K-80003

Names

[ CAS No. ]:
1292821-90-9

[ Name ]:
K-80003

[Synonym ]:
4S7931G4PP
[(1Z)-5-Fluoro-1-(4-isopropylbenzylidene)-2-methyl-1H-inden-3-yl]acetic acid
1H-Indene-3-acetic acid, 5-fluoro-2-methyl-1-[[4-(1-methylethyl)phenyl]methylene]-, (1Z)-
[5-fluoro-1-(4-isopropylbenzylidene)-2-methylinden-3-yl]acetic acid

Biological Activity

[Description]:

K-80003 is a potent inhibitor of tRXRα-dependent Akt activation and cancer cell growth.

[Related Catalog]:

Research Areas >> Cancer

[Target]

Akt


[In Vitro]

When MCF-7 cells are cotreated with K-80003, TNFα-induced colocalization of tRXRα with p85α in the cytoplasm is inhibited, resulting in tRXRα nuclear localization. Western blotting shows that K-80003-stabilized tetrameric form of tRXRα is found exclusively in the nuclear fraction, while tRXRα monomer is distributed both in the nuclear and cytoplasmic fractions[2].

[In Vivo]

K-80003 is a potent inhibitor of AKT activation by all-trans-retinoic acid. K-80003 displays enhanced efficacy in inhibiting tRXRα-dependent AKT activation and tRXRα tumor growth in animals. K-80003 has high affinity to RXRα but lacks COX inhibitory activity[1].

[Cell Assay]

MCF-7 cells cotransfected with Myc-RXRα, Myc-tRXRα, tRXRα/L433D and p85α are pretreated with or without K-80003 (5 μM) for 3 h before exposed to TNFα (10 ng/mL) for 30 min. Cells are immunostained with anti-Myc and anti-p85α antibody, and their subcellular localization revealed by confocal microscopy. HEK293T cells cotransfected with Myc-tRXRα are treated with or without K-80003 (5 μM) for 6 h. Nuclear (N) and cytoplasmic (C) fractions are prepared, subjected to BS3 crosslinking, and analysed by western blotting using anti-Myc antibody. The purity of fractions is examined by analysing the expression of nuclear PARP and cytoplasmic α-tubulin in non-crosslinked fractions. One of three similar experiments is shown[2].

[Animal admin]

Mice[1] Nude mice (BALB/c, 4-5-week old) are injected subcutaneously with 100 μL of cells (2×106). For drug treatment, mice (n=6) are treated intraperitoneally after 7 days of transplantation with Corn oil, Sulindac (60 mg/kg), or K-80003 (60 mg/kg) once every other day (six injections). Body weight and tumor sizes are measured every 4 days.

[References]

[1]. Zhou H, et al. NSAID sulindac and its analog bind RXRalpha and inhibit RXRalpha-dependent AKT signaling. Cancer Cell. 2010 Jun 15;17(6):560-73.

[2]. Chen L, et al. Modulation of nongenomic activation of PI3K signalling by tetramerization of N-terminally-cleaved RXRα. Nat Commun. 2017 Jul 17;8:16066.


[Related Small Molecules]

SB203580 | MK-2206 2HCl | SC79 | Capivasertib (AZD5363) | Honokiol | AKT inhibitor VIII | GDC-0068 | GSK690693 | Uprosertib | 1,3-Dicaffeoylquinic acid | TIC10 | Triciribine | Perifosine (KRX-0401) | afuresertib | A-443654

Chemical & Physical Properties

[ Density]:
1.2±0.1 g/cm3

[ Boiling Point ]:
491.6±40.0 °C at 760 mmHg

[ Molecular Formula ]:
C22H21FO2

[ Molecular Weight ]:
336.399

[ Flash Point ]:
251.1±27.3 °C

[ Exact Mass ]:
336.152557

[ LogP ]:
6.60

[ Vapour Pressure ]:
0.0±1.3 mmHg at 25°C

[ Index of Refraction ]:
1.615

[ Storage condition ]:
2-8℃


Related Compounds