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ChemicalBook--->CAS DataBase List--->1575596-29-0

1575596-29-0

1575596-29-0 Structure

1575596-29-0 Structure
IdentificationBack Directory
[Name]

PRN1008
[CAS]

1575596-29-0
[Synonyms]

PRN-1008-E
Rilzabrutinib
Rilzabrutinib (PRN-1008)
1-Piperidinepropanenitrile, 3-[4-amino-3-(2-fluoro-4-phenoxyphenyl)-1H-pyrazolo[3,4-d]pyrimidin-1-yl]-α-[2-methyl-2-[4-(3-oxetanyl)-1-piperazinyl]propylidene]-β-oxo-, (αE,3R)-
[Molecular Formula]

C36H40FN9O3
[MDL Number]

MFCD31631583
[MOL File]

1575596-29-0.mol
[Molecular Weight]

665.77
Chemical PropertiesBack Directory
[Boiling point ]

882.5±65.0 °C(Predicted)
[density ]

1.39±0.1 g/cm3(Predicted)
[storage temp. ]

Store at -20°C
[solubility ]

DMSO:120.0(Max Conc. mg/mL);180.24(Max Conc. mM)
[form ]

Solid
[pka]

6.24±0.70(Predicted)
[color ]

White to off-white
Safety DataBack Directory
[Symbol(GHS) ]


GHS08
[Signal word ]

Danger
[Hazard statements ]

H372
[Precautionary statements ]

P260-P264-P270-P314-P501
Hazard InformationBack Directory
[Uses]

Rilzabrutinib (PRN1008) is a reversible covalent, selective and oral active inhibitor of Bruton’s Tyrosine Kinase (BTK), with an IC50 of 1.3 nM.
[in vivo]

In vivo Rilzabrutinib demonstrates enduring pharmacodynamic effects after the compound has cleared from circulation, consistent with extended target residence time. Rilzabrutinib also reverses and completely suppresses collagen-induced arthritis in rats in a dose dependent manner which allows correlation of target occupancy and disease modification[2].

[IC 50]

BTK: 1.3 nM (IC50); BMX: 1.0 nM (IC50); ITK: 440 nM (IC50); TEC: 0.8 nM (IC50); RLK: 1.2 nM (IC50); BLK: 6.3 nM (IC50); EGFR: 520 nM (IC50); ERBB2: 3900 nM (IC50); ERBB4: 11.3 nM (IC50)
[References]

[1] Smith PF, et al. A phase I trial of PRN1008, a novel reversible covalent inhibitor of Bruton's tyrosine kinase, in healthy volunteers. Br J Clin Pharmacol. 2017 Nov;83(11):2367-2376. DOI:10.1111/bcp.13351
[2] Hill RJ, Bradshaw JM, Bisconte A, Tam D, Owens TD, Brameld KA, Smith PF, Funk JO, Goldstein DM, Nunn PA. Preclinical Characterization of PRN1008, a Novel Reversible Covalent Inhibitor of BTK that Shows Efficacy in a RAT Model of Collagen-Induced Arthritis. Annals of the Rheumatic Diseases 2015; 74(Suppl 2): 216.
Spectrum DetailBack Directory
[Spectrum Detail]

PRN1008(1575596-29-0)1HNMR
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