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ChemicalBook--->CAS DataBase List--->1457983-28-6

1457983-28-6

1457983-28-6 Structure

1457983-28-6 Structure
IdentificationBack Directory
[Name]

G-749
[CAS]

1457983-28-6
[Synonyms]

G-49
G-749
G-749, >=98%
G-749 (Free base)
8-Bromo-2-[(1-methyl-4-piperidinyl)amino]-4-[(4-phenoxyphenyl)amino]pyrido[4,3-d]pyrimidin-5(6H)-one
8-Bromo-2-[(1-methyl-4-piperidinyl)amino]-4-[(4-phenoxyphenyl)amino]pyrido[4,3-d]pyrimidin-5(6H)-one G749
[Molecular Formula]

C25H25BrN6O2
[MDL Number]

MFCD28167815
[MOL File]

1457983-28-6.mol
[Molecular Weight]

521.409
Chemical PropertiesBack Directory
[density ]

1.487±0.06 g/cm3(Predicted)
[storage temp. ]

Store at -20°C
[solubility ]

≥26.05 mg/mL in DMSO; insoluble in EtOH; insoluble in H2O
[form ]

solid
[pka]

8.32±0.40(Predicted)
[color ]

White to off-white
Safety DataBack Directory
[Symbol(GHS) ]


GHS07
[Signal word ]

Warning
[Hazard statements ]

H302-H315-H319-H335
[Precautionary statements ]

P261-P305+P351+P338
Questions And AnswerBack Directory
[Description]

G-749 is a novel and potent FLT3 inhibitor with IC50 of 0.4 nM, 0.6 nM and 1 nM for FLT3 (WT), FLT3 (D835Y), and Mer, respectively, showing lower potency against other tyrosine kinases.
[In vitro]

In FLT3-WT-bearing RS4-11 cells and FLT3-ITD-harboring MV4-11 and Molm-14 cells, G-749 potently inhibits autophosphorylation of FLT3 with IC50 of ≤8 nM. In leukemia cells, G-749 shows antiproliferative activity by inducing apoptosis. In BaF3 cell lines that stably express FLT3-ITD/N676D, FLT3-ITD/F691L, FLT3-D835Y, or FLT3-D835Y/N676D, G-749 shows strong inhibitory activity with IC50 of <10 nM, and thus overcomes drug resistance. In blasts of AML patients, G-749 also exhibits potent antileukemia activity.
[In vivo]

In MV4-11 xenograft mice, G-749 (30 mg/kg p.o.) effectively inhibits the FLT3 pathway and significant inhibits tumor growth. In an orthogonal model of bone marrow engraftment using Molm-14 cells, G-749 (20 mg/kg p.o.) also inhibits tumor growth and increases survival.
Hazard InformationBack Directory
[Uses]

G-749 is a potent FLT3 inhibitor. It shows lower potency against other tyrosine kinases.
[References]

1. lee h k, kim h w, lee i y, et al. g-749, a novel flt3 kinase inhibitor, can overcome drug resistance for the treatment of acute myeloid leukemia. blood, 2014, 123(14): 2209-2219.
Spectrum DetailBack Directory
[Spectrum Detail]

G-749(1457983-28-6)1HNMR
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