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HM43239

🥰Excellent
Catalog No. T9428Cas No. 2294874-49-8
Alias Tuspetinib

HM43239 is an orally active and selective FLT3 inhibitor with IC 50 s of 1.1 nM, 1.8 nM and 1.0 nM for FLT3 WT, FLT3 internal tandem duplication (ITD) and FLT3 D835Y kinases, respectively. HM43239 directly inhibits the kinase activity of FLT3 as a reversible Type I inhibitor and effectively modulates downstream p-STAT5 and p-ERK. HM43239 also demonstrated inhibition of SYK, JAK1/2 and TAK1. HM43239 inhibits the proliferation and induces the apoptosis of leukemic cells [1] [2] [3].

HM43239

HM43239

🥰Excellent
Purity: 98.56%
Catalog No. T9428Alias TuspetinibCas No. 2294874-49-8
HM43239 is an orally active and selective FLT3 inhibitor with IC 50 s of 1.1 nM, 1.8 nM and 1.0 nM for FLT3 WT, FLT3 internal tandem duplication (ITD) and FLT3 D835Y kinases, respectively. HM43239 directly inhibits the kinase activity of FLT3 as a reversible Type I inhibitor and effectively modulates downstream p-STAT5 and p-ERK. HM43239 also demonstrated inhibition of SYK, JAK1/2 and TAK1. HM43239 inhibits the proliferation and induces the apoptosis of leukemic cells [1] [2] [3].
Pack SizePriceAvailabilityQuantity
1 mg$64In Stock
5 mg$155In Stock
10 mg$238In Stock
25 mg$465In Stock
50 mg$665In Stock
100 mg$928In Stock
1 mL x 10 mM (in DMSO)$197In Stock
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Purity:98.56%
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Product Introduction

Bioactivity
Description
HM43239 is an orally active and selective FLT3 inhibitor with IC 50 s of 1.1 nM, 1.8 nM and 1.0 nM for FLT3 WT, FLT3 internal tandem duplication (ITD) and FLT3 D835Y kinases, respectively. HM43239 directly inhibits the kinase activity of FLT3 as a reversible Type I inhibitor and effectively modulates downstream p-STAT5 and p-ERK. HM43239 also demonstrated inhibition of SYK, JAK1/2 and TAK1. HM43239 inhibits the proliferation and induces the apoptosis of leukemic cells [1] [2] [3].
Targets&IC50
FLT3 (WT):1.1 nM, FLT3 (D835Y):1.0 nM, FLT3 (ITD):1.8 nM
In vitro
HM43239 potently inhibits the growth of acute myeloid leukemia cell lines harboring FLT3 ITD mutation like MV4-11 (IC 50 : 1.3 nM), MOLM-13 (IC 50 : 5.1 nM), and MOLM-14 (IC 50 : 2.9 nM). Besides, HM43239 inhibits KG1a cells (CD34+/CD38- cells) proliferation [1]. HM43239 induces the caspase 3/7-dependent apoptosis of leukemic stem cell (LSC) marker-expressing KG1a cells (CD34+/CD38- cells) [1]. HM43239 potently inhibits phosphorylation of SYK, STAT3, and STAT5 in KG1a cells [3].
In vivo
HM43239 exhibits the excellent dose proportional antitumor activity in mouse models xenografted with both MV4-11 and MOLM-13 cell lines without any significant toxicity [1]. HM43239 prolongs survival in FLT3 ITD/TKD double mutated xenograft mouse models [3].
AliasTuspetinib
Chemical Properties
Molecular Weight501.07
FormulaC29H33ClN6
Cas No.2294874-49-8
SmilesC[C@H]1CN(Cc2cc(Nc3ncc(Cl)c(n3)-c3c[nH]c4cc(C)ccc34)cc(c2)C2CC2)C[C@@H](C)N1
Relative Density.1.258 g/cm3 (Predicted)
Storage & Solubility Information
StoragePowder: -20°C for 3 years | In solvent: -80°C for 1 year | Shipping with blue ice.
Solubility Information
DMSO: 50 mg/mL (99.79 mM)
Solution Preparation Table
DMSO
1mg5mg10mg50mg
1 mM1.9957 mL9.9786 mL19.9573 mL99.7865 mL
5 mM0.3991 mL1.9957 mL3.9915 mL19.9573 mL
10 mM0.1996 mL0.9979 mL1.9957 mL9.9786 mL
20 mM0.0998 mL0.4989 mL0.9979 mL4.9893 mL
50 mM0.0399 mL0.1996 mL0.3991 mL1.9957 mL

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