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ZN-c3

Catalog No. T9643Cas No. 2376146-48-2

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

ZN-c3

ZN-c3

Purity: 99.80%
Catalog No. T9643Cas No. 2376146-48-2
Azenosertib (ZN-c3) is a potent and selective Wee1 inhibitor with balanced potency, ADME, and pharmacokinetic properties.[1]
Pack SizePriceAvailabilityQuantity
1 mg$97In Stock
5 mg$239In Stock
10 mg$372In Stock
25 mg$689In Stock
50 mg$1,090In Stock
100 mg$1,630In Stock
200 mg$2,190In Stock
1 mL x 10 mM (in DMSO)$277In Stock
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Purity:99.80%
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Product Introduction

Bioactivity
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]
Chemical Properties
Molecular Weight526.63
FormulaC29H34N8O2
Cas No.2376146-48-2
Storage & Solubility Information
Storagestore 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.
Solubility Information
DMSO: 50 mg/mL (94.94 mM), Sonication is recommended.
Solution Preparation Table
DMSO
1mg5mg10mg50mg
1 mM1.8989 mL9.4943 mL18.9887 mL94.9433 mL
5 mM0.3798 mL1.8989 mL3.7977 mL18.9887 mL
10 mM0.1899 mL0.9494 mL1.8989 mL9.4943 mL
20 mM0.0949 mL0.4747 mL0.9494 mL4.7472 mL
50 mM0.0380 mL0.1899 mL0.3798 mL1.8989 mL

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