| Weight | 366.41 g/mol |
|---|---|
| Formula | C19H26O7 |
| Hydrogen Acceptors | 7 |
| Hydrogen Donors | 1 |
| Aromatic Rings | 0 |
| Rotatable Bonds | 3 |
Anguidine (2270-40-8)
diacetoxyscirpenol · NSC 141537
Score:
#792 in Biochemistry
,
#2154 in Biology
,
#2649 in Chemistry
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- Efficacy of a Hydrated Sodium Calcium Aluminosilicate to Reduce the Toxicity of Aflatoxin and Diacetoxyscirpenol (Poultry Science, 1993)
- Metabolism of three trichothecene ycotoxins, T-2 toxin, diacetoxyscirpenol and deoxynivalenol, by bovne rumen microorganisms (Journal of Chromatography B: Biomedical Sciences and Applications, 1987)
- Immunosuppressive activity of Fusarium toxins. Effects on antibody synthesis and skin grafts of crude extracts, T2-toxin and diacetoxyscirpenol. (Immunology, 1979)
- Mycotoxicosis Caused by a Single Dose of T-2 Toxin or Diacetoxyscirpenol in Broiler Chickens (Veterinary Pathology, 1981)
- Thin layer chromatographic determination of aflatoxins, ochratoxins, sterigmatocystin, zearalenone, citrinin, T-2 toxin, diacetoxyscirpenol, penicillic acid, patulin, and penitrem A. (Journal - Association of Official Analytical Chemists, 1979)
- Transgenic expression of the TRI101 or PDR5 gene increases resistance of tobacco to the phytotoxic effects of the trichothecene 4,15-diacetoxyscirpenol (Plant Science, 2000)
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Predict GHS Hazards for Any Chemical in silico.
Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. - diacetoxyscirpenol
- NSC 141537
-
SMILESCC1=CC2C(CC1)(C3(C(C(C(C34CO4)O2)O)OC(=O)C)C)COC(=O)C
-
InChIKeyAUGQEEXBDZWUJY-UHFFFAOYSA-N
- Pubchem - Anguidine
- Wikipedia - Diacetoxyscirpenol
Diacetoxyscirpenol (DAS), also called anguidine, is a mycotoxin from the group of type A trichothecenes. It is a secondary metabolite product of fungi of the genus Fusarium and may cause toxicosis in farm animals.
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