GLPBio

ASTX029 (ERK1/2 inhibitor 2)

Catalog No.: GC60812Purity:>99.50%
ERK1/2-Inhibitor 2 (Beispiel 1) ist ein potenter dualer ERK1/2-Inhibitor. ERK1/2-Inhibitor 2 hat eine Anti-Krebs-AktivitÄt.

Die Produkte sind ausschließlich für Forschungszwecke bestimmt. Nicht zur Anwendung am Menschen. Wir verkaufen nicht an Patienten.


ASTX029 (ERK1/2 inhibitor 2)
Cas No.: 2095719-92-7
10mM (in 1mL DMSO)In Stock
$99.00
1
1mgIn Stock
$38.00
1
5mgIn Stock
$77.00
1
10mgIn Stock
$123.00
1
25mgIn Stock
$210.00
1
50mgIn Stock
$315.00
1

Zitate (Citations)

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    618, 1017–1023 (2023)
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    610, 366–372 (2022)
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    Cell
    187(9):2288-2304 (2024)
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    183(7):1867-1883 (2020)
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    31, 1291–1307 (2021)

Beschreibung (Description)

ASTX029 (ERK1/2 inhibitor 2) is a highly effective and selective orally bioavailable extracellular signal-regulated kinase (ERK) 1/2 inhibitor (with an IC50 of 2.7nM for ERK2) [1]. ERK1/2 is the terminal kinase in the MAPK pathway, and the activation of the ERK/MAPK pathway is very common in myeloid malignancies [2]. ASTX029 has anti-tumor activity and can be used for cancer treatment [3].

In vivo, ASTX029 (10 and 100nM; 0-72h) can induce cell cycle arrest at the G1 phase in A375 and HCT116 cells and induce apoptosis [4]. ASTX029 (0.1-5nM; 12h) significantly reduced the p-ERK level in primary microglial cells stimulated by lipopolysaccharide (LPS) and inhibited the secretion of IL-1β, IL-6 and TNF-α [5].

In vivo, ASTX029 (50μM; 1μl; intravitreal injection) significantly reduced the p-ERK level in the retina of laser-induced choroidal neovascularization (CNV) mice and reduced the lesion area of CNV [5]. ASTX029 (20-75mg/kg/day; oral) can significantly inhibit tumor growth in Colo205 (BRAFV600E-mutant colorectal cancer) tumor-bearing mice [4].

References:
[1] Munck, J., Berdini, V., Courtin, A., et al. The clinical candidate, ASTX029, is a novel, dual mechanism ERK1/2 inhibitor and has potent activity in MAPK-activated cancer cell lines and in vivo tumor models. Eur. J. Cancer 138(Suppl 2), S53 (2020)
[2] Sharma P, Piya S, Baran N, et al. P460: ERK1/2 inhibition overcomes ressitance to BCL2 inhibition in acute myeloid leukemia by impact on mitochondrial dynamics and function[J]. HemaSphere, 2023, 7(Suppl): e08176db.
[3] Hindley C J, Fazal L, Munck J M, et al. Anti-tumor activity of ASTX029, a dual mechanism inhibitor of ERK1/2, in preclinical AML models[J]. Blood, 2020, 136: 7-8.
[4] Munck JM, et al. ASTX029, a Novel Dual-mechanism ERK Inhibitor, Modulates Both the Phosphorylation and Catalytic Activity of ERK. Mol Cancer Ther. 2021 Oct;20(10):1757-1768.
[5] Zou Y, Jiang J, Li Y, et al. Immune Checkpoint PD‐L1 Modulates Retinal Microglial Activation to Alleviate Vascular Leakage in Choroidal Neovascularization via ERK[J]. Advanced Science, 2025: 2400747.

Protokoll (Protocol)

Cell experiment [1]:

Cell lines

Primary microglia cells

Preparation Method

Primary microglia cells were plated in 96-well plates at a density of 2000 cells per well and incubated in FBS-free medium for 12h prior to treatment. Treatments included ASTX029 at concentrations of 0.1, 0.5, 1, 5nM. Collect the cell culture supernatant for ELISA testing.

Reaction Conditions

0.1-5nM; 12h

Applications

ASTX029 significantly inhibited the secretion of IL-1β, IL-6 and TNF-α in primary microglial cells.
Animal experiment [1]:

Animal models

PD-L1 KO mice with a C57BL/6 background

Preparation Method

Mice were anesthetized by intraperitoneal injection of 1% pentobarbital sodium (40mg kg−1). Pupil dilation was achieved using 0.5% tropicamide eye drops. A diode laser system, designed in a slit-lamp style, employing a green laser at 532nm with a power of 100mW, a duration of 100ms, and a spot size of 100µm, was utilized. For intravitreal delivery, mice were anesthetized, and a 34-gauge needle was inserted into the vitreous space approximately 1.5mm below the limbus, and 1µL ASTX029 was administered bilaterally with a Nanofil syringe. The fundus photography and fluorescein fundus angiography (FFA) examination were conducted at 7 days post-laser photocoagulation.

Dosage form

50μM; 1μl; Intravitreal injection

Applications

ASTX029 significantly reduced the lesion area of the retina in mice with laser-induced choroidal neovascularization (CNV).

References:
[1] Zou Y, Jiang J, Li Y, et al. Immune Checkpoint PD?L1 Modulates Retinal Microglial Activation to Alleviate Vascular Leakage in Choroidal Neovascularization via ERK[J]. Advanced Science, 2025: 2400747.

Produktdokumente (Product Documents)

Purity:>99.50%Appearance:A solid

Chemische Eigenschaften (Chemical Properties)

CAS-Nr.
2095719-92-7
SMILES
ClC(C(C1=CC2=C(CN([C@H](C)C(N[C@H](CO)C3=CC(F)=CC(OC)=C3)=O)C2=O)C=C1)=N4)=CN=C4NC5CCOCC5
Summenformel
C29H31ClFN5O5
Molekulargewicht
584.04
Löslichkeit
DMSO: 250 mg/mL (428.05 mM)
Lagerung
Store at -20°C
Allgemeine Hinweise
Wählen Sie anhand der Löslichkeitsdaten des Produkts ein geeignetes Lösungsmittel. Aliquotieren Sie die Stammlösung nach der Herstellung, um wiederholte Gefrier-Auftau-Zyklen zu vermeiden.
Verwenden Sie Stammlösungen bei Lagerung bei -80°C innerhalb von 6 Monaten bzw. bei -20°C innerhalb von 1 Monat.
Zur Verbesserung der Löslichkeit das Röhrchen auf 37°C erwärmen und für eine angemessene Dauer beschallen.
Versandbedingungen
Evaluierungsmuster werden mit Kühlakkus versandt. Andere verfügbare Größen werden bei Raumtemperatur oder auf Anfrage mit Kühlakkus versandt.

Rechner (Calculators)Molarität / Verdünnung / Molekulargewicht / Einheitenumrechnung / In-vivo-Formulierung / Löslichkeit

g/mol

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