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filingDate 2010-07-01-04:00^^<http://www.w3.org/2001/XMLSchema#date>
grantDate 2015-07-09-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_b074f2d40a6dc34caf98fc3a2ec02610
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_e5e4971e1e6438746071187eec38afdb
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publicationDate 2015-07-09-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber ES-2540232-T3
titleOfInvention TOFA analogues useful in the treatment of dermatological disorders or conditions
abstract A compound of formula (I): wherein: R1 is -O-R2, wherein R2 is haloalkyl or a substituted aryl; or R1 is -O-R3-OR2, wherein R2 is optionally substituted heterocyclyl and each R3 is independently an optionally substituted alkylene chain; or R1 is RO-R3-OC (O) -N (R5) R6, -O-R3-N (R5) R6, O-R3-N- (R4) C (O) OR5 -O-R3-C ( O) OR5, -O-R3-C (O) N (R5) R6 or - N (R5) S (O) 2-R4; wherein each R3 is independently an optionally substituted alkylene chain; and R4 is optionally substituted alkyl, optionally substituted aryl, optionally substituted aralkyl, optionally substituted heteroaryl or optionally substituted heteroarylalkyl; each R5 is independently hydrogen, optionally substituted alkyl, cycloalkyl, optionally substituted aryl or optionally substituted aralkyl; and each R6 is alkyl, optionally substituted cycloalkyl, optionally substituted aralkyl or -R3-C (O) OR4; or either of R5 and R6, together with the nitrogen to which they are both attached form an optionally substituted N-heterocyclyl or an optionally substituted N-heteroaryl; as an individual stereoisomer or as a mixture thereof; or a pharmaceutically acceptable salt thereof, for use in therapy.
priorityDate 2009-07-08-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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