ProTx-I
This compound is a selective T-type calcium channel blocker with an IC50 of 0.2 μM for hCaV3.1 over hCaV3.2. It also reversibly inhibits NaV1.8 and blocks KV2.1 channels. This pharmacological profile makes it a useful research tool for studying pain signaling, neuronal excitability, and cardiovascular function in both cellular and animal models.
Product Specifications
Field of Research
Metabolism Research, Pharmacology & Drug Discovery
Molecular Weight
3987.51
Storage Conditions
-20°C
Notes
For research use only.
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