11 articles for thisTarget
The following articles (labelled with PubMed ID or TBD) are for your review
PMID
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Article Title
Organization
Functionalized N,N-Diphenylamines as Potent and Selective EPAC2 Inhibitors.
University of Texas Medical Branch
Structure-Activity Relationship Studies of Substituted 2-(Isoxazol-3-yl)-2-oxo-N'-phenyl-acetohydrazonoyl Cyanide Analogues: Identification of Potent Exchange Proteins Directly Activated by cAMP (EPAC) Antagonists.
University of Texas Medical Branch
Recent advances in the discovery of small molecules targeting exchange proteins directly activated by cAMP (EPAC).
University of Texas Medical Branch
Identification and characterization of small molecules as potent and specific EPAC2 antagonists.
University of Texas Medical Branch
5-Cyano-6-oxo-1,6-dihydro-pyrimidines as potent antagonists targeting exchange proteins directly activated by cAMP.
University of Texas Medical Branch
Chemical synthesis and biological activity of novel brominated 7-deazaadenosine-3',5'-cyclic monophosphate derivatives.
University Hospital Jena
Structure-activity relationships of 2-substituted phenyl-N-phenyl-2-oxoacetohydrazonoyl cyanides as novel antagonists of exchange proteins directly activated by cAMP (EPACs).
University of Texas Medical Branch
Exchange proteins directly activated by cAMP (EPACs): Emerging therapeutic targets.
University of Texas Medical Branch
Structure-Activity Relationship Studies with Tetrahydroquinoline Analogs as EPAC Inhibitors.
Institute For Research In Cancer and Allied Diseases
Identification of novel 2-(benzo[d]isoxazol-3-yl)-2-oxo-N-phenylacetohydrazonoyl cyanide analoguesas potent EPAC antagonists.
University of Texas Medical Branch
