JP2013523710A5 - - Google Patents
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- Publication number
- JP2013523710A5 JP2013523710A5 JP2013501951A JP2013501951A JP2013523710A5 JP 2013523710 A5 JP2013523710 A5 JP 2013523710A5 JP 2013501951 A JP2013501951 A JP 2013501951A JP 2013501951 A JP2013501951 A JP 2013501951A JP 2013523710 A5 JP2013523710 A5 JP 2013523710A5
- Authority
- JP
- Japan
- Prior art keywords
- butyl
- pyrazol
- ureido
- pyridin
- dichlorophenoxy
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Granted
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- -1 n- propyl Chemical group 0.000 claims 32
- 125000000217 alkyl group Chemical group 0.000 claims 28
- 150000001875 compounds Chemical class 0.000 claims 15
- 125000001309 chloro group Chemical group Cl* 0.000 claims 9
- 125000005843 halogen group Chemical group 0.000 claims 7
- XSQUKJJJFZCRTK-UHFFFAOYSA-N Urea Chemical compound NC(N)=O XSQUKJJJFZCRTK-UHFFFAOYSA-N 0.000 claims 6
- 239000004202 carbamide Substances 0.000 claims 6
- 229920006395 saturated elastomer Polymers 0.000 claims 6
- 229910052799 carbon Inorganic materials 0.000 claims 5
- 125000005842 heteroatom Chemical group 0.000 claims 5
- 125000000623 heterocyclic group Chemical group 0.000 claims 5
- 229910052717 sulfur Inorganic materials 0.000 claims 5
- JUJWROOIHBZHMG-UHFFFAOYSA-N Pyridine Chemical group C1=CC=NC=C1 JUJWROOIHBZHMG-UHFFFAOYSA-N 0.000 claims 4
- 125000003545 alkoxy group Chemical group 0.000 claims 4
- 125000004093 cyano group Chemical group *C#N 0.000 claims 4
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 claims 4
- 125000000171 (C1-C6) haloalkyl group Chemical group 0.000 claims 3
- 239000004480 active ingredient Substances 0.000 claims 3
- 125000002887 hydroxy group Chemical group [H]O* 0.000 claims 3
- 229910052757 nitrogen Inorganic materials 0.000 claims 3
- 125000004043 oxo group Chemical group O=* 0.000 claims 3
- VLMPAMYESBASPG-UHFFFAOYSA-N 1-[2,3-dichloro-4-[2-(methylcarbamoylamino)pyridin-4-yl]oxyphenyl]-3-[5-(1-methylcyclohexyl)-2-(4-methylphenyl)pyrazol-3-yl]urea Chemical compound C1=NC(NC(=O)NC)=CC(OC=2C(=C(Cl)C(NC(=O)NC=3N(N=C(C=3)C3(C)CCCCC3)C=3C=CC(C)=CC=3)=CC=2)Cl)=C1 VLMPAMYESBASPG-UHFFFAOYSA-N 0.000 claims 2
- 125000002947 alkylene group Chemical group 0.000 claims 2
- 125000003118 aryl group Chemical group 0.000 claims 2
- 239000003814 drug Substances 0.000 claims 2
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 claims 2
- 125000001188 haloalkyl group Chemical group 0.000 claims 2
- 229910052736 halogen Inorganic materials 0.000 claims 2
- 150000002367 halogens Chemical class 0.000 claims 2
- 125000004404 heteroalkyl group Chemical group 0.000 claims 2
- 230000000155 isotopic effect Effects 0.000 claims 2
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims 2
- 229910052760 oxygen Inorganic materials 0.000 claims 2
- 125000002924 primary amino group Chemical group [H]N([H])* 0.000 claims 2
- UMJSCPRVCHMLSP-UHFFFAOYSA-N pyridine Natural products COC1=CC=CN=C1 UMJSCPRVCHMLSP-UHFFFAOYSA-N 0.000 claims 2
- 206010039073 rheumatoid arthritis Diseases 0.000 claims 2
