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ChemicalBook--->CAS DataBase List--->2307249-33-6

2307249-33-6

2307249-33-6 Structure

2307249-33-6 Structure
IdentificationBack Directory
[Name]

BAY-885
[CAS]

2307249-33-6
[Synonyms]

BAY-885
BAY-885 USP/EP/BP
[2-amino-4-(trifluoromethoxy)phenyl]-{4-[7-(4-methylpiperazin-1-yl)pyrido[3,2-d]pyrimidin-4-yl]piperidin-1-yl}methanone
Methanone, [2-amino-4-(trifluoromethoxy)phenyl][4-[7-(4-methyl-1-piperazinyl)pyrido[3,2-d]pyrimidin-4-yl]-1-piperidinyl]-
[Molecular Formula]

C25H28F3N7O2
[MDL Number]

MFCD32067879
[MOL File]

2307249-33-6.mol
[Molecular Weight]

515.53
Questions And AnswerBack Directory
[Use]

BAY-885 is a highly potent and selective ERK5 inhibitor.
[In vitro]

BAY-885 shows potent ERK5 kinase and transcriptional inhibition in the SN12C-MEF2 reporter cell line (IC50 = 115 nM/IC90 = 691 nM) and has no effects on a reporter control cell line with constitutive luciferase expression (SN12C-CMV-luc, IC50 > 30 μM), thereby ruling out potential effects as a general inhibitor of transcription or translation.
Chemical PropertiesBack Directory
[Boiling point ]

685.0±55.0 °C(Predicted)
[density ]

1.362±0.06 g/cm3(Predicted)
[storage temp. ]

Keep in dark place,Inert atmosphere,Room temperature
[solubility ]

DMSO:23.33(Max Conc. mg/mL);45.25(Max Conc. mM)
Ethanol:8.0(Max Conc. mg/mL);15.52(Max Conc. mM)
[form ]

A solid
[pka]

7.06±0.42(Predicted)
[color ]

White to light yellow
Safety DataBack Directory
[Symbol(GHS) ]


GHS07
[Signal word ]

Warning
[Hazard statements ]

H302-H315-H319-H335
[Precautionary statements ]

P261-P280-P301+P312-P302+P352-P305+P351+P338
Spectrum DetailBack Directory
[Spectrum Detail]

BAY-885(2307249-33-6)1HNMR
Hazard InformationBack Directory
[Biological Activity]

BAY-885 is an ATP site-targetingpotent and selective ERK5 (BMK1MAPK7) inhibitor (IC50 = 35 nM with 250 μM ATP; % inhibition at 1 μM = 62/r at Fer58/human EphB343/human EphA5=20/355 kinases) with no BRD4 affinity (20 μM)nor inhibitory potency toward hERG (10 μM) and CYP enzymes (20 μM; CYP1A2CYP2C8CYP2C9CYP2D6CYP3A4). BAY-885 potently inhibits 100 ng/mL EGF-inducedERK5-dependent MEF2 activity (IC50 = 120 nM; SN12C-MEF2-luc reporter assay).
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