C5,C6-disubstituted 1H-indole-2-carboxamides: Synthesis and cytotoxic activity in the human non-small lung cancer cell line NSCLC-N16-L16

Letters in Drug Design and Discovery

Volumn 3, Issue 1, 2006, Pages 14-16

  Tsotinis, Andrew ^a   Gerasimopoulou, Maria ^a   Vlachou, Margarita ^a   Moreau, Dimitri ^b   Roussakis, Christos ^b  

^a UNIVERSITY OF ATHENS   (Greece)

^b UNIVERSITÉ DE NANTES   (France)

Author keywords

Cytotoxicity; Disubstituted 1H indole 2 carboxamides; Synthesis

Indexed keywords

4 BENZYLOXY 3 METHOXYBENZALDEHYDE; ACID; AMIDE; AMINE; AZIDE; BENZALDEHYDE DERIVATIVE; BENZYL DERIVATIVE; ESTER DERIVATIVE; INDOLE DERIVATIVE; UNCLASSIFIED DRUG;

AMIDATION; ARTICLE; CANCER CELL CULTURE; CYCLIZATION; CYTOTOXICITY; DEPROTECTION REACTION; DRUG ACTIVITY; DRUG EFFICACY; DRUG SCREENING; DRUG STRUCTURE; DRUG SYNTHESIS; HUMAN; HUMAN CELL; IC 50; IN VITRO STUDY; LUNG NON SMALL CELL CANCER; PRIORITY JOURNAL;

EID: 33645865871     PISSN: 15701808     EISSN: None     Source Type: Journal    
DOI: 10.2174/157018006775240980     Document Type: Article

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