Evidence map›Paper›PMID 25738535›Full record

ReviewMolecules (Basel, Switzerland)2015

Rational drug design and synthesis of molecules targeting the angiotensin II type 1 and type 2 receptors.

Tahsin F Kellici, Andreas G Tzakos, Thomas Mavromoustakos

Open access · goldAbstract readReview
In one paragraph

Review in Molecules (Basel, Switzerland), 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 16 papers.

0numbers the graph read from it
0cells of the map it votes in
16citing papers in PubMed
6.2field-weighted citation impact, top 3% 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

16 citing papers in PubMed, 48 citations in OpenAlex.

  1. Review
  2. Role of local angiotensin II signaling in bladder function.American journal of physiology. Renal physiology · 2024
    Review
  3. Article
  4. Review
  5. Article
  6. Losartan Interactions with 2-Hydroxypropyl-β-CD.Molecules (Basel, Switzerland) · 2022
    Article
  7. Review
  8. Rational Design and Synthesis of AT1R Antagonists.Molecules (Basel, Switzerland) · 2021
    Review
  9. Article
  10. Article
  11. Review
  12. Review
  13. Article
  14. Article
  15. Review
  16. 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

3 authors at 2 institutions in 1 country.

Tahsin F KelliciDepartment of Chemistry, National and Kapodistrian University of Athens, Panepistimiopolis Zografou 15771, Greece.
Andreas G TzakosDepartment of Chemistry, University of Ioannina, Ioannina 45110, Greece.
Thomas MavromoustakosDepartment of Chemistry, National and Kapodistrian University of Athens, Panepistimiopolis Zografou 15771, Greece. tmavrom@chem.uoa.gr.
University of Ioannina · GRNational and Kapodistrian University of Athens · GR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The angiotensin II (Ang II) type 1 and type 2 receptors (AT1R and AT2R) orchestrate an array of biological processes that regulate human health. Aberrant function of these receptors triggers pathophysiological responses that can ultimately lead to death. Therefore, it is important to design and synthesize compounds that affect beneficially these two receptors. Cardiovascular disease, which is attributed to the overactivation of the vasoactive peptide hormone Αng II, can now be treated with commercial AT1R antagonists. Herein, recent achievements in rational drug design and synthesis of molecules acting on the two AT receptors are reviewed. Quantitative structure activity relationships (QSAR) and molecular modeling on the two receptors aim to assist the search for new active compounds. As AT1R and AT2R are GPCRs and drug action is localized in the transmembrane region the role of membrane bilayers is exploited. The future perspectives in this field are outlined. Tremendous progress in the field is expected if the two receptors are crystallized, as this will assist the structure based screening of the chemical space and lead to new potent therapeutic agents in cardiovascular and other diseases.

Indexed as

Angiotensin IIAngiotensin II Type 1 Receptor BlockersAnimalsCardiovascular DiseasesDrug DesignHumansQuantitative Structure-Activity RelationshipReceptor, Angiotensin, Type 1Receptor, Angiotensin, Type 2Angiotensin IIAngiotensin II Type 1 Receptor BlockersReceptor, Angiotensin, Type 1Receptor, Angiotensin, Type 2

Identifiers

PMID25738535
PMCPMC6272512
OpenAlexW2065791710

What OpenQuestion holds

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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.