Collection of Czechoslovak Chemical Communications - digital archive 

Abstract

Solid phase methodology on benzhydrylamine resin with linkage agent and Fmoc technique was used for the synthesis of two analogs of deamino carba-1 and carba-6 oxytocin with phenylalanine in position 2 and with ornithine in position 8. The following analogs were prepared: [Phe²,Orn⁸]deamino-carba-1-oxytocin (I) and [Phe²,Orn⁸]deamino-carba-6-oxytocin (II). Moreover, analogs with δ-amino group of ornithine protected by benzyloxycarbonyl group and its corresponding sulfoxides were isolated and tested. Both deprotected analogs were found to have high uterotonic activity in vivo, and moderate pressor and antidiuretic agonistic activity. Surprisingly, in uterotonic test they are only partial agonists. The analogs with protected ornithine have preserved high uterotonic in vivo activity in contrary to the pressor activity that was strongly decreased.