
MAO-IN-M30 dihydrochloride
CAS No. 64821-19-8
MAO-IN-M30 dihydrochloride( M 30 dihydrochloride )
Catalog No. M28155 CAS No. 64821-19-8
Potent and brain selective monoamine oxidase (MAO) inhibitor (EC50 values are 37 and 57 nM for MAO-A and MAO-B, respectively).
Purity : >98% (HPLC)






Size | Price / USD | Stock | Quantity |
5MG | 141 | Get Quote |
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10MG | 203 | Get Quote |
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25MG | 338 | Get Quote |
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50MG | 505 | Get Quote |
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100MG | 710 | Get Quote |
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500MG | 1494 | Get Quote |
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1G | Get Quote | Get Quote |
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Biological Information
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Product NameMAO-IN-M30 dihydrochloride
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NoteResearch use only, not for human use.
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Brief DescriptionPotent and brain selective monoamine oxidase (MAO) inhibitor (EC50 values are 37 and 57 nM for MAO-A and MAO-B, respectively).
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DescriptionPotent and brain selective monoamine oxidase (MAO) inhibitor (EC50 values are 37 and 57 nM for MAO-A and MAO-B, respectively). Also an iron chelator with antioxidant properties. Protects cells against 6-OHDA induced apoptosis. Attenuates MPTP depletion of DA and increases striatal monoamine levels in a mouse Parkinson's disease model.(In Vitro):MAO-IN-M30 (0.25 nM; 72 hours) significantly increased cell viability to ~90% after exposure to Dexamethasone. MAO-IN-M30 treatment significantly decreases the occurrence of fragmented DNA compared to the dexamethasone-treated group in SH-SY5Y cells. MAO-IN-M30 (0-10 μM; 24 hours) enhances PC12 cell survival.(In Vivo):MAO-IN-M30 (0.5-2.5 mg/kg; p.o.; once daily for 14 consecutive days) possesses neuroprotective activities.
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In VitroMAO-IN-M30 (0.25 nM; 72 hours) significantly increased cell viability to ~90% after exposure to Dexamethasone.MAO-IN-M30 (0-10 μM; 24 hours) enhances PC12 cell survival.MAO-IN-M30 treatment significantly decreases the occurrence of fragmented DNA compared to the dexamethasone-treated group in SH-SY5Y cells. Cell Viability Assay Cell Line:SH-SY5Y cells Concentration:0.25?nM Incubation Time:72 hours Result:Significantly increased cell viability to ~90% after exposure to Dexamethasone.Cell Viability Assay Cell Line:PC12 cells Concentration:0-10 μMIncubation Time:24 hours Result:Enhanced the PC12 cell viability, the cell viability increasing to 85 ± 6 and 90 ± 7%.
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In VivoMAO-IN-M30 (0.5-2.5 mg/kg; p.o.; once daily for 14 consecutive days) possesses neuroprotective activities. Animal Model:Male C57/BL mice (20-22 g; MPTP-induced neurotoxicity in mice)Dosage:0.5, 2.5 mg/kg Administration:P.o.; once daily for 14 consecutive days Result:Significantly elevate striatal dopamine levels, reduce its metabolism, and elevate tyrosine-hydroxylase protein levels and activity. Elevated MPTP-reduced dopaminergic and transferrin receptor cell count in the SNpc.
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SynonymsM 30 dihydrochloride
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PathwayOthers
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TargetOther Targets
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Recptor——
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Research Area——
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Indication——
Chemical Information
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CAS Number64821-19-8
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Formula Weight299.2
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Molecular FormulaC14H14N2O.2HCl
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Purity>98% (HPLC)
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SolubilityIn Vitro:?DMSO : 2 mg/mL (6.68 mM)
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SMILESCN(CC#C)CC1=C2C(N=CC=C2)=C(O)C=C1.Cl.Cl
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Chemical Name——
Shipping & Storage Information
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Storage(-20℃)
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ShippingWith Ice Pack
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Stability≥ 2 years
Reference
1.Schettgen T, Weiss T, Angerer J. Biological monitoring of phenmedipham: determination of m-toluidine in urine. Arch Toxicol. 2001 May;75(3):145-9.
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