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Merck
CN
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文件

安全信息

64107

Sigma-Aldrich

羟基洋地黄毒甙

≥99% (HPLC)

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别名:
Anhydrogitalin, Bigitalin, Pseudodigitoxin
经验公式（希尔记法）:
C41H64O14
CAS号:
4562-36-1
分子量:
780.94
EC 号:
224-934-5
MDL编号:
MFCD00021173
UNSPSC代码:
12352200
PubChem化学物质编号:
329759926
NACRES:
NA.25

质量水平

100

检测方案

≥99% (HPLC)

形式

solid

应用

metabolomics
vitamins, nutraceuticals, and natural products

SMILES字符串

C[C@H]1O[C@H](C[C@H](O)[C@@H]1O)O[C@H]2[C@@H](O)C[C@@H](O[C@@H]2C)O[C@H]3[C@@H](O)C[C@@H](O[C@@H]3C)O[C@H]4CC[C@@]5(C)[C@H](CC[C@@H]6[C@@H]5CC[C@]7(C)[C@H]([C@@H](O)C[C@]67O)C8=CC(=O)OC8)C4

InChI

1S/C41H64O14/c1-19-36(47)27(42)14-33(50-19)54-38-21(3)52-34(16-29(38)44)55-37-20(2)51-32(15-28(37)43)53-24-8-10-39(4)23(13-24)6-7-26-25(39)9-11-40(5)35(22-12-31(46)49-18-22)30(45)17-41(26,40)48/h12,19-21,23-30,32-38,42-45,47-48H,6-11,13-18H2,1-5H3/t19-,20-,21-,23-,24+,25+,26-,27+,28+,29+,30+,32+,33+,34+,35+,36-,37-,38-,39+,40-,41+/m1/s1

InChI key

LKRDZKPBAOKJBT-CNPIRKNPSA-N

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相关类别

应用

Gitoxin, a cardiac glycoside from the Woolly Foxglove (Digitalis lanata), may be studied for its potential cardiac applications similar to those of digoxin. Gitoxin is a starting material for the synthesis of gitoxin derivatives with activity as cardiac glycosides.

包装

Bottomless glass bottle. Contents are inside inserted fused cone.

象形图

Skull and crossbones
GHS06

警示用语：

Danger

危险声明

H300 + H310 + H330

危险分类

Acute Tox. 2 Dermal - Acute Tox. 2 Inhalation - Acute Tox. 2 Oral

WGK

WGK 3

法规信息

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L N Kadima et al.
Archives internationales de pharmacodynamie et de therapie, 258(1), 4-14 (1982-07-01)
Absorption of 3H-gitoxin and enterohepatic recirculation of the metabolites excreted in the bile were studied in the guinea-pig. Samples were assayed either by RIA or by selective counting of the radioactivity due to tritium. When administered as hydroalcoholic solutions into
G W Ponder et al.
Journal of chromatography. A, 659(1), 177-183 (1994-01-21)
A high-performance thin-layer chromatographic (HPTLC) method for the determination of digoxin and its related compounds digoxigenin bisdigitoxoside (DBD) and gitoxin in digoxin drug substance and tablets was developed. Separation of the three compounds was accomplished on a C18 wettable reversed-phase
Isolation and mass spectrometric identification of gitoxin metabolites excreted in bile.
L N Kadima et al.
European journal of drug metabolism and pharmacokinetics, 7(2), 111-117 (1982-01-01)
Mary K Short et al.
The Journal of biological chemistry, 277(19), 16365-16370 (2002-02-21)
Antibody 26-10, obtained in a secondary immune response, binds digoxin with high affinity (K(a) = 1.3 x 10(10) M(-1)) because of extensive shape complementarity. We demonstrated previously that mutations of the hapten contact residue HTrp-100 to Arg (where H refers
J Col et al.
International journal of clinical pharmacology, therapy, and toxicology, 19(7), 314-318 (1981-07-01)
Recent studies have demonstrated that the biovailability of gitoxin could be increased to 100%. Favorable pharmacokinetic parameters for this glycoside have also been found in humans. The present paper deals with the comparative hemodynamic effect of digoxin and gitoxin on
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