Source:http://linkedlifedata.com/resource/pubmed/id/19228042
Switch to
Predicate | Object |
---|---|
rdf:type | |
lifeskim:mentions | |
pubmed:issue |
6
|
pubmed:dateCreated |
2009-3-13
|
pubmed:abstractText |
The first total synthesis of ipomoeassin F was carried out using a convergent approach that relied upon the use of Schmidt glycosidation technology for the coupling of two suitably protected monosaccharide fragments. After two steps, ring-closing metathesis was used to form the macrocyclic ring, and seven more steps then furnished ipomoeassin F. In vitro inhibitory activity against a four-panel cell line showed low nanomolar inhibitory activity.
|
pubmed:language |
eng
|
pubmed:journal | |
pubmed:citationSubset |
IM
|
pubmed:chemical | |
pubmed:status |
MEDLINE
|
pubmed:month |
Mar
|
pubmed:issn |
1523-7052
|
pubmed:author | |
pubmed:issnType |
Electronic
|
pubmed:day |
19
|
pubmed:volume |
11
|
pubmed:owner |
NLM
|
pubmed:authorsComplete |
Y
|
pubmed:pagination |
1417-20
|
pubmed:dateRevised |
2011-11-17
|
pubmed:meshHeading |
pubmed-meshheading:19228042-Antineoplastic Agents, Phytogenic,
pubmed-meshheading:19228042-Biological Agents,
pubmed-meshheading:19228042-Drug Screening Assays, Antitumor,
pubmed-meshheading:19228042-Glycoconjugates,
pubmed-meshheading:19228042-Glycosylation,
pubmed-meshheading:19228042-Humans,
pubmed-meshheading:19228042-Ipomoea,
pubmed-meshheading:19228042-Molecular Structure
|
pubmed:year |
2009
|
pubmed:articleTitle |
Total synthesis of ipomoeassin F.
|
pubmed:affiliation |
Department of Discovery Chemistry, Eisai Research Institute, 4 Corporate Drive, Andover, Massachusetts 01810, USA. maarten_postema@eri.eisai.com
|
pubmed:publicationType |
Journal Article
|