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CB-839

Cat. No. M3003

All AbMole products are for research use only, cannot be used for human consumption.

CB-839 Structure
Synonym:

Telaglenastat

Size Price Availability Quantity
1mg USD 20 In stock
2mg USD 30 In stock
5mg USD 50 In stock
10mg USD 80 In stock
25mg USD 140 In stock
50mg USD 220 In stock
100mg USD 350 In stock
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Quality Control & Documentation
Biological Activity

Telaglenastat (CB-839) is a potent, selective, and orally bioavailable glutaminase inhibitor with IC50 of 24 nM for recombinant human GAC.

In vitro: CB-839 exhibits time-dependent and slowly reversible kinetics. IC50 values for glutaminase inhibition by CB-839 following preincubation with rHu-GAC for-1 hour are < 50 nmol/L, at least 13-fold lower than with BPTES. CB-839 has antiproliferative activity in a triple-negative breast cancer (TNBC) cell line, HCC-1806, while no antiproliferative activity is observed in an estrogen receptor–positive cell line, T47D.

In vivo: In the mouse TNBC model, single agent CB-839 (200 mg/kg, p.o.) suppresses tumor growth by 61% relative to vehicle control. In the mouse JIMT-1 xenograft model, CB-839 alone (200 mg/kg, p.o.) results in 54% tumor growth inhibition (TGI) relative to vehicle control, combination of CB-839 (200 mg/kg, p.o.) with paclitaxel (10 mg/kg, p.o.) largely suppresses the regrowth of the tumors resulting in a TGI relative to vehicle control of 100%.

Product Citations
Protocol (for reference only)
Cell Experiment
Cell lines HCC1806, MDA-MB-231, and T47D cells
Preparation method For viability assays, all cell lines are treated with CB-839 at the indicated concentrations for 72 hours and analyzed for antiproliferative effects using Cell Titer Glo.
Concentrations 1 mM
Incubation time 72 h
Animal Experiment
Animal models Female Scid/Bg mice bearing TNBC or JIMT-1 xenograft
Formulation 25% (w/v) hydroxypropyl-b-cyclodextrin (HPBCD) in 10 mmol/L citrate, pH 2
Dosages 200 mg/kg
Administration p.o.
Chemical Information
Molecular Weight 571.57
Formula C26H24F3N7O3S
CAS Number 1439399-58-2
Solubility (25°C) DMSO 60 mg/mL (warmed)
Storage Powder          -20°C   3 years ;  4°C   2 years
In solvent       -80°C   6 months ;  -20°C   1 month
References

[1] Jacque N, et al. Blood. Targeting glutaminolysis has antileukemic activity in acute myeloid leukemia and synergizes with BCL-2 inhibition.

[2] Gross MI, et al. Mol Cancer Ther. Antitumor activity of the glutaminase inhibitor CB-839 in triple-negative breast cancer.

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Keywords: CB-839, Telaglenastat supplier, GluR, inhibitors, activators

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