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Structure Elucidation and in Vitro Toxicity of New Azaspiracids Isolated from the Marine Dinoflagellate Azadinium poporum

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Outgoing claims: the papers this work cites, builds on, or argues with.

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Two analogs of azaspiracid isolated from mussels, Mytilus edulis, involved in human intoxication in Ireland

inferredcites →https://doi.org/10.1002/anie.200600295openalex-snapshot

Total Synthesis and Confirmation of the Revised Structures of Azaspiracid‐2 and Azaspiracid‐3

inferredcites →https://doi.org/10.1002/rcm.3385openalex-snapshot

Discovery of new analogs of the marine biotoxin azaspiracid in blue mussels ( Mytilus edulis ) by ultra‐performance liquid chromatography/tandem mass spectrometry

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Rapid colorimetric assay for cellular growth and survival: Application to proliferation and cytotoxicity assays

inferredcites →https://doi.org/10.1016/j.hal.2005.11.004openalex-snapshot

Phytoplankton composition of the Kandalaksha Gulf, Russian White Sea: Dinophysis and lipophilic toxins in the blue mussel (Mytilus edulis)

inferredcites →https://doi.org/10.1016/j.hal.2008.06.003openalex-snapshot

Characterization of azaspiracids in plankton size-fractions and isolation of an azaspiracid-producing dinoflagellate from the North Sea

inferredcites →https://doi.org/10.1016/j.hal.2012.05.004openalex-snapshot

Blooms of Azadinium cf. spinosum Elbrächter et Tillmann (Dinophyceae) in northern shelf waters of Argentina, Southwestern Atlantic

inferredcites →https://doi.org/10.1016/j.hal.2012.10.001openalex-snapshot

First record of the genus Azadinium (Dinophyceae) from the Shetland Islands, including the description of Azadinium polongum sp. nov.

inferredcites →https://doi.org/10.1016/j.hal.2012.11.009openalex-snapshot

Morphology, phylogeny and azaspiracid profile of Azadinium poporum (Dinophyceae) from the China Sea

inferredcites →https://doi.org/10.1016/j.hal.2014.04.012openalex-snapshot

Azaspiracid variability of Azadinium poporum (Dinophyceae) from the China Sea

inferredcites →https://doi.org/10.1016/j.protis.2014.04.004openalex-snapshot

Morphological and Molecular Characterization of Three New Azadinium Species (Amphidomataceae, Dinophyceae) from the Irminger Sea

inferredcites →https://doi.org/10.1016/j.toxicon.2004.08.020openalex-snapshot

Solid phase adsorption toxin tracking (SPATT): a new monitoring tool that simulates the biotoxin contamination of filter feeding bivalves

inferredcites →https://doi.org/10.1016/j.toxicon.2005.02.015openalex-snapshot

Cytotoxic and cytoskeletal effects of azaspiracid-1 on mammalian cell lines

inferredcites →https://doi.org/10.1016/j.toxicon.2008.03.022openalex-snapshot

Confirmation by LC–MS/MS of azaspiracids in shellfish from the Portuguese north-western coast

inferredcites →https://doi.org/10.1016/j.toxicon.2009.02.008openalex-snapshot

Isolation of azaspiracid-2 from a marine sponge Echinoclathria sp. as a potent cytotoxin

inferredcites →https://doi.org/10.1016/j.toxicon.2009.07.014openalex-snapshot

First identification of azaspiracid and spirolides in Mesodesma donacium and Mulinia edulis from Northern Chile

inferredcites →https://doi.org/10.1016/j.toxicon.2012.05.007openalex-snapshot

New azaspiracids in Amphidomataceae (Dinophyceae)

inferredcites →https://doi.org/10.1016/s0021-9673(02)00003-1openalex-snapshot

Liquid chromatography with electrospray ion trap mass spectrometry for the determination of five azaspiracids in shellfish

inferredcites →https://doi.org/10.1016/s0041-0101(02)00288-xopenalex-snapshot

Detection of five new hydroxyl analogues of azaspiracids in shellfish using multiple tandem mass spectrometry

inferredcites →https://doi.org/10.1016/s0065-2164(06)59004-5openalex-snapshot

The Biosynthesis of Polyketide Metabolites by Dinoflagellates

inferredcites →https://doi.org/10.1021/ja981413ropenalex-snapshot

Azaspiracid, a New Marine Toxin Having Unique Spiro Ring Assemblies, Isolated from Irish Mussels, Mytilus edulis

inferredcites →https://doi.org/10.1021/jf2048788openalex-snapshot

Improved Isolation Procedure for Azaspiracids from Shellfish, Structural Elucidation of Azaspiracid-6, and Stability Studies

inferredcites →https://doi.org/10.1021/np500555kopenalex-snapshot

Isolation, Structure Elucidation, Relative LC-MS Response, and in Vitro Toxicity of Azaspiracids from the Dinoflagellate Azadinium spinosum

inferredcites →https://doi.org/10.1021/tx200553popenalex-snapshot

Comparative Effects of the Marine Algal Toxins Azaspiracid-1, -2, and -3 on Jurkat T Lymphocyte Cells

inferredcites →https://doi.org/10.1021/tx400434bopenalex-snapshot

Epimers of Azaspiracids: Isolation, Structural Elucidation, Relative LC-MS Response, and in Vitro Toxicity of 37-epi-Azaspiracid-1

inferredcites →https://doi.org/10.1080/09670260802578534openalex-snapshot

Azadinium spinosumgen. et sp. nov. (Dinophyceae) identified as a primary producer of azaspiracid toxins

inferredcites →https://doi.org/10.1080/09670262.2011.556753openalex-snapshot

A new non-toxic species in the dinoflagellate genusAzadinium:A. poporumsp. nov.

