Evidence map›Paper›PMID 31838328›Full record

ArticleEuropean journal of medicinal chemistry2020

Design, synthesis and discovery of andrographolide derivatives against Zika virus infection.

Feng Li, Emily M Lee, Xia Sun, Decai Wang, Hengli Tang, Guo-Chun Zhou

Abstract read
In one paragraph

Article in European journal of medicinal chemistry, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 18 papers.

0numbers the graph read from it
0cells of the map it votes in
18citing 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

18 citing papers in PubMed.

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  13. Andrographolide Suppresses Pyroptosis inOxidative medicine and cellular longevity · 2022
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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

6 authors.

Feng LiSchool of Pharmaceutical Sciences, Nanjing Tech University, Nanjing, Jiangsu, 211800, China.
Emily M LeeDepartment of Biological Science, Florida State University, Tallahassee, FL, 32306, USA.
Xia SunSchool of Pharmaceutical Sciences, Nanjing Tech University, Nanjing, Jiangsu, 211800, China.
Decai WangSchool of Pharmaceutical Sciences, Nanjing Tech University, Nanjing, Jiangsu, 211800, China.
Hengli TangDepartment of Biological Science, Florida State University, Tallahassee, FL, 32306, USA. Electronic address: tang@bio.fsu.edu.
Guo-Chun ZhouSchool of Pharmaceutical Sciences, Nanjing Tech University, Nanjing, Jiangsu, 211800, China. Electronic address: gczhou@njtech.edu.cn.

Funding

Modeling Zika virus pathogenesis and potential intervention during neural development using a human brain organoid systemU19AI131130 · NIAID · UNIVERSITY OF PENNSYLVANIA · PI MING, GUO-LI, TANG, HENGLI · 2017 to 2021
$7.7M
Perturbation of Host DNA Replication and Cell Cycle Progression by Zika VirusR01AI146342 · NIAID · FLORIDA STATE UNIVERSITY · PI TANG, HENGLI · 2019 to 2023
$1.9M
NIAID NIH HHS R01 AI146342NIAID NIH HHS U19 AI131130
6 · The paper itself

Abstract

The Zika endemic established by imported and local transmission is of significant concern and effective anti-ZIKV drugs remain an urgent unmet need. As andrographolide was identified to be an inhibitor of DENV and CHIKV and the importance of quinoline structure against infectious diseases was considered, we are interested in studying its andrographolide derivatives with quinoline moiety against Zika virus infection. In addition to screening eight in-house derivatives of andrographolide, sixteen new derivatives were designed, synthesized and tested against Zika virus infection. Among these compounds, two most potent anti-Zika compounds of 19-acetylated 14α-(5',7'-dichloro-8'-quinolyloxy) derivative 17b and 14β-(8'-quinolyloxy)-3,19- diol derivative 3 with the highest selectivity were discovered. The SAR analysis indicates that rational and optimal combined modification/s at 3-, 14-, or 19-positions can make derivatives less toxic and more potent against Zika infection, and both of 3 and 17b are suitable as leads for designing new generation of andrographolide derivatives with quinoline or its structure- and property-related moieties against Zika virus and other arboviruses.

Indexed as

Drug DesignDrug DiscoveryAntiviral AgentsDiterpenesDose-Response Relationship, DrugHumansMicrobial Sensitivity TestsMolecular StructureStructure-Activity RelationshipTumor Cells, CulturedZika VirusZika Virus InfectionandrographolideAntiviral AgentsDiterpenes14α-(8′-quinolyloxy)Andrographolide and derivativeAntiviralQuinolyloxyZika virus

Identifiers

PMID31838328
PMCPMC6980694

What OpenQuestion holds

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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.