Statements in which the resource exists as a subject.
PredicateObject
rdf:type
lifeskim:mentions
pubmed:issue
6
pubmed:dateCreated
2002-6-28
pubmed:abstractText
Six new styrylpyrone derivatives, goniolactones A-F (1-6), have been isolated from the roots of Goniothalamus cheliensis. The structures and stereochemistry of the new compounds were elucidated by interpretation of spectroscopic data and chemical methods. The relative configuration of goniolactone A (1) was determined by X-ray crystallography analysis, and the absolute configurations of goniolactones A (1) and B (2) were established by Mosher's method. Goniolactone B (2) exhibited significant cytotoxicity against A2780, HCT-8, and KB cells with IC(50) values of 7.40, 4.43, and 7.23 microM, respectively.
pubmed:language
eng
pubmed:journal
pubmed:citationSubset
IM
pubmed:chemical
pubmed:status
MEDLINE
pubmed:month
Jun
pubmed:issn
0163-3864
pubmed:author
pubmed:issnType
Print
pubmed:volume
65
pubmed:owner
NLM
pubmed:authorsComplete
Y
pubmed:pagination
835-41
pubmed:dateRevised
2006-11-15
pubmed:meshHeading
pubmed-meshheading:12088424-Annonaceae, pubmed-meshheading:12088424-Cell Line, pubmed-meshheading:12088424-Drug Screening Assays, Antitumor, pubmed-meshheading:12088424-Drugs, Chinese Herbal, pubmed-meshheading:12088424-Female, pubmed-meshheading:12088424-Humans, pubmed-meshheading:12088424-Inhibitory Concentration 50, pubmed-meshheading:12088424-Intestinal Mucosa, pubmed-meshheading:12088424-KB Cells, pubmed-meshheading:12088424-Molecular Conformation, pubmed-meshheading:12088424-Molecular Structure, pubmed-meshheading:12088424-Nuclear Magnetic Resonance, Biomolecular, pubmed-meshheading:12088424-Ovarian Neoplasms, pubmed-meshheading:12088424-Plant Roots, pubmed-meshheading:12088424-Plants, Medicinal, pubmed-meshheading:12088424-Pyrones, pubmed-meshheading:12088424-Stereoisomerism, pubmed-meshheading:12088424-Tumor Cells, Cultured
pubmed:year
2002
pubmed:articleTitle
Goniolactones A-F, six new styrylpyrone derivatives from the roots of Goniothalamus cheliensis.
pubmed:affiliation
Institute of Materia Medica, Chinese Academy of Medical Sciences and Peking Union Medical College, Beijing 100050, People's Republic of China.
pubmed:publicationType
Journal Article, Research Support, Non-U.S. Gov't