Synthesis, In silico molecular docking modeling and pharmacophore mapping of (E)-3-(4-hydroxy-2,6-dimethoxyphenyl)-1-phenylprop-2-en-1- one as potential new inhibitor of microsomal prostaglandin E synthase-1
The discovery of potent anti-inflammatory agents through inhibition of prostaglandin E2 (PGE2) via microsomal prostaglandin E2 synthase-1 (mPGES-1) blocking has been proven to be an important game changer in pharmaceutical industry in recent years. In this study, new chalcone derivative has been suc...
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| Main Authors: | , , , |
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| Format: | Book Chapter |
| Language: | en en |
| Published: |
Trans Tech Publications Ltd
2020
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| Subjects: | |
| Online Access: | http://irep.iium.edu.my/80242/1/80242_Synthesis%2C%20In%20silico%20molecular%20docking%20modeling.pdf http://irep.iium.edu.my/80242/2/80242_Synthesis%2C%20In%20silico%20molecular%20docking%20modeling_SCOPUS.pdf http://irep.iium.edu.my/80242/ https://www.scientific.net/MSF.981.247 |
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| Summary: | The discovery of potent anti-inflammatory agents through inhibition of prostaglandin E2 (PGE2) via microsomal prostaglandin E2 synthase-1 (mPGES-1) blocking has been proven to be an important game changer in pharmaceutical industry in recent years. In this study, new chalcone derivative has been successfully synthesized via Claisen-Schmidt condensation reaction. The compound was then docked into mPGES-1 active site to predict anti-inflammatory properties through ligand-enzyme interaction investigation. The data collected from in silico molecular docking simulation and pharmacophore modeling studies provide important insight on the molecular conformation and further shed light towards structural modification of the future novel mPGES-1 inhibitor. |
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