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ECI830

Catalog No. T204836 Copy Product Info
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ECI830 is a highly potent and selective oral small-molecule CDK2 inhibitor. By inhibiting CDK2 activity, ECI830 induces G1/S phase cell cycle arrest, thereby blocking DNA replication and tumor proliferation. ECI830 is suitable for use in studies of HR+/HER2- breast cancer and tumors with CCNE1 amplification.

ECI830

Copy Product Info
🥰Excellent
Catalog No. T204836

ECI830 is a highly potent and selective oral small-molecule CDK2 inhibitor. By inhibiting CDK2 activity, ECI830 induces G1/S phase cell cycle arrest, thereby blocking DNA replication and tumor proliferation. ECI830 is suitable for use in studies of HR+/HER2- breast cancer and tumors with CCNE1 amplification.

ECI830
Cas No. 3054692-62-2
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Pack SizePriceUSA StockGlobal StockQuantity
1 mg$28310-14 weeks10-14 weeks
5 mg$67610-14 weeks10-14 weeks
25 mg$1,55010-14 weeks10-14 weeks
100 mg$3,38010-14 weeks10-14 weeks
For In stock only · Estimated delivery: USA Stock (1-2 days) Global Stock (5-7 days)
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With extensive experience in compound synthesis, we can provide rapid custom synthesis services for this product according to your research needs.
For research use only—not for human use. No sales to individuals. Use as intended only.
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Product Introduction

Bioactivity
Description
ECI830 is a highly potent and selective oral small-molecule CDK2 inhibitor. By inhibiting CDK2 activity, ECI830 induces G1/S phase cell cycle arrest, thereby blocking DNA replication and tumor proliferation. ECI830 is suitable for use in studies of HR+/HER2- breast cancer and tumors with CCNE1 amplification.
In vitro
ECI830 demonstrated significant antiproliferative activity in CCNE1-amplified ovarian cancer cell lines (OVCAR3) and lung cancer cell lines (H810). [1]
The combination of ECI830 and ribociclib produced a synergistic effect in HR+/HER2– breast cancer cells, effectively inhibiting cell growth. [2]
In vivo
In a xenograft model of HR+/HER2- breast cancer cell line (MCF7) resistant to standard therapy, the combination of ECI830 and ribociclib exhibited synergistic effects, significantly inhibiting tumor growth. [1]
Treatment with ECI830 in combination with ribociclib significantly regulated pRB1 in HR+/HER2⁻ breast cancer CDX and PDX models, demonstrating potent antitumor activity. ECI830 monotherapy effectively inhibited tumor growth in CCNE1-amplified tumor models.[2]
Chemical Properties
Molecular Weight384.43
FormulaC19H24N6O3
Cas No.3054692-62-2
SmilesO=C1C2(C=3C(N1[C@H]4C[C@H](O)CCC4)=NC(NC=5C(OCC)=NNC5)=NC3)CC2
Storage & Solubility Information
StoragePowder: -20°C for 3 years | In solvent: -80°C for 1 year Shipping with blue ice/Shipping at ambient temperature.

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In Vivo Formulation Calculator (Clear solution)

Please enter your animal experiment information in the following box and click Calculate to obtain the stock solution preparation method and in vivo formula preparation method:
TargetMol | Animal experiments For example, if the intended dosage is 10 mg/kg for animals weighing 20 g , with a dosing volume of 100 μL per animal, TargetMol | Animal experiments and a total of 10 animals are to be administered, using a formulation of TargetMol | reagent 10% DMSO+ 40% PEG300+ 5% Tween 80+ 45% Saline/PBS/ddH2O , the resulting working solution concentration would be 2 mg/mL.
Stock Solution Preparation:

Dissolve 2 mg of the compound in 100 μL DMSOTargetMol | reagent to obtain a stock solution at a concentration of 20 mg/mL . If the required concentration exceeds the compound's known solubility, please contact us for technical support before proceeding.

Preparation of the In Vivo Formulation:

1) Add 100 μL of the DMSOTargetMol | reagent stock solution to 400 μL PEG300TargetMol | reagent and mix thoroughly until the solution becomes clear.

2) Add 50 μL Tween 80 and mix well until fully clarified.

3) Add 450 μL Saline,PBS or ddH2OTargetMol | reagent and mix thoroughly until a homogeneous solution is obtained.

This example is provided solely to demonstrate the use of the In Vivo Formulation Calculator and does not constitute a recommended formulation for any specific compound. Please select an appropriate dissolution and formulation strategy based on your experimental model and route of administration.
All co-solvents required for this protocol, includingDMSO, PEG300/PEG400, Tween 80, SBE-β-CD, and Corn oil, are available for purchase on the TargetMol website.
1 Enter information below:
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2 Enter the in vivo formulation:
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Please see Inhibitor Handling Instructions for more frequently ask questions. Topics include: how to prepare stock solutions, how to store products, and cautions on cell-based assays & animal experiments, etc
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