JP2007527901A5 - - Google Patents
Download PDFInfo
- Publication number
- JP2007527901A5 JP2007527901A5 JP2007502343A JP2007502343A JP2007527901A5 JP 2007527901 A5 JP2007527901 A5 JP 2007527901A5 JP 2007502343 A JP2007502343 A JP 2007502343A JP 2007502343 A JP2007502343 A JP 2007502343A JP 2007527901 A5 JP2007527901 A5 JP 2007527901A5
- Authority
- JP
- Japan
- Prior art keywords
- alkyl
- hydrogen
- substituted
- hydroxy
- alkoxy
- 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.)
- Withdrawn
Links
- 229910052739 hydrogen Inorganic materials 0.000 claims 88
- 239000001257 hydrogen Substances 0.000 claims 88
- 229910052757 nitrogen Inorganic materials 0.000 claims 74
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 claims 52
- 125000004433 nitrogen atom Chemical group N* 0.000 claims 48
- 125000004435 hydrogen atom Chemical group [H]* 0.000 claims 44
- -1 2,2-difluoroethoxy Chemical group 0.000 claims 33
- 125000000623 heterocyclic group Chemical group 0.000 claims 32
- 150000001875 compounds Chemical class 0.000 claims 28
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims 26
- NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical compound [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 claims 26
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 claims 26
- 125000005842 heteroatom Chemical group 0.000 claims 26
- 229910052760 oxygen Inorganic materials 0.000 claims 26
- 239000001301 oxygen Substances 0.000 claims 26
- 229910052717 sulfur Inorganic materials 0.000 claims 26
- 239000011593 sulfur Substances 0.000 claims 26
- 150000003839 salts Chemical class 0.000 claims 19
- 150000002431 hydrogen Chemical class 0.000 claims 18
- 125000002911 monocyclic heterocycle group Chemical group 0.000 claims 18
- 125000004076 pyridyl group Chemical group 0.000 claims 16
- 150000001204 N-oxides Chemical class 0.000 claims 14
- 125000002757 morpholinyl group Chemical group 0.000 claims 12
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 claims 11
- 101100177165 Caenorhabditis elegans har-1 gene Proteins 0.000 claims 10
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims 10
- 125000002950 monocyclic group Chemical group 0.000 claims 9
- 125000003118 aryl group Chemical group 0.000 claims 8
- 125000002887 hydroxy group Chemical group [H]O* 0.000 claims 8
- 125000001072 heteroaryl group Chemical group 0.000 claims 7
- HBAQYPYDRFILMT-UHFFFAOYSA-N 8-[3-(1-cyclopropylpyrazol-4-yl)-1H-pyrazolo[4,3-d]pyrimidin-5-yl]-3-methyl-3,8-diazabicyclo[3.2.1]octan-2-one Chemical class C1(CC1)N1N=CC(=C1)C1=NNC2=C1N=C(N=C2)N1C2C(N(CC1CC2)C)=O HBAQYPYDRFILMT-UHFFFAOYSA-N 0.000 claims 6
- 101100070530 Neurospora crassa (strain ATCC 24698 / 74-OR23-1A / CBS 708.71 / DSM 1257 / FGSC 987) het-6 gene Proteins 0.000 claims 6