- 150000003839 salts Chemical class 0.000 claims 2
- 125000000999 tert-butyl group Chemical group [H]C([H])([H])C(*)(C([H])([H])[H])C([H])([H])[H] 0.000 claims 2
- 125000006583 (C1-C3) haloalkyl group Chemical group 0.000 claims 1
- 125000003161 (C1-C6) alkylene group Chemical group 0.000 claims 1
- 125000006376 (C3-C10) cycloalkyl group Chemical group 0.000 claims 1
- 125000006552 (C3-C8) cycloalkyl group Chemical group 0.000 claims 1
- 125000006570 (C5-C6) heteroaryl group Chemical group 0.000 claims 1
- OIAZQNDOMLQBTC-UHFFFAOYSA-N 1-[5-tert-butyl-2-(4-methoxyphenyl)pyrazol-3-yl]-3-[2,3-dichloro-4-[2-(2-hydroxyethylcarbamoylamino)pyridin-4-yl]oxyphenyl]urea Chemical compound C1=CC(OC)=CC=C1N1C(NC(=O)NC=2C(=C(Cl)C(OC=3C=C(NC(=O)NCCO)N=CC=3)=CC=2)Cl)=CC(C(C)(C)C)=N1 OIAZQNDOMLQBTC-UHFFFAOYSA-N 0.000 claims 1
- PRRTTXQJXYIWIX-UHFFFAOYSA-N 1-[5-tert-butyl-2-(4-methoxyphenyl)pyrazol-3-yl]-3-[2,3-dichloro-4-[2-(2-methoxyethylcarbamoylamino)pyridin-4-yl]oxyphenyl]urea Chemical compound C1=NC(NC(=O)NCCOC)=CC(OC=2C(=C(Cl)C(NC(=O)NC=3N(N=C(C=3)C(C)(C)C)C=3C=CC(OC)=CC=3)=CC=2)Cl)=C1 PRRTTXQJXYIWIX-UHFFFAOYSA-N 0.000 claims 1
- YBGBLFUNGGROBC-UHFFFAOYSA-N 1-[5-tert-butyl-2-(4-methoxyphenyl)pyrazol-3-yl]-3-[2,3-dichloro-4-[2-(2-morpholin-4-ylethylcarbamoylamino)pyridin-4-yl]oxyphenyl]urea Chemical compound C1=CC(OC)=CC=C1N1C(NC(=O)NC=2C(=C(Cl)C(OC=3C=C(NC(=O)NCCN4CCOCC4)N=CC=3)=CC=2)Cl)=CC(C(C)(C)C)=N1 YBGBLFUNGGROBC-UHFFFAOYSA-N 0.000 claims 1
- NHMKKTQJKOFNIJ-UHFFFAOYSA-N 1-[5-tert-butyl-2-(4-methoxyphenyl)pyrazol-3-yl]-3-[2,3-dichloro-4-[2-(3-imidazol-1-ylpropylcarbamoylamino)pyridin-4-yl]oxyphenyl]urea Chemical compound C1=CC(OC)=CC=C1N1C(NC(=O)NC=2C(=C(Cl)C(OC=3C=C(NC(=O)NCCCN4C=NC=C4)N=CC=3)=CC=2)Cl)=CC(C(C)(C)C)=N1 NHMKKTQJKOFNIJ-UHFFFAOYSA-N 0.000 claims 1
- QPXKCTOLMAYCEZ-UHFFFAOYSA-N 1-[5-tert-butyl-2-(4-methoxyphenyl)pyrazol-3-yl]-3-[2,3-dichloro-4-[2-(cyclopropylcarbamoylamino)pyridin-4-yl]oxyphenyl]urea Chemical compound C1=CC(OC)=CC=C1N1C(NC(=O)NC=2C(=C(Cl)C(OC=3C=C(NC(=O)NC4CC4)N=CC=3)=CC=2)Cl)=CC(C(C)(C)C)=N1 QPXKCTOLMAYCEZ-UHFFFAOYSA-N 0.000 claims 1
- AJHNLMKJRISUFA-UHFFFAOYSA-N 1-[5-tert-butyl-2-(4-methoxyphenyl)pyrazol-3-yl]-3-[2,3-dichloro-4-[2-(ethylcarbamoylamino)pyridin-4-yl]oxyphenyl]urea Chemical compound C1=NC(NC(=O)NCC)=CC(OC=2C(=C(Cl)C(NC(=O)NC=3N(N=C(C=3)C(C)(C)C)C=3C=CC(OC)=CC=3)=CC=2)Cl)=C1 AJHNLMKJRISUFA-UHFFFAOYSA-N 0.000 claims 1
- MMMMQLITLMJIGS-UHFFFAOYSA-N 1-[5-tert-butyl-2-(4-methoxyphenyl)pyrazol-3-yl]-3-[2,3-dichloro-4-[2-(methylcarbamoylamino)pyrimidin-4-yl]oxyphenyl]urea Chemical compound CNC(=O)NC1=NC=CC(OC=2C(=C(Cl)C(NC(=O)NC=3N(N=C(C=3)C(C)(C)C)C=3C=CC(OC)=CC=3)=CC=2)Cl)=N1 MMMMQLITLMJIGS-UHFFFAOYSA-N 0.000 claims 1
- UXNCEUAZOJVHSD-UHFFFAOYSA-N 1-[5-tert-butyl-2-(4-methoxyphenyl)pyrazol-3-yl]-3-[2,3-dichloro-4-[2-[2-(dimethylamino)ethylcarbamoylamino]pyridin-4-yl]oxyphenyl]urea Chemical compound C1=CC(OC)=CC=C1N1C(NC(=O)NC=2C(=C(Cl)C(OC=3C=C(NC(=O)NCCN(C)C)N=CC=3)=CC=2)Cl)=CC(C(C)(C)C)=N1 UXNCEUAZOJVHSD-UHFFFAOYSA-N 0.000 claims 1
