Evidence map›Paper›PMID 38514617›Full record

ArticleNature communications2024

Targeted sampling of natural product space to identify bioactive natural product-like polyketide macrolides.

Darryl M Wilson, Daniel J Driedger, Dennis Y Liu, Sandra Keerthisinghe, Adrian Hermann, Christoph Bieniossek, Roger G Linington, Robert A Britton

Abstract read
In one paragraph

Article in Nature communications, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

3 citing papers in PubMed.

  1. Review
  2. Article
  3. Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

8 authors.

Darryl M WilsonDepartment of Chemistry, Simon Fraser University, Burnaby, BC, V5A 1S6, Canada.
Daniel J DriedgerDepartment of Chemistry, Simon Fraser University, Burnaby, BC, V5A 1S6, Canada.
Dennis Y LiuDepartment of Chemistry, Simon Fraser University, Burnaby, BC, V5A 1S6, Canada.
Sandra KeerthisingheCenter for High-Throughput Chemical Biology, Simon Fraser University, Burnaby, BC, V5A 1S6, Canada.
Adrian HermannRoche Pharma Research and Early Development, Roche Innovation Center Basel, F. Hoffmann-La Roche Ltd, Grenzacherstrasse 124, 4070, Basel, Switzerland.ORCID http://orcid.org/0009-0006-2487-4441
Christoph BieniossekRoche Pharma Research and Early Development, Roche Innovation Center Basel, F. Hoffmann-La Roche Ltd, Grenzacherstrasse 124, 4070, Basel, Switzerland.
Roger G LiningtonDepartment of Chemistry, Simon Fraser University, Burnaby, BC, V5A 1S6, Canada. rliningt@sfu.ca.ORCID http://orcid.org/0000-0003-1818-4971
Robert A BrittonDepartment of Chemistry, Simon Fraser University, Burnaby, BC, V5A 1S6, Canada. rbritton@sfu.ca.ORCID http://orcid.org/0000-0002-9335-0047

Funding

Gouvernement du Canada | Natural Sciences and Engineering Research Council of Canada (Conseil de Recherches en Sciences Naturelles et en Génie du Canada) 2019-06368
6 · The paper itself

Abstract

Polyketide or polyketide-like macrolides (pMLs) continue to serve as a source of inspiration for drug discovery. However, their inherent structural and stereochemical complexity challenges efforts to explore related regions of chemical space more broadly. Here, we report a strategy termed the Targeted Sampling of Natural Product space (TSNaP) that is designed to identify and assess regions of chemical space bounded by this important class of molecules. Using TSNaP, a family of tetrahydrofuran-containing pMLs are computationally assembled from pML inspired building blocks to provide a large collection of natural product-like virtual pMLs. By scoring functional group and volumetric overlap against their natural counterparts, a collection of compounds are prioritized for targeted synthesis. Using a modular and stereoselective synthetic approach, a library of polyketide-like macrolides are prepared to sample these unpopulated regions of pML chemical space. Validation of this TSNaP approach by screening this library against a panel of whole-cell biological assays, reveals hit rates exceeding those typically encountered in small molecule libraries. This study suggests that the TSNaP approach may be more broadly useful for the design of improved chemical libraries for drug discovery.

Indexed as

Biological ProductsPolyketidesDrug DiscoveryMacrolidesBiological ProductsMacrolidesPolyketides

Identifiers

PMID38514617
PMCPMC10958047

What OpenQuestion holds

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LicenceCC BY
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Registered trials

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.