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About This Item
Empirical Formula (Hill Notation):
C15H20O6
CAS Number:
Molecular Weight:
296.32
UNSPSC Code:
12352200
NACRES:
NA.77
SMILES string
O1[C@]2([C@@H]3O[C@H]4[C@@]([C@]2(C[C@H]3O)C)([C@@H](C(=O)C(=C4)C)O)CO)C1
InChI
1S/C15H20O6/c1-7-3-9-14(5-16,11(19)10(7)18)13(2)4-8(17)12(21-9)15(13)6-20-15/h3,8-9,11-12,16-17,19H,4-6H2,1-2H3/t8-,9-,11-,12-,13-,14-,15+/m1/s1
InChI key
LINOMUASTDIRTM-QGRHZQQGSA-N
biological source
Fusarium sp. (Fusarium asiaticum)
form
solution (ethanol: 2-propanol 95:5)
storage condition
protect from light
concentration
1 mg/mL
shipped in
dry ice
storage temp.
−20°C
Quality Level
Biochem/physiol Actions
Deoxynivalenol (DON) is a trichothecene mycotoxin that inhibits the synthesis of DNA and RNA as well as protein synthesis at the ribosomal level.
Deoxynivalenol (DON) is a trichothecene mycotoxin that inhibits the synthesis of DNA and RNA as well as protein synthesis at the ribosomal level. DON induces IL-6 mediated serum hyperelevation of IgA, as well as phosphorylation of extracellular signal regulated protein kinases 1 and 2 (ERK 1,2) and c-Jun N-terminal kinases 1 and 2 (JNK 1,2) in mice. An in vitro study with porcine ovarian granulosa cells suggests a dose dependent association of DON on porcine ovarian functions. It was also shown that LPS and its downstream mediators can interact with DON to modulate proliferative, cytotoxic and apoptotic outcomes in leukocytes in a tissue specific manner.
Preparation Note
Deoxynivalenol ready-made solution (1 mg/ml in Ethanol: 2-propanol 95:5) can be diluted in aqueous buffers to a working concentration of 0.1-1 μg/ml (1:1000).
signalword
Danger
hcodes
Hazard Classifications
Eye Irrit. 2 - Flam. Liq. 2
Storage Class
3 - Flammable liquids
wgk
WGK 1
flash_point_f
57.2 °F
flash_point_c
14 °C
Regulatory Information
高风险级别生物产品--毒素类产品
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