FIELD: pharmaceuticals.
SUBSTANCE: invention relates to a compound of Formula I that can inhibit NLRP3 and may find use in the treatment or prevention of a disease, disorder or condition responsive to NLRP3 inhibition. In formula, I Q represents O; R1 represents a non-aromatic heterocyclic group selected from, wherein R1 is attached to the sulfur atom of the sulfonylurea group via a ring carbon atom and where R1 may optionally be substituted by one or more substituents independently selected from -Rβ; -ORβ; -SO2Rβ; -CORβ; -COORβ; -Rα-COORβ; -CONHRβ; -CON(Rβ)2; -Rα-CON(Rβ)2;;; oxo (=O) or C1-C4 alkylene bridge; where each -Rα is independently selected from an alkylene group containing from 1 to 6 carbon atoms in its skeleton; where each -Rβ is independently selected from a C1-C6 alkyl, C2-C6 alkenyl, C2-C6 alkynyl or C3-C7 cycloalkyl group, or a 3–7 membered heterocyclic group containing one heteroatom selected from N, O or S, and any -Rβ may be optionally substituted with one or more C1-C3 alkyl, C1-C3 haloalkyl, C3-C7 cycloalkyl, -O(C1-C3 alkyl), halogen, -CN, -C≡CH or oxo (=O); where each -Rδ is independently selected from a C1-C6 alkyl group; where each m is independently selected from 1 or 2; where each n is independently selected from 1 or 2; and R2 represents .
EFFECT: invention also relates to various pharmaceutically acceptable salts of the said compound, a pharmaceutical composition containing them, their use in the manufacture of a medicinal product for treating or preventing a disease, disorder or condition responsive to NLRP3 inhibition, a method of treating such diseases and a method of inhibiting NLRP3.
26 cl, 3 tbl, 195 ex
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Authors
Dates
2023-11-29—Published
2018-07-04—Filed