10843207

Source:http://linkedlifedata.com/resource/pubmed/id/10843207

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Predicate	Object
rdf:type	pubmed:Citation
lifeskim:mentions	umls-concept:C0220781, umls-concept:C0243071, umls-concept:C0334227, umls-concept:C0441655, umls-concept:C0960969, umls-concept:C1511636, umls-concept:C1883254
pubmed:issue	10
pubmed:dateCreated	2000-10-2
pubmed:abstractText	Clausemine-A (3), isolated from the stem and root bark of Clausena excavata, was synthesized using Suzuki cross-coupling and Oxidative coupling as the key step. Compound 3, and the other two structurally related biscarbazoles 1 and 2, showed potent cytotoxic activities against a variety of human cancer cell lines in vitro.
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/Carbazoles
pubmed:status	MEDLINE
pubmed:month	May
pubmed:issn	0960-894X
pubmed:author	pubmed-author:LiuNN, pubmed-author:ZhangAA
pubmed:issnType	Print
pubmed:day	15
pubmed:volume	10
pubmed:owner	NLM
pubmed:authorsComplete	Y
pubmed:pagination	1021-3
pubmed:dateRevised	2006-11-15
pubmed:meshHeading	pubmed-meshheading:10843207-Antineoplastic Agents, pubmed-meshheading:10843207-Carbazoles, pubmed-meshheading:10843207-Drug Screening Assays, Antitumor, pubmed-meshheading:10843207-Humans, pubmed-meshheading:10843207-Tumor Cells, Cultured
pubmed:year	2000
pubmed:articleTitle	The first synthesis of clausenamine-A and cytotoxic activities of three biscarbazole analogues against cancer cells.
pubmed:affiliation	Shanghai Institute of Organic Chemistry, Chinese Academy of Sciences.
pubmed:publicationType	Journal Article, Research Support, Non-U.S. Gov't