- AHTMBXGKCASMLK-UHFFFAOYSA-N 1-[5-tert-butyl-2-(4-methoxyphenyl)pyrazol-3-yl]-3-[2,3-dichloro-4-[6-(methylcarbamoylamino)pyrimidin-4-yl]oxyphenyl]urea Chemical compound C1=NC(NC(=O)NC)=CC(OC=2C(=C(Cl)C(NC(=O)NC=3N(N=C(C=3)C(C)(C)C)C=3C=CC(OC)=CC=3)=CC=2)Cl)=N1 AHTMBXGKCASMLK-UHFFFAOYSA-N 0.000 claims 1
- SMTVTISHQTTWIJ-UHFFFAOYSA-N 1-[5-tert-butyl-2-(4-methoxyphenyl)pyrazol-3-yl]-3-[2,3-dichloro-4-[[2-(methylcarbamoylamino)pyridin-4-yl]methoxy]phenyl]urea Chemical compound C1=NC(NC(=O)NC)=CC(COC=2C(=C(Cl)C(NC(=O)NC=3N(N=C(C=3)C(C)(C)C)C=3C=CC(OC)=CC=3)=CC=2)Cl)=C1 SMTVTISHQTTWIJ-UHFFFAOYSA-N 0.000 claims 1
- USMGBMVEIONWEF-UHFFFAOYSA-N 1-[5-tert-butyl-2-(4-methoxyphenyl)pyrazol-3-yl]-3-[2-chloro-3-cyano-4-[2-(cyclopropylcarbamoylamino)pyridin-4-yl]oxyphenyl]urea Chemical compound C1=CC(OC)=CC=C1N1C(NC(=O)NC=2C(=C(C#N)C(OC=3C=C(NC(=O)NC4CC4)N=CC=3)=CC=2)Cl)=CC(C(C)(C)C)=N1 USMGBMVEIONWEF-UHFFFAOYSA-N 0.000 claims 1
- JWNUKWIUEVMBCP-UHFFFAOYSA-N 1-[5-tert-butyl-2-(4-methoxyphenyl)pyrazol-3-yl]-3-[5-[2-(methylcarbamoylamino)pyridin-4-yl]oxyquinolin-8-yl]urea Chemical compound C1=NC(NC(=O)NC)=CC(OC=2C3=CC=CN=C3C(NC(=O)NC=3N(N=C(C=3)C(C)(C)C)C=3C=CC(OC)=CC=3)=CC=2)=C1 JWNUKWIUEVMBCP-UHFFFAOYSA-N 0.000 claims 1
- MKRDTPRFOOZKLJ-UHFFFAOYSA-N 1-[5-tert-butyl-2-(4-methoxyphenyl)pyrazol-3-yl]-3-[8-[2-(methylcarbamoylamino)pyridin-4-yl]oxyquinolin-5-yl]urea Chemical compound C1=NC(NC(=O)NC)=CC(OC=2C3=NC=CC=C3C(NC(=O)NC=3N(N=C(C=3)C(C)(C)C)C=3C=CC(OC)=CC=3)=CC=2)=C1 MKRDTPRFOOZKLJ-UHFFFAOYSA-N 0.000 claims 1
- DVERJTHQZPGXQN-UHFFFAOYSA-N 1-[5-tert-butyl-2-(4-methylphenyl)pyrazol-3-yl]-3-[2,3-dichloro-4-[2-(methylcarbamoylamino)pyridin-4-yl]oxyphenyl]urea Chemical compound C1=NC(NC(=O)NC)=CC(OC=2C(=C(Cl)C(NC(=O)NC=3N(N=C(C=3)C(C)(C)C)C=3C=CC(C)=CC=3)=CC=2)Cl)=C1 DVERJTHQZPGXQN-UHFFFAOYSA-N 0.000 claims 1
- NKFGXRJEGVLHPA-UHFFFAOYSA-N 1-[5-tert-butyl-2-(4-methylphenyl)pyrazol-3-yl]-3-[2,3-dichloro-4-[2-(methylcarbamoylamino)pyrimidin-4-yl]oxyphenyl]urea Chemical compound CNC(=O)NC1=NC=CC(OC=2C(=C(Cl)C(NC(=O)NC=3N(N=C(C=3)C(C)(C)C)C=3C=CC(C)=CC=3)=CC=2)Cl)=N1 NKFGXRJEGVLHPA-UHFFFAOYSA-N 0.000 claims 1
- DUZLWGRPUKUKRC-UHFFFAOYSA-N 1-[5-tert-butyl-2-(4-methylphenyl)pyrazol-3-yl]-3-[2,3-dichloro-4-[6-(methylcarbamoylamino)pyrimidin-4-yl]oxyphenyl]urea Chemical compound C1=NC(NC(=O)NC)=CC(OC=2C(=C(Cl)C(NC(=O)NC=3N(N=C(C=3)C(C)(C)C)C=3C=CC(C)=CC=3)=CC=2)Cl)=N1 DUZLWGRPUKUKRC-UHFFFAOYSA-N 0.000 claims 1
- PARGWSHOODCFOD-UHFFFAOYSA-N 1-[5-tert-butyl-2-(4-methylphenyl)pyrazol-3-yl]-3-[2,3-dichloro-4-[6-[2-(dimethylamino)ethylcarbamoylamino]pyrimidin-4-yl]oxyphenyl]urea Chemical compound C1=NC(NC(=O)NCCN(C)C)=CC(OC=2C(=C(Cl)C(NC(=O)NC=3N(N=C(C=3)C(C)(C)C)C=3C=CC(C)=CC=3)=CC=2)Cl)=N1 PARGWSHOODCFOD-UHFFFAOYSA-N 0.000 claims 1
- OVBTUBSHWNGHEB-UHFFFAOYSA-N 1-[5-tert-butyl-2-(4-methylphenyl)pyrazol-3-yl]-3-[2,3-dichloro-4-[[2-(methylcarbamoylamino)pyridin-4-yl]methoxy]phenyl]urea Chemical compound C1=NC(NC(=O)NC)=CC(COC=2C(=C(Cl)C(NC(=O)NC=3N(N=C(C=3)C(C)(C)C)C=3C=CC(C)=CC=3)=CC=2)Cl)=C1 OVBTUBSHWNGHEB-UHFFFAOYSA-N 0.000 claims 1
- SRVVSDBSTURJMJ-UHFFFAOYSA-N 1-[5-tert-butyl-2-(4-methylphenyl)pyrazol-3-yl]-3-[5-[2-(methylcarbamoylamino)pyridin-4-yl]oxyquinolin-8-yl]urea Chemical compound C1=NC(NC(=O)NC)=CC(OC=2C3=CC=CN=C3C(NC(=O)NC=3N(N=C(C=3)C(C)(C)C)C=3C=CC(C)=CC=3)=CC=2)=C1 SRVVSDBSTURJMJ-UHFFFAOYSA-N 0.000 claims 1
