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Results for "

Deprenyl

" in MedChemExpress (MCE) Product Catalog:

5

Inhibitors & Agonists

1

Peptides

1

Isotope-Labeled Compounds

2

Click Chemistry

Cat. No. Product Name Target Research Areas Chemical Structure
  • HY-14199
    Selegiline hydrochloride
    5+ Cited Publications

    Deprenyl hydrochloride; (-)-Selegiline hydrochloride; (-)-Deprenyl hydrochloride

    Monoamine Oxidase Neurological Disease
    Selegiline (Deprenyl) hydrochloride is a potent, selective and irreversible inhibitor of MAO-B, with an IC50 of 51 nM. Selegiline hydrochloride exhibits 450-flod selectivity for MAO-B over MAO-A (IC50=23 μM). Selegiline hydrochloride can be used for the research of Parkinson's disease, Alzheimer's disease and major depressive disorder .
    Selegiline hydrochloride
  • HY-14198

    Deprenyl; (-)-Selegiline; (-)-Deprenyl

    Monoamine Oxidase Neurological Disease
    Selegiline (Deprenyl) is a potent, selective and irreversible inhibitor of MAO-B, with an IC50 of 51 nM. Selegiline exhibits 450-flod selectivity for MAO-B over MAO-A (IC50=23 μM). Selegiline can be used for the research of Parkinson's disease, Alzheimer's disease and major depressive disorder .
    Selegiline
  • HY-119532

    Desmethylselegiline

    Drug Metabolite Metabolic Disease
    Nordeprenyl is the metabolite of Deprenyl. Deprenyl is a potent, selective and irreversible inhibitor of MAO-B . Nordeprenyl is a click chemistry reagent, it contains an Alkyne group and can undergo copper-catalyzed azide-alkyne cycloaddition (CuAAc) with molecules containing Azide groups.
    Nordeprenyl
  • HY-144162S

    (Rac)-Deprenyl-d5 hydrochloride; (±)-Selegiline-d5 hydrochloride; (±)-Deprenyl-d5 hydrochloride

    Isotope-Labeled Compounds Others
    (Rac)-Selegiline-d5 (hydrochloride) is the deuterium labeled (Rac)-Selegiline hydrochloride[1].
    (Rac)-Selegiline-d5 hydrochloride
  • HY-P3350

    Bacterial Infection
    LS-BF1 is a stable and low toxic cationic antimicrobial peptide. LS-BF1 displays broad spectrum of antibacterial activity, including the challenging ESKAPE pathogens, by cell membrane disruptive mechanism. LS-BF1 shows good in vivo efficacy for elimination of bacteria in a mouse infection model[1].
    LS-BF1

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