| Name | 3,5-dichloro-N-[[(3S,4R)-1-(3,3-dimethylbutyl)-3-fluoropiperidin-4-yl]methyl]benzamide |
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| Description | TTA-P1 is a potent state-independent compound inhibiting human T-type calcium channel. T-type calcium channels play a role in diverse physiological responses including neuronal burst firing, hormone secretion, and cell growth. TTA-P1 has the potential for the research of absence epilepsy[1]. |
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| Related Catalog | |
| References |
| Molecular Formula | C19H27Cl2FN2O |
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| Molecular Weight | 389.33500 |
| Exact Mass | 388.14800 |
| PSA | 35.83000 |
| LogP | 5.33210 |