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Estropipate/雌酮硫酸酯哌嗪 {[allProObj[0].p_purity_real_show]}

货号:A340804 同义名: Piperazine estrone sulfate; Estrone sulfate piperazine salt

Estropipate, deriving from estrogen, is used to treat symptoms of menopause and to prevent osteoporosis.

HazMat Fee +

There will be a HazMat fee per item when shipping a dangerous goods. The HazMat fee will be charged to your UPS/DHL/FedEx collect account or added to the invoice unless the package is shipped via Ground service. Ship by air in Excepted Quantity (each bottle), which is up to 1g/1mL for class 6.1 packing group I or II, and up to 25g/25ml for all other HazMat items.

Type HazMat fee for 500 gram (Estimated)
Excepted Quantity USD 0.00
Limited Quantity USD 15-60
Inaccessible (Haz class 6.1), Domestic USD 80+
Inaccessible (Haz class 6.1), International USD 150+
Accessible (Haz class 3, 4, 5 or 8), Domestic USD 100+
Accessible (Haz class 3, 4, 5 or 8), International USD 200+
Estropipate/雌酮硫酸酯哌嗪 化学结构 CAS号:7280-37-7
Estropipate/雌酮硫酸酯哌嗪 化学结构
CAS号:7280-37-7
Estropipate/雌酮硫酸酯哌嗪 3D分子结构
CAS号:7280-37-7
Estropipate/雌酮硫酸酯哌嗪 化学结构 CAS号:7280-37-7
Estropipate/雌酮硫酸酯哌嗪 3D分子结构 CAS号:7280-37-7
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Estropipate/雌酮硫酸酯哌嗪 纯度/质量文件 产品仅供科研

货号:A340804 标准纯度: {[allProObj[0].p_purity_real_show]}
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Estropipate/雌酮硫酸酯哌嗪 生物活性

描述 Estropipate (EPP) is a form of estrogen, used to treat symptoms of menopause, also used to prevent osteoporosis. EPP and its free-base form (i.e., estrone sulfate) showed a potent and high degree of selectivity in inhibiting the OATP1B1-mediated transport of rosuvastatin with an IC50 value averaging 0.05 ± 0.01 and 0.12 ± 0.07 μM for human and cynomolgus monkey OATP1B1, respectively, whereas weak inhibition was observed for human and monkey OATP1B3, OATP2B1, sodium-taurocholate cotransporting polypeptide (NTCP), organic anion transporter 2, and organic cation transporter 1 with IC50 values ranging from 8.6 to 64.0 μM[2]. Estropipate (estrone-3-sulfate stabilized with piperazine) was the most selective OATP1B1 inhibitor (IC50 = 0.06 mM vs. 19.3 mM for OATP1B3)[3]. All the estrogens exerted stimulatory effects in the postmenopausal specimens that were comparable to those observed in the premenopausal proliferative-phase specimens. Estropipate, subcutaneous estradiol, and conjugated estrogens had some hyperphysiologic effects[4].

Estropipate/雌酮硫酸酯哌嗪 参考文献

[1]Bagdade JD, Subbaiah PV. Effects of estropipate treatment on plasma lipids and lipoprotein lipid composition in postmenopausal women. J Clin Endocrinol Metab. 1991 Feb;72(2):283-6.

[2]Zhang Y, Panfen E, Fancher M, Sinz M, Marathe P, Shen H. Dissecting the Contribution of OATP1B1 to Hepatic Uptake of Statins Using the OATP1B1 Selective Inhibitor Estropipate. Mol Pharm. 2019 Jun 3;16(6):2342-2353

[3]Gui C, Obaidat A, Chaguturu R, Hagenbuch B. Development of a cell-based high-throughput assay to screen for inhibitors of organic anion transporting polypeptides 1B1 and 1B3. Curr Chem Genomics. 2010 Mar 1;4:1-8

[4]Whitehead MI, Townsend PT, Pryse-Davies J, Ryder TA, King RJ. Effects of estrogens and progestins on the biochemistry and morphology of the postmenopausal endometrium. N Engl J Med. 1981 Dec 31;305(27):1599-605

Estropipate/雌酮硫酸酯哌嗪 实验方案

计算器
存储液制备 1mg 5mg 10mg

1 mM

5 mM

10 mM

2.29mL

0.46mL

0.23mL

11.45mL

2.29mL

1.15mL

22.91mL

4.58mL

2.29mL

Estropipate/雌酮硫酸酯哌嗪 技术信息

CAS号7280-37-7
分子式C22H32N2O5S
分子量 436.56
SMILES Code C[C@]1([C@](CC2)([H])[C@]3([H])CCC4=C(C=CC(OS(=O)(O)=O)=C4)[C@@]3([H])CC1)C2=O.N5CCNCC5
MDL No. MFCD00867399
别名 Piperazine estrone sulfate; Estrone sulfate piperazine salt; Ogen; Harmogen; Pipestrone
运输蓝冰
InChI Key HZEQBCVBILBTEP-ZFINNJDLSA-N
Pubchem ID 5284555
存储条件

In solvent -20°C: 3-6个月 -80°C: 12个月

Pure form Inert atmosphere, 2-8°C

溶解方案

DMSO: 105 mg/mL(240.51 mM),配合低频超声助溶,注意:DMSO长时间开封后,会吸水并导致溶解能力下降,请避免使用长期开封的DMSO

请根据您的动物给药指南选择适当的溶解方案。
以下溶解方案都请先按照体外实验的方式配制澄清的储备液,再依次添加助溶剂:
——为保证实验结果的可靠性,澄清的储备液可以根据储存条件,适当保存;体内实验的工作液,建议现用现配,当天使用; 以下溶剂前显示的百分比是指该溶剂在终溶液中的体积占比;如在配制过程中出现沉淀、析出现象,可以通过加热和/或超声的方式助溶
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