pubmed-article:14510365 | rdf:type | pubmed:Citation | lld:pubmed |
pubmed-article:14510365 | lifeskim:mentions | umls-concept:C0020205 | lld:lifeskim |
pubmed-article:14510365 | lifeskim:mentions | umls-concept:C0220781 | lld:lifeskim |
pubmed-article:14510365 | lifeskim:mentions | umls-concept:C1883254 | lld:lifeskim |
pubmed-article:14510365 | lifeskim:mentions | umls-concept:C0678594 | lld:lifeskim |
pubmed-article:14510365 | lifeskim:mentions | umls-concept:C2603343 | lld:lifeskim |
pubmed-article:14510365 | pubmed:issue | 3 | lld:pubmed |
pubmed-article:14510365 | pubmed:dateCreated | 2003-9-26 | lld:pubmed |
pubmed-article:14510365 | pubmed:abstractText | We have synthesized three types of calix[4]arene-nucleoside hybrids efficiently by amide bond formation between the amine functional groups of 1,3-diamino-calix[4]arene and the carboxyl groups of thymidine nucleoside derivatives. X-Ray crystallography of a homocoupled calix[4]arene-nucleoside hybrid revealed an interesting hydrogen bonding pattern between thymine bases and the amide linkages. We designed the calix[4]arene-oligonucleotide hybrids to be V-shaped oligodeoxyribonucleotides and synthesized them by using a calix[4]arene-nucleoside hybrid as a key building block. Thermal denaturation experiments, monitored by UV spectroscopy at 260 and 284 nm, and circular dichroism spectra of the calix[4]arene-oligonucleotide hybrids suggest that the modified oligonucleotides indeed adopt V-shaped conformations, making them suitable for use as building blocks in the construction of programmed oligonucleotide nanostructures. | lld:pubmed |
pubmed-article:14510365 | pubmed:language | eng | lld:pubmed |
pubmed-article:14510365 | pubmed:journal | http://linkedlifedata.com/r... | lld:pubmed |
pubmed-article:14510365 | pubmed:citationSubset | IM | lld:pubmed |
pubmed-article:14510365 | pubmed:chemical | http://linkedlifedata.com/r... | lld:pubmed |
pubmed-article:14510365 | pubmed:chemical | http://linkedlifedata.com/r... | lld:pubmed |
pubmed-article:14510365 | pubmed:chemical | http://linkedlifedata.com/r... | lld:pubmed |
pubmed-article:14510365 | pubmed:chemical | http://linkedlifedata.com/r... | lld:pubmed |
pubmed-article:14510365 | pubmed:chemical | http://linkedlifedata.com/r... | lld:pubmed |
pubmed-article:14510365 | pubmed:status | MEDLINE | lld:pubmed |
pubmed-article:14510365 | pubmed:author | pubmed-author:KimByeang... | lld:pubmed |
pubmed-article:14510365 | pubmed:author | pubmed-author:KimSu JeongSJ | lld:pubmed |
pubmed-article:14510365 | pubmed:author | pubmed-author:BangEun-Kyoun... | lld:pubmed |
pubmed-article:14510365 | pubmed:owner | NLM | lld:pubmed |
pubmed-article:14510365 | pubmed:authorsComplete | Y | lld:pubmed |
pubmed-article:14510365 | pubmed:pagination | 31-2 | lld:pubmed |
pubmed-article:14510365 | pubmed:dateRevised | 2006-11-30 | lld:pubmed |
pubmed-article:14510365 | pubmed:meshHeading | pubmed-meshheading:14510365... | lld:pubmed |
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pubmed-article:14510365 | pubmed:meshHeading | pubmed-meshheading:14510365... | lld:pubmed |
pubmed-article:14510365 | pubmed:meshHeading | pubmed-meshheading:14510365... | lld:pubmed |
pubmed-article:14510365 | pubmed:meshHeading | pubmed-meshheading:14510365... | lld:pubmed |
pubmed-article:14510365 | pubmed:meshHeading | pubmed-meshheading:14510365... | lld:pubmed |
pubmed-article:14510365 | pubmed:year | 2003 | lld:pubmed |
pubmed-article:14510365 | pubmed:articleTitle | Syntheses and structural studies of calix[4]arene-nucleoside and calix[4]arene-oligonucleotide hybrids. | lld:pubmed |
pubmed-article:14510365 | pubmed:affiliation | National Research Laboratory, Department of Chemistry, Division of Molecular and Life Sciences, Pohang University of Science and Technology, Pohang 790-784, Korea. | lld:pubmed |
pubmed-article:14510365 | pubmed:publicationType | Journal Article | lld:pubmed |
pubmed-article:14510365 | pubmed:publicationType | Research Support, Non-U.S. Gov't | lld:pubmed |