Shopping Cart
  • Remove All
  • TargetMol
    Your shopping cart is currently empty

Napabucasin

🥰Excellent
Catalog No. T3218Cas No. 83280-65-3
Alias BBI608

Napabucasin (BBI608) is an orally available Stat3 and Y cell stemness inhibitor.

Napabucasin

Napabucasin

🥰Excellent
Purity: 99.61%
Catalog No. T3218Alias BBI608Cas No. 83280-65-3
Napabucasin (BBI608) is an orally available Stat3 and Y cell stemness inhibitor.
Pack SizePriceAvailabilityQuantity
5 mg57 €In Stock
10 mg80 €In Stock
50 mg196 €In Stock
100 mg350 €In Stock
1 mL x 10 mM (in DMSO)64 €In Stock
Bulk & Custom
Add to Cart
Questions
View More

Related Compound Libraries of "Napabucasin"

Select Batch
Purity:99.61%
Contact us for more batch information
Resource Download
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.

Product Introduction

Bioactivity
Description
Napabucasin (BBI608) is an orally available Stat3 and Y cell stemness inhibitor.
In vitro
Napabucasin downregulates stemness gene expression driven by Stat3 and cancer stemness properties, and effectively inhibits self-renewal of stemness-high cancer cells with IC50 ranged from 0.291~1.19 μM, on inhibition on normal stem cells. [1]
In vivo
In mice bearing PaCa-2 xenografts, Napabucasin (20 mg/kg, i.p.) significantly inhibits tumor growth, relapse and metastasis. [1]
Cell Research
For cancer stem cells, spheres are dissociated and plated under cancer stem cell culture conditions on coated 96-well plates. After 72 h of culture, wells are dosed with the indicated compounds. Seventy-two hours or 24 h after dosing, CellTiter-Glo 2.0 is added to each well, and the luminescence is measured as described by the manufacturer. IC50 values are calculated by fitting a four parameter dose–response curve to normalized data using GraphPad Prism software. For bulk cells, cells are plated at 5,000 cells per well on 96-well plates. Twenty-four hours after plating, cells are treated with the indicated compounds. Viability is determined at 72 h as described above.(Only for Reference)
AliasBBI608
Chemical Properties
Molecular Weight240.21
FormulaC14H8O4
Cas No.83280-65-3
SmilesCC(=O)c1cc2c(o1)C(=O)c1ccccc1C2=O
Relative Density.1.385 g/cm3 (Predicted)
Storage & Solubility Information
StoragePowder: -20°C for 3 years | In solvent: -80°C for 1 year | Shipping with blue ice.
Solubility Information
H2O: < 1 mg/mL (insoluble or slightly soluble)
DMSO: 6.88 mg/mL (28.62 mM)
acetonitrile: 0.799 mg/ml (3.3278 mM)
Ethanol: < 1 mg/mL (insoluble or slightly soluble)
Solution Preparation Table
acetonitrile/DMSO
1mg5mg10mg50mg
1 mM4.1630 mL20.8151 mL41.6302 mL208.1512 mL
DMSO
1mg5mg10mg50mg
5 mM0.8326 mL4.1630 mL8.3260 mL41.6302 mL
10 mM0.4163 mL2.0815 mL4.1630 mL20.8151 mL
20 mM0.2082 mL1.0408 mL2.0815 mL10.4076 mL

Calculator

  • Molarity Calculator
  • Dilution Calculator
  • Reconstitution Calculator
  • Molecular Weight Calculator

In Vivo Formulation Calculator (Clear solution)

Please enter your animal experiment information in the following box and click Calculate to obtain the mother liquor preparation method and in vivo formula preparation method:
TargetMol | Animal experimentsFor example, your dosage is 10 mg/kg Each animal weighs 20 g, and the dosage volume is 100 μL . TargetMol | Animal experiments A total of 10 animals were administered, and the formula you used is 5% TargetMol | reagent DMSO+30% PEG300+5% Tween 80+60% ddH2O. So your working solution concentration is 2 mg/mL。
Mother liquor preparation method: 2 mg of drug dissolved in 50 μL DMSOTargetMol | reagent (mother liquor concentration of 40 mg/mL), if you need to configure a concentration that exceeds the solubility of the product, please contact us first.
Preparation method for in vivo formula: Take 50 μL DMSOTargetMol | reagent main solution, add 300 μLPEG300TargetMol | reagent mix well and clarify, then add 50 more μL Tween 80, mix well and clarify, then add 600 more μLddH2OTargetMol | reagent mix well and clarify
For Reference Only. Please develop an appropriate dissolution method based on your laboratory animals and route of administration.
1 Enter information below:
mg/kg
g
μL
2 Enter the in vivo formulation:
% DMSO
%
%Tween 80
%ddH2O

Dose Conversion

You can also refer to dose conversion for different animals. More Dose Conversion

Tech Support

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

Keywords

Related Tags: buy Napabucasin | purchase Napabucasin | Napabucasin cost | order Napabucasin | Napabucasin chemical structure | Napabucasin in vivo | Napabucasin in vitro | Napabucasin formula | Napabucasin molecular weight