http://rdf.ncbi.nlm.nih.gov/pubchem/patent/FR-2923485-A1

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classificationCPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07D519-04
http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/A61P35-00
classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A61K31-454
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A61P35-00
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D519-04
filingDate 2007-11-12-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_7c128a88c74f1e1096555f833836cbab
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_effb42308a1185617f5d8d17df8c2652
publicationDate 2009-05-15-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber FR-2923485-A1
titleOfInvention ANTIMITOTIC COMPOUNDS DERIVED FROM VINCA ALKALOIDS, THEIR PREPARATION AND THEIR THERAPEUTIC APPLICATION
abstract The compounds of the invention are new derivatives of the vinblastine and vinflunine family modified at positions -4, -4 ', -20', and substituted at position -12 '. These new derivatives correspond to the general formula next: in which:. R1 represents the following groups: - -C = CR <1> in which R 'represents a hydrogen atom, an alkyl group of one to six linear or branched carbon atoms, a -CH2-O-alkyl group, a group trialkylsilyl, an amino group -CH2-NXY in which X and Y independently represent a hydrogen atom or an alkyl, aryl or heteroaryl group, or can together form a 5 to 7 membered ring, - SR "in which R" represents a hydrogen atom, a linear or branched one to six-membered hydroxy-alkyl, hydroxy-alkenyl or hydroxy-alkynyl group, an optionally substituted benzyl or aryl group, in which R "'represents an OCO-Z ester function, where Z is an alkyl, alkenyl, linear or branched alkynyl group, an optionally substituted aryl or benzyl group, R2 and R3 together or independently represent a hydrogen atom or a halogen atom. R4 represents a hydrogen atom or an acetyl group .. n can take the values 1 or 2. The invention also relates to the application of these compounds or their salified forms to the treatment of cancerous pathology.
priorityDate 2007-11-12-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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