779717
19-羟基-4-雄甾烯-3,17-二酮
≥90% (HPLC)
别名:
19-羟基雄烯二酮, 4-雄甾烯-3,17-二酮-19-醇
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关于此项目
经验公式（希尔记法）:
C19H26O3
化学文摘社编号:
分子量:
302.41
Beilstein:
2567249
EC 号:
MDL编号:
UNSPSC代码:
12352103
PubChem化学物质编号:
方案
≥90% (HPLC)
表单
crystals
旋光性
[α]/D +190±5°, c = 1 in chloroform
储存温度
−20°C
SMILES字符串
C[C@]12CC[C@H]3[C@@H](CCC4=CC(=O)CC[C@]34CO)[C@@H]1CCC2=O
InChI
1S/C19H26O3/c1-18-8-7-16-14(15(18)4-5-17(18)22)3-2-12-10-13(21)6-9-19(12,16)11-20/h10,14-16,20H,2-9,11H2,1H3/t14-,15-,16-,18-,19+/m0/s1
InChI key
XGUHPTGEXRHMQQ-BGJMDTOESA-N
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包装
Bottomless glass bottle. Contents are inside inserted fused cone.
C K Sites et al.
Journal of assisted reproduction and genetics, 13(6), 505-510 (1996-07-01)
Our objective was to develop a sensitive in vitro bioassay for follicle-stimulating hormone (FSH) that does not require the housing of animals in a research facility. Porcine granulosa cells from 1- to 3-mm follicles were cultured on laminin for 48
M Numazawa et al.
Steroids, 63(2), 62-69 (1998-03-28)
Reaction of androst-5-en-17-one (1) with hypobromous acid using a short reaction time (30 min) along with a careful isolation procedure gave, for the first time, the addition product, 5 alpha-bromo-6 beta-hydroxyandrostan-17-one (3), in 43% yield. This bromohydrin was much more
M E Hähnel et al.
The Australian & New Zealand journal of obstetrics & gynaecology, 29(3 Pt 1), 238-241 (1989-08-01)
Because of the association of preeclampsia with hydatidiform mole, and since levels of 19-hydroxyandrostenedione (19-OH-A) and androstenedione (A) are raised in hypertensive diseases of pregnancy, we compared plasma 19-OH-A and A in hydatidiform mole patients with control early pregnant women.
H Sekihara et al.
The Journal of endocrinology, 138(1), 31-40 (1993-07-01)
We have reported that 19-hydroxyandrostenedione (19-OH-A-dione) amplifies the sodium-retaining action of aldosterone. To evaluate whether it also amplifies the hypertensive action of small doses of aldosterone, mononephrectomized rats were given 0.5 mg aldosterone, 10 mg 19-OH-A-dione or a combination of
H Murase et al.
The Journal of steroid biochemistry and molecular biology, 38(3), 331-337 (1991-03-01)
To verify the aldosterone amplifying action of 19-hydroxyandrostenedione (19-OH-AD), we investigated [3H]aldosterone and [3H]19-OH-AD binding to type I (mineralocorticoid) receptor in the renal cytosol of adrenalectomized and ovariectomized rat, and human mononuclear leucocytes (MNL). In the [3H]aldosterone binding study, the
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