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K03861

SKU: orb1223029

Description

AUZ454 is a potent and selective Type II FLT3 inhibitor. AUZ454 is able to override drug resistance that less potent "type I" inhibitors and "type II" first-generation FLT3 inhibitors cannot. Constitutively activated mutant FLT3 has emerged as a promising target for therapy for the subpopulation of acute myeloid leukemia (AML) patients who harbor it. The small molecule inhibitor, PKC412, targets mutant FLT3 and is currently in late-stage clinical trials. However, the identification of PKC412-resistant leukemic blast cells in the bone marrow of AML patients has propelled the development of novel and structurally distinct FLT3 inhibitors that have the potential to override drug resistance and more efficiently prevent disease progression or recurrence.

Images & Validation

Key Properties

CAS Number853299-07-7
MW501.5
Purity>98% (HPLC)
FormulaC24H26F3N7O2
SMILESCN1CCN(CC2=CC=C(NC(=O)NC3=CC=C(OC4=NC(N)=NC=C4)C=C3)C=C2C(F)(F)F)CC1
TargetCDK2(A144C)| CDK2(C118L)| CDK2(C118L/A144C)| CDK2(WT)
SolubilityDMSO : ≥ 33 mg/mL; 65.80 mM

Bioactivity

In Vitro
Cell Proliferation Assay Cell line: Caki-1 and ACHN cells. Concentration: 10 μM; 20 μM. Incubation time: 1, 2, 3, and 4 days. Result: Inhibited cell proliferation in a CDK2-dependent manner.

Storage & Handling

StorageStorage temperature: -20°C. Stability: ≥ 2 years
Expiration Date12 months from date of receipt.
DisclaimerFor research use only

Alternative Names

AUZ454 | AUZ 454 | AUZ-454 | K03861

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    853299-07-7

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    C24H26F3N7O2

    5 mg, 10 mg, 25 mg, 50 mg, 100 mg, 1 ml x 10 mM (in DMSO), 200 mg
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K03861 (orb1223029)

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Available Sizes

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200 mg
500 mg
2 mg
$ 90.00
5 mg
$ 130.00
10 mg
$ 180.00
25 mg
$ 350.00
50 mg
$ 510.00
100 mg
$ 790.00