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ChemicalBook--->CAS DataBase List--->1428569-85-0

1428569-85-0

1428569-85-0 Structure

1428569-85-0 Structure
IdentificationBack Directory
[Name]

GDC-0339
[CAS]

1428569-85-0
[Synonyms]

EOS-60554
5-amino-N-(5-((4R,5R)-4-amino-5-fluoroazepan-1-yl)-1-methyl-1H-pyrazol-4-yl)-2-(2,6-difluorophenyl)thiazole-4-carboxamide
4-Thiazolecarboxamide, 5-amino-N-[5-[(4R,5R)-4-amino-5-fluorohexahydro-1H-azepin-1-yl]-1-methyl-1H-pyrazol-4-yl]-2-(2,6-difluorophenyl)-
[Molecular Formula]

C20H22F3N7OS
[MOL File]

1428569-85-0.mol
[Molecular Weight]

465.5
Chemical PropertiesBack Directory
[density ]

1.61±0.1 g/cm3(Predicted)
[storage temp. ]

Store at -20°C
[solubility ]

DMSO : ≥ 52 mg/mL (111.71 mM)
[form ]

Solid
[pka]

9.28±0.40(Predicted)
[color ]

White to yellow
Hazard InformationBack Directory
[Uses]

GDC-0339 is a potent, orally bioavailable and well tolerated pan-Pim kinase inhibitor, with Kis of 0.03 nM, 0.1 nM and 0.02 nM for Pim1, Pim2 and Pim3, respectively. GDC-0339 is discovered as a potential treatment of multiple myeloma[1][2].
[in vivo]

GDC-0339 (1-300 mg/kg; p.o; daily; for 21 days) is efficacious in RPMI8226 and MM.1S human multiple myeloma xenograft mouse models[2].
GDC-0339 has a half-life of t1/2=0.9 h[2].

Animal Model:Female C.B-17 SCID mice, RPMI8226 human multiple myeloma xenograft mouse model[2]
Dosage:1mg/kg, 10 mg/kg, 50 mg/kg, 100 mg/kg, 200 mg/kg, 300 mg/kg
Administration:Oral administration; once daily; for 21 days
Result:Showed dose-dependent tumor growth inhibition.
[IC 50]

PIM1; PIM2; PIM3
[storage]

Store at -20°C
[References]

[1] Takahashi RH, et al. CYP1A1-Mediated Intramolecular Rearrangement of Aminoazepane in GDC-0339. Drug Metab Dispos. 2017 Oct;45(10):1084-1092. DOI:10.1124/dmd.117.076786
[2] Wang X, et al. Optimization of Pan-Pim Kinase Activity and Oral Bioavailability Leading to Diaminopyrazole (GDC-0339) for the Treatment of Multiple Myeloma. J Med Chem. 2019 Feb 28;62(4):2140-2153. DOI:10.1021/acs.jmedchem.8b01857
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