Synthesis of double-tailed (perfluoroalkyl)alkyl phosphosugars : new components for drug-carrying and -targeting systems
- Auteur
- GUILLOD, F; GREINER, J; RIESS, J. G
CNRS Univ. Nice-Sophia Antipolis, lab. chimie moléculaire, 06108 Nice, France - Source
Carbohydrate research. 1994, Vol 261, Num 1, pp 37-55 ; ref : 40 ref
- CODEN
- CRBRAT
- ISSN
- 0008-6215
- Domaine scientifique
- Biochemistry, molecular biology, biophysics; Organic chemistry
- Editeur
- Elsevier Science, Oxford
- Pays de publication
- United Kingdom
- Type de document
- Article
- Langue
- English
- Mot clé (fr)
- Aldose Animal Biocompatibilité Cible Composé aliphatique Composé amphiphile Couche bimoléculaire Phosphorylation Souris Spectre RMN Toxicité Voie intraveineuse Fluor 19 Galactopyranose 6-phosphate(1-[polyfluoroalkyl]alkyl) Galactopyranose(1,2:3,4-di-O-isopropylidène) Glucofuranose(1,2:5,6-di-O-isopropylidène) Glucopyranose 3-phosphate(1-[polyfluoroalkyl]alkyl) Glucopyranose 6-phosphate(1-[polyfluoroalkyl]alkyl) Glucopyranose(1,2,3,4-tétra-O-acétyl) Hydrogène 1 Mannopyranose 6-phosphate(1-[polyfluoroalkyl]alkyl) Mannopyranose(1,2,3,4-tétra-O-acétyl) Phosphonate(O-[1-(polyfluoroalkyl)alkyl]) Phosphore 31 Vecteur médicament carbone 13 Fluor Composé organique Mammalia Rodentia Vertebrata
- Mot clé (en)
- Aldose Animal Biocompatibility Target Aliphatic compound Amphiphilic compound Bilayer Phosphorylation Mouse NMR spectrum Toxicity Intravenous administration Drug targeting Fluorine Organic compounds Mammalia Rodentia Vertebrata
- Mot clé (es)
- Aldosa Animal Biocompatibilidad Blanco Compuesto alifático Compuesto anfifílico Capa bimolecular Fosforilación Ratón Espectro de RMN Toxicidad Vía intravenosa Fluor Compuesto orgánico Mammalia Rodentia Vertebrata
- Classification
- Pascal
- 001 Sciences exactes et technologie / 001C Chimie / 001C03 Chimie organique / 001C03C Préparations et propriétés / 001C03C07 Oses, osides et holosides. Nucléosides et nucléotides / 001C03C07A Oses et osides en c4, c5, c6, etc., diholosides et oligoholosides
- Discipline
- Organic chemistry
- Provenance
- Inist-CNRS
- Base de données
- PASCAL
- Identifiant INIST
- 4160001
Sauf mention contraire ci-dessus, le contenu de cette notice bibliographique peut être utilisé dans le cadre d’une licence CC BY 4.0 Inist-CNRS / Unless otherwise stated above, the content of this bibliographic record may be used under a CC BY 4.0 licence by Inist-CNRS / A menos que se haya señalado antes, el contenido de este registro bibliográfico puede ser utilizado al amparo de una licencia CC BY 4.0 Inist-CNRS
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DOI
10.1016/0008-6215(94)80004-9 
https://dx.doi.org/10.1016/0008-6215(94)80004-9
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