127530-40-9Relevant academic research and scientific papers
Cytotoxic ester derivatives of the mammary tumor inhibiting antiestrogen 2,3-bis(2-fluoro-4-hydroxyphenyl)-2,3-dimethylbutane
Schwarz,Hartmann,Engel,Schneider,Schonenberger
, p. 121 - 124 (2007/10/02)
The synthesis of the bis-acrylate 12, the bis-β-chloropropionate 13 and the bis-β-bromopropionate 14 of the 'partial' antiestrogen 2,3-bis(2-fluoro-4-hydroxyphenyl)-2,3-dimethylbutane (7) is described. In the case of 13 and 14 the introduction of the β-haloester-functions moderately reduces the estrogen receptor affinity of 7. However, it was quite strongly diminished in 12. The hydrolytic stability under in vitro-receptor-assay conditions decreases in the order 12 > 14 > 13. Compared with 7 the estrogenic potency of 12-14 is increased to a great extent. The title compounds cause a strong inhibition of the hormone-dependent MXT-M3.2 mouse mammary tumor.
