| Name | (3aS,6aS)-5-methylidene-3a-(naphthalen-2-ylmethyl)-1,4,6,6a-tetrahydrocyclopenta[c]furan-3-one |
|---|---|
| Synonyms |
hms3269k21
bay-36-7620 unii-0p934rsf8b |
| Description | BAY 36-7620 is a potent and noncompetitive antagonist of mGlu1 Receptor (IC50=0.16 μM) with inverse agonist activity. BAY 36-7620 inhibits tumor growth and prolongs the survival of mice with tumors by inhibiting mGlu1 receptor. BAY 36-7620 suppresses AKT phosphorylation in A549 tumors. BAY 36-762 has neuroprotective effect in acute subdural hematoma rat model.BAY 36-7620 is used in non-small cell lung cancer and breast cancer research[1][2][3][4]. |
|---|---|
| Related Catalog | |
| Target |
mGluR 1:0.16 μM (IC50) mGluR1a:0.38 μM (IC50) mGluR2:0.14 μM (IC50) mGluR 5:0.24 μM (IC50) |
| References |
| Boiling Point | 471.861ºC at 760 mmHg |
|---|---|
| Molecular Formula | C19H18O2 |
| Molecular Weight | 278.35 |
| Flash Point | 199.799ºC |
| Exact Mass | 278.13100 |
| PSA | 26.30000 |
| LogP | 3.89170 |
| Vapour Pressure | 0mmHg at 25°C |
| Index of Refraction | 1.633 |