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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/REAXYS Number:
2484202
MDL number:
UNSPSC Code:
51111800
PubChem Substance ID:
NACRES:
NA.77
En este momento no podemos mostrarle ni los precios ni la disponibilidad

Nombre del producto

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

biological source

synthetic (organic)

Quality Level

assay

≥98.00% (TLC)

form

powder

solubility

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

shipped in

ambient

storage temp.

2-8°C

SMILES string

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

InChI key

AWARIMYXKAIIGO-UYGYUSPXSA-N

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General description

β-Estradiol-6-one 6-(O-carboxymethyloxime) is a derivative of 17β-estradiol.[1]

Storage Class

11 - Combustible Solids

wgk_germany

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

Eyeshields, Gloves, type N95 (US)


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C J Meijer et al.
Virchows Archiv. B, Cell pathology including molecular pathology, 40(1), 27-37 (1982-01-01)
The present study defines criteria for determining the presence of estrogen-receptors in human breast carcinomas demonstrated by a histochemical assay using 17 beta-estradiol-carboxy-methyl-oxim-bovine serum albumen-FITC. The criteria were: 1) the percentage of cells showing fluorescence; 2) the intensity of the
M Malawer et al.
Journal of surgical oncology, 25(3), 148-152 (1984-03-01)
Hormonal receptors of giant cell tumors (GCTs) have not been previously reported. Five cases of GCT of bone were analyzed for estrogen and progesterone binding. Frozen sections were studied by a histochemical method, using 17-beta-6-CMOBSA-FITC and 11-alpha-hydroxyprogesterone-HS-BSA-TMRITC. Cytoplasmic fluorescence with
Markus Lacorn et al.
Journal of immunological methods, 297(1-2), 225-236 (2005-03-22)
17beta-estradiol (E2) concentrations are in the low pg/ml range in plasma. To develop a sensitive enzyme immunoassay (EIA) for E2-determination a highly specific antibody raised against a 6-carboxymethyl (CMO)-E2-bovine serum albumine conjugate was used. Based on 6-CMO-E2 and 6-amino-E2, four
H Zheng et al.
Yao xue xue bao = Acta pharmaceutica Sinica, 26(5), 336-340 (1991-01-01)
Estradiol conjugate has been used as a tracer to detect estrogen receptor of human mammary cancer cells. In order to look for more stable carrier of fluorescent estradiol conjugate, we substituted polyethyleneglycol (PEG) for bovine serum albumin (BSA) and synthsized
M Hill et al.
Journal of chromatography. B, Biomedical sciences and applications, 691(1), 187-191 (1997-03-28)
The conventional methods for characterization of steroid immunogens are based on the determination of the total amount of hapten bound to the protein carrier either by the UV spectroscopy or titration of unsubstituted amino groups. These methods do not allow

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