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HM43239 (Synonyms: HM43239)

Catalog No.GC63507

HM43239 es un inhibidor de FLT3 selectivo y activo por vÍa oral con IC50 de 1,1 nM, 1,8 nM y 1,0 nM para FLT3 WT, duplicaciÓn interna en tÁndem (ITD) de FLT3 y quinasas FLT3 D835Y, respectivamente. HM43239 inhibe la actividad quinasa de FLT3 como inhibidor reversible de tipo I y modula p-STAT5, p-ERK, SYK, JAK1/2 y TAK1. HM43239 inhibe la proliferaciÓn e induce la apoptosis de las células leucémicas.

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HM43239 Chemical Structure

Cas No.: 2294874-49-8;2569527-64-4

Tamaño Precio Disponibilidad Cantidad
5 mg
432,00 $
Disponible
10 mg
720,00 $
Disponible

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Sample solution is provided at 25 µL, 10mM.

Description Chemical Properties Product Documents

HM43239 is an orally active and selective FLT3 inhibitor with IC50s 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 inhibits the kinase activity of FLT3 as a reversible type I inhibitor and modulates p-STAT5, p-ERK, SYK, JAK1/2, and TAK1. HM43239 inhibits the proliferation and induces the apoptosis of leukemic cells[1][2][3].

HM43239 potently inhibits the growth of acute myeloid leukemia cell lines harboring FLT3 ITD mutation, such as MV4-11 (IC50: 1.3 nM), MOLM-13 (IC50: 5.1 nM), and MOLM-14 (IC50: 2.9 nM). HM43239 also 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].

HM43239 shows 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].

[1]. Miyoung Lee, et.al. Abstract 804: Antitumor activity of the potent and novel FLT3 inhibitor HM43239 in acute myeloid leukemia. Cancer Res July 1 2018 (78) (13 Supplement) 804.
[2]. Naval G. Daver, et.al. HM43239, a Novel Potent Small Molecule FLT3 Inhibitor, in Acute Myeloid Leukemia (AML) with FMS-like Tyrosine Kinase 3 (FLT3) Mutations: Phase 1 /2 Study. Blood 2019; 134 (Supplement_1): 1331.
[3]. JiSook Kim, et.al. Abstract 1293: HM43239, a novel FLT3 inhibitor in overcoming resistance for acute myeloid leukemia. Cancer Res July 1 2019 (79) (13 Supplement) 1293.

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Average Rating: 5 ★★★★★ (Based on Reviews and 18 reference(s) in Google Scholar.)

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