TPC2-A1-P is a powerful and membrane permeable agonist of two pore channel 2 (TPC2) with an EC 50 of 10.5 μM. TPC2-A1-P plays its role by mimicking the physiological actions of PI(3,5)P2. TPC2-A1-P also shows higher potency to induce Na 2+ mobilisation from TPC2 than TPC-A1-N ( HY-131614 ). TPC2-A1-P can be used to probe different functions of TPC2 channels in intact cells.
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