Evidence map›Paper›PMID 21825291›Full record

ArticleAntimicrobial agents and chemotherapy2011

In vitro activity of E1210, a novel antifungal, against clinically important yeasts and molds.

Mamiko Miyazaki, Takaaki Horii, Katsura Hata, Nao-Aki Watanabe, Kazutaka Nakamoto, Keigo Tanaka, Syuji Shirotori, Norio Murai, Satoshi Inoue, Masayuki Matsukura and 3 more

Open access · bronzeAbstract read
In one paragraph

Article in Antimicrobial agents and chemotherapy, 2011. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 117 papers.

0numbers the graph read from it
0cells of the map it votes in
117citing papers in PubMed
3.3field-weighted citation impact, top 7% 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

117 citing papers in PubMed, 194 citations in OpenAlex.

  1. Trial
  2. Trial
  3. Trial
  4. Review
  5. New Perspectives on Antimicrobial Agents: Fosmanogepix.Antimicrobial agents and chemotherapy · 2026
    Review
  6. Manogepix demonstrates potentAntimicrobial agents and chemotherapy · 2026
    Article
  7. Article
  8. Review
  9. Drug Discovery and Repurposing forJournal of fungi (Basel, Switzerland) · 2025
    Review
  10. Cutaneous and Lymphangitic Infection Caused byLife (Basel, Switzerland) · 2025
    Review
  11. Antimicrobial agents and chemotherapy · 2025
    Article
  12. Review
  13. Article
  14. Article
  15. Mucormycosis.Infectious disease clinics of North America · 2025
    Review
  16. Antimicrobial agents and chemotherapy · 2025
    Article
  17. Antifungal Drug Resistance.Current topics in microbiology and immunology · 2025
    Review
  18. Innovative antifungal strategies to combat drug-resistantFrontiers in cellular and infection microbiology · 2025
    Review
  19. Review
  20. Review

57 more citing papers are in PubMed but not listed here.

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

13 authors at 1 institution in 1 country.

Mamiko MiyazakiNext Generation Systems Core Function Unit, Eisai Product Creation Systems, Eisai Co., Ltd., 5-1-3 Tokodai, Tsukuba, Ibaraki, Japan. m3-miyazaki@hhc.eisai.co.jp
Takaaki Horii
Katsura Hata
Nao-Aki Watanabe
Kazutaka Nakamoto
Keigo Tanaka
Syuji Shirotori
Norio Murai
Satoshi Inoue
Masayuki Matsukura
Shinya Abe
Kentaro Yoshimatsu
Makoto Asada
Eisai (Japan) · JP

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

E1210 is a new antifungal compound with a novel mechanism of action and broad spectrum of antifungal activity. We investigated the in vitro antifungal activities of E1210 compared to those of fluconazole, itraconazole, voriconazole, amphotericin B, and micafungin against clinical fungal isolates. E1210 showed potent activities against most Candida spp. (MIC(90) of ≤0.008 to 0.06 μg/ml), except for Candida krusei (MICs of 2 to >32 μg/ml). E1210 showed equally potent activities against fluconazole-resistant and fluconazole-susceptible Candida strains. E1210 also had potent activities against various filamentous fungi, including Aspergillus fumigatus (MIC(90) of 0.13 μg/ml). E1210 was also active against Fusarium solani and some black molds. Of note, E1210 showed the greatest activities against Pseudallescheria boydii (MICs of 0.03 to 0.13 μg/ml), Scedosporium prolificans (MIC of 0.03 μg/ml), and Paecilomyces lilacinus (MICs of 0.06 μg/ml) among the compounds tested. The antifungal action of E1210 was fungistatic, but E1210 showed no trailing growth of Candida albicans, which has often been observed with fluconazole. In a cytotoxicity assay using human HK-2 cells, E1210 showed toxicity as low as that of fluconazole. Based on these results, E1210 is likely to be a promising antifungal agent for the treatment of invasive fungal infections.

Indexed as

AminopyridinesAmphotericin BAntifungal AgentsAspergillusCandidaCell LineEchinocandinsFluconazoleFungiFusariumHumansIsoxazolesItraconazoleLipopeptidesMicafunginMicrobial Sensitivity TestsAminopyridinesAmphotericin BAntifungal AgentsAPX001AEchinocandinsFluconazoleIsoxazolesItraconazoleLipopeptidesMicafunginPyrimidinesTriazolesVoriconazole

Identifiers

PMID21825291
PMCPMC3186989
OpenAlexW2114599108

What OpenQuestion holds

Textmetadata
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.