FIELD: pharmaceutical chemistry.
SUBSTANCE: group of inventions relates to the field of pharmaceutical chemistry, and it is the use of a compound of the formula A1 (its pharmaceutically acceptable salt) or 6-(2-chloro-6-methylpyridine-4-yl)-5-(4-fluorophenyl)-1,2,4-triazine-3-amine (its pharmaceutically acceptable salt) in the manufacture of a drug for the treatment of cancer mediated by the activity of A1 receptor and/or A2a receptor. In the formula A1, A is CyAA or HetAA; CyAA is a 6-element aromatic carbocyclic system, where CyAA group has a substituent R4a at position 3 relatively to the point of attachment to a triazine ring, and, if necessary, has one or more additional substituent R4a; HetAA is a 6-element heterocyclic group, which can be aromatic, fully saturated or partially unsaturated, and which contains one or two heteroatoms selected from O and N, while HetAA group has a substituent R4b at position 3 relatively to the point of attachment to the triazine ring, and, if necessary, has one or more additional substituent R4b; B is CyBB or HetBB; CyBB is phenyl optionally having one or more substituent R4c; HetBB is a 6-element aromatic heterocyclic group that contains one or two N atoms; R4a-R4c are as specified in the claims. It is provided that compound A1 is not 5-(2-chlorophenyl)-6-(3,4-dimethoxyphenyl)-[1,2,4]triazine-3-ylamine or 5-(2-chlorophenyl)-6-(3,4,5-trimethoxyphenyl)-[1,2,4]triazine-3-ylamine.
EFFECT: use of 1,2,4-triazine-3-amine derivatives in the production of a drug for the treatment of cancer mediated by the activity of A1 receptor and/or A2a receptor.
18 cl, 1 tbl, 7 ex
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Authors
Dates
2022-05-12—Published
2011-02-07—Filed