http://rdf.ncbi.nlm.nih.gov/pubchem/patent/ES-2579855-T3
Outgoing Links
Predicate | Object |
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assignee | http://rdf.ncbi.nlm.nih.gov/pubchem/patentassignee/MD5_239b1fe8a19ef004b8c47c090a9c16d5 |
classificationCPCInventive | http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07D471-04 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07D498-08 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07D451-02 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/A61K31-5377 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07D491-08 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/A61P43-00 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/A61K31-444 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/A61P35-00 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/A61P35-04 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/A61K31-437 |
classificationIPCInventive | http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A61K31-4745 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D413-14 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A61P35-00 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D401-04 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D471-04 |
filingDate | 2012-06-21-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
grantDate | 2016-08-17-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
inventor | http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_1485553a3771d6e9c3e1c555f277f70e http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_b4e78c042240ac7ecec80644506ac84f http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_b210fc2ae9c7647e052e8bba5c27fed4 http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_176a3b313695eca6b3509596ee2ebfdd http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_f9efd143608cdf867bcb464c492ee446 http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_cb541e6dc48cf0b5b7da86e301aed7f8 http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_758337335d0482932384f462714fb7a6 http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_ac32d06a8bf35e869509daf44cf02640 http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_1d37d4ad3cae46b5cb55e6d0bfadc38e http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_3ddb269fe87548923df330d906b3376a http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_07a01e6d26f3aefec3f4a1c8e257b4ec http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_19ba935b1281076a4a4f4e5299d99dcd http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_6615efb6f05eccbdafff171c4dbdf079 http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_657baa2d4a4b6be1e4eff83a48b418d4 http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_9067ef6e6d8d04a8935bb188e579061b http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_f11eed39045f0904669f89f6fb801094 http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_fbbcf4cfb99826efddfc3d036b2f1431 http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_43ff6fc4151f7458835c6e493224dc11 |
publicationDate | 2016-08-17-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
publicationNumber | ES-2579855-T3 |
titleOfInvention | Substituted imidazopyridinyl-aminopyridine compounds |
abstract | A compound of formula I: ** Formula ** or a pharmaceutically acceptable salt or ester thereof, in which: X is NRNRN ', GOLD, SRS or ** Formula ** in which ** Formula ** is attached to the imidazopyridinyl ring of formula I in the position indicated by "**"; RO and RS are each independently C6-C10 aryl unsubstituted or substituted; RN is (CH2) mRhc or C6-C10 aryl unsubstituted or substituted; RN 'is H; or RN and RN ', together with the nitrogen atom to which they are attached, form an unsubstituted or substituted morpholine; m is 1, 2, 3 or 4; Rhc is an unsubstituted or substituted heterocycle comprising a 6-membered ring and 1 or 2 heteroatoms selected from N, O and S; and Rph is substituted C3-C6 alkyl or unsubstituted C4-C6 alkyl; wherein: said substituted aryl and substituted heterocycle are substituted at one or more positions of the ring with alkyl, alkenyl, alkynyl, halogen, hydroxy, alkoxy, alkylcarbonyloxy, arylcarbonyloxy, alkoxycarbonyloxy, aryloxycarbonyloxy, carboxylate, alkylcarbonyl, alkylaminocarbonylaminocarbonylaminocarbonylaminocarbonylaminocarbonylaminocarbonylamino alkylcarbonyl, arylcarbonyl, aralkylcarbonyl, alkenylcarbonyl, alkoxycarbonyl, aminocarbonyl, alkylthiocarbonyl, phosphate, phosphonate, phosphinate, amino (including alkylamino, dialkylamino, arylamino, diarylamino and alkylamino), acylamino (including alkylcarbonylamino, arylcarbonylamino, imylcarbonylamino, amylcarbonylamino, imylcarbonylamino, imylcarbonylamino, amylaminocarbonylamino sulfhydryl, alkylthio, arylthio, thiocarboxylate, sulfates, alkylsulfinyl, sulfonate, sulfamoyl, sulfonamido, nitro, trifluoromethyl, cyano, azido, heterocyclyl, alkylaryl or an aromatic or heteroaromatic moiety; said substituted morpholine is substituted with one or more groups, each of which is independently selected from hydroxyl, halogen (including fluorine, chlorine, bromine and iodine), cyano, nitro, unsubstituted amino, C1-C6 alkylamino, di-alkylamino C1-C6 unsubstituted or substituted, C1-C6 alkyl unsubstituted or substituted (including methyl, ethyl, n-propyl, i-propyl, n-butyl, i-butyl, s-butyl, t-butyl, n-pentyl, s-pentyl and n-hexyl), and unsubstituted or substituted C1-C6 alkoxy (including methoxy, ethoxy, n-propyloxy, i-propyloxy, n-butoxy and t-butoxy); said substituted alkoxy is substituted with alkenyl, alkynyl, halogen, hydroxy, alkylcarbonyloxy, arylcarbonyloxy, alkoxycarbonyloxy, aryloxycarbonyloxy, carboxylate, alkylcarbonyl, arylcarbonyl, alkoxycarbonyl, aminocarbonyl, alkylaminocarbonyl, dialkylaminocarbonyloxy, alkylaminocarbonyloxy, alkyloxycarbonyloxy, alkylaminocarbonyloxy, alkyloxycarbonyloxy, alkyloxycarbonyloxy, alkylaminocarbonyloxy, alkylaminocarbonyloxy, alkylaminocarbonyloxy, alkylaminocarbonyloxy, alkylaminocarbonyloxy, alkylaminocarbonyloxy, alkylaminocarbonyloxy, alkylarylcarbonate, alkylaryloxycarbonyl, alkylaryloxycarbonyl, alkylaryloxycarbonyl, alkylaryloxycarbonyl, , dialkylamino, arylamino, diarylamino and alkylamino), acylamino (including alkylcarbonylamino, arylcarbonylamino, carbamoyl and ureido), amidino, imino, sulfhydryl, alkylthio, arylthio, thiocarboxylate, sulfates, alkylsulfinyl, sulfonate, sulfamoyl, sulfonifluoromethyl, nitroamidooromethyl azido, heterocyclyl, alkylaryl, or an aromatic or heteroaromatic moiety; and said substituted alkyl, substituted alkylamino or substituted dialkylamino have substituents that replace one or more hydrogen atoms in one or more carbons of the main hydrocarbon chain, wherein the substituents are alkyl, alkenyl, alkynyl, halogen, hydroxy, alkylcarbonyloxy, arylcarbonyloxy, alkoxycarbonyloxy, aryloxycarbonyloxy, carboxylate, alkylcarbonyl, arylcarbonyl, alkoxycarbonyl, aminocarbonyl, alkylaminocarbonyl, dialkylaminocarbonyl, alkylthiocarbonyl, alkoxyl, phosphate, phosphonate, phosphinate, amino (including alkylamino, dialkylamino, arylamino, diarylamino and alkylarylamino), acylamino (including alkylcarbonylamino, arylcarbonylamino , carbamoyl and ureido), amidino, imino, sulfhydryl, alkylthio, arylthio, thiocarboxylate, sulfates, alkylsulfinyl, sulfonate, sulfamoyl, sulfonamido, nitro, trifluoromethyl, cyano, azido, heterocyclyl, alkylaryl, or an aromatic or heteroaromatic moiety. |
priorityDate | 2011-06-24-04:00^^<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: 91.