Evidence map›Paper›PMID 27314508›Full record

ReviewChemical reviews2016

Structure, Chemical Synthesis, and Biosynthesis of Prodiginine Natural Products.

Dennis X Hu, David M Withall, Gregory L Challis, Regan J Thomson

Abstract readReview
In one paragraph

Review in Chemical reviews, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 58 papers.

0numbers the graph read from it
0cells of the map it votes in
58citing 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

58 citing papers in PubMed.

  1. Review
  2. Article
  3. Article
  4. Breeding ofBiodesign research · 2026
    Article
  5. Review
  6. Metacycloprodigiosin produced by a high-yieldOrganic & biomolecular chemistry · 2026
    Article
  7. Article
  8. Article
  9. Article
  10. Review
  11. Promising Prodiginins Biological Activities.Chemistry & biodiversity · 2025
    Review
  12. Article
  13. Review
  14. Article
  15. Article
  16. An Algerian Soil-LivingJournal of fungi (Basel, Switzerland) · 2024
    Article
  17. Article
  18. Article
  19. Article
  20. Review
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

4 authors.

Dennis X HuDepartment of Chemistry, Northwestern University , Evanston, Illinois 60208, United States.
David M WithallDepartment of Chemistry, University of Warwick , Coventry CV4 7AL, United Kingdom.
Gregory L ChallisDepartment of Chemistry, University of Warwick , Coventry CV4 7AL, United Kingdom.
Regan J ThomsonDepartment of Chemistry, Northwestern University , Evanston, Illinois 60208, United States.

Funding

New Methods for the Concise Synthesis of Bioactive Polycyclic MoleculesR01GM085322 · NIGMS · NORTHWESTERN UNIVERSITY · PI THOMSON, REGAN JAMES · 2009 to 2013
$1.4M
NIGMS NIH HHS R01 GM085322
6 · The paper itself

Abstract

The prodiginine family of bacterial alkaloids is a diverse set of heterocyclic natural products that have likely been known to man since antiquity. In more recent times, these alkaloids have been discovered to span a wide range of chemical structures that possess a number of interesting biological activities. This review provides a comprehensive overview of research undertaken toward the isolation and structural elucidation of the prodiginine family of natural products. Additionally, research toward chemical synthesis of the prodiginine alkaloids over the last several decades is extensively reviewed. Finally, the current, evidence-based understanding of the various biosynthetic pathways employed by bacteria to produce prodiginine alkaloids is summarized.

Indexed as

AlkaloidsBacteriaBiological ProductsProdigiosinSerratia marcescensAlkaloidsBiological ProductsprodiginineProdigiosin

Identifiers

PMID27314508
PMCPMC5555159

What OpenQuestion holds

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Registered trials

None linked

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.