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G007-LK

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Catalog No. T6842Cas No. 1380672-07-0

G007-LK is a selective inhibitor of TNKS1 and TNKS2, with IC50s of 46 nM and 25 nM, respectively.

G007-LK

G007-LK

🥰Excellent
Purity: 98.62%
Catalog No. T6842Cas No. 1380672-07-0
G007-LK is a selective inhibitor of TNKS1 and TNKS2, with IC50s of 46 nM and 25 nM, respectively.
Pack SizePriceAvailabilityQuantity
1 mg$45In Stock
2 mg$64In Stock
5 mg$100In Stock
10 mg$169In Stock
25 mg$351In Stock
50 mg$558In Stock
100 mg$785In Stock
1 mL x 10 mM (in DMSO)$125In Stock
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Purity:98.62%
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Product Introduction

Bioactivity
Description
G007-LK is a selective inhibitor of TNKS1 and TNKS2, with IC50s of 46 nM and 25 nM, respectively.
Targets&IC50
TNKS2:25 nM, TNKS1:46 nM
In vitro
G007-LK demonstrated anti-tumor efficacy in xenograft and genetically engineered CRC models. In the COLO-320DM model, it reduced levels of tankyrases 1 and 2, stabilized AXIN1 and AXIN2, and decreased β-catenin levels. G007-LK treatment increased the expression of KRT20 and TM4SF4 in COLO-320DM tumors. Administered at 20 mg/kg twice daily, G007-LK achieved a 61% inhibition of tumor growth. Additionally, it reduced Wnt/β-catenin signaling and cell proliferation in normal intestinal tissue.
In vivo
G007-LK inhibits Wnt/β-catenin signaling by preventing poly(ADP-ribosyl)ation-dependent AXIN degradation, thus promoting β-catenin destabilization. In cell culture, it completely blocks ligand-driven Wnt/β-catenin signaling and demonstrates inhibition of approximately 50% in APC mutation-driven signaling across most CRC cell lines. G007-LK reduces mitotic COLO-320DM cells from 24% to 12% and S-phase HCT-15 cells from 28% to 18% at a concentration of 0.2 μM. It also inhibits colony formation in CRC cell lines COLO-320DM and SW403. Furthermore, G007-LK suppresses organ growth with an IC50 of 80 nM.
Kinase Assay
TNKS1 and TNKS2 in vitro biochemical assays: G007-LK inhibitory activity at various doses (duplicates) is tested twice by TNKS1, TNSK2 Chemiluminescent Assay Kits, and the luminescence is measured.
Cell Research
Cell lines: APC-mutant CRC cell lines COLO-320DM. Concentrations: ~0.2 μM. Method: For colony formation assays,cells are seeded at 500 cells/well in 2 mL medium.Cell line in triplicate wells is treated with either 0.06% DMSO or compound in 0.06% DMSO and incubated for up to 17 days or until colonies became sufficiently large to quantify.Colonies are stained with 200 μL of 12 mM 3-(4,5-dimethylthiazol-2-yl)-2,5-diphenyltetrazolium bromide to each well for 1 h,and colony numbers are quantitated with a GelCount scanner at 1200 dpi resolution.
Animal Research
Animal Models: Human APC –mutant CRC xenograft COLO-320DM. Formulation: 15% DMSO,17.5% Cremophor EL,8.75% ethanol,8.75% Miglyol 810N,50% PBS. Dosages: 20 mg/kg. Administration: intraperitoneal injection twice daily
Chemical Properties
Molecular Weight529.96
FormulaC25H16ClN7O3S
Cas No.1380672-07-0
SmilesCS(=O)(=O)c1ccc(nc1)-c1nnc(\C=C\c2nnc(o2)-c2ccc(cc2)C#N)n1-c1ccccc1Cl
Relative Density.1.47 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
Ethanol: < 1 mg/mL (insoluble or slightly soluble)
H2O: < 1 mg/mL (insoluble or slightly soluble)
DMSO: 93 mg/mL (175.5 mM)
Solution Preparation Table
DMSO
1mg5mg10mg50mg
1 mM1.8869 mL9.4347 mL18.8693 mL94.3467 mL
5 mM0.3774 mL1.8869 mL3.7739 mL18.8693 mL
10 mM0.1887 mL0.9435 mL1.8869 mL9.4347 mL
20 mM0.0943 mL0.4717 mL0.9435 mL4.7173 mL
50 mM0.0377 mL0.1887 mL0.3774 mL1.8869 mL
100 mM0.0189 mL0.0943 mL0.1887 mL0.9435 mL

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