ChemicalBook--->CAS DataBase List--->2248666-66-0

2248666-66-0

2248666-66-0 Structure

2248666-66-0 Structure
IdentificationBack Directory
[Name]

PF429242 dihydrochloride
[CAS]

2248666-66-0
[Synonyms]

PF 429242-HCl
PF429242,PF-429242 dihydrochloride,PF429242 dihydrochloride,Virus Protease,inhibit,PF 429242,Inhibitor,Fatty Acid Synthase (FASN),PF-429242
[Molecular Formula]

C??H??Cl?N?O?
[MOL File]

2248666-66-0.mol
[Molecular Weight]

446.03
Chemical PropertiesBack Directory
[storage temp. ]

Store at -20°C
[solubility ]

DMF: 30 mg/ml; DMSO: 30 mg/ml; Ethanol: 30 mg/ml; PBS (pH 7.2): 10 mg/ml
[form ]

A crystalline solid
[color ]

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


GHS07,GHS08,GHS09
[Signal word ]

Danger
[Hazard statements ]

H303-H315-H319-H335-H410-H372
[Precautionary statements ]

P261-P264-P271-P273-P280-P302+P352-P304+P340+P312-P305+P351+P338-P312-P332+P313-P337+P313-P391-P403+P233-P405-P501
Hazard InformationBack Directory
[Description]

PF-429242 is an inhibitor of site-1 protease with an IC50 value of 170 nM for human recombinant site-1 protease. It is selective for site-1 protease over trypsin, elastase, proteinase K, plasmin, kallikren, factor XIa, thrombin, and furin at concentrations up to 100 μM. PF-429242 completely inhibits proteolytic processing and nuclear translocation of sterol regulatory element-binding protein (SREBP) in HepG2 cells at a concentration of 10 μM. It also reduces expression of HMG-CoA synthase and fatty acid synthase (EC50s = 0.3 and 2 μM, respectively) and inhibits cholesterol synthesis (EC50 = 600 nM) in HepG2 cells and reduces cholesterol and fatty acid synthesis in CD-1 mice. PF-429242 inhibits replication of dengue virus serotypes 1-4 in infected HeLa cells. It also reduces growth of T98G, U87-MG, and A172 glioblastoma cells (IC50s = 0.32, 15.2, and 27.6 μM, respectively).
[storage]

Store at -20°C
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