ChemicalBook--->CAS DataBase List--->1820565-69-2

1820565-69-2

1820565-69-2 Structure

1820565-69-2 Structure
IdentificationBack Directory
[Name]

N-(4-((1R,3S,5S)-3-amino-5-methylcyclohexyl)pyridin-3-yl)-6-(2,6-difluorophenyl)-5-fluoropicolinamide
[CAS]

1820565-69-2
[Synonyms]

EOS-62253
PIM-447 2HCl
LGH-447 dihydrochloride
PIM-447 (dihydrochloride)
[Molecular Formula]

C24H23F3N4O
[MDL Number]

MFCD30489747
[MOL File]

1820565-69-2.mol
[Molecular Weight]

440.461
Chemical PropertiesBack Directory
[storage temp. ]

Store at -20°C
[solubility ]

Water:50.0(Max Conc. mg/mL);97.39(Max Conc. mM)
[form ]

Solid
[color ]

White to off-white
Hazard InformationBack Directory
[Uses]

PIM447 dihydrochloride (LGH447 dihydrochloride) is a potent, orally available, and selective pan-PIM kinase inhibitor, with Ki values of 6, 18, and 9 pM for PIM1, PIM2, and PIM3, respectively. PIM447 dihydrochloride displays dual antimyeloma and bone-protective effects. PIM447 dihydrochloride induces apoptosis[1][2].
[in vivo]

PIM447 (oral gavage; 100 mg/kg; 5 times/week) clearly controlls tumor progression and the serum levels of hIgλ secreted by RPMI-8226-luc cells in mouse model of bone marrow-disseminated human multiple myeloma[1].

Animal Model:RPMI-8226-luc cells are injected intravenously into 6-week-old female NODSCID-IL-2Rγ-/-(NSG) mice[1]
Dosage:100 mg/kg
Administration:oral gavage; 100 mg/kg; 5 times/week
Result:Was well tolerated, as the body weight of mice did not decrease by more than 10%. Increased bone volume density and trabecular number and reduced trabecular separation relative to vehicle group.
[IC 50]

PIM1; PIM2; PIM3
[References]

[1] Paíno T et al. The novel pan-PIM kinase inhibitor, PIM447, displays dual anti-myeloma and bone protective effects, and potently synergizes with current standards of care. Clin Cancer Res. 2016 Jul 20. DOI:10.1158/1078-0432.CCR-16-0230
[2] Burger MT et al. Identification of N-(4-((1R,3S,5S)-3-Amino-5-methylcyclohexyl)pyridin-3-yl)-6-(2,6-difluorophenyl)-5-fluoropicolinamide (PIM447), a Potent and Selective Proviral Insertion Site of Moloney Murine Leukemia (PIM) 1, 2, and 3 Kinase Inhibitor in Clinical Trials for Hematological Malignancies. J Med Chem. 2015 Nov 12;58(21):8373-86. DOI:10.1021/acs.jmedchem.5b01275
[3] Peters TL et al. Control of translational activation by PIM kinase in activated B-cell diffuse large B-cell lymphoma confers sensitivity to inhibition by PIM447. Oncotarget. 2016 Aug 20 DOI:10.18632/oncotarget.11457
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