ChemicalBook--->CAS DataBase List--->300670-16-0

300670-16-0

300670-16-0 Structure

300670-16-0 Structure
IdentificationBack Directory
[Name]

N-(4-BROMOPHENYL)-3-{[(4-BROMOPHENYL)AMI
[CAS]

300670-16-0
[Synonyms]

C2-8 (polyQ aggregation inhibitor C2-8)
N-(4-BROMOPHENYL)-3-{[(4-BROMOPHENYL)AMI
Polyglutamine Aggregation Inhibitor III, C2-8
Benzamide, N-(4-bromophenyl)-3-(((4-bromophenyl)amino)sulfonyl)
N-(4-Bromophenyl)-3-[[(4-bromophenyl)amino]sulfonyl]benzamide >=98% (HPLC), solid
[Molecular Formula]

C19H14Br2N2O3S
[MDL Number]

MFCD00355835
[MOL File]

300670-16-0.mol
[Molecular Weight]

510.2
Chemical PropertiesBack Directory
[density ]

1.760±0.06 g/cm3(Predicted)
[storage temp. ]

2-8°C
[solubility ]

DMSO: ~20 mg/mL
[form ]

solid
[pka]

7.49±0.10(Predicted)
[color ]

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


GHS07
[Signal word ]

Warning
[Hazard statements ]

H319-H413
[Precautionary statements ]

P273-P305+P351+P338
[Hazard Codes ]

Xi
[Risk Statements ]

36
[Safety Statements ]

26
[WGK Germany ]

3
Hazard InformationBack Directory
[Description]

C2-8 is an inhibitor of polyglutamine (polyQ) aggregation (IC50s = 25 and 0.05 μM for recombinant HDQ51 and in PC12 cells, respectively). It also inhibits polyQ aggregation in organotypic hippocampal slice cultures isolated from R6/2 transgenic mice and reduces neurodegeneration in a dose-dependent manner in a Drosophila model of Huntington''s disease. C2-8 (100 and 200 mg/kg) reduces huntingtin aggregate size, reduces neuronal atrophy, and improves motor performance in a rotarod test in the R6/2 transgenic mouse model of Huntington''s disease.
[Uses]

C2-8 is an inhibitor of polyglutamine (polyQ) aggregation (IC50s=25 and 0.05 μM for recombinant HDQ51 and in PC12 cells, respectively). It also inhibits polyQ aggregation in organotypic hippocampal slice cultures isolated from R6/2 transgenic mice and reduces neurodegeneration in a dose-dependent manner in a Drosophila model of Huntington's disease. C2-8 (100 and 200 mg/kg) reduces huntingtin aggregate size, reduces neuronal atrophy, and improves motor performance in a rotarod test in the R6/2 transgenic mouse model of Huntington's disease.
[storage]

Store at -20°C
[References]

[1] Zhang, et al. A potent small molecule inhibits polyglutamine aggregation in Huntington’s disease neurons and suppresses neurodegeneration in vivo. Proc. Natl. Acad. Sci. USA 102(3), 892-897 (2005).
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