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871307-18-5

871307-18-5 Structure

871307-18-5 Structure
IdentificationBack Directory
[Name]

4-[(3-Chloro-4-fluorophenyl)amino]-6-[(3-pyridinylmethyl)amino]-1,7-naphthyridine-3-carbonitrile
[CAS]

871307-18-5
[Synonyms]

TC-S 7006
Tpl2-IN-2p
Tpl2 Kinase Inhibitor
Tpl2 Kinase Inhibitor 1
4-(3-chloro-4-fluorophenylamino)-6-(pyridin-3-ylmethylamino)-1,7-naphthyridine-3-carbonitrile
4-[(3-Chloro-4-fluorophenyl)amino]-6-[(3-pyridinylmethyl)amino]-1,7-naphthyridine-3-carbonitrile
1,7-Naphthyridine-3-carbonitrile, 4-[(3-chloro-4-fluorophenyl)amino]-6-[(3-pyridinylmethyl)amino]-
[Molecular Formula]

C21H14ClFN6
[MOL File]

871307-18-5.mol
[Molecular Weight]

404.83
Chemical PropertiesBack Directory
[density ]

1.45
[storage temp. ]

Sealed in dry,2-8°C
[solubility ]

DMF: 1 mg/ml; DMF:PBS(pH7.2) (1:2): 0.33 mg/ml; DMSO: 1 mg/ml
[form ]

A crystalline solid
Hazard InformationBack Directory
[Description]

Tpl2 kinase inhibitor is an inhibitor of tumor progression locus 2 (Tpl2; IC50 = 0.05 μM). It is selective for Tpl2 over MEK, p38 MAPK, Src, MK2, and PKC (IC50s = >40, 180, >400, 110, and >400 μM, respectively). Tpl2 kinase inhibitor inhibits LPS-induced TNF-α production in isolated human monocytes and whole blood (IC50s = 0.7 and 8.5 μM, respectively). It enhances differentiation induced by 1,25-dihydroxy vitamin D3 (calcitriol; ) in HL-60 and U937 leukemia cells when used at a concentration of 5 μM. Tpl2 kinase inhibitor (5 μM) inhibits the proliferation of KG-1a leukemia cells.
[Uses]

TC-S 7006 is a Tpl2 kinase inhibitor.
[storage]

Store at -20°C
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