Home - Products - Others - Other Targets - 2,7-dihydroxy-3,4-dimethoxyphenanthrene

2,7-dihydroxy-3,4-dimethoxyphenanthrene

CAS No. 86630-46-8

2,7-dihydroxy-3,4-dimethoxyphenanthrene( ——— )

Catalog No. M38756 CAS No. 86630-46-8

Nudol is a phenanthrene compound that has anti-cancer activity. Nudol inhibits cell proliferation, induces cell apoptosis. Nudol inhibits MMP-2M and MMP-9 activity (Ki: 988.9 nM, 1.76 μM, respectively). Nudol can be used in the research of cancers, such as osteosarcoma.

Purity : >98% (HPLC)

COA Datasheet HNMR HPLC MSDS Handing Instructions
Size Price / USD Stock Quantity
25MG Get Quote Get Quote
50MG Get Quote Get Quote
100MG Get Quote Get Quote

Biological Information

  • Product Name
    2,7-dihydroxy-3,4-dimethoxyphenanthrene
  • Note
    Research use only, not for human use.
  • Brief Description
    Nudol is a phenanthrene compound that has anti-cancer activity. Nudol inhibits cell proliferation, induces cell apoptosis. Nudol inhibits MMP-2M and MMP-9 activity (Ki: 988.9 nM, 1.76 μM, respectively). Nudol can be used in the research of cancers, such as osteosarcoma.
  • Description
    Nudol is a natural product.
  • In Vitro
    Nudol (0-40 μM, 24-72 h) decreases cell viability in several cancer cell lines.Nudol (0-20 μM, 24/48 h) suppresses the cell migration and causes cell cycle arrest at G2/M phase in U2OS cells.Nudol (20 μM, 48 h) induces cell apoptosis through the caspase-dependent pathway in U2OS cells.Nudol (compound 4) inhibits MMP-2 and MMP-9 activity with Ki values of 988.9 nM and 1.76 μM respectively.Cell Viability Assay Cell Line:U2OS, MG63, MDA-MB-231, MCF-7, and A549 cells Concentration:0, 10, 20, 30, 40 μM Incubation Time:24, 48, and 72 h Result:Decreased the cell viability of osteosarcoma cells in dose- and time-dependent manners.Cell Cycle Analysis Cell Line:U2OS cells Concentration:0, 5, 10, 20 μM Incubation Time:24, 48, and 72 h Result:Triggered G2/M phase arrest by decreasing cell cycle-related proteins (CDK1, CDK2, CDK4, and CDK10).Western Blot Analysis Cell Line:U2OS cells Concentration:0, 5, 10, 20, 40 μM Incubation Time:24, 48, and 72 h Result:Increased the protein level of cytochrome c.Down-regulated anti-apoptotic Bcl-2, accompanied by an increased level of pro-apoptotic Bax.
  • In Vivo
    ———
  • Synonyms
    ———
  • Pathway
    Others
  • Target
    Other Targets
  • Recptor
    ———
  • Research Area
    ———
  • Indication
    ———

Chemical Information

  • CAS Number
    86630-46-8
  • Formula Weight
    270.279
  • Molecular Formula
    C16H14O4
  • Purity
    >98% (HPLC)
  • Solubility
    ———
  • SMILES
    ———
  • Chemical Name
    ——

Shipping & Storage Information

  • Storage
    (-20℃)
  • Shipping
    With Ice Pack
  • Stability
    ≥ 2 years

Reference

1. Yuying Zhang, et al. Nudol, a phenanthrene derivative from Dendrobium nobile, induces cell cycle arrest and apoptosis and inhibits migration in osteosarcoma cells. Drug Des Devel Ther. 2019 Jul 29;13:2591-2601. ?
molnova catalog
related products
  • Acetyl-(Tyr1,D-Arg2)...

    Acetyl-(D-Arg2)-GRF (1-29) amide (human) is an antagonist of growth hormone releasing factor (GRF). Acetyl-(D-Arg2)-GRF (1-29) amide (human) inhibits the release of growth hormone (GH) and can be used for endocrine research.

  • TMPD dihydrochloride

    TMPD dihydrochloride is an active substrate of enzymatically convert redox and an electron donor for the reduction of heme peroxidases.

  • G-Protein antagonist...

    Substance P-related peptide that inhibits binding of G proteins to their receptors. Competitively and reversibly inhibits M2 muscarinic receptor activation of Gi or Go and inhibits Gs activation by β-adrenoceptors.