Bay 36-7620 structure
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Common Name | Bay 36-7620 | ||
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CAS Number | 232605-26-4 | Molecular Weight | 278.35 | |
Density | N/A | Boiling Point | 471.861ºC at 760 mmHg | |
Molecular Formula | C19H18O2 | Melting Point | N/A | |
MSDS | N/A | Flash Point | 199.799ºC |
Use of Bay 36-7620BAY 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]. |
Name | (3aS,6aS)-5-methylidene-3a-(naphthalen-2-ylmethyl)-1,4,6,6a-tetrahydrocyclopenta[c]furan-3-one |
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Synonym | More Synonyms |
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]. |
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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 |
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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 |
hms3269k21 |
bay-36-7620 |
unii-0p934rsf8b |