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    products/biochemicals/h89-dihydrochloride-kinase-inhibitor-ab120341.pdf

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H89 dihydrochloride, Kinase inhibitor (ab120341)

  • Datasheet
  • SDS
  • COA
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Chemical Structure - H89 dihydrochloride, Kinase inhibitor (ab120341)
  • Functional Studies - H89 dihydrochloride, Kinase inhibitor (ab120341)

Key features and details

  • Kinase inhibitor
  • CAS Number: 130964-39-5
  • Soluble in DMSO to 100 mM and in water to 25 mM (with heating)
  • Form / State: Solid
  • Source: Synthetic

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Overview

  • Product name

    H89 dihydrochloride, Kinase inhibitor
  • Description

    Kinase inhibitor
  • Biological description

    Kinase inhibitor, commonly used as a protein kinase A inhibitor (IC50 = 135 nM). Also inhibits other kinases, including MSK1 , S6K1 and ROCKII (IC50 values are 120, 80 and 270 nM, respectively).

  • CAS Number

    130964-39-5
  • Chemical structure

    Chemical Structure

Properties

  • Chemical name

    N-[2-[[3-(4-Bromophenyl)-2-propen-1-yl]amino]ethyl]-5-isoquinolinesulfonamide dihydrochloride
  • Molecular weight

    519.28
  • Molecular formula

    C20H20BrN3O2S.2HCl
  • PubChem identifier

    5702541
  • Storage instructions

    Store at -20°C. Store under desiccating conditions. The product can be stored for up to 12 months.
  • Solubility overview

    Soluble in DMSO to 100 mM and in water to 25 mM (with heating)
  • Handling

    Wherever possible, you should prepare and use solutions on the same day. However, if you need to make up stock solutions in advance, we recommend that you store the solution as aliquots in tightly sealed vials at -20°C. Generally, these will be useable for up to one month. Before use, and prior to opening the vial we recommend that you allow your product to equilibrate to room temperature for at least 1 hour.

    Refer to SDS for further information.

    Need more advice on solubility, usage and handling? Please visit our frequently asked questions (FAQ) page for more details.

  • SMILES

    C1=CC2=C(C=CN=C2)C(=C1)S(=O)(=O)NCCNC/C=C/C3=CC=C(C=C3)Br.Cl.Cl
  • Source

    Synthetic

  • Research areas

    • Cell Biology
    • Apoptosis
    • Intracellular
    • Kinases
    • Signal Transduction
    • Protein Phosphorylation
    • Ser / Thr Kinases
    • PKA
    • Signal Transduction
    • Protein Phosphorylation
    • Ser / Thr Kinases
    • PKB / AKT
    • Signal Transduction
    • Protein Phosphorylation
    • Ser / Thr Kinases
    • Other Kinases
    • Signal Transduction
    • Second Messenger
    • Nucleotide Messenger
    • cAMP
    • Cancer
    • Signal transduction
    • Protein phosphorylation
    • Serine/threonine kinases
    • Other
    • Cancer
    • Signal transduction
    • Protein phosphorylation
    • Serine/threonine kinases
    • AKT
    • Cardiovascular
    • Atherosclerosis
    • Diabetes associated
    • Cardiovascular
    • Heart
    • Cardiac metabolism
    • Cancer
    • Cancer Metabolism
    • Metabolic signaling pathway
    • Metabolism of lipids and lipoproteins
    • Cancer
    • Cancer Metabolism
    • Metabolic signaling pathway
    • Integration of energy metabolism
    • Biochemicals
    • Product Range
    • Just Add Water
    • Biochemicals
    • Chemical Type
    • Biochemicals
    • Biochemicals
    • Pharmacology
    • Enzymes
    • Kinase
    • General
    • Inhibitors
    • Biochemicals
    • Pharmacology
    • Enzymes
    • Kinase
    • Protein Kinase A
    • Inhibitors
    • Biochemicals
    • Pharmacology
    • Signaling
    • Signal transduction
    • Inositol & cAMP signaling
    • Protein Kinase A
    • Inhibitors
    • Metabolism
    • Pathways and Processes
    • Metabolic signaling pathways
    • Lipid and lipoprotein metabolism
    • Lipid metabolism
    • Metabolism
    • Pathways and Processes
    • Metabolic signaling pathways
    • Energy transfer pathways
    • Integration of energy
    • Metabolism
    • Types of disease
    • Diabetes
    • Metabolism
    • Types of disease
    • Heart disease
    • Biochemicals
    • Research Area
    • Heart disease
    • Signaling
    • Inositol & cAMP signaling
    • Protein Kinase A
    • Inhibitors
    • Biochemicals
    • Research Area
    • Pain & inflammation
    • Signaling
    • Inositol & cAMP signaling
    • Protein Kinase A
    • Inhibitors
    • Biochemicals
    • Research Area
    • Alzheimer's Disease
    • Signaling
    • Signal transduction
    • Inositol & cAMP signaling
    • Protein Kinase A
    • Inhibitors
    • Biochemicals
    • Research Area
    • Diabetes
    • Signaling
    • Signal transduction
    • Inositol & cAMP signaling
    • Protein Kinase A
    • Inhibitors
    • Biochemicals
    • Research Area
    • Hypertension
    • Signaling
    • Signal transduction
    • Inositol & cAMP signaling
    • Protein Kinase A
    • Inhibitors
    • Biochemicals
    • Research Area
    • Obesity
    • Signaling
    • Signal transduction
    • Inositol & cAMP signaling
    • Protein Kinase A
    • Inhibitors
    • Biochemicals
    • Research Area
    • Respiratory disease
    • Signaling
    • Inositol & cAMP signaling
    • Protein Kinase A
    • Inhibitors
    • Biochemicals
    • Research Area
    • Stroke
    • Signaling
    • Signal transduction
    • Inositol & cAMP signaling
    • Protein Kinase A
    • Inhibitors
    • Biochemicals
    • Research Area
    • Cancer
    • Signal transduction
    • Inositol & cAMP signaling
    • Protein Kinase A
    • Inhibitors

