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Poloxime

Catalog No. T16559Cas No. 17302-61-3

Poloxime is a hydrolysis product of poloxin and is a non-ATP-competitive Plk1 inhibitor. It also has moderate Plk1 inhibitory activity.

Poloxime

Poloxime

Catalog No. T16559Cas No. 17302-61-3
Poloxime is a hydrolysis product of poloxin and is a non-ATP-competitive Plk1 inhibitor. It also has moderate Plk1 inhibitory activity.
Pack SizePriceAvailabilityQuantity
2 mg$395 days
5 mg$627-10 days
10 mg$927-10 days
25 mg$1397-10 days
50 mg$1777-10 days
100 mg$2977-10 days
1 mL x 10 mM (in DMSO)$687-10 days
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Product Introduction

Bioactivity
Description
Poloxime is a hydrolysis product of poloxin and is a non-ATP-competitive Plk1 inhibitor. It also has moderate Plk1 inhibitory activity.
In vitro
Poloxime (100 μM) suppresses phosphopeptide binding to the polo-box domain (PBD) of polo-like kinase 1 [2].
Chemical Properties
Molecular Weight179.22
FormulaC10H13NO2
Cas No.17302-61-3
Storage & Solubility Information
StoragePowder: -20°C for 3 years | In solvent: -80°C for 1 year | Shipping with blue ice.
Solubility Information
DMSO: 100 mg/mL (557.97 mM)
Solution Preparation Table
DMSO
1mg5mg10mg50mg
1 mM5.5797 mL27.8987 mL55.7973 mL278.9867 mL
5 mM1.1159 mL5.5797 mL11.1595 mL55.7973 mL
10 mM0.5580 mL2.7899 mL5.5797 mL27.8987 mL
20 mM0.2790 mL1.3949 mL2.7899 mL13.9493 mL
50 mM0.1116 mL0.5580 mL1.1159 mL5.5797 mL
100 mM0.0558 mL0.2790 mL0.5580 mL2.7899 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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