Z0292
α-玉米赤霉醇
~98% (HPLC), powder, mycotoxin
别名:
2,4-二羟基-6-(6α,10-二羟基十一烷基)苯甲酸 μ-内酯
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关于此项目
经验公式（希尔记法）:
C18H26O5
化学文摘社编号:
分子量:
322.40
NACRES:
NA.77
PubChem Substance ID:
UNSPSC Code:
12352200
EC Number:
247-769-0
MDL number:
产品名称
α-玉米赤霉醇, ~98% (HPLC)
InChI key
DWTTZBARDOXEAM-GXTWGEPZSA-N
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
SMILES string
C[C@H]1CCC[C@H](O)CCCCCc2cc(O)cc(O)c2C(=O)O1
biological source
synthetic (organic)
sterility
non-sterile
assay
~98% (HPLC)
form
powder
drug control
regulated under CDSA - not available from Sigma-Aldrich Canada
technique(s)
UHPLC: suitable
solubility
methanol: 1.96-2.04 mg/mL, clear, colorless to faintly yellow
shipped in
ambient
storage temp.
−20°C
Quality Level
signalword
Danger
hcodes
Hazard Classifications
Repr. 2 - Skin Corr. 1B
存储类别
8A - Combustible corrosive hazardous materials
wgk
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
Eyeshields, Gloves, type P3 (EN 143) respirator cartridges
法规信息
涉药品监管产品
此项目有
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
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
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
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
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
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