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Results for "

serotonin metabolism

" in MedChemExpress (MCE) Product Catalog:
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Cat. No. 상품명 Target 연구분야 Chemical Structure
  • HY-14197
    Clorgyline
    5+ Cited Publications

    M&B 9302

    		 Monoamine Oxidase Neurological Disease
    Clorgyline (M&B 9302) is an orally active, blood-brain barrier permeable and selective monoamine oxidase A (MAO-A) inhibitor. Clorgyline's selective inhibition of MAO-A leads to reduced metabolism of neurotransmitters such as serotonin (5-hydroxytryptamine), which accumulates in the brain. Clorgyline can be used in the study of depression and neurodegenerative diseases .
    Clorgyline
  • HY-G0002
    Lurasidone metabolite 14326

    		Drug Metabolite Dopamine Receptor 5-HT Receptor Neurological Disease
    Lurasidone metabolite 14326 is a minor active metabolite of Lurasidone (HY-B0032A) generated via metabolism by CYP3A4. Lurasidone metabolite 14326 shares similar receptor-binding properties with Lurasidone, acting as an antagonist of the dopamine D2 receptor (dopamine D2 receptor), an antagonist of the serotonin 5-HT2A and 5-HT7 receptors (5-HT2A and 5-HT7 receptor), and a partial agonist of the serotonin 5-HT1A receptor. Lurasidone metabolite 14326 can be used in the research of schizophrenia and bipolar depression .
    Lurasidone metabolite 14326
  • HY-W707780
    Nor mianserin hydrochloride

    		Serotonin Transporter Cardiovascular Disease Neurological Disease Inflammation/Immunology
    Nor mianserin hydrochloride, demethylated derivative of Mianserin (HY-B0188), is a serotonin antagonist. Nor mianserin hydrochloride can be used for the research of diseases related to serotonin metabolism disorders and histamine metabolism disorders .
    Nor mianserin hydrochloride
  • HY-115418
    Alentemol hydrobromide

    U-68553B

    		 Dopamine Receptor Neurological Disease
    Alentemol (hydrobromide) is a dopamine antagonist and dihydrophenalene analog with dimethylamino substitution and an orthophenolic hydroxy group relative to the amino nitrogen. Alentemol (hydrobromide) does not impair escape response at a dose that completely suppresses conditioned avoidance in rats .
    Alentemol hydrobromide

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