Vacuolin-1

CAT:
804-HY-118630-01
Size:
5 mg
  • Availability: 24/48H Stock Items & 2 to 6 Weeks non Stock Items.
  • Dry Ice Shipment: No
Vacuolin-1 - image 1

Vacuolin-1

  • Description :

    Vacuolin-1 is a potent and cell-permeable lysosomal exocytosis inhibitor. Vacuolin-1 blocks the Ca2+-dependent exocytosis of lysosomes and prevents the release of lysosomal content without affecting the process of resealing. vacuolin‐1 is a potent and selective PIKfyve inhibitor and inhibits late‐stage autophagy by impairing lysosomal maturation. Vacuolin-1 can induce vacuole formation and increase the percentage of enucleated cells[1][2][4].
  • UNSPSC :

    12352005
  • Hazard Statement :

    H302, H315, H319, H335
  • Target :

    Autophagy; PIKfyve
  • Type :

    Reference compound
  • Related Pathways :

    Autophagy; PI3K/Akt/mTOR
  • Applications :

    COVID-19-immunoregulation
  • Field of Research :

    Cancer
  • Assay Protocol :

    https://www.medchemexpress.com/vacuolin-1.html
  • Purity :

    98.54
  • Solubility :

    DMSO : 10 mg/mL (ultrasonic; warming; heat to 60°C)
  • Smiles :

    IC1=CC(/C=N/NC2=NC(N(C3=CC=CC=C3)C4=CC=CC=C4)=NC(N5CCOCC5)=N2)=CC=C1
  • Molecular Formula :

    C26H24IN7O
  • Molecular Weight :

    577.42
  • Precautions :

    H302, H315, H319, H335
  • References & Citations :

    [1]Jan Cerny, et al.The small chemical vacuolin-1 inhibits Ca (2+) -dependent lysosomal exocytosis but not cell resealing. EMBO Rep. 2004 Sep;5 (9) :883-8.|[2]Osamu Sano, et al. Vacuolin-1 inhibits autophagy by impairing lysosomal maturation via PIKfyve inhibition. FEBS Lett. 2016 Jun;590 (11) :1576-85.|[3]Yingying Lu, et al. Vacuolin-1 potently and reversibly inhibits autophagosome-lysosome fusion by activating RAB5A. Autophagy|[4]Keerthivasan G, et al. Vesicle trafficking plays a novel role in erythroblast enucleation. Blood. 2010 Oct 28;116 (17) :3331-40.
  • Shipping Conditions :

    Blue Ice
  • Storage Conditions :

    -20°C (Powder, stored under nitrogen)
  • Scientific Category :

    Reference compound1
  • Clinical Information :

    No Development Reported
  • CAS Number :

    [351986-85-1]

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