| pubmed-article:1761417 | rdf:type | pubmed:Citation | lld:pubmed |
| pubmed-article:1761417 | lifeskim:mentions | umls-concept:C0004927 | lld:lifeskim |
| pubmed-article:1761417 | lifeskim:mentions | umls-concept:C0376525 | lld:lifeskim |
| pubmed-article:1761417 | lifeskim:mentions | umls-concept:C0024485 | lld:lifeskim |
| pubmed-article:1761417 | lifeskim:mentions | umls-concept:C2603343 | lld:lifeskim |
| pubmed-article:1761417 | lifeskim:mentions | umls-concept:C1516050 | lld:lifeskim |
| pubmed-article:1761417 | lifeskim:mentions | umls-concept:C0050496 | lld:lifeskim |
| pubmed-article:1761417 | lifeskim:mentions | umls-concept:C0059508 | lld:lifeskim |
| pubmed-article:1761417 | lifeskim:mentions | umls-concept:C0243072 | lld:lifeskim |
| pubmed-article:1761417 | pubmed:issue | 11 | lld:pubmed |
| pubmed-article:1761417 | pubmed:dateCreated | 1992-2-11 | lld:pubmed |
| pubmed-article:1761417 | pubmed:abstractText | Complete 1H and 13C NMR assignments are presented for eremomycin (1) and some of its desglycosylated derivatives 2, 3 and compared to the structurally closely related glycopeptide vancomycin. Primary structure and stereochemistry of eremomycin is corroborated by the present high field total correlation spectroscopy, NOESY and heteronuclear multiple-bond correlation NMR methods. A rough motional characterization of the title compound is attempted by 13C-T1 and 13C-[1H] NOE measurements. Dimerization of eremomycin is observed both in DMSO-d6-CCl4 and D2O solutions. Complexation with cell wall analogue dipeptide Ac-D-Ala-D-Ala is also demonstrated. | lld:pubmed |
| pubmed-article:1761417 | pubmed:language | eng | lld:pubmed |
| pubmed-article:1761417 | pubmed:journal | http://linkedlifedata.com/r... | lld:pubmed |
| pubmed-article:1761417 | pubmed:citationSubset | IM | lld:pubmed |
| pubmed-article:1761417 | pubmed:chemical | http://linkedlifedata.com/r... | lld:pubmed |
| pubmed-article:1761417 | pubmed:chemical | http://linkedlifedata.com/r... | lld:pubmed |
| pubmed-article:1761417 | pubmed:chemical | http://linkedlifedata.com/r... | lld:pubmed |
| pubmed-article:1761417 | pubmed:chemical | http://linkedlifedata.com/r... | lld:pubmed |
| pubmed-article:1761417 | pubmed:status | MEDLINE | lld:pubmed |
| pubmed-article:1761417 | pubmed:month | Nov | lld:pubmed |
| pubmed-article:1761417 | pubmed:issn | 0021-8820 | lld:pubmed |
| pubmed-article:1761417 | pubmed:author | pubmed-author:BerdnikovaT... | lld:pubmed |
| pubmed-article:1761417 | pubmed:author | pubmed-author:SztaricskaiFF | lld:pubmed |
| pubmed-article:1761417 | pubmed:author | pubmed-author:BattaGG | lld:pubmed |
| pubmed-article:1761417 | pubmed:author | pubmed-author:RüdelCC | lld:pubmed |
| pubmed-article:1761417 | pubmed:author | pubmed-author:KövérK EKE | lld:pubmed |
| pubmed-article:1761417 | pubmed:issnType | Print | lld:pubmed |
| pubmed-article:1761417 | pubmed:volume | 44 | lld:pubmed |
| pubmed-article:1761417 | pubmed:owner | NLM | lld:pubmed |
| pubmed-article:1761417 | pubmed:authorsComplete | Y | lld:pubmed |
| pubmed-article:1761417 | pubmed:pagination | 1208-21 | lld:pubmed |
| pubmed-article:1761417 | pubmed:dateRevised | 2006-11-15 | lld:pubmed |
| pubmed-article:1761417 | pubmed:meshHeading | pubmed-meshheading:1761417-... | lld:pubmed |
| pubmed-article:1761417 | pubmed:meshHeading | pubmed-meshheading:1761417-... | lld:pubmed |
| pubmed-article:1761417 | pubmed:meshHeading | pubmed-meshheading:1761417-... | lld:pubmed |
| pubmed-article:1761417 | pubmed:meshHeading | pubmed-meshheading:1761417-... | lld:pubmed |
| pubmed-article:1761417 | pubmed:meshHeading | pubmed-meshheading:1761417-... | lld:pubmed |
| pubmed-article:1761417 | pubmed:meshHeading | pubmed-meshheading:1761417-... | lld:pubmed |
| pubmed-article:1761417 | pubmed:year | 1991 | lld:pubmed |
| pubmed-article:1761417 | pubmed:articleTitle | An NMR study of eremomycin and its derivatives. Full 1H and 13C assignment, motional behavior, dimerization and complexation with Ac-D-Ala-D-Ala. | lld:pubmed |
| pubmed-article:1761417 | pubmed:affiliation | Research Group for Antibiotics, Hungarian Academy of Sciences, Debrecen. | lld:pubmed |
| pubmed-article:1761417 | pubmed:publicationType | Journal Article | lld:pubmed |
| pubmed-article:1761417 | pubmed:publicationType | Comparative Study | lld:pubmed |
| pubmed-article:1761417 | pubmed:publicationType | Research Support, Non-U.S. Gov't | lld:pubmed |
