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Medicinal Chemistry Research

, Volume 28, Issue 10, pp 1783–1795 | Cite as

Synthesis, sciatic nerve block activity evaluation and molecular docking of fluoro-substituted lidocaine analogs as local anesthetic agents

  • Wen LiEmail author
  • Ying Yan
  • Yingjie Chang
  • Lina Ding
  • Hongmin Liu
  • Qidong YouEmail author
Original Article
  • 25 Downloads

Abstract

Thirty fluoro-substituted lidocaine analogs (10ae, 11ae, 14a–e, 15a–e, 18a–e and 19a–e) were synthesized, and their sciatic nerve block activity were evaluated as local anesthesia. Most of the compounds displayed significant potency, and compound 10a in particular was much more potent than the parent lidocaine. Fifteen analogs including 10a demonstrated pKa values of 7.5–7.8 suitable for local anesthesia. Compound 10a, 14e, and lidocaine were docked into three target receptors of local anesthetics by molecular docking studies to delineate structure-activity relationships and explain the differences in activities. Hydrophobic interactions and hydrogen bonds were identified key to molecular binding, suggesting that optimization of these interactions and/or trifluoro-substitution at the benzene ring of lidocaine could enhance the properties of lidocine analogs for local anesthesia.

Keywords

Lidocaine Synthesis Local anesthetic activity Molecular docking 

Notes

Acknowledgements

This work was supported by a grant from Jiangsu Hengrui Pharmaceutical Com. Ltd and a foundation on the integration of industry, education, and research of He’nan science and technology commission (No. 152107000041). The authors are grateful to Dr J.H. Fu (Pharmaceutical School, China Pharmaceutical University) for the determination of biological activity. We thank Amy Tong from Liwen Bianji, Edanz Editing China (www.liwenbianji.cn/ac), for editing the English draft of this paper.

Compliance with ethical standards

Conflict of interest

The authors declare that they have no conflict of interest.

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Copyright information

© Springer Science+Business Media, LLC, part of Springer Nature 2019

Authors and Affiliations

  1. 1.School of Pharmaceutical SciencesZhengzhou UniversityZhengzhouPR China
  2. 2.Jiangsu Key Laboratory of Drug Design and Optimization and Department of Medicinal ChemistryChina Pharmaceutical UniversityNanjingPR China
  3. 3.Collaborative Innovation Center of New Drug Research and Safety EvaluationHenan Province & Key Laboratory of Technology of Drug Preparation (Zhengzhou University), Ministry of Education & Key Laboratory of Henan Province for Drug Quality and EvaluationZhengzhouPR China

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