ChemicalBook--->CAS DataBase List--->1293395-67-1

1293395-67-1

1293395-67-1 Structure

1293395-67-1 Structure
IdentificationBack Directory
[Name]

PF-5006739
[CAS]

1293395-67-1
[Synonyms]

PF-5006739
PF 5006739;PF5006739
PF-5006739 >=98% (HPLC)
4-[5-(4-fluorophenyl)-3-[1-(1,2-oxazol-3-ylmethyl)piperidin-4-yl]imidazol-4-yl]pyrimidin-2-amine
4-[4-(4-Fluorophenyl)-1-[1-(3-isoxazolylmethyl)-4-piperidinyl]-1H-imidazol-5-yl]-2-pyrimidinamine
2-Pyrimidinamine, 4-[4-(4-fluorophenyl)-1-[1-(3-isoxazolylmethyl)-4-piperidinyl]-1H-imidazol-5-yl]-
[Molecular Formula]

C22H22FN7O
[MDL Number]

MFCD28386023
[MOL File]

1293395-67-1.mol
[Molecular Weight]

419.45
Chemical PropertiesBack Directory
[storage temp. ]

room temp
[solubility ]

Soluble in DMSO
[form ]

powder
[color ]

white to beige
Safety DataBack Directory
[RIDADR ]

UN 2811 6.1 / PGIII
Hazard InformationBack Directory
[Biochem/physiol Actions]

PF-5006739 is a potent inhibitor of casein kinases 1 delta (CK1δ) and 1 epsilon (CK1ε), key regulators of the suprachiasmatic nucleus (SCN) central clock and also linked to the development of drug addiction through PERIOD proteins (PER1–3) and dopamine- and cAMP-regulated neuronal phosphoprotein (DARPP-32) modulation. PF-5006739 has low nM in vitro potency for CK1δ/ε (IC50 values of 3.9 nM for CK1δ and 17.0 nM for CK1ε) and high kinome selectivity. PF-5006739 induced profound phase delays in circadian periodicity in both nocturnal and diurnal animal models and attenuated opioid drug-seeking behavior in a rodent operant reinstatement model.
[storage]

Store at +4°C
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