Synthesis and biological activities of novel β-Carbolines as PDE5 inhibitors

Synthesis and biological activities of novel β-Carbolines as PDE5 inhibitors Furoyl and Benzofuroyl Pyrroloquinolones as Potent and Selective PDE5 Inhibitors for Treatment of Erectile Dysfunction Discovery of furyl/thienyl β-carboline derivatives as potent and selective PDE5 inhibitors with excellent vasorelaxant effect Quinolines as extremely potent and selective PDE5 inhibitors as potential agents for treatment of erectile dysfunction Pyrimidinylpyrroloquinolones as Highly Potent and Selective PDE5 Inhibitors for Treatment of Erectile Dysfunction The Discovery of Tadalafil:  A Novel and Highly Selective PDE5 Inhibitor. 1: 5,6,11,11a-Tetrahydro-1H-imidazo[1‘,5‘:1,6]pyrido[3,4-b]indole-1,3(2H)-dione Analogues Quinazolines as potent and highly selective PDE5 inhibitors as potential therapeutics for male erectile dysfunction Design and synthesis of furyl/thineyl pyrroloquinolones based on natural alkaloid perlolyrine, lead to the discovery of potent and selective PDE5 inhibitors 2-Phenylquinazolin-4(3H)-one, a class of potent PDE5 inhibitors with high selectivity versus PDE6 Structure−Activity Relationships of N-Acyl Pyrroloquinolone PDE-5 Inhibitors