Molecular Formula | C8H13NO2 |
Molar Mass | 155.19 |
Density | 1.256±0.06 g/cm3(Predicted) |
Melting Point | >300°C(lit.) |
Boling Point | 295.5±23.0 °C(Predicted) |
Solubility | Aqueous Acid (Slightly) |
Appearance | Solid |
Color | White |
pKa | 2.58±0.20(Predicted) |
Storage Condition | Keep in dark place,Sealed in dry,Room Temperature |
WGK Germany | 3 |
biological activity | BCH (2-aminocicyclo-(2,2,1)-heptane-2-carboxylic acid, LAT1-IN-1) it is a selective, competitive inhibitor of system L amino acid transporter 1 (LAT1). BCH (LAT1-IN-1) induces apoptosis in cancer cells. |
Target | Value |
Cell Line: | KYSE30 and KYSE150 esophageal cancer cells KYSE30 and KYSE150 cells KYSE30 and KYSE150 cells |
Concentration: | 1 mM, 3 mM, 5 mM, 10 mM, 20 mM, 30 mM, 40 mM, 50 mM, or 100 mM 30 mM 30 mM |
Incubation Time: | 3 days 24 and 48 hours 0 hour, 0.5 hour, 1 hour, 3 hours, 6 hours, 24 hours |
Result: | Cell proliferation was suppressed in a dose-dependent manner. Cell cycle arrest. Phosphorylation of 4E-BP1 and p70S6K was decreased. The amount of mTOR, 4E-BP1, and p70S6K proteins was slightly decreased. Significantly delayed tumor growth and decreased glucose metabolism. |
Animal Model: | Male BALB/c nude mice (5-week-old) with KYSE150 cells |
Dosage: | 200 mg/kg |
Administration: | Intravenous injection; daily; for 14 days |
uses | inhibitors of amino acid transmembrane transport. |