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Glasdegib(PF-04449913)
本产品不向个人销售,仅用作科学研究,不用于任何人体实验及非科研性质的动物实验。
Glasdegib(PF-04449913)图片
CAS NO:1095173-27-5
规格:≥98%
包装与价格:
包装价格(元)
2mg电议
5mg电议
10mg电议
25mg电议
50mg电议
100mg电议
500mg电议

产品介绍
理化性质和储存条件
Molecular Weight (MW)374.44
FormulaC21H22N6O
CAS No.1095173-27-5 (free base)
Storage-20℃ for 3 years in powder form
-80℃ for 2 years in solvent
Solubility (In vitro)DMSO: 47 mg/mL (125.5 mM)
Water:<1 mg/mL
Ethanol:<1 mg/mL
SMILES CodeO=C(NC1=CC=C(C#N)C=C1)N[C@H]2C[C@H](C3=NC4=CC=CC=C4N3)N(C)CC2
SynonymsPF 04449913; PF-4449913; PF-04449913; PF4449913; PF04449913; PF 4449913; daurismo
实验参考方法
In Vitro

In vitro activity: In vitro microsomal assays, PF-04449913 have high clearance in rat and low clearance in dog and human, without inhibiting any of the major cytochrome P450 isoforms.


Kinase Assay: Glasdegib (formerly known as PF-04449913) is a novel potent, and orally bioavailable small-molecule inhibitor of Smoothened (Smo) in the Hedgehog (Hh) signaling pathway with IC50 of 5 nM. The Hh signaling pathway plays an important role in cellular growth, differentiation and repair. Constitutive activation of Hh pathway signaling has been observed in various types of cancers. Glasdegib significantly reduces medulloblastoma growth in a Ptch1+/-p53+/- allograft model at doses that decreased murine Shh target gene expression. In stromal co-culture experiments, FACS analysis demonstrates a significant reduction in BC LSC by PF-04449913 when compared with normal progenitors.


Cell Assay: In the Hedgehog (Hh) signaling pathway, the combination of Hh ligands and their receptor Patched leads to the activation of smoothened and subsequently activation of three transcription factors Gli1, Gli2 and Gli3. It then leads to the proliferation of cells. As an antagonist of smoothened, PF-04449913 is developed for treatment of cancer.

In VivoIn rat and dog, PF-04449913 shows high clearance, and good oral bioavailability
Animal modelRat, dog
Formulation & DosageDissolved in 10% EtOH/20% PEG400/70% PBS (i.v.); 0.5% methylcellulose in water (p.o.); 1 mg/kg (Rat); 0.5 mg/kg (dog i.v.); 3 mg/kg (dog p.o.); i.v. or p.o. administration
ReferencesACS Med Chem Lett. 2011 Dec 21;3(2):106-11.