Evidence map›Paper›PMID 27077842›Full record

ArticleMolecules (Basel, Switzerland)2016

Phenolic Constituents of Medicinal Plants with Activity against Trypanosoma brucei.

Ya Nan Sun, Joo Hwan No, Ga Young Lee, Wei Li, Seo Young Yang, Gyongseon Yang, Thomas J Schmidt, Jong Seong Kang, Young Ho Kim

Open access · goldAbstract read
In one paragraph

Article in Molecules (Basel, Switzerland), 2016. 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
2.6field-weighted citation impact, top 11% 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, 19 citations in OpenAlex.

  1. In Silico and In Vitro Search for Dual Inhibitors of theMolecules (Basel, Switzerland) · 2023
    Article
  2. Anti-Frontiers in microbiology · 2023
    Article
  3. Review
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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

9 authors at 4 institutions in 2 countries.

Ya Nan SunCollege of Pharmacy, Chungnam National University, Daejeon 305-764, Korea. yanansun@163.com.
Joo Hwan NoLeishmania Research Laboratory, Institut Pasteur Korea, 696 Sampyeong-dong, Bundang-gu, Seongnam-si, Gyeonggi 463-400, Korea. joohwan.no@ip-korea.org.
Ga Young LeeCollege of Pharmacy, Chungnam National University, Daejeon 305-764, Korea. lakasis@lycos.co.kr.
Wei LiSchool of Biotechnology, Yeungnam University, Gyeongsan, Gyeongbuk 712-749, Korea. hasaegawa@ynu.ac.kr.
Seo Young YangCollege of Pharmacy, Chungnam National University, Daejeon 305-764, Korea. syyang@cnu.ac.kr.
Gyongseon YangLeishmania Research Laboratory, Institut Pasteur Korea, 696 Sampyeong-dong, Bundang-gu, Seongnam-si, Gyeonggi 463-400, Korea. gyongseon.yang@ip-korea.org.
Thomas J SchmidtInstitute of Pharmaceutical Biology and Phytochemistry (IPBP), University of Münster, PharmaCampus, Corrensstrasse 48, D-48149 Münster, Germany. thomschm@uni-muenster.de.
Jong Seong KangCollege of Pharmacy, Chungnam National University, Daejeon 305-764, Korea. kangjss@cnu.ac.kr.
Young Ho KimCollege of Pharmacy, Chungnam National University, Daejeon 305-764, Korea. yhk@cnu.ac.kr.
Chungnam National University · KRInstitut Pasteur Korea · KRUniversity of Münster · DEYeungnam University · KR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Neglected tropical diseases (NTDs) affect over one billion people all over the world. These diseases are classified as neglected because they impact populations in areas with poor financial conditions and hence do not attract sufficient research investment. Human African Trypanosomiasis (HAT or sleeping sickness), caused by the parasite Trypanosoma brucei, is one of the NTDs. The current therapeutic interventions for T. brucei infections often have toxic side effects or require hospitalization so that they are not available in the rural environments where HAT occurs. Furthermore, parasite resistance is increasing, so that there is an urgent need to identify novel lead compounds against this infection. Recognizing the wide structural diversity of natural products, we desired to explore and identify novel antitrypanosomal chemotypes from a collection of natural products obtained from plants. In this study, 440 pure compounds from various medicinal plants were tested against T. brucei by in a screening using whole cell in vitro assays. As the result, twenty-two phenolic compounds exhibited potent activity against cultures of T. brucei. Among them, eight compounds-4, 7, 11, 14, 15, 18, 20, and 21-showed inhibitory activity against T. brucei, with IC50 values below 5 µM, ranging from 0.52 to 4.70 μM. Based on these results, we attempt to establish some general trends with respect to structure-activity relationships, which indicate that further investigation and optimization of these derivatives might enable the preparation of potentially useful compounds for treating HAT.

Indexed as

AnimalsBiological ProductsHumansPhenolsPlants, MedicinalTrypanocidal AgentsTrypanosoma brucei bruceiTrypanosomiasis, AfricanBiological ProductsPhenolsTrypanocidal Agentsmedicinal plantsneglected tropical diseasesphenolic constituentsQSARTrypanosoma brucei

Identifiers

PMID27077842
PMCPMC6273235
OpenAlexW2341903388

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.