GLPBio

ASTX029 (ERK1/2 inhibitor 2)

Catalog No.: GC60812Purity:>99.50%
مثبط ERK1 / 2 2 (مثال 1) هو مثبط مزدوج قوي ERK1 / 2. مثبط ERK1 / 2 له نشاط مضاد للسرطان.

المنتجات مخصصة للاستخدام البحثي فقط، وليست للاستخدام البشري. نحن لا نبيع للمرضى.


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

المراجع (Citations)

لا تتوفر حاليًا مراجع لهذا المنتج. فيما يلي مجموعة مختارة من المنشورات التي تستشهد بمنتجات GlpBio.
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    632, 686–694 (2024)
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    Nature
    618, 1017–1023 (2023)
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    Nature
    610, 366–372 (2022)
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    Cell
    187(9):2288-2304 (2024)
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    Cell
    183(7):1867-1883 (2020)
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    388(6745) (2025)
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    33, 904–922 (2023)
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    31, 1291–1307 (2021)

الوصف (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.

البروتوكول (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.

وثائق المنتج (Product Documents)

Purity:>99.50%Appearance:A solid

الخصائص الكيميائية (Chemical Properties)

رقم CAS
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
الصيغة الجزيئية
C29H31ClFN5O5
الوزن الجزيئي
584.04
الذوبانية
DMSO: 250 mg/mL (428.05 mM)
التخزين
Store at -20°C
إرشادات عامة
اختر مذيبًا مناسبًا وفقًا لبيانات ذوبانية المنتج. بعد التحضير، قسّم المحلول المخزون إلى أجزاء لتجنب دورات التجميد والذوبان المتكررة.
استخدم المحاليل المخزونة خلال 6 أشهر عند حفظها في -80°C، أو خلال شهر واحد عند حفظها في -20°C.
لتحسين الذوبانية، سخّن الأنبوب إلى 37°C وعرّضه للموجات فوق الصوتية لمدة مناسبة.
شروط الشحن
تُشحن عينات التقييم مع عبوات تبريد. وتُشحن الأحجام الأخرى المتاحة في درجة حرارة الغرفة، أو مع عبوات تبريد عند الطلب.

الحاسبات (Calculators)المولارية / التخفيف / الوزن الجزيئي / تحويل الوحدات / تركيبة داخل الجسم الحي / الذوبانية

g/mol

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