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Biochemicals

Cryptotanshinone, STAT3 inhibitor (ab120666)

Cryptotanshinone, STAT3 inhibitor (ab120666)
  • ChIP - Anti-Histone H3 antibody - Nuclear Loading Control and ChIP Grade (ab1791)

Key features and details

  • STAT3 inhibitor with diverse biological activities
  • CAS Number: 35825-57-1
  • Purity: > 97%
  • Soluble in DMSO to 10 mM
  • Form / State: Solid
  • Source: Salvia miltiorrhiza

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Overview

  • Product name

    Cryptotanshinone, STAT3 inhibitor
  • Description

    STAT3 inhibitor with diverse biological activities
  • Biological description

    STAT3 inhibitor (IC50 = 4.6 μM). Cell-permeable, naturally occuring constitutent of Salvia miltiorrhiza with diverse biological activities. Shows anticancer, antibacterial, anti-inflammatory, antidiabetes and antiobesity activity. Attenuates amyloid plaque deposition in the brain.

  • Purity

    > 97%
  • CAS Number

    35825-57-1
  • Chemical structure

    Chemical Structure

Properties

  • Chemical name

    (R)-(-)-1,6,6-Trimethyl-1,2,6,7,8,9-hexahydrophenanthro[1,2-b]furan-10,11-dione
  • Molecular weight

    296.37
  • Molecular formula

    C19H20O3
  • Storage instructions

    Store at -20°C. It is important to note that this product is reported to be light sensitive. Store In the Dark. Store under desiccating conditions.
  • Solubility overview

    Soluble in DMSO to 10 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.

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

  • Source

    Salvia miltiorrhiza

  • Research areas

    • Biochemicals
    • Chemical Type
    • Biochemicals
    • Biochemicals
    • Pharmacology
    • Signaling
    • Amyloidogenesis
    • Biochemicals
    • Pharmacology
    • Signaling
    • Signal transduction
    • JAK/STAT
    • STAT
    • Inhibitors
    • Biochemicals
    • Research Area
    • Heart disease
    • Signaling
    • Amyloidogenesis
    • Biochemicals
    • Research Area
    • Heart disease
    • Signaling
    • Cytokine and NF-κB signaling
    • STAT
    • Inhibitors
    • Biochemicals
    • Research Area
    • Pain & inflammation
    • Signaling
    • Amyloidogenesis
    • Biochemicals
    • Research Area
    • Pain & inflammation
    • Signaling
    • Cytokine and NF-κB signaling
    • STAT
    • Inhibitors
    • Biochemicals
    • Research Area
    • Alzheimer's Disease
    • Signaling
    • Amyloidogenesis
    • Biochemicals
    • Research Area
    • Alzheimer's Disease
    • Signaling
    • Signal transduction
    • JAK/STAT signaling
    • STAT
    • Inhibitors
    • Biochemicals
    • Research Area
    • Diabetes
    • Signaling
    • Amyloidogenesis
    • Biochemicals
    • Research Area
    • Diabetes
    • Signaling
    • Signal transduction
    • JAK/STAT signaling
    • STAT
    • Inhibitors
    • Biochemicals
    • Research Area
    • Hypertension
    • Signaling
    • Amyloidogenesis
    • Biochemicals
    • Research Area
    • Hypertension
    • Signaling
    • Signal transduction
    • JAK/STAT signaling
    • STAT
    • Inhibitors
    • Biochemicals
    • Research Area
    • Obesity
    • Signaling
    • Amyloidogenesis
    • Biochemicals
    • Research Area
    • Obesity
    • Signaling
    • Signal transduction
    • JAK/STAT signaling
    • STAT
    • Inhibitors
    • Biochemicals
    • Research Area
    • Respiratory disease
    • Signaling
    • Amyloidogenesis
    • Biochemicals
    • Research Area
    • Respiratory disease
    • Signaling
    • Cytokine and NF-κB signaling
    • STAT
    • Inhibitors
    • Biochemicals
    • Research Area
    • Stroke
    • Signaling
    • Amyloidogenesis
    • Biochemicals
    • Research Area
    • Stroke
    • Signaling
    • Signal transduction
    • JAK/STAT signaling
    • STAT
    • Inhibitors
    • Biochemicals
    • Pharmacology
    • Receptors & Transporters
    • Enzyme-Linked Receptors
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    • Other
    • Biochemicals
    • Pharmacology
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    • DNA, RNA & protein synthesis
    • Transcription factors
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    • Stem Cells
    • JAK/STAT
    • Biochemicals
    • Research Area
    • Cancer
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    • Biochemicals
    • Research Area
    • Cancer
    • Signal transduction
    • JAK/STAT
    • STAT
    • Inhibitors
    • Biochemicals
    • Research Area
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    • Pharmacology
    • Signaling
    • Immunomodulators
    • Immunomodulators & Immunosuppressants
    • Biochemicals
    • Pharmacology
    • Signaling
    • Immunomodulators
    • Antibacterial

Images

  • Functional Studies - Cryptotanshinone, STAT3 inhibitor (ab120666)
    Functional Studies - Cryptotanshinone, STAT3 inhibitor (ab120666)

    MCF7 cells were incubated at 37°C for 4h with vehicle control (0 µM) and different concentrations of cryptotanshinone (ab120666). Increased expression of JNK1+JNK2 (phospho T183 + Y185) in MCF7cells correlates with an increase in cryptotanshinone concentration, as described in literature.

    Whole cell lysates were prepared with RIPA buffer (containing protease inhibitors and sodium orthovanadate), 10 µg of each were loaded on the gel and the WB was run under reducing conditions. After transfer the membrane was blocked for an hour using 5% BSA before being incubated with ab4821 at at 1/1000 dilution and ab8227 at 1 µg/ml overnight at 4°C. Antibody binding was detected using an anti-rabbit antibody conjugated to HRP (ab97051) at 1/10000 dilution and visualised using ECL development solution.

Please note: All products are "FOR RESEARCH USE ONLY. NOT FOR USE IN DIAGNOSTIC PROCEDURES"
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