Evidence map›Paper›PMID 29094937›Full record

ArticleJournal of medicinal chemistry2017

Structure-Based Design and Discovery of New M

Inbar Fish, Anne Stößel, Katrin Eitel, Celine Valant, Sabine Albold, Harald Huebner, Dorothee Möller, Mary J Clark, Roger K Sunahara, Arthur Christopoulos and 2 more

Abstract read
In one paragraph

Article in Journal of medicinal chemistry, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 10 papers.

0numbers the graph read from it
0cells of the map it votes in
10citing 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

10 citing papers in PubMed.

  1. Trial
  2. Article
  3. Review
  4. Article
  5. Article
  6. Article
  7. Article
  8. Novel MBritish journal of pharmacology · 2020
    Article
  9. Article
  10. 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

12 authors.

Inbar FishDepartment of Pharmaceutical Chemistry, University of California, San Francisco , San Francisco, California 94158, United States.
Anne StößelDepartment of Chemistry and Pharmacy, Medicinal Chemistry, Emil Fischer Center, Friedrich Alexander University , Schuhstraße 19, 91052 Erlangen, Germany.
Katrin EitelDepartment of Chemistry and Pharmacy, Medicinal Chemistry, Emil Fischer Center, Friedrich Alexander University , Schuhstraße 19, 91052 Erlangen, Germany.
Celine ValantDrug Discovery Biology, Monash Institute of Pharmaceutical Sciences, Monash University , Parkville Victoria 3052, Australia.
Sabine AlboldDrug Discovery Biology, Monash Institute of Pharmaceutical Sciences, Monash University , Parkville Victoria 3052, Australia.
Harald HuebnerDepartment of Chemistry and Pharmacy, Medicinal Chemistry, Emil Fischer Center, Friedrich Alexander University , Schuhstraße 19, 91052 Erlangen, Germany.
Dorothee MöllerDepartment of Chemistry and Pharmacy, Medicinal Chemistry, Emil Fischer Center, Friedrich Alexander University , Schuhstraße 19, 91052 Erlangen, Germany.
Mary J ClarkDepartment of Pharmacology, University of California, San Diego , La Jolla, California 92093, United States.
Roger K SunaharaDepartment of Pharmacology, University of California, San Diego , La Jolla, California 92093, United States.
Arthur ChristopoulosDrug Discovery Biology, Monash Institute of Pharmaceutical Sciences, Monash University , Parkville Victoria 3052, Australia.
Brian K ShoichetDepartment of Pharmaceutical Chemistry, University of California, San Francisco , San Francisco, California 94158, United States.ORCID 0000-0002-6098-7367
Peter GmeinerDepartment of Chemistry and Pharmacy, Medicinal Chemistry, Emil Fischer Center, Friedrich Alexander University , Schuhstraße 19, 91052 Erlangen, Germany.ORCID 0000-0002-4127-197X

Funding

Development and Testing of New Computational Methods for Ligand Discovery and MechanismR35GM122481 · NIGMS · UNIVERSITY OF CALIFORNIA, SAN FRANCISCO · PI Brian K Shoichet · 2017 to 2026
$8.5M
Structure-based discovery of allosteric ligands for G Protein Coupled ReceptorsU19GM106990 · NIGMS · STANFORD UNIVERSITY · PI GMEINER, PETER · 2013 to 2017
$6.3M
NIGMS NIH HHS R35 GM122481NIGMS NIH HHS U19 GM106990
6 · The paper itself

Abstract

Muscarinic receptor agonists are characterized by apparently strict restraints on their tertiary or quaternary amine and their distance to an ester or related center. On the basis of the active state crystal structure of the muscarinic M

Indexed as

AcetylcholineAnimalsArrestinBenzofuransCarbacholCHO CellsCricetulusDrug DesignHEK293 CellsHumansIsoxazolesLigandsMolecular Docking SimulationMuscarinic AgonistsN-MethylscopolamineQuaternary Ammonium Compounds2-(2,3-dihydrobenzofuran-6-yl)-N,N,N-trimethylethan-1-aminiumAcetylcholineArrestinBenzofuransCarbacholiperoxoIsoxazolesLigandsMuscarinic Agonistsnicotinic receptor alpha4beta2N-MethylscopolamineQuaternary Ammonium CompoundsReceptor, Muscarinic M1Receptor, Muscarinic M2Receptor, Muscarinic M3Receptors, NicotinicTritium

Identifiers

PMID29094937
PMCPMC5836741

What OpenQuestion holds

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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.