FIELD: chemistry.
SUBSTANCE: invention relates to novel polyheterocyclic compounds of formulas Ia or Ib, given below, stereoisomers, pharmaceutically acceptable salts or their mixture, where m=0.1 or 2; n=0.1 or 2; p=0.1 or 2; q=0.1 or 2; r=0. 1, 2 or 3; stands for a single bond or a double bond; and stands for a double bond in a macrocyclic internal combination with cyclopropyl formyl; stands for a single bond in a cycle D, E, E1 and G, where D and G independently stand for oxygen, E and E1 independently stand for C(Ra)(Rb); R10 stands for hydrogen; Ra, Rb and Rc independently on each other stand for hydrogen; when r=0 E is absent, D and E1 are directly bound; L stands for methylene (CRbRc); T stands for nitrogen (N) or CH; U stands for carbon (C); W stands for oxygen; X stands for oxygen; Y stands for nitrogen (N) or CH; Z stands for OH; C1-C20 alkyl-sulphonylamido, C3-C20-cycloalkyl-sulphonylamido; R1 and R2 independently stand for C1-C20-alkyl, C3-C20 cycloalkyl, C6-C12 arylamine, C1-C20 alkoxycarbonyl-amino, C2-C20 heterocyclic sulphonylamide ring; R3, R4, R5, R6 - independently stand for H; R7, R8 and R9 independently stand for H. The compounds inhibit replication of protease NS3 of the hepatitis C virus.
EFFECT: improved properties of the compounds.
7 cl, 1 tbl, 11 dwg, 118 ex
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Authors
Dates
2014-12-20—Published
2011-01-27—Filed