XL228

XL228 is a protein kinase inhibitor with IC50 of 5 nM, 1.4 nM, 3.1 nM, 1.6 nM, 6.1 nM and 2 nM for wild-type ABL kinase, ABL T315I, Aurora A, IGF-1R, SRC and LYN, respectively.

XL228 Chemical Structure

XL228 Chemical Structure

CAS: 898280-07-4

Purity & Quality Control

Batch: S127201 DMSO] 88 mg/mL] false] Ethanol] 30 mg/mL] false] Water] Insoluble] false Purity: 99.85%
99.85

XL228 Related Products

Signaling Pathway

Choose Selective Bcr-Abl Inhibitors

Biological Activity

Description XL228 is a protein kinase inhibitor with IC50 of 5 nM, 1.4 nM, 3.1 nM, 1.6 nM, 6.1 nM and 2 nM for wild-type ABL kinase, ABL T315I, Aurora A, IGF-1R, SRC and LYN, respectively.
Targets
ABL T315I [1]
(Cell-free assay)
IGF-1R [1]
(Cell-free assay)
LYN [1]
(Cell-free assay)
Aurora A [1]
(Cell-free assay)
wild-type ABL kinase [1]
(Cell-free assay)
Click to View More Targets
1.4 nM 1.6 nM 2 nM 3.1 nM 5 nM
NCT Number Recruitment Conditions Sponsor/Collaborators Start Date Phases
NCT00526838 Terminated
Cancer|Lymphoma
Exelixis
September 2007 Phase 1
NCT00464113 Terminated
Chronic Myeloid Leukemia|Leukemia Lymphoblastic Acute Philadelphia-Positive
Exelixis
May 2007 Phase 1

Chemical Information & Solubility

Molecular Weight 437.54 Formula

C22H31N9O

CAS No. 898280-07-4 SDF --
Smiles CC(C)C1=NOC(=C1)CNC2=NC(=CC(=N2)N3CCN(C)CC3)NC4=N[NH]C(=C4)C5CC5
Storage (From the date of receipt) 3 years -20°C powder

In vitro
Batch:

DMSO : 88 mg/mL ( (201.12 mM); Moisture-absorbing DMSO reduces solubility. Please use fresh DMSO.)

Ethanol : 30 mg/mL

Water : Insoluble


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In vivo
Batch:

Add solvents to the product individually and in order.


In vivo Formulation Calculator

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In vivo Formulation Calculator (Clear solution)

Step 1: Enter information below (Recommended: An additional animal making an allowance for loss during the experiment)

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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.

Tech Support

Answers to questions you may have can be found in the inhibitor handling instructions. Topics include how to prepare stock solutions, how to store inhibitors, and issues that need special attention for cell-based assays and animal experiments.

Handling Instructions

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