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pubmed-article:10999256pubmed:abstractTextAmphiphilic complementary nucleobase derivatives, containing n-octadecyloxymethyl substituents at the N1 position of pyrimidine and N9 of purine, dissolved in chloroform form non-specific lyotropic mesophases, which were analyzed by optical polarizing microscopy. Molecular modeling studies visualize hypothetical horizontal and vertical nucleobase hydrogen-bonding and stacking arrangements, as well as aliphatic long-chain interstrand interaction.lld:pubmed
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pubmed-article:10999256pubmed:authorpubmed-author:HoffmannSSlld:pubmed
pubmed-article:10999256pubmed:authorpubmed-author:MeisterW VWVlld:pubmed
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pubmed-article:10999256pubmed:pagination1185-91lld:pubmed
pubmed-article:10999256pubmed:dateRevised2006-11-15lld:pubmed
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pubmed-article:10999256pubmed:year2000lld:pubmed
pubmed-article:10999256pubmed:articleTitleSelf-assembly and lyomesophases formed by long-chain alkoxymethyl-nucleobase derivatives.lld:pubmed
pubmed-article:10999256pubmed:affiliationMartin Luther University Halle-Wittenberg, Institute of Biochemistry, Halle, Saale, Germany. meister@biochemtech.uni-halle.delld:pubmed
pubmed-article:10999256pubmed:publicationTypeJournal Articlelld:pubmed
pubmed-article:10999256pubmed:publicationTypeResearch Support, Non-U.S. Gov'tlld:pubmed