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ZLY025

Catalog No. T216008 Copy Product Info
🥰Excellent
ZLY025 is an efficient, orally active CCNK degrader with a DC50 value of 42.7 nM. It exhibits broad-spectrum antiproliferative activity against various tumor cells, with IC50 values ranging from 0.08 to 2.45 μM. ZLY025 can induce apoptosis and cause G1 phase arrest. It is applicable for cancer research, including studies on lung cancer.

ZLY025

Copy Product Info
🥰Excellent
Catalog No. T216008

ZLY025 is an efficient, orally active CCNK degrader with a DC50 value of 42.7 nM. It exhibits broad-spectrum antiproliferative activity against various tumor cells, with IC50 values ranging from 0.08 to 2.45 μM. ZLY025 can induce apoptosis and cause G1 phase arrest. It is applicable for cancer research, including studies on lung cancer.

ZLY025
Cas No. 3070379-34-6
Pack SizePriceUSA StockGlobal StockQuantity
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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
ZLY025 is an efficient, orally active CCNK degrader with a DC50 value of 42.7 nM. It exhibits broad-spectrum antiproliferative activity against various tumor cells, with IC50 values ranging from 0.08 to 2.45 μM. ZLY025 can induce apoptosis and cause G1 phase arrest. It is applicable for cancer research, including studies on lung cancer.
In vitro
ZLY025 exhibits broad-spectrum antiproliferative activity against various tumor cell lines, including those of lung cancer, breast cancer, liver cancer, and leukemia, with IC50 values ranging from 0.08 to 2.45μM. ZLY025 (125-500 nM; 24 h) induces apoptosis and G1 phase arrest in A549 cells. Additionally, ZLY025 (30-1000 nM; 8-24 h) reduces the expression of CCNK, CDK12, p-CTD, and BRCA1 in A549 cells.
In vivo
ZLY025 administered at 0-40 mg/kg by gavage once daily for 17 days exhibits dose-dependent tumor growth inhibition in the BALB/c nude mouse A549 xenograft model. Additionally, ZLY025 at 200 mg/kg given orally by gavage once daily for 14 days demonstrates very low subacute toxicity in ICR mice.
Chemical Properties
Molecular Weight299.35
FormulaC15H13N3O2S
Cas No.3070379-34-6
SmilesO=C(NC1=NC=C(S1)C)CC=2C=CC(=CC2)C3=NC=CO3
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:
% DMSO
%
% Tween 80
% Saline/PBS/ddH2O

Dose Conversion

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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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