Glycosyl-nucleolipids as new bioinspired amphiphiles

dc.contributor.author	Latxague, Laurent
dc.contributor.author	Patwa, Amit
dc.contributor.author	Amigues, Eric
dc.contributor.author	Barthélémy, Philippe
dc.date.accessioned	2019-06-13T07:40:02Z
dc.date.available	2019-06-13T07:40:02Z
dc.date.issued	2013-09-30
dc.identifier.issn	1420-3049 (P-ISSN)
dc.identifier.uri	http://27.109.7.66:8080/xmlui/handle/123456789/578
dc.description	Molecules, Vol-18, Issue-10, 2013, p. 12241-12263	en_US
dc.description.abstract	Four new Glycosyl-NucleoLipid (GNL) analogs featuring either a single fluorocarbon or double hydrocarbon chains were synthesized in good yields from azido thymidine as starting material. Physicochemical studies (surface tension measurements, differential scanning calorimetry) indicate that hydroxybutanamide-based GNLs feature endothermic phase transition temperatures like the previously reported double chain glycerol-based GNLs. The second generation of GNFs featuring a free nucleobase reported here presents a better surface activity (lower lim) compared to the first generation of GNFs.	en_US
dc.language.iso	en_US	en_US
dc.publisher	MDPI	en_US
dc.subject	Nucleolipid	en_US
dc.subject	Nucleoside	en_US
dc.subject	Glycosyl	en_US
dc.subject	Fluorocarbon	en_US
dc.subject	Amphiphiles	en_US
dc.subject	Surface tension	en_US
dc.title	Glycosyl-nucleolipids as new bioinspired amphiphiles	en_US
dc.type	Article	en_US