Evidence map›Paper›PMID 24402176›Full record

ArticleMarine drugs2014

Induced marine fungus Chondrostereum sp. as a means of producing new sesquiterpenoids chondrosterins I and J by using glycerol as the carbon source.

Hou-Jin Li, Wen-Han Jiang, Wan-Ling Liang, Jia-Xin Huang, Yu-Fei Mo, Yan-Qing Ding, Chi-Keung Lam, Xiao-Jun Qian, Xiao-Feng Zhu, Wen-Jian Lan

Abstract read
In one paragraph

Article in Marine drugs, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 14 papers.

0numbers the graph read from it
0cells of the map it votes in
14citing 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

14 citing papers in PubMed.

  1. Article
  2. Review
  3. Article
  4. Species Diversity and Secondary Metabolites ofMolecules (Basel, Switzerland) · 2021
    Review
  5. Article
  6. Review
  7. Review
  8. Review
  9. Article
  10. Review
  11. Article
  12. Review
  13. Article
  14. 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

10 authors.

Hou-Jin LiSchool of Chemistry and Chemical Engineering, Sun Yat-Sen University, Guangzhou 510275, China. ceslhj@mail.sysu.edu.cn.
Wen-Han JiangSchool of Chemistry and Chemical Engineering, Sun Yat-Sen University, Guangzhou 510275, China. natprodjwh@gmail.com.
Wan-Ling LiangSchool of Chemistry and Chemical Engineering, Sun Yat-Sen University, Guangzhou 510275, China. natprodlwl@gmail.com.
Jia-Xin HuangSchool of Chemistry and Chemical Engineering, Sun Yat-Sen University, Guangzhou 510275, China. natprodhjx1@gmail.com.
Yu-Fei MoSchool of Chemistry and Chemical Engineering, Sun Yat-Sen University, Guangzhou 510275, China. marinemyf@yahoo.com.
Yan-Qing DingSchool of Chemistry and Chemical Engineering, Sun Yat-Sen University, Guangzhou 510275, China. marinedyq@gmail.com.
Chi-Keung LamSchool of Chemistry and Chemical Engineering, Sun Yat-Sen University, Guangzhou 510275, China. cklam@mail.sysu.edu.cn.
Xiao-Jun QianSchool of Chemistry and Chemical Engineering, Sun Yat-Sen University, Guangzhou 510275, China. marineqxj@gmail.com.
Xiao-Feng ZhuSchool of Chemistry and Chemical Engineering, Sun Yat-Sen University, Guangzhou 510275, China. zhuxfeng@mail.sysu.edu.cn.
Wen-Jian LanSchool of Chemistry and Chemical Engineering, Sun Yat-Sen University, Guangzhou 510275, China. lanwj@mail.sysu.edu.cn.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Chondrostereum sp., a marine fungus isolated from a soft coral Sarcophyton tortuosum, can yield hirsutane framework sesquiterpenoids. However, the metabolites profiles vary dramatically with the composition change of the culture media. This fungus was cultured in a liquid medium containing glycerol as the carbon source, and two new metabolites, chondrosterins I and J (1 and 2), were obtained. Their structures were elucidated primarily based on MS, NMR and X-ray single-crystal diffraction data. By comparison with the known hirsutane sesquiterpenoids, chondrosterins I and J have unique structural features, including a methyl was migrated from C-2 to C-6, and the methyl at C-3 was carboxylated. Compound 2 exhibited potent cytotoxic activities against the cancer cell lines CNE-1 and CNE-2 with the IC50 values of 1.32 and 0.56 μM.

Indexed as

Antineoplastic AgentsCell Line, TumorChromatography, High Pressure LiquidCircular DichroismCrystallography, X-RayCulture MediaDrug Screening Assays, AntitumorGlycerolHumansMagnetic Resonance SpectroscopyModels, MolecularPolyporaceaeSesquiterpenesSpectrophotometry, InfraredSpectrophotometry, UltravioletTetrazolium SaltsAntineoplastic Agentschondrosterin JCulture MediaGlycerolSesquiterpenesTetrazolium SaltsThiazolesthiazolyl blue

Identifiers

PMID24402176
PMCPMC3917267

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.