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Monoamine Oxidase

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Monoamine Oxidase

Chemical Structure Cat. No. Product Name CAS No.
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.
Isatin Chemical Structure
BCP15996 Isatin 91-56-5
Isatin is a potent inhibitor of monoamine oxidase (MAO) with an IC50 of 3 μM. Also binds to central benzodiazepine receptors (IC50 against clonazepam, 123 μM). Also acts as an antagonist of both atrial natriuretic peptide stimulated and nitric oxide-stimulated guanylate cyclase activity. Shows effect on the serotonergic system.
Vafidemstat Chemical Structure
BCP29383 Vafidemstat 1357362-02-7
Vafidemstat, also known as ORY 2001, is a lysine-specific histone demethylase (LSD1) inhibitor.
Lazabemide Chemical Structure
BCP21224 Lazabemide 103878-84-8
Lazabemide is a reversible and selective inhibitor of monoamine oxidase B (MAO-B). Lazabemide is potentially an antiparkinsonian agent.
Eprobemide Chemical Structure
BCP30208 Eprobemide 87940-60-1
Eprobemide is a non-competitive reversible inhibitor of monoamine oxidase A.
Moclobemide Chemical Structure
BCP15783 Moclobemide 71320-77-9
Moclobemide(Ro111163) is a reversible monoamine oxidase inhibitor (MAOI) selective for isoform A (RIMA) used to treat major depressive disorder.
Safinamide Chemical Structure
BCP12082 Safinamide 133865-89-1
Safinamide (EMD 1195686; FCE 26743) selectively and reversibly inhibits MAO-B with IC50 of 98 nM, exhibits 5918-fold selectivity against MAO-A.
Safinamide mesylate Chemical Structure
BCP16018 Safinamide mesylate 202825-46-5
Safinamide Mesylate is mesylate salt of Safinamide, selectively and reversibly inhibits MAO-B with IC50 of 98 nM, exhibits 5918-fold selectivity against MAO-A.
Mofegiline hydrochloride Chemical Structure
BCP23694 Mofegiline hydrochloride 120635-25-8
Mofegiline HCl (MDL72974A) is a potent and selective enzyme-activated irreversible inhibitor of MAO-B; shows marked selectivity for the B form (IC50 = 680 and 3.6 nM for MAO-A and MAO-B, respectively.
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