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KPT-6566

SKU: orb1301363

Description

KPT-6566

Images & Validation

Key Properties

CAS Number881487-77-0
MW443.54
Purity97.81% (May vary between batches)
FormulaC22H21NO5S2
SMILESCC(C)(C)c1ccc(cc1)S(=O)(=O)\N=C1/C=C(SCC(O)=O)C(=O)c2ccccc12
TargetOthers
Solubility10% DMSO+90% Saline:1 mg/mL (2.25 mM);DMSO:120 mg/mL (270.55 mM)

Bioactivity

Target IC50
PIN1 PPIase:640 nM
In Vitro
KPT-6566 covalently binds to the catalytic site of PIN1,inhibited the PPIase activity of PIN1 and turned out to have an IC50 of 0.64 μM. This interaction results in the release of a quinone-mimicking drug that generates reactive oxygen species and DNA damage, inducing cell death specifically in cancer cells.
Cell Research
For IC50 determination, human recombinant PIN1 was preincubated with different concentrations of KPT-6566 and PPIase activity was measured after 180 min. K values of PPIase activity were plotted against inhibitor concentration in a semi-logarithmic plot.

Storage & Handling

Storage-20°C
Expiration Date12 months from date of receipt.
DisclaimerFor research use only

Alternative Names

ROS, pin1, anti- proliferation, breast epithelial, DNA damage, Cyclin D1, inhibit, KPT 6566, KPT6566, KPT-6566, Inhibitor

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Key Properties

No computed properties available.

Protocol Information

Available Sizes

Select a size below

1 mg
$ 140.00
1 ml x 10 mM (in DMSO)
$ 330.00
5 mg
$ 340.00
10 mg
$ 430.00
25 mg
$ 590.00
50 mg
$ 730.00
100 mg
$ 940.00
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