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Inavolisib

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Catalog No. T15375Cas No. 2060571-02-8
Alias RG6114, GDC-0077

Inavolisib (GDC-0077) is an orally available selective PI3Kα inhibitor with an IC50 value of 0.038 nM.It exerts its activity by binding to the ATP-binding site of PI3K, thereby inhibiting the phosphorylation of PIP2 to PIP3.

Inavolisib

Inavolisib

🥰Excellent
Purity: 99.83%
Catalog No. T15375Alias RG6114, GDC-0077Cas No. 2060571-02-8
Inavolisib (GDC-0077) is an orally available selective PI3Kα inhibitor with an IC50 value of 0.038 nM.It exerts its activity by binding to the ATP-binding site of PI3K, thereby inhibiting the phosphorylation of PIP2 to PIP3.
Pack SizePriceAvailabilityQuantity
1 mg$80In Stock
5 mg$223In Stock
10 mg$392In Stock
25 mg$668In Stock
50 mg$1,090In Stock
100 mg$1,890In Stock
1 mL x 10 mM (in DMSO)$425In Stock
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Purity:99.83%
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Product Introduction

Bioactivity
Description
Inavolisib (GDC-0077) is an orally available selective PI3Kα inhibitor with an IC50 value of 0.038 nM.It exerts its activity by binding to the ATP-binding site of PI3K, thereby inhibiting the phosphorylation of PIP2 to PIP3.
Targets&IC50
PI3Kα:0.038 nM
In vitro
METHODS: Cell viability was assayed using Inavolisib (GDC-00777) up to 100 μmol/L in a panel of cancer cell lines.
RESULTS Inavolisib (GDC-00777) is a stronger cellular antiproliferative inducer. [1]
In vivo
METHODS: p110a protein depletion was studied in a p110a mutant xenograft breast cancer model using Inavolisib (GDC-0077) at a single oral dose of 50 mg/kgDC-0077.
RESULTS Inavolisib (GDC-0077) depleted p110a protein expression for up to 8 hours. [1]
AliasRG6114, GDC-0077
Chemical Properties
Molecular Weight407.37
FormulaC18H19F2N5O4
Cas No.2060571-02-8
SmilesC[C@H](Nc1ccc2-c3nc(cn3CCOc2c1)N1[C@@H](COC1=O)C(F)F)C(N)=O
Relative Density.1.63 g/cm3 (Predicted)
Storage & Solubility Information
Storagestore at low temperature,keep away from direct sunlight | Powder: -20°C for 3 years | In solvent: -80°C for 1 year | Shipping with blue ice.
Solubility Information
10% DMSO+40% PEG300+5% Tween 80+45% Saline: 10 mg/mL (24.55 mM), In vivo: Please add the solvents sequentially, clarifying the solution as much as possible before adding the next one. Dissolve by heating and/or sonication if necessary. Working solution is recommended to be prepared and used immediately.
DMSO: 100 mg/mL (245.48 mM), Sonication is recommended.
Solution Preparation Table
DMSO
1mg5mg10mg50mg
50 mM0.0491 mL0.2455 mL0.4910 mL2.4548 mL
100 mM0.0245 mL0.1227 mL0.2455 mL1.2274 mL

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TargetMol | Animal experimentsFor example, your dosage is 10 mg/kg Each animal weighs 20 g, and the dosage volume is 100 μL . TargetMol | Animal experiments A total of 10 animals were administered, and the formula you used is 5% TargetMol | reagent DMSO+30% PEG300+5% Tween 80+60% ddH2O. So your working solution concentration is 2 mg/mL。
Mother liquor preparation method: 2 mg of drug dissolved in 50 μL DMSOTargetMol | reagent (mother liquor concentration of 40 mg/mL), if you need to configure a concentration that exceeds the solubility of the product, please contact us first.
Preparation method for in vivo formula: Take 50 μL DMSOTargetMol | reagent main solution, add 300 μLPEG300TargetMol | reagent mix well and clarify, then add 50 more μL Tween 80, mix well and clarify, then add 600 more μLddH2OTargetMol | reagent mix well and clarify
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