- 125000000217 alkyl group Chemical group 0.000 claims 5
- 125000004397 aminosulfonyl group Chemical group NS(=O)(=O)* 0.000 claims 5
- 125000002619 bicyclic group Chemical group 0.000 claims 5
- KCNKJCHARANTIP-SNAWJCMRSA-N allyl-{4-[3-(4-bromo-phenyl)-benzofuran-6-yloxy]-but-2-enyl}-methyl-amine Chemical compound C=1OC2=CC(OC/C=C/CN(CC=C)C)=CC=C2C=1C1=CC=C(Br)C=C1 KCNKJCHARANTIP-SNAWJCMRSA-N 0.000 claims 4
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 claims 4
- 125000001449 isopropyl group Chemical group [H]C([H])([H])C([H])(*)C([H])([H])[H] 0.000 claims 4
- 125000000956 methoxy group Chemical group [H]C([H])([H])O* 0.000 claims 4
- 125000000719 pyrrolidinyl group Chemical group 0.000 claims 4
- 125000001559 cyclopropyl group Chemical group [H]C1([H])C([H])([H])C1([H])* 0.000 claims 3
- 239000008194 pharmaceutical composition Substances 0.000 claims 3
- 229920006395 saturated elastomer Polymers 0.000 claims 3
- 125000004200 2-methoxyethyl group Chemical group [H]C([H])([H])OC([H])([H])C([H])([H])* 0.000 claims 2
- 125000003545 alkoxy group Chemical group 0.000 claims 2
- 125000001995 cyclobutyl group Chemical group [H]C1([H])C([H])([H])C([H])(*)C1([H])[H] 0.000 claims 2
- 125000004786 difluoromethoxy group Chemical group [H]C(F)(F)O* 0.000 claims 2
- 238000004519 manufacturing process Methods 0.000 claims 2
- 125000002943 quinolinyl group Chemical group N1=C(C=CC2=CC=CC=C12)* 0.000 claims 2
- 208000023504 respiratory system disease Diseases 0.000 claims 2
- YMNZIHGNPNDDNZ-UHFFFAOYSA-N 2-[4-[4-(2-hydroxy-8,9-dimethoxy-1,2,3,4,4a,10b-hexahydrophenanthridin-6-yl)benzoyl]piperazin-1-yl]-1-morpholin-4-ylethanone Chemical compound C1=2C=C(OC)C(OC)=CC=2C2CC(O)CCC2N=C1C(C=C1)=CC=C1C(=O)N(CC1)CCN1CC(=O)N1CCOCC1 YMNZIHGNPNDDNZ-UHFFFAOYSA-N 0.000 claims 1
- WECVSESKDKJTAC-UHFFFAOYSA-N 2-[4-[4-(2-hydroxy-8,9-dimethoxy-1,2,3,4,4a,10b-hexahydrophenanthridin-6-yl)benzoyl]piperazin-1-yl]-1-pyrrolidin-1-ylethanone Chemical compound C1=2C=C(OC)C(OC)=CC=2C2CC(O)CCC2N=C1C(C=C1)=CC=C1C(=O)N(CC1)CCN1CC(=O)N1CCCC1 WECVSESKDKJTAC-UHFFFAOYSA-N 0.000 claims 1
- PUEUAIGMUIWFSO-UHFFFAOYSA-N 2-[4-[4-(2-hydroxy-8,9-dimethoxy-1,2,3,4,4a,10b-hexahydrophenanthridin-6-yl)benzoyl]piperazin-1-yl]-n-pyridin-2-ylacetamide Chemical compound C1=2C=C(OC)C(OC)=CC=2C2CC(O)CCC2N=C1C(C=C1)=CC=C1C(=O)N(CC1)CCN1CC(=O)NC1=CC=CC=N1 PUEUAIGMUIWFSO-UHFFFAOYSA-N 0.000 claims 1
- HNFUFRMJVMPCPK-UHFFFAOYSA-N 2-[4-[4-[9-(difluoromethoxy)-2-hydroxy-8-methoxy-1,2,3,4,4a,10b-hexahydrophenanthridin-6-yl]benzoyl]piperazin-1-yl]-1-morpholin-4-ylethanone Chemical compound N=1C2CCC(O)CC2C=2C=C(OC(F)F)C(OC)=CC=2C=1C(C=C1)=CC=C1C(=O)N(CC1)CCN1CC(=O)N1CCOCC1 HNFUFRMJVMPCPK-UHFFFAOYSA-N 0.000 claims 1
