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filingDate 2001-12-11-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_093482677a89a161320b34671f53a8a9
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_75986b83dad970ef011846eddfc0829a
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_25f460848885908bbac4f5b776fda5c5
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_a1b2da561a1a6b41ed2bbcbdb572b556
publicationDate 2003-06-13-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber FR-2833266-A1
titleOfInvention NOVEL PHOSPHONATE DERIVATIVES, PROCESS FOR THEIR PREPARATION, THEIR USE AS MODULATORS OF TGAMMA9 DELTA2 LYMPHOCYTE ACTIVITY
abstract The invention relates to novel phosphonate derivatives corresponding to the formula (I) below, in which A represents a linear, branched or cyclic alkyl group, saturated or unsaturated C 1 -C 50, this alkyl group may carry one or of several aromatic groups, it may comprise one or more ether bridges, one or more functions chosen from: a carboxylic acid, an ester, an amide, a nitrile, a hydroxyl, an aldehyde, a ketone, a halogen, an amine, a thiol, a thio-ketone, an episulfide, a selenol, a seleno-ketone, a sulfide, a sulfone, a sulfoxide, it may carry one or more heterocycles, n is an integer ranging from 1 to 4, X represents a group chosen from a hydrogen atom and a pharmaceutically acceptable organic or inorganic cationic group, B represents a group chosen from: X andwherein X and A have the same meaning as above, to their method of preparation, their use as modulating ligands of γ9δ2 T lymphocytes and pharmaceutical compositions comprising them.
priorityDate 2001-12-11-04:00^^<http://www.w3.org/2001/XMLSchema#date>
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Total number of triples: 395.