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ChemicalBook--->CAS DataBase List--->1002304-34-8

1002304-34-8

1002304-34-8 Structure

1002304-34-8 Structure
IdentificationBack Directory
[Name]

AMG-208
[CAS]

1002304-34-8
[Synonyms]

CS-191
AMG-208
AMG-208, >=98%
AMG208; AMG 208
AMG-208 USP/EP/BP
AMG-208;AMG208; AMG 208
7-Methoxy-4-[(6-phenyl-1,2,4-triazolo[4,3-b]pyridazin-3-yl)methoxy]quinoline
Quinoline, 7-Methoxy-4-[(6-phenyl-1,2,4-triazolo[4,3-b]pyridazin-3-yl)Methoxy]-
7-Methoxy-4-[(6-phenyl-1,2,4-triazolo[4,3-b]pyridazin-3-yl)methoxy]quinoline AMG 208
[Molecular Formula]

C22H17N5O2
[MDL Number]

MFCD17215205
[MOL File]

1002304-34-8.mol
[Molecular Weight]

383.41
Chemical PropertiesBack Directory
[density ]

1.34
[storage temp. ]

Store at -20°C
[solubility ]

insoluble in EtOH; insoluble in H2O; ≥3.83 mg/mL in DMSO
[form ]

solid
[pka]

5.98±0.27(Predicted)
[color ]

White to off-white
Hazard InformationBack Directory
[Uses]

AMG-208 is an orally active c-Met/RON dual selective inhibitor with an IC50 of 9 nM for c-Met. AMG-208 is a CYP3A4 inhibitor with an IC50 of 32 μM. AMG-208 has anti-cancer activity[1][2][3].
[Definition]

ChEBI: A member of the class of quinolines that is 7-methoxyquinoline substituted at position 4 by a (6-phenyl[1,2,4]triazolo[4,3-b]pyridazin-3-yl)methoxy group. AMG exhibits antitumour activity, particularly in prostate cancer.
[in vivo]

In male Sprague Dawley rats, AMG-208 (0.5 mg/kg i.v.) shows a high bioavailability with Cl of 0.37 L/h/kg, Vss of 0.38 L/kg and T1/2 of 1 hour[1].

[target]

Met
[IC 50]

CYP3A4: 32 μM (IC50); c-Met: 9 nM (IC50)
[References]

[1] Albrecht BK, et al. Discovery and optimization of triazolopyridazines as potent and selective inhibitors of the c-Met kinase. J Med Chem. 2008, 51(10), 2879-2882. DOI:10.1021/jm800043g
[2] Boezio AA, et al. Discovery and optimization of potent and selective triazolopyridazine series of c-Met inhibitors. Bioorg Med Chem Lett. 2009, 19(22), 6307-6312. DOI:10.1016/j.bmcl.2009.09.096
[3] Liu X, et al. Developing c-MET pathway inhibitors for cancer therapy: progress and challenges. Trends Mol Med. 2010,16(1), 37-45. DOI:10.1016/j.molmed.2009.11.005
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