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Azenosertib (ZN-c3) is a potent and selective Wee1 inhibitor with balanced potency, ADME, and pharmacokinetic properties.[1]

| Pack Size | Price | USA Warehouse | Global Warehouse | Quantity |
|---|---|---|---|---|
| 1 mg | $97 | In Stock | In Stock | |
| 5 mg | $239 | In Stock | In Stock | |
| 10 mg | $372 | In Stock | In Stock | |
| 25 mg | $689 | In Stock | In Stock | |
| 50 mg | $1,090 | In Stock | In Stock | |
| 100 mg | $1,630 | - | In Stock | |
| 200 mg | $2,190 | - | In Stock | |
| 1 mL x 10 mM (in DMSO) | $277 | In Stock | In Stock |
| Description | Azenosertib (ZN-c3) is a potent and selective Wee1 inhibitor with balanced potency, ADME, and pharmacokinetic properties.[1] |
| In vitro | METHODS: Azenosertib (ZN-c3) was used to treat cancer cells H23 for three days and A427 for four days, and the proliferation of cancer cells was observed. RESULTS Azenosertib (ZN-c3) inhibited the proliferation of cancer cells H23 and A427, with IC50 of 103 and 75 nM. [1] |
| In vivo | The pharmacokinetic data of Azenosertib (10 mg/kg, oral) showed that the plasma exposure rate of Azenosertib in the beagle dog model was Cmax = 2.1 μM, the half-life T1/2 was 2.3 h, the AUC0-24 h was 9.7 μM·h, and the oral availability was F=142%; Azenosertib (80 mg/kg, oral for 28 days) inhibited the tumor growth of A427 xenograft tumors in the NOD/SCID mouse model[1] |
| Molecular Weight | 526.63 |
| Formula | C29H34N8O2 |
| Cas No. | 2376146-48-2 |
| Smiles | C(C=C)N1N(C=2C(C1=O)=CN=C(NC3=CC=C(C=C3)N4CCN(C)CC4)N2)C=5N=C6C(=CC5)CC[C@@]6(CC)O |
| Storage | store at low temperature,keep away from direct sunlight | Powder: -20°C for 3 years | In solvent: -80°C for 1 year | Shipping with blue ice/Shipping at ambient temperature. | ||||||||||||||||||||||||||||||
| Solubility Information | DMSO: 50 mg/mL (94.94 mM), Sonication is recommended. | ||||||||||||||||||||||||||||||
| In Vivo Formulation | 10% DMSO+40% PEG300+5% Tween 80+45% Saline: 5 mg/mL (9.49 mM), Sonication is recommended. Please add the solvents sequentially, clarifying the solution as much as possible before adding the next one. Dissolve by heating and/or sonication if necessary. Working solution is recommended to be prepared and used immediately. The formulation provided above is for reference purposes only. In vivo formulations may vary and should be modified based on specific experimental conditions. | ||||||||||||||||||||||||||||||
Solution Preparation Table | |||||||||||||||||||||||||||||||
DMSO
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