Vomitoxin
Title: Vomitoxin
CAS Registry Number: 51481-10-8
CAS Name: 12,13-Epoxy-3,7,15-trihydroxytrichothec-9-en-8-one
Additional Names: deoxynivalenol; dehydronivalenol
Molecular Formula: C15H20O6
Molecular Weight: 296.32
Percent Composition: C 60.80%, H 6.80%, O 32.40%
Literature References: Isoln of the trichothecene mycotoxin from Fusarium roseum and structure: N. Morooka et al., J. Food Hyg. Soc. Japan 13, 368 (1972); T. Yoshizawa, N. Morooka, Agric. Biol. Chem. 37, 2933 (1973). Isoln from F. graminearum: R. F. Vesonder et al., Appl. Microbiol. 26, 1008 (1973); eidem, Appl. Environ. Microbiol. 31, 280 (1976). Emetic and refusal activity in swine: D. M. Forsyth et al., ibid. 34, 547 (1977). HPLC analysis: G. A. Bennett et al., J. Am. Oil Chem. Soc. 58, 1002A (1981). Implicated as a chemical warfare agent with nivalenol, q.v. in Southeast Asia: N. Wade, Science 214, 34 (1981).
Properties: Fine needles from ethyl acetate + petr ether, mp 151-153°. [a]D25+6.35° (c = 0.07 in ethanol). uv max (ethanol): 218 nm (e 4500). LD50 i.p. in male, female mice (mg/kg): 70.0, 76.7 (Yoshizawa, Morooka).
Melting point: mp 151-153°
Optical Rotation: [a]D25+6.35° (c = 0.07 in ethanol)
Absorption maximum: uv max (ethanol): 218 nm (e 4500)
Toxicity data: LD50 i.p. in male, female mice (mg/kg): 70.0, 76.7 (Yoshizawa, Morooka)

Others monographs:
Ethinamate1-Naphthylamine-5-sulfonic AcidBeeswaxN,N'-Carbonyldiimidazole
3'-Adenylic AcidN,N'-DimethylthioureaSuintn-Butyl n-Butyrate
DihydroactinidiolideIdoxuridineKitolParthenolide
AcetamidePentrylImatinibSkatole
©2016 DrugLead US FDA&EMEA