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Merck

E0251

Sigma-Aldrich

Estrone 3-sulfate sodium salt

contains ~35% Tris as stabilizer

Synonym(e):

1,3,5(10)-Estratrien-17-one 3-sulfate

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About This Item

Lineare Formel:
C18H21O5SNa
CAS-Nummer:
Molekulargewicht:
372.41
MDL-Nummer:
UNSPSC-Code:
12352202
PubChem Substanz-ID:
NACRES:
NA.77

Biologische Quelle

synthetic (organic)

Qualitätsniveau

Sterilität

non-sterile

Assay

≥98% (TLC)

Form

powder

Enthält

~35% Tris as stabilizer

Methode(n)

inhibition assay: suitable

Löslichkeit

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

Versandbedingung

ambient

Lagertemp.

−20°C

SMILES String

[Na].[H][C@]12CC[C@]3(C)C(=O)CC[C@@]3([H])[C@]1([H])CCc4cc(OS(O)(=O)=O)ccc24

InChI

1S/C18H22O5S.Na.H/c1-18-9-8-14-13-5-3-12(23-24(20,21)22)10-11(13)2-4-15(14)16(18)6-7-17(18)19;;/h3,5,10,14-16H,2,4,6-9H2,1H3,(H,20,21,22);;/t14-,15-,16+,18+;;/m1../s1

InChIKey

GQZNDBBLTDOIBE-DLEHHZMWSA-N

Leistungsmerkmale und Vorteile

This compound is a featured product for ADME Tox research. Click here to discover more featured ADME Tox products. Learn more about bioactive small molecules for other areas of research at sigma.com/discover-bsm.

Verpackung

Packungsgrösse basiert auf dem Steroidgehalt

Piktogramme

Health hazard

Signalwort

Danger

Gefahreneinstufungen

Carc. 2 - Lact. - Repr. 1A

Lagerklassenschlüssel

6.1C - Combustible acute toxic Cat.3 / toxic compounds or compounds which causing chronic effects

WGK

WGK 3

Flammpunkt (°F)

Not applicable

Flammpunkt (°C)

Not applicable


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Die Dokumentenbibliothek aufrufen

Christopher A Pearl et al.
Domestic animal endocrinology, 33(4), 451-459 (2006-10-13)
The steroid hormone regulation of the epididymis in a high estrogen producing animal like the boar is not currently understood. To test the hypothesis that the boar epididymis is an estrogen and androgen responsive tissue, the presence of estrogen and
E S M Silva et al.
Theriogenology, 86(7), 1749-1756 (2016-08-09)
The present study evaluated the influence of different regimens of estradiol benzoate (EB) treatments followed by a single dose of long-acting progesterone (LA P4) on plasma estrogen and P4 concentrations in noncyclic mares prepared as embryo recipients. Twenty-one anestrous mares
Emre Karakus et al.
Frontiers in pharmacology, 9, 941-941 (2018-09-07)
Estrogens play a pivotal role in the development and proliferation of hormone-dependent breast cancer. Apart from free estrogens, which can directly activate the estrogen receptor (ER) of tumor cells, sulfo-conjugated steroids, which maintain high plasma concentrations even after menopause, first
Takashi Nozawa et al.
Pharmaceutical research, 22(10), 1634-1641 (2005-09-24)
The aim of the study is to suppress the progress of estrogen-dependent breast cancer by inhibiting the membrane transporter, which mediates the internalization of estrone-3-sulfate as estrogen precursor in the cancer cells. The uptake of estrone-3-sulfate by estrogen-dependent breast cancer
Maria Karlgren et al.
Journal of medicinal chemistry, 55(10), 4740-4763 (2012-05-01)
The hepatic organic anion transporting polypeptides (OATPs) influence the pharmacokinetics of several drug classes and are involved in many clinical drug-drug interactions. Predicting potential interactions with OATPs is, therefore, of value. Here, we developed in vitro and in silico models

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