Your shopping cart is currently empty

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.


| Pack Size | Price | USA Stock | Global Stock | Quantity |
|---|---|---|---|---|
| 1 mg | $283 | 10-14 weeks | 10-14 weeks | |
| 5 mg | $676 | 10-14 weeks | 10-14 weeks | |
| 25 mg | $1,550 | 10-14 weeks | 10-14 weeks | |
| 100 mg | $3,380 | 10-14 weeks | 10-14 weeks |
| 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] |
| Molecular Weight | 384.43 |
| Formula | C19H24N6O3 |
| Cas No. | 3054692-62-2 |
| Smiles | O=C1C2(C=3C(N1[C@H]4C[C@H](O)CCC4)=NC(NC=5C(OCC)=NNC5)=NC3)CC2 |
| Storage | Powder: -20°C for 3 years | In solvent: -80°C for 1 year Shipping with blue ice/Shipping at ambient temperature. |
Dissolve 2 mg of the compound in 100 μL DMSO
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.
1) Add 100 μL of the DMSO
stock solution to 400 μL PEG300
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 ddH2O
and mix thoroughly until a homogeneous solution is obtained.
| Size | Quantity | Unit Price | Amount | Operation |
|---|

Copyright © 2015-2026 TargetMol Chemicals Inc. All Rights Reserved.