AMIDINE DERIVATIVES, MIXTURE OF THEIR ISOMERS OR SEPARATE ISOMERS AND SALTS, PHARMACEUTICAL COMPOSITION SHOWING ANTAGONISTIC EFFECT WITH RESPECT TO LEUKOTRIENE-B4

FIELD: organic chemistry, pharmacy. SUBSTANCE: invention relates to derivatives of amidine of the formula (I) where R1 and R2 are similar or distinct and mean hydrogen, halide, alkyl, phenyl possibly substituted with halogen, alkyl, alkoxyl or acyl, OR5 where R5 - H, alkyl, phenyl possibly substitut...

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Hauptverfasser: EHRNST-OTTO RENT, FRANTS BIRKE, RAL'F ANDERSKEVITTS, KURT SHROMM, ARMIN FJUGNER, FRANK KHIMMEL'SBAKH
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creator EHRNST-OTTO RENT
FRANTS BIRKE
RAL'F ANDERSKEVITTS
KURT SHROMM
ARMIN FJUGNER
FRANK KHIMMEL'SBAKH
description FIELD: organic chemistry, pharmacy. SUBSTANCE: invention relates to derivatives of amidine of the formula (I) where R1 and R2 are similar or distinct and mean hydrogen, halide, alkyl, phenyl possibly substituted with halogen, alkyl, alkoxyl or acyl, OR5 where R5 - H, alkyl, phenyl possibly substituted with halogen, alkyl, alkoxyl or acyl, group SO2R6 where R6 - alkyl, phenyl, COR6; or R1 and R2 together mean groups -CR8=CR9-CH= CH-, -CH=CR8-CR9=CH- or -CR8=CH--CR9=CH- bound with adjacent carbon atoms of benzene ring where R8 and R9 mean H, OH, alkyl, alkoxy, acyl or -O--CHR10-CH2 where R10 - H, alkyl or -CO--CH2-CH2-O-; R3 - hydroxyl, H, alkyl, alkoxy or acyl, phenyl; R4 - H or alkoxy; A - one of group X1-A-X2 (a) or X2-A2-X3 (b) where A1 is C2-4-alkylene, cis- or trans--CH2--CH= CH--CH2-, or , ; A2 is C1-5-alkylene; X1 - O, imino, sulfur, sulfinyl, carbonyl, methylene; X2 - oxygen or sulfur atom, imino-group or ; X3 is NH-CO, CO-NH or SO2-NH; B - a group CH=CH or CH=N, a mixture of their isomers, or separate isomers and their salts. Pharmaceutical composition has compounds of the formula (I) as an active component and shows antagonistic effect with respect to leukotriene-B4 and can be used, in part, for treatment of patients with asthma and ulcer colitis. EFFECT: improved method of synthesis. 11 cl, 5 tbl, 29 ex
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SUBSTANCE: invention relates to derivatives of amidine of the formula (I) where R1 and R2 are similar or distinct and mean hydrogen, halide, alkyl, phenyl possibly substituted with halogen, alkyl, alkoxyl or acyl, OR5 where R5 - H, alkyl, phenyl possibly substituted with halogen, alkyl, alkoxyl or acyl, group SO2R6 where R6 - alkyl, phenyl, COR6; or R1 and R2 together mean groups -CR8=CR9-CH= CH-, -CH=CR8-CR9=CH- or -CR8=CH--CR9=CH- bound with adjacent carbon atoms of benzene ring where R8 and R9 mean H, OH, alkyl, alkoxy, acyl or -O--CHR10-CH2 where R10 - H, alkyl or -CO--CH2-CH2-O-; R3 - hydroxyl, H, alkyl, alkoxy or acyl, phenyl; R4 - H or alkoxy; A - one of group X1-A-X2 (a) or X2-A2-X3 (b) where A1 is C2-4-alkylene, cis- or trans--CH2--CH= CH--CH2-, or , ; A2 is C1-5-alkylene; X1 - O, imino, sulfur, sulfinyl, carbonyl, methylene; X2 - oxygen or sulfur atom, imino-group or ; X3 is NH-CO, CO-NH or SO2-NH; B - a group CH=CH or CH=N, a mixture of their isomers, or separate isomers and their salts. Pharmaceutical composition has compounds of the formula (I) as an active component and shows antagonistic effect with respect to leukotriene-B4 and can be used, in part, for treatment of patients with asthma and ulcer colitis. 