Evidence map›Paper›PMID 37582235›Full record

ArticleACS pharmacology & translational science2022

Development of Ultrapure and Potent Tannic Acids as a Pan-coronal Antiviral Therapeutic.

Po-Chang Shih, Yi-Wen Mao, Jhe-Wei Hu, Han-Yi Hsieh, Tsai-Miao Shih, Lu-Ping Lu, Wei-Hua Chang, Chan-Hui Huang, Chia-Hung Lin, Chih-Hung Lin and 11 more

Open access · hybridAbstract read
In one paragraph

Article in ACS pharmacology & translational science, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing papers in PubMed
0.9field-weighted citation impact, top 26% 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

5 citing papers in PubMed, 9 citations in OpenAlex.

  1. Article
  2. Review
  3. Review
  4. Review
  5. 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

21 authors at 3 institutions in 2 countries.

Po-Chang ShihDepartment of Research and Development, SyneuRx International (Taiwan) Corp., New Taipei City 22175, Taiwan.ORCID https://orcid.org/0000-0002-6124-5090
Yi-Wen MaoDepartment of Research and Development, SyneuRx International (Taiwan) Corp., New Taipei City 22175, Taiwan.
Jhe-Wei HuDepartment of Research and Development, SyneuRx International (Taiwan) Corp., New Taipei City 22175, Taiwan.
Han-Yi HsiehDepartment of Research and Development, SyneuRx International (Taiwan) Corp., New Taipei City 22175, Taiwan.
Tsai-Miao ShihDepartment of Research and Development, SyneuRx International (Taiwan) Corp., New Taipei City 22175, Taiwan.
Lu-Ping LuDepartment of Research and Development, SyneuRx International (Taiwan) Corp., New Taipei City 22175, Taiwan.
Wei-Hua ChangDepartment of Research and Development, SyneuRx International (Taiwan) Corp., New Taipei City 22175, Taiwan.
Chan-Hui HuangDepartment of Research and Development, SyneuRx International (Taiwan) Corp., New Taipei City 22175, Taiwan.
Chia-Hung LinDepartment of Research and Development, SyneuRx International (Taiwan) Corp., New Taipei City 22175, Taiwan.
Chih-Hung LinDepartment of Research and Development, SyneuRx International (Taiwan) Corp., New Taipei City 22175, Taiwan.
Peng TanDepartment of Research and Development, SyneuRx International (Taiwan) Corp., New Taipei City 22175, Taiwan.
Ya-Ching YangDepartment of Research and Development, SyneuRx International (Taiwan) Corp., New Taipei City 22175, Taiwan.
Ming-Hong ChienDepartment of Research and Development, SyneuRx International (Taiwan) Corp., New Taipei City 22175, Taiwan.
Chen-Che SuDepartment of Research and Development, SyneuRx International (Taiwan) Corp., New Taipei City 22175, Taiwan.
Cheng-Hsin YehDepartment of Research and Development, SyneuRx International (Taiwan) Corp., New Taipei City 22175, Taiwan.
Pei-Yun ChuangDepartment of Research and Development, SyneuRx International (Taiwan) Corp., New Taipei City 22175, Taiwan.
Tien-Lan HsiehDepartment of Research and Development, SyneuRx International (Taiwan) Corp., New Taipei City 22175, Taiwan.
Ching-Cheng WangDepartment of Research and Development, SyneuRx International (Taiwan) Corp., New Taipei City 22175, Taiwan.
Po-Shiuan HsiehInstitute of Physiology, National Defense Medical Center, Taipei City 11490, Taiwan.
Teh-Ying ChouDepartment of Pathology and Laboratory Medicine, Taipei Veterans General Hospital, Taipei City 112, Taiwan.
Guochuan Emil TsaiDepartment of Research and Development, SyneuRx International (Taiwan) Corp., New Taipei City 22175, Taiwan.ORCID https://orcid.org/0000-0002-5124-3841
National Yang Ming Chiao Tung University · TWTri-Service General Hospital · TWUniversity of California, Los Angeles · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The rampageous transmission of SARS-CoV-2 has been devastatingly impacting human life and public health since late 2019. The waves of pandemic events caused by distinct coronaviruses at present and over the past decades have prompted the need to develop broad-spectrum antiviral drugs against them. In this study, our Pentarlandir ultrapure and potent tannic acids (UPPTA) showed activities against two coronaviral strains, SARS-CoV-2 and HCoV-OC43, the earliest-known coronaviruses. The mode of inhibition of Pentarlandir UPPTA is likely to act on 3-chymotrypsin-like protease (3CLpro) to prevent viral replication, as supported by results of biochemical analysis, a 3CLpro assay, and a "gain-of-function" 3CLpro overexpressed cell-based method. Even in the 3CLpro overexpressed environment, Pentarlandir UPPTA remained its antiviral characteristic. Utilizing cell-based virucidal and cytotoxicity assays, the 50% effective concentrations (EC

Identifiers

PMID37582235
PMCPMC9128009
OpenAlexW4280629325

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
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.