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质量水平
方案
≥98% (CP)
表单
powder
技术
mass spectrometry (MS): suitable
储存温度
−20°C
SMILES字符串
C[C@]12CC[C@@H](O)C[C@H]1CC[C@H]3[C@@H]4CC[C@H](C(=O)CO)[C@@]45C[C@H](O[C@@H]5O)[C@H]23
InChI
1S/C21H32O5/c1-20-7-6-12(23)8-11(20)2-3-13-14-4-5-15(16(24)10-22)21(14)9-17(18(13)20)26-19(21)25/h11-15,17-19,22-23,25H,2-10H2,1H3/t11-,12-,13+,14+,15-,17+,18-,19+,20+,21-/m1/s1
InChI key
JDEYOKPHRJVBQO-BMDKAXIVSA-N
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相关类别
包装
This product may be available from bulk stock and can be packaged on demand. For information on pricing, availability and packaging, please contact Stable Isotopes Customer Service.
警示用语：
Warning
危险声明
预防措施声明
危险分类
Skin Sens. 1
储存分类代码
11 - Combustible Solids
WGK
WGK 3
闪点(°F)
Not applicable
闪点(°C)
Not applicable
T Miyazaki et al.
Endocrinologia japonica, 32(4), 505-509 (1985-08-01)
After a large amount of aldosterone was injected into a male rabbit, urine was collected for 48 h. Separation of urinary aldosterone metabolites into monoglucosiduronate fraction and monosulphate fraction was carried out by a combination of countercurrent distribution and DEAE-Sephadex
High-performance liquid chromatography in the radioimmunoassay of urinary tetrahydroaldosterone.
O B Holland et al.
Journal of chromatography, 385, 393-396 (1987-01-09)
J Wacker et al.
Endocrine research, 21(1-2), 197-202 (1995-02-01)
In the present study the aldosterone-18-glucuronide and tetrahydroaldosterone values in 24 hour urine collections of healthy nonpregnant women, women with normal pregnancies and women with pregnancy induced hypertension (PIH) were compared. In pregnancy an elevated excretion of both aldosterone metabolites
M Egfjord et al.
Metabolism: clinical and experimental, 42(4), 470-476 (1993-04-01)
The effect of uremia on hepatic metabolism of aldosterone was studied in the isolated perfused liver of female Wistar rats. Uremia was induced by five-sixths partial nephrectomy 4 weeks before experiments. Isolated livers of normal and uremic rats were perfused
T Miyazaki et al.
Endocrinologia japonica, 34(2), 161-169 (1987-04-01)
Analysis of urinary metabolites of [1, 2-3H]-aldosterone was performed in the male guinea-pig. Separation of urinary metabolites was carried out by countercurrent distribution followed by DEAE-Sephadex A-25 column chromatography. A major component was obtained which was both hydrolyzable with sulphatase
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