Pheophorbide A

CAT:
804-HY-125665-01
Size:
5 mg
  • Availability: 24/48H Stock Items & 2 to 6 Weeks non Stock Items.
  • Dry Ice Shipment: No
Pheophorbide A - image 1

Pheophorbide A

  • Description :

    Pheophorbide A is an intermediate product in the chlorophyll degradation pathway. Pheophorbide A can be used as a photosensitizer. Pheophorbide A is a lymphatic vascular activator. Pheophorbide A has antitumor activity. Pheophorbide A can be used for human lymphatic vascular insufficiencies research[1][2][3].
  • UNSPSC :

    12352005
  • Hazard Statement :

    H302, H315, H319, H335
  • Target :

    Apoptosis
  • Type :

    Natural Products
  • Related Pathways :

    Apoptosis
  • Applications :

    Cancer-programmed cell death
  • Field of Research :

    Cancer; Cardiovascular Disease
  • Assay Protocol :

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

    95.0
  • Solubility :

    DMSO : 2 mg/mL (ultrasonic; warming; heat to 60°C) |Methanol : < 1 mg/mL (ultrasonic; warming; heat to 60°C)
  • Smiles :

    O=C([C@@H]1/C(C(NC(/C=C2C(CC)=C3C)=C4C)=C4C1=O)=C(N=C(/C=C(C(C)=C/5C=C)\NC5=C/C3=N/2)[C@H]6C)\[C@H]6CCC(O)=O)OC
  • Molecular Formula :

    C35H36N4O5
  • Molecular Weight :

    592.68
  • Precautions :

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

    [1]Jihye Kim, et al. Pheophorbide a identified in an Eupatorium perfoliatum extract is a novel lymphatic vascular activator. Biomed Pharmacother. 2022 Mar;147:112664.|[2]Tang PM, et al. Pheophorbide a, an active compound isolated from Scutellaria barbata, possesses photodynamic activities by inducing apoptosis in human hepatocellular carcinoma. Cancer Biol Ther. 2006 Sep;5 (9) :1111-6.|[3]Ahn MY, et al. Pheophorbide a-mediated photodynamic therapy induces apoptotic cell death in murine oral squamous cell carcinoma in vitro and in vivo. Oncol Rep. 2012 Jun;27 (6) :1772-8.
  • Shipping Conditions :

    Blue Ice
  • Storage Conditions :

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

    Natural Products
  • Clinical Information :

    No Development Reported
  • CAS Number :

    [15664-29-6]

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