secreted protein that functions primarily through interaction with its receptor kinases, ALK and LTK, triggering phosphorylation cascades that lead to the activation of downstream signaling pathways. ALK is well-characterized for its role in neurodevelopment and the pathogenesis of certain cancers, such as anaplastic large-cell lymphoma, neuroblastoma, and non-small cell lung cancer, where it can be mutated or aberrantly expressed.
The binding of ALKAL1 to ALK activates the kinase domain of ALK, which then phosphorylates specific intracellular proteins, leading to the activation of signaling pathways involved in cell proliferation and survival, such as the PI3K/AKT and MEK/ERK pathways. This activation can contribute to the development and maintenance of the nervous system but can also be co-opted in cancerous processes where ALK is mutated or overexpressed.LTK's functions are less well-understood but are believed to be involved in hematopoiesis and immune responses. ALKAL1's interaction with LTK suggests a role in these processes, although detailed mechanisms remain to be fully elucidated.
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| Product Name | CAS # | Catalog # | QUANTITY | Price | Citations | RATING |
|---|---|---|---|---|---|---|
5-Chloro-N2-(2-isopropoxy-5-methyl-4-(piperidin-4-yl)phenyl)-N4-(2-(isopropylsulfonyl)phenyl)pyrimidine-2,4-diamine | 1032900-25-6 | sc-505041 | 1 mg | $230.00 | ||
Ceritinib selectively inhibits ALK tyrosine kinase activity, resulting in reduced tumor cell proliferation in ALK-expressing cells. | ||||||
CH5424802 | 1256580-46-7 | sc-364461 sc-364461A | 5 mg 50 mg | $191.00 $902.00 | ||
Alectinib is an oral inhibitor of ALK, effectively targeting ALK phosphorylation and downstream signaling pathways. | ||||||
Lorlatinib | 1454846-35-5 | sc-507437 | 5 mg | $135.00 | ||
Lorlatinib is a third-generation ALK inhibitor, effective against most known resistant ALK mutations. | ||||||
Entrectinib | 1108743-60-7 | sc-507438 | 5 mg | $180.00 | ||
Entrectinib targets ALK, ROS1, and NTRK, inhibiting their kinase activity and blocking signal transduction. | ||||||
TAE684 | 761439-42-3 | sc-364626 sc-364626A | 5 mg 50 mg | $188.00 $988.00 | 2 | |
TAE684 is a highly selective ALK inhibitor, effective in cell lines dependent on ALK activity. | ||||||
GSK 690693 | 937174-76-0 | sc-363280 sc-363280A | 10 mg 50 mg | $255.00 $1071.00 | 4 | |
GSK1838705A inhibits ALK, IGF-1R, and the insulin receptor, disrupting signaling pathways essential for tumor cell survival. | ||||||