Quinoclamine


CAS No. : 2797-51-5

2797-51-5
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Cat. No. : HY-121632
M.Wt: 207.62
Formula: C10H6ClNO2
Purity: >98 %
Solubility: DMSO : 250 mg/mL (ultrasonic)
Introduction of 2797-51-5 :

Quinoclamine, a naphthoquinone derivative, is a NF-κB inhibitor. Quinoclamine exhibits anti-cancer activity[1][2]. IC50 & Target: NF-κB[2] In Vitro: Quinoclamine causes differentiation of U-937 cells into macrophage-like cells[1].
Quinoclamine inhibits NF-κB activities in HepG2 cells, with an IC50 of 1.7 μM[2].
Quinoclamine (1-4 μM; 30 minutes ) suppresses endogenous NF-κB activity in HepG2 cells through the inhibition of IκB-α phosphorylation and p65 translocation[2].
Quinoclamine inhibits induced NF-κB activities in lung and breast cancer cell lines[2].
Quinoclamine affects the expression levels of genes involved in cell cycle or apoptosis[2].
Quinoclamine down-regulates the expressions of UDP glucuronosyltransferase genes involved in phase II drug metabolism[2].

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