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.
Triphenylthylene, tamoxifen analog; SERM.
Aureothricin is a member of the dithiolopyrrolo...
Adenosine A2A agonist.
Fermentation impurity
Naturally occurring sesteterpenoid.
Selective cannabinoid receptor 2 (CB2) inverse ...
Calcium channel blocker.
Diterpene found in brewed, unfiltered coffee; F...
Peptide; NMDA partial agonist.
Mixture of pyrantel, a thiophene, and pamoic ac...
Phytoestrogen, isoflavone found in various plan...
NLRP3 and caspase-1 inhibitor.
Ansamycin; bacterial DNA-dependent RNA polymera...
Isoxazole derivative; HSP90 inhibitor.
Immunodominant peptide epitope occurring in mul...
HDM2 inhibitor
Indoleamine-2,3-dioxygenase inhibitor.
Antacid; pepsin inhibitor. Assay (Polysaccharid...