Evidence map›Paper›PMID 33556871›Full record

ReviewBiomedicine & pharmacotherapy = Biomedecine & pharmacotherapie2021

An update review of emerging small-molecule therapeutic options for COVID-19.

Dengke Tian, Yuzhi Liu, Chengyuan Liang, Liang Xin, Xiaolin Xie, Dezhu Zhang, Minge Wan, Han Li, Xueqi Fu, Hong Liu and 1 more

Abstract readReview
In one paragraph

Review in Biomedicine & pharmacotherapy = Biomedecine & pharmacotherapie, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 36 papers.

0numbers the graph read from it
0cells of the map it votes in
36citing 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

36 citing papers in PubMed.

  1. Article
  2. Review
  3. Review
  4. Review
  5. Targeting the Main Protease (MACS chemical biology · 2024
    Article
  6. Article
  7. Article
  8. A Tale of Two Proteases: MPharmaceuticals (Basel, Switzerland) · 2023
    Review
  9. Article
  10. Small molecules in the treatment of COVID-19.Signal transduction and targeted therapy · 2022
    Review
  11. Review
  12. Review
  13. Article
  14. Design, synthesis and docking study of Vortioxetine derivatives as a SARS-CoV-2 main protease inhibitor.Daru : journal of Faculty of Pharmacy, Tehran University of Medical Sciences · 2022
    Article
  15. Article
  16. Article
  17. Article
  18. Article
  19. Article
  20. 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

11 authors.

Dengke TianSchool of Life Sciences, Jilin University, Changchun, 130012, PR China.
Yuzhi LiuFaculty of Pharmacy, Shaanxi University of Science & Technology, Xi'an, 710021, PR China.
Chengyuan LiangSchool of Life Sciences, Jilin University, Changchun, 130012, PR China; Faculty of Pharmacy, Shaanxi University of Science & Technology, Xi'an, 710021, PR China. Electronic address: chengyuanliang@gmail.com.
Liang XinFaculty of Pharmacy, Shaanxi University of Science & Technology, Xi'an, 710021, PR China.
Xiaolin XieShaanxi Panlong Pharmaceutical Group Co., Ltd., Xi'an, 710025, PR China.
Dezhu ZhangShaanxi Panlong Pharmaceutical Group Co., Ltd., Xi'an, 710025, PR China.
Minge WanSchool of Medicine and Pharmacy, Shaanxi University of Business & Commerce, Xi'an 712046, PR China.
Han LiFaculty of Pharmacy, Shaanxi University of Science & Technology, Xi'an, 710021, PR China.
Xueqi FuSchool of Life Sciences, Jilin University, Changchun, 130012, PR China.
Hong LiuZhuhai Jinan Selenium Source Nanotechnology Co., Ltd., Hengqin New Area, Zhuhai, 519030, PR China. Electronic address: sesource_liuhong@163.com.
Wenqiang CaoZhuhai Jinan Selenium Source Nanotechnology Co., Ltd., Hengqin New Area, Zhuhai, 519030, PR China. Electronic address: sesource_cwq@163.com.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The SARS-CoV-2 outbreak and pandemic that began near the end of 2019 has posed a challenge to global health. At present, many candidate small-molecule therapeutics have been developed that can inhibit both the infection and replication of SARS-CoV-2 and even potentially relieve cytokine storms and other related complications. Meanwhile, host-targeted drugs that inhibit cellular transmembrane serine protease (TMPRSS2) can prevent SARS-CoV-2 from entering cells, and its combination with chloroquine and dihydroorotate dehydrogenase (DHODH) inhibitors can limit the spread of SARS-CoV-2 and reduce the morbidity and mortality of patients with COVID-19. The present article provides an overview of these small-molecule therapeutics based on insights from medicinal chemistry research and focuses on RNA-dependent RNA polymerase (RdRp) inhibitors, such as the nucleoside analogues remdesivir, favipiravir and ribavirin. This review also covers inhibitors of 3C-like protease (3CL

Indexed as

Antiviral AgentsCOVID-19COVID-19 Drug TreatmentSARS-CoV-2Enzyme InhibitorsHumansMolecular Targeted TherapyTherapies, InvestigationalAntiviral AgentsEnzyme Inhibitors3C-like protease (3CL(pro))CoronavirusesPapain-like protease (PL(pro))RNA-dependent RNA polymerase (RdRp)SARS-CoV-2Transmembrane serine protease (TMPRSS2)

Identifiers

PMID33556871
PMCPMC7857046

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.