Evidence map›Paper›PMID 30134555›Full record

ReviewMolecules (Basel, Switzerland)2018

Linear Triquinane Sesquiterpenoids: Their Isolation, Structures, Biological Activities, and Chemical Synthesis.

Yi Qiu, Wen-Jian Lan, Hou-Jin Li, Liu-Ping Chen

Abstract readReview
In one paragraph

Review in Molecules (Basel, Switzerland), 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 11 papers.

0numbers the graph read from it
0cells of the map it votes in
11citing 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

11 citing papers in PubMed.

  1. Review
  2. Article
  3. Article
  4. Article
  5. Article
  6. Review
  7. IUCrData · 2021
    Article
  8. Review
  9. Total Synthesis of the Diterpene Waihoensene.Angewandte Chemie (International ed. in English) · 2021
    Article
  10. Article
  11. 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

4 authors.

Yi QiuSchool of Chemistry, Sun Yat-sen University, Guangzhou 510275, China. qiuyi0771@163.com.
Wen-Jian LanSchool of Pharmaceutical Sciences, Sun Yat-sen University, Guangzhou 510006, China. lanwj@mail.sysu.edu.cn.
Hou-Jin LiSchool of Chemistry, Sun Yat-sen University, Guangzhou 510275, China. ceslhj@mail.sysu.edu.cn.ORCID 0000-0003-3026-6128
Liu-Ping ChenSchool of Chemistry, Sun Yat-sen University, Guangzhou 510275, China. cesclp@mail.sysu.edu.cn.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Linear triquinane sesquiterpenoids represent an important class of natural products. Most of these compounds were isolated from fungi, sponges, and soft corals, and many of them displayed a wide range of biological activities. On account of their structural diversity and complexity, linear triquinane sesquiterpenoids present new challenges for chemical structure identification and total synthesis. 118 linear triquinane sesquiterpenoids were classified into 8 types, named types I⁻VIII, based on the carbon skeleton and the position of carbon substituents. Their isolation, structure elucidations, biological activities, and chemical synthesis were reviewed. This paper cited 102 articles from 1947 to 2018.

Indexed as

AnimalsAnti-Infective AgentsAntineoplastic AgentsBiological ProductsCell SurvivalChemistry Techniques, SyntheticHumansMicrobial Sensitivity TestsMolecular StructureSesquiterpenesStructure-Activity RelationshipAnti-Infective AgentsAntineoplastic AgentsBiological ProductsSesquiterpenesbiological activitycapnellenehirsutaneisolationlinear triquinane sesquiterpenoidstructuresynthesis

Identifiers

PMID30134555
PMCPMC6225328

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.