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GDC0084

SKU: orb1303870

Description

GDC-0084 (RG7666) is a selective PI3K inhibitor that blocks the PI3K/AKT signaling pathway, suppressing tumor cell proliferation and survival. It is utilized in oncology research for studying pathway biology and has demonstrated antitumor activity in both in vitro assays and in vivo xenograft models.

Research Area

Signal Transduction

Images & Validation

Key Properties

CAS Number1382979-44-3
MW382.42
Purity≥95%
FormulaC18H22N8O2
SMILESCC1(C)OCCn2c1nc1c(nc(nc21)-c1cnc(N)nc1)N1CCOCC1
TargetPI3K,mTOR
SolubilityEthanol:< 1 mg/mL (insoluble or slightly soluble);H2O:< 1 mg/mL (insoluble or slightly soluble);DMSO:3.83 mg/mL (10.02 mM)

Bioactivity

Target IC50
mTOR:70 nM(Ki app)|PI3Kγ:10 nM(Ki app)|PI3Kα:2 nM(Ki app)|PI3Kβ:46 nM(Ki app)|PI3Kδ:3 nM(Ki app)
In Vivo
In human microsomal and stem cell cultures, GDC-0084 showed good metabolic stability and inhibited pAKT, a key signal of the PI3K pathway, in normal brain tissues.GDC-0084 inhibited the proliferation of a variety of glioma cells (IC50: 0.3-1.1 μM).The binding rate of GDC-0084 to plasma proteins was low, and the free fraction of GDC-0084 in CD-1 mouse plasma was 29.5±2.0%. was 29.5±2.7% (n=3,5 μM), while the binding rate to brain tissue was higher in CD-1 mice with a free fraction of only 6.7±1% (n=3).
In Vitro
In human microsomal and stem cell cultures, GDC-0084 showed good metabolic stability and inhibited pAKT, a key signal of the PI3K pathway, in normal brain tissues.GDC-0084 inhibited the proliferation of a variety of glioma cells (IC50: 0.3-1.1 μM).The binding rate of GDC-0084 to plasma proteins was low, and the free fraction of GDC-0084 in CD-1 mouse plasma was 29.5±2.0%. was 29.5±2.7% (n=3,5 μM), while the binding rate to brain tissue was higher in CD-1 mice with a free fraction of only 6.7±1% (n=3).
Cell Research
For transport studies, cells are seeded on 24-well Millicell plates 4 days prior to use(polyethylene terephtalate membrane, 1 μm pore size) at a seeding density of 1.3×105 cells/ml). GDC-0084 is tested at 5 μM in the apical-tobasolateral (A-B) and basolateral-to-apical (B-A) directions. The compound is dissolved in transport buffer consisting of Hanks' balanced salt solution with 10 mM HEPES. Lucifer Yellow is used as the paracellular and monolayer integrity marker. GDC-0084 concentrations in the donor and receiving compartments are determined by liquid chromatography-tandem mass spectrometry (LC-MS/MS) analysis. The apparent permeability (Papp), in the apical to A-B and B-A directions, is calculated after 2-hour incubation.(Only for Reference)

Storage & Handling

StoragePowder: -20°C for 3 years | In solvent: -80°C for 1 year | Shipping with blue ice/Shipping at ambient temperature.
Expiration Date12 months from date of receipt.
DisclaimerFor research use only

Alternative Names

GDC 0084, GDC0084, GDC-0084, mTOR, Paxalisib, RG 7666, RG7666, RG-7666, PI3Kα, PI3Kβ, PI3Kγ, PI3Kδ
Quality Guarantee

Quality Guarantee

Explore bioreagents carefree to elevate your research. All our products are rigorously tested for performance. If a product does not perform as described on its datasheet, our scientific support team will provide expert troubleshooting, a prompt replacement, or a refund. For full details, please see our Terms & Conditions and Buying Guide. Contact us at [email protected].

Key Properties

No computed properties available.

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GDC0084 (orb1303870)

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% DMSO +
%+
% Tween 80 +
%

Available Sizes

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2 mg
$ 80.00
1 ml x 10 mM (in DMSO)
$ 90.00
5 mg
$ 100.00
10 mg
$ 130.00
25 mg
$ 220.00
50 mg
$ 340.00
100 mg
$ 610.00
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