92445-90-4Relevant academic research and scientific papers
COMPOUNDS (CYSTEIN BASED LIPOPEPTIDES) AND COMPOSITIONS AS TLR2 AGONISTS USED FOR TREATING INFECTIONS, INFLAMMATIONS, RESPIRATORY DISEASES ETC.
-
, (2011/10/13)
The invention provides a novel class of compounds viz. generally lipopeptides like Pam3CSK4, immunogenic compositions and pharmaceutical compositions comprising such compounds and methods of using such compounds to treat or prevent diseases or disorders associated with Toll-Like Receptors 2. In one aspect, the compounds are useful as adjuvants for enhancing the effectiveness a vaccine.
Synthesis and antitumor activity of ether glycero-phospholipids bearing a carbamate moiety at the sn-2 position: Selective sensitivity against prostate cancer cell lines
Byun, Hoe-Sup,Bittman, Robert,Samadder, Pranati,Arthur, Gilbert
experimental part, p. 1045 - 1052 (2011/02/21)
Analogues of 1-O-hexadecyl-sn-3-glycerophosphonocholine (compounds 1-4) or sn-3-glycerophosphocholine (compound 5) bearing a carbamate or dicarbamate moiety at the sn-2 position were synthesized and evaluated for their antiproliferative activity against c
SYNTHESIS OF GLYCEROLIPID CARBAMATES AND DICARBAMATES AND THEIR USE AS ANTITUMOR COMPOUNDS
-
Page/Page column 18-19, (2008/06/13)
The syntheses and in vitro antitumor properties of carbamate-containing, dicarbamate-containing, and ureido-containing phospholipid compounds that have an ether linkage at the C-1 position of a glycerol backbone, a carbamate, dicarbamate, or ureido moiety
Self-organizing properties of natural and related synthetic glycolipids
Dumoulin, Fabienne,Lafont, Dominique,Boullanger, Paul,Mackenzie, Grahame,Mehl, Georg H.,Goodby, John W.
, p. 13737 - 13748 (2007/10/03)
In this article we report on the syntheses, self-organizing properties, and structures of a variety of cerebrosides and related synthetic glycolipids. The thermotropic and lyotropic liquid crystalline properties of the materials were evaluated in detail. All of the families of materials studied exhibited columnar mesophases. In the dry state the aliphatic chains were found to be located on the exterior of the columns, whereas in the wet state the reverse was the case with the polar headgroups on the exterior. Thus, the aliphatic chains act almost like hydrocarbon solvents in the dry state.
