- Signaling Pathways
- Neuronal Signaling
- Monoamine Oxidase
Monoamine Oxidase
MAO
Monoamine Oxidase Isoform Specific Products
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Monoamine Oxidase Inhibitors
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Monoamine Oxidase Activators
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Monoamine Oxidase Modulators
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Monoamine Oxidase Chemicals
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Monoamine Oxidase Substrate
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Monoamine Oxidase Ligands
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Monoamine Oxidase Related Products (515)
Related Products (515)
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Antibodies (2)
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Monoamine Oxidase Isoform Comparison
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GSK-LSD1 dihydrochloride (Standard)
0 ImagesCat. No.: HY-100546ARCAS No.: 2102933-95-7GSK-LSD1 (dihydrochloride) (Standard) is the analytical standard of GSK-LSD1 (dihydrochloride) (HY-100546A). This product is intended for research and analytical applications. GSK-LSD1 dihydrochloride is a potent, selective and irreversible lysine specific demethylase 1 (LSD1) inhibitor with an IC50 of 16 nM. -
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MD 780236 free base
0 ImagesCat. No.: HY-129444CAS No.: 73423-36-6MD 780236 free base is a substrate and selective inhibitor of monoamine oxidase B (MAO-B), competitive with phenylethylamine and 5-hydroxytryptamine (5-HT). -
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Safinamide-d5
0 ImagesCat. No.: HY-70057S4Synonyms: FCE 26743-d5; EMD 1195686-d5Safinamide-d5 (FCE 26743-d5) is deuterium labeled Safinamide. Safinamide is a potent, selective, and reversible monoamine oxidase B (MAO-B) inhibitor (IC50=0.098 μM) over MAO-A (IC50=580 μM). Safinamide also blocks sodium channels and modulates glutamate (Glu) release, showing a greater affinity at depolarized (IC50=8?μM) than at resting (IC50=262?μM) potentials. Safinamide has neuroprotective and neurorescuing effects and can be used for the study of parkinson disease, ischemia stroke etc.al. -
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- Methyl piperate
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Caroxazone
0 ImagesCat. No.: HY-119774CAS No.: 18464-39-6Caroxazone is a reversible inhibitor for monoamine oxidase (MAO). Caroxazone exhibits activity as an antidepressant agent. -
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4-Chlorochalcone
0 ImagesCat. No.: HY-W325160CAS No.: 956-04-74-Chlorochalcone (Compound 3) is a monoamine oxidase inhibitor (hMAO-B: IC50 = 0.082 μM, hMAO-A: IC50 = 9.95 μM). 4-Chlorochalcone also exhibits inhibitory activity against cholinesterase (AChE: IC50 = 2.79 μM). 4-Chlorochalcone is a chalcone derivative. -
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Acacetin 7-O-(6-O-malonylglucoside)
0 ImagesCat. No.: HY-N13041CAS No.: 155049-92-6Acacetin 7-O-(6-O-malonylglucoside) is a monoamine oxidase inhibitor with strong inhibitory effects on monoamine oxidase A (MAO-A) and monoamine oxidase B (MAO-B) with IC50 values of 2.34 and 1.87 μM, respectively. Acacetin 7-O-(6-O-malonylglucoside) is a reversible MAO inhibitor that can be used in the research of neurodegenerative diseases and affective disorders. -
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2,6-Dimethoxybenzylamine hydrochloride
0 ImagesCat. No.: HY-W017118ACAS No.: 34967-23-22,6-Dimethoxybenzylamine hydrochloride (Compound 5) exhibits reversible inhibitory activity against copper amine oxidase (CAO), that inhibits benzylamine oxidase (BAO) and monoamine oxidase B (MAO B) with IC50 of 120 μM and 190 μM. -
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RS 8359 (Standard)
0 ImagesCat. No.: HY-14260RCAS No.: 105365-76-2RS 8359 (Standard) is the analytical standard of RS 8359. This product is intended for research and analytical applications. RS 8359 is a selective and reversible MAO-A inhibitor, with antidepressant activity. -
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Tranylcypromine
0 ImagesTranylcypromine (SKF 385) is a potent monoamine oxidase (MAO) inhibitor. -
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MAO-B-IN-57
0 ImagesCat. No.: HY-183437CAS No.: 1522345-35-2MAO-B-IN-57 is a selective MAO-B inhibitor with an IC50 of 41.38 nM against human MAO-B. MAO-B-IN-57 shows no significant in vitro cytotoxicity and can significantly increase the survival rate of PC12 cells damaged by 6-OHDA. MAO-B-IN-57 can be used in studies related to Parkinson's disease. -
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MDL 72394
0 ImagesCat. No.: HY-188168CAS No.: 99630-95-2Synonyms: FMMTMDL 72394 (FMMT) is an orally active, blood-brain barrier-penetrant amino acid-based prodrug compound. MDL 72394 is decarboxylated by aromatic L-amino acid decarboxylase to generate the active metabolite MDL 72392 (HY-182727), which is a covalent irreversible MAO inhibitor. MDL 72394 is transported into the brain and synaptosomes via the L-neutral amino acid transport system and the norepinephrine transporter. MDL 72394 selectively inhibits MAO in noradrenergic and dopaminergic neurons without inhibiting serotonergic neurons. MDL 72394 increases hypothalamic extracellular 5-HT, tissue 5-HT, and pineal melatonin biosynthesis, and decreases 5-HIAA. MDL 72394 can be used in research related to MAO-mediated diseases, such as depression. -
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MD 770222
0 ImagesCat. No.: HY-124464CAS No.: 70133-35-6MD 770222, a major plasma O-demethyl metabolite of Cimoxatone (HY-15386), is an orally active, selective and reversible MAO A inhibitor. MD 770222 shows less potent than Cimoxatone. -
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6,7-Dimethylisatin
0 ImagesCat. No.: HY-W029600CAS No.: 20205-43-06,7-Dimethylisatin (compound 1l), an Isatin (HY-Y0265) analogue, is a potent MAO inhibitor with IC50s of 20.3 μM and 6.74 μM for MAO-A and MAO-B, respectively. 6,7-Dimethylisatin has the potential for depression, Alzheimer's disease and Parkinson's disease research. -
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MAO-B-IN-1
0 ImagesCat. No.: HY-U00343CAS No.: 1124198-17-9MAO-B-IN-1 is an inhibitor of monoamine oxidase B, used for the research of neurological diseases. -
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Sorry. There is currently no product that acts on isoform Bcl-2, Bcl-W and Bim together.Please
try each isoform separately.