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ChemicalBook--->CAS DataBase List--->1892576-58-7

1892576-58-7

1892576-58-7 Structure

1892576-58-7 Structure
IdentificationBack Directory
[Name]

PF-06747711
[CAS]

1892576-58-7
[Synonyms]

PF-06747711
RORC2 Inverse Agonist
PF06747711,PF 06747711
PF-06747711 >=98% (HPLC)
Benzamide, 3-cyano-N-[1-methyl-3-[1-(2-methyl-1-oxopropyl)-4-piperidinyl]-4-(trifluoromethyl)-1H-pyrrolo[2,3-b]pyridin-5-yl]-
[Molecular Formula]

C26H26F3N5O2
[MDL Number]

MFCD31697703
[MOL File]

1892576-58-7.mol
[Molecular Weight]

497.51
Chemical PropertiesBack Directory
[Boiling point ]

621.8±55.0 °C(Predicted)
[density ]

1.34±0.1 g/cm3(Predicted)
[storage temp. ]

Store at -20°C
[solubility ]

DMSO: 41.67 mg/mL (83.76 mM)
[form ]

Solid
[pka]

10.27±0.43(Predicted)
[color ]

White to off-white
Safety DataBack Directory
[Symbol(GHS) ]


GHS07
[Signal word ]

Warning
[Hazard statements ]

H302-H315-H319-H335
[Precautionary statements ]

P261-P280-P301+P312-P302+P352-P305+P351+P338
Hazard InformationBack Directory
[Uses]

PF-06747711 is a potent, selective, and orally active retinoic acid receptor-related orphan C2 (RORC2, also known as RORγt) inverse agonist, with an IC50 of 4.1 nM. Anti-skin inflammatory activity[1].
[Biological Activity]

PF-06747711 is a mono-imine compound. It regulates gene expression in signaling pathways by targeting a nuclear hormone receptor. It is also used to tre at psoriasis.''PF-06747711 is a potent and selective RORC2 modulator.
[in vivo]

PF-06747711 (10, 30, and 100 mg/kg, p.o., daily over 5 days) inhibits ear swelling in a dose-dependent manner in mice[1].

Animal Model:8?10 week old female Balb/c mice[1]
Dosage:10, 30, and 100 mg/kg
Administration:P.O. daily over 5 days
Result:Inhibited ear swelling, and caused a maximum inhibition of 46% at 100 mg/kg.
[References]

[1] Schnute ME, et al. Discovery of 3-Cyano- N-(3-(1-isobutyrylpiperidin-4-yl)-1-methyl-4-(trifluoromethyl)-1 H-pyrrolo[2,3- b]pyridin-5-yl)benzamide: A Potent, Selective, and Orally Bioavailable Retinoic Acid Receptor-Related Orphan Receptor C2 Inverse Agonist. J Med Chem. 2018 Sep 9. DOI:10.1021/acs.jmedchem.8b00392
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