Authors: Worachartcheewan, Apilak
Prachayasittikul, Veda
Prachayasittikul, Supaluk
Tantivit, Visanu
Yeeyahya, Chareef
Prachayasittikul, Virapong
Title: Rational design of novel coumarins
Other Titles: a potential trend for antioxidants in cosmetics
Language (ISO): en
Abstract: Coumarins are well-known for their antioxidant effect and aromatic property, thus, they are one of ingredients commonly added in cosmetics and personal care products. Quantitative structure-activity relationships (QSAR) modeling is an in silico method widely used to facilitate rational design and structural optimization of novel drugs. Herein, QSAR modeling was used to elucidate key properties governing antioxidant activity of a series of the reported coumarin-based antioxidant agents (1-28). Several types of descriptors (calculated from 4 softwares i.e., Gaussian 09, Dragon, PaDEL and Mold2 softwares) were used to generate three multiple linear regression (MLR) models with preferable predictive performance (Q2LOO-CV = 0.813-0.908; RMSELOO-CV = 0.150-0.210; Q2Ext = 0.875-0.952; RMSEExt = 0.104-0.166). QSAR analysis indicated that number of secondary amines (nArNHR), polarizability (G2p), electronegativity (D467, D580, SpMin2_Bhe, and MATS8e), van der Waals volume (D491 and D461), and H-bond potential (SHBint4) are important properties governing antioxidant activity. The constructed models were also applied to guide in silico rational design of an additional set of 69 structurally modified coumarins with improved antioxidant activity. Finally, a set of 9 promising newly design compounds were highlighted for further development. Structure-activity analysis also revealed key features required for potent activity which would be useful for guiding the future rational design. In overview, our findings demonstrated that QSAR modeling could possibly be a facilitating tool to enhance successful development of bioactive compounds for health and cosmetic applications.
Subject Headings: coumarin
antioxidant activity
rational design
Issue Date: 2020-02-26
Rights link:
Provenance: IfADo - Leibniz Research Centre for Working Environment and Human Factors, Dortmund
Appears in Collections:Original Articles 2020

Files in This Item:
File Description SizeFormat 
Worachartcheewan_26022020_proof.pdfDNB445.1 kBAdobe PDFView/Open

This item is protected by original copyright

This item is licensed under a Creative Commons License Creative Commons