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Merck

K2126

Sigma-Aldrich

β-Estradiol-6-one 6-(O-carboxymethyloxime)

≥98.00% (TLC), powder

Sinónimos:

β-Estradiol-6-(O-carboxymethyl)oxime, 1,3,5(10)-Estratriene-3,17β-diol-6-one6-(O-carboxymethyloxime), 3,17β-Dihydroxy-1,3,5(10)-estratriene 6-(O-carboxymethyl)oxime, 6-Ketoestradiol 6-(O-carboxymethyloxime)

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About This Item

Fórmula empírica (notación de Hill):
C20H25NO5
Número de CAS:
Peso molecular:
359.42
Beilstein:
2484202
Número MDL:
Código UNSPSC:
51111800
ID de la sustancia en PubChem:
NACRES:
NA.77

Nombre del producto

β-Estradiol-6-one 6-(O-carboxymethyloxime),

origen biológico

synthetic (organic)

Nivel de calidad

Ensayo

≥98.00% (TLC)

Formulario

powder

solubilidad

ethanol: 19.60-20.40 mg/mL, clear, colorless to faintly yellow

Condiciones de envío

ambient

temp. de almacenamiento

2-8°C

cadena SMILES

C[C@]12CC[C@H]3[C@@H](C\C(=N\OCC(O)=O)c4cc(O)ccc34)[C@@H]1CC[C@@H]2O

InChI

1S/C20H25NO5/c1-20-7-6-13-12-3-2-11(22)8-15(12)17(21-26-10-19(24)25)9-14(13)16(20)4-5-18(20)23/h2-3,8,13-14,16,18,22-23H,4-7,9-10H2,1H3,(H,24,25)/b21-17-/t13-,14-,16+,18+,20+/m1/s1

Clave InChI

AWARIMYXKAIIGO-UYGYUSPXSA-N

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Descripción general

β-Estradiol-6-one 6-(O-carboxymethyloxime) is a derivative of 17β-estradiol.

Código de clase de almacenamiento

11 - Combustible Solids

Clase de riesgo para el agua (WGK)

WGK 3

Punto de inflamabilidad (°F)

Not applicable

Punto de inflamabilidad (°C)

Not applicable

Equipo de protección personal

Eyeshields, Gloves, type N95 (US)


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F Mao et al.
Yao xue xue bao = Acta pharmaceutica Sinica, 26(8), 611-614 (1991-01-01)
According to the character of structure and activity of the test reagents I-IV, two new reagents V and VI for detecting estrogen receptor of human mammary cancer cells were synthesized. This simplifies the route of synthesis and increases activity. Key
M Bourtourault et al.
Research communications in chemical pathology and pharmacology, 72(3), 273-284 (1991-06-01)
Female rats were immunized with mixed 17 beta-estradiol-6-carboxymethyloxime-bovine serum albumin and testosterone-3-carboxymethyloxime-bovine serum albumin. All the animals produced antibodies against the 2 haptens and were better immunized against 17 beta-estradiol than against testosterone. Nevertheless the disappearance of cyclic ovarian function
Mingzhe Liu et al.
Journal of bioscience and bioengineering, 111(5), 564-568 (2011-02-01)
Antibodies were covalently conjugated with poly(ethylene glycol) (PEG) and the properties of the PEGylated antibodies in organic media were investigated. Two types of monoclonal antibody were used in this study. One was a monoclonal antibody (abzyme) that was prepared against
C M Furnival et al.
The British journal of surgery, 70(8), 457-459 (1983-08-01)
The performance of a fluorescent cytochemical oestrogen receptor (ER) assay has been compared with an established dextran-coated charcoal ER assay in 85 cases of primary breast cancer. Both assays were performed on tissue samples from the same tumour, by independent
May L Chiu et al.
Biotechnology and applied biochemistry, 58(1), 75-82 (2011-03-31)
A convenient homogeneous enzyme immunoassay for estradiol is described. Unlike heterogeneous immunoassays, which require time-consuming separation steps or expensive automated systems, homogeneous immunoassays, wherein all reagents are freely suspended in bulk solution, can be simple and fast without costly instrumentation.

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