Evidence map›Paper›PMID 33178313›Full record

ArticleEvidence-based complementary and alternative medicine : eCAM2020

Revealing the Pharmacological Mechanism of

FengZhi Liu, Qian Zhao, Suxian Liu, Yingzhi Xu, Dongrui Zhou, Ying Gao, Lingqun Zhu

Open access · hybridAbstract read
In one paragraph

Article in Evidence-based complementary and alternative medicine : eCAM, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing papers in PubMed
1.7field-weighted citation impact, top 14% 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

6 citing papers in PubMed, 11 citations in OpenAlex.

  1. Combined treatment withFrontiers in pharmacology · 2026
    Article
  2. Article
  3. Galgravin Isolated fromInternational journal of molecular sciences · 2023
    Article
  4. Article
  5. Review
  6. 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

7 authors at 3 institutions in 1 country.

FengZhi LiuKey Laboratory of Chinese Internal Medicine of Ministry of Education and Beijing, Dongzhimen Hospital, Beijing University of Chinese Medicine, Beijing 100700, China.ORCID https://orcid.org/0000-0003-2760-5934
Qian ZhaoPharmaceutical Science, Beijing University Health Science Center, Beijing 100089, China.
Suxian LiuLonghua Hospital Shanghai University of Traditional Chinese Medicine, Shanghai 200032, China.
Yingzhi XuKey Office of Encephalopathy TCM Research, Dongzhimen Hospital, Beijing University of Chinese Medicine, Beijing 100700, China.
Dongrui ZhouKey Laboratory of Chinese Internal Medicine of Ministry of Education and Beijing, Dongzhimen Hospital, Beijing University of Chinese Medicine, Beijing 100700, China.
Ying GaoKey Office of Encephalopathy TCM Research, Dongzhimen Hospital, Beijing University of Chinese Medicine, Beijing 100700, China.ORCID https://orcid.org/0000-0003-3525-9939
Lingqun ZhuKey Laboratory of Chinese Internal Medicine of Ministry of Education and Beijing, Dongzhimen Hospital, Beijing University of Chinese Medicine, Beijing 100700, China.ORCID https://orcid.org/0000-0001-7293-2526
Beijing University of Chinese Medicine · CNShanghai University of Traditional Chinese Medicine · CNShenzhen University Health Science Center · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

aimStroke is the second significant cause for death, with ischemic stroke (IS) being the main type threatening human being's health. METHODS AND MATERIALS: ADME (absorbed, distributed, metabolized, and excreted) is an important property for screening-related compounds in AT, which were screening out of TCMSP, TCMID, Chemistry Database, and literature from CNKI. Then, these targets related to screened compounds were predicted via Swiss Targets, when AT-related targets database was established. The gene targets related to IS were collected from DisGeNET and GeneCards. IS-AT is a common protein interactive network established by STRING Database. Gene Ontology (GO) and Kyoto Encyclopedia of Genes and Genomes (KEGG) pathway enrichment were analysed by IS-AT common target genes. Cytoscape software was used to establish a visualized network for active compounds-core targets and core target proteins-proteins interactive network. Furthermore, we drew a signal pathway picture about its effect to reveal the basic mechanism of AT against IS systematically.

resultsThere were 53 active compounds screened from AT, inferring the main therapeutic substances as follows: bisasaricin, 3-cyclohexene-1-methanol-

conclusionAT had a therapeutic effect for ischemic via multicomponent, multitarget, and multisignal pathway, which provided a novel research aspect for AT against IS.

Identifiers

PMID33178313
PMCPMC7648688
OpenAlexW3097522053

What OpenQuestion holds

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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.