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TQFL13

Catalog No. T213013 Copy Product Info
🥰Excellent
TQFL13 is a derivative of Thymoquinone (TQ) with notable anti-breast cancer activity. It exhibits higher cytotoxicity against breast cancer cells (BT549, MDA-MB-231, 4T1), induces apoptosis, and arrests the cell cycle at the S and G2/G1 phases. TQFL13 demonstrates dose-dependent antitumor activity in murine breast cancer xenograft models and is useful for breast cancer research.

TQFL13

Copy Product Info
🥰Excellent
Catalog No. T213013

TQFL13 is a derivative of Thymoquinone (TQ) with notable anti-breast cancer activity. It exhibits higher cytotoxicity against breast cancer cells (BT549, MDA-MB-231, 4T1), induces apoptosis, and arrests the cell cycle at the S and G2/G1 phases. TQFL13 demonstrates dose-dependent antitumor activity in murine breast cancer xenograft models and is useful for breast cancer research.

TQFL13
Cas No. 2822560-46-1
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
TQFL13 is a derivative of Thymoquinone (TQ) with notable anti-breast cancer activity. It exhibits higher cytotoxicity against breast cancer cells (BT549, MDA-MB-231, 4T1), induces apoptosis, and arrests the cell cycle at the S and G2/G1 phases. TQFL13 demonstrates dose-dependent antitumor activity in murine breast cancer xenograft models and is useful for breast cancer research.
In vitro
TQFL13 exhibits cytotoxicity against BT549, MDA-MB-231, and 4T1 breast cancer cells with low toxicity to normal MCF-10A cells. At concentrations of 0-160 μM over 24 hours, the IC50 values are 23.80 μM, 37.55 μM, 17.59 μM, and >100 μM respectively; at 48 hours, the IC50 values alter to 12.35 μM, 12.14 μM, 12.21 μM, and >100 μM. At concentrations of 0-20 μM for 24 hours, TQFL13 induces apoptosis in 4T1 cells and causes cell cycle arrest in BT549 and MDA-MB-231 cells at the S phase and G2/G1 phase. Additionally, TQFL13, at 2.5-5 μM for up to 54 hours, inhibits the growth, migration, and invasion of 4T1 cells.
In vivo
TQFL13 (3.75-15 mg/kg, intraperitoneal injection, from the 4th day after 4T1 cell implantation in the mammary fat pad until the 30th day) exhibits antitumor activity in a BALB/c mouse xenograft model of breast cancer.
Chemical Properties
Molecular Weight357.41
FormulaC20H23NO5
Cas No.2822560-46-1
SmilesO=C1C=C(C(=O)C(N=CC2=CC=C(OC)C(OC)=C2OC)=C1C)C(C)C
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
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