The Pseudo‐Natural Product Tafbromin Selectively Targets the TAF1 Bromodomain 2

Abstract: Phenotypic assays detect small‐molecule bioactivity at functionally relevant cellular sites, and inherently cover a variety of targets and mechanisms of action. They can uncover new small molecule‐target pairs and may give rise to novel biological insights. By means of an osteoblast differentiation assay which employs a Hedgehog (Hh) signaling agonist as stimulus and which monitors an endogenous marker for osteoblasts, we identified a pyrrolo[3,4‐g]quinoline (PQ) pseudo‐natural product (PNP) class of osteogenesis inhibitors. The most potent PQ, termed Tafbromin, impairs canonical Hh signaling and modulates osteoblast differentiation through binding to the bromodomain 2 of the TATA‐box binding protein‐associated factor 1 (TAF1). Tafbromin is the most selective TAF1 bromodomain 2 ligand and promises to be an invaluable tool for the study of biological processes mediated by TAF1 (2) bromodomains.

Standort
Deutsche Nationalbibliothek Frankfurt am Main
Umfang
Online-Ressource
Sprache
Englisch

Erschienen in
The Pseudo‐Natural Product Tafbromin Selectively Targets the TAF1 Bromodomain 2 ; day:04 ; month:07 ; year:2024 ; extent:13
Angewandte Chemie ; (04.07.2024) (gesamt 13)

Urheber
Patil, Sohan
Cremosnik, Gregor
Dötsch, Lara
Flegel, Jana
Schulte, Britta
Maier, Kerstin C.
Žumer, Kristina
Cramer, Patrick
Janning, Petra
Sievers, Sonja
Ziegler, Slava
Waldmann, Herbert

DOI
10.1002/ange.202404645
URN
urn:nbn:de:101:1-2407081442060.672301600293
Rechteinformation
Open Access; Der Zugriff auf das Objekt ist unbeschränkt möglich.
Letzte Aktualisierung
14.08.2025, 10:46 MESZ

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