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PF-06273340

Catalog No. T19649Cas No. 1402438-74-7
Alias PF-6273340, PF6273340, PF 6273340, PF 06273340

PF-06273340 is an effective, Selective, and Peripherally Restricted Pan-Trk inhibitor (IC50: Trk-A = 6 nM; Trk-B = 4 nM; Trk-C = 3 nM). PF-06273340 has low metabolic turnover in HLM and hHep is a good substrate for efflux transporters P-gp (ER = 35.7) and BCRP (ER = 4.0) and has moderate passive permeability (RRCK Papp = 5.4 × 10 6 cm s 1).

PF-06273340

PF-06273340

Purity: 98.00%
Catalog No. T19649Alias PF-6273340, PF6273340, PF 6273340, PF 06273340Cas No. 1402438-74-7
PF-06273340 is an effective, Selective, and Peripherally Restricted Pan-Trk inhibitor (IC50: Trk-A = 6 nM; Trk-B = 4 nM; Trk-C = 3 nM). PF-06273340 has low metabolic turnover in HLM and hHep is a good substrate for efflux transporters P-gp (ER = 35.7) and BCRP (ER = 4.0) and has moderate passive permeability (RRCK Papp = 5.4 × 10 6 cm s 1).
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Purity:98.00%
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Product Introduction

Bioactivity
Description
PF-06273340 is an effective, Selective, and Peripherally Restricted Pan-Trk inhibitor (IC50: Trk-A = 6 nM; Trk-B = 4 nM; Trk-C = 3 nM). PF-06273340 has low metabolic turnover in HLM and hHep is a good substrate for efflux transporters P-gp (ER = 35.7) and BCRP (ER = 4.0) and has moderate passive permeability (RRCK Papp = 5.4 × 10 6 cm s 1).
AliasPF-6273340, PF6273340, PF 6273340, PF 06273340
Chemical Properties
Molecular Weight479.92
FormulaC23H22ClN7O3
Cas No.1402438-74-7
Storage & Solubility Information
Storagestore at low temperature | Powder: -20°C for 3 years | In solvent: -80°C for 1 year | Shipping with blue ice.
Solubility Information
H2O: Insoluble
DMSO: 90 mg/mL (187.53 mM)
Ethanol: 1 mg/mL (2.08 mM)
Solution Preparation Table
Ethanol/DMSO
1mg5mg10mg50mg
1 mM2.0837 mL10.4184 mL20.8368 mL104.1840 mL
DMSO
1mg5mg10mg50mg
5 mM0.4167 mL2.0837 mL4.1674 mL20.8368 mL
10 mM0.2084 mL1.0418 mL2.0837 mL10.4184 mL
20 mM0.1042 mL0.5209 mL1.0418 mL5.2092 mL
50 mM0.0417 mL0.2084 mL0.4167 mL2.0837 mL
100 mM0.0208 mL0.1042 mL0.2084 mL1.0418 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
For Reference Only. Please develop an appropriate dissolution method based on your laboratory animals and route of administration.
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