- LFHYTFLZVJJDAQ-UHFFFAOYSA-N 2-[4-[4-[9-(difluoromethoxy)-2-hydroxy-8-methoxy-1,2,3,4,4a,10b-hexahydrophenanthridin-6-yl]benzoyl]piperazin-1-yl]-n,n-dimethylacetamide Chemical compound N=1C2CCC(O)CC2C=2C=C(OC(F)F)C(OC)=CC=2C=1C(C=C1)=CC=C1C(=O)N1CCN(CC(=O)N(C)C)CC1 LFHYTFLZVJJDAQ-UHFFFAOYSA-N 0.000 claims 1
- 125000003762 3,4-dimethoxyphenyl group Chemical group [H]C1=C([H])C(OC([H])([H])[H])=C(OC([H])([H])[H])C([H])=C1* 0.000 claims 1
- XVKSYVWQNHHKQV-KJXAQDMKSA-N 3-[(2r,4ar,10br)-9-ethoxy-2-hydroxy-8-methoxy-1,2,3,4,4a,10b-hexahydrophenanthridin-6-yl]-n-cyclobutylbenzamide Chemical compound N([C@@H]1CC[C@@H](O)C[C@@H]1C=1C=C(C(=CC=11)OC)OCC)=C1C(C=1)=CC=CC=1C(=O)NC1CCC1 XVKSYVWQNHHKQV-KJXAQDMKSA-N 0.000 claims 1
- UKPIEGKUSRBBTE-SYYKKAFVSA-N 3-[(2r,4ar,10br)-9-ethoxy-2-hydroxy-8-methoxy-1,2,3,4,4a,10b-hexahydrophenanthridin-6-yl]-n-cyclopropylbenzamide Chemical compound N([C@@H]1CC[C@@H](O)C[C@@H]1C=1C=C(C(=CC=11)OC)OCC)=C1C(C=1)=CC=CC=1C(=O)NC1CC1 UKPIEGKUSRBBTE-SYYKKAFVSA-N 0.000 claims 1
- XUIVMRIGLWWQOM-UHFFFAOYSA-N 4-(2-hydroxy-8,9-dimethoxy-1,2,3,4,4a,10b-hexahydrophenanthridin-6-yl)-n,n-dimethylbenzamide Chemical compound C1=2C=C(OC)C(OC)=CC=2C2CC(O)CCC2N=C1C1=CC=C(C(=O)N(C)C)C=C1 XUIVMRIGLWWQOM-UHFFFAOYSA-N 0.000 claims 1
- UZXMBYVZKPCTEZ-UHFFFAOYSA-N 4-(2-hydroxy-8,9-dimethoxy-1,2,3,4,4a,10b-hexahydrophenanthridin-6-yl)-n-(2-morpholin-4-ylethyl)benzamide Chemical compound C1=2C=C(OC)C(OC)=CC=2C2CC(O)CCC2N=C1C(C=C1)=CC=C1C(=O)NCCN1CCOCC1 UZXMBYVZKPCTEZ-UHFFFAOYSA-N 0.000 claims 1
- YACLYEFFJHPPGX-UHFFFAOYSA-N 4-(2-hydroxy-8,9-dimethoxy-1,2,3,4,4a,10b-hexahydrophenanthridin-6-yl)-n-(2-pyridin-3-ylethyl)benzamide Chemical compound C1=2C=C(OC)C(OC)=CC=2C2CC(O)CCC2N=C1C(C=C1)=CC=C1C(=O)NCCC1=CC=CN=C1 YACLYEFFJHPPGX-UHFFFAOYSA-N 0.000 claims 1
- RCIFXRMESZRVKK-UHFFFAOYSA-N 4-(2-hydroxy-8,9-dimethoxy-1,2,3,4,4a,10b-hexahydrophenanthridin-6-yl)-n-(2-pyridin-4-ylethyl)benzamide Chemical compound C1=2C=C(OC)C(OC)=CC=2C2CC(O)CCC2N=C1C(C=C1)=CC=C1C(=O)NCCC1=CC=NC=C1 RCIFXRMESZRVKK-UHFFFAOYSA-N 0.000 claims 1
- RKRBIYOSFUFIEF-UHFFFAOYSA-N 4-(2-hydroxy-8,9-dimethoxy-1,2,3,4,4a,10b-hexahydrophenanthridin-6-yl)-n-(3-morpholin-4-ylpropyl)benzamide Chemical compound C1=2C=C(OC)C(OC)=CC=2C2CC(O)CCC2N=C1C(C=C1)=CC=C1C(=O)NCCCN1CCOCC1 RKRBIYOSFUFIEF-UHFFFAOYSA-N 0.000 claims 1
- JZYDHQRZQOEWIN-UHFFFAOYSA-N 4-(2-hydroxy-8,9-dimethoxy-1,2,3,4,4a,10b-hexahydrophenanthridin-6-yl)-n-(4-methylpiperazin-1-yl)benzamide Chemical compound C1=2C=C(OC)C(OC)=CC=2C2CC(O)CCC2N=C1C(C=C1)=CC=C1C(=O)NN1CCN(C)CC1 JZYDHQRZQOEWIN-UHFFFAOYSA-N 0.000 claims 1
- NVFYVOYKTAOECP-YVWKXTFCSA-N 4-[(2r,4ar,10br)-9-(difluoromethoxy)-2-hydroxy-8-methoxy-1,2,3,4,4a,10b-hexahydrophenanthridin-6-yl]-n-cyclopropylbenzamide Chemical compound C=1([C@H]2C[C@H](O)CC[C@H]2N=2)C=C(OC(F)F)C(OC)=CC=1C=2C(C=C1)=CC=C1C(=O)NC1CC1 NVFYVOYKTAOECP-YVWKXTFCSA-N 0.000 claims 1
