Description
AMG-208 is an inhibitor of c-MET and Ron that exhibits anticancer chemotherapeutic activity in prostate cancer models in vitro and in vivo.
Product Unit Size | Cost | Quantity | Stock |
---|
AMG-208 is an inhibitor of c-MET and Ron that exhibits anticancer chemotherapeutic activity in prostate cancer models in vitro and in vivo.
Cas No. | 1002304-34-8 |
---|---|
Purity | ≥98% |
Formula | C22H17N5O2 |
Formula Wt. | 383.40 |
Chemical Name | 7-methoxy-4-[(6-phenyl-[1,2,4]triazolo[4,3-b]pyridazin-3-yl)methoxy]quinoline |
IUPAC Name | 7-methoxy-4-[(6-phenyl-[1,2,4]triazolo[4,3-b]pyridazin-3-yl)methoxy]quinoline |
Synonym | AMG208; AMG 208 |
Solubility | DMSO 0.25 mg/mL (0.65 mM) Water Insoluble Ethanol Insoluble |
Appearance | White to off white powder |
Store Temp | -20°C |
---|---|
Ship Temp | Ambient |
MSDS | |
---|---|
Info Sheet |
Liu X, Newton RC, Scherle PA. Developing c-MET pathway inhibitors for cancer therapy: progress and challenges. Trends Mol Med. 2010 Jan;16(1):37-45. PMID: 20031486.
Albrecht BK, Harmange JC, Bauer D, et al. Discovery and optimization of triazolopyridazines as potent and selective inhibitors of the c-Met kinase. J Med Chem. 2008 May 22;51(10):2879-82. PMID: 18426196.
Benzyl taxol analog; potential microtubule depo...
Triterpene saponin found in species of Panax.
Mycotoxin derivative; actin polymerization inhi...
Antimicrobial peptide found in Vespula lewisii,...
Pyrrolidone; NMDA and mGluR5 agonist, N-type an...
PDK1 and Akt inhibitor.
Fluoroquinolone; bacterial DNA gyrase and helic...
Iron chelator.
Valsartan impurity
Endogenous opioid peptide; μOR agonist.
Coumarin, more potent isomer; VKORC1 inhibitor....
PKC and PKD activator, carcinogen.
Thiazole; proteasome inhibitor, protein translo...
MELK inhibitor.
Benzamide; HDAC1 inhibitor.
Nucleoside (deoxycytidine) analog; ribonucleoti...
Endogenous peptide hormone, glugagon fragment; ...
Triazole; gibberellin inhibitor, potential 14-Î...
Synthetic glutathione peroxidase mimetic; yeast...
AT1 inhibitor.