Description
TGX-221 is an inhibitor of PI3Kβ. It exhibits high selectivity to clear cell renal cell carcinoma with VHL and SETD2 mutations. It also inhibits cell migration and invasion, and induces apoptosis in human glioblastoma cells.
TGX-221 is an inhibitor of PI3Kβ. It exhibits high selectivity to clear cell renal cell carcinoma with VHL and SETD2 mutations. It also inhibits cell migration and invasion, and induces apoptosis in human glioblastoma cells.
| Cas No. | 663619-89-4 |
|---|---|
| Formula | C21H24N4O2 |
| Formula Wt. | 364.44 |
| IUPAC Name | 9-(1-anilinoethyl)-7-methyl-2-morpholin-4-ylpyrido[1,2-a]pyrimidin-4-one |
| Solubility | DMSO 12 mg/mL (32.92 mM) Water Insoluble Ethanol Insoluble |
| Appearance | Light Yellow Powder |
| Store Temp | -20°C |
|---|---|
| Ship Temp | Ambient |
| MSDS | |
|---|---|
| Info Sheet |
Feng C., Sun Y., PI3Kβ inhibitor TGX221 selectively inhibits renal cell carcinoma cells with both VHL and SETD2 mutations and links multiple pathways. Sci Rep. 5:9465 (2015). PMID: 25853938.
Yang X., Yang J., TGX-221 inhibits proliferation and induces apoptosis in human glioblastoma cells. Oncol Rep. 38(5):2836-2842. PMID: 29048665.
L-type Ca2+ channel blocker.
TRPV4 agonist
Bisphosphonate.
GSK-3β, HGK, and CDK inhibitor.
Endogenous steroid hormone, estradiol metabolit...
RET, EGFR, VEGFR2 inhibitor.
Tyrphostin; IGF-1R inhibitor.
Fatty acid metabolite of chlorophyll; RXR and P...
Vitamin E analog, antioxidant.
α-glucosidase inhibitor, potential GLP-1 agoni...
Fibrate; PPARα agonist.
Alkaloid found in Galanthus, Narcissus, Leucoju...
nNOS inhibitor.
Coccidiostat; dihydrofolate reductase inhibitor...
Nucleoside (guanosine) analog; DNA chain termin...
CDK4/6 inhibitor.
Mixture of Ginkgolides A, B and C, found in Gin...
p110δ PI3K inhibitor.
A third-generation ALK inhibitor.
NS3/4A serine protease inhibitor.