- USWDEAODPRGOFK-UHFFFAOYSA-N 1-[5-tert-butyl-2-(4-methylphenyl)pyrazol-3-yl]-3-[8-[[2-(methylcarbamoylamino)pyridin-4-yl]methoxy]quinolin-5-yl]urea Chemical compound C1=NC(NC(=O)NC)=CC(COC=2C3=NC=CC=C3C(NC(=O)NC=3N(N=C(C=3)C(C)(C)C)C=3C=CC(C)=CC=3)=CC=2)=C1 USWDEAODPRGOFK-UHFFFAOYSA-N 0.000 claims 1
- CSEFAOSXZQCHNC-UHFFFAOYSA-N 1-[5-tert-butyl-2-[4-(hydroxymethyl)phenyl]pyrazol-3-yl]-3-[2,3-dichloro-4-[2-(2-morpholin-4-ylethylcarbamoylamino)pyridin-4-yl]oxyphenyl]urea Chemical compound C=1C=C(CO)C=CC=1N1N=C(C(C)(C)C)C=C1NC(=O)NC(C(=C1Cl)Cl)=CC=C1OC(C=1)=CC=NC=1NC(=O)NCCN1CCOCC1 CSEFAOSXZQCHNC-UHFFFAOYSA-N 0.000 claims 1
- BSMRUQMZPUPKCC-UHFFFAOYSA-N 1-[5-tert-butyl-2-[4-(hydroxymethyl)phenyl]pyrazol-3-yl]-3-[2,3-dichloro-4-[2-(cyclopropylcarbamoylamino)pyridin-4-yl]oxyphenyl]urea Chemical compound C=1C=C(CO)C=CC=1N1N=C(C(C)(C)C)C=C1NC(=O)NC(C(=C1Cl)Cl)=CC=C1OC(C=1)=CC=NC=1NC(=O)NC1CC1 BSMRUQMZPUPKCC-UHFFFAOYSA-N 0.000 claims 1
- VVBJANIWLGGZJB-UHFFFAOYSA-N 1-[5-tert-butyl-2-[4-(hydroxymethyl)phenyl]pyrazol-3-yl]-3-[2,3-dichloro-4-[2-(methylcarbamoylamino)pyrimidin-4-yl]oxyphenyl]urea Chemical compound CNC(=O)NC1=NC=CC(OC=2C(=C(Cl)C(NC(=O)NC=3N(N=C(C=3)C(C)(C)C)C=3C=CC(CO)=CC=3)=CC=2)Cl)=N1 VVBJANIWLGGZJB-UHFFFAOYSA-N 0.000 claims 1
- NFEGIIQSUSSDLM-UHFFFAOYSA-N 1-[5-tert-butyl-2-[4-(hydroxymethyl)phenyl]pyrazol-3-yl]-3-[2,3-dichloro-4-[2-[2-(dimethylamino)ethylcarbamoylamino]pyridin-4-yl]oxyphenyl]urea Chemical compound C1=NC(NC(=O)NCCN(C)C)=CC(OC=2C(=C(Cl)C(NC(=O)NC=3N(N=C(C=3)C(C)(C)C)C=3C=CC(CO)=CC=3)=CC=2)Cl)=C1 NFEGIIQSUSSDLM-UHFFFAOYSA-N 0.000 claims 1
- DKVWSSQEESVPSA-UHFFFAOYSA-N 1-[5-tert-butyl-2-[4-(hydroxymethyl)phenyl]pyrazol-3-yl]-3-[2,3-dichloro-4-[6-(methylcarbamoylamino)pyrimidin-4-yl]oxyphenyl]urea Chemical compound C1=NC(NC(=O)NC)=CC(OC=2C(=C(Cl)C(NC(=O)NC=3N(N=C(C=3)C(C)(C)C)C=3C=CC(CO)=CC=3)=CC=2)Cl)=N1 DKVWSSQEESVPSA-UHFFFAOYSA-N 0.000 claims 1
- YZZUDFVTYXDQEJ-UHFFFAOYSA-N 1-[5-tert-butyl-2-[4-(hydroxymethyl)phenyl]pyrazol-3-yl]-3-[5-[2-(methylcarbamoylamino)pyridin-4-yl]oxyquinolin-8-yl]urea Chemical compound C1=NC(NC(=O)NC)=CC(OC=2C3=CC=CN=C3C(NC(=O)NC=3N(N=C(C=3)C(C)(C)C)C=3C=CC(CO)=CC=3)=CC=2)=C1 YZZUDFVTYXDQEJ-UHFFFAOYSA-N 0.000 claims 1
- KEUPSXIYJHLGEW-UHFFFAOYSA-N 1-[5-tert-butyl-2-[4-(hydroxymethyl)phenyl]pyrazol-3-yl]-3-[8-[2-(methylcarbamoylamino)pyridin-4-yl]oxyquinolin-5-yl]urea Chemical compound C1=NC(NC(=O)NC)=CC(OC=2C3=NC=CC=C3C(NC(=O)NC=3N(N=C(C=3)C(C)(C)C)C=3C=CC(CO)=CC=3)=CC=2)=C1 KEUPSXIYJHLGEW-UHFFFAOYSA-N 0.000 claims 1
- ZLAAPNRAYFZHNK-UHFFFAOYSA-N 1-methyl-3-pyridin-2-ylurea Chemical compound CNC(=O)NC1=CC=CC=N1 ZLAAPNRAYFZHNK-UHFFFAOYSA-N 0.000 claims 1
- 125000005955 1H-indazolyl group Chemical group 0.000 claims 1
- XIPWBCORXDYDEH-UHFFFAOYSA-N 3-[4-[4-[[5-tert-butyl-2-(4-methoxyphenyl)pyrazol-3-yl]carbamoylamino]-2,3-dichlorophenoxy]pyridin-2-yl]-1,1-dimethylurea Chemical compound C1=CC(OC)=CC=C1N1C(NC(=O)NC=2C(=C(Cl)C(OC=3C=C(NC(=O)N(C)C)N=CC=3)=CC=2)Cl)=CC(C(C)(C)C)=N1 XIPWBCORXDYDEH-UHFFFAOYSA-N 0.000 claims 1
