- 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 (511)
Related Products (511)
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Antibodies (2)
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Monoamine Oxidase Isoform Comparison
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7-Hydroxy-3,4-dihydro-2(1H)-quinolinone
0 ImagesSynonyms: 3,4-Dihydro-7-hydroxy-2(1H)-quinolinone -
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- 2614W94
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PF9601N
0 ImagesPF9601N, an monoamine oxidase B (MAO-B) inhibitor, possesses neuroprotective properties in several in vitro and in vivo models of Parkinson's disease (PD). PF9601N can be used for the research of neurodegenerative diseases mediated by excitotoxicity. PF9601N is a click chemistry reagent, it contains an Alkyne group and can undergo copper-catalyzed azide-alkyne cycloaddition (CuAAc) with molecules containing Azide groups. -
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Pheniprazine
0 ImagesCat. No.: HY-W224327CAS No.: 55-52-7Synonyms: β-PhenylisopropylhydrazinePheniprazine is a potent and long acting inhibitor of monoamine oxidase. Pheniprazine has the potential for the research of depression. -
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- HDAC-MB
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MAO-B-IN-18
0 ImagesMAO-B-IN-18 is a potent and selective MAO B inhibitor with IC50s of 52 nM and 14 μM for hMAO B and hMAO A, respectively. MAO-B-IN-18 enables promising cytoprotective effects against hydrogen peroxide insults in neuroblastoma and astrocytes cultures. -
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Glicoricone
0 ImagesCat. No.: HY-N9329CAS No.: 161099-37-2Glicoricone, a phenolic compound, is isolated from a species of licorice. Glicoricone is an inhibitor of monoamine oxidase (MAO), with an IC50 of 140 μM. Glicoricone binds to estrogen receptor (ER) and shows estrogen antagonist activity. -
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Gaultherin
0 ImagesGaultherin is an orally active non-steroidal anti-inflammatory agent. Gaultherin selectively inhibits NF-κB, MAPK, COX-2 (IC50 = 0.35 mg/mL), LOX (IC50 = 0.56 mg/mL) and HYAL (IC50 = 28.58 μg/mL) to exert anti-inflammatory, antipyretic and analgesic effects. Gaultherin exhibits modest direct antioxidant capacity, greater in cell-based models. Gaultherin does not affect COX-1 so that avoids the common gastrointestinal side effects of Aspirin (HY-14654). -
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Modaline sulfate
0 ImagesModaline sulfate is a MAO inhibitor, used in the treatment of depression. -
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MAO-IN-1
0 ImagesMAO-IN-1 is a monoamine oxidase B (MAO B) inhibitor with an IC50 of 20 nM. -
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Amitraz (Standard)
0 ImagesCat. No.: HY-B1111RCAS No.: 33089-61-1Synonyms: BTS-27419 (Standard)Amitraz (Standard) is the analytical standard of Amitraz. This product is intended for research and analytical applications. Amitraz is a non-systemic acaricide and insecticide with alpha-adrenergic agonist activity that interacts with octopamine receptors in the central nervous system and inhibits monoamine oxidase and prostaglandin synthesis. -
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2-APB hydrochloride
0 Images2-APB is an analog of 6-APB, a benzofuran derivative and a psychoactive substance. Certain benzofuran derivatives have monoamine oxidase-A inhibitory activity . -
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MAO-B-IN-64
0 ImagesCat. No.: HY-189245MAO-B-IN-64 is an orally active, blood-brain barrier-permeable reversible competitive inhibitor of monoamine oxidase B, with an IC50 of 0.35 nM against human MAO-B and a Ki of 0.22 nM for human MAO-B. MAO-B-IN-64 exhibits antioxidant effects by scavenging free radicals. MAO-B-IN-64 exerts anti-neuroinflammatory effects by inhibiting the release of pro-inflammatory factors. MAO-B-IN-64 acts as an H2S donor by releasing hydrogen sulfide. MAO-B-IN-64 can be applied in the research of Parkinson's disease. -
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Lenumlostat hydrochloride
0 ImagesCat. No.: HY-107422ACAS No.: 2098884-53-6Synonyms: PAT-1251 hydrochloride; GB2064 hydrochloridePAT-1251 Hydrochloride is a potent, selective and oral lysyl oxidase-like 2 (LOXL2) inhibitor, with IC50s of 0.71 and 1.17 μM for hLOXL2 and hLOXL3, respectively, and also potently inhibits mouse, rat, and dog LOXL2 (IC50s, 0.10, 0.12, and 0.16 μM, respectively). PAT-1251 Hydrochloride is used in the research of fibrotic diseases. -
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- MC4762
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(S)-Rasagiline mesylate
0 ImagesCat. No.: HY-14200ACAS No.: 202464-88-8Synonyms: TVP1022 mesylate; S-PAI mesylate(S)-Rasagiline (TVP1022) mesylate is the relatively inactive S-enantiomer form of Rasagiline mesylate. Rasagiline mesylate is a highly potent selective irreversible MAO inhibitor with IC50s of 4.43 nM and 412 nM for rat brain MAO B and A activity, respectively. -
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MAO A/HDAC-IN-1
0 ImagesCat. No.: HY-142706CAS No.: 3031466-56-2MAO A/HDAC-IN-1 is a dual?inhibitor?of monoamine oxidase A (MAO A) and HDAC. MAO A/HDAC-IN-1 can be used for glioma research. MAO A/HDAC-IN-1 is a click chemistry reagent, it contains an Alkyne group and can undergo copper-catalyzed azide-alkyne cycloaddition (CuAAc) with molecules containing Azide groups. -
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PXS-5505
0 ImagesSynonyms: LOX-IN-3 dihydrochloride monohydratePXS-5505 (LOX-IN-3 dihydrochloride monohydrate) (Compound 33) is an orally active lysyl oxidase (LOX) inhibitor. PXS-5505 can be used for fibrosis, cancer and angiogenesis research. -
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RS 2232
0 ImagesCat. No.: HY-123129CAS No.: 85073-83-2RS 2232 is an orally active, competitive 5-HT deamination inhibitor with a Ki of 0.054 μM. RS-2232 exhibits reversible and specific inhibition of type A monoamine oxidase. RS 2232 can be used in brain research. -
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hMAO-B-IN-7
0 ImagesCat. No.: HY-157400CAS No.: 2955577-14-5hMAO-B-IN-7 (compound 11n) is a potent and blood–brain barrier (BBB) penetrable inhibitor of human monoamine oxidase-B (hMAO-B), with the IC50 value of 0.79±0.05 μM. hMAO-B-IN-7 can be used for Alzheimer’s disease (AD) and Parkinson’s disease (PD) research. -
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Sorry. There is currently no product that acts on isoform Bcl-2, Bcl-W and Bim together.Please
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