Evidence map›Paper›PMID 34122859›Full record

ArticleChemical science2020

Steric and stereoscopic disulfide construction for cross-linkage

Wen-Chao Gao, Jun Tian, Yu-Zhu Shang, Xuefeng Jiang

Abstract read
In one paragraph

Article in Chemical science, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 14 papers.

0numbers the graph read from it
0cells of the map it votes in
14citing 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

14 citing papers in PubMed.

  1. Article
  2. Article
  3. Article
  4. Article
  5. Review
  6. Article
  7. Article
  8. Article
  9. Radical approaches to C-S bonds.Nature reviews. Chemistry · 2023
    Review
  10. Article
  11. Article
  12. Article
  13. Article
  14. 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

4 authors.

Wen-Chao GaoShanghai Key Laboratory of Green Chemistry and Chemical Process, Department of Chemistry, East China Normal University Shanghai 200062 P. R. China xfjiang@chem.ecnu.edu.cn.ORCID https://orcid.org/0000-0002-1382-6210
Jun TianCollege of Biomedical Engineering, Taiyuan University of Technology Taiyuan 030024 P. R. China.
Yu-Zhu ShangCollege of Biomedical Engineering, Taiyuan University of Technology Taiyuan 030024 P. R. China.
Xuefeng JiangShanghai Key Laboratory of Green Chemistry and Chemical Process, Department of Chemistry, East China Normal University Shanghai 200062 P. R. China xfjiang@chem.ecnu.edu.cn.ORCID https://orcid.org/0000-0002-1849-6572

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Disulfide bonds are a significant motif in life and drug-delivery systems. In particular, steric hindrance and stereoscopic disulfide linkers are closely associated with the stability of antibody-drug conjugates, which affects the potency, selectivity, and pharmacokinetics of drugs. However, limited availability and diversity of tertiary thiols impede the construction of steric and stereoscopic disulfides for cross-linkage in biochemistry and pharmaceuticals. Through modulating the mask effect of disulfurating reagents, we develop a facile and robust strategy for construction of diverse steric and stereoscopic disulfides

Identifiers

PMID34122859
PMCPMC8152801

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Registered trials

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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.