Diclofensine

CAS No. 67165-56-4

Diclofensine( Ro 8-4650 )

Catalog No. M20755 CAS No. 67165-56-4

Diclofensine inhibits the uptake of serotonin noradrenaline and dopamine.

Purity : >98% (HPLC)

COA Datasheet HNMR HPLC MSDS Handing Instructions
Size Price / USD Stock Quantity
5MG 43 In Stock
10MG 73 In Stock
25MG 132 In Stock
50MG 200 In Stock
100MG 300 In Stock
200MG Get Quote In Stock
500MG Get Quote In Stock
1G Get Quote In Stock

Biological Information

  • Product Name
    Diclofensine
  • Note
    Research use only, not for human use.
  • Brief Description
    Diclofensine inhibits the uptake of serotonin noradrenaline and dopamine.
  • Description
    Diclofensine inhibits the uptake of serotonin noradrenaline and dopamine.
  • In Vitro
    ——
  • In Vivo
    ——
  • Synonyms
    Ro 8-4650
  • Pathway
    Membrane Transporter/Ion Channel
  • Target
    Monoamine Transporter
  • Recptor
    Monoamine transporter
  • Research Area
    ——
  • Indication
    ——

Chemical Information

  • CAS Number
    67165-56-4
  • Formula Weight
    322.2
  • Molecular Formula
    C17H17Cl2NO
  • Purity
    >98% (HPLC)
  • Solubility
    ——
  • SMILES
    COc1ccc2C(CN(C)Cc2c1)c1ccc(Cl)c(Cl)c1
  • Chemical Name
    ——

Shipping & Storage Information

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

Reference

1.Cherpillod C Omer L M O . A Controlled Trial with Diclofensine a New Psychoactive Drug in the Treatment of Depression[J]. Journal of International Medical Research 1981 9(5):324-329.
molnova catalog
related products
  • Vanoxerine

    Vanoxerine (GBR-12909, I-893, Boxeprazine) is a highly potent inhibitor of dopamine uptake in vitro in tissue slices obtained from rat neostriatum with IC50 of 40-50 nM.

  • Tetrabenazine Metabo...

    Tetrabenazine Metabolite ((-)-β-HTBZ), a vesicles monoamine transporter 2 (VMAT2) inhibitor, is an active metabolite of Tetrabenazine.

  • Lenumlostat

    Lenumlostat is an orally available, selective and potent lysyl oxidase-like protein 2 (LOXL2) inhibitor with inhibitory effects on hLOXL2, hLOXL3 and LOXL2 for the study of fibrotic diseases.