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ChemicalBook--->CAS DataBase List--->1887161-80-9

1887161-80-9

1887161-80-9 Structure

1887161-80-9 Structure
IdentificationBack Directory
[Name]

RORγt Inverse agonist 6
[CAS]

1887161-80-9
[Synonyms]

RORγt Inverse agonist 6
[Molecular Formula]

C28H29ClN6O5
[MDL Number]

MFCD32263437
[MOL File]

1887161-80-9.mol
[Molecular Weight]

565.02
Chemical PropertiesBack Directory
[density ]

1.46±0.1 g/cm3(Predicted)
[storage temp. ]

Store at -20°C
[solubility ]

DMSO : 50 mg/mL (88.49 mM; Need ultrasonic)
[form ]

Solid
[pka]

11.82±0.70(Predicted)
[color ]

White to off-white
Hazard InformationBack Directory
[Uses]

RORγt Inverse agonist 6 (compound 43) is a RORγt inverse agonist for the study of Th17-driven autoimmune diseases. RORγt Inverse agonist 6 (compound 43) suppresses IL-17A gene expression by IL-23 stimulation in vivo[1].
[Biological Activity]

RORγt Inverse agonist 6 (compound 43) is a RORγt inverse agonist for the study of Th17-driven autoimmune diseases. RORγt Inverse agonist 6 (compound 43) suppresses IL-17A gene expression by IL-23 stimulation in vivo[1]. RORγt Inverse agonist 6 (compound 43) suppresses IL-17A gene expression by IL-23 stimulation in a mouse pharmacodynamics model[1].RORγt Inverse agonist 6 (compound 43) exhibits improved drug exposure (mouse AUC: 1289 ng?h/mL at 1 mg/kg, po)[1].RORγt Inverse agonist 6 (compound 43, 30 mg/kg, po, b.i.d) inhibits the expression level of IL-17A by 59% compared to the vehicle after the oral administration at the tested dose[1].
[in vivo]

RORγt Inverse agonist 6 (compound 43) suppresses IL-17A gene expression by IL-23 stimulation in a mouse pharmacodynamics model[1].
RORγt Inverse agonist 6 (compound 43) exhibits improved drug exposure (mouse AUC: 1289 ng?h/mL at 1 mg/kg, po)[1].
RORγt Inverse agonist 6 (compound 43, 30 mg/kg, po, b.i.d) inhibits the expression level of IL-17A by 59% compared to the vehicle after the oral administration at the tested dose[1].

Animal Model:Mice[1].
Dosage:30 mg/kg.
Administration:Orally twice: at 30 min before and 8 h after IL-23 administration.
Result:Inhibited the expression level of IL-17A by 59% compared to the vehicle after the oral administration at the tested dose.
[storage]

Store at -20°C
[References]

[1]. Sato A, et al. Design and Synthesis of Conformationally Constrained RORγt Inverse Agonists. ChemMedChem. 2019 Oct 28.
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