- MDRDQUUSTQLWDS-UHFFFAOYSA-N 4-[3-tert-butyl-5-[[2,3-dichloro-4-[2-(methylcarbamoylamino)pyridin-4-yl]oxyphenyl]carbamoylamino]pyrazol-1-yl]benzoic acid Chemical compound C1=NC(NC(=O)NC)=CC(OC=2C(=C(Cl)C(NC(=O)NC=3N(N=C(C=3)C(C)(C)C)C=3C=CC(=CC=3)C(O)=O)=CC=2)Cl)=C1 MDRDQUUSTQLWDS-UHFFFAOYSA-N 0.000 claims 1
- LRFVTYWOQMYALW-UHFFFAOYSA-N 9H-xanthine Chemical class O=C1NC(=O)NC2=C1NC=N2 LRFVTYWOQMYALW-UHFFFAOYSA-N 0.000 claims 1
- 206010006187 Breast cancer Diseases 0.000 claims 1
- 208000026310 Breast neoplasm Diseases 0.000 claims 1
- 206010006458 Bronchitis chronic Diseases 0.000 claims 1
- 206010006895 Cachexia Diseases 0.000 claims 1
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 claims 1
- 208000006545 Chronic Obstructive Pulmonary Disease Diseases 0.000 claims 1
- 206010009900 Colitis ulcerative Diseases 0.000 claims 1
- 206010009944 Colon cancer Diseases 0.000 claims 1
- 208000001333 Colorectal Neoplasms Diseases 0.000 claims 1
- 206010010741 Conjunctivitis Diseases 0.000 claims 1
- 206010010744 Conjunctivitis allergic Diseases 0.000 claims 1
- 201000003883 Cystic fibrosis Diseases 0.000 claims 1
- 206010012434 Dermatitis allergic Diseases 0.000 claims 1
- 206010012442 Dermatitis contact Diseases 0.000 claims 1
- 206010014561 Emphysema Diseases 0.000 claims 1
- 201000009794 Idiopathic Pulmonary Fibrosis Diseases 0.000 claims 1
- QPJVMBTYPHYUOC-UHFFFAOYSA-N Methyl benzoate Natural products COC(=O)C1=CC=CC=C1 QPJVMBTYPHYUOC-UHFFFAOYSA-N 0.000 claims 1
- 206010033645 Pancreatitis Diseases 0.000 claims 1
- 201000004681 Psoriasis Diseases 0.000 claims 1
- CZPWVGJYEJSRLH-UHFFFAOYSA-N Pyrimidine Chemical group C1=CN=CN=C1 CZPWVGJYEJSRLH-UHFFFAOYSA-N 0.000 claims 1
- 206010039085 Rhinitis allergic Diseases 0.000 claims 1
- 208000005718 Stomach Neoplasms Diseases 0.000 claims 1
- 201000006704 Ulcerative Colitis Diseases 0.000 claims 1
- 125000002015 acyclic group Chemical group 0.000 claims 1
- 125000002723 alicyclic group Chemical group 0.000 claims 1
- 208000002205 allergic conjunctivitis Diseases 0.000 claims 1
- 201000010105 allergic rhinitis Diseases 0.000 claims 1
- 208000006673 asthma Diseases 0.000 claims 1
- 125000004429 atom Chemical group 0.000 claims 1
- 208000024998 atopic conjunctivitis Diseases 0.000 claims 1
- 201000008937 atopic dermatitis Diseases 0.000 claims 1
- 208000010668 atopic eczema Diseases 0.000 claims 1
- 229940125388 beta agonist Drugs 0.000 claims 1
- 206010006451 bronchitis Diseases 0.000 claims 1
- 125000000484 butyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 claims 1
- 125000002837 carbocyclic group Chemical group 0.000 claims 1
- 125000004432 carbon atom Chemical group C* 0.000 claims 1
- 125000002915 carbonyl group Chemical group [*:2]C([*:1])=O 0.000 claims 1
- 239000000969 carrier Substances 0.000 claims 1
- 208000029771 childhood onset asthma Diseases 0.000 claims 1
- 208000007451 chronic bronchitis Diseases 0.000 claims 1
- 208000010247 contact dermatitis Diseases 0.000 claims 1
- 208000035250 cutaneous malignant susceptibility to 1 melanoma Diseases 0.000 claims 1
- 125000000753 cycloalkyl group Chemical group 0.000 claims 1
- 239000003085 diluting agent Substances 0.000 claims 1