- MKHFCVWOMJXTEO-GZGNHOFSSA-N 4-[(2r,4ar,10br)-9-ethoxy-2-hydroxy-8-methoxy-1,2,3,4,4a,10b-hexahydrophenanthridin-6-yl]-n,n-di(propan-2-yl)benzamide Chemical compound N([C@@H]1CC[C@@H](O)C[C@@H]1C=1C=C(C(=CC=11)OC)OCC)=C1C1=CC=C(C(=O)N(C(C)C)C(C)C)C=C1 MKHFCVWOMJXTEO-GZGNHOFSSA-N 0.000 claims 1
- OPVBRSGHFDVMEI-SYYKKAFVSA-N 4-[(2r,4ar,10br)-9-ethoxy-2-hydroxy-8-methoxy-1,2,3,4,4a,10b-hexahydrophenanthridin-6-yl]-n-cyclopropylbenzamide Chemical compound N([C@@H]1CC[C@@H](O)C[C@@H]1C=1C=C(C(=CC=11)OC)OCC)=C1C(C=C1)=CC=C1C(=O)NC1CC1 OPVBRSGHFDVMEI-SYYKKAFVSA-N 0.000 claims 1
- KFVCBHFHQZURCC-VCOUNFBDSA-N 4-[(2s,4as,10bs)-2-hydroxy-8,9-dimethoxy-1,2,3,4,4a,10b-hexahydrophenanthridin-6-yl]-n-(2,6-dimethoxypyridin-3-yl)benzamide Chemical compound COC1=NC(OC)=CC=C1NC(=O)C1=CC=C(C=2C3=CC(OC)=C(OC)C=C3[C@@H]3C[C@@H](O)CC[C@@H]3N=2)C=C1 KFVCBHFHQZURCC-VCOUNFBDSA-N 0.000 claims 1
- KAPRORPOJQQGSS-UHFFFAOYSA-N 4-[9-(difluoromethoxy)-2-hydroxy-8-methoxy-1,2,3,4,4a,10b-hexahydrophenanthridin-6-yl]-n,n-bis(2-methoxyethyl)benzamide Chemical compound C1=CC(C(=O)N(CCOC)CCOC)=CC=C1C(C1=CC(OC)=C(OC(F)F)C=C11)=NC2C1CC(O)CC2 KAPRORPOJQQGSS-UHFFFAOYSA-N 0.000 claims 1
- WZWASYKSBHYSMD-UHFFFAOYSA-N 4-[9-(difluoromethoxy)-2-hydroxy-8-methoxy-1,2,3,4,4a,10b-hexahydrophenanthridin-6-yl]-n,n-dimethylbenzamide Chemical compound N=1C2CCC(O)CC2C=2C=C(OC(F)F)C(OC)=CC=2C=1C1=CC=C(C(=O)N(C)C)C=C1 WZWASYKSBHYSMD-UHFFFAOYSA-N 0.000 claims 1
- SIHYCKIFAZZFAY-UHFFFAOYSA-N [4-(2-hydroxy-8,9-dimethoxy-1,2,3,4,4a,10b-hexahydrophenanthridin-6-yl)phenyl]-(4-pyridin-4-ylpiperazin-1-yl)methanone Chemical compound C1=2C=C(OC)C(OC)=CC=2C2CC(O)CCC2N=C1C(C=C1)=CC=C1C(=O)N(CC1)CCN1C1=CC=NC=C1 SIHYCKIFAZZFAY-UHFFFAOYSA-N 0.000 claims 1
- KPYRBBMXZVVEEI-UHFFFAOYSA-N [4-[9-(difluoromethoxy)-2-hydroxy-8-methoxy-1,2,3,4,4a,10b-hexahydrophenanthridin-6-yl]phenyl]-(4-pyridin-4-ylpiperazin-1-yl)methanone Chemical compound N=1C2CCC(O)CC2C=2C=C(OC(F)F)C(OC)=CC=2C=1C(C=C1)=CC=C1C(=O)N(CC1)CCN1C1=CC=NC=C1 KPYRBBMXZVVEEI-UHFFFAOYSA-N 0.000 claims 1
- JBWUXNPUPYMVSG-UHFFFAOYSA-N [4-[9-(difluoromethoxy)-2-hydroxy-8-methoxy-1,2,3,4,4a,10b-hexahydrophenanthridin-6-yl]phenyl]-[4-(2-morpholin-4-ylethyl)piperazin-1-yl]methanone Chemical compound N=1C2CCC(O)CC2C=2C=C(OC(F)F)C(OC)=CC=2C=1C(C=C1)=CC=C1C(=O)N(CC1)CCN1CCN1CCOCC1 JBWUXNPUPYMVSG-UHFFFAOYSA-N 0.000 claims 1
- UOKFXGYLDDAFLR-UHFFFAOYSA-N [4-[9-(difluoromethoxy)-2-hydroxy-8-methoxy-1,2,3,4,4a,10b-hexahydrophenanthridin-6-yl]phenyl]-[4-[2-(dimethylamino)ethyl]piperazin-1-yl]methanone Chemical compound N=1C2CCC(O)CC2C=2C=C(OC(F)F)C(OC)=CC=2C=1C(C=C1)=CC=C1C(=O)N1CCN(CCN(C)C)CC1 UOKFXGYLDDAFLR-UHFFFAOYSA-N 0.000 claims 1
- 125000002777 acetyl group Chemical group [H]C([H])([H])C(*)=O 0.000 claims 1
