FIELD: medicine. SUBSTANCE: acetic acid derivatives of formula: HN (NH)C-X-Y-CO-Z-CH(Q′)COOQ′ wherein Q′ is hydrogen, phenylene; Q′ is hydrogen, phenyl lower alkyl; X is 1,4-phenylene, 2,5- pyridilene or 1,4-piperidinylene attached via hydrocarbon atom in position 4 to group Y. Y is group of formula: -(CH2)0-2-CONHCH(Q3)(CH2)1-31-CONHCH2CH(Q4),, compound of formula 1 or compound of formula 2 or formulae 3 and 4; Q3 is hydrogen, methyl, phenyl, COOH or -CONH(CH2)2COOH; Q4 is hydrogen, methyl or phenyl; Z is 1,4- piperazinylene, 1,4-piperidinylene at attached via nitrogen atom in position 1 to group CO, or group of formula 5; Q′ is hydrogen, methyl, phenyl or COO lower alkyl; R″′ is residue attached via aminogroup of alpha- aminocarboxylic acid, or residue of ester of said acid or group of formula: -NHCH2CH2Ar or COR″′-carbamoyl or pyrrolidinoyl, Ar-phenyl unsubstituted or substituted with carboxy group of group -O(CH2)1-4COOH or hydrates thereof, or solvates thereof, or pharmaceutically acceptable salts thereof. Structure of compounds of formula 1,2,3,4 and 5. EFFECT: improved properties of the title compounds. 8 cl, 3 tbl
Title |
Year |
Author |
Number |
DERIVATIVES OF N-ACYL-α-AMINO ACID OR THEIR PHYSIOLOGICALLY ACCEPTABLE SALTS, SIMPLE ETHERS OR ESTERS, AMIDES OR HYDRATES AND COMPOSITION INHIBITING ADHESIVE PROTEINS BINDING WITH PLATELETS AND PLATELET AGGREGATION |
1992 |
- Leo Alig[Ch]
- Paul Khadvari[Ch]
- Marianne Khjurtseler[Ch]
- Marsel Mjuller[Ch]
- Beat Shtejner[Ch]
- Tomas Veller[Ch]
|
RU2097378C1 |
GLYCINE DERIVATIVES OR THEIR PHYSIOLOGICALLY ACCEPTABLE SALTS SHOWING CAPABILITY TO INHIBIT FIBRINOGEN BINDING IN FIBRINOGEN PLATELET RECEPTOR |
1990 |
- Leo Alig[Ch]
- Albrekht Edenkhofer[Ch]
- Marsel Mjuller[Ch]
- Arnold Chechiak[De]
- Tomas Ueller[Ch]
|
RU2024549C1 |
METHOD OF SYNTHESIS OF CARBOXYLIC OR SULFONIC ACID AMIDES OR THEIR PHYSIOLOGICALLY COMPATIBLE SALTS |
1990 |
- Leo Alig[Ch]
- Albrekht Edenkhofer[Ch]
- Marsel Mjuller[Ch]
- Arnold Trtsekiak[De]
- Tomas Veller[Ch]
|
RU2072986C1 |
SULFONEAMIDOCARBOXAMIDES, THEIR HYDRATES AND PHYSIOLOGICALLY ACCEPTABLE SALTS, PHARMACEUTICAL COMPOSITION ON SAID |
1993 |
- Zhan Akermann
- David Banner
- Klaus Gubernator
- Kurt Khil'Pert
- Zherar Shmid
|
RU2133739C1 |
ACETIC ACID DERIVATIVES |
1994 |
- Alig Leo
- Khadvari Pol'
- Khjurtseler Mjuller Marianne
- Mjuller Marsel'
- Shtajner Beat
- Veller Tomas
|
RU2151768C1 |
(S)-1-[(10-CHLORO-6,7-DIHYDRO-4-OXO-3-PHENYL-4H-BENZO[A]QUINO- -LIZINE-1-YL)-CARBONYL]-3-ETHOXYPYRROLIDINE, (S)-1-[(10-CHLORO-6,7-DIHYDRO-4-OXO-3-PHENYL-4H-BENZO[A]QUINOLIZINE-1-YL)- -CARBONYL]-3-HYDROXYPYRROLIDINE AS AN INTERMEDIATE COMPOUND, COMPOSITION SHOWING HYPNOTIC NONSEDATIVE ACTION |
1992 |
- Rikhard Rajmund Shershlikht[De]
- Ul'Rikh Vidmer[Ch]
|
RU2073678C1 |
AMINO ACID DERIVATIVES AND PHARMACEUTICALLY ACCEPTABLE BASIC SALTS THEREOF METHODS OF PREPARING AMINO ACID DERIVATIVES AND PHARMACEUTICAL COMPOSITION HAVING ANTIVIRAL ACTIVITY |
1992 |
- Dzhosef Armstrong Martin[Gb]
- Garez Dzhon Tomas[Gb]
|
RU2109731C1 |
DERIVATIVES OF THIAZOLE, METHOD OF THEIR SYNTHESIS, COMPOSITION BASED ON THEREOF AND INTERMEDIATE COMPOUND |
1999 |
- Leo Alig
- Al'Brekht Ehdenkhofer
- Kurt Khil'Pert
- Tomas Veller
|
RU2166503C2 |
METHOD OF SYNTHESIS OF TRIAZOLO-[4,3-A]-[1,4]-DIAZEPINES |
1988 |
|
RU2071962C1 |
DERIVATIVES OF ARYLSULFONEAMIDE OR THEIR SALTS AND PHARMACEUTICAL COMPOSITION SHOWING ANTIPROTECTIVE, ANTIHYPERTENSION AND VASOSPAMOLYTIC, IN PART, ANTIISCHEMIC ACTION |
1992 |
- Kaspar Burri[Ch]
- Martin Klozel'[Fr]
- Val'Ter Fishli[Ch]
- Zhorzh Khirt[Fr]
- Bernd Mikhael' Leffler[De]
- Genri Ramuz[Ch]
|
RU2083567C1 |