FIELD: chemistry, pharmaceutics.
SUBSTANCE: claimed invention relates to novel azaheterocycles of general formula 1.1-13 and 2, as well as their pharmaceutically acceptable salts, which possess anti-carcinogenic activity, pharmaceutical composition with their application and combinatorial and focused libraries including novel azaheterocycles. In general formulae 1.1-1.3 and 2.
.
For compounds 1.1-1.3 each of R1 a R2 a independently on each other represent possibly substituted C1-C6alkyl; each of R1 d, R2 d, R3 d, R4 d, R5 d, R6 d and R7 d independently on each other represent substitutes of cyclic system, preferably hydrogen atom, or for compounds 1.1 and 1.3 independently R1 d and R2 d, R3 d and R4 d, R5 d and R6 d together with atoms with which they are bound can form through R1 d and R2 d, R3 d and R4 d, R5 d and R6 d respectively, possibly substituted aromatic cycle, such as benzole, 5-6-member heterocycle which includes, at least, one of heteroatoms, selected from S; or for compounds 1.2 independently R1 d and R2 d, R3 d and R4 d, R4 d and R5 d, R6 d and R7 d together with atoms with which they are bound can form through R1 d and R2 d, R3 d and R4 d, R4 d and R5 d, R6 d and R7 d respectively, possibly substituted aromatic cycle, such as benzole, 5-6-member heterocycle which includes, at least, one of heteroatoms, selected from S; for compound 2 R1 a represents amino group substitute, excluding hydrogen atom, such as possibly substituted C1-C6alkyl, possibly substituted phenyl; R2 a represents possibly substituted C1-C6alkyl; R3 a represents amino group substitute, such as hydrogen atom, possibly substituted C1-C6alkyl; Rn d represents one or two substitutes of cyclic system, preferably hydrogen atom, solid line with accompanying it dotted line represent single or double bond.
EFFECT: obtaining novel azaheterocycles and their pharmaceutically acceptable salts, which possess anti-carcinogenic activity.
9 cl, 4 dwg, 3 tbl, 7 ex
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Authors
Dates
2009-01-27—Published
2007-06-19—Filed