Evidence map›Paper›PMID 29389125›Full record

ArticleJournal of natural products2018

Biomimetic Stereoselective Sulfa-Michael Addition Leads to Platensimycin and Platencin Sulfur Analogues against Methicillin-Resistant Staphylococcus aureus.

Lin Qiu, Kai Tian, Zhongqing Wen, Youchao Deng, Dingding Kang, Haoyu Liang, Xiangcheng Zhu, Ben Shen, Yanwen Duan, Yong Huang

Abstract read
In one paragraph

Article in Journal of natural products, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers.

0numbers the graph read from it
0cells of the map it votes in
8citing 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

8 citing papers in PubMed.

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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.

Lin QiuXiangya International Academy of Translational Medicine and ‡Xiangya Hospital, Central South University , Changsha, Hunan 410013, People's Republic of China.
Kai TianXiangya International Academy of Translational Medicine and ‡Xiangya Hospital, Central South University , Changsha, Hunan 410013, People's Republic of China.
Zhongqing WenXiangya International Academy of Translational Medicine and ‡Xiangya Hospital, Central South University , Changsha, Hunan 410013, People's Republic of China.
Youchao DengXiangya International Academy of Translational Medicine and ‡Xiangya Hospital, Central South University , Changsha, Hunan 410013, People's Republic of China.
Dingding KangXiangya International Academy of Translational Medicine and ‡Xiangya Hospital, Central South University , Changsha, Hunan 410013, People's Republic of China.
Haoyu LiangXiangya International Academy of Translational Medicine and ‡Xiangya Hospital, Central South University , Changsha, Hunan 410013, People's Republic of China.
Xiangcheng ZhuXiangya International Academy of Translational Medicine and ‡Xiangya Hospital, Central South University , Changsha, Hunan 410013, People's Republic of China.
Ben ShenXiangya International Academy of Translational Medicine and ‡Xiangya Hospital, Central South University , Changsha, Hunan 410013, People's Republic of China.ORCID 0000-0002-9750-5982
Yanwen DuanXiangya International Academy of Translational Medicine and ‡Xiangya Hospital, Central South University , Changsha, Hunan 410013, People's Republic of China.
Yong HuangXiangya International Academy of Translational Medicine and ‡Xiangya Hospital, Central South University , Changsha, Hunan 410013, People's Republic of China.ORCID 0000-0002-3163-1716

Funding

Discovery and biosynthesis of diterpenoid natural products in actinomycetalsR01GM114353 · NIGMS · SCRIPPS FLORIDA · PI SHEN, BEN · 2016 to 2019
$1.8M
NIGMS NIH HHS R01 GM114353
6 · The paper itself

Abstract

Several sulfur-containing platensimycin (PTM) and platencin (PTN) analogues, with activities comparable to the parent natural products, have recently been discovered from microorganisms, implying a biomimetic route to diversify the PTM and PTN scaffolds for structure-activity relationship study. We present here a substrate-directed and scaleable semisynthetic strategy to make PTM and PTN sulfur analogues with excellent diasteroselectivity, without using any chiral catalysts. Most of the sulfur analogues showed strong activities against clinical Staphylococcus aureus isolates, with minimum inhibitory concentrations of 0.5-2 μg mL

Indexed as

AdamantaneAminobenzoatesAminophenolsAnilidesAnti-Bacterial AgentsBiological ProductsBiomimeticsMethicillin-Resistant Staphylococcus aureusMicrobial Sensitivity TestsPolycyclic CompoundsStructure-Activity RelationshipSulfurAdamantaneAminobenzoatesAminophenolsAnilidesAnti-Bacterial AgentsBiological ProductsplatencinplatensimycinPolycyclic CompoundsSulfur

Identifiers

PMID29389125
PMCPMC6245554

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.