- 201000010099 disease Diseases 0.000 claims 1
- 208000037265 diseases, disorders, signs and symptoms Diseases 0.000 claims 1
- 125000001153 fluoro group Chemical group F* 0.000 claims 1
- 206010017758 gastric cancer Diseases 0.000 claims 1
- 125000001072 heteroaryl group Chemical group 0.000 claims 1
- 125000000592 heterocycloalkyl group Chemical group 0.000 claims 1
- 229910052739 hydrogen Inorganic materials 0.000 claims 1
- 208000036971 interstitial lung disease 2 Diseases 0.000 claims 1
- 125000001449 isopropyl group Chemical group [H]C([H])([H])C([H])(*)C([H])([H])[H] 0.000 claims 1
- 201000001441 melanoma Diseases 0.000 claims 1
- 229940095102 methyl benzoate Drugs 0.000 claims 1
- WBTMEQBEZBHVLX-UHFFFAOYSA-N n-[4-[2,3-dichloro-4-[[5-(1-methylcyclohexyl)-2-(4-methylphenyl)pyrazol-3-yl]carbamoylamino]phenoxy]pyridin-2-yl]pyrrolidine-1-carboxamide Chemical compound C1=CC(C)=CC=C1N1C(NC(=O)NC=2C(=C(Cl)C(OC=3C=C(NC(=O)N4CCCC4)N=CC=3)=CC=2)Cl)=CC(C2(C)CCCCC2)=N1 WBTMEQBEZBHVLX-UHFFFAOYSA-N 0.000 claims 1
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Applications Claiming Priority (3)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| GBGB1005589.5A GB201005589D0 (en) | 2010-04-01 | 2010-04-01 | Novel compounds |
| GB1005589.5 | 2010-04-01 | ||
| PCT/GB2011/050668 WO2011121366A1 (en) | 2010-04-01 | 2011-04-01 | Pyrazole p38 map kinase inhibitors |
Publications (3)
| Publication Number | Publication Date |
|---|---|
| JP2013523710A JP2013523710A (ja) | 2013-06-17 |
| JP2013523710A5 true JP2013523710A5 (https=) | 2014-05-08 |
| JP5902668B2 JP5902668B2 (ja) | 2016-04-13 |
Family
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| JP2013501951A Active JP5902668B2 (ja) | 2010-04-01 | 2011-04-01 | ピラゾール系ｐ３８ＭＡＰキナーゼ阻害剤 |
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| US (3) | US20130029990A1 (https=) |
| EP (1) | EP2556065B1 (https=) |
| JP (1) | JP5902668B2 (https=) |
| ES (1) | ES2532764T3 (https=) |
| GB (1) | GB201005589D0 (https=) |
| WO (1) | WO2011121366A1 (https=) |
Families Citing this family (41)
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| AU2008337286B2 (en) | 2007-12-19 | 2014-08-07 | Cancer Research Technology Limited | Pyrido[2,3-b]pyrazine-8-substituted compounds and their use |
| GB0905955D0 (en) * | 2009-04-06 | 2009-05-20 | Respivert Ltd | Novel compounds |
| NZ601085A (en) | 2010-02-01 | 2015-04-24 | Cancer Rec Tech Ltd | 1-(5-tert-butyl-2-phenyl-2h-pyrazol-3-yl)-3-[2-fluoro-4-(1-methyl-2-oxo-2,3-dihydro-1h-imidazo[4,5-b]pyridin-7-yloxy)-phenyl]-urea and related compounds and their use in therapy |
| GB201005589D0 (en) | 2010-04-01 | 2010-05-19 | Respivert Ltd | Novel compounds |
| WO2011124923A2 (en) | 2010-04-08 | 2011-10-13 | Respivert Limited | Novel compounds |
| EP2556068B1 (en) | 2010-04-08 | 2019-01-23 | Respivert Limited | P38 map kinase inhibitors |
| GB201009731D0 (en) * | 2010-06-10 | 2010-07-21 | Pulmagen Therapeutics Inflamma | Kinase inhibitors |
| GB201010193D0 (en) | 2010-06-17 | 2010-07-21 | Respivert Ltd | Medicinal use |
| US8933228B2 (en) | 2010-06-17 | 2015-01-13 | Respivert, Ltd. | Respiratory formulations and compounds for use therein |
