Matches in SemOpenAlex for { <https://semopenalex.org/work/W2022631293> ?p ?o ?g. }
- W2022631293 endingPage "12" @default.
- W2022631293 startingPage "1" @default.
- W2022631293 abstract "A series of racemic 16:0 disaturated N-substituted diether phosphonolipid analogs of glycerophospholipids have been synthesized and purified. Isosteric methylene substitution at three of the four ester sites (carboxyl, phosphate) of conventional glycerophospholipids enhanced the hydrophobicity of analog compounds compared with dipalmitoyl phosphatidylcholine (DPPC), the major glycerophospholipid component of lung surfactant. Further substitutions at the nitrogen headgroup also contributed to hydrophobicity/hydrophilicity characteristics, as well as allowing graded variations in headgroup size among the members of the diether phosphonolipid analog series. Interfacial property studies showed that these compounds had significant differences in surface activity characteristics compared with DPPC, including increased adsorption and respreading facility, plus an enhanced ability to generate low surface tension (less than 1 to 4 mN/m) on an oscillating bubble apparatus at 37 degrees C. In addition, pressure-volume mechanical studies in surfactant-deficient excised rat lungs showed that the diether phosphonate analog of DPPC could partially restore pressure-volume characteristics toward normal, both as a pure component and in binary mixtures with palmitoyl-oleoyl phosphatidylglycerol. These findings suggest that selected analog compounds, synthesized with relatively small structural modifications from biologic glycerophospholipids, may have eventual applications as components of synthetic exogenous lung surfactants. Of more immediate importance, analog molecules with defined structural variations are convenient molecular probes for developing structure-surface activity correlates for phospholipid-like surfactants and for investigating the specificity of interactions between glycerophospholipids and other compounds such as proteins." @default.
- W2022631293 created "2016-06-24" @default.
- W2022631293 creator A5008052979 @default.
- W2022631293 creator A5008325152 @default.
- W2022631293 creator A5015316695 @default.
- W2022631293 creator A5020672465 @default.
- W2022631293 creator A5037580907 @default.
- W2022631293 creator A5045715531 @default.
- W2022631293 creator A5054328852 @default.
- W2022631293 creator A5071826171 @default.
- W2022631293 date "1991-06-01" @default.
- W2022631293 modified "2023-09-26" @default.
- W2022631293 title "Chemical synthesis and surface activity of lung surfactant phospholipid analogs. II. Racemic N-substituted diether phospholipids" @default.
- W2022631293 cites W160000646 @default.
- W2022631293 cites W1917099971 @default.
- W2022631293 cites W1966184825 @default.
- W2022631293 cites W1970418468 @default.
- W2022631293 cites W1978468660 @default.
- W2022631293 cites W1985973395 @default.
- W2022631293 cites W1990550159 @default.
- W2022631293 cites W1998860125 @default.
- W2022631293 cites W2008280284 @default.
- W2022631293 cites W2012448047 @default.
- W2022631293 cites W2017069757 @default.
- W2022631293 cites W2017468295 @default.
- W2022631293 cites W2025219534 @default.
- W2022631293 cites W2032083637 @default.
- W2022631293 cites W2042467899 @default.
- W2022631293 cites W2061485665 @default.
- W2022631293 cites W2061595163 @default.
- W2022631293 cites W2074483025 @default.
- W2022631293 cites W2085938353 @default.
- W2022631293 cites W2135361385 @default.
- W2022631293 cites W2261863169 @default.
- W2022631293 cites W2324312308 @default.
- W2022631293 cites W2427625331 @default.
- W2022631293 cites W3024947858 @default.
- W2022631293 cites W4375199581 @default.
- W2022631293 doi "https://doi.org/10.1016/0005-2760(91)90048-m" @default.
- W2022631293 hasPubMedId "https://pubmed.ncbi.nlm.nih.gov/2054372" @default.
- W2022631293 hasPublicationYear "1991" @default.
- W2022631293 type Work @default.
- W2022631293 sameAs 2022631293 @default.
- W2022631293 citedByCount "23" @default.
- W2022631293 countsByYear W20226312932013 @default.
- W2022631293 countsByYear W20226312932014 @default.
- W2022631293 countsByYear W20226312932016 @default.
- W2022631293 countsByYear W20226312932021 @default.
- W2022631293 crossrefType "journal-article" @default.
- W2022631293 hasAuthorship W2022631293A5008052979 @default.
- W2022631293 hasAuthorship W2022631293A5008325152 @default.
- W2022631293 hasAuthorship W2022631293A5015316695 @default.
- W2022631293 hasAuthorship W2022631293A5020672465 @default.
- W2022631293 hasAuthorship W2022631293A5037580907 @default.
- W2022631293 hasAuthorship W2022631293A5045715531 @default.
- W2022631293 hasAuthorship W2022631293A5054328852 @default.
- W2022631293 hasAuthorship W2022631293A5071826171 @default.
- W2022631293 hasConcept C161790260 @default.
- W2022631293 hasConcept C178790620 @default.
- W2022631293 hasConcept C185592680 @default.
- W2022631293 hasConcept C2776330855 @default.
- W2022631293 hasConcept C2776952329 @default.
- W2022631293 hasConcept C2777454769 @default.
- W2022631293 hasConcept C2778918659 @default.
- W2022631293 hasConcept C2779191827 @default.
- W2022631293 hasConcept C2780726299 @default.
- W2022631293 hasConcept C2909522894 @default.
- W2022631293 hasConcept C41625074 @default.
- W2022631293 hasConcept C55493867 @default.
- W2022631293 hasConcept C58226133 @default.
- W2022631293 hasConcept C65165184 @default.
- W2022631293 hasConcept C71240020 @default.
- W2022631293 hasConceptScore W2022631293C161790260 @default.
- W2022631293 hasConceptScore W2022631293C178790620 @default.
- W2022631293 hasConceptScore W2022631293C185592680 @default.
- W2022631293 hasConceptScore W2022631293C2776330855 @default.
- W2022631293 hasConceptScore W2022631293C2776952329 @default.
- W2022631293 hasConceptScore W2022631293C2777454769 @default.
- W2022631293 hasConceptScore W2022631293C2778918659 @default.
- W2022631293 hasConceptScore W2022631293C2779191827 @default.
- W2022631293 hasConceptScore W2022631293C2780726299 @default.
- W2022631293 hasConceptScore W2022631293C2909522894 @default.
- W2022631293 hasConceptScore W2022631293C41625074 @default.
- W2022631293 hasConceptScore W2022631293C55493867 @default.
- W2022631293 hasConceptScore W2022631293C58226133 @default.
- W2022631293 hasConceptScore W2022631293C65165184 @default.
- W2022631293 hasConceptScore W2022631293C71240020 @default.
- W2022631293 hasIssue "1" @default.
- W2022631293 hasLocation W20226312931 @default.
- W2022631293 hasLocation W20226312932 @default.
- W2022631293 hasOpenAccess W2022631293 @default.
- W2022631293 hasPrimaryLocation W20226312931 @default.
- W2022631293 hasRelatedWork W2032169846 @default.
- W2022631293 hasRelatedWork W2054489835 @default.
- W2022631293 hasRelatedWork W2065024022 @default.
- W2022631293 hasRelatedWork W2089155826 @default.
- W2022631293 hasRelatedWork W2110122657 @default.
- W2022631293 hasRelatedWork W2164616370 @default.