3-spiro-indolin-2-one derivatives as vasopressin and/or oxytocin receptor ligands

Under the present invention involves a dihydro-indol-ketone derivatives: where: w represents a-CH2-or-SO2-groups; Cy with their carbon to form the key link of non-aromatic saturated or unsaturated hydrocarbon rings in the C3-C12, the Central Visual case may be heavy or be of one or more (C1-C7) alkyl substituted, described substituent can be replaced one or more times on the same carbon atoms or alkyl substituted by C3-C6 Spiro; T representatives (C1-C4) Sub-alkyl, alkylidene group depends on the specific situation (C3-C6) Asia naphthenic discontinuous, alkylidene group depending on the specific circumstances of the case are described (C1-C3) alkyl replaced one or more times on the same carbon atoms; or t representatives directly connected to key; Z representative of particular amino; R1, R2, and R3 and R4, or such as hydrogen or halogens, alkyl substituents. The invention available compounds against leaf after vasopressin and/or drug oxytocin receptor affinity.