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    products/biochemicals/ipa-3-group-i-p21-activated-kinase-pak-inhibitor-ab141014.pdf

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Epigenetics and Nuclear Signaling Chromatin Binding Proteins Methyl Lysine
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IPA 3, Group I, p21-activated kinase (PAK) inhibitor (ab141014)

  • Datasheet
  • SDS
  • COA
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Chemical Structure - IPA 3, Group I, p21-activated kinase (PAK) inhibitor (ab141014)

    Key features and details

    • Group I, p21-activated kinase (PAK) inhibitor
    • CAS Number: 42521-82-4
    • Purity: > 97%
    • Soluble in DMSO to 100 mM and in ethanol to 25 mM
    • Form / State: Solid
    • Source: Synthetic

    Overview

    • Product name

      IPA 3, Group I, p21-activated kinase (PAK) inhibitor
    • Description

      Group I, p21-activated kinase (PAK) inhibitor
    • Biological description

      Group I, p21-activated kinase (PAK) inhibitor (IC50 = 2.5 μM). Non-ATP competitive, allosteric inhibition in vivo. Selectivity over >200 other kinases.

    • Purity

      > 97%
    • CAS Number

      42521-82-4
    • Chemical structure

      Chemical Structure

    Properties

    • Chemical name

      1,1'-Dithiobis-2-naphthalenol
    • Molecular weight

      350.45
    • Molecular formula

      C20H14O2S2
    • PubChem identifier

      521106
    • Storage instructions

      Store at +4°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 ethanol to 25 mM
    • 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.

       Toxic, 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

      Oc4ccc1ccccc1c4SSc3c(O)ccc2ccccc23
    • Source

      Synthetic

    • Research areas

      • Epigenetics and Nuclear Signaling
      • Chromatin Binding Proteins
      • Methyl Lysine
      • Epigenetics and Nuclear Signaling
      • Transcription
      • Domain Families
      • Zinc Finger
      • Signal Transduction
      • Protein Phosphorylation
      • Ser / Thr Kinases
      • Other Kinases
      • Signal Transduction
      • Signaling Pathway
      • G Protein Signaling
      • Small G Proteins
      • Regulators
      • Signal Transduction
      • Signaling Pathway
      • Nuclear Signaling
      • Nuclear Hormone Receptors
      • Estrogen
      • Signal Transduction
      • Metabolism
      • Energy Metabolism
      • Epigenetics and Nuclear Signaling
      • Nuclear Signaling Pathways
      • Nuclear Receptors
      • Estrogen
      • Signal Transduction
      • Signaling Pathway
      • Nuclear Signaling
      • Nuclear Hormone Receptors
      • Vitamin D Receptor
      • Epigenetics and Nuclear Signaling
      • Nuclear Signaling Pathways
      • Nuclear Receptors
      • Vitamin D Receptor
      • Cancer
      • Signal transduction
      • Nuclear signaling
      • Nuclear hormone receptors
      • Estrogen
      • Cancer
      • Signal transduction
      • Nuclear signaling
      • Nuclear hormone receptors
      • Other
      • Cancer
      • Oncoproteins/suppressors
      • Tumor suppressors
      • Other
      • Cardiovascular
      • Heart
      • Cardiac arrhythmias
      • Cardiovascular
      • Heart
      • Hypertrophy
      • Other
      • Cancer
      • Cancer Metabolism
      • Metabolic signaling pathway
      • Integration of energy metabolism
      • Biochemicals
      • Chemical Type
      • Biochemicals
      • Biochemicals
      • Pharmacology
      • Signaling
      • Apoptosis & cell cycle
      • Other
      • Metabolism
      • Pathways and Processes
      • Mitochondrial Metabolism
      • Mitochondrial Biogenesis
      • Metabolism
      • Pathways and Processes
      • Metabolic signaling pathways
      • Nucleotide metabolism
      • Molecular processes
      • Mitochondrial transcription
      • Metabolism
      • Pathways and Processes
      • Metabolic signaling pathways
      • Energy transfer pathways
      • Energy Metabolism
      • Metabolism
      • Pathways and Processes
      • Metabolic signaling pathways
      • Energy transfer pathways
      • Integration of energy
      • Biochemicals
      • Research Area
      • Heart disease
      • Signaling
      • Apoptosis & cell cycle
      • Other
      • Biochemicals
      • Research Area
      • Pain & inflammation
      • Signaling
      • Apoptosis & cell cycle
      • Other
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      • Research Area
      • Alzheimer's Disease
      • Apoptosis & cell cycle
      • Other
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      • Research Area
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      • Apoptosis & cell cycle
      • Other
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      • Research Area
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      • Apoptosis & cell cycle
      • Other
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      • Research Area
      • Diabetes
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      • Other
      • Biochemicals
      • Research Area
      • Diabetes
      • Signaling
      • Apoptosis & cell cycle
      • Other
      • Biochemicals
      • Research Area
      • Heart disease
      • Apoptosis & cell cycle
      • Other
      • Biochemicals
      • Research Area
      • Hypertension
      • Apoptosis & cell cycle
      • Other
      • Biochemicals
      • Research Area
      • Hypertension
      • Signaling
      • Apoptosis & cell cycle
      • Other
      • Biochemicals
      • Research Area
      • Obesity
      • Apoptosis & cell cycle
      • Other
      • Biochemicals
      • Research Area
      • Obesity
      • Signaling
      • Apoptosis & cell cycle
      • Other
      • Biochemicals
      • Research Area
      • Pain & inflammation
      • Apoptosis & cell cycle
      • Other
      • Biochemicals
      • Research Area
      • Respiratory disease
      • Apoptosis & cell cycle
      • Other
      • Biochemicals
      • Research Area
      • Respiratory disease
      • Signaling
      • Apoptosis & cell cycle
      • Other
      • Biochemicals
      • Research Area
      • Stroke
      • Apoptosis & cell cycle
      • Other
      • Biochemicals
      • Research Area
      • Stroke
      • Signaling
      • Apoptosis & cell cycle
      • Other
      • Biochemicals
      • Pharmacology
      • Enzymes
      • Kinase
      • PAK
      • Inhibitors
      • Biochemicals
      • Pharmacology
      • Signaling
      • Signal transduction
      • PI3K/Akt signaling
      • p21
      • Inhibitors
      • Biochemicals
      • Research Area
      • Cancer
      • Signal transduction
      • PI3K/Akt signaling
      • p21
      • Inhibitors

    Images

    • Chemical Structure - IPA 3, Group I, p21-activated kinase (PAK) inhibitor (ab141014)
      Chemical Structure - IPA 3, Group I, p21-activated kinase (PAK) inhibitor (ab141014)
      2D chemical structure image of ab141014, IPA 3, Group I, p21-activated kinase (PAK) inhibitor

    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 (1)

    Publishing research using ab141014? Please let us know so that we can cite the reference in this datasheet.

    ab141014 has been referenced in 1 publication.

    • Liu JS  et al. ß-elemene enhances the radiosensitivity of gastric cancer cells by inhibiting Pak1 activation. World J Gastroenterol 21:9945-56 (2015). PubMed: 26379399

    Customer reviews and Q&As

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