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Chemical Structure
Chemical Structure
Chemical Structure

Neobavaisoflavone [41060-15-5]

Research Use Only
AG-CN2-0498
AdipoGen Life Sciences
CAS Number41060-15-5
Product group Chemicals
Estimated Purity>98%
Molecular Weight322.4
Price on request
Packing Size
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Overview

  • Supplier
    AdipoGen Life Sciences
  • Product Name
    Neobavaisoflavone [41060-15-5]
  • Delivery Days Customer
    10
  • CAS Number
    41060-15-5
  • Certification
    Research Use Only
  • Estimated Purity
    >98%
  • Hazard Information
    Non-hazardous
  • Molecular Formula
    C20H18O4
  • Molecular Weight
    322.4
  • Scientific Description
    Antibiotic. Antibacterial and antifungal compound. Displays antibiotic activity against Gram-negative multidrug resistant bacteria. Anticancer compound. DNA polymerase inhibitor. Enhances TRAIL-induced apoptosis via inhibition of metastasis. Anti-inflammatory agent inhibiting IL-6-induced STAT3 activation and phosphorylation. Platelet aggregation inhibitor. Human carboxylesterase 1&2 and UDP-glucuronosyltransferase 1A1 inhibitor, enzymes important in drug metabolism. Antioxidant. Inhibits the production of nitric oxide (NO), reactive oxygen species (ROS) and reactive nitrogen species (RNS). Neuroprotective. Exerts protective effects against H2O2-induced neuronal cell damage. Shows osteogenic acitivty. - Chemical. CAS: 41060-15-5. Formula: C20H18O4. MW: 322.4. Isolated from Psoralea corylifolia sp. Antibiotic. Antibacterial and antifungal compound. Displays antibiotic activity against Gram-negative multidrug resistant bacteria. Anticancer compound. DNA polymerase inhibitor. Enhances TRAIL-induced apoptosis via inhibition of metastasis. Anti-inflammatory agent inhibiting IL-6-induced STAT3 activation and phosphorylation. Platelet aggregation inhibitor. Human carboxylesterase 1&2 and UDP-glucuronosyltransferase 1A1 inhibitor, enzymes important in drug metabolism. Antioxidant. Inhibits the production of nitric oxide (NO), reactive oxygen species (ROS) and reactive nitrogen species (RNS). Neuroprotective. Exerts protective effects against H2O2-induced neuronal cell damage. Shows osteogenic acitivty.
  • SMILES
    OC1=CC=C(C(C(C2=CC=C(O)C(C/C=C(C)/C)=C2)=CO3)=O)C3=C1
  • Storage Instruction
    2°C to 8°C,-20°C
  • UNSPSC
    12352200

References

  • Prenylated isoflavanone from the roots of Erythrina sigmoidea: A.E. Nkengfack, et al.; Phytochemistry 36, 1047 (1994)
  • Antiplatelet flavonoids from seeds of Psoralea corylifolia: W.J. Tsai, et al.; J. Nat. Prod. 59, 671 (1996)
  • DNA polymerase and topoisomerase II inhibitors from Psoralea corylifolia: N.J. Sun, et al.; J. Nat. Prod. 61, 362 (1998)
  • Studies on the chemical constituents of Psoralea corylifolia L.: B. Ruan, et al.; J. Asian Nat. Prod. Res. 9, 41 (2007)
  • The combination of TRAIL and isoflavones enhances apoptosis in cancer cells: J. Bronikowska, et al.; Molecules 15, 2000 (2010)
  • Inhibition of inflammatory mediators by neobavaisoflavone in activated RAW264.7 macrophages: E. Szliszka, et al.; Molecules 16, 3701 (2011)
  • Neobavaisoflavone stimulates osteogenesis via p38-mediated up-regulation of transcription factors and osteoid genes expression in MC3T3-E1 cells: M.-J. Don, et al.; Phytomed. 19, 551, (2012)
  • Phenolic compounds isolated from Psoralea corylifolia inhibit IL-6-induced STAT3 activation: S.W. Lee, et al.; Planta Med. 78, 903 (2012)
  • Neobavaisoflavone sensitizes apoptosis via the inhibition of metastasis in TRAIL-resistant human glioma U373MG cells: Y.J. Kim, et al.; Life Sci. 95, 101 (2014)
  • Activity of three cytotoxic isoflavonoids from Erythrina excelsa and Erythrina senegalensis (neobavaisoflavone, sigmoidin H and isoneorautenol) toward multi-factorial drug resistant cancer cells: V. Kuete, et al.; Phytomed. 21, 682 (2014)