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Building Bridges in a Series of Estrogen Receptor Degraders: An Application of Metathesis in Medicinal Chemistry.


ABSTRACT: Herein we report the use of metathesis to construct a novel tetracyclic core in a series of estrogen receptor degraders. This improved the chemical stability, as assessed using an NMR-MS based assay, and gave a molecule with excellent physicochemical properties and pharmacokinetics in rat. X-ray crystallography established minimal perturbation of the bridged compounds relative to the unbridged analogues in the receptor binding pocket. Unfortunately, despite retaining excellent binding to ER?, this adversely affected the ability of the compounds to degrade the receptor.

SUBMITTER: Scott JS 

PROVIDER: S-EPMC6792171 | biostudies-literature | 2019 Oct

REPOSITORIES: biostudies-literature

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Building Bridges in a Series of Estrogen Receptor Degraders: An Application of Metathesis in Medicinal Chemistry.

Scott James S JS   Breed Jason J   Carbajo Rodrigo J RJ   Davey Paul R PR   Greenwood Ryan R   Huynh Hoan K HK   Klinowska Teresa T   Morrow Christopher J CJ   Moss Thomas A TA   Polanski Radoslaw R   Nissink J Willem M JWM   Varnes Jeffrey J   Yang Bin B  

ACS medicinal chemistry letters 20190923 10


Herein we report the use of metathesis to construct a novel tetracyclic core in a series of estrogen receptor degraders. This improved the chemical stability, as assessed using an NMR-MS based assay, and gave a molecule with excellent physicochemical properties and pharmacokinetics in rat. X-ray crystallography established minimal perturbation of the bridged compounds relative to the unbridged analogues in the receptor binding pocket. Unfortunately, despite retaining excellent binding to ERα, th  ...[more]

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