Digoxin

Chemodex
Product Code: CDX-D0175
Supplier: Chemodex
CodeSizePrice
CDX-D0175-G0011 g£121.00
Quantity:
CDX-D0175-G0055 g£450.00
Quantity:
Prices exclude any Taxes / VAT

Overview

Regulatory Status: RUO
Shipping:
Ambient
Storage:
+4°C

Images

1 / 1
Chemical Structure

Chemical Structure

Further Information

Alternate Names/Synonyms:
12beta-Hydroxydigitoxin; NSC 95100
Appearance:
White powder.
CAS:
20830-75-5
Class:
6.1
EClass:
32160000
Form (Short):
liquid
GHS Symbol:
GHS06
Handling Advice:
Keep cool and dry.Protect from light and moisture.
Hazards:
H300, H330
InChi:
InChI=1S/C41H64O14/c1-19-36(47)28(42)15-34(50-19)54-38-21(3)52-35(17-30(38)44)55-37-20(2)51-33(16-29(37)43)53-24-8-10-39(4)23(13-24)6-7-26-27(39)14-31(45)40(5)25(9-11-41(26,40)48)22-12-32(46)49-18-22/h12,19-21,23-31,33-38,42-45,47-48H,6-11,13-18H2,1-5H3/t19-,20-,21-,23-,24+,25-,26-,27+,28+,29+,30+,31-,33+,34+,35+,36-,37-,38-,39+,40+,41+/m1/s1
InChiKey:
LTMHDMANZUZIPE-PUGKRICDSA-N
Long Description:
Chemical. CAS: 20830-75-5. Formula: C41H64O14. MW: 780.94. Synthetic. Cardiac glycoside from the leaves of Digitalis lanata. It is used to treat cardiac arrhythmias. It is often used as a model substrate of P-glycoprotein (Pgp) (0.01-10µM) and an inhibitor of Na+/K+-ATPase. Inhibits membrane-bound alpha-subunits of the Na+/K+ ATPase pump in myocytes. The primary mechanism of action involves inhibition of the Na+/K+ ATPase, mainly in the myocardium. This inhibition causes an increase in intracellular sodium levels, resulting in a reversal of the action of the sodium-calcium exchanger, which causes an increase in the intracellular calcium concentration. This leads to a decrease in heart rate and increased storage of calcium in the sarcoplasmic reticulum, causing a corresponding increase in the release of calcium during each action potential.
MDL:
MFCD00003674
Molecular Formula:
C41H64O14
Molecular Weight:
780.94
Package Type:
Vial
PG:
II
Precautions:
P260, P264, P284, P301, P310, P310
Product Description:
Cardiac glycoside from the leaves of Digitalis lanata. It is used to treat cardiac arrhythmias. It is often used as a model substrate of P-glycoprotein (Pgp) (0.01-10µM) and an inhibitor of Na+/K+-ATPase. Inhibits membrane-bound alpha-subunits of the Na+/K+ ATPase pump in myocytes. The primary mechanism of action involves inhibition of the Na+/K+ ATPase, mainly in the myocardium. This inhibition causes an increase in intracellular sodium levels, resulting in a reversal of the action of the sodium-calcium exchanger, which causes an increase in the intracellular calcium concentration. This leads to a decrease in heart rate and increased storage of calcium in the sarcoplasmic reticulum, causing a corresponding increase in the release of calcium during each action potential.
Purity:
>95% (HPLC)
Signal word:
Danger
SMILES:
[H][C@@]1(C[C@H](O)[C@H](O[C@@]2([H])C[C@H](O)[C@H](O[C@@]3([H])C[C@H](O)[C@H](O)[C@@H](C)O3)[C@@H](C)O2)[C@@H](C)O1)O[C@H]1CC[C@@]2(C)[C@]([H])(CC[C@]3([H])[C@]2([H])C[C@@H](O)[C@]2(C)[C@H](CC[C@]32O)C2=CC(=O)OC2)C1
Solubility Chemicals:
Soluble in DMSO (100mM) or methanol.
Source / Host:
Synthetic.
Transportation:
Excepted Quantity
UN Nummer:
UN 3462
UNSPSC Category:
Biochemical Reagents
UNSPSC Number:
12352200
Use & Stability:
Stable for at least 2 years after receipt when stored at -20°C.

References

(1) R.G. Woolfson, et al.; Kidney Int. 46, 297 (1994) | (2) S. Reddy, et al.; Curr. Opin. Cardiol. 12, 233 (1997) | (3) K. Kjeldsen & H. Bundgaard; Ann. N Y Acad. Sci. 986, 702 (2003) | (4) M. Gheorghiade, et al.; Circulation 109, 2959 (2004) | (5) M. Ehle, et al.; Crit. Pathw. Cardiol. 10, 93 (2011) | (6) R.J. Biggar; Clin. Cancer Res. 18, 2133 (2012) | (7) A.M. Nader & D.R. Foster; J. Clin. Pharmacol. 54, 3 (2014) | (8) G.A. Ewy; Am. J. Med. 128, 1272 (2015)

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