Guanfu base A

CAT:
804-HY-N1483-01
Size:
5 mg
  • Availability: 24/48H Stock Items & 2 to 6 Weeks non Stock Items.
  • Dry Ice Shipment: No
Guanfu base A - image 1

Guanfu base A

  • Description :

    Guanfu base A is an antiarrhythmic alkaloid isolated from Aconitum coreanum and is a potent noncompetitive CYP2D6 inhibitor, with a Ki of 1.20 μM in human liver microsomes (HLMs) and a Ki of 0.37 μM for the human recombinant form (rCYP2D6) . Guanfu base A is also a potent competitive inhibitor of CYP2D in monkey (Ki of 0.38 μM) and dog (Ki of 2.4 μM) microsomes[1]. Guanfu base A also inhibits HERG channel current[2].
  • CAS Number :

    [1394-48-5]
  • UNSPSC :

    12352005
  • Target :

    Potassium Channel
  • Type :

    Natural Products
  • Related Pathways :

    Membrane Transporter/Ion Channel
  • Applications :

    Neuroscience-Neuromodulation
  • Field of Research :

    Cardiovascular Disease
  • Assay Protocol :

    https://www.medchemexpress.com/guanfu-base-a.html
  • Purity :

    98.10
  • Solubility :

    DMSO : 100 mg/mL (ultrasonic)
  • Smiles :

    O[C@@]12C3[C@]45[C@@]([C@@H]6O)([H])C1(CC([C@@]6([H])[C@H]2OC(C)=O)=C)C[C@@]7([H])[C@]4([H])[C@@](C)(C[C@H](OC(C)=O)C5)C[N@]37
  • Molecular Formula :

    C24H31NO6
  • Molecular Weight :

    429.51
  • References & Citations :

    [1]Sun J, et al. Guanfu base A, an antiarrhythmic alkaloid of Aconitum coreanum, Is a CYP2D6 inhibitor of human, monkey, and dog isoforms. Drug Metab Dispos. 2015 May;43 (5) :713-24.|[2]Huang X, et al. Comparative effects of Guanfu base A and Guanfu base G on HERG K+ channel. J Cardiovasc Pharmacol. 2012 Jan;59 (1) :77-83.
  • Shipping Conditions :

    Room Temperature
  • Storage Conditions :

    4°C (Powder, sealed storage, away from moisture and light)
  • Scientific Category :

    Natural Products
  • Clinical Information :

    No Development Reported

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