Home - Products - Others - Other Targets - 4-Hepten-3-one, 7-(4-hydroxy-3-methoxyphenyl)-1-phenyl-, (4E)-

4-Hepten-3-one, 7-(4-hydroxy-3-methoxyphenyl)-1-phenyl-, (4E)-

CAS No. 478314-07-7

4-Hepten-3-one, 7-(4-hydroxy-3-methoxyphenyl)-1-phenyl-, (4E)-( ——— )

Catalog No. M39815 CAS No. 478314-07-7

4-Hepten-3-one, 7-(4-hydroxy-3-methoxyphenyl)-1-phenyl-, (4E)-

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
200MG Get Quote Get Quote
500MG Get Quote Get Quote
1G Get Quote Get Quote

Biological Information

  • Product Name
    4-Hepten-3-one, 7-(4-hydroxy-3-methoxyphenyl)-1-phenyl-, (4E)-
  • Note
    Research use only, not for human use.
  • Brief Description
    4-Hepten-3-one, 7-(4-hydroxy-3-methoxyphenyl)-1-phenyl-, (4E)-
  • Description
    4-Hepten-3-one, 7-(4-hydroxy-3-methoxyphenyl)-1-phenyl-, (4E)-
  • In Vitro
    ———
  • In Vivo
    ———
  • Synonyms
    ———
  • Pathway
    Others
  • Target
    Other Targets
  • Recptor
    ———
  • Research Area
    ———
  • Indication
    ———

Chemical Information

  • CAS Number
    478314-07-7
  • Formula Weight
    ———
  • Molecular Formula
    ———
  • Purity
    >98% (HPLC)
  • Solubility
    ———
  • SMILES
    ———
  • Chemical Name
    ——

Shipping & Storage Information

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

Reference

molnova catalog
related products
  • Ajugasterone C

    Ajugasterone C shows significant inhibitory effect at 100 mg/kg dose on rat paw oedema development due to carrageenan-induced inflammation in Sprague Dawley rats.

  • C 101248

    C 101248 is a selective and potent inhibitor targeting both mouse and human tandem pore domain halothane-inhibited K+ channel 1 (THIK-1, IC50= 50 nM), without affecting the K2P family members (TREK-1, TWIK-2) and Kv2.1.

  • Adoprazine

    Adoprazine is a potential atypical antipsychotic bearing potent D2 receptor antagonist and 5-HT1A receptor agonist properties.