- SYGWYBOJXOGMRU-UHFFFAOYSA-N chembl233051 Chemical group C1=CC=C2C3=CC(C(N(CCN(C)C)C4=O)=O)=C5C4=CC=CC5=C3SC2=C1 SYGWYBOJXOGMRU-UHFFFAOYSA-N 0.000 claims 1
- 201000010099 disease Diseases 0.000 claims 1
- 208000037265 diseases, disorders, signs and symptoms Diseases 0.000 claims 1
- 239000003937 drug carrier Substances 0.000 claims 1
- 229910052731 fluorine Inorganic materials 0.000 claims 1
- 239000011737 fluorine Substances 0.000 claims 1
- 229910052736 halogen Inorganic materials 0.000 claims 1
- 150000002367 halogens Chemical group 0.000 claims 1
- 230000001404 mediated effect Effects 0.000 claims 1
- 125000004573 morpholin-4-yl group Chemical group N1(CCOCC1)* 0.000 claims 1
- ZEPPGNZXTBBYJH-UHFFFAOYSA-N n'-[4-(2-hydroxy-8,9-dimethoxy-1,2,3,4,4a,10b-hexahydrophenanthridin-6-yl)benzoyl]morpholine-4-carbohydrazide Chemical compound C1=2C=C(OC)C(OC)=CC=2C2CC(O)CCC2N=C1C(C=C1)=CC=C1C(=O)NNC(=O)N1CCOCC1 ZEPPGNZXTBBYJH-UHFFFAOYSA-N 0.000 claims 1
- KFVCBHFHQZURCC-UHFFFAOYSA-N n-(2,6-dimethoxypyridin-3-yl)-4-(2-hydroxy-8,9-dimethoxy-1,2,3,4,4a,10b-hexahydrophenanthridin-6-yl)benzamide Chemical compound COC1=NC(OC)=CC=C1NC(=O)C1=CC=C(C=2C3=CC(OC)=C(OC)C=C3C3CC(O)CCC3N=2)C=C1 KFVCBHFHQZURCC-UHFFFAOYSA-N 0.000 claims 1
- NVFYVOYKTAOECP-UHFFFAOYSA-N n-cyclopropyl-4-[9-(difluoromethoxy)-2-hydroxy-8-methoxy-1,2,3,4,4a,10b-hexahydrophenanthridin-6-yl]benzamide Chemical compound N=1C2CCC(O)CC2C=2C=C(OC(F)F)C(OC)=CC=2C=1C(C=C1)=CC=C1C(=O)NC1CC1 NVFYVOYKTAOECP-UHFFFAOYSA-N 0.000 claims 1
- 239000000546 pharmaceutical excipient Substances 0.000 claims 1
- 229940124531 pharmaceutical excipient Drugs 0.000 claims 1
- 208000017520 skin disease Diseases 0.000 claims 1
Applications Claiming Priority (3)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| EP04100990 | 2004-03-10 | ||
| EP04106677 | 2004-12-17 | ||
| PCT/EP2005/051054 WO2005087745A1 (en) | 2004-03-10 | 2005-03-09 | Novel amido-substituted hydroxy-6-phenylphenanthridines and their use as pde4 inhibitors |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| JP2007527901A JP2007527901A (ja) | 2007-10-04 |
| JP2007527901A5 true JP2007527901A5 (https=) | 2008-04-24 |
Family
ID=34965034
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP2007502343A Withdrawn JP2007527901A (ja) | 2004-03-10 | 2005-03-09 | アミド置換された新規のヒドロキシ−６−フェニルフェナントリジン及びｐｄｅ４インヒビターとしてのそれらの使用 |
Country Status (15)
| Country | Link |
|---|---|
| US (1) | US20070185149A1 (https=) |
| EP (1) | EP1725534A1 (https=) |
| JP (1) | JP2007527901A (https=) |
| KR (1) | KR20060130697A (https=) |
| CN (1) | CN1926113B (https=) |
| AR (1) | AR049324A1 (https=) |
| AU (1) | AU2005221832A1 (https=) |
| BR (1) | BRPI0508481A (https=) |
| CA (1) | CA2558391A1 (https=) |
| IL (1) | IL177496A0 (https=) |
| MX (1) | MXPA06009892A (https=) |
