ChemicalBook--->CAS DataBase List--->877874-85-6

877874-85-6

877874-85-6 Structure

877874-85-6 Structure
IdentificationBack Directory
[Name]

KG5
[CAS]

877874-85-6
[Synonyms]

KG5
2-methylsulfanyl-6-[4-[3-[3-(trifluoromethyl)anilino]-1H-1,2,4-triazol-5-yl]phenoxy]pyrimidin-4-amine
2-(Methylthio)-6-[4-[5-[[3-(trifluoromethyl)phenyl]amino]-1H-1,2,4-triazol-3-yl]phenoxy]-4-pyrimidinamine
4-Pyrimidinamine, 2-(methylthio)-6-[4-[5-[[3-(trifluoromethyl)phenyl]amino]-1H-1,2,4-triazol-3-yl]phenoxy]-
B-Raf,antiangiogenic,KIT,c-Kit,KG5,CD135,Raf kinases,Raf,PDGFR,Cluster of differentiation antigen 135,Platelet-derived growth factor receptor,Fms like tyrosine kinase 3,metastasis,c-Raf,FLT3,PDGFRβ,inhibit,anticancer,phosphorylation,SCFR,Inhibitor,KG 5,CD117,KG-5
[Molecular Formula]

C20H16F3N7OS
[MDL Number]

MFCD22124522
[MOL File]

877874-85-6.mol
[Molecular Weight]

459.45
Chemical PropertiesBack Directory
[Boiling point ]

654.0±65.0 °C(Predicted)
[density ]

1.54±0.1 g/cm3(Predicted)
[storage temp. ]

Store at -20°C
[solubility ]

Soluble in DMSO
[form ]

Solid
[pka]

9.54±0.40(Predicted)
[color ]

White to off-white
[SMILES]

NC1=CC(OC2=CC=C(C3=NN=C(NC4=CC(C(F)(F)F)=CC=C4)N3)C=C2)=NC(SC)=N1
Safety DataBack Directory
[WGK Germany ]

WGK 3
[Storage Class]

11 - Combustible Solids
Hazard InformationBack Directory
[Uses]

KG 5 is orally active drug that stabilizes inactive state of PDGFRβ/B-RAF and inhibits tumor angiogenesis.
[in vivo]

KG5 (Compound 6; 100 mg/kg; oral administration; daily; for 26 days) treatment prevents tumor growth in an orthotopic renal cell carcinoma model[1].
KG5 (Compound 6; 50 mg/kg; i.p.; twice daily) treatment completely blocks angiogenesis relative to vehicle control in mice (injected with Matrigel containing bFGF). Pharmacokinetic analysis of the dose and formulation of KG5 used indicated a Cmax of 3.6 μg/mL, T1/2 of 11.5 h, and an area under the concentration time curve (AUC0-12h) of 14.7 μg?h/mL[1].
KG5 (Compound 6; 1 μM) disrupts a late step in angiogenesis during zebrafish embryogenesis[1].

Animal Model:Male Nu/Nu mice injected with SN12C-RFP cells[1]
Dosage:100 mg/kg
Administration:Oral administration; daily; for 26 days
Result:Prevented tumor growth in an orthotopic renal cell carcinoma model.
[IC 50]

B-Raf; PDGFRβ: 520 nM (Kd); FLT3: 52 nM (Kd); KIT: 170 nM (Kd); PDGFRα: 300 nM (Kd); c-Raf
[storage]

Store at -20°C
Spectrum DetailBack Directory
[Spectrum Detail]

KG5(877874-85-6)1HNMR
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