http://rdf.ncbi.nlm.nih.gov/pubchem/patent/EP-1266899-B1

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filingDate 1995-04-14-04:00^^<http://www.w3.org/2001/XMLSchema#date>
grantDate 2007-01-03-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_6bc5e16b0445e8fae1070ce6f2d25c92
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_31d07253d7ddce5158d0001f1394178a
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_4403a50f182f76ea6e7fe72097780a71
publicationDate 2007-01-03-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber EP-1266899-B1
titleOfInvention Rapamycin hdroxyesters, process for their preparation and pharmaceutical compositions containing them
abstract A compound of structure (I) nwherein R 1 and R 2 are each, independently, hydrogen or - CO(CR 3 R 4 ) b (CR 5 R 6 ) d CR 7 R 8 R 9 ; nR 3 and R 4 are each, independently, hydrogen, alkyl, alkenyl, alkynyl, trifluoromethyl, or -F; nR 5 and R 6 are each, independently, hydrogen, alkyl, alkenyl, alkynyl, -(CR 3 R 4 ) f OR 10 , -CF 3 , -F, or -CO 2 R 11 , or R 5 and R 6 may be taken together to form X or a cycloalkyl ring that is optionally mono-, di-, or tri-substituted with - (CR 3 R 4 ) f OR 10 ; nR 7 is hydrogen, alkyl, alkenyl, alkynyl, -(CR 3 R 4 ) f OR 10 , -CF 3 , -F, or -CO 2 R 11 ; nR 8 and R 9 are each, independently, hydrogen, alkyl, alkenyl, alkynyl, -(CR 3 R 4 ) f OR 10 , -CF 3 , -F, or -CO 2 R 11 , or R 8 and R 9 may be taken together to form X or a cycloalkyl ring that is optionally mono-, di-, or tri-substituted with -(CR 3 R 4 ) f OR 10 ; nR 10 is hydrogen, alkyl, alkenyl, alkynyl, tri-(alkyl)silyl, tri-(alkyl)silylethyl, triphenylmethyl, benzyl, alkoxymethyl, tri-(alkyl)silylethoxymethyl, chloroethyl, or tetrahydropyranyl; nR 11 is hydrogen, alkyl, alkenyl, alkynyl, or phenylalkyl; nX is 5-(2,2-dialkyl)[1,3]dioxanyl, 5-(2,2-dicycloalkyl)[1,3]dioxanyl, 4-(2,2-dialkyl)[1,3]-dioxanyl, 4-(2,2-dicycloalkyl)[1,3]dioxanyl, 4-(2,2-dialkyl)[1,3]dioxalanyl, or 4-(2,2-dicycloalkyl)[1,3]dioxalanyl; nb = 0-6; nd = 0-6; and nf = 0-6 nwith the proviso that R 1 and R 2 are both not hydrogen and further provided that either R 1 or R 2 contains at least one -(CR 3 R 4 ) f OR 10 , X, or -(CR 3 R 4 ) f OR 10 substituted cycloalkyl group, or a pharmaceutically acceptable salt thereof which is useful as an immunosuppressive, antiinflammatory, antifungal, antiproliferative, and antitumor agent.
priorityDate 1994-04-18-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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