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1421502-62-6

1421502-62-6 Structure

1421502-62-6 Structure
IdentificationBack Directory
[Name]

(2-(6-(2-ETHYL-5-FLUORO-4-HYDROXYPHENYL)-1H-INDAZOL-3-YL)-3,4,6,7-TETRAHYDRO-5H-IMIDAZO[4,5-C]PYRIDIN-5-YL)(5-(PIPERIDIN-1-YL)PYRAZIN-2-YL)METHANONE
[CAS]

1421502-62-6
[Synonyms]

PF 6263276
PF06263276,PF 06263276
PF-06263276 (PF 6263276)
PF-06263276 >=98% (HPLC)
(2-(6-(2-ETHYL-5-FLUORO-4-HYDROXYPHENYL)-1H-INDAZOL-3-YL)-3,4,6,7-TETRAHYDRO-5H-IMIDAZO[4,5-C]PYRIDIN-5-YL)(5-(PIPERIDIN-1-YL)PYRAZIN-2-YL)METHANONE
Methanone, [2-[6-(2-ethyl-5-fluoro-4-hydroxyphenyl)-1H-indazol-3-yl]-3,4,6,7-tetrahydro-5H-imidazo[4,5-c]pyridin-5-yl][5-(1-piperidinyl)-2-pyrazinyl]-
[Molecular Formula]

C31H31FN8O2
[MDL Number]

MFCD30718580
[MOL File]

1421502-62-6.mol
[Molecular Weight]

566.63
Chemical PropertiesBack Directory
[Boiling point ]

921.1±65.0 °C(Predicted)
[density ]

1.394±0.06 g/cm3(Predicted)
[storage temp. ]

room temp
[solubility ]

Soluble in DMSO
[form ]

powder
[pka]

8.54±0.25(Predicted)
[color ]

white to beige
Hazard InformationBack Directory
[Uses]

PF-06263276 (PF 6263276) is a potent and selective pan-JAK inhibitor, with IC50s of 2.2 nM, 23.1 nM, 59.9 nM and 29.7 nM for JAK1, JAK2, JAK3 and TYK2, respectively. PF-06263276 inhibits pSTAT3 and TYK2 pathway. PF-06263276 has a protective effect against ear skin inflammation[1].
[Biological Activity]

PF-06263276 is an inhibitor of the Janus kinase (JAK) enzymes 123 and tyrosine kinase 2 (TYK2). PF-06263276 has been investigated for the treatment of psoriasis.
[in vivo]

PF-06263276 (0.3-100 μg/animal; i.t.) can dose-dependently inhibit the increase of lung pSTAT3 in the pharmacodynamic model of IL-6-induced lung pSTAT3 response in mice, with an ED50 of approximately 3 μg/animal[1].
PF-06263276 (4% solution; topical administration; multiple times; 11 days) can significantly reduce ear swelling by 48% in the IL-23-induced mouse ear skin inflammation model and inhibit the JAK2/TYK2 pathway[1].

[IC 50]

JAK1: 2.2 nM (IC50); JAK2: 23.1 nM (IC50); JAK3: 59.9 nM (IC50); Tyk2: 29.7 nM (IC50)
[storage]

Store at -20°C
[References]

[1] Jones P, et al. Design and Synthesis of a Pan-Janus Kinase Inhibitor Clinical Candidate (PF-06263276) Suitable for Inhaled and Topical Delivery for the Treatment of Inflammatory Diseases of the Lungs and Skin. J Med Chem. 2017 Jan 26;60(2):767-786. DOI:10.1021/acs.jmedchem.6b01634
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