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Potential Inhibitor to Abnormal Involuntary Movement Disorder:<br />

Dimethoxy-Terphenyl and 3-(4-Methoxy-Phenyl)-Dibenzofuran Targeting<br />

Monoamine Oxidase B<br />

Goh Meng Shien<br />

Supervisor: Dr. Muhamad Fairus Bin Hassim<br />

Co-supervisor: Dr. Fatimah Binti Hashim<br />

Bachelor of Science (Biological Sciences)<br />

School of Fundamental Science<br />

Abnormal involuntary movements (AIM) disorder is symptom of Parkinson and seizure.<br />

Usually associated with false signalling of monoamine oxidase B (MAOB) associated<br />

pathway in synapse. Our study identifies new terphenyl-based compounds that<br />

interact with MOAB. Cytotoxicity of dimethoxy-terphenyl (14MP) and 3-(4-Methoxyphenyl)-dibenzofuran<br />

(FD1) were assessed. Through computational approach, we<br />

identified potential proteins that interacted with the compounds and characterized the<br />

type of interaction. Cytotoxic assessment using MTT shows minimal cytotoxicity to<br />

NIH-3T3 and RAW264.7, however 14MP is more toxic than FD1. Homologous database<br />

screening to find proteins targeted by these compounds shows that 14MP has the<br />

highest probability to interact with MAOB and amyloid precursor-like proteins (APLPs).<br />

While for FD1 are inducible nitric oxide synthase (P35228) and MAOB. However,<br />

further molecular docking analysis shows that MAOB has the highest binding affinity<br />

with 14MP and FD1. Thus, indicate potential inhibitor for MAOB from false breaking<br />

down dopamine hence causing AIM.<br />

360 | U M T U N D E R G R A D U A T E R E S E A R C H D A Y 2018

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