Evidence map›Paper›PMID 31744211›Full record

ReviewMolecules (Basel, Switzerland)2019

Spirocyclic Motifs in Natural Products.

Evgeny Chupakhin, Olga Babich, Alexander Prosekov, Lyudmila Asyakina, Mikhail Krasavin

Abstract readReview
In one paragraph

Review in Molecules (Basel, Switzerland), 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 44 papers.

0numbers the graph read from it
0cells of the map it votes in
44citing 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

44 citing papers in PubMed.

  1. Article
  2. Review
  3. Article
  4. Article
  5. Article
  6. Article
  7. Article
  8. Article
  9. Annulative endoperoxidation of tetronates.Organic & biomolecular chemistry · 2025
    Article
  10. Article
  11. Article
  12. Article
  13. A Review of Approaches Developed for Spiroether Synthesis.Topics in current chemistry (Cham) · 2025
    Review
  14. Article
  15. Article
  16. Article
  17. Article
  18. Article
  19. Article
  20. 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

5 authors.

Evgeny ChupakhinImmanuel Kant Baltic Federal University, 236016 Kaliningrad, Alexandra Nevskogo 14, Russia.
Olga BabichImmanuel Kant Baltic Federal University, 236016 Kaliningrad, Alexandra Nevskogo 14, Russia.
Alexander ProsekovKemerovo State University, 650000 Krasnaya, Kemerovo, Russia.
Lyudmila AsyakinaKemerovo State University, 650000 Krasnaya, Kemerovo, Russia.
Mikhail KrasavinImmanuel Kant Baltic Federal University, 236016 Kaliningrad, Alexandra Nevskogo 14, Russia.

Funding

Ministry of Education and Science of the Russian Federation RFMEFI57718X0285
6 · The paper itself

Abstract

Spirocyclic motifs are emerging privileged structures for drug discovery. They are also omnipresent in the natural products domain. However, until today, no attempt to analyze the structural diversity of various spirocyclic motifs occurring in natural products and their relative populations with unique compounds reported in the literature has been undertaken. This review aims to fill that void and analyze the diversity of structurally unique natural products containing spirocyclic moieties of various sizes.

Indexed as

Models, ChemicalBiological ProductsSpiro CompoundsStructure-Activity RelationshipBiological ProductsSpiro Compoundsbiological activitychemical diversitynatural productsprivileged structuresspirocycles

Identifiers

PMID31744211
PMCPMC6891393

What OpenQuestion holds

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Read underepoch 390

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.