Parthenolide and its photochemically synthesized 1(10)Z isomer: Chemical reactivity and structure-activity relationship studies in human leucocyte chemotaxis

Bioorganic and Medicinal Chemistry

Volumn 11, Issue 7, 2003, Pages 1503-1510

  Neukirch, Hannes ^a   Kaneider, Nicole C ^b   Wiedermann, Christian J ^b   Guerriero, Antonio ^a   D'Ambrosio, Michele ^a  

^a UNIVERSITY OF TRENTO   (Italy)

^b UNIVERSITY OF INNSBRUCK   (Austria)

Author keywords

[No Author keywords available]

Indexed keywords

11,13 DIHYDROPARTHENOLIDE; 2,3,6,7,7A,8,10A,10B OCTAHYDRO 1A,5 DIMETHYL 8 METHYLENEOXIRENO[9,10]CYCLODECA[1,2 B]FURAN 9(1AH) ONE; 2,3,6,7,7A,8,10A,10B OCTAHYDRO 1A,5,8 TRIMETHYLOXIRENO[9,10]CYCLODECA[1,2 B]FURAN 9(1AH) ONE; 2,3,6,7,7A,8,10A,10B OCTAHYDRO 8 (METHOXYMETHYL) 1A,5 DIMETHYLOXIRENO[9,10]CYCLODECA[1,2 B]FURAN 9(1AH) ONE; 3A,4,5,8,11,11A HEXAHYDRO 11 HYDROXY 6,10 DIMETHYL 3 METHYLENECYCLODECA[B]FURAN 2(3H) ONE; 3A,4,5,8,9,10,11,11A OCTAHYDRO 11 HYDROXY 10 METHOXY 6,10 DIMETHYL 3 METHYLENECYCLODECA[B]FURAN 2(3H) ONE; 3A,4,5,8,9,10,11,11A OCTAHYDRO 11 HYDROXY 6 METHYL 3,10 BIS(METHYLENE)CYCLODECA[B]FURAN 2(3H) ONE; ANTIINFLAMMATORY AGENT; DECAHYDRO 9 HYDROXY 6 METHOXY 6,8A DIMETHYL 3 METHYLENECYCLOBUTA[6,7]CYCLOOCTA[1,2 B]FURAN 2(3H) ONE; DECAHYDRO 9 HYDROXY 6 METHOXY 6,9 DIMETHYLAZULENO[4,5 B]FURAN 2(3H) ONE; FURAN DERIVATIVE; PARTHENOLIDE; UNCLASSIFIED DRUG;

ANTIINFLAMMATORY ACTIVITY; ARTICLE; CHEMOTAXIS; CONTROLLED STUDY; CYCLIZATION; DRUG DESIGN; DRUG SELECTIVITY; DRUG SYNTHESIS; HUMAN; HUMAN CELL; IN VITRO STUDY; ISOMER; LEUKOCYTE; NEUTROPHIL CHEMOTAXIS; PHARMACOPHORE; PHOTOCHEMISTRY; STRUCTURE ACTIVITY RELATION;

ANTI-INFLAMMATORY AGENTS, NON-STEROIDAL; CATALYSIS; CHEMOTAXIS, LEUKOCYTE; HUMANS; INDICATORS AND REAGENTS; ISOMERISM; MODELS, MOLECULAR; MOLECULAR CONFORMATION; PHOTOCHEMISTRY; SESQUITERPENES; STRUCTURE-ACTIVITY RELATIONSHIP;

EID: 0037375657     PISSN: 09680896     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0968-0896(02)00553-9     Document Type: Article

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