Results 131 to 140 of about 997 (174)

New approach methodologies to enhance human health risk assessment of immunotoxic properties of chemicals - a PARC (Partnership for the Assessment of Risk from Chemicals) project. [PDF]

Front Toxicol
Snapkow I, Smith NM, Arnesdotter E, Beekmann K, Blanc EB, Braeuning A, Corsini E, Sollner Dolenc M, Duivenvoorde LPM, Sundstøl Eriksen G, Franko N, Galbiati V, Gostner JM, Grova N, Gutleb AC, Hargitai R, Janssen AWF, Krapf SA, Lindeman B, Lumniczky K, Maddalon A, Mollerup S, Parráková L, Pierzchalski A, Pieters RHH, Silva MJ, Solhaug A, Staal YCM, Straumfors A, Szatmári T, Turner JD, Vandebriel RJ, Zenclussen AC, Barouki R.   +33 more
europepmc   +1 more source

Mycotoxins and Fungal Toxins: Current Status and Future Perspectives. [PDF]

Toxins (Basel)
Wang J, Tolosa J, Wang W, Yang X.
europepmc   +1 more source

Ueber die Chemie der Enniatine

, 1948
openaire   +2 more sources

Some of the next articles are maybe not open access.

Related searches:

Production of enniatin A

Canadian Journal of Microbiology, 1973
Growth of a strain of Fusarium sambucinum in surface culture on a specially developed medium gave high yields of enniatins, from which enniatin A, free from the B and C homologues, could be obtained by column chromatography in yields of 1 g or more per liter of culture.
T K, Audhya, D W, Russel
openaire   +2 more sources

Biosynthesis and biological activity of enniatins

Die Pharmazie, 2007
Enniatins are N-methylated cyclohexadepsipeptides (CHDPs), composed of three units each of N-methylated branched-chain L-amino acid and L-2-hydroxy acid arranged in an alternate fashion. These low-molecular secondary metabolites are produced by Fusarium species, typical mycotoxin producing fungi. Enniatins are known for their ionophoric, phytotoxic and
Firáková, S., Proksa, B., Sturdíková, M.   +2 more
openaire   +2 more sources

The structure of enniatins and related antibiotics

Tetrahedron, 1963
Abstract The synthesis of cyclotetradepsipeptides the structure of which has previously been assigned to antibiotics of the enniatin group is described. It was found that these antibiotics cannot be represented by the formulas (I)–(VI).
M M, Shemyakin, Y A, Ovchinnkov, V T, Ivanov, A A, Kiryushkin   +3 more
openaire   +2 more sources

Enniatin A1, enniatin B1 and beauvericin on HepG2: Evaluation of toxic effects

Food and Chemical Toxicology, 2015
Hepatotoxicity of three Fusarium mycotoxins, beauvericin (BEA) and two enniatins (ENNs) ENN A1 and ENN B1, in hepatocarcinoma cells (HepG2) were evaluated and compared. Concentrations used were 1.5 and 3 μM at 24, 48 and 72 h for each mycotoxin. Flow cytometry was used to examine enniatins effects on cell proliferation, to characterize the cell cycle ...
Ana, Juan-García, María-José, Ruiz, Guillermina, Font, Lara, Manyes   +3 more
openaire   +2 more sources

Investigation of the electrophysiological properties of enniatins

Archives of Biochemistry and Biophysics, 2004
Enniatins are cyclohexadepsipeptides produced by various species of the genus Fusarium, and are known to have ionophoric, antibiotic, and in vitro hypolipidaemic properties. With the patch clamp technique in the inside-out mode it could be shown that enniatin easily incorporates into the cell membrane in which it forms cation-selective pores.
Kamyar, Majid-Reza, Rawnduzi, Pakiza, Studenik, Christian, Kouri, Katerina, Lemmens, Rosa   +4 more
openaire   +3 more sources

Fate of enniatins and deoxynivalenol during pasta cooking

Food Chemistry, 2016
The fate of deoxynivalenol and enniatins was studied during cooking of commercially available dry pasta in the Netherlands in 2014. Five samples containing relatively high levels of deoxynivalenol and/or enniatins were selected for the cooking experiment.
Monique De Nijs, Hans G J Mol
exaly   +4 more sources

Synthesis of enniatin B

Experientia, 1963
Die Struktur von Enniatin B, eines antimikrobiellen Wirkstoffes aus Fusarienstammen (ETH, Zurich), wird durch Synthese als die eines Cyclohexapeptolids bewiesen (vgl. X).
Pl. A. Plattner, K. Vogler, R. O. Studer, P. Quitt, W. Keller-Schierlein   +4 more
openaire   +1 more source