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1.
J Org Chem ; 81(6): 2364-71, 2016 Mar 18.
Artículo en Inglés | MEDLINE | ID: mdl-26926714

RESUMEN

A new strategy for the synthesis of acyl ß-C-glycosides is described. The reactivity of glyconitriles toward organometallic reagents such as organomagnesium or organolithium derivatives was studied, affording acyl ß-C-glycosides in moderate to good yields. In this study, glycal formation was efficiently prevented by deprotonating the hydroxyl group in position 2 of the glyconitriles during the process.

2.
J Med Chem ; 55(3): 1227-41, 2012 Feb 09.
Artículo en Inglés | MEDLINE | ID: mdl-22243602

RESUMEN

We propose here the synthesis and biological evaluation of 3,4-dideoxy-GalCer derivatives. The absence of the 3- and 4-hydroxyls on the sphingoid base is combined with the introduction of mono or difluoro substituent at C3 (analogues 8 and 9, respectively) to evaluate their effect on the stability of the ternary CD1d/GalCer/TCR complex which strongly modulate the immune responses. Biological evaluations were performed in vitro on human cells and in vivo in mice and results discussed with support of modeling studies. The fluoro 3,4-dideoxy-GalCer analogues appears as partial agonists compared to KRN7000 for iNKT cell activation, inducing T(H)1 or T(H)2 biases that strongly depend of the mode of antigen presentation, including human vs mouse differences. We evidenced that if a sole fluorine atom is not able to balance the loss of the 3-OH, the presence of a difluorine group at C3 of the sphingosine can significantly restore human iNKT activation.


Asunto(s)
Adyuvantes Inmunológicos/síntesis química , Galactosilceramidas/síntesis química , Células T Asesinas Naturales/efectos de los fármacos , Adyuvantes Inmunológicos/química , Adyuvantes Inmunológicos/farmacología , Animales , Células Presentadoras de Antígenos/efectos de los fármacos , Células Presentadoras de Antígenos/inmunología , Células Presentadoras de Antígenos/metabolismo , Antígenos CD1d/inmunología , Antígenos CD1d/metabolismo , Línea Celular , Femenino , Galactosilceramidas/química , Galactosilceramidas/inmunología , Galactosilceramidas/metabolismo , Galactosilceramidas/farmacología , Humanos , Enlace de Hidrógeno , Ratones , Ratones Endogámicos C57BL , Modelos Moleculares , Células T Asesinas Naturales/inmunología , Células T Asesinas Naturales/metabolismo , Estabilidad Proteica , Receptores de Antígenos de Linfocitos T/inmunología , Receptores de Antígenos de Linfocitos T/metabolismo , Especificidad de la Especie , Estereoisomerismo , Relación Estructura-Actividad , Células TH1/efectos de los fármacos , Células TH1/inmunología , Células TH1/metabolismo , Células Th2/efectos de los fármacos , Células Th2/inmunología , Células Th2/metabolismo
3.
Bioorg Chem ; 38(2): 43-7, 2010 Apr.
Artículo en Inglés | MEDLINE | ID: mdl-20060997

RESUMEN

3,6-Anhydro-1-(aryl or alkylamino)-1-deoxy-D-sorbitol derivatives have been prepared in four steps from isosorbide, a by-product from the starch industry. The inhibitory activities of these new compounds have been evaluated towards 13 glycosidases. A first lead-compound was identified, which inhibited beta-N-acetylglucosaminidase from bovine kidney (82% inhibition at 1mM).


Asunto(s)
Inhibidores Enzimáticos/síntesis química , Glicósido Hidrolasas/antagonistas & inhibidores , Sorbitol/síntesis química , Animales , Bovinos , Inhibidores Enzimáticos/química , Inhibidores Enzimáticos/farmacología , Glicósido Hidrolasas/metabolismo , Isosorbida/química , Riñón/enzimología , Sorbitol/análogos & derivados , Sorbitol/farmacología
4.
J Org Chem ; 67(23): 8191-6, 2002 Nov 15.
Artículo en Inglés | MEDLINE | ID: mdl-12423150

RESUMEN

A water-soluble version of N,N'-dimethyl-1,2-diphenylethane-1,2-diamine was prepared by introduction of phosphonic acid moieties on the para position of the aromatic rings. Preliminary investigation of the catalytic properties of the iridium complex of this ligand under biphasic conditions showed that this system compared well with the homogeneous counterpart for the asymmetric hydrogenation of ketones but with noticeably higher reaction rates for the biphasic system.

5.
Bioorg Med Chem Lett ; 12(14): 1841-4, 2002 Jul 22.
Artículo en Inglés | MEDLINE | ID: mdl-12086830

RESUMEN

Different types of heterogenized catalysts were involved in asymmetric reactions. Hydrogen transfer reduction was performed with amino alcohols derived from poly((S)-(GMA-co-EGDMA or DVB)) and hydrogenation with BINAP grafted onto PEG or copolymerized with isocyanates as ligands. Attempts of catalysts recycling are reported.


Asunto(s)
Amino Alcoholes/química , Hidrógeno/química , Naftalenos/química , Polímeros/química , Rutenio/química , Acetoacetatos/química , Acetofenonas/química , Catálisis , Hidrogenación , Oxidación-Reducción , Estereoisomerismo
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