BindingDB

The first public molecular recognition database, BindingDB supports research, education and practice in drug discovery, pharmacology and related fields.

BindingDB contains 3.2M data for 1.4M Compounds and 11.4K Targets. Of those, 1.6M data for 745K Compounds and 4.7K Targets were curated by BindingDB curators. BindingDB is a FAIRsharing resource.

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23 articles for J Heering

The following articles (labelled with PubMed ID or TBD) are for your review

PMID
Data
Article Title
Organization
Thermodynamic properties of leukotriene AEBI
Goethe-University Frankfurt
N-Benzylbenzamides: A Novel Merged Scaffold for Orally Available Dual Soluble Epoxide Hydrolase/Peroxisome Proliferator-Activated Receptor¿ Modulators.EBI
Goethe-University Frankfurt
Tuning RXR Modulators for PGC1α Recruitment.EBI
Ludwig-Maximilians-Universitat (LMU) Munchen
Development of a Potent and Selective G2A (GPR132) Agonist.EBI
Fraunhofer Institute for Translational Medicine and Pharmacology ITMP
Structure-Based Design of Dual Partial Peroxisome Proliferator-Activated Receptor γ Agonists/Soluble Epoxide Hydrolase Inhibitors.EBI
Goethe-University
Design of a Potent TLX Agonist by Rational Fragment Fusion.EBI
Goethe University Frankfurt
Combined Cardioprotective and Adipocyte Browning Effects Promoted by the Eutomer of Dual sEH/PPARγ Modulator.EBI
Goethe University
Propranolol Activates the Orphan Nuclear Receptor TLX to Counteract Proliferation and Migration of Glioblastoma Cells.EBI
Goethe-University Frankfurt
Development and Profiling of Inverse Agonist Tools for the Neuroprotective Transcription Factor Nurr1.EBI
Goethe University Frankfurt
Discovery of Irbesartan Derivatives as BLT2 Agonists by Virtual Screening.EBI
Fraunhofer Institute For Translational Medicine and Phamacology Itmp
Demonstrating Ligandability of the LC3A and LC3B Adapter Interface.EBI
Goethe-University Frankfurt
Fragment-like Chloroquinolineamines Activate the Orphan Nuclear Receptor Nurr1 and Elucidate Activation Mechanisms.EBI
Goethe University
Design, Synthesis, and Structure-Activity Relationship Studies of Dual Inhibitors of Soluble Epoxide Hydrolase and 5-Lipoxygenase.EBI
Goethe-University of Frankfurt
First Structure-Activity Relationship Study of Potent BLT2 Agonists as Potential Wound-Healing Promoters.EBI
Fraunhofer Ime
Photohormones Enable Optical Control of the Peroxisome Proliferator-Activated Receptor γ (PPARγ).EBI
New York University
l-Thyroxin and the Nonclassical Thyroid Hormone TETRAC Are Potent Activators of PPARγ.EBI
Goethe-University Frankfurt
Discovery of the First in Vivo Active Inhibitors of the Soluble Epoxide Hydrolase Phosphatase Domain.EBI
Goethe-University Frankfurt
Tuning Nuclear Receptor Selectivity of Wy14,643 towards Selective Retinoid X Receptor Modulation.EBI
Goethe University Frankfurt
Structure optimization of a new class of PPARγ antagonists.EBI
Fraunhofer Institute For Molecular Biology and Applied Ecology Ime
A Selective Modulator of Peroxisome Proliferator-Activated Receptor γ with an Unprecedented Binding Mode.EBI
Goethe-University Frankfurt
Computer-Assisted Discovery and Structural Optimization of a Novel Retinoid X Receptor Agonist Chemotype.EBI
Goethe-University Frankfurt
Nonacidic Farnesoid X Receptor Modulators.EBI
Goethe-University Frankfurt
A Dual Modulator of Farnesoid X Receptor and Soluble Epoxide Hydrolase To Counter Nonalcoholic Steatohepatitis.EBI
Goethe-University Frankfurt