Combinational Synthesis for the Expedited Discovery of Novel Selective Antiestrogens for Breast Cancer Prevention and Therapy
Abstract
We have conceived of an approach to prepare by combinatorial methods, libraries of novel ligands for the estrogen receptor, by the creation of simple amide or five-membered ring heterocyclic core structures that display peripheral substitutes (phenols, aliphatic groups, etc.) commonly found in non-steroidal estrogens. These novel estrogens might be useful in the treatment or prevention of breast cancer. We have made good progress on the preparation of novel estrogen of the diphenyl carboxamide class, the diphenylsulfonamide class, the phenyl benzylcarboxamide and sulfonamide classes, and the pyrazole, oxazole, thiazole, and imidazole classes. Members of some classes have high affinity for the estrogen receptor, and some of them show high binding and potency selectivity for the estrogen receptor subtype alpha and other selectivity for the subtype beta. We have also developed a convenient solid phase synthesis of the pyrazole class, so that we can prepare conveniently and rapidly larger libraries of the members of what appear presently to be the most promising of these classes of novel estrogens.
Document Details
- Document Type
- Technical Report
- Publication Date
- Sep 01, 1999
- Accession Number
- ADB257384
Entities
People
- John Katzenellenbogen
Organizations
- University of Illinois Urbana–Champaign