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dc.contributor.authorPrins, Louis H.A.
dc.contributor.authorPetzer, Jacobus P.
dc.contributor.authorMalan, Sarel F.
dc.date.accessioned2012-02-29T09:49:49Z
dc.date.available2012-02-29T09:49:49Z
dc.date.issued2010en_US
dc.identifier.citationPrins, L.H.A. et al. 2010. Inhibition of monoamine oxidase by indole and benzofuran derivatives. European journal of medicinal chemistry, 45(10):4458-4466. [https://doi.org/10.1016/j.ejmech.2010.07.005]en_US
dc.identifier.issn0223-5234en_US
dc.identifier.issn1768-3254en_US
dc.identifier.urihttp://hdl.handle.net/10394/5995
dc.identifier.urihttps://www.sciencedirect.com/science/article/pii/S022352341000485X
dc.identifier.urihttps://doi.org/10.1016/j.ejmech.2010.07.005
dc.description.abstractMonoamine oxidase (MAO) is an important drug target for the treatment of neurological disorders. A series of indole and benzofuran derivatives were synthesised and evaluated as inhibitors of the two MAO isoforms, MAO-A and MAO-B. In general, the derivatives were found to be selective MAO-B inhibitors with Ki values in the nanoMolar (nM) to microMolar (μM) concentration range. The most potent MAO-B inhibitor, 3,4-dichloro-N-(2-methyl-1H-indol-5-yl)benzamide, exhibited a Ki value of 0.03 μM and was 99 fold more selective for the B isoform. We conclude that these indole and benzofuran derivatives are promising reversible MAO-B inhibitors with a possible role in the treatment of neurodegenerative diseases such as Parkinson’s disease (PD)
dc.language.isoen
dc.publisherElsevieren_US
dc.subjectMonoamine oxidase (MAO)
dc.subjectIndole derivatives
dc.subjectBenzofuran derivatives
dc.subjectParkinson’s disease (PD)
dc.subjectMolecular docking
dc.subjectLigandFit
dc.titleInhibition of monoamine oxidase by indole and benzofuran derivativesen_US
dc.contributor.researchID10199667 - Malan, Sarel Francois
dc.contributor.researchID10727388 - Petzer, Jacobus Petrus
dc.contributor.researchID12256129 - Prins, Louis Hendrik Albertus


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