FIELD: medicine; pharmaceuticals.
SUBSTANCE: present invention refers to a compound of general formula (I) and its pharmaceutically acceptable salt, which can find application in modulation of sphingosine-1-phosphate receptors (S1P). In formula (I) X1, X2, X3 and X4 are CR1; is selected from and ; Z is -O- or -OCH2-; each R1 is independently selected from a group consisting of hydrogen, halogen and C1-C6 alkyl substituted by halogen; each R2 is independently selected from the group consisting of halogen and C1-C6 alkyl substituted by halogen; R3 is selected from the group consisting of hydrogen and C1-C6 alkyl; n equals 0–4 and p equals 0 or 1. Present invention also relates to a pharmaceutical composition for modulating sphingosine-1-phosphate (S1P) receptor activity, comprising a pharmaceutically acceptable diluent, excipient or binder and compound of formula (I) or its pharmaceutically acceptable salt. Described also is use of compounds of formula (I) and their pharmaceutically acceptable salts for treating a disease, disorder or condition, where the disease, disorder or condition is selected from multiple sclerosis, ulcerative colitis and Crohn's disease.
EFFECT: heterocyclic compounds for treating a disease are disclosed.
21 cl, 2 dwg, 1 tbl, 20 ex
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Authors
Dates
2020-07-21—Published
2016-11-11—Filed