Literature DB >> 25074019

Biology-oriented synthesis: harnessing the power of evolution.

Hilde van Hattum1, Herbert Waldmann.   

Abstract

For scientists to gain a better understanding of nature, biological research is greatly aided by small-molecule modulators that perturb protein activity without fundamentally altering the underlying biological systems. The number of possible interfering molecules, however, is so vast that, due to limitations in existing matter and time required for synthesis, they cannot be covered comprehensively. Because proteins and their cognate natural product ligands and substrates co-evolved, these naturally occurring ligands can serve as structural starting points to explore the biologically relevant chemical space. To this end, known natural products are structurally classified on the basis of their core scaffolds and hierarchically arranged in the "natural product tree", which can be annotated for bioactivity and intuitively navigated with currently available software. Biologically relevant scaffolds inspire the synthesis of compound libraries enriched in biological activity. This Perspective describes the development of "biology-oriented synthesis" as a guiding principle to harness the power of evolution in the quest for novel bioactive small molecules for chemical biology research and drug discovery.

Mesh:

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Year:  2014        PMID: 25074019     DOI: 10.1021/ja505861d

Source DB:  PubMed          Journal:  J Am Chem Soc        ISSN: 0002-7863            Impact factor:   15.419


  28 in total

Review 1.  Discovery of novel drug targets and their functions using phenotypic screening of natural products.

Authors:  Junghwa Chang; Ho Jeong Kwon
Journal:  J Ind Microbiol Biotechnol       Date:  2015-09-12       Impact factor: 3.346

2.  The natural productome.

Authors:  Andrea M E Palazzolo; Claire L W Simons; Martin D Burke
Journal:  Proc Natl Acad Sci U S A       Date:  2017-05-22       Impact factor: 11.205

Review 3.  Counting on natural products for drug design.

Authors:  Tiago Rodrigues; Daniel Reker; Petra Schneider; Gisbert Schneider
Journal:  Nat Chem       Date:  2016-04-25       Impact factor: 24.427

4.  Re-engineering natural products to engage new biological targets.

Authors:  Stephen E Motika; Paul J Hergenrother
Journal:  Nat Prod Rep       Date:  2020-11-18       Impact factor: 13.423

5.  Bridging the gap between natural product synthesis and drug discovery.

Authors:  Nathanyal J Truax; Daniel Romo
Journal:  Nat Prod Rep       Date:  2020-10-26       Impact factor: 13.423

6.  Cheminformatic characterization of natural products from Panama.

Authors:  Dionisio A Olmedo; Mariana González-Medina; Mahabir P Gupta; José L Medina-Franco
Journal:  Mol Divers       Date:  2017-08-22       Impact factor: 2.943

7.  Impact of a five-dimensional framework on R&D productivity at AstraZeneca.

Authors:  Paul Morgan; Dean G Brown; Simon Lennard; Mark J Anderton; J Carl Barrett; Ulf Eriksson; Mark Fidock; Bengt Hamrén; Anthony Johnson; Ruth E March; James Matcham; Jerome Mettetal; David J Nicholls; Stefan Platz; Steve Rees; Michael A Snowden; Menelas N Pangalos
Journal:  Nat Rev Drug Discov       Date:  2018-01-19       Impact factor: 84.694

8.  Re-Engineering of Yohimbine's Biological Activity through Ring Distortion: Identification and Structure-Activity Relationships of a New Class of Antiplasmodial Agents.

Authors:  Nicholas G Paciaroni; David L Perry; Verrill M Norwood; Claribel Murillo-Solano; Jennifer Collins; Srinivasarao Tenneti; Debopam Chakrabarti; Robert W Huigens
Journal:  ACS Infect Dis       Date:  2020-01-16       Impact factor: 5.084

9.  A Tryptoline Ring-Distortion Strategy Leads to Complex and Diverse Biologically Active Molecules from the Indole Alkaloid Yohimbine.

Authors:  Nicholas G Paciaroni; Ranjala Ratnayake; James H Matthews; Verrill M Norwood; Austin C Arnold; Long H Dang; Hendrik Luesch; Robert W Huigens
Journal:  Chemistry       Date:  2017-02-03       Impact factor: 5.236

10.  Access to a Structurally Complex Compound Collection via Ring Distortion of the Alkaloid Sinomenine.

Authors:  Alfredo Garcia; Bryon S Drown; Paul J Hergenrother
Journal:  Org Lett       Date:  2016-09-21       Impact factor: 6.005

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