Z0417
β-玉米赤霉醇
~98% (HPLC), nonsteroidal estrogen, powder
别名:
2,4-二羟基-6-（6β1,10-二羟基十一基 ] 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
UNSPSC Code:
12352200
PubChem Substance ID:
NACRES:
NA.77
MDL number:
产品名称
β-玉米赤霉醇, ~98% (HPLC)
SMILES string
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-JSGCOSHPSA-N
sterility
non-sterile
assay
~98% (HPLC)
form
powder
drug control
regulated under CDSA - not available from Sigma-Aldrich Canada
availability
not available in Canada
solubility
methanol: 19.60-20.40 mg/mL, clear, colorless to faintly yellow
shipped in
ambient
storage temp.
−20°C
Quality Level
Gene Information
rat ... Ar(24208)
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
Erika Pfeiffer et al.
Molecular nutrition & food research, 54(10), 1468-1476 (2010-04-17)
Glucuronidation constitutes an important pathway in the phase II metabolism of the mycotoxin zearalenone (ZEN) and the growth promotor α-zearalanol (α-ZAL, zeranol), but the enzymology of their formation is yet unknown. In the present study, ZEN, α-ZAL and four of
B H Migdalof et al.
Xenobiotica; the fate of foreign compounds in biological systems, 13(4), 209-221 (1983-04-01)
The disposition of [3H]zeranol has been studied in the female Wistar rat, New Zealand rabbit, beagle dog, rhesus monkey and man. The blood elimination half-life of total radioactivity in rabbit was 26 h, monkey 18 h and man 22 h.
F M Launay et al.
Food additives and contaminants, 21(1), 52-62 (2004-01-28)
A method is described for the quantitative determination of the veterinary drug zeranol, its epimer taleranol and the mycotoxins zearalenone, alpha-zearalenol and beta-zearalenol in bovine urine. The method is based on liquid chromatography coupled to negative-ion electrospray mass spectrometry-mass spectrometry
H Malekinejad et al.
Veterinary research communications, 30(4), 445-453 (2006-02-28)
The enzymes 3alpha- and 3beta-hydroxysteroid dehydrogenase (3alpha- and 3beta-HSD) play a pivotal role in synthesis of various steroid hormones including oestradiol and testosterone. The structure of the mycotoxin zearalenone resembles many characteristics of steroids and binds to oestrogen receptors as
Zearalenones: characterization of the estrogenic potencies and receptor interactions of a series of fungal beta-resorcylic acid lactones.
B S Katzenellenbogen et al.
Endocrinology, 105(1), 33-40 (1979-07-01)
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