FIELD: pharmaceuticals.
SUBSTANCE: invention relates to a compound of formula (IА) or a pharmaceutically acceptable salt thereof. In formula (I): n is either 1, 2, 3 or 4; structural unit selected from the group consisting of , ring A is selected from the group consisting of 5–6 membered heteroaryl; each R1 is independently selected from the group consisting of H, F, Cl, Br, I, C1-6 alkyl, C1-6 alkoxy and C3-6 cycloalkyl, with C1-6 alkyl, C1-6 alkoxy and C3-6 cycloalkyl are optionally substituted with 1, 2 or 3 R; each R2 is independently selected from the group consisting of H, F, Cl, Br, I, COOH, and C1-3 alkyl, with C1-3 alkyl optionally substituted with 1, 2, or 3 R; each R is independently selected from the group consisting of F, Cl, Br, I, OH, C1-3 alkyl and C1-3 alkoxy, with C1-3 alkyl and C1-3 alkoxy optionally substituted with 1, 2 or 3 R'; every R' independently selected from the group consisting of F, Cl, Br, I and OH; A 5–6 membered heteroaryl contains 1, 2, 3 or 4 heteroatoms or heteroradicals independently selected from the group consisting of -NH-, -O- and N; and Z1 is N, Z2 and Z3 are CH; Z2 is N, Z1 and Z3 are CH; Z3 is N, Z1 and Z2 are CH; Z1 and Z2 are N, Z3 is CH; Z2 and Z 3 are N, Z1 is CH; or Z1 and Z3 are N, Z2 is CH. Also the use of the said compound for the manufacture of a medicinal product is proposed.
EFFECT: proposed compound can be used as an ATR inhibitor.
15 cl, 1 dwg, 4 tbl, 61 ex
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Authors
Dates
2023-07-03—Published
2019-02-02—Filed