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

BindingDB contains 2.8M data for 1.2M Compounds and 9.2K Targets. Of those, 1,346K data for 622K Compounds and 4.5K Targets were curated by BindingDB curators. BindingDB is a FAIRsharing resource.

If BindingDB was of value to your research, please take a moment to donate to this nonprofit project. Your donation will let us provide you with more data and improved service.

Advanced Search

22 articles for thisTarget


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

PMID
Data
Article Title
Organization
Benzo[b]thiophene-2-carboxamide derivatives as potent urotensin-II receptor antagonists.EBI
Korea Research Institute Of Chemical Technology
Urotensin II((4-11)) Azasulfuryl Peptides: Synthesis and Biological Activity.EBI
Universit£
Lead optimization of P5U and urantide: discovery of novel potent ligands at the urotensin-II receptor.EBI
University Of Naples&Quot;Federico Ii&Quot
Synthesis and SAR of thieno[3,2-b]pyridinyl urea derivatives as urotensin-II receptor antagonists.EBI
Korea Research Institute Of Chemical Technology
Development and pharmacological characterization of conformationally constrained urotensin II-related peptide agonists.EBI
Universit£
Deconstruction of sulfonamide inhibitors of the urotensin receptor (UT) and design and synthesis of benzylamine and benzylsulfone antagonists.EBI
Boehringer Ingelheim Pharmaceuticals
Aminoalkoxybenzyl pyrrolidines as novel human urotensin-II receptor antagonists.EBI
Glaxosmithkline
Further studies at neuropeptide s position 5: discovery of novel neuropeptide S receptor antagonists.EBI
National Institute Of Neuroscienc
New insight into the binding mode of peptide ligands at Urotensin-II receptor: structure-activity relationships study on P5U and urantide.EBI
University Of Naples Federico Ii
N-alkyl-5H-pyrido[4,3-b]indol-1-amines and derivatives as novel urotensin-II receptor antagonists.EBI
Glaxosmithkline
Structure-activity relationships of a novel series of urotensin II analogues: identification of a urotensin II antagonist.EBI
University Of Rouen
Identification of new agonists of urotensin-II from a cyclic peptide library.EBI
Prism Bio. Lab.
2-Aminomethyl piperidines as novel urotensin-II receptor antagonists.EBI
Glaxosmithkline
Development of potent and selective small-molecule human Urotensin-II antagonists.EBI
Glaxosmithkline
Urotensin-II receptor modulators as potential drugs.EBI
Johnson & Johnson Pharmaceutical Research & Development
Nonpeptide urotensin-II receptor antagonists: a new ligand class based on piperazino-phthalimide and piperazino-isoindolinone subunits.EBI
Johnson & Johnson Pharmaceutical Research & Development
Urotensin-II receptor antagonists: synthesis and SAR of N-cyclic azaalkyl benzamides.EBI
Glaxosmithkline
Potent and selective small-molecule human urotensin-II antagonists with improved pharmacokinetic profiles.EBI
Glaxosmithkline
Phenylpiperidine-benzoxazinones as urotensin-II receptor antagonists: synthesis, SAR, and in vivo assessment.EBI
Johnson & Johnson Pharmaceutical Research & Development
Architecture of the human urotensin II receptor: comparison of the binding domains of peptide and non-peptide urotensin II agonists.EBI
Università
Identification of nonpeptidic urotensin II receptor antagonists by virtual screening based on a pharmacophore model derived from structure-activity relationships and nuclear magnetic resonance studies on urotensin II.EBI
Aventis Pharma Germany
Synthesis of Novel Oxazolo[4,5-b]pyridine-2-one based 1,2,3-triazoles as Glycogen Synthase Kinase-3ß Inhibitors with Anti-inflammatory Potential.BDB
Hamdard University (Jamia Hamdard)