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16 articles for thisTarget


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

PMID
Data
Article Title
Organization
Synthesis, evaluation and structure-activity relationship of new 3-carboxamide coumarins as FXIIa inhibitors.EBI
University of Namur
Indoleamine 2,3-dioxygenase inhibitory activity of derivatives of marine alkaloid tsitsikammamine A.EBI
University of Namur
Tryptophan 2,3-dioxygenase (TDO) inhibitors. 3-(2-(pyridyl)ethenyl)indoles as potential anticancer immunomodulators.EBI
University of Namur
Indanesulfonamides as carbonic anhydrase inhibitors and anticonvulsant agents: structure-activity relationship and pharmacological evaluation.EBI
University of Namur
Carbonic anhydrase inhibitors: anticonvulsant sulfonamides incorporating valproyl and other lipophilic moieties.EBI
University of Namur
Discovery and preliminary SARs of keto-indoles as novel indoleamine 2,3-dioxygenase (IDO) inhibitors.EBI
University of Namur
Indol-2-yl ethanones as novel indoleamine 2,3-dioxygenase (IDO) inhibitors.EBI
University of Namur
NF-kappaB inducing kinase (NIK) inhibitors: identification of new scaffolds using virtual screening.EBI
University of Namur
Ligand-based and structure-based virtual screening to identify carbonic anhydrase IX inhibitors.EBI
University of Namur
Recent developments of carbonic anhydrase inhibitors as potential anticancer drugs.EBI
University of Namur
Investigation of mechanism-based thrombin inhibitors: Implications of a highly conserved water molecule for the binding of coumarins within the S pocket.EBI
University of Namur
3,6-disubstituted coumarins as mechanism-based inhibitors of thrombin and factor Xa.EBI
University of Namur
Factor XII/XIIa inhibitors: Their discovery, development, and potential indications.EBI
University of Namur
Synthesis of 4- and 5-arylthiazolinethiones as inhibitors of indoleamine 2,3-dioxygenase.EBI
University of Namur
ERK inhibitorsBDB
Merck Sharp & Dohme
Heterodimeric tacrine-based acetylcholinesterase inhibitors: investigating ligand-peripheral site interactions.BDB
Hong Kong University of Science and Technology