Evidence map›Paper›PMID 34873311›Full record

ArticleThe Journal of antibiotics2022

Isolation of new derivatives of the 20-membered macrodiolide bispolide from Kitasatospora sp. MG372-hF19.

Yasuko Kohda, Shuichi Sakamoto, Maya Umekita, Tomoyuki Kimura, Yumiko Kubota, Rie Arisaka, Yuko Shibuya, Hideyuki Muramatsu, Ryuichi Sawa, Shingo Dan and 2 more

Abstract read
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In one paragraph

Article in The Journal of antibiotics, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
0.2field-weighted citation impact, top 50% 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

2 citing papers in PubMed, 3 citations in OpenAlex.

  1. Article
  2. Review
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

12 authors at 2 institutions in 1 country.

Yasuko KohdaInstitute of Microbial Chemistry (BIKAKEN), Numazu, Microbial Chemistry Research Foundation, Shizuoka, Japan.
Shuichi SakamotoInstitute of Microbial Chemistry (BIKAKEN), Numazu, Microbial Chemistry Research Foundation, Shizuoka, Japan. sakamotos@bikaken.or.jp.ORCID 0000-0001-9396-9475
Maya UmekitaInstitute of Microbial Chemistry (BIKAKEN), Laboratory of Microbiology, Microbial Chemistry Research Foundation, Tokyo, Japan.
Tomoyuki KimuraInstitute of Microbial Chemistry (BIKAKEN), Laboratory of Molecular Structure Analysis, Microbial Chemistry Research Foundation, Tokyo, Japan.
Yumiko KubotaInstitute of Microbial Chemistry (BIKAKEN), Laboratory of Molecular Structure Analysis, Microbial Chemistry Research Foundation, Tokyo, Japan.
Rie ArisakaInstitute of Microbial Chemistry (BIKAKEN), Laboratory of Microbiology, Microbial Chemistry Research Foundation, Tokyo, Japan.
Yuko ShibuyaInstitute of Microbial Chemistry (BIKAKEN), Laboratory of Microbiology, Microbial Chemistry Research Foundation, Tokyo, Japan.
Hideyuki MuramatsuInstitute of Microbial Chemistry (BIKAKEN), Laboratory of Microbiology, Microbial Chemistry Research Foundation, Tokyo, Japan.ORCID 0000-0001-5900-2113
Ryuichi SawaInstitute of Microbial Chemistry (BIKAKEN), Laboratory of Molecular Structure Analysis, Microbial Chemistry Research Foundation, Tokyo, Japan.
Shingo DanDivision of Molecular Pharmacology, Cancer Chemotherapy Center, Japanese Foundation for Cancer Research, Tokyo, Japan.
Manabu KawadaInstitute of Microbial Chemistry (BIKAKEN), Numazu, Microbial Chemistry Research Foundation, Shizuoka, Japan.ORCID 0000-0001-9348-4240
Masayuki IgarashiInstitute of Microbial Chemistry (BIKAKEN), Laboratory of Microbiology, Microbial Chemistry Research Foundation, Tokyo, Japan. igarashim@bikaken.or.jp.ORCID 0000-0002-1562-6685
Microbial Chemistry Research Foundation · JPJapanese Foundation For Cancer Research · JP

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

New three macrocyclic diolides, named bispolides C-E (1-3), were isolated from a fermentation broth of the actinomycete strain MG372-hF19, which produces an indole glycoside and leptomycins as we reported previously. The absolute structures of compounds 1-3 were elucidated by NMR and X-ray crystallography. Compounds 1-3 diverge from the known nine bispolides in their different alkylation patterns on the 20-membered macrocyclic diolide skeleton and the side chain in their planar structures. Furthermore, compounds 1-3 exhibited antibacterial activity against methicillin-resistant Staphylococcus aureus and vancomycin-resistant Enterococci and cytotoxic activity against human cancer cell lines. Among them, compound 3 has the most potent biological activities against bacteria and tumor cells. Additionally, using a membrane-potential-sensitive fluorescence probe, we found that compounds 1-3 and elaiophylin have a similar effect on membrane potential in A549 human lung cancer cells.

Indexed as

A549 CellsActinobacteriaAlkylationAnti-Bacterial AgentsAntibiotics, AntineoplasticCell Line, TumorCrystallography, X-RayDrug Screening Assays, AntitumorEnterococcusHumansMacrolidesMagnetic Resonance SpectroscopyMethicillin-Resistant Staphylococcus aureusMicrobial Sensitivity TestsMolecular StructureStreptomycetaceaeAnti-Bacterial AgentsAntibiotics, AntineoplasticMacrolides

Identifiers

PMID34873311
OpenAlexW4200478633

What OpenQuestion holds

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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.