ChemicalBook--->CAS DataBase List--->887401-93-6

887401-93-6

887401-93-6 Structure

887401-93-6 Structure
IdentificationBack Directory
[Name]

INCB 3284 diMesylate
[CAS]

887401-93-6
[Synonyms]

CS-352
INCB3284
Dimesylate
INCB3284 mesylate
INCB 3284 biMesylate
INCB 3284 diMesylate
INCB 3284 dimesylate, >=98%
N-[2-[[(3R)-1-[4-hydroxy-4-(6-methoxypyridin-3-yl)cyclohexyl]pyrrolidin-3-yl]amino]-2-oxoethyl]-3-(trifluoromethyl)benzamide
N-[2-[[(3R)-1-[4-hydroxy-4-(6-methoxypyridin-3-yl)cyclohexyl]pyrrolidin-3-yl]amino]-2-oxoethyl]-3-(trifluoromethyl)benzamide,methanesulfonic acid
N-[2-[[(3R)-1-[trans-4-Hydroxy-4-(6-methoxy-3-pyridinyl)cyclohexyl]-3-pyrrolidinyl]amino]-2-oxoethyl]-3-(trifluoromethyl)-benzamide dimethanesulfonate
N-[2-({(3R)-1-[trans-4-Hydroxy-4-(6-Methoxy-3-pyridinyl)cyclohexyl]-3-pyrrolidinyl}aMino)-2-oxoethyl]-3-(trifluoroMethyl)benzaMide Methanesulfonate (1:2)
[Molecular Formula]

C26H31F3N4O4
[MDL Number]

MFCD20926352
[MOL File]

887401-93-6.mol
[Molecular Weight]

520.544
Chemical PropertiesBack Directory
[storage temp. ]

Store at -20°C
[solubility ]

DMF:11.0(Max Conc. mg/mL);15.43(Max Conc. mM)
DMSO:57.19(Max Conc. mg/mL);80.24(Max Conc. mM)
PBS (pH 7.2):5.0(Max Conc. mg/mL);7.02(Max Conc. mM)
Water:71.28(Max Conc. mg/mL);100.0(Max Conc. mM)
[form ]

Powder
[color ]

Colorless to light yellow
[InChIKey]

PNPNUHKICDECDH-SEBNIYPMSA-N
Safety DataBack Directory
[Symbol(GHS) ]

Exclamation Mark (GHS07)
GHS07
[Signal word ]

Warning
[Hazard statements ]

H302-H315-H319-H335
[Precautionary statements ]

P261-P305+P351+P338
[WGK Germany ]

WGK 3
[Storage Class]

11 - Combustible Solids
Hazard InformationBack Directory
[Uses]

Dimesylate is a potent, selective, and orally bioavailable hCCR2 antagonist.
[Biological Activity]

Primary Target
human CCR2 (hCCR2)''Target IC50: 3.7 nM4.7 nMand 84 nM for different assays.
[in vivo]

INCB 3284 (1 mg/kg/day, ip) reduces liver damage, and decreases microglia activation in AOM-treated mice via inhibition on CCR2. INCB 3284 also significantly reduces the pERK1/2 to tERK1/2 ratio, as well as G-protein signaling pathway activity and proinflammatory cytokine production in cortex lysates from mice administed with azoxymethane[2].

[IC 50]

MCP-1-hCCR2: 3.7 nM (IC50)
[storage]

Store at -20°C
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