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ChemicalBook--->CAS DataBase List--->300815-41-2

300815-41-2

300815-41-2 Structure

300815-41-2 Structure
IdentificationBack Directory
[Name]

RS 102895
[CAS]

300815-41-2
[Synonyms]

RS 102895 HYDROCHLORIDE
1'-(4-(trifluoromethyl)phenethyl)spiro[benzo[d][1,3]oxazine-4,4'-piperidin]-2(1H)-one
1'-[2-[4-(trifluoromethyl)phenyl]ethyl]-spiro[4h-3,1-benzoxazine-4,4'-peperidin]-2(1h)-one
Spiro[4H-3,1-benzoxazine-4,4'-piperidin]-2(1H)-one, 1'-[2-[4-(trifluoromethyl)phenyl]ethyl]-
1'-(4-(TrifluoroMethyl)phenethyl)spiro[benzo[d][1,3]oxazine-4,4'-piperidin]-2(1H)-one hydrochloride
1'-[2-[4-(trifluoromethyl)phenyl]ethyl]spiro[1H-3,1-benzoxazine-4,4'-piperidine]-2-one,hydrochloride
1'-[2-[4-(TRIFLUOROMETHYL)PHENYL]ETHYL]-SPIRO[4H-3,1-BENZOXAZINE-4,4'-PIPERIDIN]-2(1H)-ONE HYDROCHLORIDE
[Molecular Formula]

C21H21F3N2O2
[MDL Number]

MFCD08703093
[MOL File]

300815-41-2.mol
[Molecular Weight]

390.4
Chemical PropertiesBack Directory
[Boiling point ]

446.1±45.0 °C(Predicted)
[density ]

1.33±0.1 g/cm3 (20 ºC 760 Torr)
[storage temp. ]

Desiccate at RT
[solubility ]

DMSO: 18 mg/mL, clear, colorless
[form ]

powder
[pka]

13.46±0.20(Predicted)
[color ]

white
Safety DataBack Directory
[Safety Statements ]

22-24/25
[WGK Germany ]

3
Hazard InformationBack Directory
[Uses]

RS 102895 is a CCR2-selective chemokine receptor inhibitor.
[Biological Activity]

CCR2-selective chemokine receptor antagonist (IC 50 values are 0.36 and 17.8 μ M for inhibition of human recombinant CCR2b and CCR1 receptors respectively). Blocks MCP-1-stimulated calcium influx and chemotaxis with IC 50 values of 32 nM and 1.7 μ M respectively. Also inhibits α 1A , α 1D and 5-HT 1A receptors.
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