3,5-Dichloro-N-((1-((2,2-dimethyltetrahydro-2H-pyran-4-yl)methyl)-4-fluoropiperidin-4-yl)methyl)benzamide structure
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Common Name | 3,5-Dichloro-N-((1-((2,2-dimethyltetrahydro-2H-pyran-4-yl)methyl)-4-fluoropiperidin-4-yl)methyl)benzamide | ||
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CAS Number | 918430-49-6 | Molecular Weight | 431.37 | |
Density | 1.25g/cm3 | Boiling Point | 510.1°C at 760 mmHg | |
Molecular Formula | C21H29Cl2FN2O2 | Melting Point | N/A | |
MSDS | N/A | Flash Point | 262.3°C |
Use of 3,5-Dichloro-N-((1-((2,2-dimethyltetrahydro-2H-pyran-4-yl)methyl)-4-fluoropiperidin-4-yl)methyl)benzamide(Rac)-TTA-P2 is the inactive isomer of TTA-P2 (HY-10035), and can be used as an experimental control. TTA-P2 (T-Type calcium channel inhibitor) is a potent inhibitor of T-Type calcium channel. TTA-P2 penetrates well the CNS and blocks the native T-type currents in deep cerebellar nuclear neurons, the window current is completely abolished both for wild-type and mutant Cav3.1 channels. TTA-P2 has the potential for the research of neurology disease[1]. |
Name | 3,5-Dichloro-N-({1-[(2,2-dimethyltetrahydro-2H-pyran-4-yl)methyl] -4-fluoro-4-piperidinyl}methyl)benzamide |
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Synonym | More Synonyms |
Description | (Rac)-TTA-P2 is the inactive isomer of TTA-P2 (HY-10035), and can be used as an experimental control. TTA-P2 (T-Type calcium channel inhibitor) is a potent inhibitor of T-Type calcium channel. TTA-P2 penetrates well the CNS and blocks the native T-type currents in deep cerebellar nuclear neurons, the window current is completely abolished both for wild-type and mutant Cav3.1 channels. TTA-P2 has the potential for the research of neurology disease[1]. |
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Related Catalog | |
References |
Density | 1.25g/cm3 |
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Boiling Point | 510.1°C at 760 mmHg |
Molecular Formula | C21H29Cl2FN2O2 |
Molecular Weight | 431.37 |
Flash Point | 262.3°C |
Exact Mass | 430.15900 |
PSA | 45.06000 |
LogP | 5.24520 |
MFCD11977740 |