| CN103917536B (zh) | 2011-10-03 | 2016-07-06 | 瑞斯比维特有限公司 | 1-吡唑基-3-(4-((2-(苯氨基)嘧啶-4-基)氧基)萘-1-基)脲用作p38 MAP激酶抑制剂 |
| EP2578582A1 (en) | 2011-10-03 | 2013-04-10 | Respivert Limited | 1-Pyrazolyl-3-(4-((2-anilinopyrimidin-4-yl)oxy)napththalen-1-yl)ureas as p38 MAP kinase inhibitors |
| KR20140105459A (ko) * | 2011-12-09 | 2014-09-01 | 키에시 파르마슈티시 엣스. 피. 에이. | 키나아제 억제제 |
| DK2788349T3 (en) * | 2011-12-09 | 2017-01-30 | Chiesi Farm Spa | kinase inhibitors |
| WO2014015056A2 (en) * | 2012-07-17 | 2014-01-23 | Washington University | Anti-mucus drugs and uses therefor |
| GB201214750D0 (en) | 2012-08-17 | 2012-10-03 | Respivert Ltd | Compounds |
| US20150225373A1 (en) | 2012-08-29 | 2015-08-13 | Respivert Limited | Kinase inhibitors |
| US20150210722A1 (en) | 2012-08-29 | 2015-07-30 | Respivert Limited | Kinase inhibitors |
| EP2890701B1 (en) | 2012-08-29 | 2017-03-29 | Respivert Limited | Kinase inhibitors |
| GB201215357D0 (en) | 2012-08-29 | 2012-10-10 | Respivert Ltd | Compounds |
| WO2014076484A1 (en) | 2012-11-16 | 2014-05-22 | Respivert Limited | Kinase inhibitors |
| EP2970190A1 (en) | 2013-03-14 | 2016-01-20 | Respivert Limited | Kinase inhibitors |
| US9771353B2 (en) | 2013-04-02 | 2017-09-26 | Topivert Pharma Limited | Kinase inhibitors based upon N-alkyl pyrazoles |
| KR102283876B1 (ko) | 2013-04-02 | 2021-07-29 | 옥슬러 액퀴지션즈 리미티드 | 키나제 저해제로서 유용한 우레아 유도체 |
| WO2015035223A1 (en) | 2013-09-09 | 2015-03-12 | Peloton Therapeutics, Inc. | Aryl ethers and uses thereof |
| GB201320729D0 (en) | 2013-11-25 | 2014-01-08 | Cancer Rec Tech Ltd | Therapeutic compounds and their use |
| GB201320732D0 (en) | 2013-11-25 | 2014-01-08 | Cancer Rec Tech Ltd | Methods of chemical synthesis |
| EP3083604A1 (en) | 2013-12-20 | 2016-10-26 | Respivert Limited | Urea derivatives useful as kinase inhibitors |
| ES2677595T3 (es) | 2014-02-14 | 2018-08-03 | Respivert Limited | Compuestos heterocíclicos aromáticos como compuestos antiinflamatorios |
| MA40774A (fr) | 2014-10-01 | 2017-08-08 | Respivert Ltd | Dérivés de diaryle-urée en tant qu'inhibiteurs de kinase p38 |
| US10807948B2 (en) | 2015-03-11 | 2020-10-20 | Peloton Therapeutics, Inc. | Aromatic compounds and uses thereof |
| WO2016145045A1 (en) | 2015-03-11 | 2016-09-15 | Peloton Therapeutics, Inc. | Compositions for use in treating glioblastoma |
| WO2016144826A1 (en) | 2015-03-11 | 2016-09-15 | Peloton Therapeutics, Inc. | Substituted pyridines and uses thereof |
| US10278942B2 (en) | 2015-03-11 | 2019-05-07 | Peloton Therapeutics, Inc. | Compositions for use in treating pulmonary arterial hypertension |
| WO2016168510A1 (en) | 2015-04-17 | 2016-10-20 | Peloton Therapeutics, Inc. | Combination therapy of a hif-2-alpha inhibitor and an immunotherapeutic agent and uses thereof |
| CN108290139B (zh) | 2015-10-01 | 2021-12-31 | 孟山都技术公司 | 卤代硝基芳香族化合物的催化氢化方法 |
| CA3015978A1 (en) | 2016-04-06 | 2017-10-12 | Topivert Pharma Limited | Kinase inhibitors |
| US11407771B2 (en) | 2018-05-30 | 2022-08-09 | Washington University | Mitogen-activated protein kinase inhibitors, methods of making, and methods of use thereof |
