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pubmed-article:12639576pubmed:abstractTextA series of N(2)-furoyl and N(2)pyrimidinyl beta-carbolines was discovered to possess potent inhibitory activity against PDE5. During the synthesis we developed a tandem resin quenching protocol, which allowed us to synthesize large number of target compounds in a rapid fashion. Representative compounds exhibit superior selectivity to sildenafil versus other isozymes of PDEs, and demonstrated in vivo efficacy in increasing introcavernosal pressure in dogs.lld:pubmed
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pubmed-article:12639576pubmed:articleTitleSynthesis and biological activities of novel beta-carbolines as PDE5 inhibitors.lld:pubmed
pubmed-article:12639576pubmed:affiliationJohnson & Johnson Pharmaceutical Research & Development L.L.C., 1000 Route 202, Raritan, NJ 08869, USA. zsui@prius.jnj.comlld:pubmed
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