µ-TRTX-Hd1a, a spider venom-derived compound, selectively inhibits the human NaV 1.7 channel by functioning as a gating modifier, interacting with the S3b-S4 paddle motif within domain II of the channel [1].
Molecular Weight:
3822.33
Formula:
C160H246N46O51S6
Target:
Sodium Channel
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