Peptides Codex
Home
Spider-venom peptide family (toxins)

Huwentoxin

Huwentoxins are a family of neurotoxic peptides from the venom of the Chinese bird spider, most sharing the highly stable inhibitor cystine-knot (ICK) fold. Different members target voltage-gated calcium or sodium channels; huwentoxin-IV, for example, selectively blocks tetrodotoxin-sensitive sodium channels including Nav1.7. This makes them valuable research tools for studying pain signaling. This page is educational and not medical advice.

By The Peptides Codex Editorial TeamReviewed July 10, 2026
Length
n/a
Class
Spider-venom peptide family (toxins)
Function
Inhibitor cystine-knot peptides that modulate voltage-gated ion channels
Context
Research tools for ion-channel and pain studies

A family of disulfide-knotted spider peptides, several of which block the pain channel Nav1.7.

Also known as: HWTX · HwTx-IV · mu-theraphotoxin-Hs2a

Part of the Foundational & therapeutic peptides cluster

Overview

Huwentoxins are a family of neurotoxic peptides from the venom of the Chinese bird spider, most sharing the highly stable inhibitor cystine-knot (ICK) fold. Different members target voltage-gated calcium or sodium channels; huwentoxin-IV, for example, selectively blocks tetrodotoxin-sensitive sodium channels including Nav1.7. This makes them valuable research tools for studying pain signaling. This page is educational and not medical advice.

Source & context

Biological / chemical source: Venom of the Chinese bird spider (Cyriopagopus schmidti / Haplopelma schmidti)

Primary research or clinical context: Research tools for ion-channel and pain studies

Cystine-knot scaffold

Most huwentoxins fold into an inhibitor cystine knot, in which three disulfide bonds form a ring threaded by a third bridge. This gives exceptional stability across pH and temperature, a property that makes ICK peptides attractive templates for engineering selective, protease-resistant channel modulators.

Channel targets and pain research

Individual huwentoxins act on N-type calcium channels or on voltage-gated sodium channels. Huwentoxin-IV inhibits Nav1.7, a channel central to pain sensation, so it is studied as a probe and lead for non-opioid analgesic research. These remain investigational tools rather than approved medicines.

FAQ about Huwentoxin

What is Huwentoxin?+

Huwentoxins are a family of neurotoxic peptides from the venom of the Chinese bird spider, most sharing the highly stable inhibitor cystine-knot (ICK) fold. Different members target voltage-gated calcium or sodium channels; huwentoxin-IV, for example, selectively blocks tetrodotoxin-sensitive sodium channels including Nav1.7. This makes them valuable research tools for studying pain signaling. This page is educational and not medical advice.

Is Huwentoxin an approved medicine?+

Huwentoxin is discussed here as a research / educational topic. Research tools for ion-channel and pain studies. This is not medical advice.

What is the typical length of Huwentoxin?+

Huwentoxin is not a classic amino-acid chain peptide in the same sense; see the profile for classification details.

Related peptides

References & further reading

  1. 1.Wikipedia — Huwentoxin
  2. 2.UniProtKB — Huwentoxin-IV / Mu-theraphotoxin-Hs2a, Cyriopagopus schmidti (P83303)
Disclaimer: Educational content only. Not medical advice. Not instructions for human use. Research peptides and unapproved products may be restricted or illegal to market for human consumption in your jurisdiction. Consult qualified professionals and applicable law.
You might also like: All peptides · Atlas · Research · Tools
Cite this: Peptides Codex — Huwentoxin educational profile.
Tip: Use browser print (Ctrl/Cmd + P) for a clean PDF of this page.