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E1636

Sigma-Aldrich

β-Estradiol 3,17-disulfate dipotassium salt

≥95%

Sinônimo(s):

1,3,5(10)-Estratriene 3,17β-disulfate, 3,17β-Dihydroxy-1,3,5(10)-estratriene disulfate

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About This Item

Fórmula linear:
C18H22O8S2K2
Número CAS:
17046-60-5
Peso molecular:
508.69
Número MDL:
MFCD00058502
Código UNSPSC:
51111800
ID de substância PubChem:
24894425
NACRES:
NA.77
fonte biológica:
synthetic
Formulário:
powder
Ensaio:
≥95%

fonte biológica

synthetic

Ensaio

≥95%

Formulário

powder

técnica(s)

inhibition assay: suitable

solubilidade

water: 50 mg/mL, clear, colorless

Condições de expedição

ambient

temperatura de armazenamento

−20°C

cadeia de caracteres SMILES

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

InChI

1S/C18H24O8S2.K.H/c1-18-9-8-14-13-5-3-12(25-27(19,20)21)10-11(13)2-4-15(14)16(18)6-7-17(18)26-28(22,23)24;;/h3,5,10,14-17H,2,4,6-9H2,1H3,(H,19,20,21)(H,22,23,24);;/t14-,15-,16+,17+,18+;;/m1../s1

chave InChI

CPIZVUIARARPNO-LBARCDFESA-N

Ações bioquímicas/fisiológicas

Among other effects, this conjugated estrogen selectively inhibits glutathione S-transferases.

Código de classe de armazenamento

11 - Combustible Solids

Classe de risco de água (WGK)

WGK 3

Ponto de fulgor (°F)

Not applicable

Ponto de fulgor (°C)

Not applicable

Equipamento de proteção individual

Eyeshields, Gloves, type N95 (US)

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Certificados de análise (COA)

Lot/Batch Number
BGBB6707V
078K37773
078K37772
078K37771
078K3777

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J J Barycki et al.
Archives of biochemistry and biophysics, 345(1), 16-31 (1997-09-01)
3beta-(Iodoacetoxy)dehydroisoandrosterone (3beta-IDA), an analogue of the electrophilic substrate, Delta5-androstene-3,17-dione, as well as an analogue of several other steroid inhibitors of glutathione S-transferase, was tested as an affinity label of rat liver glutathione S-transferase, isozyme 1-1. A time-dependent loss of enzyme
Angelo Quaranta et al.
PloS one, 4(11), e7699-e7699 (2009-11-06)
Dramatic declines in amphibian populations have been described all over the world since the 1980s. The evidence that the sensitivity to environmental threats is greater in amphibians than in mammals has been generally linked to the observation that amphibians are
J D Bain et al.
Steroids, 43(6), 603-619 (1984-06-01)
The efficiencies for estrogen conjugate hydrolysis were compared between enzyme hydrolysis, acid solvolysis and a new method, ammonolysis. Samples included: 1) crystalline 1,3,5(10)-estratriene-3, 17 beta-diol disulfate (estradiol 3,17-disulfate), 2) squirrel monkey urine collected following an intravenous injection of [2,4,6,7-H] 1,3,5(10)-estratriene-3,17
A H Maas et al.
Nederlands tijdschrift voor geneeskunde, 145(2), 65-69 (2001-02-28)
Coronary heart disease develops on average 10-15 years later in women than in men and is uncommon before menopause. 17 beta-estradiol has atheroprotective properties through rapid vasodilatory effects on the endothelium by stimulating nitric monoxide production and longer-term actions by
Fanfan Zhou et al.
European journal of pharmaceutical sciences : official journal of the European Federation for Pharmaceutical Sciences, 27(5), 518-523 (2005-11-01)
Human organic anion transporter 4 (hOAT4) belongs to a family of organic anion transporters which play critical roles in the body disposition of clinically important drugs, including anti-HIV therapeutics, anti-tumor drugs, antibiotics, anti-hypertensives, and anti-inflammatories. hOAT4 is expressed in the
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