Statements in which the resource exists as a subject.
PredicateObject
rdf:type
lifeskim:mentions
pubmed:issue
9
pubmed:dateCreated
2001-9-28
pubmed:abstractText
Artemisinic acid (2) was modified through allylic oxidation at C-3 or conjugate addition at C-13 to afford 12 methyl artemisinate derivatives (4-15). Photooxidation of the derivatives yielded eight new artemisinin analogues, including 13-cyanoartemisinin (16), 13-methoxycarbonyl artemisinin (17), 13-methoxyartemisinin (18), 13-ethylsulfonylartemisinin (19), 13-nitromethylartemisinin (20), 13-(1-nitroethyl)artemisinin (21), (3R)-3-hydroxyartemisinin (22), and (3R)-3-acetoxyartemisinin (23). Among the analogues, only compound 20 had antimalarial activity comparable to artemisinin (1).
pubmed:language
eng
pubmed:journal
pubmed:citationSubset
IM
pubmed:chemical
pubmed:status
MEDLINE
pubmed:month
Sep
pubmed:issn
0163-3864
pubmed:author
pubmed:issnType
Print
pubmed:volume
64
pubmed:owner
NLM
pubmed:authorsComplete
Y
pubmed:pagination
1201-5
pubmed:dateRevised
2006-11-15
pubmed:meshHeading
pubmed-meshheading:11575956-Animals, pubmed-meshheading:11575956-Antimalarials, pubmed-meshheading:11575956-Artemisinins, pubmed-meshheading:11575956-Chloroquine, pubmed-meshheading:11575956-Chromatography, Thin Layer, pubmed-meshheading:11575956-Drug Resistance, Microbial, pubmed-meshheading:11575956-Drugs, Chinese Herbal, pubmed-meshheading:11575956-Gas Chromatography-Mass Spectrometry, pubmed-meshheading:11575956-Humans, pubmed-meshheading:11575956-KB Cells, pubmed-meshheading:11575956-Magnetic Resonance Spectroscopy, pubmed-meshheading:11575956-Molecular Structure, pubmed-meshheading:11575956-Plasmodium falciparum, pubmed-meshheading:11575956-Sesquiterpenes, pubmed-meshheading:11575956-Spectrophotometry, Infrared, pubmed-meshheading:11575956-Spectroscopy, Fourier Transform Infrared, pubmed-meshheading:11575956-Stereoisomerism, pubmed-meshheading:11575956-Structure-Activity Relationship
pubmed:year
2001
pubmed:articleTitle
Synthesis of new artemisinin analogues from artemisinic acid modified at C-3 and C-13 and their antimalarial activity.
pubmed:affiliation
Graduate School of Agricultural Biotechnology, Seoul National University, Suwon 441-744, Korea.
pubmed:publicationType
Journal Article, Comparative Study, In Vitro, Research Support, Non-U.S. Gov't