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AZ7550 trimesylate salt

Catalog No. T13564L2Cas No. 2319837-99-3
Alias AZ7550 trimesylate salt (1421373-99-0 free base), AZ7550 Mesylate

AZ7550 trimesylate salt (AZ7550 Mesylate) is the active metabolite of ositinib, AZ7550 trimesylate salt inhibits IGF1R activity and can be used in the study of non-small cell lung cancer.

AZ7550 trimesylate salt

AZ7550 trimesylate salt

Purity: 99.24%
Catalog No. T13564L2Alias AZ7550 trimesylate salt (1421373-99-0 free base), AZ7550 MesylateCas No. 2319837-99-3
AZ7550 trimesylate salt (AZ7550 Mesylate) is the active metabolite of ositinib, AZ7550 trimesylate salt inhibits IGF1R activity and can be used in the study of non-small cell lung cancer.
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1 mg$149In Stock
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Purity:99.24%
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Product Introduction

Bioactivity
Description
AZ7550 trimesylate salt (AZ7550 Mesylate) is the active metabolite of ositinib, AZ7550 trimesylate salt inhibits IGF1R activity and can be used in the study of non-small cell lung cancer.
Targets&IC50
ACK1:156 nM, FLT3:302 nM, FES:449 nM, ALK:420 nM, MNK2:228 nM, MLK1:88 nM, IGF-1R:1.6 μM, ERB4:195 nM, BRK:843 nM, IRR:840 nM
In vitro
AZ7550 trimesylate salt (Compound 28) demonstrates a potency and selectivity profile broadly similar to the parent compound AZD9291. Inhibiting the double mutant (DM) cell line H1975, activating mutant (AM) cell line PC9, and wild-type (WT) cell line LoVo, AZ7550 trimesylate salt exhibits IC50s of 45, 26, and 786 nM, respectively. Moreover, it inhibits the antiproliferative cell lines H1975 (DM), PC9 (AM), and Calu3 (WT) with GI50s of 19, 15, and 537 nM, respectively[1].
AliasAZ7550 trimesylate salt (1421373-99-0 free base), AZ7550 Mesylate
Chemical Properties
Molecular Weight773.9
FormulaC30H43N7O11S3
Cas No.2319837-99-3
Storage & Solubility Information
Storagekeep away from moisture | Powder: -20°C for 3 years | In solvent: -80°C for 1 year | Shipping with blue ice.
Solubility Information
DMSO: 20 mg/mL (25.84 mM), Sonication is recommended.
Solution Preparation Table
DMSO
1mg5mg10mg50mg
1 mM1.2922 mL6.4608 mL12.9216 mL64.6078 mL
5 mM0.2584 mL1.2922 mL2.5843 mL12.9216 mL
10 mM0.1292 mL0.6461 mL1.2922 mL6.4608 mL
20 mM0.0646 mL0.3230 mL0.6461 mL3.2304 mL

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Please enter your animal experiment information in the following box and click Calculate to obtain the mother liquor preparation method and in vivo formula preparation method:
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
For Reference Only. Please develop an appropriate dissolution method based on your laboratory animals and route of administration.
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