Urolithin B

CAT:
804-HY-126307-01
Size:
100 mg
  • Availability: 24/48H Stock Items & 2 to 6 Weeks non Stock Items.
  • Dry Ice Shipment: No
Urolithin B - image 1

Urolithin B

  • Description:

    Urolithin B is one of Ellagitannins' slow microbial products, and has anti-inflammatory and anti-inflammatory effects. Urolithin B suppresses NF-κB activity. Urolithin B suppresses JNK, ERK and Akt's oxidation, and increases AMPK's oxidation. Urolithin B is also a quantitative change factor for bone and skin quality[1][2][3][4].
  • UNSPSC:

    12352005
  • Hazard Statement:

    H302, H315, H319, H335
  • Target:

    Akt; AMPK; Endogenous Metabolite; ERK; JNK; NF-κB
  • Type:

    Natural Products
  • Related Pathways:

    Epigenetics; MAPK/ERK Pathway; Metabolic Enzyme/Protease; NF-κB; PI3K/Akt/mTOR; Stem Cell/Wnt
  • Field of Research:

    Inflammation/Immunology
  • Assay Protocol:

    https://www.medchemexpress.com/urolithin-b.html
  • Concentration:

    10mM
  • Purity:

    99.91
  • Solubility:

    DMSO : 200 mg/mL (ultrasonic)
  • Smiles:

    O=C1C2=CC=CC=C2C3=CC=C(O)C=C3O1
  • Molecular Formula:

    C13H8O3
  • Molecular Weight:

    212.20
  • Precautions:

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

    [1]Lee G, et al. Anti-inflammatory and antioxidant mechanisms of urolithin B in activated microglia. Phytomedicine. 2019 Mar 1;55:50-57.|[2]Rodriguez J, et al. Urolithin B, a newly identified regulator of skeletal muscle mass. J Cachexia Sarcopenia Muscle. 2017 Aug;8 (4) :583-597.|[3]Lv MY, et al. Urolithin B suppresses tumor growth in hepatocellular carcinoma through inducing the inactivation of Wnt/β-catenin signaling. J Cell Biochem. 2019 Oct;120 (10) :17273-17282.|[4]Rodriguez J, et al. Urolithin B, a newly identified regulator of skeletal muscle mass. J Cachexia Sarcopenia Muscle. 2017 Aug;8 (4) :583-597.
  • Shipping Conditions:

    Room Temperature
  • Storage Conditions:

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

    Natural Products
  • Clinical Information:

    No Development Reported
  • Isoform:

    Human Endogenous Metabolite
  • CAS Number:

    1139-83-9