ChemicalBook--->CAS DataBase List--->1242156-23-5

1242156-23-5

1242156-23-5 Structure

1242156-23-5 Structure
IdentificationBack Directory
[Name]

RN486
[CAS]

1242156-23-5
[Synonyms]

RN486
RN468
RN486/RN-486
RN486 LM-2078
RN486 TFA Salt
6-Cyclopropyl-8-fluoro-2-(2-(hydroxymethyl)-3-(1-methyl-5-(5-(4-methylpiperazin-1-yl)pyridin-2
6-cyclopropyl-8-fluoro-2-(2-(hydroxyMethyl)-3-(1-Methyl-5-(5-(4-Methylpiperazin-1-yl)pyridin-2-ylaMino)-6-oxo-1,6-dihydropyridin-3-yl)phenyl)isoquinolin-1(2H)-one
6-cyclopropyl-8-fluoro-2-(2-(hydroxyMethyl)-3-(1-Methyl-5-((5-(4-Methylpiperazin-1-yl)pyridin-2-yl)aMiNA)-6-oxo-1,6-dihydropyridin-3-yl)phenyl)isoquiNAlin-1(2H)-one
6-Cyclopropyl-2-[3-[1,6-dihydro-1-methyl-5-[[5-(4-methyl-1-piperazinyl)-2-pyridinyl]amino]-6-oxo-3-pyridinyl]-2-(hydroxymethyl)phenyl]-8-fluoro-1(2H)-isoquinolinone
[EINECS(EC#)]

200-110-4
[Molecular Formula]

C35H35FN6O3
[MDL Number]

MFCD24682729
[MOL File]

1242156-23-5.mol
[Molecular Weight]

606.689
Chemical PropertiesBack Directory
[Boiling point ]

868.6±65.0 °C(Predicted)
[density ]

1.378±0.06 g/cm3(Predicted)
[storage temp. ]

Store at -20°C
[solubility ]

≥30.35 mg/mL in DMSO with gentle warming; insoluble in H2O; insoluble in EtOH
[form ]

solid
[pka]

13.95±0.10(Predicted)
[CAS DataBase Reference]

1242156-23-5
Questions And AnswerBack Directory
[Biological activity]

RN486 is an effective BTK inhibitor with an IC50 of 4 nM.
[In vitro]

RN486 not only potently and selectively inhibits the Btk enzyme, but also displays functional activities in human cell-based assays in multiple cell types, blocking Fcε receptor cross-linking-induced degranulation in mast cells (IC50 = 2.9 nM), Fcγ receptor engagement-mediated tumor necrosis factor α production in monocytes (IC50 = 7.0 nM), and B cell antigen receptor-induced expression of an activation marker, CD69, in B cells in whole blood (IC50 = 21.0 nM). RN486 is able to block the signaling of BCR as demonstrated by a marked inhibition of phosphorylation of both Btk and PLCγ2 in B cells. RN486 displays a selective B cell inhibitory profile in BioMAP Systems.
[In vivo]

RN486 displays similar functional activities in rodent models, effectively preventing type I and type III hypersensitivity responses. More importantly, RN486 produces robust anti-inflammatory and bone-protective effects in mouse CIA and rat adjuvant-induced arthritis (AIA) models. In the AIA model, RN486 inhibits both joint and systemic inflammation either alone or in combination with methotrexate, reducing both paw swelling and inflammatory markers in the blood.
Hazard InformationBack Directory
[Uses]

RN 486 is a Bruton’s tyrosine kinase (Btk) inhibitor, blocking receptor cross-linking-induced degranulation in mast cells. May be used in the prevention of arthritis and other autoimmune diseases.
[storage]

Store at -20°C
Spectrum DetailBack Directory
[Spectrum Detail]

RN486(1242156-23-5)1HNMR
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