| AU2019351494B2 (en) * | 2018-09-29 | 2025-03-13 | Jiangsu Yahong Meditech Co., Ltd. | Nitroxoline prodrug and use thereof |
| WO2020113094A1 (en) | 2018-11-30 | 2020-06-04 | Nuvation Bio Inc. | Pyrrole and pyrazole compounds and methods of use thereof |
| KR20220038696A (ko) * | 2019-07-19 | 2022-03-29 | 아나제네시스 바이오테크놀로지스 에스.에이.에스. | 폴리방향족 우레아 유도체 및 근육 질환 치료에서의 이들의 용도 |
| EP4029501A1 (en) | 2021-01-19 | 2022-07-20 | Anagenesis Biotechnologies | Combination of polyaromatic urea derivatives and glucocorticoid or hdac inhibitor for the treatment of diseases or conditions associated with muscle cells and/or satellite cells |
Family Cites Families (18)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US20080300281A1 (en) * | 1997-12-22 | 2008-12-04 | Jacques Dumas | Inhibition of p38 Kinase Activity Using Aryl and Heteroaryl Substituted Heterocyclic Ureas |
| UA73492C2 (en) | 1999-01-19 | 2005-08-15 | Aromatic heterocyclic compounds as antiinflammatory agents | |
| CN101010315A (zh) | 2004-04-30 | 2007-08-01 | 拜耳制药公司 | 用于治疗癌症的取代的吡唑基脲衍生物 |
| PL1778686T3 (pl) | 2004-08-12 | 2009-04-30 | Pfizer | Pochodne triazolopirydynylosulfanylowe jako inhibitory kinazy MAP P38 |
| GB0500435D0 (en) | 2005-01-10 | 2005-02-16 | Novartis Ag | Organic compounds |
| DE102005015253A1 (de) * | 2005-04-04 | 2006-10-05 | Merck Patent Gmbh | Pyrazolderivate |
| DE102005037499A1 (de) * | 2005-08-09 | 2007-02-15 | Merck Patent Gmbh | Pyrazolderivate |
| JP2009518298A (ja) * | 2005-12-01 | 2009-05-07 | バイエル ヘルスケア リミティド ライアビリティ カンパニー | 癌治療に有用な尿素化合物 |
| CA2637172A1 (en) | 2006-01-27 | 2007-08-09 | Array Biopharma Inc. | Pyridin-2-amine derivatives and their use as glucokinase activators |
| CA2627692A1 (en) | 2006-01-30 | 2007-08-02 | Irm Llc | Spiro imidazole derivatives as ppar modulators |
| US20070194939A1 (en) | 2006-02-21 | 2007-08-23 | Alvarez Frank D | Healthcare facilities operation |
| GB0818033D0 (en) * | 2008-10-02 | 2008-11-05 | Respivert Ltd | Novel compound |
| MY159230A (en) * | 2008-10-02 | 2016-12-30 | Respivert Ltd | P38 map kinase inhibitors |
| JP5670912B2 (ja) * | 2008-12-11 | 2015-02-18 | レスピバート・リミテツド | ｐ３８ＭＡＰキナーゼ阻害剤 |
| GB0905955D0 (en) * | 2009-04-06 | 2009-05-20 | Respivert Ltd | Novel compounds |
| GB201005589D0 (en) | 2010-04-01 | 2010-05-19 | Respivert Ltd | Novel compounds |
| WO2011124923A2 (en) | 2010-04-08 | 2011-10-13 | Respivert Limited | Novel compounds |
| EP2556068B1 (en) | 2010-04-08 | 2019-01-23 | Respivert Limited | P38 map kinase inhibitors |
-
2010
- 2010-04-01 GB GBGB1005589.5A patent/GB201005589D0/en not_active Ceased
-
2011
- 2011-04-01 JP JP2013501951A patent/JP5902668B2/ja active Active
- 2011-04-01 EP EP11713510.3A patent/EP2556065B1/en active Active
- 2011-04-01 US US13/638,640 patent/US20130029990A1/en not_active Abandoned
- 2011-04-01 WO PCT/GB2011/050668 patent/WO2011121366A1/en not_active Ceased
- 2011-04-01 ES ES11713510.3T patent/ES2532764T3/es active Active
-
2016
- 2016-01-18 US US14/997,820 patent/US9771354B2/en active Active
-
2017
- 2017-08-29 US US15/689,075 patent/US10000471B2/en active Active
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