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Documenti fondamentali

D9404

Sigma-Aldrich

Digitoxigenin

Sinonimo/i:

3β,14-Dihydroxy-5β,20(22)-cardenolide, 3,14,21-Trihydroxy-20(22)-norcholenic acid lactone, 5β,20(22)-Cardenolide-3β,14-diol

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About This Item

Formula empirica (notazione di Hill):
C23H34O4
Numero CAS:
Peso molecolare:
374.51
Beilstein:
95448
Numero CE:
Numero MDL:
Codice UNSPSC:
12161900
ID PubChem:
NACRES:
NA.25

Descrizione

non-ionic

Livello qualitativo

Saggio

≥97.0% (TLC)

Stato

powder

PM

374.51 g/mol

Punto di fusione

253 °C (lit.)

Stringa SMILE

[H][C@]12CC[C@]3([H])[C@]([H])(CC[C@]4(C)[C@]([H])(CC[C@]34O)C5=CC(=O)OC5)[C@@]1(C)CC[C@H](O)C2

InChI

1S/C23H34O4/c1-21-8-5-16(24)12-15(21)3-4-19-18(21)6-9-22(2)17(7-10-23(19,22)26)14-11-20(25)27-13-14/h11,15-19,24,26H,3-10,12-13H2,1-2H3/t15-,16+,17-,18+,19-,21+,22-,23+/m1/s1
XZTUSOXSLKTKJQ-CESUGQOBSA-N

Informazioni sul gene

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Descrizione generale

Digitoxigenin is the aglycone of digitoxin.

Applicazioni

Digitoxigenin has been used in a study to assess its stereochemical effects in cancer cytotoxicity. It has also been used in a study to investigate the advantage of gold(I)-catalyzed glycosidation of glycosyl o-alkyl benzoates to assemble digitoxin.

Pittogrammi

Skull and crossbones

Avvertenze

Danger

Indicazioni di pericolo

Classi di pericolo

Acute Tox. 2 Oral

Codice della classe di stoccaggio

6.1A - Combustible acute toxic Cat. 1 and 2 / very toxic hazardous materials

Classe di pericolosità dell'acqua (WGK)

WGK 3

Dispositivi di protezione individuale

Eyeshields, Faceshields, Gloves, type P2 (EN 143) respirator cartridges


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Certificati d'analisi (COA)

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g-Strophanthin phyproof® Reference Substance

PHL80207

g-Strophanthin

Digitoxin European Pharmacopoeia (EP) Reference Standard

D1800000

Digitoxin

Convallatoxin ≥65%

Sigma-Aldrich

C9140

Convallatoxin

Bufalin

Sigma-Aldrich

B0261

Bufalin

Digoxin United States Pharmacopeia (USP) Reference Standard

USP

1200000

Digoxin

T Warashina et al.
Chemical & pharmaceutical bulletin, 48(4), 516-524 (2000-04-27)
Twenty-nine new oxypregnane glycosides were obtained along with two known cardenolides, frugoside and gofruside, and three known 12-O-acylated pregnane glycosides from the roots of Asclepias incarnata L. (Asclepiadaceae). By detailed studies of the 1H- and 13C-NMR spectra, the structures were
P De Weer et al.
The Journal of general physiology, 117(4), 315-328 (2001-03-30)
The steady-state voltage and [Na(+)](o) dependence of the electrogenic sodium pump was investigated in voltage-clamped internally dialyzed giant axons of the squid, Loligo pealei, under conditions that promote the backward-running mode (K(+)-free seawater; ATP- and Na(+)-free internal solution containing ADP
The crystal structure of digitoxigenin, C23H34O4
Isabella Karle and J. Karle
Acta Crystallographica Section B, Structural Crystallography and Crystal Chemistry, B25, 434-434 (1969)
Maoquan Zhou et al.
Organic letters, 8(19), 4339-4342 (2006-09-08)
A convergent and stereocontrolled route to trisaccharide natural product digitoxin has been developed. The route is amenable to the preparation of both the digitoxigen mono- and bisdigitoxoside. This route featured the iterative application of the palladium-catalyzed glycosylation reaction, reductive 1,3-transposition
A Babes et al.
Biophysical journal, 79(5), 2557-2571 (2000-10-29)
We have used admittance analysis together with the black lipid membrane technique to analyze electrogenic reactions within the Na(+) branch of the reaction cycle of the Na(+)/K(+)-ATPase. ATP release by flash photolysis of caged ATP induced changes in the admittance

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