“…A number of analgesic peptides from its venom have been reported; for most of them, it can be assumed that they could target VGSCs by virtue of their primary structure homology and similar scaffold with so-called long-chain sodium channel toxins (Goudet et al, 2002). They are: BmK ITAP, an excitatory insect-selective toxin (Xiong et al, 1999); BmK dITAP3, a depressant insect-selective toxin (Guan et al, 2001a) with an analgesic effect in mice; BmK AGAP, an antitumor analgesic peptide showing inhibitory effect on both visceral and somatic pain (Liu et al, 2003); BmK Ang P1 (Guan et al, 2001b); BmK AngM1 (Cao et al, 2004); BmK AS (Chen and Ji, 2002); BmK IT2 ; BmK I1; BmK I4; and BmK I6 (Guan et al, 2000). All of these are peptides for which analgesic properties in mice have been demonstrated.…”