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filingDate 1990-06-07-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_1a74588a552852d2ef00e14a0be4594f
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_250eac0d38fe8a0cdc3ac7c8a3afeb5b
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_acdc6fee00e3527fafd9417f4eb5f653
publicationDate 1990-12-12-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber EP-0402259-A1
titleOfInvention Anthracyclines, process for their preparation and medicaments containing them
abstract R 1 représente un atome d'hydrogène, un groupe COR 4 , dans lequel R 4 représente un groupe alkyle en C 1 -C 8 ; R 2 représente un atome d'hydrogène ou un atome d'iode ; R 3 représente un groupe azide, un groupe morpholino, une amine primaire, une amine secondaire NHR 6 dans laquelle R 6 représente un groupe COCF 3 , un groupe COCH 3 , un groupe phtalimido, une amine tertiaire NR 7 R 7 , dans laquelle R 7 est un benzyle, un méthyle, un aminonitrile ; Rs représente un atome d'hydrogène, un groupe acyle en C 2 -C 4 éventuellement substitué, un groupe benzyle éventuellement substitué. These anthracyclines are represented by the formula I below: in which R 1 represents a hydrogen atom, a COR 4 group, in which R 4 represents a C 1 -C 8 alkyl group; R 2 represents a hydrogen atom or an iodine atom; R 3 represents an azide group, a morpholino group, a primary amine, a secondary amine NHR 6 in which R 6 represents a COCF 3 group, a COCH 3 group, a phthalimido group, a tertiary amine NR 7 R 7 , in which R 7 is benzyl, methyl, aminonitrile; Rs represents a hydrogen atom, an optionally substituted C 2 -C 4 acyl group, an optionally substituted benzyl group.
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priorityDate 1989-06-07-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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