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ARRY-382 CSF-1R inhibitor

Cat.No.S3570

ARRY-382 is a highly selective, oral inhibitor of the CSF1R with an IC50 of 9 nM.
ARRY-382 CSF-1R inhibitor Chemical Structure

Chemical Structure

Molecular Weight: 564.68

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Quality Control

Batch: S357001 DMSO]5 mg/mL]false]Ethanol]5 mg/mL]false]Water]Insoluble]false Purity: 99.16%
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99.16

Solubility

In vitro
Batch:

DMSO : 5 mg/mL (8.85 mM)
(Moisture-contaminated DMSO may reduce solubility. Use fresh, anhydrous DMSO.)

Ethanol : 5 mg/mL

Water : Insoluble

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In vivo
Batch:

In vivo Formulation Calculator (Clear solution)

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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.

Chemical Information, Storage & Stability

Molecular Weight 564.68 Formula

C32H36N8O2

Storage (From the date of receipt) 3 years -20°C powder
CAS No. 1313407-95-2 -- Storage of Stock Solutions

Synonyms N/A Smiles CN1CCN(CCOC2=CC3=NC=C([N]3C=C2)C(=O)NC4=C5C(=CC=C4)[N](CC6=CC=CC(=N6)C)N=C5C7CC7)CC1

Mechanism of Action

Targets/IC50/Ki
CSF1R
9 nM
In vitro

ARRY-382 is a highly selective, oral inhibitor of the CSF1R with an IC50 of 9 nM.

References

Clinical Trial Information

(data from https://clinicaltrials.gov, updated on 2024-05-22)

NCT Number Recruitment Conditions Sponsor/Collaborators Start Date Phases
NCT02880371 Terminated
Advanced Solid Tumors
Pfizer
September 1 2016 Phase 1|Phase 2

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