Octacosane

CAT:
804-HY-W272217-01
Size:
5 g
  • Availability: 24/48H Stock Items & 2 to 6 Weeks non Stock Items.
  • Dry Ice Shipment: No
Octacosane - image 1

Octacosane

  • Description :

    Octacosane is an endogenous metabolite with antibacterial activity. Octacosane shows high cytotoxicity against murine melanoma B16F10-Nex2 cells besides inducing protection against a grafted subcutaneous melanoma. Octacosane has the larvicidal activity against mosquito Culex quinquefasciatus with the LC50 concentration of 7.2 mg/l[1][2][3].
  • Product Name Alternative :

    N-Octacosane; NSC 5549
  • UNSPSC :

    12352211
  • Hazard Statement :

    H304, H411
  • Target :

    Bacterial; Endogenous Metabolite
  • Type :

    Reference compound
  • Related Pathways :

    Anti-infection; Metabolic Enzyme/Protease
  • Applications :

    COVID-19-immunoregulation
  • Field of Research :

    Cancer; Inflammation/Immunology
  • Assay Protocol :

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

    98.0
  • Solubility :

    Ethanol : < 1 mg/mL (ultrasonic; warming; heat to 60°C)
  • Smiles :

    CCCCCCCCCCCCCCCCCCCCCCCCCCCC
  • Molecular Formula :

    C28H58
  • Molecular Weight :

    394.76
  • Precautions :

    H304, H411
  • References & Citations :

    [1]Carlos R Figueiredo, et al. Pyrostegia venusta heptane extract containing saturated aliphatic hydrocarbons induces apoptosis on B16F10-Nex2 melanoma cells and displays antitumor activity in vivo. Pharmacogn Mag. 2014 Apr;10 (Suppl 2) :S363-76. |[2]S Rajkumar, et al. Mosquitocidal activities of octacosane from Moschosma polystachyum Linn (lamiaceae) . J Ethnopharmacol. 2004 Jan;90 (1) :87-9.|[3]Sameh S M Soliman, et al. Effective targeting of breast cancer cells (MCF7) via novel biogenic synthesis of gold nanoparticles using cancer-derived metabolites. PLoS One. 2020 Oct 6;15 (10) :e0240156.
  • Shipping Conditions :

    Room Temperature
  • Storage Conditions :

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

    Reference compound1
  • Clinical Information :

    No Development Reported
  • Isoform :

    Human Endogenous Metabolite
  • CAS Number :

    [630-02-4]

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