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    Digoxin

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      Digoxin

      SKU
      D0175

      Category: Phytochemicals

      Synonyms
      12β-Hydroxydigitoxin , NSC 95100
      20830-75-5
      CAS-Number
      C41H64O14
      Molecular Formula
      780.94
      Molecular Weight

      For Research Use Only. Not Intended for Diagnostic or Therapeutic Use.

      • Product Data
      • Handling
      • Safety Information
      • Details

      Specifications

      Purity
      ≥95% (HPLC)
      Appearance
      White powder
      Identity
      1H-NMR

      Properties

      Solvents
      DMSO, methanol, dilute alcohol, a mixture of chloroform and alcohol, and water (0.06 mg/ml at 25 °C)
      Melting Point
      248-250°C
      Density
      ~1.4 g/cm3

      Documentation

      Safety Data Sheet (SDS)
      CDX D0175 MSDS_V1.2.pdf
      Safety Data Sheet (SDS)
      CDX D0175 MSDS.pdf
      Shipping
      AMBIENT
      Short Term Storage
      RT
      Long Term Storage
      RT
      Handling Advice
      Protect from light and moisture.
      Use / Stability
      Stable for at least 2 years after receipt when stored at RT.
      Hazard statements
      H300 + H330
      Precautionary statements
      P260-P264-P284-P301 + P310-P310
      GHS Symbol
      GHS06
      Signal word
      Danger
      RIDADR
      UN3462 6.1
      Transportation
      Packing Group II
      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) (0.01-10 µM) and an inhibitor of Na+/K+-ATPase. Inhibits membrane-bound ?-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.
      Smiles
      O=C1OC/C(=C/1)[C@H]2CC[C@@]8(O)[C@]2(C)[C@H](O)C[C@H]7[C@H]8CC[C@H]6[C@]7(C)CC[C@H](O[C@@H]5O[C@H](C)[C@@H](O[C@@H]4O[C@@H]([C@@H](O[C@@H]3O[C@@H]([C@@H](O)[C@@H](O)C3)C)[C@@H](O)C4)C)[C@@H](O)C5)C6
      InChi Key
      LTMHDMANZUZIPE-PUGKRICDSA-N
      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)

      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) (0.01-10 µM) and an inhibitor of Na+/K+-ATPase. Inhibits membrane-bound ?-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.

      Artikelnummer: D0175 Kategorie: Phytochemicals
      • Zusätzliche Informationen

      Zusätzliche Informationen

      Synonyms

      12β-Hydroxydigitoxin, NSC 95100

      Purity

      ≥95% (HPLC)

      Appearance

      White powder

      CAS-Number

      20830-75-5

      Molecular Formula

      C41H64O14

      Molecular Weight

      780.94

      Identity

      1H-NMR

      Solvents

      DMSO, methanol, dilute alcohol, a mixture of chloroform and alcohol, and water (0.06 mg/ml at 25 °C)

      Melting Point

      248-250°C

      Density

      ~1.4 g/cm3

      Smiles

      O=C1OC/C(=C/1)[C@H]2CC[C@@]8(O)[C@]2(C)[C@H](O)C[C@H]7[C@H]8CC[C@H]6[C@]7(C)CC[C@H](O[C@@H]5O[C@H](C)[C@@H](O[C@@H]4O[C@@H]([C@@H](O[C@@H]3O[C@@H]([C@@H](O)[C@@H](O)C3)C)[C@@H](O)C4)C)[C@@H](O)C5)C6

      InChi Key

      LTMHDMANZUZIPE-PUGKRICDSA-N

      Shipping

      AMBIENT

      Short Term Storage

      RT

      Long Term Storage

      RT

      Handling Advice

      Protect from light and moisture.

      Use / Stability

      Stable for at least 2 years after receipt when stored at RT.

      Hazard statements

      H300 + H330

      Precautionary statements

      P260-P264-P284-P301 + P310-P310

      GHS Symbol

      GHS06

      Signal word

      Danger

      RIDADR

      UN3462 6.1

      Transportation

      Packing Group II

      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)

      Quantity

      1 g, 5 g, Bulk

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