Literature DB >> 10969968

Identification of thioether intermediates in the reductive transformation of gonyautoxins into saxitoxins by thiols.

S Sato1, R Sakai, M Kodama.   

Abstract

O-Sulfate group of gonyautoxin I and IV is transformed into methylene to form neosaxitoxin by thiols such as glutathione, a common cellular scavenger, in mild conditions. We isolated the intermediate of this conversion and propose that this reaction proceeds through formation of thiohemiketal, 1,2 shift to form stable thioether intermediate, and then redox exchange at sulfur atom to form the final product.

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Year:  2000        PMID: 10969968     DOI: 10.1016/s0960-894x(00)00332-2

Source DB:  PubMed          Journal:  Bioorg Med Chem Lett        ISSN: 0960-894X            Impact factor:   2.823


  4 in total

Review 1.  Recent progress in neuroactive marine natural products.

Authors:  Ryuichi Sakai; Geoffrey T Swanson
Journal:  Nat Prod Rep       Date:  2014-01-17       Impact factor: 13.423

2.  Preparation of calibration standards of N1-H paralytic shellfish toxin analogues by large-scale culture of cyanobacterium Anabaena circinalis (TA04).

Authors:  Ryuichi Watanabe; Toshiyuki Suzuki; Yasukatsu Oshima
Journal:  Mar Drugs       Date:  2011-03-22       Impact factor: 5.118

3.  Determination of Gonyautoxin-4 in Echinoderms and Gastropod Matrices by Conversion to Neosaxitoxin Using 2-Mercaptoethanol and Post-Column Oxidation Liquid Chromatography with Fluorescence Detection.

Authors:  Marisa Silva; Verónica Rey; Ana Botana; Vitor Vasconcelos; Luis Botana
Journal:  Toxins (Basel)       Date:  2015-12-30       Impact factor: 4.546

4.  Novel Polyclonal Antibody Raised against Tetrodotoxin Using Its Haptenic Antigen Prepared from 4,9-anhydrotetrodotoxin Reacted with 1,2-Ethaneditiol and Further Reacted with Keyhole Limpet Hemocyanin.

Authors:  Shigeru Sato; Suzuka Takaishi; Ko Yasumoto; Shugo Watabe
Journal:  Toxins (Basel)       Date:  2019-09-20       Impact factor: 4.546

  4 in total

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