Evidence map›Paper›PMID 35450381›Full record

ArticleACS medicinal chemistry letters2022

Design, Synthesis, and Evaluation of PD-1/PD-L1 Antagonists Bearing a Benzamide Scaffold.

Lu Lu, Zhihao Qi, Tianyu Wang, Xiangyu Zhang, Kuojun Zhang, Kaizhen Wang, Yao Cheng, Yibei Xiao, Zheng Li, Sheng Jiang

Open access · greenAbstract read
In one paragraph

Article in ACS medicinal chemistry letters, 2022. 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
2.3field-weighted citation impact, top 10% 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

8 citing papers in PubMed, 22 citations in OpenAlex.

  1. Article
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  4. Design, Synthesis, and Evaluation of 8-(ACS medicinal chemistry letters · 2024
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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 at 2 institutions in 2 countries.

Lu LuState Key Laboratory of Natural Medicines, Department of Medicinal Chemistry and Department of Biomedical Engineering, China Pharmaceutical University, Nanjing 210009, China.
Zhihao QiState Key Laboratory of Natural Medicines, Department of Medicinal Chemistry and Department of Biomedical Engineering, China Pharmaceutical University, Nanjing 210009, China.
Tianyu WangState Key Laboratory of Natural Medicines, Department of Medicinal Chemistry and Department of Biomedical Engineering, China Pharmaceutical University, Nanjing 210009, China.
Xiangyu ZhangState Key Laboratory of Natural Medicines, Department of Medicinal Chemistry and Department of Biomedical Engineering, China Pharmaceutical University, Nanjing 210009, China.
Kuojun ZhangState Key Laboratory of Natural Medicines, Department of Medicinal Chemistry and Department of Biomedical Engineering, China Pharmaceutical University, Nanjing 210009, China.
Kaizhen WangState Key Laboratory of Natural Medicines, Department of Medicinal Chemistry and Department of Biomedical Engineering, China Pharmaceutical University, Nanjing 210009, China.
Yao ChengState Key Laboratory of Natural Medicines, Department of Medicinal Chemistry and Department of Biomedical Engineering, China Pharmaceutical University, Nanjing 210009, China.
Yibei XiaoState Key Laboratory of Natural Medicines, Department of Medicinal Chemistry and Department of Biomedical Engineering, China Pharmaceutical University, Nanjing 210009, China.
Zheng LiCenter for Bioenergetics, Houston Methodist Research Institute, 6670 Bertner, Houston, Texas 77030, United States.
Sheng JiangState Key Laboratory of Natural Medicines, Department of Medicinal Chemistry and Department of Biomedical Engineering, China Pharmaceutical University, Nanjing 210009, China.ORCID https://orcid.org/0000-0002-4550-5024
China Pharmaceutical University · CNHouston Methodist · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Several antibodies targeting programmed cell death-1 (PD-1)/programmed cell death-ligand 1 (PD-L1) have been approved by the U.S. Food and Drug Administration (FDA) for cancer therapy. Although many small-molecule inhibitors of the PD-1/PD-L1 pathway have been reported, no small-molecule inhibitors have been approved for cancer treatment. In this work, a series of novel benzamide derivatives were designed, synthesized, and evaluated to find effective inhibitors of the PD-1/PD-L1 interaction. The most potent compound

Identifiers

PMID35450381
PMCPMC9014519
OpenAlexW4221055326

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.