Abcam, ab142082, NVP-TAE684, ALK inhibitor

Size: 5mg
MW 614.2 Da, Purity >98%. Highly potent, selective ALK inhibitor in vitro (IC 50 = 2 nM). Suppresses lymphomagenesis in vivo . Down-regulates CD30 expression. Antitumor agent. Potent LRRK2 kinase inhibitor (IC 50 = 7.8 nM).
Key facts
CAS number:761439-42-3,
Purity:>98%,
Form:SolidSee storage information,
Molecular weight:614.2 Da,
Molecular formula:C30H40ClN7O3S,
PubChem:16038120,
Nature:Synthetic,
Solubility:Soluble in DMSO,
Biochemical name:5-chloro-N4-(2-(isopropylsulfonyl)phenyl)-N2-(2-methoxy-4-(4-(4-methylpiperazin-1-yl)piperidin-1-yl)phenyl)pyrimidine-2,4-diamine,
Biological description:Highly potent, selective ALK inhibitor in vitro (IC50 = 2 nM). Suppresses lymphomagenesis in vivo. Down-regulates CD30 expression. Antitumor agent. Potent LRRK2 kinase inhibitor (IC50 = 7.8 nM).,
Canonical smiles:CC(C)S(=O)(=O)C1=CC=CC=C1NC2=NC(=NC=C2Cl)NC3=C(C=C(C=C3)N4CCC(CC4)N5CCN(CC5)C)OC,
InChi:InChI=1S/C30H40ClN7O3S/c1-21(2)42(39,40)28-8-6-5-7-26(28)33-29-24(31)20-32-30(35-29)34-25-10-9-23(19-27(25)41-4)37-13-11-22(12-14-37)38-17-15-36(3)16-18-38/h5-10,19-22H,11-18H2,1-4H3,(H2,32,33,34,35),
InChiKey:QQWUGDVOUVUTOY-UHFFFAOYSA-N,
IUPAC Name:5-chloro-2-N-[2-methoxy-4-[4-(4-methylpiperazin-1-yl)piperidin-1-yl]phenyl]-4-N-(2-propan-2-ylsulfonylphenyl)pyrimidine-2,4-diamine

Product details:
This product is manufactured by BioVision, an Abcam company and was previously called 1683 NVP-TAE684. 1683-5 is the same size as the 5 mg size of ab142082.

Properties and Storage Information:
Shipped at conditions-Ambient - Can Ship with Ice, Appropriate long-term storage conditions--20°C, Storage information-Store under desiccating conditions, The product can be stored for up to 12 months

Supplementary Information:
This supplementary information is collated from multiple sources and compiled automatically.
ALK also known as Anaplastic Lymphoma Kinase is a receptor tyrosine kinase with a molecular mass of approximately 176 kDa. ALK plays an important role in cell signaling and is involved in the regulation of cell growth. It predominantly expresses in the nervous system but also appears in other tissues like the liver and small intestine. The PAK proteins including PAK1 PAK2 and PAK3 function as serine/threonine kinases important for various cellular processes and are expressed in tissues such as the brain and heart. Other targets in this group like MAP4K6 CaMKII PHKG2 MAP4K5 and MAP4K3/GLK function as kinases participating in signal transduction.
Biological function summary
These proteins help regulate critical cellular events like differentiation apoptosis and cytoskeletal reorganization. ALK often forms part of signaling complexes that control cellular communication. CaMKII which is calcium/calmodulin-dependent protein kinase II uniquely regulates synaptic signaling and memory function. PAK proteins mediate pathways that control cytoskeletal dynamics while MAP4K proteins participate in MAP kinase pathways that regulate cell proliferation and survival.
Pathways
These kinases integrate into significant signaling cascades such as the MAPK/ERK pathway and the PI3K/Akt pathway. The MAPK/ERK pathway involving proteins like MAP4K6 and MAP4K5 plays an important role in transmitting signals from growth factors outside the cell to the DNA in the nucleus affecting cell division and differentiation. PAK proteins also link to the PI3K/Akt pathway which influences many cellular processes including metabolism and survival. These pathways emphasize their influence in critical regulatory processes in the cell.
ALK mutations and rearrangements associate strongly with certain cancers such as non-small cell lung cancer and anaplastic large cell lymphoma. The aberrant activation of ALK leads to uncontrolled cell proliferation and survival which is a hallmark of cancer. PAK proteins relate to neurological disorders like Alzheimer's due to their role in cytoskeletal regulation and neuronal signaling. In these diseases interactions with other proteins like EGFR in the case of ALK and tau proteins for PAK1 highlight their relevance in disease mechanisms.