Top Suppliers:I want be here
  • DC Chemicals Limited
  • China
  • Product Name: STK16-IN-1
  • Price: $500.0/100mg $800.0/250mg $1600.0/1g
  • Purity: 98.0%
  • Stocking Period: 3 Day
  • Contact: Tony Cao

1223001-53-3

1223001-53-3 structure
1223001-53-3 structure
  • Name: STK16-IN-1
  • Chemical Name: STK16-IN-1
  • CAS Number: 1223001-53-3
  • Molecular Formula: C17H12FN3O
  • Molecular Weight: 293.295
  • Catalog: Research Areas Cancer
  • Create Date: 2018-06-02 14:42:10
  • Modify Date: 2024-01-12 18:54:51
  • STK16-IN-1 is a STK16 kinase inhibitor with an IC50 of 295 nM.

Name STK16-IN-1
Synonyms 1-(4-Fluoro-3-methylphenyl)-1,7-dihydro-2H-pyrrolo[2,3-h][1,6]naphthyridin-2-one
2H-Pyrrolo[2,3-h]-1,6-naphthyridin-2-one, 1-(4-fluoro-3-methylphenyl)-1,7-dihydro-
Description STK16-IN-1 is a STK16 kinase inhibitor with an IC50 of 295 nM.
Related Catalog
Target

IC50: 295 nM (STK16)[1]

In Vitro STK16-IN-1, which exhibits potent inhibitory activity against STK16 kinase (IC50=0.295 μM) with excellent selective across the kinome as assessed using the KinomeScanTM profiling assay. STK16-IN-1 inhibits mTOR kinase with an IC50 of 5.56 μM. In MCF-7 cells, treatment with STK16-IN-1 results in a reduction in cell number and accumulation of binucleated cells, which can be recapitulated by RNAi knockdown of STK16. Co-treatment of STK16-IN-1 with chemotherapeutics such as cisplatin, doxorubicin, colchicine and paclitaxel results in a slight potentiation of the anti-proliferative effects of the chemotherapeutics. STK16-IN-1 provides a useful tool compound for further elucidating the biological functions of STK16)[1].
Kinase Assay STK16-IN-1 is generally prepared with 1:3 serial dilutions for 4 concentrations (100 nM, 50 nM, 20 nM, and 10 nM); 6 concentrations are used (1 mM to 10 μM) for ATP competition experiments. The kinase reaction is performed with 1×kinase reaction buffer. Reactions in each well are started immediately by adding ATP and kept going for half an hour under 37°C. After the plate cooled for 5 minutes at room temperature, 5 μL of ADP-Glo reagent is added into each well to stop the reaction and consume the remaining ADP within 40 minutes. At the end, 10 μL of kinase detection reagent is added into the well and incubated for 1 hour to produce a luminescence signal[1].
Cell Assay MCF-7, HCT116, HeLa cells are treated with STK16-IN-1 (0, 5, 10 μM) for 72 hours and apoptotic cells are analyzed by flow cytometry using Annexin V/PI apoptosis detection kit[1].
References

[1]. Liu F, et al. Discovery of a Highly Selective STK16 Kinase Inhibitor. ACS Chem Biol. 2016 Jun 17;11(6):1537-43.

Density 1.4±0.1 g/cm3
Boiling Point 552.4±50.0 °C at 760 mmHg
Molecular Formula C17H12FN3O
Molecular Weight 293.295
Flash Point 287.9±30.1 °C
Exact Mass 293.096436
LogP 3.41
Vapour Pressure 0.0±1.5 mmHg at 25°C
Index of Refraction 1.713
Storage condition 2-8℃