Synthesis and cytostatic properties of some 6H-indolo[2,3-b][1,8] naphthyridine derivatives

Archiv der Pharmazie

Volumn 337, Issue 8, 2004, Pages 434-439

  Mastalarza, Henryk ^a   Jasztold Howorko, Ryszard ^a,c   Rulko, Felicja ^a   Croisy, Alain ^b   Carrez, Daniele ^b  

^a WROCLAW MEDICAL UNIVERSITY   (Poland)

^b INSTITUT CURIE   (France)

^c Dept of Organ Chem of Medicine ^*  (Poland)

Author keywords

6H Indolo 2,3 b 1,8 naphthyridines; Cytotoxicity; Synthesis

Indexed keywords

1 METHYL 6H INDOLO[2,3 B][1,8]NAPHTHYRIDINE; 3 ACETYLAMINO 11 METHYL 6H INDOLO[2,3 B][1,8]NAPHTHYRIDINE; 3 ACETYLAMINO 5,11 DIMETHYL 6H INDOLO[2,3 B][1,8]NAPHTHYRIDINE; 3 ACETYLAMINO 5,6,11 TRIMETHYL 6H INDOLO[2,3 B][1,8]NAPHTHYRIDINE METHYLSULFATE; 3 ACETYLAMINO 6,11 DIMETHYL 6H INDOLO[2,3 B][1,8]NAPHTHYRIDINE; ELLIPTICINE; HETEROCYCLIC COMPOUND; NAPHTHYRIDINE DERIVATIVE; UNCLASSIFIED DRUG;

ANTINEOPLASTIC ACTIVITY; ARTICLE; CONTROLLED STUDY; CYTOSTASIS; DRUG SCREENING; DRUG SYNTHESIS; HUMAN; HUMAN CELL; IN VITRO STUDY; METHODOLOGY; PRIORITY JOURNAL; TUMOR CELL LINE;

ANTINEOPLASTIC AGENTS; CELL DIVISION; CELL LINE, TUMOR; DRUG SCREENING ASSAYS, ANTITUMOR; HUMANS; INDICATORS AND REAGENTS; INDOLES; MAGNETIC RESONANCE SPECTROSCOPY; NAPHTHYRIDINES; STRUCTURE-ACTIVITY RELATIONSHIP;

EID: 4544240169     PISSN: 03656233     EISSN: None     Source Type: Journal    
DOI: 10.1002/ardp.200200696     Document Type: Article

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