Agonist (Ovulation Induction) and Post-Coital Contraceptive Properties of [D-Ala6] and [D-Trp6]-Lhrh Series

Abstract

Seven derivatives of LH-RH, representing the [D-Ala⁶] or [D-Trp⁶] series, with or without a Fujino modification, were evaluated for ovulation-inducing (agonist) and post-coital contraceptive activity in rats. Six of these analogues had a high degree of agonist and pregnancy-terminating potency. In general, several modifications can result in a particular series of composite molecules that possess a biologic potency greater than each of its predecessors; this correlation of structure with activity was more consistent in the [D-Ala⁶]-series than in the [D-Trp⁶]-series. The relationship between structural modifications, resistance to enzyme degradation (based on literature reports) and increased biologic potency is discussed.