| NO (1) | NO20064415L (https=) |
| NZ (1) | NZ549254A (https=) |
| TW (1) | TW200600499A (https=) |
| WO (1) | WO2005087745A1 (https=) |
Families Citing this family (17)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JP4587294B2 (ja) | 2002-08-29 | 2010-11-24 | ニコメッド ゲゼルシャフト ミット ベシュレンクテル ハフツング | Ｐｄｅ４インヒビターとしての２−ヒドロキシ−６−フェニルフェナントリジン |
| ATE353217T1 (de) | 2002-08-29 | 2007-02-15 | Altana Pharma Ag | 3-hydroxy-6-phenylphenanthridine als pde-4 inhibitoren |
| GB0316915D0 (en) | 2003-07-18 | 2003-08-20 | Glaxo Group Ltd | Compounds |
| CA2556086C (en) | 2004-02-18 | 2014-04-01 | Altana Pharma Ag | Novel guanidinyl-substituted hydroxy-6-phenylphenenthridines as effective phosphodiesterase (pde) 4 inhibitors |
| AR049419A1 (es) * | 2004-03-03 | 2006-08-02 | Altana Pharma Ag | Hidroxi-6-fenilfenantridinas sustituidas con heterociclilo |
| PL2589599T4 (pl) | 2004-03-03 | 2015-06-30 | Takeda Gmbh | Nowe hydroksy-6-heteroarylofenantrydyny i ich zastosowanie jako inhibitorów PDE4 |
| EP1791847A2 (en) | 2004-09-08 | 2007-06-06 | Altana Pharma AG | Novel 3-thia-10-aza-phenanthrene derivatives |
| ATE508130T1 (de) | 2004-09-08 | 2011-05-15 | Nycomed Gmbh | 3-oxa-10-aza-phenanthrene als pde4- oder pde3/4- inhibitoren |
| PL1856093T3 (pl) * | 2005-03-02 | 2010-05-31 | Takeda Gmbh | Chlorowodorek (2R,4aR,10bR)-6-(2,6-dimetoksy-pirydyn-3-ylo)-9-etoksy-8-metoksy-1,2,3,4,4a,10b-heksahydrofenantrydyn-2-olu |
| GB0601951D0 (en) | 2006-01-31 | 2006-03-15 | Novartis Ag | Organic compounds |
| JP2010508315A (ja) | 2006-10-30 | 2010-03-18 | ノバルティス アーゲー | 抗炎症剤としてのヘテロ環式化合物 |
| ES2460897T3 (es) | 2007-10-04 | 2014-05-14 | F. Hoffmann-La Roche Ag | Derivados de ciclopropil aril amida y usos de los mismos |
| AU2009203693B2 (en) | 2008-01-11 | 2012-06-07 | Novartis Ag | Pyrimidines as kinase inhibitors |
| EP2406210A1 (en) * | 2009-03-09 | 2012-01-18 | Basf Se | Process for preparing substituted 2-nitrobiphenyls |
| UY33597A (es) | 2010-09-09 | 2012-04-30 | Irm Llc | Compuestos y composiciones como inhibidores de la trk |
| WO2012034095A1 (en) | 2010-09-09 | 2012-03-15 | Irm Llc | Compounds and compositions as trk inhibitors |
| MA34969B1 (fr) | 2011-02-25 | 2014-03-01 | Irm Llc | Composes et compositions en tant qu inibiteurs de trk |
Family Cites Families (25)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| DE69231395T3 (de) * | 1991-09-20 | 2005-07-21 | Glaxo Group Ltd., Greenford | Neue medizinische Indikation für Tachykinin-Antagonisten |
| BR9707233A (pt) * | 1996-01-31 | 1999-07-20 | Byk Gulden Lomberg Chem Fab | Fenantridinas |
| US6127378A (en) * | 1996-03-26 | 2000-10-03 | Byk Gulden Lomberg Chemische Fabrik Gmbh | Phenanthridines substituted in the 6 position |
| PL189641B1 (pl) * | 1996-11-11 | 2005-09-30 | Altana Pharma Ag | Benzonaftyrydyny, środki farmaceutyczne je zawierające oraz zastosowanie benzonaftyrydyn |
