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5. Steroidal affinity labels of the estrogen receptor. 3. Estradiol 11 beta-n-alkyl derivatives bearing a terminal electrophilic group: antiestrogenic and cytotoxic properties. Lobaccaro C; Pons JF; Duchesne MJ; Auzou G; Pons M; Nique F; Teutsch G; Borgna JL J Med Chem; 1997 Jul; 40(14):2217-27. PubMed ID: 9216841 [TBL] [Abstract][Full Text] [Related]
6. Steroidal affinity labels of the estrogen receptor. 2. 17 alpha-[(Haloacetamido)alkyl]estradiols. el Garrouj D; Aliau S; Aumelas A; Borgna JL J Med Chem; 1995 Jun; 38(13):2339-48. PubMed ID: 7608900 [TBL] [Abstract][Full Text] [Related]
7. Differential interactions of estrogens and antiestrogens at the 17 beta-hydroxy or counterpart function with the estrogen receptor. Borgna JL; Scali J Eur J Biochem; 1991 Aug; 199(3):575-85. PubMed ID: 1868844 [TBL] [Abstract][Full Text] [Related]
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11. 11 beta-chloromethyl-[3H]estradiol-17 beta: a very high affinity, reversible ligand for the estrogen receptor. Bindal RD; Carlson KE; Reiner GC; Katzenellenbogen JA J Steroid Biochem; 1987 Oct; 28(4):361-70. PubMed ID: 3669657 [TBL] [Abstract][Full Text] [Related]
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14. 2-Arylindenes and 2-arylindenones: molecular structures and considerations in the binding orientation of unsymmetrical nonsteroidal ligands to the estrogen receptor. Anstead GM; Wilson SR; Katzenellenbogen JA J Med Chem; 1989 Sep; 32(9):2163-71. PubMed ID: 2769689 [TBL] [Abstract][Full Text] [Related]
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17. Steroidal affinity labels of the estrogen receptor. 1. 17 alpha-(Bromoacetoxy)alkyl/alkynylestradiols. el Garrouj D; Aumelas A; Borgna JL J Med Chem; 1993 Oct; 36(20):2973-83. PubMed ID: 8411015 [TBL] [Abstract][Full Text] [Related]
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