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532959-63-0

532959-63-0 Structure

532959-63-0 Structure
IdentificationBack Directory
[Name]

N-[4-(4-Amino-2-ethyl-1H-imidazo[4,5-c]quinolin-1-yl)butyl]-methylesulfonamide
[CAS]

532959-63-0
[Synonyms]

3M-852A
PF-4878691
PF-4878691 (3M-852A)
Toll-like Receptor (TLR),inhibit,PF4878691,PF 4878691,PF-4878691,Inhibitor
N-(4-(4-Amino-2-ethyl-1H-imidazo[4,5-c]quinolin-1-yl)butyl)methanesulfonamide
N-[4-(4-Amino-2-ethyl-1H-imidazo[4,5-c]quinolin-1-yl)butyl]-methyl sulfonamide
N-[4-(4-Amino-2-ethyl-1H-imidazo[4,5-c]quinolin-1-yl)butyl]-methylesulfonamide
Methanesulfonamide, N-[4-(4-amino-2-ethyl-1H-imidazo[4,5-c]quinolin-1-yl)butyl]-
N-[4-(4-Amino-2-ethyl-1H-imidazo[4,5-c]quinolin-1-yl)butyl]-methyl sulfonamide,immunomodulator, immune response modifier
[Molecular Formula]

C17H23N5O2S
[MDL Number]

MFCD30533308
[MOL File]

532959-63-0.mol
[Molecular Weight]

361.46
Chemical PropertiesBack Directory
[Boiling point ]

632.3±65.0 °C(Predicted)
[density ]

1.38±0.1 g/cm3(Predicted)
[storage temp. ]

Store at -20°C
[solubility ]

Soluble in DMSO
[form ]

Solid
[pka]

11.32±0.40(Predicted)
[color ]

White to off-white
Hazard InformationBack Directory
[Uses]

PF-4878691 (3M-852A) is an orally active TLR7 agonist. PF-4878691 has the innate immune response activity, antiviral efficacy against HCV, and can be used for the research of cancer[1][2].
[in vivo]

PF-4878691 (10-150 mg, Oral gavage, single dose) induces pharmacology in BALB/c mice and C57bl/6 J mice[1].

Animal Model:BALB/c mice , C57bl/6 J mice[3]
Dosage:30 mg/kg, 60 mg/kg, 90 mg/kg, 150 mg/kg
Administration:Oral gavage (p.o.)
Result:Induced dose and time dependant lymphopenia and 2,5,oligoadenylate synthetase (2,5,OAS). Caused cardiovascular changes. Significantly increased TLR7 receptor RNA.
[IC 50]

TLR7; IL-6; IL-8; IL-1β; IL-2
[storage]

Store at -20°C
[References]

[1] Fidock MD, et al. The innate immune response, clinical outcomes, and ex vivo HCV antiviral efficacy of a TLR7 agonist (PF-4878691). Clin Pharmacol Ther. 2011 Jun;89(6):821-9. DOI:10.1038/clpt.2011.60
[2] Birmachu W, et al. Transcriptional networks in plasmacytoid dendritic cells stimulated with synthetic TLR 7 agonists [J]. BMC immunology, 2007, 8: 1-19.
[3] Horscroft NJ, et al. Antiviral applications of Toll-like receptor agonists. J Antimicrob Chemother. 2012 Apr;67(4):789-801. DOI:10.1093/jac/dkr588
Spectrum DetailBack Directory
[Spectrum Detail]

N-[4-(4-Amino-2-ethyl-1H-imidazo[4,5-c]quinolin-1-yl)butyl]-methylesulfonamide(532959-63-0)1HNMR
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