| pubmed-article:15987143 | rdf:type | pubmed:Citation | lld:pubmed |
| pubmed-article:15987143 | lifeskim:mentions | umls-concept:C0030551 | lld:lifeskim |
| pubmed-article:15987143 | lifeskim:mentions | umls-concept:C0028128 | lld:lifeskim |
| pubmed-article:15987143 | lifeskim:mentions | umls-concept:C0011957 | lld:lifeskim |
| pubmed-article:15987143 | lifeskim:mentions | umls-concept:C1708715 | lld:lifeskim |
| pubmed-article:15987143 | lifeskim:mentions | umls-concept:C2346689 | lld:lifeskim |
| pubmed-article:15987143 | lifeskim:mentions | umls-concept:C2349975 | lld:lifeskim |
| pubmed-article:15987143 | pubmed:issue | 14 | lld:pubmed |
| pubmed-article:15987143 | pubmed:dateCreated | 2005-6-30 | lld:pubmed |
| pubmed-article:15987143 | pubmed:abstractText | [reaction: see text] The synthesis and characterization of a series of symmetric bis-dialkyldiamine-based diazeniumdiolates, RN[N(O)NO(-)Na(+)](CH(2))(x)()N[N(O)NO(-)Na(+)]R', are reported. Preparation of corresponding intramolecular diazeniumdiolates of the form RN[N(O)NO](-)(CH(2))(x)()NH(2)(+)R' with alkyl groups > (CH(2))(4)CH(3) have been shown previously to lack stability. In contrast, sodium-stabilized bis-diazeniumdiolates of such lipophilic species can be readily formed when these same diamines are reacted with NO in basic media. The resulting compounds release 4 mol of NO per mole of original diamine. This approach enables the synthesis of more lipophilic NO donors than previously possible. | lld:pubmed |
| pubmed-article:15987143 | pubmed:grant | http://linkedlifedata.com/r... | lld:pubmed |
| pubmed-article:15987143 | pubmed:language | eng | lld:pubmed |
| pubmed-article:15987143 | pubmed:journal | http://linkedlifedata.com/r... | lld:pubmed |
| pubmed-article:15987143 | pubmed:citationSubset | IM | lld:pubmed |
| pubmed-article:15987143 | pubmed:chemical | http://linkedlifedata.com/r... | lld:pubmed |
| pubmed-article:15987143 | pubmed:chemical | http://linkedlifedata.com/r... | lld:pubmed |
| pubmed-article:15987143 | pubmed:chemical | http://linkedlifedata.com/r... | lld:pubmed |
| pubmed-article:15987143 | pubmed:chemical | http://linkedlifedata.com/r... | lld:pubmed |
| pubmed-article:15987143 | pubmed:chemical | http://linkedlifedata.com/r... | lld:pubmed |
| pubmed-article:15987143 | pubmed:status | MEDLINE | lld:pubmed |
| pubmed-article:15987143 | pubmed:month | Jul | lld:pubmed |
| pubmed-article:15987143 | pubmed:issn | 1523-7060 | lld:pubmed |
| pubmed-article:15987143 | pubmed:author | pubmed-author:MeyerhoffMark... | lld:pubmed |
| pubmed-article:15987143 | pubmed:author | pubmed-author:ReynoldsMelis... | lld:pubmed |
| pubmed-article:15987143 | pubmed:author | pubmed-author:ZhouZhengrong... | lld:pubmed |
| pubmed-article:15987143 | pubmed:author | pubmed-author:OhBong KBK | lld:pubmed |
| pubmed-article:15987143 | pubmed:issnType | Print | lld:pubmed |
| pubmed-article:15987143 | pubmed:day | 7 | lld:pubmed |
| pubmed-article:15987143 | pubmed:volume | 7 | lld:pubmed |
| pubmed-article:15987143 | pubmed:owner | NLM | lld:pubmed |
| pubmed-article:15987143 | pubmed:authorsComplete | Y | lld:pubmed |
| pubmed-article:15987143 | pubmed:pagination | 2813-6 | lld:pubmed |
| pubmed-article:15987143 | pubmed:dateRevised | 2007-11-14 | lld:pubmed |
| pubmed-article:15987143 | pubmed:meshHeading | pubmed-meshheading:15987143... | lld:pubmed |
| pubmed-article:15987143 | pubmed:meshHeading | pubmed-meshheading:15987143... | lld:pubmed |
| pubmed-article:15987143 | pubmed:meshHeading | pubmed-meshheading:15987143... | lld:pubmed |
| pubmed-article:15987143 | pubmed:meshHeading | pubmed-meshheading:15987143... | lld:pubmed |
| pubmed-article:15987143 | pubmed:meshHeading | pubmed-meshheading:15987143... | lld:pubmed |
| pubmed-article:15987143 | pubmed:meshHeading | pubmed-meshheading:15987143... | lld:pubmed |
| pubmed-article:15987143 | pubmed:meshHeading | pubmed-meshheading:15987143... | lld:pubmed |
| pubmed-article:15987143 | pubmed:year | 2005 | lld:pubmed |
| pubmed-article:15987143 | pubmed:articleTitle | Bis-diazeniumdiolates of dialkyldiamines: enhanced nitric oxide loading of parent diamines. | lld:pubmed |
| pubmed-article:15987143 | pubmed:affiliation | The University of Michigan, Department of Chemistry, Ann Arbor, Michigan 48109-1055, USA. | lld:pubmed |
| pubmed-article:15987143 | pubmed:publicationType | Journal Article | lld:pubmed |
| pubmed-article:15987143 | pubmed:publicationType | Research Support, U.S. Gov't, P.H.S. | lld:pubmed |
| pubmed-article:15987143 | pubmed:publicationType | Research Support, N.I.H., Extramural | lld:pubmed |
| http://linkedlifedata.com/r... | pubmed:referesTo | pubmed-article:15987143 | lld:pubmed |
