ChemicalBook--->CAS DataBase List--->1370261-98-5

1370261-98-5

1370261-98-5 Structure

1370261-98-5 Structure
IdentificationBack Directory
[Name]

PRT062607 acetate
[CAS]

1370261-98-5
[Synonyms]

P50515 Acetate
P505-15 Acetate
P505 15 Acetate
PRT062607 acetate
4-((3-(2H-1,2,3-Triazol-2-yl)phenyl)amino)-2-(((1R,2S)-2-aminocyclohexyl)amino)pyrimidine-5-carboxamide acetate
[Molecular Formula]

C21H27N9O3
[MDL Number]

MFCD23105961
[MOL File]

1370261-98-5.mol
[Molecular Weight]

453.51
Chemical PropertiesBack Directory
[form ]

Solid
[color ]

Off-white to light yellow
Hazard InformationBack Directory
[Uses]

PRT062607 (P505-15) acetate is an orally available Syk inhibitor (IC50: 1 nM) that inhibits inflammation and induction Apoptosis. PRT062607 acetate exerts potent antitumor activity in tumor xenograft mouse models[1].[2].
[in vivo]

PRT062607 acetate produced dose-dependent anti-inflammatory activity in two rodent models of rheumatoid arthritis. PRT062607 acetate (15, 30 mg/kg; po; bid; 5 d) causes SYK inhibition in mice and prevents BCR-induced splenomegaly in mice[1].
PRT062607 acetate (15 mg/kg; po ; bid; 5 d) SYK inhibition in mice prevents Ramos tumor formation in mouse xenograft models[1].
PRT062607 acetate (10-20 mg/kg; po; bid) prevents BCR mediated splenomegaly and significantly inhibited NHL tumor growth in xenograft models[2].

Animal Model:anti-IgD Stimulated Mouse Inflammation Model[1]
Dosage:10 mg/kg, 15 mg/kg, 20 mg/kg
Administration:po; bid for 5 days
Result:Suppressed mouse B-cell activation following stimulation with this anti-IgD.
Animal Model:Ramos Tumor Xenograft Model in NOD/SCID mice[1]
Dosage:15 mg/kg, 30 mg/kg
Administration:po; bid; terminated when tumor weights began reaching approximately 1.5 mg, at which time tumors were excised and weighed.
Result:Protected mouse from Ramos tumor growth in vivo.
[IC 50]

Lck: 249 nM (IC50, [2]); PAK5: 166 nM (IC50, [2])
[References]

[1] Spurgeon SE, et al. The selective SYK inhibitor P505-15 (PRT062607) inhibits B cell signaling and function in vitro and in vivo and augments the activity of fludarabine in chronic lymphocytic leukemia. J Pharmacol Exp Ther. 2013 Feb;344(2):378-87. DOI:10.1124/jpet.112.200832
[2] Coffey G, et al. Specific inhibition of spleen tyrosine kinase suppresses leukocyte immune function and inflammation in animal models of rheumatoid arthritis. J Pharmacol Exp Ther. 2012 Feb;340(2):350-9. DOI:10.1124/jpet.111.188441
Spectrum DetailBack Directory
[Spectrum Detail]

PRT062607 acetate(1370261-98-5)1HNMR
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