所有图片(1)
别名:
2,4-二羟基-6-(6α,10-二羟基十一烷基)苯甲酸 μ-内酯
经验公式（希尔记法）:
C18H26O5
CAS号:
分子量:
322.40
EC 号:
MDL编号:
UNSPSC代码:
12352200
PubChem化学物质编号:
NACRES:
NA.77
推荐产品
生物来源
synthetic (organic)
质量水平
无菌性
non-sterile
检测方案
~98% (HPLC)
形式
powder
药品控制
regulated under CDSA - not available from Sigma-Aldrich Canada
技术
UHPLC: suitable
溶解性
methanol: 1.96-2.04 mg/mL, clear, colorless to faintly yellow
运输
ambient
储存温度
−20°C
SMILES字符串
C[C@H]1CCC[C@H](O)CCCCCc2cc(O)cc(O)c2C(=O)O1
InChI
1S/C18H26O5/c1-12-6-5-9-14(19)8-4-2-3-7-13-10-15(20)11-16(21)17(13)18(22)23-12/h10-12,14,19-21H,2-9H2,1H3/t12-,14+/m0/s1
InChI key
DWTTZBARDOXEAM-GXTWGEPZSA-N
警示用语：
Danger
危险声明
危险分类
Repr. 2 - Skin Corr. 1B
WGK
WGK 3
闪点(°F)
Not applicable
闪点(°C)
Not applicable
个人防护装备
Eyeshields, Gloves, type P3 (EN 143) respirator cartridges
法规信息
监管及禁止进口产品
C Mastri et al.
Journal of steroid biochemistry, 23(3), 279-289 (1985-09-01)
It is now well established that the mycotoxin zearalenone and some of its derivatives possess oestrogenic activity. In the present study, the binding characteristics of [3H]zearalanol (P-1496) to different classes of sites including [1] the oestrogen receptor, [2] the higher
Mario Thevis et al.
Drug testing and analysis, 3(11-12), 777-783 (2011-11-19)
Zeranol ((7R,11S)-7,15,17-trihydroxy-11-methyl-12-oxabicyclo[12.4.0]octadeca-1(14),15,17-trien-13-one, also referred to as 7α-zearalanol, Ralone®, Frideron®, Ralgro®, etc.) is a semi-synthetic estrogenic veterinary drug with growth-promoting properties. Its use regarding animal husbandry has been prohibited in the European Union since 1981 and, due to its anabolic effects
Yosra Ayed et al.
Mutation research, 726(1), 42-46 (2011-09-06)
Zearalenone (ZEN) is a non-steroidal estrogenic mycotoxin produced by Fusarium fungi. It contaminates different components of the food chain and can cause serious economic and public health problems. The major metabolites of ZEN in various animal species are alpha- and
Zhanhui Wang et al.
Journal of molecular recognition : JMR, 24(5), 815-823 (2011-08-04)
The molecular recognition of hapten-antibody is a fundamental event in competitive immunoassay, which guarantees the sensitivity and specificity of immunoassay for the detection of haptens. The aim of this study is to investigate the correlation between binding ability of one
Michele Solfrizzo et al.
Analytical and bioanalytical chemistry, 401(9), 2831-2841 (2011-09-06)
Humans and animals can be simultaneously exposed through the diet to different mycotoxins, including aflatoxins, ochratoxin A, deoxynivalenol, zearalenone, and fumonisins, which are the most important. Evaluation of the frequency and levels of human and animal exposure to these mycotoxins
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