| WO1999005112A1 (en) * | 1997-07-25 | 1999-02-04 | Byk Gulden Lomberg Chemische Fabrik Gmbh | Substituted 6-alkylphenanthridines |
| JP2001510827A (ja) * | 1997-07-25 | 2001-08-07 | ビイク グルデン ロンベルク ヒエーミツシエ フアブリーク ゲゼルシヤフト ミツト ベシユレンクテル ハフツング | 置換６−フェニルフェナントリジン |
| PT998460E (pt) * | 1997-07-25 | 2004-07-30 | Altana Pharma Ag | Novos derivados de tetrazole |
| DK1075477T3 (da) * | 1998-05-05 | 2003-06-30 | Altana Pharma Ag | Nye benzonaphthyridin-N-oxider |
| ES2241571T3 (es) * | 1999-01-15 | 2005-11-01 | Altana Pharma Ag | N-oxidos de fenantrinida con actividad inhividora de pde-iv. |
| DE60020079T2 (de) * | 1999-01-15 | 2006-01-19 | Altana Pharma Ag | Phenanthridin-N-oxide mit PDE-IV-hemmender Wirkung |
| TR200501553T2 (tr) * | 1999-01-15 | 2005-06-21 | Altana Pharma Ag | PDE-IV inhibe edici aktivitesi olan fenilfenantridinler |
| ES2236288T3 (es) * | 2000-07-14 | 2005-07-16 | Altana Pharma Ag | 6-heteroarilfenantridinas. |
| US6936622B2 (en) * | 2001-02-21 | 2005-08-30 | Altana Pharma Ag | 6-phenylbenzonaphthyridines |
| CA2495597A1 (en) * | 2002-08-17 | 2004-03-04 | Altana Pharma Ag | Novel phenanthridines |
| JP4587294B2 (ja) * | 2002-08-29 | 2010-11-24 | ニコメッド ゲゼルシャフト ミット ベシュレンクテル ハフツング | Ｐｄｅ４インヒビターとしての２−ヒドロキシ−６−フェニルフェナントリジン |
| ATE353217T1 (de) * | 2002-08-29 | 2007-02-15 | Altana Pharma Ag | 3-hydroxy-6-phenylphenanthridine als pde-4 inhibitoren |
| US20060110819A1 (en) * | 2002-09-30 | 2006-05-25 | Lomas Lee O | Apparatus and method for expression and capture of biomolecules and complexes on adsorbent surfaces |
| AR049419A1 (es) * | 2004-03-03 | 2006-08-02 | Altana Pharma Ag | Hidroxi-6-fenilfenantridinas sustituidas con heterociclilo |
| AU2005220034A1 (en) * | 2004-03-09 | 2005-09-15 | Nycomed Gmbh | Novel isoamido-substituted hydroxy-6-phenylphenanthridines and their use as PDE4 inhibitors |
| CA2558390A1 (en) * | 2004-03-10 | 2005-09-22 | Altana Pharma Ag | Novel thio-containing hydroxy-6-phenylphenanthridines and their use as pde4 inhibitors |
| WO2005085203A1 (en) * | 2004-03-10 | 2005-09-15 | Altana Pharma Ag | Novel difluoroethoxy-substituted hydroxy-6-phenylphenanthridines and their use as pde4 inhibitors |
| US20080119505A1 (en) * | 2005-02-01 | 2008-05-22 | Altana Pharma Ag | Novel 6-Pyridylphenanthridines |
| PL1856093T3 (pl) * | 2005-03-02 | 2010-05-31 | Takeda Gmbh | Chlorowodorek (2R,4aR,10bR)-6-(2,6-dimetoksy-pirydyn-3-ylo)-9-etoksy-8-metoksy-1,2,3,4,4a,10b-heksahydrofenantrydyn-2-olu |
| US20080167316A1 (en) * | 2005-03-02 | 2008-07-10 | Altana Pharma Ag | 6-Heteroaryl-1,2,3,4,4A, 10B-Hexahydrophenanthridines as Pde4-Inhibitors for the Treatment of Inflammatory Disorders |
| CA2599368A1 (en) * | 2005-03-09 | 2006-09-14 | Nycomed Gmbh | Amido-substituted 6-phenylphenanthridines |
