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22191-97-5

22191-97-5 Structure

22191-97-5 Structure
IdentificationBack Directory
[Name]

2-(4-Aminophenyl)quinoline
[CAS]

22191-97-5
[Synonyms]

4-(2-quinolyl)aniline
4-quinolin-2-ylaniline
2-(4-Aminophenyl)quinoline
[4-(2-quinolyl)phenyl]amine
4-(2-Quinolinyl)benzenamine
(4-Quinolin-2-ylphenyl)amine
Benzenamine, 4-(2-quinolinyl)-
BF-170 hydrochloride >=98% (HPLC), solid
[Molecular Formula]

C15H12N2
[MDL Number]

MFCD08705340
[MOL File]

22191-97-5.mol
[Molecular Weight]

220.27
Chemical PropertiesBack Directory
[storage temp. ]

-20°C
[solubility ]

H2O: soluble10mg/mL
[form ]

solid
[color ]

orange
[Water Solubility ]

H2O: 10mg/mL
Safety DataBack Directory
[Hazard Codes ]

Xn
[Risk Statements ]

22-37/38-41
[Safety Statements ]

26
[WGK Germany ]

3
Hazard InformationBack Directory
[Uses]

BF-170 is a selective tau fibril binding agent with an EC50 of 221 nM. It exhibits good blood-brain barrier permeability, and after intravenous injection in mice, the concentration in brain tissue reaches 9.1% ID/g within 2 minutes (with a brain clearance rate of 0.25% ID/g after 30 minutes). BF-170 can be used as a probe for tau protein pathology imaging in Alzheimer's disease (AD). It plays an important role in early-stage AD research and holds potential for imaging studies of tau-related neurodegenerative diseases[1].
[Biological Activity]

BF-170 is a new probe for neurofibrillary tangles (tau fibrils). It exhibits greater binding affinity to tau than to Aβ fibrilsEC50 = 221 nM vs. EC50 = 786 nM (Ki for Aβ > 5,000 nM). BF-170 demonstrates fast clearance from the brain; clearly visualizes neurofibrillary tanglesneuropil threadsand paired helical filament-type neuritis. BF-70 may become one of the candidate compounds for in vivo imaging of tau pathology associated with Alzheimerμs disease and is a useful tool in distinguishing among tau and Aβ fibrils specifically in AD.
[References]

[1] Okamura N, et al. Quinoline and benzimidazole derivatives: candidate probes for in vivo imaging of tau pathology in Alzheimer's disease. J Neurosci. 2005 Nov 23;25(47):10857-62. DOI:10.1523/JNEUROSCI.1738-05.2005
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