Evidence map›Paper›PMID 35056776›Full record

ArticleMolecules (Basel, Switzerland)2022

Structural Basis of 2-Phenylamino-4-phenoxyquinoline Derivatives as Potent HIV-1 Non-Nucleoside Reverse Transcriptase Inhibitors.

Arthit Makarasen, Suwicha Patnin, Pongsit Vijitphan, Nanthawan Reukngam, Panita Khlaychan, Mayuso Kuno, Pakamas Intachote, Busakorn Saimanee, Suchada Sengsai, Supanna Techasakul

Abstract read
In one paragraph

Article in Molecules (Basel, Switzerland), 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
5citing papers in PubMed, 1 pooled it
–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

5 citing papers in PubMed, 1 synthesis or guideline pooled it.

  1. Recent Advances in Nitrogen-Containing Heterocyclic Scaffolds as Antiviral Agents.Medicinal chemistry (Shariqah (United Arab Emirates)) · 2024
    Pooled it
  2. Article
  3. Article
  4. Evolution of Antiretroviral Drug Rilpivirine and Approach to Oncology.International journal of molecular sciences · 2023
    Review
  5. 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

10 authors.

Arthit MakarasenLaboratory of Organic Synthesis, Department of Chemistry, Chulabhorn Research Institute, Bangkok 10210, Thailand.
Suwicha PatninLaboratory of Organic Synthesis, Department of Chemistry, Chulabhorn Research Institute, Bangkok 10210, Thailand.
Pongsit VijitphanLaboratory of Organic Synthesis, Department of Chemistry, Chulabhorn Research Institute, Bangkok 10210, Thailand.ORCID 0000-0002-1957-9644
Nanthawan ReukngamLaboratory of Organic Synthesis, Department of Chemistry, Chulabhorn Research Institute, Bangkok 10210, Thailand.
Panita KhlaychanLaboratory of Organic Synthesis, Department of Chemistry, Chulabhorn Research Institute, Bangkok 10210, Thailand.
Mayuso KunoDepartment of Chemistry, Faculty of Science, Srinakharinwirot University, Bangkok 10110, Thailand.
Pakamas IntachoteBiological Activity Test and Screening Unit, Central Facilities, Chulabhorn Research Institute, Bangkok 10210, Thailand.
Busakorn SaimaneeBiological Activity Test and Screening Unit, Central Facilities, Chulabhorn Research Institute, Bangkok 10210, Thailand.
Suchada SengsaiBiological Activity Test and Screening Unit, Central Facilities, Chulabhorn Research Institute, Bangkok 10210, Thailand.
Supanna TechasakulLaboratory of Organic Synthesis, Department of Chemistry, Chulabhorn Research Institute, Bangkok 10210, Thailand.

Funding

Chulabhorn Research Institute 313/2220Thailand Research Fund 313/2220
6 · The paper itself

Abstract

New target molecules, namely, 2-phenylamino-4-phenoxyquinoline derivatives, were designed using a molecular hybridization approach, which was accomplished by fusing the pharmacophore structures of three currently available drugs: nevirapine, efavirenz, and rilpivirine. The discovery of disubstituted quinoline indicated that the pyridinylamino substituent at the 2-position of quinoline plays an important role in its inhibitory activity against HIV-1 RT. The highly potent HIV-1 RT inhibitors, namely, 4-(2',6'-dimethyl-4'-formylphenoxy)-2-(5″-cyanopyridin-2″ylamino)quinoline (

Indexed as

Models, MolecularBinding SitesChemistry Techniques, SyntheticDose-Response Relationship, DrugEnzyme ActivationHIV-1HIV Reverse TranscriptaseHumansMolecular ConformationMolecular Docking SimulationMolecular Dynamics SimulationMolecular StructureProtein BindingQuinolinesReverse Transcriptase InhibitorsStructure-Activity RelationshipHIV Reverse TranscriptasequinolineQuinolinesReverse Transcriptase Inhibitorsanti-cancercytotoxicHIV-1molecular dockingquinoline

Identifiers

PMID35056776
PMCPMC8781960

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.