Toxins as Marine-Based Drug Discovery II

A special issue of Marine Drugs (ISSN 1660-3397).

Deadline for manuscript submissions: closed (31 May 2021) | Viewed by 424

Special Issue Editor


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Guest Editor
Toxicology and Pharmacology, Department Pharmaceutical Sciences, Catholic University Leuven, Herestraat 49 box 922, 3000 Leuven, Belgium
Interests: peptide toxin; small molecules; voltage-gated ion channel; electrophysiology; pharmacology; venom; drug discovery
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Special Issue Information

Dear Colleagues,

Marine organisms can be seen as an untapped cocktail of biologically-active compounds, being increasingly recognized as an emerging source of therapeutics. Marine organisms have evolved the most sophisticated chemistry and neuropharmacology for their own biological purposes by producing a structural and functional diversity of bioactive molecules. These toxins are highly selective ligands for a wide range of ion channels and receptors. Therefore, they represent interesting lead compounds for the development of, for example, analgesics, anti-cancer drugs, drugs for neurological disorders, such as multiple sclerosis, Parkinson’s disease and Alzheimer’s disease among others.

In consideration of the success of the Special Issue on “Toxins as Marine-Based Drug Discovery” (https://www.mdpi.com/journal/marinedrugs/special_issues/toxins_marine_drug_discovery), and the relevant interest on the topic, we are pleased to announce the second version of this Special Issue.

This Special Issue of /Marine Drugs/ will provide a comprehensive look at marine toxins and toxin inspired leads and will focus on the mechanism of action and structure-function of marine neurotoxins and their targets, including, but not limited to, recent developments related to the emergence of marine organisms as an underutilized source of highly evolved bioactive peptides and small molecules with clinical potential.

As the Guest Editor, I invite colleagues working on marine bioactive peptides and compounds to contribute to this Special Issue of /Marine Drugs/ with interesting papers showing significant advances within this field.

Sincerely,

Dr. Steve Peigneur
Guest Editor

Manuscript Submission Information

Manuscripts should be submitted online at www.mdpi.com by registering and logging in to this website. Once you are registered, click here to go to the submission form. Manuscripts can be submitted until the deadline. All submissions that pass pre-check are peer-reviewed. Accepted papers will be published continuously in the journal (as soon as accepted) and will be listed together on the special issue website. Research articles, review articles as well as short communications are invited. For planned papers, a title and short abstract (about 100 words) can be sent to the Editorial Office for announcement on this website.

Submitted manuscripts should not have been published previously, nor be under consideration for publication elsewhere (except conference proceedings papers). All manuscripts are thoroughly refereed through a single-blind peer-review process. A guide for authors and other relevant information for submission of manuscripts is available on the Instructions for Authors page. Marine Drugs is an international peer-reviewed open access monthly journal published by MDPI.

Please visit the Instructions for Authors page before submitting a manuscript. The Article Processing Charge (APC) for publication in this open access journal is 2900 CHF (Swiss Francs). Submitted papers should be well formatted and use good English. Authors may use MDPI's English editing service prior to publication or during author revisions.

Keywords

  • Neurotoxins
  • Marine natural compounds
  • Sodium channels
  • Potassium channels
  • Calcium channels
  • Chloride ion channels
  • TRP channels
  • ASIC channels
  • opiate receptors
  • acetylcholine receptors
  • NMDA receptors
  • Antibiotics
  • Antimicrobial peptides
  • Gastropod venom peptides
  • Sea anemone toxins

Related Special Issues

Published Papers

There is no accepted submissions to this special issue at this moment.
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