Jan S. Tytgat

Leuven, VLG 3000, Belgium

Last Updated: 09/26/2026

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Found 229 publications

Electrophysiological Characterization of the Venom and Toxins from the Scorpion Tityus championi Targeting Voltage-Gated Sodium Channels and Molecular Modeling of Tch3, a Toxin with Therapeutic Potential for Pain Relief.

Electrophysiological Characterization of the Venom and Toxins from the Scorpion Tityus championi Targeting Voltage-Gated Sodium Channels and Molecular Modeling of Tch3, a Toxin with Therapeutic Potential for Pain Relief.

Journal: Biomolecules

Published: March 04, 2026

Alanine Mutagenesis Identifies Specific Amino Acids of Nemertide Alpha-1 Activity and Its Binding to Target Receptors.

Alanine Mutagenesis Identifies Specific Amino Acids of Nemertide Alpha-1 Activity and Its Binding to Target Receptors.

Journal: Journal of natural products

Published: December 17, 2025

Identification and functional characterization of a Nav-targeting peptide NavTx-Bg1 from sea anemone Bunodosoma goanense (Vennam & den Hartog, 1993) transcriptome.

Identification and functional characterization of a Nav-targeting peptide NavTx-Bg1 from sea anemone Bunodosoma goanense (Vennam & den Hartog, 1993) transcriptome.

Journal: Toxicon : official journal of the International Society on Toxinology

Published: November 04, 2025

The diversity of insecticide target site mutations in Apis mellifera.

The diversity of insecticide target site mutations in Apis mellifera.

Journal: BMC genomics

Published: August 29, 2025

The Helix Ring Peptide U11 from the Venom of the Ant, Tetramorium bicarinatum, Acts as a Putative Pore-Forming Toxin, Not a New Kv1.3 Channel Blocker. Comment on Boy et al. A New Kv1.3 Channel Blocker from the Venom of the Ant Tetramorium bicarinatum. Toxins 2025, 17, 379.

The Helix Ring Peptide U11 from the Venom of the Ant, Tetramorium bicarinatum, Acts as a Putative Pore-Forming Toxin, Not a New Kv1.3 Channel Blocker. Comment on Boy et al. A New Kv1.3 Channel Blocker from the Venom of the Ant Tetramorium bicarinatum. Toxins 2025, 17, 379.

Journal: Toxins

Published: August 22, 2025

Exploring the unknown activity of the Huwentoxin-II spider toxin family: A screening of Ap1 toxins from Acanthoscurria paulensis venom.

Exploring the unknown activity of the Huwentoxin-II spider toxin family: A screening of Ap1 toxins from Acanthoscurria paulensis venom.

Journal: International journal of biological macromolecules

Published: August 07, 2025

Discovery of new neutrophil elastase inhibitors through Meloidae genome and transcriptome analyses.

Discovery of new neutrophil elastase inhibitors through Meloidae genome and transcriptome analyses.

Journal: Bioorganic chemistry

Published: July 22, 2025

LaIT6: A Novel Insect-Selective K+-Channel Toxin from Liocheles australasiae Scorpion Venom.

LaIT6: A Novel Insect-Selective K+-Channel Toxin from Liocheles australasiae Scorpion Venom.

Journal: Molecules (Basel, Switzerland)

Published: June 26, 2025

Pharmacological characterization of vampire bat-derived CGRP at the human CGRP receptor in the Xenopus oocyte system.

Pharmacological characterization of vampire bat-derived CGRP at the human CGRP receptor in the Xenopus oocyte system.

Journal: Toxicon : official journal of the International Society on Toxinology

Published: April 23, 2025

Biodiversity2Drugs-Renaissance of exploring nature-derived peptides for GPCR ligand discovery.

Biodiversity2Drugs-Renaissance of exploring nature-derived peptides for GPCR ligand discovery.

Journal: British journal of pharmacology

Published: April 01, 2025

Spider venom peptides with unique fold selectively block Shaker-type potassium channels.

Spider venom peptides with unique fold selectively block Shaker-type potassium channels.

Journal: Cellular and molecular life sciences : CMLS

Published: March 07, 2025

The major component of Heteractis magnifica sea anemone venom, RpIII, exhibits strong subtype selectivity for insects over mammalian voltage-gated sodium channels.

The major component of Heteractis magnifica sea anemone venom, RpIII, exhibits strong subtype selectivity for insects over mammalian voltage-gated sodium channels.

Journal: Neuropharmacology

Published: January 31, 2025

Showing 1-12 of 229

Last Updated: 09/26/2026