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Merck
CN

R2153

Sigma-Aldrich

RU 26752

≥98% (HPLC), solid

别名:

17α-Hydroxy-3-oxo-7α-propylpregn-4-ene-21-carboxylic acid γ-lactone

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关于此项目

经验公式(希尔记法):
C25H36O3
化学文摘社编号:
分子量:
384.55
MDL编号:
UNSPSC代码:
51111800
PubChem化学物质编号:
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方案

≥98% (HPLC)

表单

solid

溶解性

DMSO: soluble 20 mg/mL at 60 °C (warming up for 20 minutes)

储存温度

−20°C

SMILES字符串

[H][C@]12CC[C@@]3(C)[C@@]([H])(CC[C@@]34CCC(=O)O4)[C@]1([H])[C@H](CCC)CC5=CC(=O)CC[C@]25C

InChI

1S/C25H36O3/c1-4-5-16-14-17-15-18(26)6-10-23(17,2)19-7-11-24(3)20(22(16)19)8-12-25(24)13-9-21(27)28-25/h15-16,19-20,22H,4-14H2,1-3H3/t16-,19+,20+,22-,23+,24+,25-/m1/s1

InChI key

MOFIIHQCTIJVBB-JEHIOXJOSA-N

生化/生理作用

Mineralocorticoid receptor antagonist.
RU 26752 is a mineralocorticoid receptor antagonist.

象形图

Exclamation mark

警示用语:

Warning

危险声明

预防措施声明

危险分类

Acute Tox. 4 Oral - Aquatic Chronic 4

储存分类代码

11 - Combustible Solids

WGK

WGK 3

闪点(°F)

Not applicable

闪点(°C)

Not applicable

个人防护装备

dust mask type N95 (US), Eyeshields, Gloves

法规信息

新产品
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历史批次信息供参考:

分析证书(COA)

Lot/Batch Number

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Saaeha Rauz et al.
Investigative ophthalmology & visual science, 44(4), 1643-1651 (2003-03-27)
In peripheral sodium-transporting tissues, the serum- and glucocorticoid-regulated kinase (SGK) isoform-1 is an early corticosteroid target gene in the activation of epithelial sodium channels (ENaCs). Sodium transport across the human ocular nonpigmented and pigmented ciliary epithelial bilayer (NPE-PE) is essential
A Souque et al.
The Journal of steroid biochemistry and molecular biology, 57(5-6), 315-321 (1996-03-01)
To investigate the role of sulfhydryl groups in the interaction of agonists and antagonists with the human mineralocorticoid receptor (hMR) the effect of methyl methanethiosulfonate (MMTS) on free and liganded-hMR was examined. hMR was expressed in insect cells (Sf9) using
Sanjay Rajagopalan et al.
The Medical clinics of North America, 87(2), 441-457 (2003-04-16)
Based upon the results of the RALES trial and accumulating evidence about the role of aldosterone and aldosterone receptor antagonism in various disease states, the authors anticipate that aldosterone receptor antagonists will become standard therapy, along with ACE inhibitors and
M Mirshahi et al.
Biochemical and biophysical research communications, 270(3), 811-815 (2000-04-25)
PCR analysis and Western blotting revealed the expression of the mineralocorticoid receptor (MCR) and the epithelial sodium channel (ENaC) genes at the level of RNA, DNA, and protein in several leukemic cell lines, fibroblasts from human cornea, and epithelial cells
G Lazar et al.
Biochimica et biophysica acta, 1033(1), 41-48 (1990-01-29)
Cardiac cytosol from adrenalectomized rats was radiolabelled with 10 nM tritiated RU 26752, R 5020 or aldosterone, to saturate the mineralocorticoid receptor (MCR) in the presence of 1 microM RU 38486 to block the glucocorticoid and progestin receptors. Free steroids

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