Honokiol

CAT:
804-HY-N0003-01
Size:
50 mg
  • Availability: 24/48H Stock Items & 2 to 6 Weeks non Stock Items.
  • Dry Ice Shipment: No
Honokiol - image 1

Honokiol

  • Description:

    Honokiol is a bioactive, biphenolic phytochemical that possesses potent antioxidative, anti-inflammatory, antiangiogenic, and anticancer activities by targeting a variety of signaling molecules. It inhibits the activation of Akt. Honokiol can readily cross the blood brain barrier[1][2][3][4].
  • Product Name Alternative:

    NSC 293100
  • UNSPSC:

    12352005
  • Hazard Statement:

    H318, H410
  • Target:

    Akt; Autophagy; ERK; HCV
  • Type:

    Natural Products
  • Related Pathways:

    Anti-infection; Autophagy; MAPK/ERK Pathway; PI3K/Akt/mTOR; Stem Cell/Wnt
  • Applications:

    Cancer-Kinase/protease
  • Field of Research:

    Cancer
  • Assay Protocol:

    https://www.medchemexpress.com/honokiol.html
  • Purity:

    99.94
  • Solubility:

    DMSO : ≥ 50 mg/mL
  • Smiles:

    OC1=C (CC=C) C=C (C2=CC (CC=C) =CC=C2O) C=C1
  • Molecular Formula:

    C18H18O2
  • Molecular Weight:

    266.33
  • Precautions:

    H318, H410
  • References & Citations:

    [1]Chang KH, et al. Honokiol-induced apoptosis and autophagy in glioblastoma multiforme cells. Oncol Lett. 2013 Nov;6 (5) :1435-1438.|[2]Godugu C, et al. Honokiol nanomicellar formulation produced increased oral bioavailability and anticancer effects in triple negative breast cancer (TNBC) . Colloids Surf B Biointerfaces. 2017 Jan 23;153:208-219|[3]Lee TY, et al. Honokiol as a specific collagen receptor glycoprotein VI antagonist on human platelets: Functional ex vivo and in vivo studies. Sci Rep. 2017 Jan 5;7:40002|[4]Zhai H, et al. Honokiol-induced neurite outgrowth promotion depends on activation of extracellular signal-regulated kinases (ERK1/2) . Eur J Pharmacol. 2005 Jun 1;516 (2) :112-7.
  • Shipping Conditions:

    Room Temperature
  • Storage Conditions:

    -20°C, 3 years; 4°C, 2 years (Powder)
  • Scientific Category:

    Natural Products
  • Clinical Information:

    Phase 3
  • Isoform:

    ERK1; ERK2
  • CAS Number:

    35354-74-6