EMD 66684EMD 66684 - High-quality laboratory reagent available from Gentaur. Catalog: 804-HY-103247.804-HY-103247804-HY-103247Business & Industrial > Science & LaboratoryEMD 66684
Gentaur
EUR12027-02-25

EMD 66684

CAT:
804-HY-103247
Size:
1 Each
  • Availability: 24/48H Stock Items & 2 to 6 Weeks non Stock Items.
  • Dry Ice Shipment: No
EMD 66684 - image 1

EMD 66684

  • Description:

    EMD 66684 is an antagonist of Angiotensin II Type 1 (AT1) receptor. EMD 66684 shows potent binding affinities for the AT1 subtype Ang II receptor with an IC50 value of 0.7 nM. EMD 66684 also serves as an antiischemic cytoprotectant [1]-[5].
  • UNSPSC:

    12352005
  • Target:

    Angiotensin Receptor
  • Type:

    Reference compound
  • Related Pathways:

    GPCR/G Protein
  • Applications:

    Neuroscience-Neuromodulation
  • Field of Research:

    Cardiovascular Disease
  • Assay Protocol:

    https://www.medchemexpress.com/emd-66684.html
  • Solubility:

    10 mM in DMSO
  • Smiles:

    O=C1C2=C(C=CN1CC(N(C)C)=O)N=C(CCCC)N2CC3=CC=C(C4=C(C5=NN=NN5)C=CC=C4)C=C3.Cl
  • Molecular Formula:

    C28H31ClN8O2
  • Molecular Weight:

    547.05
  • References & Citations:

    [1]Westfall TC, et al. Interactions of neuropeptide y, catecholamines, and angiotensin at the vascular neuroeffector junction. Adv Pharmacol. 2013;68:115-39.|[2]Qu L, et al. Systematic characterization of AT1 receptor antagonists with label-free dynamic mass redistribution assays. J Pharmacol Toxicol Methods. 2020 Mar-Apr;102:106682.|[3]Mederski WW, et al. Non-peptide angiotensin II receptor antagonists: synthesis and biological activity of a series of novel 4,5-dihydro-4-oxo-3H-imidazo[4,5-c]pyridine derivatives. J Med Chem. 1994 May 27;37 (11) :1632-45.|[4]Byku M, et al. Nerve stimulation induced overflow of neuropeptide Y and modulation by angiotensin II in spontaneously hypertensive rats. Am J Physiol Heart Circ Physiol. 2008 Nov;295 (5) :H2188-97.|[5]Avkran M, et al. Treatment of ischemia with an angiotensin II antagonist: UK, GB2337701. 1999-12-01.
  • Shipping Conditions:

    Room temperature
  • Scientific Category:

    Reference compound1
  • Clinical Information:

    No Development Reported
  • Isoform:

    AT1 Receptor; AT2 Receptor
  • CAS Number:

    [1216884-39-7]