CAS NO: | 5975-78-0 |
包装 | 价格(元) |
1mg | 电议 |
5mg | 电议 |
Cas No. | 5975-78-0 |
别名 | 玉米赤霉酮 |
化学名 | (3S)-3,4,5,6,9,10,11,12-octahydro-14,16-dihydroxy-3-methyl-1H-2-benzoxacyclotetradecin-1,7(8H)-dione |
Canonical SMILES | OC1=C(C(O[C@@H](C)CCCC(CCCCC2)=O)=O)C2=CC(O)=C1 |
分子式 | C18H24O5 |
分子量 | 320.4 |
溶解度 | Soluble in DMSO |
储存条件 | Store at -20℃ |
General tips | For obtaining a higher solubility , please warm the tube at 37 ℃ and shake it in the ultrasonic bath for a while. |
Shipping Condition | Evaluation sample solution : ship with blue ice All other available size: ship with RT , or blue ice upon request |
产品描述 | Zearalanone (ZAN) is an estrogen receptor agonist and also an androgen receptor antagonist [1]. Zearalenone (ZEN), a β-resorcyclic acid lactone (RAL), is a non-steroidal estrogenic mycotoxin biosynthesized by several Fusarium species. Zearalenone (ZEN) is the well-known mycotoxin present in numerous agricultural products [1][2][3][4]. In the human endometrial Ishikawa cell line, zearalenone (ZEN) exhibited strong oestrogenicity [4].When incubated Fusarium semitectum on sorghum, the ratio of ZAN to ZEN remained constant after 5 days, suggesting that ZAN might not be suitable for use as an internal standard [5]. Zearalanone, a major phase I metabolite of zearalenone (ZEN), is an estrogen receptor agonist and also an androgen receptor antagonist. In MCF-7 cells, Zearalanone strongly induced cell proliferation with EC50 value of 1.21 nM and showed significant estrogenic activity. Zearalanone behaved as full hERα agonist. In PALM cells, Zearalanone acted as a hAR antagonist that strongly inhibited the luciferase activity induced by 0.3 nM of R1881, the synthetic androgen [1]. References: |