| Name | TPC2-A1-N |
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| Description | TPC2-A1-N is a novel, lipophilic, membrane permeable isoform-selective small molecule agonist of two-pore channel 2 (TPC2). TPC2-A1-N plays its role by mimicking the physiological actions of NAADP and PI(3,5)P2?through independent binding sites. TPC2-A1-N has inverse effects on key lysosomal activities and increases the pH in the lysosomal lumen in a TPC2-dependent manner. |
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| Molecular Formula | C17H9Cl2F3N2O2 |
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| Molecular Weight | 401.17 |