Images

  • Chemical Structure - H89 dihydrochloride, Kinase inhibitor (ab120341)
    Chemical Structure - H89 dihydrochloride, Kinase inhibitor (ab120341)
    2D chemical structure image of ab120341, H89 dihydrochloride, Kinase inhibitor
  • Functional Studies - H89 dihydrochloride, Kinase inhibitor (ab120341)
    Functional Studies - H89 dihydrochloride, Kinase inhibitor (ab120341)Image from Tagashira, Hideki et al., PLOS One., 10(6):e0128678. Fig 8.; doi: 10.1371/journal.pone.0128678. Reproduced under the Creative Commons license http://creativecommons.org/licenses/by/4.0/

    Normal human melanocytes (NHMs) were treated with ab120341 at the indicated concentrations to test if the inhibition of MSK1 activation results in the down-regulated MITF and EDNRB expression in UVB-exposed NHMs. ab120341 was added immediately after UVB irradiation and cells were cultured for 6h (for MITF, A) or 24 h (for EDNRB, B). Total mRNAs were purified and Real-time RT-PCR was carried out with MITF or EDNRB primer and β-actin primer as the internal control. Error bars represent S.D. from triplicate experiments. *P<0.05 and **P<0.01 against NHMs UVB-irradiated in the absence of H89, respectively.

    Tagashira, Hideki et al., PLOS One., 10(6):e0128678. Fig 8.; doi: 10.1371/journal.pone.0128678.

Protocols

To our knowledge, customised protocols are not required for this product. Please try the standard protocols listed below and let us know how you get on.

Click here to view the general protocols

Datasheets and documents

  • SDS download

  • Datasheet download

    Download
  • COA

References (5)

Publishing research using ab120341? Please let us know so that we can cite the reference in this datasheet.

ab120341 has been referenced in 5 publications.

  • Wu K  et al. Activity- and sleep-dependent regulation of tonic inhibition by Shisa7. Cell Rep 34:108899 (2021). PubMed: 33761345
  • Vaena S  et al. Aging-dependent mitochondrial dysfunction mediated by ceramide signaling inhibits antitumor T cell response. Cell Rep 35:109076 (2021). PubMed: 33951438
  • Chen J  et al. Cyp2aa9 regulates haematopoietic stem cell development in zebrafish. Sci Rep 6:26608 (2016). PubMed: 27197559
  • Tagashira H  et al. UVB Stimulates the Expression of Endothelin B Receptor in Human Melanocytes via a Sequential Activation of the p38/MSK1/CREB/MITF Pathway Which Can Be Interrupted by a French Maritime Pine Bark Extract through a Direct Inactivation of MSK1. PLoS One 10:e0128678 (2015). PubMed: 26030901
  • Zhang L  et al. The slow afterhyperpolarization: a target of ß1-adrenergic signaling in hippocampus-dependent memory retrieval. J Neurosci 33:5006-16 (2013). PubMed: 23486971

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