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TDZD-8

SKU: orb1300998

Description

TDZD-8

Research Area

Signal Transduction, Stem Cell & Developmental Biology

Images & Validation

Key Properties

CAS Number327036-89-5
MW222.26
Purity99.61%
FormulaC10H10N2O2S
SMILESCn1sc(=O)n(Cc2ccccc2)c1=O
TargetGSK-3
SolubilityH2O:< 1 mg/mL (insoluble or slightly soluble);10% DMSO+40% PEG300+5% Tween 80+45% Saline:2 mg/mL (9 mM);DMSO:70 mg/mL (314.95 mM);Ethanol:44.5 mg/mL (200.22 mM)

Bioactivity

Target IC50
GSK-3β:2 μM
In Vitro
TDZD-8 acts as a noncompetitive inhibitor of ATP or GS-1 binding. TDZD-8 shows no inhibition of PKA, PKC, Cdk-1/cyclin B or CK-II in kinase assays. TDZD-8 specifically induces cell death of primary leukemia specimens. TDZD-8 ablates leukemia progenitor and stem cells. TDZD-8 treatment induces oxidative stress. TDZD-8 induces cell death with extremely rapid cell death kinetics showing loss of membrane integrity. TDZD-8 inhibits PKC and FLT3 in primary AML specimens.

Storage & Handling

StoragePowder: -20°C for 3 years | In solvent: -80°C for 1 year | Shipping with blue ice/Shipping at ambient temperature.
Expiration Date12 months from date of receipt.
DisclaimerFor research use only

Alternative Names

Glycogen synthase kinase 3, Glycogen synthase kinase-3, GSK3, GSK-3, GSK-3b Inhibitor I, GSK-3beta Inhibitor I, GSK-3β, GSK-3β Inhibitor I, Inhibitor, NP 01139, NP01139, NP-01139, inhibit, TDZD-8, TDZD 8, TDZD8

Similar Products

  • TDZD-8 [orb1225303]

    >98% (HPLC)

    327036-89-5

    222.3

    C10H10N2O2S

    5 mg, 10 mg, 25 mg, 50 mg, 100 mg, 1 g, 500 mg, 200 mg
Quality Guarantee

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Key Properties

No computed properties available.

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TDZD-8 (orb1300998)

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% DMSO +
%+
% Tween 80 +
%

Available Sizes

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1 ml x 10 mM (in DMSO)
$ 90.00
5 mg
$ 90.00
10 mg
$ 100.00
25 mg
$ 120.00
50 mg
$ 170.00
100 mg
$ 240.00
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