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HTH-01-091

Catalog No. T24152Cas No. 2000209-42-5
Alias HTH01-091, HTH-01091, HTH 01-091, HTH 01091

HTH-01-091 is a potent and selective maternal embryonic leucine zipper kinase (MELK) inhibitor (IC50: 10.5 nM) that also inhibits PIM1/2/3, RIPK2, DYRK3, smMLCK, and CLK2. It can be used to study breast cancer.

HTH-01-091

HTH-01-091

Purity: 98.40%
Catalog No. T24152Alias HTH01-091, HTH-01091, HTH 01-091, HTH 01091Cas No. 2000209-42-5
HTH-01-091 is a potent and selective maternal embryonic leucine zipper kinase (MELK) inhibitor (IC50: 10.5 nM) that also inhibits PIM1/2/3, RIPK2, DYRK3, smMLCK, and CLK2. It can be used to study breast cancer.
Pack SizePriceAvailabilityQuantity
1 mg$296In Stock
5 mg$728In Stock
10 mg$987In Stock
25 mg$1,530In Stock
50 mg$1,980In Stock
100 mg$2,500In Stock
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Purity:98.40%
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Product Introduction

Bioactivity
Description
HTH-01-091 is a potent and selective maternal embryonic leucine zipper kinase (MELK) inhibitor (IC50: 10.5 nM) that also inhibits PIM1/2/3, RIPK2, DYRK3, smMLCK, and CLK2. It can be used to study breast cancer.
Targets&IC50
DYRK4:41.8 nM, mTOR:632 nM, Pim1:60.6 nM, CDK7:1230 nM
In vitro
HTH-01-091 (0-10 μM, 1 h) dose-dependently decreased MELK pull-down by streptavidin beads, demonstrating that the compound is cell permeable and binds to MELK in an ATP-competitive fashion causes MELK degradation.[1]
HTH-01-091 (1 μM) selectively inhibits 4% of the kinases over 90%[1].
HTH-01-091 (0-10 μM, 3 days) exhibits minor antiproliferative effects in breast cancer cells[1].
AliasHTH01-091, HTH-01091, HTH 01-091, HTH 01091
Chemical Properties
Molecular Weight499.43
FormulaC26H28Cl2N4O2
Cas No.2000209-42-5
Storage & Solubility Information
StoragePowder: -20°C for 3 years | In solvent: -80°C for 1 year | Shipping with blue ice.
Solubility Information
DMSO: 5 mg/mL (10 mM)
Solution Preparation Table
DMSO
1mg5mg10mg50mg
1 mM2.0023 mL10.0114 mL20.0228 mL100.1141 mL
5 mM0.4005 mL2.0023 mL4.0046 mL20.0228 mL
10 mM0.2002 mL1.0011 mL2.0023 mL10.0114 mL

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