Vergleich

FL-411

ArtNr CS-0034229-10mg
Hersteller ChemScene
Menge 10mg
Kategorie
Typ Molecules
Specific against other
ECLASS 10.1 32169090
ECLASS 11.0 32169090
UNSPSC 12000000
Similar products 2118944-88-8
Lieferbar
Alternative Names
BRD4-IN-1
CAS
2118944-88-8
Purity
>98%
Formula
C18H19N3O2S
MWt
341.43
Solubility
DMSO : 5.4 mg/mL (15.82 mM; Need ultrasonic); H2O : < 0.1 mg/mL (insoluble)
Clinical Information
No Development Reported
Pathway
Epigenetics
Target
Epigenetic Reader Domain
Biological Activity
FL-411 is a potent and selective BRD4 inhibitor with an IC50 of 0.43+/-0.09 uM for BRD4(1). IC50 & Target: IC50: 0.43+/-0.09 uM (BRD4(1))[1] In Vitro: FL-411 is a selective BRD4 inhibitor. Binding affinities of FL-411 are measured by TR-FRET against the first and second bromodomains of BRD2(1), BRD4(1), and BRD4(2) with IC50s of 24.60+/-0.70 uM, 0.47+/-0.02 uM, 0.93+/-0.05 uM, respectively. FL-411 possesses a good BRD4(1) inhibition activity (IC50=0.43+/-0.09 uM), antiproliferative activity (MCF-7, IC50=1.62+/-0.06 uM; MDA-MB-231, IC50=3.27+/-0.14 uM), and autophagic activity (42.29% in MCF-7 cells), as well as displays a low toxicity against MCF10A cells). FL-411 induces ATG5-dependent autophagy-associated cell death (ACD) by blocking BRD4-AMPK interaction and thus activating AMPK-mTOR-ULK1-modulated autophagic pathway in breast cancer cells[1]. In Vivo: To evaluate the antitumor activity of FL-411 in vivo, two breast tumor xenograft models, namely, MCF-7 and MDA-MB-231 cell lines models, are used. The in vivo study is conducted using three different doses of FL-411: 25 mg/kg, 50 mg/kg, and 100 mg/kg. In all the models, FL-411 shows significant tumor growth inhibition in a dose-dependent manner as determined by 80% and 76% tumor growth inhibition ratio in MCF-7 and MDA-MB-231 cell models, respectively. A remarkable loss of tumor weights is observed in all dose groups (p<0.001). FL-411 displays no obvious effects on the body weight of all the treatment groups. To examine whether FL-411-mediated inhibition of tumor growth in vivo is associated with reduced cell proliferation and the increased autophagy-associated cell death, tumor tissues from control and FL-411-treated mice are processed for the immunohistochemical analysis of Ki-67 and LC3. FL-411 treatment obviously reduces the number of Ki-67 (p<0.001) positive cells as well as increases autophagy levels, which is determined by increased LC3 expression (p<0.001)[1].

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Alle Produkte sind nur für Forschungszwecke bestimmt. Nicht für den menschlichen, tierärztlichen oder therapeutischen Gebrauch.

Menge: 10mg
Lieferbar: In stock
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