Evidence map›Paper›PMID 32547398›Full record

ArticleFrontiers in pharmacology2020

Identification of Structural Features for the Inhibition of OAT3-Mediated Uptake of Enalaprilat by Selected Drugs and Flavonoids.

Yao Ni, Zelin Duan, Dandan Zhou, Shuai Liu, Huida Wan, Chunshan Gui, Hongjian Zhang

Open access · goldAbstract read
In one paragraph

Article in Frontiers in pharmacology, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 13 papers.

0numbers the graph read from it
0cells of the map it votes in
13citing papers in PubMed
1.1field-weighted citation impact, top 20% 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

13 citing papers in PubMed, 21 citations in OpenAlex.

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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

7 authors at 1 institution in 1 country.

Yao NiCollege of Pharmaceutical Sciences, Soochow University, Suzhou, China.
Zelin DuanCollege of Pharmaceutical Sciences, Soochow University, Suzhou, China.
Dandan ZhouCollege of Pharmaceutical Sciences, Soochow University, Suzhou, China.
Shuai LiuCollege of Pharmaceutical Sciences, Soochow University, Suzhou, China.
Huida WanCollege of Pharmaceutical Sciences, Soochow University, Suzhou, China.
Chunshan GuiCollege of Pharmaceutical Sciences, Soochow University, Suzhou, China.
Hongjian ZhangCollege of Pharmaceutical Sciences, Soochow University, Suzhou, China.
Soochow University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Enalaprilat is the active metabolite of enalapril, a widely used antihypertension drug. The human organic anion transporter 3 (OAT3), which is highly expressed in the kidney, plays a critical role in the renal clearance of many drugs. While urinary excretion is the primary elimination route of enalaprilat, direct involvement of OAT3 has not been reported so far. In the present study, OAT3-mediated uptake of enalaprilat was first characterized, and the inhibition of OAT3 transport activity was then examined for a number of flavonoid and drug molecules with diverse structures. A varying degree of inhibition potency was demonstrated for flavonoids, with IC

Indexed as

enalaprilatflavonoidherb-drug interactionorganic anion transporter 3 (OAT3)three-dimensional quantitative structure-activity relationship

Identifiers

PMID32547398
PMCPMC7271668
OpenAlexW3032412073

What OpenQuestion holds

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LicenceCC BY
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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.