| pubmed-article:17239591 | rdf:type | pubmed:Citation | lld:pubmed |
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| pubmed-article:17239591 | lifeskim:mentions | umls-concept:C1999216 | lld:lifeskim |
| pubmed-article:17239591 | lifeskim:mentions | umls-concept:C1883254 | lld:lifeskim |
| pubmed-article:17239591 | lifeskim:mentions | umls-concept:C0243071 | lld:lifeskim |
| pubmed-article:17239591 | lifeskim:mentions | umls-concept:C0205250 | lld:lifeskim |
| pubmed-article:17239591 | lifeskim:mentions | umls-concept:C0679622 | lld:lifeskim |
| pubmed-article:17239591 | lifeskim:mentions | umls-concept:C1707689 | lld:lifeskim |
| pubmed-article:17239591 | lifeskim:mentions | umls-concept:C0205314 | lld:lifeskim |
| pubmed-article:17239591 | lifeskim:mentions | umls-concept:C0205460 | lld:lifeskim |
| pubmed-article:17239591 | pubmed:issue | 6 | lld:pubmed |
| pubmed-article:17239591 | pubmed:dateCreated | 2007-2-23 | lld:pubmed |
| pubmed-article:17239591 | pubmed:abstractText | Novel analogues of the V-ATPase inhibitors archazolid A and B with modifications of the free hydroxyl groups and the side chain were designed by molecular modeling, synthesized by derivatization of the parent natural product and evaluated for V-ATPase inhibition and growth inhibition of murine connective tissue cells. | lld:pubmed |
| pubmed-article:17239591 | pubmed:language | eng | lld:pubmed |
| pubmed-article:17239591 | pubmed:journal | http://linkedlifedata.com/r... | lld:pubmed |
| pubmed-article:17239591 | pubmed:citationSubset | IM | lld:pubmed |
| pubmed-article:17239591 | pubmed:chemical | http://linkedlifedata.com/r... | lld:pubmed |
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| pubmed-article:17239591 | pubmed:status | MEDLINE | lld:pubmed |
| pubmed-article:17239591 | pubmed:month | Mar | lld:pubmed |
| pubmed-article:17239591 | pubmed:issn | 0960-894X | lld:pubmed |
| pubmed-article:17239591 | pubmed:author | pubmed-author:WieczorekHelm... | lld:pubmed |
| pubmed-article:17239591 | pubmed:author | pubmed-author:MencheDirkD | lld:pubmed |
| pubmed-article:17239591 | pubmed:author | pubmed-author:HussMarkusM | lld:pubmed |
| pubmed-article:17239591 | pubmed:author | pubmed-author:SasseFlorenzF | lld:pubmed |
| pubmed-article:17239591 | pubmed:author | pubmed-author:HassfeldJorma... | lld:pubmed |
| pubmed-article:17239591 | pubmed:issnType | Print | lld:pubmed |
| pubmed-article:17239591 | pubmed:day | 15 | lld:pubmed |
| pubmed-article:17239591 | pubmed:volume | 17 | lld:pubmed |
| pubmed-article:17239591 | pubmed:owner | NLM | lld:pubmed |
| pubmed-article:17239591 | pubmed:authorsComplete | Y | lld:pubmed |
| pubmed-article:17239591 | pubmed:pagination | 1732-5 | lld:pubmed |
| pubmed-article:17239591 | pubmed:dateRevised | 2008-1-16 | lld:pubmed |
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| pubmed-article:17239591 | pubmed:year | 2007 | lld:pubmed |
| pubmed-article:17239591 | pubmed:articleTitle | Design, synthesis, and biological evaluation of novel analogues of archazolid: a highly potent simplified V-ATPase inhibitor. | lld:pubmed |
| pubmed-article:17239591 | pubmed:affiliation | Helmholtz-Zentrum für Infektionsforschung GmbH, Medizinische Chemie, Inhoffenstrasse 7, 38124 Braunschweig, Germany. dirk.menche@heimholtz-hzi.de | lld:pubmed |
| pubmed-article:17239591 | pubmed:publicationType | Journal Article | lld:pubmed |
| pubmed-article:17239591 | pubmed:publicationType | Research Support, Non-U.S. Gov't | lld:pubmed |
| http://linkedlifedata.com/r... | http://linkedlifedata.com/r... | pubmed-article:17239591 | lld:chembl |
