Istaroxime

CAT:
804-HY-15718
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  • Availability: 24/48H Stock Items & 2 to 6 Weeks non Stock Items.
  • Dry Ice Shipment: No
Istaroxime - image 1

Istaroxime

  • UNSPSC Description:

    Istaroxime (PST2744) is a potent inhibitor of Na+,K+-ATPase with IC50 of 0.11 μM.
  • Target Antigen:

    Na+/K+ ATPase
  • Type:

    Reference compound
  • Related Pathways:

    Membrane Transporter/Ion Channel
  • Applications:

    Neuroscience-Neuromodulation
  • Field of Research:

    Cardiovascular Disease
  • Assay Protocol:

    https://www.medchemexpress.com/Istaroxime.html
  • Solubility:

    10 mM in DMSO
  • Smiles:

    O=C1CC[C@@]2([H])[C@]3([H])CC([C@@]4([H])C/C(CC[C@]4(C)[C@@]3([H])CC[C@@]21C)=N/OCCN)=O
  • Molecular Weight:

    360.49
  • References & Citations:

    [1]Gobbini M, et al. Novel analogues of istaroxime, a potent inhibitor of Na+,K+-ATPase: synthesis and structure-activity relationship. J Med Chem. 2008 Aug 14;51(15):4601-8.|[2]Gobbini M, et al. Novel analogues of Istaroxime, a potent inhibitor of Na(+),K(+)-ATPase: Synthesis, structure-activity relationship and 3D-quantitative structure-activity relationship of derivatives at position 6 on the androstane scaffold. Bioorg Med Ch|[3]Micheletti R, et al. Pharmacological profile of the novel inotropic agent (E,Z)-3-((2-aminoethoxy)imino)androstane-6,17-dione hydrochloride (PST2744). J Pharmacol Exp Ther. 2002 Nov;303(2):592-600.Pnas nexus . 2023 Dec 22.|Biochem Pharmacol. 2020 Oct;180:114122.|Biochem Pharmacol. 2023 Mar 24;211:115516.|Front Pharmacol. 2020 Dec 14.|J Am Heart Assoc. 2021 Jul 3;e018833.
  • Shipping Conditions:

    Room temperature
  • Clinical Information:

    Phase 2
  • CAS Number:

    203737-93-3