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Home Cardiovascular Heart Autophagy PF 04449913 maleate - ≥98%(HPLC), high purity , Smoothened homolog antagonist, CAS No.2030410-25-2, Smoothened homolog antagonist
PF 04449913 maleate - ≥98%(HPLC), high purity , Smoothened homolog antagonist, CAS No.2030410-25-2, Smoothened homolog antagonist
Basic Description Synonyms GLASDEGIB MALEATE [JAN] | 2030410-25-2 (maleate) | Glasdegib maleate | 1-((2R,4R)-2-(1H-Benzimidazol-2-yl)-1-methylpiperidin-4-yl)-3-(4-cyanophenyl)urea maleate salt | 2030410-25-2 | D11107 | DTXSID301027747 | 1-((2R,4R)-2-(1H-Benzimidazol-2-yl)-1-methylp Specifications & Purity ≥98%(HPLC) Biochemical and Physiological Mechanisms Potent Smo antagonist (IC50= 5 nM). Attenuates the leukemia-initiation potential of AML cells in a serial transplantation mouse model. Also eliminates self-propagation capacity of AML cells. Storage Temp Store at 2-8°C Shipped In Wet ice Action Type ANTAGONIST Mechanism of action Smoothened homolog antagonist
Names and Identifiers IUPAC Name 1-[(2R,4R)-2-(1H-benzimidazol-2-yl)-1-methylpiperidin-4-yl]-3-(4-cyanophenyl)urea;(Z)-but-2-enedioic acid INCHI InChI=1S/C21H22N6O.C4H4O4/c1-27-11-10-16(24-21(28)23-15-8-6-14(13-22)7-9-15)12-19(27)20-25-17-4-2-3-5-18(17)26-20;5-3(6)1-2-4(7)8/h2-9,16,19H,10-12H2,1H3,(H,25,26)(H2,23,24,28);1-2H,(H,5,6)(H,7,8)/b;2-1-/t16-,19-;/m1./s1 InChi Key VJCVKWFBWAVYOC-UIXXXISESA-N Canonical SMILES CN1CCC(CC1C2=NC3=CC=CC=C3N2)NC(=O)NC4=CC=C(C=C4)C#N.C(=CC(=O)O)C(=O)O Isomeric SMILES CN1CC[C@H](C[C@@H]1C2=NC3=CC=CC=C3N2)NC(=O)NC4=CC=C(C=C4)C#N.C(=C\C(=O)O)\C(=O)O PubChem CID 122640033 Molecular Weight 490.51
Chemical and Physical Properties Solubility Solvent:DMSO, Max Conc. mg/mL: 49.05, Max Conc. mM: 100
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