Evidence map›Paper›PMID 20543968›Full record

ReviewFuture medicinal chemistry2010

Small-molecule modulators of inward rectifier K+ channels: recent advances and future possibilities.

Gautam Bhave, Daniel Lonergan, Brian A Chauder, Jerod S Denton

Open access · greenAbstract readReview
In one paragraph

Review in Future medicinal chemistry, 2010. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 30 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
30citing papers in PubMed, 1 pooled it
1.8field-weighted citation impact, top 16% 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

30 citing papers in PubMed, 1 synthesis or guideline pooled it, 50 citations in OpenAlex.

  1. Pooled it
  2. Article
  3. Article
  4. Article
  5. AsKC11, a Kunitz Peptide fromMarine drugs · 2022
    Article
  6. Review
  7. Weak Electromagnetic Fields Accelerate Fusion of Myoblasts.International journal of molecular sciences · 2021
    Article
  8. Article
  9. Review
  10. Article
  11. Expression, localization, and functional properties of inwardly rectifying KAmerican journal of physiology. Renal physiology · 2020
    Review
  12. Article
  13. Article
  14. Article
  15. Inhibitors of the Renal Outer Medullary Potassium Channel.ACS medicinal chemistry letters · 2015
    Article
  16. Article
  17. Review
  18. Cardiac ion channels.Channels (Austin, Tex.) · 2015
    Review
  19. Article
  20. 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

4 authors at 1 institution in 1 country.

Gautam BhaveDepartment of Anesthesiology, Vanderbilt University Medical Center, Nashville, TN 37232, USA.
Daniel Lonergan
Brian A Chauder
Jerod S Denton
Vanderbilt University Medical Center · US

Funding

The Vanderbilt Specialized Chemistry Center for Accelerated Probe DevelopmentU54MH084659 · NIMH · VANDERBILT UNIVERSITY · PI MEILER, JENS · 2008 to 2013
$24.1M
Molecular pharmacology and physiology of kidney potassium transportR01DK082884 · NIDDK · VANDERBILT UNIVERSITY · PI DENTON, JEROD S. · 2010 to 2014
$1.3M
Identification of novel modulators of ROMK K+ channel activityR21NS057041 · NINDS · VANDERBILT UNIVERSITY · PI DENTON, JEROD S · 2006 to 2006
$77k
NIDDK NIH HHS R01 DK082884NIMH NIH HHS 1U54MH084659-01NIMH NIH HHS U54 MH084659NINDS NIH HHS 1R21NS5704111NINDS NIH HHS R21 NS057041
6 · The paper itself

Abstract

Inward rectifier potassium (Kir) channels have been postulated as therapeutic targets for several common disorders including hypertension, cardiac arrhythmias and pain. With few exceptions, however, the small-molecule pharmacology of this family is limited to nonselective cardiovascular and neurologic drugs with off-target activity toward inward rectifiers. Consequently, the actual therapeutic potential and 'drugability' of most Kir channels has not yet been determined experimentally. The purpose of this review is to provide a comprehensive summary of publicly disclosed Kir channel small-molecule modulators and highlight recent targeted drug-discovery efforts toward Kir1.1 and Kir2.1. The review concludes with a brief speculation on how the field of Kir channel pharmacology will develop over the coming years and a discussion of the increasingly important role academic laboratories will play in this progress.

Indexed as

AnimalsDrug DiscoveryHumansModels, MolecularPotassium Channels, Inwardly RectifyingSmall Molecule LibrariesPotassium Channels, Inwardly RectifyingSmall Molecule Libraries

Identifiers

PMID20543968
PMCPMC2883187
OpenAlexW2050133219

What OpenQuestion holds

Textmetadata
LicenceTDM
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.