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16α-hydroxy Estrone Sale

(Synonyms: 16ALPHA-羟基雌酚酮,16αOHE) 目录号 : GC41950

A hydroxylated metabolite of estrone

16α-hydroxy Estrone Chemical Structure

Cas No.:566-76-7

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1mg
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5mg
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10mg
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Sample solution is provided at 25 µL, 10mM.

Description

The naturally-occurring estrogens are estrone , estradiol , and estriol . 16α-hydroxy Estrone (16α-OHE1) is a hydroxylated metabolite of E1 as well as an interconversion product with E2. E1 is 16α-hydroxylated by cytochrome P450 (CYP) isoforms, including CYP1A1, CYP3A5, CYP3A4, and CYP3A7, with CYP3A5 being breast-specific. 16α-OHE1 is sulphatized or glucuronidated before excretion. It is increased in rheumatoid arthritis and decreased by physical activity. Unlike the parent estrogens and other hydroxylated metabolites of E1, 16α-OHE1 binds covalently and persistently activates estrogen receptors. In addition, this metabolite increases cell proliferation and does not suppress TNF-α secretion, whereas other estrogen metabolites are not pro-proliferative and have marked effects on TNF-α secretion. The levels of 16α-OHE1 are increased in some forms of hormone therapy. Because hormone therapy increases breast cancer risk, 16α-OHE1 has been implicated as a risk factor for breast cancer, although supportive data remains elusive.

化学性质

Cas No. 566-76-7 SDF
别名 16ALPHA-羟基雌酚酮,16αOHE
Canonical SMILES O=C1[C@H](O)C[C@@]2([H])[C@]3([H])CCC4=CC(O)=CC=C4[C@@]3([H])CC[C@@]21C
分子式 C18H22O3 分子量 286.4
溶解度 DMF: 30 mg/ml,DMF:PBS (pH 7.2) (1:5): 0.15 mg/ml,DMSO: 20 mg/ml 储存条件 Store at -20°C
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1 mg 5 mg 10 mg
1 mM 3.4916 mL 17.4581 mL 34.9162 mL
5 mM 0.6983 mL 3.4916 mL 6.9832 mL
10 mM 0.3492 mL 1.7458 mL 3.4916 mL
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