Evidence map›Paper›PMID 26525642›Full record

ArticleTetrahedron2015

Spiroscytalin, a new tetramic acid and other metabolites of mixed biogenesis from Scytalidium cuboideum.

Arlene A Sy-Cordero, Mario Figueroa, Huzefa A Raja, Maria Elena Meza Aviña, Mitchell P Croatt, Audrey F Adcock, David J Kroll, Mansukh C Wani, Cedric J Pearce, Nicholas H Oberlies

Abstract read
In one paragraph

Article in Tetrahedron, 2015. 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. Article
  2. Article
  3. Mycobiology · 2025
    Article
  4. Article
  5. Penicillides fromMolecules (Basel, Switzerland) · 2024
    Review
  6. Article
  7. Review
  8. Article
  9. qNMR for profiling the production of fungal secondary metabolites.Magnetic resonance in chemistry : MRC · 2017
    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

10 authors.

Arlene A Sy-CorderoUniversity of North Carolina at Greensboro, Department of Chemistry and Biochemistry, Greensboro, NC 27402, United States.
Mario FigueroaFacultad de Química, Universidad Nacional Autónoma de México, Mexico DF 04510, Mexico.
Huzefa A RajaUniversity of North Carolina at Greensboro, Department of Chemistry and Biochemistry, Greensboro, NC 27402, United States.
Maria Elena Meza AviñaUniversity of North Carolina at Greensboro, Department of Chemistry and Biochemistry, Greensboro, NC 27402, United States.
Mitchell P CroattUniversity of North Carolina at Greensboro, Department of Chemistry and Biochemistry, Greensboro, NC 27402, United States.
Audrey F AdcockDepartment of Pharmaceutical Sciences, BRITE, North Carolina Central University, Durham, NC 27707, United States.
David J KrollDepartment of Pharmaceutical Sciences, BRITE, North Carolina Central University, Durham, NC 27707, United States.
Mansukh C WaniNatural Products Laboratory, Research Triangle Institute, Research Triangle Park, NC 27709, United States.
Cedric J PearceMycosynthetix, Inc., Hillsborough, NC 27279, United States.
Nicholas H OberliesUniversity of North Carolina at Greensboro, Department of Chemistry and Biochemistry, Greensboro, NC 27402, United States.

Funding

Project 3:Isolation Chemistry of Filamentous Fungi and Biological EvaluationP01CA125066 · NCI · OHIO STATE UNIVERSITY · PI JIMMY ORJALA · 2007 to 2026
$27.2M
NCI NIH HHS P01 CA125066
6 · The paper itself

Abstract

Spiroscytalin (1), a new tetramic acid that possesses an uncommon spiro-ring fusion between a polyketide-derived octalin ring system and a 2,4-pyrrolidinedione, along with two known compounds, leporin B (2) and purpactin A (3), were isolated from a solid phase culture of the fungus Scytalidium cuboideum (MSX 68345). The molecular connectivity of 1-3 was determined using NMR spectroscopy and mass spectrometry. The relative configurations of 1 and 2 were determined by NOESY experiments. The absolute configuration of 1 was determined by electronic circular dichroism (ECD) via a combination of experimental measurements and computational calculations. While leporin B was known, it displayed activities that had not been reported previously, including cytotoxicity against three human tumor cell lines and antibacterial activity against Candida albicans and Staphylococcus aureus.

Indexed as

Leporin BPurpactin AScytalidium cuboideumTetramic acid

Identifiers

PMID26525642
PMCPMC4624200

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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.