Evidence map›Paper›PMID 28573254›Full record

ReviewAfrican journal of traditional, complementary, and alternative medicines : AJTCAM2017

STRUCTURAL CHARACTERISTICS AND ANTIHYPERTENSIVE EFFECTS OF ANGIOTENSIN-I-CONVERTING ENZYME INHIBITORY PEPTIDES IN THE RENIN-ANGIOTENSIN AND KALLIKREIN KININ SYSTEMS.

Sivananthan Manoharan, Adawiyah Suriza Shuib, Noorlidah Abdullah

Open access · diamondAbstract readReview
In one paragraph

Review in African journal of traditional, complementary, and alternative medicines : AJTCAM, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 12 papers.

0numbers the graph read from it
0cells of the map it votes in
12citing papers in PubMed
2.5field-weighted citation impact, top 10% 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

12 citing papers in PubMed, 57 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

3 authors at 1 institution in 1 country.

Sivananthan ManoharanInstitute of Biological Sciences, Faculty of Science, University of Malaya, 50603 Kuala Lumpur.
Adawiyah Suriza ShuibInstitute of Biological Sciences, Faculty of Science, University of Malaya, 50603 Kuala Lumpur.
Noorlidah AbdullahInstitute of Biological Sciences, Faculty of Science, University of Malaya, 50603 Kuala Lumpur.
University of Malaya · MY

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundThe commercially available synthetic angiotensin-I-converting enzyme (ACE) inhibitors are known to exert negative side effects which have driven many research groups globally to discover the novel ACE inhibitors.

methodLiterature search was performed within the PubMed, ScienceDirect.com and Google Scholar.

resultsThe presence of proline at the C-terminal tripeptide of ACE inhibitor can competitively inhibit the ACE activity. The effects of other amino acids are less studied leading to difficulties in predicting potent peptide sequences. The broad specificity of the enzyme may be due to the dual active sites observed on the somatic ACE. The inhibitors may not necessarily competitively inhibit the enzyme which explains why some reported inhibitors do not have the common ACE inhibitor characteristics. Finally, the

conclusionThe relationship between peptide amino acid sequence and inhibitory activity,

Indexed as

Amino AcidsAngiotensin-Converting Enzyme InhibitorsAnimalsAntihypertensive AgentsCatalytic DomainHumansHypertensionKallikrein-Kinin SystemPeptidesPeptidyl-Dipeptidase ARenin-Angiotensin SystemStructure-Activity RelationshipAmino AcidsAngiotensin-Converting Enzyme InhibitorsAntihypertensive AgentsPeptidesPeptidyl-Dipeptidase AACE inhibitorAngiotensin-I-converting enzymeAntihypertensive activityBioactive peptides

Identifiers

PMID28573254
PMCPMC5446464
OpenAlexW2589950995

What OpenQuestion holds

Textmetadata
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.