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ZK824859 hydrochloride (2271122-53-1 free base)

Catalog No. T13409L
Alias ZK824859 hydrochloride

ZK824859 hydrochloride is an oral available and selective inhibitor of urokinase plasminogen activator (uPA)(IC50s of 79 nM, 1580 nM and 1330 nM for human uPA, tPA, and plasmin, respectively).

ZK824859 hydrochloride (2271122-53-1 free base)

ZK824859 hydrochloride (2271122-53-1 free base)

Catalog No. T13409LAlias ZK824859 hydrochloride
ZK824859 hydrochloride is an oral available and selective inhibitor of urokinase plasminogen activator (uPA)(IC50s of 79 nM, 1580 nM and 1330 nM for human uPA, tPA, and plasmin, respectively).
Pack SizePriceAvailabilityQuantity
5 mg$398Backorder
10 mg$663Backorder
50 mg$1,850Backorder
100 mg$2,905Backorder
200 mgInquiryBackorder
500 mgInquiryBackorder
1 mL x 10 mM (in DMSO)$439Backorder
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Product Introduction

Bioactivity
Description
ZK824859 hydrochloride is an oral available and selective inhibitor of urokinase plasminogen activator (uPA)(IC50s of 79 nM, 1580 nM and 1330 nM for human uPA, tPA, and plasmin, respectively).
Targets&IC50
uPA (human):79 nM , Plasmin (human):1330 nM , TPA (human):1580 nM
In vitro
ZK824859 is 5 fold less potent and has lost selectivity in mouse: uPA with IC50 of 410?nM; tPA with IC50 of 910?nM; plasmin with IC50 of 1600?nM compared to human IC50 of 79?nM, 1580?nM and 1330?nM respectively.
AliasZK824859 hydrochloride
Chemical Properties
Molecular Weight464.89
FormulaC23H23ClF2N2O4
Storage & Solubility Information
StoragePowder: -20°C for 3 years | In solvent: -80°C for 1 year | Shipping with blue ice.
Solubility Information
DMSO: 125 mg/mL (268.88 mM)
Solution Preparation Table
DMSO
1mg5mg10mg50mg
1 mM2.1510 mL10.7552 mL21.5105 mL107.5523 mL
5 mM0.4302 mL2.1510 mL4.3021 mL21.5105 mL
10 mM0.2151 mL1.0755 mL2.1510 mL10.7552 mL
20 mM0.1076 mL0.5378 mL1.0755 mL5.3776 mL
50 mM0.0430 mL0.2151 mL0.4302 mL2.1510 mL
100 mM0.0215 mL0.1076 mL0.2151 mL1.0755 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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