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Monoamine Oxidase

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Monoamine Oxidase

Chemical Structure Cat. No. Product Name CAS No.
Phenelzine Sulfate Chemical Structure
 BCP44466 Phenelzine Sulfate 156-51-4
Phenelzine Sulfate is a hydrazine derivative and a potent non-selective monoamine oxidase (MAO) inhibitor with anxiolytic and antidepressant properties.
Contezolid Chemical Structure
 BCP42163 Contezolid 1112968-42-9
Contezolid is a monoamine oxidase-A (MAO-A) Inhibitor potentially for the treatment of acute bacterial skin.
Selegiline hydrochloride Chemical Structure
 BCP38874 Selegiline hydrochloride 14611-52-0
Selegiline hydrochloride is a selective, irreversible inhibitor of Type B monoamine oxidase. It is used in newly diagnosed patients with Parkinson's disease. It may slow progression of the clinical disease and delay the requirement for levodopa therapy. It also may be given with levodopa upon onset of disability.
PF 9601N Chemical Structure
 BCP37785 PF 9601N 133845-63-3
PF 9601N is a selective and potent monoamine oxidase B inhibitor that exhibit anti-Parkinsonian effects in several models of PD.
PXS-5153A dihydrochloride Chemical Structure
 BCP36149 PXS-5153A dihydrochloride 2125956-82-1
PXS-5153A is a novel mechanism based, fast-acting, dual LOXL2/LOXL3 inhibitor, which was used to interrogate the role of these enzymes in models of collagen crosslinking and fibrosis.
Tranylcipromine Chemical Structure
 BCP35142 Tranylcipromine 155-09-9
Tranylcypromine, an amphetamine derivative, has been found to be a MAO inhibitor that could be used an antidepressant agent and anxiolytic drug.
Toloxatone Chemical Structure
 BCP32681 Toloxatone 29218-27-7
Toloxatone is a reversible monoamine oxidase A (MAOA) inhibitor. Antidepressant.
Pirlindole Chemical Structure
 BCP32097 Pirlindole 60762-57-4
Pirlindole is a highly selective reversible inhibitor of monoamine oxidase type A.
SL251188 Chemical Structure
 BCP18119 SL251188 185835-97-6
SL-251188 is a monoamine oxidase B (MAO-B) inhibitor potentially for treatment of Alzheimer's dementia and smoking cessation. SL-25.1188 is characterized in vivo by reversible binding, high brain uptake, and very slow plasma metabolism.
TB5 Chemical Structure
 BCP24913 TB5 948841-07-4
TB5 is a potent, selective and reversible inhibitor of hMAO-B with a Ki value of 0.11±0.01 μM.
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