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Telaglenastat

Catalog No. T6797   CAS 1439399-58-2
Synonyms: CB 839, CB839, CB-839

Telaglenastat (CB 839) (IC50 of 24 nM), an effective, specific, and oral inhibitor, which is bioavailable glutaminase, for recombinant human GAC.

All products from TargetMol are for Research Use Only. Not for Human or Veterinary or Therapeutic Use.
Telaglenastat Chemical Structure
Telaglenastat, CAS 1439399-58-2
Pack Size Availability Price/USD Quantity
2 mg In stock $ 32.00
5 mg In stock $ 47.00
10 mg In stock $ 72.00
25 mg In stock $ 128.00
50 mg In stock $ 222.00
100 mg In stock $ 369.00
500 mg In stock $ 869.00
1 g In stock $ 1,190.00
1 mL * 10 mM (in DMSO) In stock $ 59.00
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Purity: 100%
Purity: 99.89%
Purity: 99.87%
Purity: 99.86%
Purity: 97.57%
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Biological Description
Chemical Properties
Storage & Solubility Information
Description Telaglenastat (CB 839) (IC50 of 24 nM), an effective, specific, and oral inhibitor, which is bioavailable glutaminase, for recombinant human GAC.
Targets&IC50 Glutaminase:24 nM
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.[1]
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%.[1]
Kinase Assay Inhibition of CB-839 on rHu-GAC: The enzymatic activity is measured in assay buffer containing 50 mM Tris-Acetate pH 8.6, 150 mM K2HPO4 , 0.25 mM EDTA, 0.1 mg/mL bovine serum albumin, 1 mM DTT, 2 mM NADP+ and 0.01% Triton X-100. To measure inhibition, the inhibitor (prepared in DMSO) is first pre-mixed with glutamine and glutamate dehydrogenase (GDH) and reactions are initiated by the addition of rHu-GAC. Final reactions contains 2 nM rHu-GAC, 10 mM glutamine, 6 units/mL GDH and 2% DMSO. Generation of NADPH is monitored by fluorescence (Ex340/Em460 nm) every minute for 15 minutes on a SpectraMax M5e plate reader. Relative fluorescence units (RFU) are converted to units of NADPH concentration (μM) using a standard curve of NADPH. Each assay plate incorporates control reactions that monitores the conversion of glutamate (1 to 75 μM) plus NADP+ to α-ketoglutarate plus NADPH by GDH. Under these assay conditions, up to 75 μM glutamate is stoichiometrically converts to α-ketoglutarate/NADPH by GDH. Initial reaction velocities are calculated by fitting the first 5 minutes of each progress curve to a straight line. Inhibition curves are fitted to a four-parameter dose response equation of the form: % activity = Bottom + (Top-Bottom)/(1+10^((LogIC50-X)*HillSlope)).
Cell Research 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.(Only for Reference)
Synonyms CB 839, CB839, CB-839
Molecular Weight 571.57
Formula C26H24F3N7O3S
CAS No. 1439399-58-2

Storage

Powder: -20°C for 3 years | In solvent: -80°C for 1 year

Solubility Information

H2O: < 1 mg/mL (insoluble or slightly soluble)

Ethanol: < 1 mg/mL (insoluble or slightly soluble)

DMSO: 93 mg/mL (162.7 mM)

TargetMolReferences and Literature

1. Gross MI, et al. Mol Cancer Ther. 2014, 13(4):890-901. 2. Caiola E, Colombo M, Sestito G, et al. Glutaminase Inhibition on NSCLC Depends on Extracellular Alanine Exploitation[J]. Cells. 2020, 9(8): 1766.

TargetMolCitations

1. Caiola E, Colombo M, Sestito G, et al. Glutaminase Inhibition on NSCLC Depends on Extracellular Alanine Exploitation. Cells. 2020, 9(8): 1766

Related compound libraries

This product is contained In the following compound libraries:
Anti-Cancer Active Compound Library Drug Repurposing Compound Library Anti-Cancer Drug Library Inhibitor Library Anti-Cancer Clinical Compound Library Anti-Breast Cancer Compound Library Bioactive Compounds Library Max Anti-Cancer Compound Library Anti-Lung Cancer Compound Library Protease Inhibitor Library

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Keywords

Telaglenastat 1439399-58-2 Autophagy Metabolism Proteases/Proteasome transporter Glutaminase CB 839 antiproliferative HCC-1806 TNBC breast Inhibitor splice cell PDAC CB839 variants selective cancer triple-negative CB-839 inhibit inhibitor

 

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