FIELD: chemistry.
SUBSTANCE: invention relates to compounds of formula (II):
or a pharmaceutically acceptable salt or tautomer thereof, where: X is O or OH; W is N; L is -(C(R5)2)mY1(C(R5)2)p-; Y1 is S; R1 is absent or represents C6-C10 arylene; each R5 in each occurrence is independently H; each R6 in each occurrence is independently H; R7 is A or C; A is -(C(R6)2) r tetrazole, C is -(C(R6)2)rC6-C10 aryl, wherein said aryl is substituted with one to three substitutes, each independently selected from halogen and OH; Rc is H or -CN; Rd is CF3, -(C(R6)2)tC6-C10 aryl; Rf is H; Rj is absent; each m, p, q and r is independently 0, 1 or 2; each t is 1 or 2; and is a single bond or a double bond, which are capable of inhibiting decarboxylase activity of semialdehyde α-amino-β-carboxymuconic acid (ACMSD). Present application also describes pharmaceutical compositions, use of said compounds as a medicinal agent.
EFFECT: compounds are suitable for preventing and/or treating diseases and disorders associated with disorders of NAD+ biosynthesis, for example, metabolic disorders, neurodegenerative diseases, chronic inflammatory diseases, renal diseases and diseases associated with aging.
54 cl, 1 tbl, 98 ex
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Authors
Dates
2025-06-03—Published
2019-11-19—Filed