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Development of Chemistry-Based Screening Platform for Access to Mirror-Image Library of Natural Products

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  • © 2018

Overview

  • Nominated as an outstanding Ph.D. thesis by Kyoto University
  • Describes a pioneering chemistry-based screening process for drug discovery
  • Provides valuable insights for the field of organic chemistry, especially regarding the total synthesis of natural products and proteins
  • Includes supplementary material: sn.pub/extras

Part of the book series: Springer Theses (Springer Theses)

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Table of contents (4 chapters)

Keywords

About this book

This thesis mainly describes the development of a screening process for a mirror-image library of chiral natural products. It demonstrates how, by using mirror-image proteins for the screening of available natural products, unavailable mirror-image isomers of natural products can be screened in a mirror process. Moreover, as mirror-image isomers including target proteins and natural products are mainly prepared by means of chemical synthesis, the screening strategy presented here suggests the importance of organic chemistry.

Natural products are commonly used as valuable resources for drug discovery. However, as they are mostly produced as single enantiomeric forms, researchers have tested o


nly natural products bearing one stereochemistry available in nature. As natural products and their enantiomers have identical physicochemical properties and different biological activities, mirror-image isomers of natural products are promising candidates for novel medicinal resources.

In an effort to identify anticancer agents from the mirror-image library, chemical protein syntheses of some target oncoproteins, MDM2, MDMX and Grb2, and their applications to the chemical array screening process were achieved. In the course of this process the NP843 enantiomer, which is the enantiomer of an α-tocopherol derivative, was successfully identified as a novel MDM2-p53 interaction inhibitor. These results clearly show that a mirror-image library of chiral natural products represents an invaluable medicinal resource. Accordingly, the chemistry-based screening strategy described in this thesis will be of great interest to a broad range of chemists involved in natural product, medicinal, and synthetic chemistry.

Authors and Affiliations

  • Graduate School of Pharmaceutical Sciences, Kyoto University, Kyoto, Japan

    Taro Noguchi

Bibliographic Information

  • Book Title: Development of Chemistry-Based Screening Platform for Access to Mirror-Image Library of Natural Products

  • Authors: Taro Noguchi

  • Series Title: Springer Theses

  • DOI: https://doi.org/10.1007/978-981-10-6623-8

  • Publisher: Springer Singapore

  • eBook Packages: Chemistry and Materials Science, Chemistry and Material Science (R0)

  • Copyright Information: Springer Nature Singapore Pte Ltd. 2018

  • Hardcover ISBN: 978-981-10-6622-1Published: 16 November 2017

  • Softcover ISBN: 978-981-13-4917-1Published: 23 December 2018

  • eBook ISBN: 978-981-10-6623-8Published: 03 November 2017

  • Series ISSN: 2190-5053

  • Series E-ISSN: 2190-5061

  • Edition Number: 1

  • Number of Pages: XIV, 80

  • Number of Illustrations: 28 b/w illustrations, 18 illustrations in colour

  • Topics: Medicinal Chemistry, Organic Chemistry, Pharmaceutical Sciences/Technology

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