| pubmed-article:497363 | rdf:type | pubmed:Citation | lld:pubmed |
| pubmed-article:497363 | lifeskim:mentions | umls-concept:C0020792 | lld:lifeskim |
| pubmed-article:497363 | lifeskim:mentions | umls-concept:C0683140 | lld:lifeskim |
| pubmed-article:497363 | lifeskim:mentions | umls-concept:C0009030 | lld:lifeskim |
| pubmed-article:497363 | lifeskim:mentions | umls-concept:C0022023 | lld:lifeskim |
| pubmed-article:497363 | lifeskim:mentions | umls-concept:C0033568 | lld:lifeskim |
| pubmed-article:497363 | lifeskim:mentions | umls-concept:C0439962 | lld:lifeskim |
| pubmed-article:497363 | lifeskim:mentions | umls-concept:C1704332 | lld:lifeskim |
| pubmed-article:497363 | lifeskim:mentions | umls-concept:C0870883 | lld:lifeskim |
| pubmed-article:497363 | lifeskim:mentions | umls-concept:C0376315 | lld:lifeskim |
| pubmed-article:497363 | lifeskim:mentions | umls-concept:C0449851 | lld:lifeskim |
| pubmed-article:497363 | lifeskim:mentions | umls-concept:C1524063 | lld:lifeskim |
| pubmed-article:497363 | lifeskim:mentions | umls-concept:C1707959 | lld:lifeskim |
| pubmed-article:497363 | lifeskim:mentions | umls-concept:C0701898 | lld:lifeskim |
| pubmed-article:497363 | pubmed:issue | 8 | lld:pubmed |
| pubmed-article:497363 | pubmed:dateCreated | 1980-1-28 | lld:pubmed |
| pubmed-article:497363 | pubmed:abstractText | The synthetic prostaglandin analogue cloprostenol has been prepared radiolabelled with 14C. The isotopic abundance of 14C at position C-15 was greater than 90% of the theoretical maximum. We have utilizted the high abundance of the 14C isotope for metabolism studies by preparing mixtures of [12C]:[14C]cloprostenol such that fragments detected by mass spectrometry contained characteristic isotope clusters analogous to those often obtained using stable isotopes. | lld:pubmed |
| pubmed-article:497363 | pubmed:language | eng | lld:pubmed |
| pubmed-article:497363 | pubmed:journal | http://linkedlifedata.com/r... | lld:pubmed |
| pubmed-article:497363 | pubmed:citationSubset | IM | lld:pubmed |
| pubmed-article:497363 | pubmed:chemical | http://linkedlifedata.com/r... | lld:pubmed |
| pubmed-article:497363 | pubmed:chemical | http://linkedlifedata.com/r... | lld:pubmed |
| pubmed-article:497363 | pubmed:chemical | http://linkedlifedata.com/r... | lld:pubmed |
| pubmed-article:497363 | pubmed:chemical | http://linkedlifedata.com/r... | lld:pubmed |
| pubmed-article:497363 | pubmed:status | MEDLINE | lld:pubmed |
| pubmed-article:497363 | pubmed:month | Aug | lld:pubmed |
| pubmed-article:497363 | pubmed:issn | 0306-042X | lld:pubmed |
| pubmed-article:497363 | pubmed:author | pubmed-author:BourneG RGR | lld:pubmed |
| pubmed-article:497363 | pubmed:author | pubmed-author:MossS RSR | lld:pubmed |
| pubmed-article:497363 | pubmed:author | pubmed-author:PhillipsP JPJ | lld:pubmed |
| pubmed-article:497363 | pubmed:author | pubmed-author:WhiteD FDF | lld:pubmed |
| pubmed-article:497363 | pubmed:author | pubmed-author:WebsterJ TJT | lld:pubmed |
| pubmed-article:497363 | pubmed:issnType | Print | lld:pubmed |
| pubmed-article:497363 | pubmed:volume | 6 | lld:pubmed |
| pubmed-article:497363 | pubmed:owner | NLM | lld:pubmed |
| pubmed-article:497363 | pubmed:authorsComplete | Y | lld:pubmed |
| pubmed-article:497363 | pubmed:pagination | 359-60 | lld:pubmed |
| pubmed-article:497363 | pubmed:dateRevised | 2006-11-15 | lld:pubmed |
| pubmed-article:497363 | pubmed:meshHeading | pubmed-meshheading:497363-A... | lld:pubmed |
| pubmed-article:497363 | pubmed:meshHeading | pubmed-meshheading:497363-R... | lld:pubmed |
| pubmed-article:497363 | pubmed:meshHeading | pubmed-meshheading:497363-F... | lld:pubmed |
| pubmed-article:497363 | pubmed:meshHeading | pubmed-meshheading:497363-C... | lld:pubmed |
| pubmed-article:497363 | pubmed:meshHeading | pubmed-meshheading:497363-T... | lld:pubmed |
| pubmed-article:497363 | pubmed:meshHeading | pubmed-meshheading:497363-M... | lld:pubmed |
| pubmed-article:497363 | pubmed:meshHeading | pubmed-meshheading:497363-T... | lld:pubmed |
| pubmed-article:497363 | pubmed:meshHeading | pubmed-meshheading:497363-P... | lld:pubmed |
| pubmed-article:497363 | pubmed:meshHeading | pubmed-meshheading:497363-C... | lld:pubmed |
| pubmed-article:497363 | pubmed:year | 1979 | lld:pubmed |
| pubmed-article:497363 | pubmed:articleTitle | Ion cluster techniques in drug metabolism: an example of the use of mixtures of the [12C]:[14C] isotopic forms of the synthetic prostaglandin cloprostenol ('Estrumate') to facilitate metabolite identification. | lld:pubmed |
| pubmed-article:497363 | pubmed:publicationType | Journal Article | lld:pubmed |
