Results 191 to 200 of about 9,044 (210)
Some of the next articles are maybe not open access.

Trichodermadiene: a new trichothecene

Tetrahedron Letters, 1980
A new trichothecene, trichodermadiene (3), possessing a dienic ester side chain has been isolated and characterized.
Eugene P. Mazzola   +4 more
openaire   +2 more sources

Chromatography of Trichothecene Mycotoxins

Journal of Liquid Chromatography, 1986
Abstract Trichothecene mycotoxins occur in agricultural commodities and can cause problems from feed refusal to death in animals. This paper describes chromatographic methods for selective analysis for trichothecene mycotoxins. These methods include gas chromatography (GC), thin layer chromatography (TLC), and high pressure liquid chromatography (HPLC).
W. Hyde   +3 more
openaire   +2 more sources

Trichothecene Mycotoxins

2009
Publisher Summary Trichothecene mycotoxins are a family of tetracyclic sesquiterpenoid substances comprising over 200 compounds of widely varying toxicity. The epoxy group at C-12 and C-13 is considered essential for toxicity. Trichothecenes are broadly divided into two groups, the macrocyclic and nonmacrocyclic, based on the presence or absence of a ...
Val R. Beasley, Wanda M. Haschek
openaire   +2 more sources

HPLC-MS-Method for A-Trichothecenes

Mycotoxin Research, 2001
Gaschromatography with electron capture detection belongs to the most important methods for analysing the A-trichothecenes T-2 toxin, HT-2 toxin and diacetoxyscirpenol. The need of a derivatisation for these mycotoxins prior detection is the main disadvantage of this method.
Binder M, Thimm N, Handl J
openaire   +3 more sources

Systemic Effects of Topically Applied Trichothecenes I. Comparative Study of Various Trichothecenes in Mice

Journal of Veterinary Medicine Series A, 1986
SummaryT‐2 toxin, HT‐2 toxin, Diacetoxyscirpenol (DAS), Roridin A, Verrucarin A and 3‐Acetyl‐deoxynivalenol (3‐AcDON) were dissolved in dimethyl sulfoxide and applied topically to mice. For a mortality study, groups of 10–20 male mice received either 5, 10, 20, 30 or 40 mg toxin/kg BW. Further, mixtures of trichothecenes were applied, e. g.: T‐2 toxin +
H. B. Schiefer   +2 more
openaire   +3 more sources

Trichothecene Production byTrichoderma brevicompactum

Journal of Agricultural and Food Chemistry, 2005
Trichoderma brevicompactum, T. viride, T. harzianum, T. atroviride, T. longibrachiatum, T. erinaceum, T. citrinoviride, and Hypocrea lutea were screened for production of trichothecenes after growth on one or several solid and liquid media. Trichothecenes were detected by liquid chromatography combined with online UV/vis spectroscopy and electrospray ...
Doustmorad Zafari   +3 more
openaire   +3 more sources

Hydroxylations of trichothecene rings in the biosynthesis of Fusarium trichothecenes: evolution of alternative pathways in the nivalenol chemotype

Environmental Microbiology, 2016
SummaryFusarium sporotrichioides genes FsTri11, FsTri13, and FsTri1 encode cytochrome P450 monooxygenases (CYPs) responsible for hydroxylations at C‐15, C‐4, and C‐8 of the trichothecene skeleton, respectively. However, the corresponding genes of nivalenol (NIV)‐chemotype Fusarium graminearum remain to be functionally elucidated.
Makoto Fujimura   +13 more
openaire   +3 more sources

State of the art of trichothecenes analysis

Toxicology Letters, 2004
Methods to analyze trichothecenes should be fast, reliable and economical. The known methods can be divided into two categories: the 'instrumental methods' as gas chromatography (GC) and high performance liquid chromatography (HPLC) and the so called 'fast methods' like thin layer chromatography (TLC), enzyme-linked immunosorbant analyses (ELISA) and ...
openaire   +3 more sources

Novel rearrangements of macrocyclic trichothecenes

Tetrahedron Letters, 1990
Abstract Myrotoxin B ( 1 ) readily undergoes electrophilic addition of water and BrOH to give myrotoxin B hydrate ( 5 ) and the bromohydrin 2 , respectively. When these hemiketals are treated with DBU in THF, they undergo novel rearrangements apparently via their open chain hydroxyketone forms. Myrotoxin B hydrate ( 5 ) gives a spirocyclic ketal 6
Ming Zeng   +2 more
openaire   +2 more sources

Biotransformation of Trichothecenes: The Role of Intestinal Microflora in the Metabolism and Toxicity of Trichothecene Mycotoxins

1990
The trichothecene mycotoxins are a group of tetracyclic sesquiterpenoid compounds characterized by a six-membered oxygen ring, an epoxide in the 12,13 position and an olefinic bond in the 9,10 position. They are produced by a variety of fungi including Stachybotrys, Myrothecium, Trichothecium, and particularly species of the genus Fusarium ...
C. Helaszek   +2 more
openaire   +2 more sources

Home - About - Disclaimer - Privacy