Structure-guided synthesis of tamoxifen analogs with improved selectivity for the orphan ERRgamma.

Article Details

Citation

Chao EY, Collins JL, Gaillard S, Miller AB, Wang L, Orband-Miller LA, Nolte RT, McDonnell DP, Willson TM, Zuercher WJ

Structure-guided synthesis of tamoxifen analogs with improved selectivity for the orphan ERRgamma.

Bioorg Med Chem Lett. 2006 Feb 15;16(4):821-4. Epub 2005 Nov 22.

PubMed ID
16307879 [ View in PubMed
]
Abstract

The design and synthesis of 4-hydroxytamoxifen (4-OHT) derivatives are described. The binding affinities of these compounds toward the orphan estrogen-related receptor gamma and the classical estrogen receptor alpha demonstrate that analogs bearing hydroxyalkyl groups display improved binding selectivity profiles compared with that of 4-OHT. An X-ray crystal structure of one of the designed compounds bound to ERRgamma LBD confirms the molecular basis of the selectivity.

DrugBank Data that Cites this Article

Polypeptides
NameUniProt ID
Estrogen-related receptor gammaP62508Details