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HSD1590

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Catalog No. T39944Cas No. 2379279-96-4

HSD1590 is a highly effective and potent inhibitor of ROCK1 and ROCK2, with IC50 values of 1.22 nM and 0.51 nM, respectively. It demonstrates exceptional binding affinity to ROCK, with Kd values below 2 nM. Moreover, HSD1590 showcases minimal cytotoxicity, making it an ideal compound for various applications.

HSD1590

HSD1590

😃Good
Catalog No. T39944Cas No. 2379279-96-4
HSD1590 is a highly effective and potent inhibitor of ROCK1 and ROCK2, with IC50 values of 1.22 nM and 0.51 nM, respectively. It demonstrates exceptional binding affinity to ROCK, with Kd values below 2 nM. Moreover, HSD1590 showcases minimal cytotoxicity, making it an ideal compound for various applications.
Pack SizePriceAvailabilityQuantity
5 mg405 €7-10 days
1 mL x 10 mM (in DMSO)395 €7-10 days
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Product Introduction

Bioactivity
Description
HSD1590 is a highly effective and potent inhibitor of ROCK1 and ROCK2, with IC50 values of 1.22 nM and 0.51 nM, respectively. It demonstrates exceptional binding affinity to ROCK, with Kd values below 2 nM. Moreover, HSD1590 showcases minimal cytotoxicity, making it an ideal compound for various applications.
Targets&IC50
ROCK1:1.22 nM (IC50), ROCK2:0.51 nM (IC50)
In vitro
HSD1590, when administered at concentrations ranging from 0.5 to 1 μM for 24 hours, significantly reduces migration, an effect not attributed to cellular mortality but to the inhibition of live cell movement, as further confirmed by studies at concentrations of 0.5-10 μM over 12-24 hours. Cell viability assays using MDA-MB-23 cells at these concentrations for the specified durations demonstrate about 80% viability at 12 hours, declining to 63% after 24 hours, underscoring the compound's effectiveness in inhibiting migration without causing substantial cell death.
Chemical Properties
Molecular Weight359.19
FormulaC20H18BN3O3
Cas No.2379279-96-4
Relative Density.1.43 g/cm3 (Predicted)
Storage & Solubility Information
StoragePowder: -20°C for 3 years | In solvent: -80°C for 1 year | Shipping with blue ice.

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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
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