Protein Structure-Based Design, Synthesis Strategy and In Vitro Pharmacological Characterization of Estrogen Receptor α and β Selective Compounds

Author:

Hillisch A.,Peters O.,Kosemund D.,Müller G.,Walter A.,Elger W.,Fritzemeier K.-H.

Publisher

Springer Berlin Heidelberg

Reference21 articles.

1. Brzozowski AM et al. (1997) Molecular basis of agonism and antagonism in the oestrogen receptor. Nature 389:753–758

2. Dechering K, Boersma C, Mosselman S (2000) Estrogen receptors alpha and beta: two receptors of a kind? Curr Med Chem 7:561–576

3. Fritzemeier K.-H., Kollenkirchen U, Kosemund D, Müller G (2000) 19-Nor17 alpha-pregna-1,3,5 (10)-trien-17 beta-ols of a 21,16 alpha-lactone ring. WO0226763, 4 Oct 2000

4. Fritzemeier KH, Hegele-Hartung C (1999) In vitro and in vivo models to characterize estrogens and antiestrogens. In: Oettel M, Schillinger, E (eds) Handbook of experimental pharmacology, vol 135/II. Estrogens and antiestrogens II. Springer, Berlin Heidelberg

5. Fuhrmann U, Slater EP, Fritzemeier KH (1995) Characterization of the novel progestin gestodene by receptor binding studies and transactivation assays. Contraception 51:45–52

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