10328288

Source:http://linkedlifedata.com/resource/pubmed/id/10328288

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Predicate	Object
rdf:type	pubmed:Citation
lifeskim:mentions	umls-concept:C0220781, umls-concept:C0441655, umls-concept:C1511636, umls-concept:C1883254
pubmed:issue	8
pubmed:dateCreated	1999-8-3
pubmed:abstractText	6-Chloro-7-arylamino-5,8-isoquinolinediones were newly synthesized and evaluated for in vitro cytotoxic activities against five human solid tumor cell lines. Among them, 5b, 5c and 5d exhibited potent activities against the cell lines HCT-15 and SK-MEL-2.
pubmed:language	eng
pubmed:journal	http://linkedlifedata.com/resource/pubmed/journal/9107377
pubmed:citationSubset	IM
pubmed:chemical	http://linkedlifedata.com/resource/pubmed/chemical/Antineoplastic Agents, http://linkedlifedata.com/resource/pubmed/chemical/Isoquinolines
pubmed:status	MEDLINE
pubmed:month	Apr
pubmed:issn	0960-894X
pubmed:author	pubmed-author:JungS HSH, pubmed-author:LeeC OCO, pubmed-author:LeeI KIK, pubmed-author:RyuC KCK
pubmed:issnType	Print
pubmed:day	19
pubmed:volume	9
pubmed:owner	NLM
pubmed:authorsComplete	Y
pubmed:pagination	1075-80
pubmed:dateRevised	2006-11-15
pubmed:meshHeading	pubmed-meshheading:10328288-Antineoplastic Agents, pubmed-meshheading:10328288-Humans, pubmed-meshheading:10328288-Inhibitory Concentration 50, pubmed-meshheading:10328288-Isoquinolines, pubmed-meshheading:10328288-Tumor Cells, Cultured
pubmed:year	1999
pubmed:articleTitle	Synthesis and cytotoxic activities of 6-chloro-7-arylamino-5,8-isoquinolinediones.
pubmed:affiliation	College of Pharmacy, Ewha Womans University, Seodaemunku, Seoul, Korea.
pubmed:publicationType	Journal Article, Research Support, Non-U.S. Gov't