Search results for "Amide"
showing 10 items of 3119 documents
Intestinal CD36. A lipid-sensor involved in the processing of chylomicrons in rodents
2011
International audience; CD36 is a multifunctional glycoprotein which binds nanomolar concentrations of long-chain fatty acids (LCFA) and is highly expressed on the luminal surface of enterocytes. Despite of its implication in oleoylethanolamide (OEA) and chylomicron synthesis, CD36 function in small intestine remains incompletely understood. Our in vivo data demonstrated that CD36 gene deletion in mice did not affect intestinal LCFA uptake. CD36 protein disappeared early from the luminal side of intestinal villi during the post-prandial period but only when the diet contained lipids. This drop was significant 1 h after a lipid supply and was associated with ubiquitination of CD36. Using CHO…
CCDC 1425258: Experimental Crystal Structure Determination
2016
Related Article: T. Mäkelä, K. Rissanen|2016|Dalton Trans.|45|6481|doi:10.1039/C6DT00414H
CCDC 656319: Experimental Crystal Structure Determination
2008
Related Article: F.Cuenot, M.Meyer, E.Espinosa, A.Bucaille, R.Burgat, R.Guilard, C.Marichal-Westrich|2008|Eur.J.Inorg.Chem.||267|doi:10.1002/ejic.200700819
CCDC 855065: Experimental Crystal Structure Determination
2013
Related Article: O.Plietzsch, A.Schade, A.Hafner, J.Huuskonen, K.Rissanen, M.Nieger, T.Muller, S.Brase|2013|Eur.J.Org.Chem.|2013|283|doi:10.1002/ejoc.201201162
Synthesis and stereochemical studies of 2-substituted thiazolidine-4-carboxamide derivatives
2000
A series of new 2-substituted thiazolidine-4-carboxamide derivatives which have potentially useful immunological properties, have been synthesized in a stereoselective manner by coupling 2-subsituted thiazolidine-4-carboxylic acids with amines or amino esters. The structure of these compounds was established by combination of NMR methods and by X-ray analysis.
CCDC 853880: Experimental Crystal Structure Determination
2012
Related Article: L.Kaufmann, E.V.Dzyuba, F.Malberg, N.L.Low, M.Groschke, B.Brusilowskij, J.Huuskonen, K.Rissanen, B.Kirchner, C.A.Schalley|2012|Org.Biomol.Chem.|10|5954|doi:10.1039/c2ob25196e
Physico-chemical investigation of the state of cyanamide confined in AOT and lecithin reversed micelles
2004
Sodium bis(2-ethylhexyl)sulfosuccinate (AOT) and lecithin reversed micelles containing cyanamide have been investigated by small-angle X-ray scattering, FT-IR, and 1H NMR spectroscopy at various cyanamide-to-surfactant molar ratio (X) and at fixed surfactant concentration (0.1 mol kg-1). Experimental data are consistent with a model of cyanamide molecules confined in reversed micelles, quite uniformly distributed among them and mainly located among surfactant headgroups. SAXS data analysis leads also to hypothesize a unidimensional growth of the reversed micelles with increasing the X value. Moreover, the cyanamide state and the cyanamide/cyanamide interactions in reversed micelles have bee…
CCDC 854391: Experimental Crystal Structure Determination
2012
Related Article: B.Os'mialowski, E.Kolehmainen, R.Dobosz, R.Gawinecki, R.Kauppinen, A.Valkonen, J.Koivukorpi, K.Rissanen|2010|J.Phys.Chem.A|114|10421|doi:10.1021/jp1063116
CCDC 1954699: Experimental Crystal Structure Determination
2019
Related Article: A. Aydin, S.T. Celikesir, M. Akkurt, M. Saylam, V. Pabuccuoglu|2019|Acta Crystallogr.,Sect.E:Cryst.Commun.|75|1531|doi:10.1107/S2056989019012908
2-cinnamamido, 2-(3-phenylpropiolamido) and 2-(3-phenylpropanamido)benzamides: synthesis, antiproliferative activity and mechanism of action
2013
Several new 2-cinnamamido, 2-(3-phenylpropiolamido) and 2-(3-phenylpropanamido)benzamides were synthesized by stirring in pyridine the opportune acid chlorides with the appropriate anthranilamide derivatives. Some of the synthesized compounds were evaluated for their in vitro antiproliferative activity against a panel of 5 human cell lines (K562 human chronic myelogenous leukemia cells, MCF-7 breast cancer cells, HTC-116 and HT26 colon cancer cells and NCI H460 non-small cell lung cancer cells).