Please use this identifier to cite or link to this item:
https://doi.org/10.3390/md15120352
DC Field | Value | |
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dc.title | Liposomal circular dichroism (L-Cd) of arenoyl derivatives of sphingolipids. Amplification of cotton effects in ordered lipid bilayers | |
dc.contributor.author | Molinski, T.F | |
dc.contributor.author | Broaddus, C.D | |
dc.contributor.author | Morinaka, B.I | |
dc.date.accessioned | 2020-10-27T10:17:50Z | |
dc.date.available | 2020-10-27T10:17:50Z | |
dc.date.issued | 2017 | |
dc.identifier.citation | Molinski, T.F, Broaddus, C.D, Morinaka, B.I (2017). Liposomal circular dichroism (L-Cd) of arenoyl derivatives of sphingolipids. Amplification of cotton effects in ordered lipid bilayers. Marine Drugs 15 (12) : 352. ScholarBank@NUS Repository. https://doi.org/10.3390/md15120352 | |
dc.identifier.issn | 16603397 | |
dc.identifier.uri | https://scholarbank.nus.edu.sg/handle/10635/181233 | |
dc.description.abstract | Liposomal circular dichroism (L-CD) of acyclic amino alcohols exhibit amplification of Cotton effects when measured in highly uniform, unilamellar liposomes. The effect is likely due to intermolecular associations—H-aggregates—that self-assemble spontaneously within the lipid bilayer, and persists over long time scales. L-CD spectra of N,O,O-tri-(6′methoxy-2′naphthoyl)-D-erythro-sphingosine, or the corresponding dihydro-derivative (sphinganine), shows ~10-fold amplification of magnitudes of Cotton effects over conventional CD spectra recorded in isotropic solution. © 2017 by the authors. | |
dc.rights | Attribution 4.0 International | |
dc.rights.uri | http://creativecommons.org/licenses/by/4.0/ | |
dc.source | Unpaywall 20201031 | |
dc.subject | aminoalcohol | |
dc.subject | arenoyl derivative | |
dc.subject | liposome | |
dc.subject | n, O,O' tri (6' methoxy 2' naphthoyl) dextro erythro sphingosine | |
dc.subject | sphinganine | |
dc.subject | sphingolipid | |
dc.subject | sphingosine | |
dc.subject | unclassified drug | |
dc.subject | carboxylic acid | |
dc.subject | liposome | |
dc.subject | sphingolipid | |
dc.subject | Article | |
dc.subject | chemical analysis | |
dc.subject | chemical structure | |
dc.subject | circular dichroism | |
dc.subject | lipid bilayer | |
dc.subject | molecular interaction | |
dc.subject | synthesis | |
dc.subject | analogs and derivatives | |
dc.subject | chemistry | |
dc.subject | circular dichroism | |
dc.subject | lipid bilayer | |
dc.subject | procedures | |
dc.subject | stereoisomerism | |
dc.subject | Acids, Acyclic | |
dc.subject | Circular Dichroism | |
dc.subject | Lipid Bilayers | |
dc.subject | Liposomes | |
dc.subject | Sphingolipids | |
dc.subject | Sphingosine | |
dc.subject | Stereoisomerism | |
dc.type | Article | |
dc.contributor.department | PHARMACY | |
dc.description.doi | 10.3390/md15120352 | |
dc.description.sourcetitle | Marine Drugs | |
dc.description.volume | 15 | |
dc.description.issue | 12 | |
dc.description.page | 352 | |
Appears in Collections: | Elements Staff Publications |
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