| pubmed-article:17020289 | rdf:type | pubmed:Citation | lld:pubmed |
| pubmed-article:17020289 | lifeskim:mentions | umls-concept:C0002068 | lld:lifeskim |
| pubmed-article:17020289 | lifeskim:mentions | umls-concept:C0012512 | lld:lifeskim |
| pubmed-article:17020289 | lifeskim:mentions | umls-concept:C0086860 | lld:lifeskim |
| pubmed-article:17020289 | lifeskim:mentions | umls-concept:C0018164 | lld:lifeskim |
| pubmed-article:17020289 | pubmed:issue | 21 | lld:pubmed |
| pubmed-article:17020289 | pubmed:dateCreated | 2006-10-5 | lld:pubmed |
| pubmed-article:17020289 | pubmed:abstractText | [reaction: see text] A concise synthesis of a gramicidin S analogue with trisubstituted (E)-alkene dipeptide isostere (TEADI) replacements at both d-Phe-Pro positions was realized. Conformational analysis demonstrated that TEADIs can serve as type II beta-turn promoters in a cyclic scaffold and successfully mimic a proline residue. | lld:pubmed |
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| pubmed-article:17020289 | pubmed:language | eng | lld:pubmed |
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| pubmed-article:17020289 | pubmed:citationSubset | IM | lld:pubmed |
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| pubmed-article:17020289 | pubmed:status | MEDLINE | lld:pubmed |
| pubmed-article:17020289 | pubmed:month | Oct | lld:pubmed |
| pubmed-article:17020289 | pubmed:issn | 1523-7060 | lld:pubmed |
| pubmed-article:17020289 | pubmed:author | pubmed-author:WipfPeterP | lld:pubmed |
| pubmed-article:17020289 | pubmed:author | pubmed-author:WeisblumBerna... | lld:pubmed |
| pubmed-article:17020289 | pubmed:author | pubmed-author:XiaoJingboJ | lld:pubmed |
| pubmed-article:17020289 | pubmed:issnType | Print | lld:pubmed |
| pubmed-article:17020289 | pubmed:day | 12 | lld:pubmed |
| pubmed-article:17020289 | pubmed:volume | 8 | lld:pubmed |
| pubmed-article:17020289 | pubmed:owner | NLM | lld:pubmed |
| pubmed-article:17020289 | pubmed:authorsComplete | Y | lld:pubmed |
| pubmed-article:17020289 | pubmed:pagination | 4731-4 | lld:pubmed |
| pubmed-article:17020289 | pubmed:dateRevised | 2010-9-16 | lld:pubmed |
| pubmed-article:17020289 | pubmed:meshHeading | pubmed-meshheading:17020289... | lld:pubmed |
| pubmed-article:17020289 | pubmed:meshHeading | pubmed-meshheading:17020289... | lld:pubmed |
| pubmed-article:17020289 | pubmed:meshHeading | pubmed-meshheading:17020289... | lld:pubmed |
| pubmed-article:17020289 | pubmed:meshHeading | pubmed-meshheading:17020289... | lld:pubmed |
| pubmed-article:17020289 | pubmed:meshHeading | pubmed-meshheading:17020289... | lld:pubmed |
| pubmed-article:17020289 | pubmed:meshHeading | pubmed-meshheading:17020289... | lld:pubmed |
| pubmed-article:17020289 | pubmed:meshHeading | pubmed-meshheading:17020289... | lld:pubmed |
| pubmed-article:17020289 | pubmed:meshHeading | pubmed-meshheading:17020289... | lld:pubmed |
| pubmed-article:17020289 | pubmed:meshHeading | pubmed-meshheading:17020289... | lld:pubmed |
| pubmed-article:17020289 | pubmed:year | 2006 | lld:pubmed |
| pubmed-article:17020289 | pubmed:articleTitle | Trisubstituted (E)-alkene dipeptide isosteres as beta-turn promoters in the gramicidin S cyclodecapeptide scaffold. | lld:pubmed |
| pubmed-article:17020289 | pubmed:affiliation | Department of Chemistry and Center for Chemical Methodologies & Library Development, University of Pittsburgh, Pittsburgh, Pennsylvania 15260, USA. | lld:pubmed |
| pubmed-article:17020289 | pubmed:publicationType | Journal Article | lld:pubmed |
| pubmed-article:17020289 | pubmed:publicationType | Research Support, Non-U.S. Gov't | lld:pubmed |
| pubmed-article:17020289 | pubmed:publicationType | Research Support, N.I.H., Extramural | lld:pubmed |
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