SCOPUS 정보 검색 플랫폼

Volumn 9, Issue 8, 2001, Pages 2155-2164

Cytotoxic activities of novel hexahydroindolizino[8,7-b]indole derivatives prepared by 1,3-dipolar cycloaddition reactions of 3,4-dihydro-β-carboline ylides

(9) Bertrand, Martial a Poissonnet, Guillaume a Théret Bettiol, Marie Hélène a Gaspard, Christiane a Werner, Georges H a Pfeiffer, Bruno b Renard, Pierre b Léonce, Stéphane c Dodd, Robert H a

a CNRS (France)

b ADIR (France)

c INSTITUT DE RECHERCHES SERVIER (France)

Author keywords

[No Author keywords available]

Indexed keywords

3,4 DIHYDRO BETA CARBOLINE; 6 BENZYLOXY 3,4 DIHYDRO BETA CARBOLINE; 8 BENZYLOXY 1,2,3,5,6,11B HEXAHYDROINDOLIZINO[8,7 B]INDOLE 1 CARBONITRILE; 8 BENZYLOXY 1,2,3,5,6,11B HEXAHYDROINDOLIZINO[8,7 B]INDOLE 2 CARBONITRILE; 9 BENZYL 3,4 DIHYDRO BETA CARBOLINE; BETA CARBOLINE DERIVATIVE; DOXORUBICIN; HEXAHYDROINDOLIZINO[8,7 B]INDOLE DERIVATIVE; INDOLE DERIVATIVE; UNCLASSIFIED DRUG;

ANIMAL CELL; ARTICLE; CANCER GROWTH; CELL CYCLE; CHEMICAL REACTION; CONTROLLED STUDY; CYCLIZATION; CYTOTOXICITY; DRUG SYNTHESIS; GROWTH INHIBITION; HUMAN; HUMAN CELL; IC 50; LEUKEMIA L 1210; MOUSE; NONHUMAN;

ANTINEOPLASTIC AGENTS; CARBOLINES; CELL CYCLE; CELL SURVIVAL; HUMANS; INDOLES; K562 CELLS;

EID: 0034907490 PISSN: 09680896 EISSN: None Source Type: Journal
DOI: 10.1016/S0968-0896(01)00119-5 Document Type: Article

Times cited : (15)

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