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  • DC Chemicals Limited
  • China
  • Product Name: GSK-805
  • Price: $Inquiry/100mg $1100.0/250mg $2200.0/1g
  • Purity: 98.0%
  • Stocking Period: 3 Day
  • Contact: Tony Cao

1426802-50-7

1426802-50-7 structure
1426802-50-7 structure
  • Name: ROR gamma-t-IN-1
  • Chemical Name: N-[2,6-Dichloro-2'-(trifluoromethoxy)-4-biphenylyl]-2-[4-(ethylsulfonyl)phenyl]acetamide
  • CAS Number: 1426802-50-7
  • Molecular Formula: C23H18Cl2F3NO4S
  • Molecular Weight: 532.359
  • Catalog: Signaling Pathways Metabolic Enzyme/Protease ROR
  • Create Date: 2018-06-25 14:30:59
  • Modify Date: 2024-01-12 06:03:16
  • GSK805 is a potent, orally bioavailable RORγγ Inhibitor with pIC50 of 8.4 and >8.2 for RORγ FRET assay and Th17 assay.

Name N-[2,6-Dichloro-2'-(trifluoromethoxy)-4-biphenylyl]-2-[4-(ethylsulfonyl)phenyl]acetamide
Synonyms MFCD28902182
Benzeneacetamide, N-[2,6-dichloro-2'-(trifluoromethoxy)[1,1'-biphenyl]-4-yl]-4-(ethylsulfonyl)-
N-[2,6-Dichloro-2'-(trifluoromethoxy)-4-biphenylyl]-2-[4-(ethylsulfonyl)phenyl]acetamide
ROR gamma-t-IN-1
Description GSK805 is a potent, orally bioavailable RORγγ Inhibitor with pIC50 of 8.4 and >8.2 for RORγ FRET assay and Th17 assay.
Related Catalog
Target

IC50: 8.4 (RORγt)[1].

Animal Admin Animal administration[1] GSK805 are orally administered once daily at 3 doses (1, 3, and 10 mg/kg) to EAE mice from the day of immunization. Compared to the control, the treatment with 9a or 9g resulted in a delay and significant reduction in clinical severity of EAE in a dose-dependent manner. Compared to thiazole ketone amide 2, which only showed EAE efficacy up to day 20 at 100 mg/kg twice daily dosing,32 the biaryl amides 9a and 9g are much more efficacious. This could be attributed to their good in vitro activities as well as much improved oral exposure and CNS penetration. However, it should be noted that although 9g had more brain exposure than 9a, it exhibited less efficacy than 9a in EAE experiments, indicating that there might be additional factors such as "free" brain concentration affecting in vivo efficacy[1].
References

[1]. Wang Y, et al. Discovery of Biaryl Amides as Potent, Orally Bioavailable, and CNS Penetrant RORγt Inhibitors. ACS Med Chem Lett. 2015 May 26;6(7):787-792.

Density 1.4±0.1 g/cm3
Boiling Point 617.1±55.0 °C at 760 mmHg
Molecular Formula C23H18Cl2F3NO4S
Molecular Weight 532.359
Flash Point 327.0±31.5 °C
Exact Mass 531.028564
LogP 5.41
Vapour Pressure 0.0±1.8 mmHg at 25°C
Index of Refraction 1.581