http://rdf.ncbi.nlm.nih.gov/pubchem/patent/ES-2598653-T3

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filingDate 2013-03-14-04:00^^<http://www.w3.org/2001/XMLSchema#date>
grantDate 2017-01-30-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_57892ba425b2bb20c178b82fa5b2a46a
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publicationDate 2017-01-30-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber ES-2598653-T3
titleOfInvention Liver X receptor modulators
abstract A compound represented by the following structural formula: ** Formula ** or a pharmaceutically acceptable salt thereof, wherein: X is N or CRc; R1 is alkyl or -NRaRb; R2 is H; halogen; -CN; -NRC (O) R; -C (O) OR; -C (O) NRaRb; monocyclic heteroaromatic optionally substituted with one or more groups selected from alkyl, -CN, -NRC (O) R, -C (O) OR, -C (O) NRaRb and halogen; monocyclic non-aromatic heterocycle optionally substituted with one or more groups selected from alkyl, halogen, -CN and> = O; or alkyl optionally substituted with one or more groups selected from halogen, hydroxy, alkoxy, -NRaRb, -NRC (O) R, -NRC (O) O (alkyl), -NRC (O) N (R) 2, -C (O) OR, thiol, alkylthiol, nitro, -CN,> = O, -OC (O) H, -OC (O) (alkyl), -OC (O) O (alkyl), -OC (O) N (R) 2 and -C (O) NRaRb; R3 is alkyl, haloalkyl, hydroxyalkyl, alkoxyalkyl, cycloalkyl, monocyclic non-aromatic heterocycle, monocyclic heteroaromatic or phenyl, wherein the phenyl, the monocyclic non-aromatic heterocycle and the monocyclic heteroaromatic group represented by R3 are optionally substituted with one or more groups selected from alkyl, halogen, haloalkyl, alkoxy, haloalkoxy, nitro and -CN; R4 is halogen, -CN, -OR, -SR, -N (R) 2, -C (O) R, -C (O) OR, -OC (O) O (alkyl), -C (O) O (haloalkyl), -OC (O) R, -C (O) N (R) 2, -OC (O) N (R) 2, -NRC (O) R, -NRC (O) O (alkyl), -S (O) R, -SO2R, -SO2N (R) 2, -NRS (O) R, -NRSO2R, -NRC (O) N (R) 2, -NRSO2N (R) 2, haloalkyl, haloalkoxy, cycloalkoxy , cycloalkyl, monocyclic non-aromatic heterocycle, monocyclic heteroaromatic or alkyl, wherein the monocyclic non-aromatic heterocycle, the monocyclic heteroaromatic and the alkyl group represented by R4 are optionally substituted with one or more groups selected from -CN, -OR, -SR, -N (R) 2,> = O, -C (O) R, -C (O) OR, -C (O) O (haloalkyl), -OC (O) R, -OC (O) O (alkyl ), -C (O) N (R) 2, -OC (O) N (R) 2, -NRC (O) R, -NRC (O) O (alkyl), -S (O) R, -SO2R , -SO2N (R) 2, -NRS (O) R, -NRSO2R, -NRC (O) N (R) 2 and -NRSO2N (R) 2; Each R is independently H or alkyl; Ra and Rb are independently H, alkyl or Ra and Rb can be taken together with the nitrogen to which they are attached to form a monocyclic non-aromatic heterocycle; and Rc is H, alkyl, or halogen.
priorityDate 2012-03-16-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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Total number of triples: 760.