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CAL-101 (Idelalisib) PI3Kδ inhibitor

Cat.No.S2226

Idelalisib (CAL-101) is a selective p110δ inhibitor with IC50 of 2.5 nM in cell-free assays; shown to have 40- to 300-fold greater selectivity for p110δ than p110α/β/γ, and 400- to 4000-fold more selectivity to p110δ than C2β, hVPS34, DNA-PK and mTOR. Idelalisib also stimulates autophagy.
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Quality Control

Batch: Purity: 99.93%
99.93

Solubility in DMSO or Water

In vitro
Batch:

DMSO : 83 mg/mL (199.79 mM)
(Moisture-contaminated DMSO may reduce solubility. Use fresh, anhydrous DMSO.)

Water : Insoluble

Ethanol : Insoluble

The solubility data above are all experimental results (not literature values).

Molarity Calculator

Mass Concentration Volume Molecular Weight
Dilution Calculator Molecular Weight Calculator

In vivo
Batch:

In vivo Formulation Calculator (Clear solution)

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Calculation results:

Working concentration: mg/ml;

Method for preparing DMSO master liquid: mg drug pre-dissolved in μL DMSO ( Master liquid concentration mg/mL, Please contact us first if the concentration exceeds the DMSO solubility of the batch of drug. )

Method for preparing in vivo formulation: Take μL DMSO master liquid, next addμL PEG300, mix and clarify, next addμL Tween 80, mix and clarify, next add μL ddH2O, mix and clarify.

Method for preparing in vivo formulation: Take μL DMSO master liquid, next add μL Corn oil, mix and clarify.

Note: 1. Please make sure the liquid is clear before adding the next solvent.
2. Be sure to add the solvent(s) in order. You must ensure that the solution obtained, in the previous addition, is a clear solution before proceeding to add the next solvent. Physical methods such
as vortex, ultrasound or hot water bath can be used to aid dissolving.

Read more about CAL-101 (Idelalisib) solubility in DMSO or water

Working Concentrations for Cell Culture Treatment

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Mechanism of Action

Information CAL-101 (Idelalisib) is a potent, selective PI3Kδ inhibitor. It affects the PI3K/AKT/mTOR signaling pathway by binding to the kinase ATP-binding cleft and reducing AKT phosphorylation, effectively inhibiting tumor cell proliferation and promoting apoptosis in hematological malignancies.

Read more about CAL-101 (Idelalisib) IC50 for cell-based and cell-free assays

Primary Applications and Mechanism of Action

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Chemical Information, Storage & Stability

Molecular Weight 415.42 Formula

C22H18FN7O

Storage (From the date of receipt)
CAS No. 870281-82-6 Download SDF Storage of Stock Solutions

Synonyms GS-1101 Smiles CCC(C1=NC2=C(C(=CC=C2)F)C(=O)N1C3=CC=CC=C3)NC4=NC=NC5=C4NC=N5

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Read more comparative analysis about CAL-101 (Idelalisib)

Tech Support

Handling Instructions

Tel: +1-832-582-8158 Ext:3

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Frequently Asked Questions

Question 1:
What is the recommended dose and the route of administration for it in mouse studies?

Answer:
According to the following paper, it can be used by I.V. administration at the concentration of 40 mg/kg. https://www.ncbi.nlm.nih.gov/pubmed/24625684