Evidence map›Paper›PMID 26771621›Full record

ArticleMarine drugs2016

Five New Cytotoxic Metabolites from the Marine Fungus Neosartorya pseudofischeri.

Wen-Jian Lan, Sheng-Jiao Fu, Meng-Yang Xu, Wan-Ling Liang, Chi-Keung Lam, Guo-Hua Zhong, Jun Xu, De-Po Yang, Hou-Jin Li

Open access · goldAbstract read
In one paragraph

Article in Marine drugs, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 18 papers.

0numbers the graph read from it
0cells of the map it votes in
18citing papers in PubMed
4.9field-weighted citation impact, top 6% of its field
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

18 citing papers in PubMed, 41 citations in OpenAlex.

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  7. Biosynthesis of Terpenoid-Pyrrolobenzoxazine Hybrid Natural Product CJ-12662.Angewandte Chemie (International ed. in English) · 2022
    Article
  8. Article
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  10. Review
  11. Review
  12. Hybrid Polyketides from aMarine drugs · 2019
    Article
  13. Article
  14. Article
  15. Article
  16. Article
  17. Article
  18. 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

9 authors at 2 institutions in 1 country.

Wen-Jian LanSchool of Pharmaceutical Sciences, Sun Yat-sen University, Guangzhou 510006, China. lanwj@mail.sysu.edu.cn.
Sheng-Jiao FuLab of Insect Toxicology, South China Agricultural University, Guangzhou 510642, China. marnatprod2015@yeah.net.
Meng-Yang XuSchool of Pharmaceutical Sciences, Sun Yat-sen University, Guangzhou 510006, China. xumy3@mail2.sysu.edu.cn.
Wan-Ling LiangSchool of Pharmaceutical Sciences, Sun Yat-sen University, Guangzhou 510006, China. natprodlwl@gmail.com.
Chi-Keung LamSchool of Chemistry and Chemical Engineering, Sun Yat-sen University, Guangzhou 510275, China. cklam@mail.sysu.edu.cn.
Guo-Hua ZhongLab of Insect Toxicology, South China Agricultural University, Guangzhou 510642, China. guohuazhong@scau.edu.cn.
Jun XuSchool of Pharmaceutical Sciences, Sun Yat-sen University, Guangzhou 510006, China. junxu@biochemomes.com.
De-Po YangSchool of Pharmaceutical Sciences, Sun Yat-sen University, Guangzhou 510006, China. lssydp@mail.sysu.edu.cn.
Hou-Jin LiSchool of Chemistry and Chemical Engineering, Sun Yat-sen University, Guangzhou 510275, China. ceslhj@mail.sysu.edu.cn.
Sun Yat-sen University · CNSouth China Agricultural University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The marine fungus Neosartorya pseudofischeri was isolated from Acanthaster planci from the South China Sea. In a preliminary bioactivity screening, the crude methanol extract of the fungal mycelia showed significant inhibitory activity against the Sf9 cell line from the fall armyworm Spodoptera frugiperda. Five novel compounds, including 5-olefin phenylpyropene A (1), 13-dehydroxylpyripyropene A (4), deacetylsesquiterpene (7), 5-formyl-6-hydroxy-8-isopropyl-2- naphthoic acid (9) and 6,8-dihydroxy-3-((1E,3E)-penta-1,3-dien-1-yl)isochroman-1-one (10), together with eleven known compounds, phenylpyropene A (2) and C (3), pyripyropene A (5), 7-deacetylpyripyropene A (6), (1S,2R,4aR,5R,8R,8aR)-1,8a-dihydroxy-2-acetoxy-3,8-dimethyl-5- (prop-1-en-2-yl)-1,2,4a, 5,6,7,8,8a-octahydronaphthalene (8), isochaetominine C (11), trichodermamide A (12), indolyl-3-acetic acid methyl ester (13), 1-acetyl-β-carboline (14), 1,2,3,4-tetrahydro-6-hydroxyl-2-methyl-l,3,4-trioxopyrazino[l,2-a]-indole (15) and fumiquinazoline F (16), were obtained. The structures of these compounds were determined mainly by MS and NMR data. The absolute configuration of 9 was assigned by the single-crystal X-ray diffraction studies. Compounds 1-11 and 15 showed significant cytotoxicity against the Sf9 cells from S. frugiperda.

Indexed as

NeosartoryaAnimalsAntineoplastic AgentsCell Line, TumorChinaDrug Screening Assays, AntitumorHumansInsecticidesSeawaterSesquiterpenesSpodopteraStructure-Activity RelationshipX-Ray DiffractionAntineoplastic AgentsInsecticidesSesquiterpenescytotoxic activitymarine fungusNeosartorya pseudofischeriphenylpyropenepyripyropenesesquiterpene

Identifiers

PMID26771621
PMCPMC4728515
OpenAlexW2233065225

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.