Evidence map›Paper›PMID 22198732›Full record

ArticleNature chemical biology2011

Skepinone-L is a selective p38 mitogen-activated protein kinase inhibitor.

Solveigh C Koeberle, Johannes Romir, Stefan Fischer, Andreas Koeberle, Verena Schattel, Wolfgang Albrecht, Christian Grütter, Oliver Werz, Daniel Rauh, Thilo Stehle and 1 more

Abstract read
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Article in Nature chemical biology, 2011. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 50 papers.

0numbers the graph read from it
0cells of the map it votes in
50citing 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

50 citing papers in PubMed.

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  13. Candida albicans-induced leukotriene biosynthesis in neutrophils is restricted to the hyphal morphology.FASEB journal : official publication of the Federation of American Societies for Experimental Biology · 2021
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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

11 authors.

Solveigh C KoeberleInstitute of Pharmacy, University of Tübingen, Tübingen, Germany.
Johannes Romir
Stefan Fischer
Andreas Koeberle
Verena Schattel
Wolfgang Albrecht
Christian Grütter
Oliver Werz
Daniel Rauh
Thilo Stehle
Stefan A Laufer

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Until now, a lack of inhibitors with high potency and selectivity in vivo has hampered investigation of the p38 mitogen-activated protein kinase (MAPK) signaling pathway. We describe the design of skepinone-L, which is, to our knowledge, the first ATP-competitive p38 MAPK inhibitor with excellent in vivo efficacy and selectivity. Therefore, skepinone-L is a valuable probe for chemical biology research, and it may foster the development of a unique class of kinase inhibitors.

Indexed as

Adenosine TriphosphateAnimalsBinding, CompetitiveDibenzocycloheptenesDrug DesignMiceModels, Molecularp38 Mitogen-Activated Protein KinasesProtein Interaction Domains and MotifsProtein Kinase InhibitorsAdenosine TriphosphateDibenzocycloheptenesp38 Mitogen-Activated Protein KinasesProtein Kinase Inhibitorsskepinone-L

Identifiers

PMID22198732

What OpenQuestion holds

Textmetadata
Read underepoch 390

Registered trials

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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.