“…The spectrum of toxins of most species includes TTX and two of its equilibrium analogues (4-epiTTX and 4,9-anhydroTTX). In Kulikovia manchenkoi, body extracts possessed 5,6,11-trideoxyTTX, 11-deoxyTTX, and 5-deoxyTTX [8]; in Yininemertes pratensis, body extracts possessed 5,11-dideoxyTTX and 11-norTTX-6(S)-ol [7]. The most toxic nemertean, C. simula, contains up to 13 TTX analogues, 11 of which are non-equilibrium: 11-norTTX-6(s)-ol, 11-deoxyTTX, 11-norTTX-6(r)-ol, 5,6,11-trideoxyTTX, 5-deoxyTTX, 11-oxoTTX, 4,9-anhydro-8-epi-5,6,11-trideoxyTTX, 1-hydroxy-8-epi-5,6,11-trideoxyTTX, 4,9-anhydro-5,6,11-trideoxyTTX, 6,11-dideoxyTTX, and 4,9-anhydro-11-oxoTTX [8,11,13].…”