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SUBSTANCE: invention relates to derivatives of amidine of the formula (I) where R1 and R2 are similar or distinct and mean hydrogen, halide, alkyl, phenyl possibly substituted with halogen, alkyl, alkoxyl or acyl, OR5 where R5 - H, alkyl, phenyl possibly substituted with halogen, alkyl, alkoxyl or acyl, group SO2R6 where R6 - alkyl, phenyl, COR6; or R1 and R2 together mean groups -CR8=CR9-CH= CH-, -CH=CR8-CR9=CH- or -CR8=CH--CR9=CH- bound with adjacent carbon atoms of benzene ring where R8 and R9 mean H, OH, alkyl, alkoxy, acyl or -O--CHR10-CH2 where R10 - H, alkyl or -CO--CH2-CH2-O-; R3 - hydroxyl, H, alkyl, alkoxy or acyl, phenyl; R4 - H or alkoxy; A - one of group X1-A-X2 (a) or X2-A2-X3 (b) where A1 is C2-4-alkylene, cis- or trans--CH2--CH= CH--CH2-, or , ; A2 is C1-5-alkylene; X1 - O, imino, sulfur, sulfinyl, carbonyl, methylene; X2 - oxygen or sulfur atom, imino-group or ; X3 is NH-CO, CO-NH or SO2-NH; B - a group CH=CH or CH=N, a mixture of their isomers, or separate isomers and their salts. 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SUBSTANCE: invention relates to derivatives of amidine of the formula (I) where R1 and R2 are similar or distinct and mean hydrogen, halide, alkyl, phenyl possibly substituted with halogen, alkyl, alkoxyl or acyl, OR5 where R5 - H, alkyl, phenyl possibly substituted with halogen, alkyl, alkoxyl or acyl, group SO2R6 where R6 - alkyl, phenyl, COR6; or R1 and R2 together mean groups -CR8=CR9-CH= CH-, -CH=CR8-CR9=CH- or -CR8=CH--CR9=CH- bound with adjacent carbon atoms of benzene ring where R8 and R9 mean H, OH, alkyl, alkoxy, acyl or -O--CHR10-CH2 where R10 - H, alkyl or -CO--CH2-CH2-O-; R3 - hydroxyl, H, alkyl, alkoxy or acyl, phenyl; R4 - H or alkoxy; A - one of group X1-A-X2 (a) or X2-A2-X3 (b) where A1 is C2-4-alkylene, cis- or trans--CH2--CH= CH--CH2-, or , ; A2 is C1-5-alkylene; X1 - O, imino, sulfur, sulfinyl, carbonyl, methylene; X2 - oxygen or sulfur atom, imino-group or ; X3 is NH-CO, CO-NH or SO2-NH; B - a group CH=CH or CH=N, a mixture of their isomers, or separate isomers and their salts. Pharmaceutical composition has compounds of the formula (I) as an active component and shows antagonistic effect with respect to leukotriene-B4 and can be used, in part, for treatment of patients with asthma and ulcer colitis. EFFECT: improved method of synthesis. 11 cl, 5 tbl, 29 ex</abstract><edition>6</edition><oa>free_for_read</oa></addata></record>
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subjects ACYCLIC OR CARBOCYCLIC COMPOUNDS
CHEMISTRY
HETEROCYCLIC COMPOUNDS
HUMAN NECESSITIES
HYGIENE
MEDICAL OR VETERINARY SCIENCE
METALLURGY
ORGANIC CHEMISTRY
PREPARATIONS FOR MEDICAL, DENTAL, OR TOILET PURPOSES
SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS ORMEDICINAL PREPARATIONS
title AMIDINE DERIVATIVES, MIXTURE OF THEIR ISOMERS OR SEPARATE ISOMERS AND SALTS, PHARMACEUTICAL COMPOSITION SHOWING ANTAGONISTIC EFFECT WITH RESPECT TO LEUKOTRIENE-B4
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