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Glasdegib (PF-04449913)
Cat. No.:
OB0225WX-2670
Appearance:
Solid
Purity:
≥99%
Identity:
Confirmed by NMR, and HPLC.
Size:
Add to basket
Product Overview
Description:
Glasdegib is an orally bioavailable small molecule that acts as a potent inhibitor of the Smoothened (Smo) receptor with an IC50 of 5 nM.
Synonym:
Glasdegib; 1095173-27-5; PF-04449913; PF 04449913; 1-((2R,4R)-2-(1H-benzo[d]iMidazol-2-yl)-1-Methylpiperidin-4-yl)-3-(4-cyanophenyl)urea; glasdegibum; 1-[(2R,4R)-2-(1H-benzimidazol-2-yl)-1-methylpiperidin-4-yl]-3-(4-cyanophenyl)urea; Glasdegib (PF-04449913); PF-4449913; PF-913; 1-((2R,4R)-2-(1H-benzimidazol-2-yl)-1-methylpiperidin-4-yl)-3-(4-cyanophenyl)urea; N-[(2R,4R)-2-(1H-benzimidazol-2-yl)-1-methylpiperidin-4-yl]-N'-(4-cyanophenyl)urea; Urea, N-[(2R,4R)-2-(1H-benzimidazol-2-yl)-1-methyl-4-piperidinyl]-N'-(4-cyanophenyl)-; N-[(2R,4R)-2-(1H-Benzimidazol-2-yl)-1-methyl-4-piperidinyl]-N'-(4-cyanophenyl)-urea, ; PF 04449913; MFCD25976839
CAS No.:
1095173-27-5
Compound CID:
25166913
Formula:
C21H22N6
Formula Weight:
374.44
Specification
Stability:
3 years in powder form.
Storage:
Storage at -20°C.
Applications:
Glasdegib is used in stem cell and oncology research as an orally active Smoothened (Smo) inhibitor to investigate the regulation of the Hedgehog signaling pathway in myeloid malignancies.
Library Information
Target:
Hedgehog/Smoothened
Receptor:
Smo
Pathways:
Stem cells & Wnt
Plate Number:
L6700-08
Empty Location:
a1-h1; a12-h12
Container:
96-well plate
Formulation:
10mM DMSO
DMSO Max Solubility:
47 mg/mL; 125.52 mM
ALogP:
2.363
HBA_Count:
2
HBD_Count:
3
Rotatable Bond:
3





