ChemicalBook--->CAS DataBase List--->911392-40-0

911392-40-0

911392-40-0 Structure

911392-40-0 Structure
IdentificationBack Directory
[Name]

Nivalenol-13C15 solution
[CAS]

911392-40-0
[Synonyms]

13C15-Nivalenol
Nivalenol-13C15 solution
13C15]-Nivalenol-25 μg/mL in ACN
[EINECS(EC#)]

804-499-3
[Molecular Formula]

C15H20O7
[MDL Number]

MFCD26142914
[MOL File]

911392-40-0.mol
[Molecular Weight]

327.2
Chemical PropertiesBack Directory
[density ]

1.582±0.10 g/cm3(Temp: 25 °C; Press: 760 Torr)(predicted)
[Fp ]

2℃
[storage temp. ]

-20°C
[solubility ]

Acetonitrile: Soluble
Safety DataBack Directory
[Symbol(GHS) ]


GHS02,GHS07
[Signal word ]

Danger
[Hazard statements ]

H225-H302+H312+H332-H319
[Precautionary statements ]

P210-P280-P305+P351+P338
[Hazard Codes ]

F,Xn
[Risk Statements ]

11-20/21/22-36
[Safety Statements ]

16-36/37
[RIDADR ]

UN 1648 3 / PGII
[WGK Germany ]

2
Hazard InformationBack Directory
[Uses]

Nivalenol-13C15 is the 13C labeled Nivalenol (HY-N6801)[1]. Nivalenol, classified as type B trichotecenes toxins produced by Fusarium graminearum, is a fungal metabolite present in agricultural product[2]. Nivalenol induces cell death through caspase-dependent mechanisms and via the intrinsic apoptotic pathway. Nivalenol affects the immune system, causes emesis, growth retardation, reproductive disorders and has a haematotoxic/myelotoxic effect[3].
[storage]

Store at -20°C
[References]

[1] Russak EM, et al. Impact of Deuterium Substitution on the Pharmacokinetics of Pharmaceuticals. Ann Pharmacother. 2019 Feb;53(2):211-220. DOI:10.1177/1071100718790255
[2] Bry?a M, et al. Natural Occurrence of Nivalenol, Deoxynivalenol, and Deoxynivalenol-3-Glucoside in Polish Winter Wheat. Toxins (Basel). 2018 Feb 13;10(2). DOI:10.3390/toxins10020081
[3] Aupanun S, et al. Individual and combined mycotoxins deoxynivalenol, nivalenol, and fusarenon-X induced apoptosis in lymphoid tissues of mice after oral exposure. Toxicon. 2019 Jul;165:83-94. DOI:10.1016/j.toxicon.2019.04.017
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