4-(5-Chloro-2(3H)-benzoxazolon-3-yl) Butanoic Acid Derivatives: Synthesis, Antinociceptive and Anti-inflammatory Properties

Archiv der Pharmazie

Volumn 336, Issue 10, 2003, Pages 477-482

  Gulcan, Hayrettin Ozan ^a   Kupeli, Esra ^a   Unlu, Serdar ^a   Yesilada, Erdem ^a   Sahin, Mustafa Fethi ^a  

^a GAZI UNIVERSITY   (Turkey)

Author keywords

2(3H) Benzoxazolone; Anti inflammatory; Antinociceptive; Butanamides; Synthesis

Indexed keywords

1 [4 [5 CHLORO 2(3H) BENZOXAZOLON 3 YL]BUTANOYL] 4 (2 FLUOROPHENYL)PIPERAZINE; 1 [4 [5 CHLORO 2(3H) BENZOXAZOLON 3 YL]BUTANOYL] 4 (2 METHOXYPHENYL)PIPERAZINE; 1 [4 [5 CHLORO 2(3H) BENZOXAZOLON 3 YL]BUTANOYL] 4 (2 PYRIDINYL)PIPERAZINE; 1 [4 [5 CHLORO 2(3H) BENZOXAZOLON 3 YL]BUTANOYL] 4 (4 FLUOROPHENYL)PIPERAZINE; 1 [4 [5 CHLORO 2(3H) BENZOXAZOLON 3 YL]BUTANOYL] 4 BENZYLPIPERAZINE; 1 [4 [5 CHLORO 2(3H) BENZOXAZOLON 3 YL]BUTANOYL] 4 BENZYLPIPERIDINE; 1 [4 [5 CHLORO 2(3H) BENZOXAZOLON 3 YL]BUTANOYL] 4 PHENYLPIPERAZINE; 1 [4 [5 CHLORO 2(3H) BENZOXAZOLON 3 YL]BUTANOYL] 4 PIPERONYLPIPERAZINE; 1,4 BENZOQUINONE; 2 BENZOXAZOLONE DERIVATIVE; 4 [5 CHLORO 2(3H) BENZOXAZOLINON 3 YL]BUTANOIC ACID; 4 [5 CHLORO 2(3H) BENZOXAZOLON 3 YL]BUTANOIC ACID; ACETYLSALICYLIC ACID; AMIDE; BUTYRIC ACID DERIVATIVE; CARBOXYLIC ACID; CARRAGEENAN; ETHYL 4 [5 CHLORO 2(3H) BENZOXAZOLON 3 YL]BUTANOATE; INDOMETACIN; N [4 [5 CHLORO 2(3H) BENZOXAZOLON 3 YL]BUTANOYL]MORPHOLINE; N [4 [5 CHLORO 2(3H) BENZOXAZOLON 3 YL]BUTANOYL]PIPERIDINE; UNCLASSIFIED DRUG;

AMIDATION; ANALYTIC METHOD; ANIMAL EXPERIMENT; ANIMAL MODEL; ANIMAL TISSUE; ANTIINFLAMMATORY ACTIVITY; ANTINOCICEPTION; ARTICLE; CHEMICAL STRUCTURE; CONTROLLED STUDY; DRUG SCREENING; DRUG STRUCTURE; DRUG SYNTHESIS; ELEMENTAL ANALYSIS; INFRARED SPECTROSCOPY; MALE; MOUSE; NONHUMAN; PRIORITY JOURNAL; PROTON NUCLEAR MAGNETIC RESONANCE; STRUCTURE ACTIVITY RELATION;

ANALGESICS; ANIMALS; ANTI-INFLAMMATORY AGENTS, NON-STEROIDAL; BUTYRIC ACIDS; DISEASE MODELS, ANIMAL; EDEMA; MAGNETIC RESONANCE SPECTROSCOPY; MALE; MICE; MOLECULAR STRUCTURE; OXAZOLES; PAIN; STRUCTURE-ACTIVITY RELATIONSHIP;

EID: 0242492560     PISSN: 03656233     EISSN: None     Source Type: Journal    
DOI: 10.1002/ardp.200300722     Document Type: Article

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