-
2005
- 2005-03-09 EP EP05740073A patent/EP1725534A1/en not_active Withdrawn
- 2005-03-09 AU AU2005221832A patent/AU2005221832A1/en not_active Abandoned
- 2005-03-09 BR BRPI0508481-4A patent/BRPI0508481A/pt not_active IP Right Cessation
- 2005-03-09 CN CN2005800068554A patent/CN1926113B/zh not_active Expired - Fee Related
- 2005-03-09 US US10/591,480 patent/US20070185149A1/en not_active Abandoned
- 2005-03-09 MX MXPA06009892A patent/MXPA06009892A/es not_active Application Discontinuation
- 2005-03-09 JP JP2007502343A patent/JP2007527901A/ja not_active Withdrawn
- 2005-03-09 CA CA002558391A patent/CA2558391A1/en not_active Abandoned
- 2005-03-09 NZ NZ549254A patent/NZ549254A/en unknown
- 2005-03-09 KR KR1020067020318A patent/KR20060130697A/ko not_active Ceased
- 2005-03-09 WO PCT/EP2005/051054 patent/WO2005087745A1/en not_active Ceased
- 2005-03-10 TW TW094107344A patent/TW200600499A/zh unknown
- 2005-03-11 AR ARP050100931A patent/AR049324A1/es unknown
-
2006
- 2006-08-15 IL IL177496A patent/IL177496A0/en unknown
- 2006-09-29 NO NO20064415A patent/NO20064415L/no not_active Application Discontinuation
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| JP2007527901A5 (https=) | ||
| CN102459223B (zh) | 5-吡啶-3-基-1，3-二氢-吲哚-2-酮衍生物及其作为醛固酮合成酶和/或cyp11b1调节剂的用途 | |
| DK2609091T3 (en) | Pharmaceutically active compounds as AXL inhibitors | |
| CN112351780A (zh) | Ptpn11的取代的杂环抑制剂 | |
| TW444013B (en) | Quinoline and quinazoline compounds useful in treating benign prostatic hyperplasia | |
| EP4051386A1 (en) | Small molecule degraders of helios and methods of use | |
| CN101622241B (zh) | 苯并咪唑化合物及其医药用途 | |
| JP2012525332A5 (https=) | ||
| JP2012510989A5 (https=) | ||
| JP2006520805A5 (https=) | ||
| BR112020025073A2 (pt) | moduladores de montagem de capsídeo da hepatite b | |
| CN107428690A (zh) | 可用于治疗癌症的突变idh1抑制剂 | |
| RU2015154987A (ru) | Гетероциклические производные | |
| JP2012502067A5 (https=) | ||
| AU2009224533A1 (en) | Azabicyclic carboxamide derivatives, preparation thereof and therapeutic use thereof | |
| RU2009148673A (ru) | Производные пиразинона и их применение для лечения легочных заболеваний | |
| TW200403223A (en) | Novel compounds | |
| JP2016501203A (ja) | インドールアミン２，３−ジオキシゲナーゼの阻害剤として有用な化合物 | |
| KR20140002709A (ko) | Ｆａａｈ 저해제 | |
| CA2901332A1 (en) | Trk-inhibiting compound | |
| JP2008540637A5 (https=) | ||
| AU2010310518A1 (en) | mGluR4 allosteric potentiators, compositions, and methods of treating neurological dysfunction | |
| RU2013154117A (ru) | Производные 1-фенил-2-пиридинилалкильных спиртов в качестве ингибиторов фосфодиэстеразы | |
| CN101312720A (zh) | 2-氨基苯甲酰胺衍生物 | |
| JP2023538608A (ja) | 線維症の処置のためのｔｌｒ９阻害剤阻害剤としての１ｈ－ピロロ［３，２－ｃ］ピリジンおよび１ｈ－ピロロ［２，３－ｃ］ピリジン誘導体 |