Esmolol

CAT:
804-HY-B1392A
Size:
1 Each

For Laboratory Research Only. Not for Clinical or Personal Use.

  • Availability: 24/48H Stock Items & 2 to 6 Weeks non Stock Items.
  • Dry Ice Shipment: No
Esmolol - image 1

Esmolol

  • Description:

    Esmolol is an ultra-short-acting cardioselective β1-adrenergic blocker. Esmolol exerts its antiarrhythmic effect by activating Neurokinin 1 Receptor. Esmolol attenuates post resuscitation myocardial dysfunction. Esmolol improves diabetic wound healing by inhibiting aldose reductase and the production of advanced glycation end products and promoting fibroblast migration. Esmolol can be used to study cardiac diseases such as arrhythmias and diabetic foot ulcers[1][2][3].
  • UNSPSC:

    12352005
  • Hazard Statement:

    H302-H315-H319-H335
  • Target:

    Adrenergic Receptor; Aldose Reductase; Apoptosis; Caspase; Neurokinin Receptor
  • Type:

    Reference compound
  • Related Pathways:

    Apoptosis; GPCR/G Protein; Metabolic Enzyme/Protease; Neuronal Signaling
  • Applications:

    Neuroscience-Neurodegeneration
  • Field of Research:

    Cancer; Endocrinology; Cardiovascular Disease
  • Assay Protocol:

    https://www.medchemexpress.com/esmolol.html
  • Smiles:

    O=C(OC)CCC1=CC=C(OCC(O)CNC(C)C)C=C1
  • Molecular Formula:

    C16H25NO4
  • Molecular Weight:

    295.37
  • Precautions:

    P261-P280-P302+P352
  • References & Citations:

    [1]Kulkarni SA, et al. Novel topical esmolol hydrochloride improves wound healing in diabetes by inhibiting aldose reductase, generation of advanced glycation end products, and facilitating the migration of fibroblasts. Front Endocrinol (Lausanne) . 2022 Aug 23;13:926129. |[2]Wang LL, et al. Esmolol activates endogenous neurokinin activity inhibiting infarction-induced arrhythmias in rats: novel mechanisms of anti-arrhythmia. Regul Pept. 2013 Sep 10;186:116-22. |[3]Zhang Q, et al. Combination of epinephrine with esmolol attenuates post-resuscitation myocardial dysfunction in a porcine model of cardiac arrest. PLoS One. 2013 Dec 18;8 (12) :e82677.
  • Shipping Conditions:

    Room temperature
  • Scientific Category:

    Reference compound1
  • Clinical Information:

    Launched
  • Isoform:

    Caspase 3; β adrenergic receptor
  • CAS Number:

    [81147-92-4]