Evidence map›Paper›PMID 35704446›Full record

ArticleAngewandte Chemie (International ed. in English)2022

Total Synthesis of Kibdelomycin.

Chi He, Yu Wang, Cheng Bi, David S Peters, Timothy J Gallagher, Johannes Teske, Jason S Chen, Rachel Corsetti, Anthony D'Onofrio, Kim Lewis and 1 more

Abstract read
In one paragraph

Article in Angewandte Chemie (International ed. in English), 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing 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

3 citing papers in PubMed.

  1. Review
  2. Article
  3. Total Synthesis of Kibdelomycin.Angewandte Chemie (International ed. in English) · 2022
    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

11 authors.

Chi HeDepartment of Chemistry, Scripps Research, 10550N. Torrey Pines Road, La Jolla, CA 92122, USA.
Yu WangDepartment of Chemistry, Scripps Research, 10550N. Torrey Pines Road, La Jolla, CA 92122, USA.
Cheng BiDepartment of Chemistry, Scripps Research, 10550N. Torrey Pines Road, La Jolla, CA 92122, USA.
David S PetersDepartment of Chemistry, Scripps Research, 10550N. Torrey Pines Road, La Jolla, CA 92122, USA.
Timothy J GallagherDepartment of Chemistry, Scripps Research, 10550N. Torrey Pines Road, La Jolla, CA 92122, USA.
Johannes TeskeDepartment of Chemistry, Scripps Research, 10550N. Torrey Pines Road, La Jolla, CA 92122, USA.
Jason S ChenDepartment of Chemistry, Scripps Research, 10550N. Torrey Pines Road, La Jolla, CA 92122, USA.
Rachel CorsettiDepartment of Biology, Northeastern University, 360 Huntington Avenue, Boston, Ma 02115, USA.
Anthony D'OnofrioDepartment of Biology, Northeastern University, 360 Huntington Avenue, Boston, Ma 02115, USA.
Kim LewisDepartment of Biology, Northeastern University, 360 Huntington Avenue, Boston, Ma 02115, USA.
Phil S BaranDepartment of Chemistry, Scripps Research, 10550N. Torrey Pines Road, La Jolla, CA 92122, USA.ORCID 0000-0001-9193-9053

Funding

Scalable Synthesis and New Bond DisconnectionsR35GM118176 · NIGMS · SCRIPPS RESEARCH INSTITUTE, THE · PI BARAN, PHIL S · 2016 to 2025
$11.5M
NIGMS NIH HHS GM-118176NIGMS NIH HHS R35 GM118176
6 · The paper itself

Abstract

A modular total synthesis of kibdelomycin is disclosed that should enable structure-activity relationship (SAR) studies of this interesting class of antibiotics. The route uses simple building blocks and addresses lingering questions about its structural assignment and relationship to amycolamicin, a recently described natural product reported to have a similar structure. Initial antibacterial assays reveal that both C-22 epimers (the N-glycosidic linkage) of the natural product have similar activity while structurally truncated analogs lose activity.

Indexed as

Biological ProductsPyrrolidinonesAnti-Bacterial AgentsPyrrolesStructure-Activity RelationshipAnti-Bacterial AgentsBiological ProductskibdelomycinPyrrolesPyrrolidinonesAntibioticsGlycosidationModular SynthesisTotal Synthesis

Identifiers

PMID35704446
PMCPMC9357209

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.