| Source: | Giberella zeae | | Synonyms | FES, Compound F-2, Toxin F2. IUPAC name: （3S,11E）-14,16-dihydroxy-3-methyl-3,4,5,6,9,10-hexahydro-1H-2-benzoxacyclotetradecine-1,7（8H）-dione | | Description: | Zearalenone is a naturally occurring estrogen, a mycotoxin from resorcylic acid lactone group. It is named after the species name of the fungus that produces it. | | CAS number: | 17924-92-4 | | Merck index: | 13,10169 | | Molecular weight: | 318.4 | | Structure: | 
| | Molecular Formula: | C18H22O5 | Solubility
information: | Solubility of Zearalenone in water is about 0.002g/100ml. Zearalenone is slightly soluble in hexane and progressively more in benzene, acetonitrile, dichloromethane, methanol, acetone. | | Specifications | | | Appearance: | White powder | | Purity: | At least 98% by TLC, HPLC | | λmax: | （in methanol） 236,274,316. | | Melting point: | 159°C - 163°C | | Solubility: | Clear colourless solution at 5mg/ml Methanol | | Storage: | -20°C. | | Applications: | The resorcylic acid lactones have estrogenic activity.
Zearalenone and its derivates were used as veterinary anabolic or estrogen substitutes. | | Classification: | A resorcylic acid lactone
Mycotoxin | | Related products: | Deoxynivalenol （Vomitoxin）, Brefeldin | | Warnings: |  | | | For Research use only. Not for Human or Drug use
GMP/API grade available on request
7AAD by Fermentek is not produced from or contains any ingredients from animal origin.
No genetically modified organisms are used. | | Publications | | | | Songsermsakul P, Sontag G, Cichna-Markl M, Zentek J, Razzazi-Fazeli E.
Determination of zearalenone and its metabolites in urine, plasma and faeces of horses by HPLC-APCI-MS.
J Chromatogr B Analyt Technol Biomed Life Sci. 2006 Jul 7 | | | Ding X, Lichti K, Staudinger JL.
The mycoestrogen zearalenone induces CYP3A through activation of the pregnane X receptor.
Toxicol Sci. 2006 Jun;91（2）:448-55 | |
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