FIELD: pharmaceuticals.
SUBSTANCE: invention relates to a compound of formula (I-a2) or (I-a3) or a pharmaceutically acceptable salt thereof, where Z represents a group of formula (iv), L3 represents an unsubstituted C1-C6 alkylene, C1-C6 alkylene, substituted by methyl, unsubstituted hetero-C1-C6 alkylene containing an O atom as a heteroatom, or hetero-C1-C6 alkylene containing an O atom as a heteroatom, substituted by methyl; R3b represents hydrogen; R3a represents unsubstituted C1-C6 alkyl or C1-C6 alkyl substituted with 1–3 fluorine atoms or a methoxy group; R2 represents hydrogen; each of R11a and R11b independently represents hydrogen; R6a and R6b are each hydrogen, unsubstituted C1-C6 alkyl or halogen; Y represents -O-; RZ5 represents hydrogen; and R Z6 is in each case independently hydrogen or unsubstituted C1-C6 alkyl. The invention relates to a pharmaceutical composition with activity against the NMDA receptor, containing a pharmaceutically acceptable carrier and an effective amount of a compound of the invention or a pharmaceutically acceptable salt thereof. The invention also provides a method of treating, ameliorating or controlling a disease or condition mediated by an NMDA receptor, which comprises administering to a patient in need of such treatment, amelioration or control a therapeutically effective amount of a compound of the invention or a pharmaceutically acceptable salt or a pharmaceutical composition thereof.
EFFECT: obtaining 3α- and 3β-hydroxysteroids with NMDA receptor activity.
19 cl, 1 tbl, 37 ex
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Authors
Dates
2023-11-24—Published
2012-09-07—Filed