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FL118

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Catalog No. T77701Cas No. 135415-73-5
Alias FL-118, FL 118, 10,11-(Methylenedioxy)-20(S)-camptothecin

FL118 is a novel survivin inhibitor that inhibits cancer stem cell-like properties.FL118 is a novel camptothecin analog with anticancer activity that inhibits epithelial-mesenchymal transition through the Wnt/β-catenin signaling pathway, thereby inhibiting migration and invasion of human breast cancer cells.

FL118

FL118

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Purity: 97.14%
Catalog No. T77701Alias FL-118, FL 118, 10,11-(Methylenedioxy)-20(S)-camptothecinCas No. 135415-73-5
FL118 is a novel survivin inhibitor that inhibits cancer stem cell-like properties.FL118 is a novel camptothecin analog with anticancer activity that inhibits epithelial-mesenchymal transition through the Wnt/β-catenin signaling pathway, thereby inhibiting migration and invasion of human breast cancer cells.
Pack SizePriceUSA WarehouseGlobal WarehouseQuantity
1 mg$73In StockIn Stock
5 mg$156In StockIn Stock
10 mg$197In StockIn Stock
25 mg$396In StockIn Stock
50 mg$488In StockIn Stock
100 mg$787-In Stock
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In Stock Estimated shipping dateUSA Warehouse[1-2 days] Global Warehouse[5-7 days]
All TargetMol products are for research purposes only and cannot be used for human consumption. We do not provide products or services to individuals. Please comply with the intended use and do not use TargetMol products for any other purpose.
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Purity:97.14%
Appearance:Solid
Color:Yellow
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Product Introduction

Bioactivity
Description
FL118 is a novel survivin inhibitor that inhibits cancer stem cell-like properties.FL118 is a novel camptothecin analog with anticancer activity that inhibits epithelial-mesenchymal transition through the Wnt/β-catenin signaling pathway, thereby inhibiting migration and invasion of human breast cancer cells.
In vitro
FL118 (0-200 nM; 24, 48, and 72 h) suppresses cell proliferation and migration in ES-2 and SK-O-V3 cells, influencing CYGB expression and inhibiting the PI3K/AKT/mTOR pathway, altering vimentin and E-cadherin levels in ovarian cancer cells. FL118 (0-500 nM; 0-72 h) induces dephosphorylation and degradation of DDX5, regulating survivin, McL-1, XIAP, cIAP2, c-Myc, and mKras expression. FL118 (0-1 μM; 24, 48 h) exhibits cytotoxicity against A549, MDA-MB-231, and RM-1 cell lines, enhancing PARP cleavage and triggering apoptosis in A549 cells, primarily arresting them at the G2/M phase.
In vivo
FL118 (5 and 10 mg/kg; p.o.; once a week; 20 days; female BALB/c nude mice) dose-dependently suppressed ES-2 tumor growth by upregulating CYGB expression.[1] Additionally, FL118 (0-1.5 mg/kg; i.p.; once every other day; five times) effectively eliminated human colon and head-and-neck tumors resistant to irinotecan or topotecan.[4] FL118 (1.5 mg/kg; i.v.; once) also demonstrated favorable pharmacokinetic profiles.[4]
SynonymsFL-118, FL 118, 10,11-(Methylenedioxy)-20(S)-camptothecin
Chemical Properties
Molecular Weight392.36
FormulaC21H16N2O6
Cas No.135415-73-5
SmilesC(C)[C@]1(O)C2=C(C(=O)N3C(=C2)C=4C(C3)=CC=5C(N4)=CC6=C(C5)OCO6)COC1=O
Relative Density.no data available
Storage & Solubility Information
StoragePowder: -20°C for 3 years | In solvent: -80°C for 1 year | Shipping with blue ice/Shipping at ambient temperature.
Solubility Information
DMSO: 2 mg/mL (5.1 mM), Sonication and heating are recommended.
Solution Preparation Table
DMSO
1mg5mg10mg50mg
1 mM2.5487 mL12.7434 mL25.4868 mL127.4340 mL
5 mM0.5097 mL2.5487 mL5.0974 mL25.4868 mL

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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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