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ChemicalBook--->CAS DataBase List--->866269-28-5

866269-28-5

866269-28-5 Structure

866269-28-5 Structure
IdentificationBack Directory
[Name]

methyl 2-[3-({[3-(6-amino-2-butoxy-8-oxo-8,9-dihydro-7H-purin-9-yl)propyl][3-(morpholin-4-yl)propyl]amino}methyl)phenyl]acetate
[CAS]

866269-28-5
[Synonyms]

AZD8848
AZD8848,AZD-8848
methyl 2-[3-({[3-(6-amino-2-butoxy-8-oxo-8,9-dihydro-7H-purin-9-yl)propyl][3-(morpholin-4-yl)propyl]amino}methyl)phenyl]acetate
[EINECS(EC#)]

642-434-9
[Molecular Formula]

C29H43N7O5
[MDL Number]

MFCD18633259
[MOL File]

866269-28-5.mol
[Molecular Weight]

569.696
Chemical PropertiesBack Directory
[storage temp. ]

Store at -20°C
[form ]

Solid
[color ]

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


GHS08
[Signal word ]

Danger
[Hazard statements ]

H372
[Precautionary statements ]

P260-P264-P270-P314-P501
Hazard InformationBack Directory
[Uses]

AZD8848 is a selective toll-like receptor 7 (TLR7) anteagent agonist which is developed for the research of asthma and allergic rhinitis[1].
[in vivo]

AZD8848 (0.1-1 mg/kg; intratracheal) has a good pharmacokinetics in the Brown Norway rat[1].
? AZD8848 (0.3 mg/kg; Intratracheal) suppresses the ovalbumin (OVA) challenge in the rat allergy model[1].

Animal Model:Brown Norway rat allergy model[1]
Dosage:0.1 mg/kg, 1 mg/kg
Administration:Intratracheal (24 hours prior to and 24 hours after the OVA challenge)
Result:Suppressed OVA challenge in a dose-dependent manner.
Animal Model:Brown Norway rat[1]
Dosage:0.3 mg/kg (Pharmacokinetic Analysis)
Administration:Intratracheal
Result:Has a very short half-life (0.2 min) in rat blood and declined slowly after this point and levels above 1000 nmol/kg were maintained for over 5 hours.
[IC 50]

TLR7
[References]

[1] Delaney S, et al. Tolerability in man following inhalation dosing of the selective TLR7 agonist, AZD8848. BMJ Open Respir Res. 2016 Feb 23;3(1):e000113. DOI:10.1136/bmjresp-2015-000113
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