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By considering published structural information we have designed high throughput biaryl lipophilic acid arrays leveraging facile chemistry to expedite their synthesis. We rapidly identified multiple hits which were of suitable IP agonist potency. These relatively simple and strategically undecorated molecules present an ideal opportunity for optimization towards our target candidate profile.

作者:Stephen C, McKeown;Steven J, Charlton;Brian, Cox;Helen, Fitch;Christopher D, Howson;Catherine, Leblanc;Arndt, Meyer;Elizabeth M, Rosethorne;Emily, Stanley

来源:Bioorganic & medicinal chemistry letters 2014 年 24卷 10期

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作者:
Stephen C, McKeown;Steven J, Charlton;Brian, Cox;Helen, Fitch;Christopher D, Howson;Catherine, Leblanc;Arndt, Meyer;Elizabeth M, Rosethorne;Emily, Stanley
来源:
Bioorganic & medicinal chemistry letters 2014 年 24卷 10期
标签:
IP agonist PGI(2) agonist Prostanoid Pulmonary arterial hypertension
By considering published structural information we have designed high throughput biaryl lipophilic acid arrays leveraging facile chemistry to expedite their synthesis. We rapidly identified multiple hits which were of suitable IP agonist potency. These relatively simple and strategically undecorated molecules present an ideal opportunity for optimization towards our target candidate profile.