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ChemicalBook--->CAS DataBase List--->2743427-26-9

2743427-26-9

2743427-26-9 Structure

2743427-26-9 Structure
IdentificationBack Directory
[Name]

INDEX NAME NOT YET ASSIGNED
[CAS]

2743427-26-9
[Synonyms]

GSK215
[Molecular Formula]

C50H59F3N10O6S
[MOL File]

2743427-26-9.mol
[Molecular Weight]

985.14
Chemical PropertiesBack Directory
[Boiling point ]

1103.2±65.0 °C(Predicted)
[density ]

1.317±0.06 g/cm3(Predicted)
[storage temp. ]

Store at -20°C
[solubility ]

DMSO : 250 mg/mL (253.77 mM; Need ultrasonic)
[form ]

Solid
[pka]

13.97±0.40(Predicted)
[color ]

Off-white to light yellow
[InChIKey]

ZGSWGXNEXAXEGV-VSAGVCMVNA-N
Hazard InformationBack Directory
[Biological Activity]

GSK215 is a potent and selective PROTAC focal adhesion kinase (FAK) degrader. GSK215 is designed by a binder for the VHL E3 ligase and the FAK inhibitor VS-4718. GSK215 induces rapid and prolonged FAK degradation, giving a long-lasting effect on FAK levels and a marked pharmacokinetic/pharmacodynamics (PK/PD) disconnect[1]. GSK215 (0.1-1000 nM; 2 hours) effectively increases the FAK degradation by >90% and determines a DC50 of 1.3 nM[1]. GSK215 (8mg/kg; i.h.) treatment shows the Cmax and tmax values of 526 ng/mL and 0.33 hours, respectively[1].
[in vitro]

GSK215 (0.1-1000 nM; 2 h) effectively increases the FAK degradation by >90% and determines a DC50 of 1.3 nM in A549 cells. Its induced degradation is proteasome and ubiquitin-dependent. GSK215 (above 100 nM, 6h) primarily reduces kinases CDK7, RPS6KA3, MET, and GAK. This compound (100 nM, 48 h) inhibits migration, invasion, and collagen deposition in A549 cells.
[storage]

Store at -20°C
[References]

[1]. Law RP, Nunes J, Chung CW, et al. Discovery and Characterisation of Highly Cooperative FAK-Degrading PROTACs [published online ahead of print, 2021 Aug 20]. Angew Chem Int Ed Engl. 2021;10.1002/anie.202109237.
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