PMID

Data

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

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