3-Acetyldeoxynivalenol

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For research use only. Not intended for any clinical use
CATAP50722388
CAS50722-38-8
Structure: 
MDL NumberMFCD00135964
Molecular Weight338.35
InChI KeyADFIQZBYNGPCGY-HTJQZXIKSA-N
Descriptionfrom Fusarium roseum
Size1MG, 5MG
Storage Conditions2-8°C

1Biosynthesis of the Trichothecene 3-acetyldeoxynivalenol. Is Isotrichodermin a Biosynthetic Precursor?

L O Zamir, A Nikolakakis, K A Devor, F Sauriol

J Biol Chem. 1996 Nov 1;271(44):27353-9.

PMID: 8910312

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1Comparative Study of Deoxynivalenol, 3-acetyldeoxynivalenol, and 15-acetyldeoxynivalenol on Intestinal Transport and IL-8 Secretion in the Human Cell Line Caco-2

Tomoyuki Kadota, Hiroko Furusawa, Satoshi Hirano, Osamu Tajima, Yoichi Kamata, Yoshiko Sugita-Konishi

Toxicol In Vitro. 2013 Sep;27(6):1888-95.

PMID: 23792671

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1Mycotoxins: Occurrence, Toxicology, and Exposure Assessment

S Marin, A J Ramos, G Cano-Sancho, V Sanchis

Food Chem Toxicol. 2013 Oct;60:218-37.

PMID: 23907020

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1Oral Bioavailability, Hydrolysis, and Comparative Toxicokinetics of 3-Acetyldeoxynivalenol and 15-Acetyldeoxynivalenol in Broiler Chickens and Pigs

Nathan Broekaert, Mathias Devreese, Thomas De Mil, Sophie Fraeyman, Gunther Antonissen, Siegrid De Baere, Patrick De Backer, An Vermeulen, Siska Croubels

J Agric Food Chem. 2015 Oct 7;63(39):8734-42.

PMID: 26343882

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1Sphaerodes Mycoparasitica Biotrophic Mycoparasite of 3-acetyldeoxynivalenol- And 15-acetyldeoxynivalenol-producing Toxigenic Fusarium Graminearum Chemotypes

Vladimir Vujanovic, Yit Kheng Goh

FEMS Microbiol Lett. 2011 Mar;316(2):136-43.

PMID: 21204935

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