2013
DOI: 10.1016/j.cca.2013.07.005
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Nodularins in poisoning

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Cited by 55 publications
(30 citation statements)
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“…They also possess the (2S,3S,8S,9S)-3-amino-9-methoxy-2,6,8-trimethyl-10-phenyldeca-4,6-dienoic acid (ADDA) functional group common to the microcystin class of cyanotoxins (Chorus and Bartram, 1999;Chen et al, 2013). There are at least 12 known nodularins Carmichael, 1997;Mazur-Marzec et al, 2006;Chen et al, 2013) of which nodularin-R is the most common (Chen et al, 2013).…”
Section: Introductionmentioning
confidence: 99%
See 1 more Smart Citation
“…They also possess the (2S,3S,8S,9S)-3-amino-9-methoxy-2,6,8-trimethyl-10-phenyldeca-4,6-dienoic acid (ADDA) functional group common to the microcystin class of cyanotoxins (Chorus and Bartram, 1999;Chen et al, 2013). There are at least 12 known nodularins Carmichael, 1997;Mazur-Marzec et al, 2006;Chen et al, 2013) of which nodularin-R is the most common (Chen et al, 2013).…”
Section: Introductionmentioning
confidence: 99%
“…Mouse toxicology studies have reported LD 50 's via i.p. injection for nodularins ranging from 30 to >2000 mg nodularin/kg bw Chen et al, 2013).…”
Section: Introductionmentioning
confidence: 99%
“…Once ingested, MCs are concentrated in hepatic tissues, where they bind to the catalytic subunit of protein phosphatases, triggering hepatotoxicity. The main mechanism of action for NODs also involves protein phosphates and can lead to high tumorogenic activity [11,12]. The NODs, mostly synthesized by the cyanobacteria Nodularia spumigena, are chemically similar to MCs because they are also cyclic pentapeptides (Adda-D-Glu-MeDhb-D-MeAsp-L-Arg); however, fewer than 10 analogs have been described to date.…”
Section: Introductionmentioning
confidence: 99%
“…The NODs, mostly synthesized by the cyanobacteria Nodularia spumigena, are chemically similar to MCs because they are also cyclic pentapeptides (Adda-D-Glu-MeDhb-D-MeAsp-L-Arg); however, fewer than 10 analogs have been described to date. The main mechanism of action for NODs also involves protein phosphates and can lead to high tumorogenic activity [11,12]. Different CYNs producing microorganisms have been identified, including Cylindrospermopsis, Aphanizomenon, Umezakia, Raphidiopsis, Anabaena, and Lygnbya [13].…”
Section: Introductionmentioning
confidence: 99%
“…They are similar to microcystins in structure and mechanism of toxicity and, for the purposes of this discussion, are considered equivalent to microcystins (Namikoshi et al, 1994;Chen et al, 2013). The frequency of microcystin-producing HABs appears to be increasing in most regions in association with the expansion of intensive agriculture, industrial development, and urbanization.…”
Section: Introductionmentioning
confidence: 95%