55955-33-4Relevant academic research and scientific papers
N-Oxyamide-linked glycoglycerolipid coated AuNPs for receptor-targeting imaging and drug delivery
Chen, Na,Yu, Zhi-Hao,Zhou, Dan,Hu, Xi-Le,Zang, Yi,He, Xiao-Peng,Li, Jia,Xie, Juan
supporting information, p. 2284 - 2287 (2016/02/18)
The synthesis of a series of new N-oxyamide-linked glycoglycerolipids and their assembly with gold nanoparticles for receptor-targeting imaging and drug delivery are reported.
Synthesis and anti-herpes simplex viral activity of monoglycosyl diglycerides
Janwitayanuchit, Wicharn,Suwanborirux, Khanit,Patarapanich, Chamnan,Pummangura, Sunibhond,Lipipun, Vimolmas,Vilaivan, Tirayut
, p. 1253 - 1264 (2007/10/03)
Based on the discovery of antiviral β-galactosyl diglycerides from Clinacanthus nutans leaves, 19 monoglycosyl diglycerides were synthesized and examined for inhibitory effect on herpes simplex virus types 1 and 2 (HSV-1, HSV-2). A study of the structure-
Synthesis and mesogenic properties of glycosyl diacylglycerols.
von Minden,Morr,Milkereit,Heinz,Vill
, p. 55 - 80 (2007/10/03)
We synthesised glycosyl diacylglycerols bearing unsaturated or chiral methyl branched fatty acid chains. The thermotropism was measured with polarising microscopy and additionally the lyotropism with the contact preparation method. The synthesised compoun
CHEMOENZYMATIC SYNTHESIS OF 1-O-ACYL-3-O-(6'-O-ACYL-β-D-GALACTOPYRANOSYL)-SN-GLYCEROL
Morimoto, Takashi,Nagatsu, Akito,Murakami, Nobutoshi,Sakakibara, Jinsaku
, p. 6443 - 6450 (2007/10/02)
Convenient synthesis of 1-O-acyl-3-O-(6'-O-acyl-β-D-galactopyranosyl)sn-glycerol was studied.The lipase from Achromobacter sp. catalyzed acylation of 3-O-β-D-galactopyranosyl-sn-glycerol, which contains two primary hydroxyl functions, proceeded regioselectively to furnish 1-O-acyl-3-O-β-D-galactopyranosyl-sn-glycerol.
SYNTHESIS OF A TEICHOIC ACID FRAGMENT OF BACILLUS VAR. NIGER W.M. BY A PHOSPHOTRIESTER APPROACH
van Boeckel, C.A.A.,Visser, G. M.,Hermans, J.P.G.,van Boom, J.H.
, p. 4743 - 4746 (2007/10/02)
Three properly-protected derivatives, one non-terminal and two terminal units, of 3-O-(2,3,4,6-tetra-O-acetyl-β-D-glucopyranosyl)-sn-glycerol have been joined together by two interglyceridic phosphotriester linkages to afford, after removal of all pro
