Download MendeleyBenzopyrans as selective estrogen receptor beta agonists (SERBAs). Part 3: synthesis of cyclopentanone and cyclohexanone intermediates for C-ring modification.
Richardson, T.I., Dodge, J.A., Durst, G.L., Pfeifer, L.A., Shah, J., Wang, Y., Durbin, J.D., Krishnan, V., Norman, B.H.(2007) Bioorg Med Chem Lett 17: 4824-4828
- PubMed: 17614275
- DOI: https://doi.org/10.1016/j.bmcl.2007.06.052
- Primary Citation of Related Structures:
2Q70, 2Z4B - PubMed Abstract:
Benzopyrans are selective estrogen receptor (ER) beta agonists (SERBAs), which bind the ER subtypes alpha and beta in opposite orientations. Here we describe the syntheses of cyclopentanone and cyclohexanone intermediates for SAR studies of the C-ring on the benzopyran scaffold. Modification of the C-ring disrupts binding to ERalpha, thus improving ERbeta selectivity up to 100-fold. X-ray cocrystal structures confirm previously observed binding modes.
Organizational Affiliation:
Lilly Research Laboratories, Eli Lilly and Company, Lilly Corporate Center, Indianapolis, IN 46285, USA. t_richardson@lilly.com
