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Z19024498

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Catalog No. T218824 Copy Product Info
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Z19024498 serves as a thermosensitizer and can inhibit SAFB granule formation under heat stress conditions. Additionally, it enhances heat stress-induced apoptosis (Apoptosis) and exhibits anticancer activity against cervical cancer when used in conjunction with heat stress.

Z19024498

Cas No. 1005147-23-8
Pack SizePriceUSA StockGlobal StockQuantity
10 mgInquiry10-14 weeks10-14 weeks
50 mgInquiry10-14 weeks10-14 weeks
For In stock only · Estimated delivery: USA Stock (1-2 days) Global Stock (5-7 days)
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For research use only—not for human use. No sales to individuals. Use as intended only.
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Product Introduction

Bioactivity
Description
Z19024498 serves as a thermosensitizer and can inhibit SAFB granule formation under heat stress conditions. Additionally, it enhances heat stress-induced apoptosis (Apoptosis) and exhibits anticancer activity against cervical cancer when used in conjunction with heat stress.
In vitro
Z19024498 significantly enhances the inhibition of HeLa cell growth induced by heat stress when pre-incubated at 37°C for 1 hour, co-incubated under 43°C heat stress for 1 hour, and followed by recovery for 24 hours at 37°C without the compound. Additionally, Z19024498 inhibits the formation of independent SAFB granules in HeLa cells subjected to heat stress (IC50 = 10.7 μM) when used at concentrations of 0-20 μM, with pre-incubation at 37°C for 1 hour, followed by co-incubation at 43°C for 1 hour.
In vivo
Administering Z19024498 (3 mg/kg; intraperitoneal injection; twice) on its own can slightly reduce tumor volume and extend survival in mice with HeLa xenografts. Combined with heat stress, it significantly inhibits tumor growth.
Chemical Properties
Molecular Weight332.23
FormulaC14H19Cl2N3O2
Cas No.1005147-23-8
SmilesO=C1C(Cl)=C(Cl)C=NN1CC(=O)NC2CCCC(C)C2C
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
Related Tags: Z19024498 in vivo | Z19024498 in vitro | Z19024498 formula | Z19024498 molecular weight