11β-Substituted Estradiol Derivatives. 2. Potential Carbon-11- and Iodine-Labeled Probes for the Estrogen Receptor

Elio Napolitano, Rita Fiaschi, Kathryn E. Carlson, John A. Katzenellenbogen

Research output: Contribution to journalArticlepeer-review

Abstract

Four new classes of 11β-substituted estradiol and estriol derivatives (cyanoalkyl, ethynyl, propynyl, and iodovinyl) have been synthesized, and their binding affinity for the estrogen receptor has been evaluated. The binding affinity values indicate that the estrogen receptor has tolerance for estradiol derivatives bearing 11β-groups whose size, rigidity, and polarity are limited. The estradiol derivatives have higher affinity than the estriol derivatives. The potential of these agents as imaging agent for estrogen receptor-positive breast tumors is discussed. On the basis of the results of this and a previously reported study (Napolitano, E.; Fiaschi, R.; Carlson, K. E.; Katzenellenbogen, J. A. 11β-Substituted Estradiol Derivatives, Potential High-Affinity Carbon-11-Labeled Probes for the Estrogen Receptor: A Structure-Affinity Relationship Study. J. Med. Chem. 1995, 38, 429-434), a general strategy for designing high-affinity probes for the estrogen receptor is proposed.

Original languageEnglish (US)
Pages (from-to)2774-2779
Number of pages6
JournalJournal of Medicinal Chemistry
Volume38
Issue number14
DOIs
StatePublished - Jul 1 1995

ASJC Scopus subject areas

  • Molecular Medicine
  • Drug Discovery

Fingerprint

Dive into the research topics of '11β-Substituted Estradiol Derivatives. 2. Potential Carbon-11- and Iodine-Labeled Probes for the Estrogen Receptor'. Together they form a unique fingerprint.

Cite this