inferredcites →https://doi.org/10.1111/j.1550-7408.2011.00600.xopenalex-snapshot

First Report of the Photosynthetic Dinoflagellate Genus A zadinium in the P acific O cean: Morphology and Molecular Characterization of A zadinium cf. poporum

inferredcites →https://doi.org/10.1111/jpy.12104openalex-snapshot

A new potentially toxic A zadinium species ( D inophyceae) from the M editerranean Sea, A . dexteroporum sp. nov.

inferredcites →https://doi.org/10.1139/m62-029openalex-snapshot

STUDIES OF MARINE PLANKTONIC DIATOMS: I. CYCLOTELLA NANA HUSTEDT, AND DETONULA CONFERVACEA (CLEVE) GRAN.

inferredcites →https://doi.org/10.1271/bbb.65.740openalex-snapshot

Structures of Azaspiracid Analogs, Azaspiracid-4 and Azaspiracid-5, Causative Toxins of Azaspiracid Poisoning in Europe

inferredcites →https://doi.org/10.2216/13-178.1openalex-snapshot

Azadinium dalianense , a new dinoflagellate species from the Yellow Sea, China

inferredcites →https://doi.org/10.2216/ph09-35.1openalex-snapshot

Azadinium obesum (Dinophyceae), a new nontoxic species in the genus that can produce azaspiracid toxins

inferredcites →https://doi.org/10.2983/0730-8000(2006)25[1067:fdoaim]2.0.co;2openalex-snapshot

FIRST DETECTION OF AZASPIRACIDS IN MUSSELS IN NORTH WEST AFRICA

inferredcites →https://doi.org/10.3354/ame01603openalex-snapshot

Feeding by heterotrophic protists and copepods on the photosynthetic dinoflagellate Azadinium cf. poporum from western Korean waters

inferredcites →https://doi.org/10.3390/md10061360openalex-snapshot

Production and Isolation of Azaspiracid-1 and -2 from Azadinium spinosum Culture in Pilot Scale Photobioreactors

inferredcites →https://doi.org/10.3390/md6020039openalex-snapshot

Azaspiracid Shellfish Poisoning: A Review on the Chemistry, Ecology, and Toxicology with an Emphasis on Human Health Impacts

inferredcites →https://doi.org/10.3724/sp.j.1123.2010.00363openalex-snapshot

Determination of azaspiracid-1 in shellfishes by liquid chromatography with tandem mass spectrometry

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Incoming claims: where this work appears in other papers’ reference lists and arguments.

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inferred← citeshttps://doi.org/10.1007/s00216-016-0037-4openalex-snapshot

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inferred← citeshttps://doi.org/10.1016/j.ejop.2026.126182openalex-snapshot

Azadinium fusiforme, a new species of Amphidomataceae from Korean and Japanese coastal waters that lacks azaspiracid production

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Toxigenic algae and associated phycotoxins in two coastal embayments in the Ebro Delta (NW Mediterranean)

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Amphidoma languida (Amphidomatacea, Dinophyceae) with a novel azaspiracid toxin profile identified as the cause of molluscan contamination at the Atlantic coast of southern Spain

inferred← citeshttps://doi.org/10.1016/j.hal.2017.08.004openalex-snapshot

Identification of Azadinium species and a new azaspiracid from Azadinium poporum in Puget Sound, Washington State, USA

inferred← citeshttps://doi.org/10.1016/j.hal.2018.08.011openalex-snapshot

Diversity, distribution, and azaspiracids of Amphidomataceae (Dinophyceae) along the Norwegian coast

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Two novel azaspiracids from Azadinium poporum, and a comprehensive compilation of azaspiracids produced by Amphidomataceae, (Dinophyceae)

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Structure and toxicity of AZA-59, an azaspiracid shellfish poisoning toxin produced by Azadinium poporum (Dinophyceae)

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Production of the dinoflagellate Amphidoma languida in a large scale photobioreactor and structure elucidation of its main metabolite AZA-39

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Phylogeny and ultrastructure of a non-toxigenic dinoflagellate Amphidoma fulgens sp. nov. (Amphidomataceae, Dinophyceae), with a wide distribution across Asian Pacific

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Diversity of amphidomatacean dinoflagellates in Japan, with a description of Azadinium inconspicuum sp. nov. and azaspiracid components in Azadinium poporum ribotypes

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New azaspiracid analogues detected as bi-charged ions in Azadinium poporum (Amphidomataceae, Dinophyceae) isolated from Japanese coastal waters

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Coordination regulation of enhanced performance reveals the tolerance mechanism of Chlamys farreri to azaspiracid toxicity

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Complex profiles of azaspiracid analogues in two culture strains of Azadinium poporum (Amphidomataceae, Dinophyceae) isolated from Japanese coastal waters determined by LC-MS/MS

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Azaspiracid-59 accumulation and transformation in mussels (Mytilus edulis) after feeding with Azadinium poporum (Dinophyceae)

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A Practical ELISA for Azaspiracids in Shellfish via Development of a New Plate-Coating Antigen

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