INHIBITORS OF ENZYMES CONVERTING 1beta-INTERLEUKIN

FIELD: organic chemistry, biochemistry, medicine. SUBSTANCE: invention relates to compounds of the general formulas alpha- and beta-: and , wherein n = 0, 1 or 2; m and m' represent 1 or 2; R11 means: or ; R2' = R2 is hydrogen atom; R3 is -CH2Ar or 5-15-membered nonaromatic monocyclic grou...

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Hauptverfasser: GOLEK DZHULIAN M.S, LIVINGSTON DEHVID DZH, DAFFI DZHON P, MERKO MARK A, ZELLE ROBERT E, BEMIZ GAJ V, FRIDMAN VOL'F GERMAN, MALLIKAN MAJKL D
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creator GOLEK DZHULIAN M.S
LIVINGSTON DEHVID DZH
DAFFI DZHON P
MERKO MARK A
ZELLE ROBERT E
BEMIZ GAJ V
FRIDMAN VOL'F GERMAN
MALLIKAN MAJKL D
description FIELD: organic chemistry, biochemistry, medicine. SUBSTANCE: invention relates to compounds of the general formulas alpha- and beta-: and , wherein n = 0, 1 or 2; m and m' represent 1 or 2; R11 means: or ; R2' = R2 is hydrogen atom; R3 is -CH2Ar or 5-15-membered nonaromatic monocyclic group that can comprise from 0 to 2 endocyclic nitrogen atoms; R4 is unbranched (C1-5)-alkyl group; R5 is taken among group including -C(0)R7, -C(0)OR9, -C(0)C(0)R7; R7 is taken among the group: phenyl, naphthyl, isoquinoline being phenyl can be substituted with halogen atom, (C1-6)-alkoxy group, 1,2-methylenedioxy-group or N(H)C(O)-(C1-6)-alkyl; R9 is taken independently among direct -alkyl group optionally substituted with phenyl; R12 and R13 are taken independently among the group including R7, -C(O)-R7 and C(O)-N(H)-R7; or R12 and R13 form in common 4-8-membered saturated cyclic group. Invention relates to pharmaceutical composition used for inhibition of activity of enzyme converting 1beta-interleukin (ICE), to method for inhibition of activity of ICE, to methods for treatment or prophylaxis of IL-mediated diseases. EFFECT: valuable medicinal properties of compounds. 14 cl, 1 tbl
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SUBSTANCE: invention relates to compounds of the general formulas alpha- and beta-: and , wherein n = 0, 1 or 2; m and m' represent 1 or 2; R11 means: or ; R2' = R2 is hydrogen atom; R3 is -CH2Ar or 5-15-membered nonaromatic monocyclic group that can comprise from 0 to 2 endocyclic nitrogen atoms; R4 is unbranched (C1-5)-alkyl group; R5 is taken among group including -C(0)R7, -C(0)OR9, -C(0)C(0)R7; R7 is taken among the group: phenyl, naphthyl, isoquinoline being phenyl can be substituted with halogen atom, (C1-6)-alkoxy group, 1,2-methylenedioxy-group or N(H)C(O)-(C1-6)-alkyl; R9 is taken independently among direct -alkyl group optionally substituted with phenyl; R12 and R13 are taken independently among the group including R7, -C(O)-R7 and C(O)-N(H)-R7; or R12 and R13 form in common 4-8-membered saturated cyclic group. Invention relates to pharmaceutical composition used for inhibition of activity of enzyme converting 1beta-interleukin (ICE), to method for inhibition of activity of ICE, to methods for treatment or prophylaxis of IL-mediated diseases. 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SUBSTANCE: invention relates to compounds of the general formulas alpha- and beta-: and , wherein n = 0, 1 or 2; m and m' represent 1 or 2; R11 means: or ; R2' = R2 is hydrogen atom; R3 is -CH2Ar or 5-15-membered nonaromatic monocyclic group that can comprise from 0 to 2 endocyclic nitrogen atoms; R4 is unbranched (C1-5)-alkyl group; R5 is taken among group including -C(0)R7, -C(0)OR9, -C(0)C(0)R7; R7 is taken among the group: phenyl, naphthyl, isoquinoline being phenyl can be substituted with halogen atom, (C1-6)-alkoxy group, 1,2-methylenedioxy-group or N(H)C(O)-(C1-6)-alkyl; R9 is taken independently among direct -alkyl group optionally substituted with phenyl; R12 and R13 are taken independently among the group including R7, -C(O)-R7 and C(O)-N(H)-R7; or R12 and R13 form in common 4-8-membered saturated cyclic group. 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subjects CHEMISTRY
HUMAN NECESSITIES
HYGIENE
MEDICAL OR VETERINARY SCIENCE
METALLURGY
ORGANIC CHEMISTRY
PEPTIDES
PREPARATIONS FOR MEDICAL, DENTAL, OR TOILET PURPOSES
SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS ORMEDICINAL PREPARATIONS
title INHIBITORS OF ENZYMES CONVERTING 1beta-INTERLEUKIN
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