AU2007338409B2 - Cycloalkylamine substituted isoquinolone and isoquinolinone derivatives - Google Patents
Cycloalkylamine substituted isoquinolone and isoquinolinone derivatives Download PDFInfo
- Publication number
- AU2007338409B2 AU2007338409B2 AU2007338409A AU2007338409A AU2007338409B2 AU 2007338409 B2 AU2007338409 B2 AU 2007338409B2 AU 2007338409 A AU2007338409 A AU 2007338409A AU 2007338409 A AU2007338409 A AU 2007338409A AU 2007338409 B2 AU2007338409 B2 AU 2007338409B2
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- Australia
- Prior art keywords
- alkyl
- alkylene
- aryl
- heterocyclyl
- compound according
- 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.)
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- VDBNYAPERZTOOF-UHFFFAOYSA-N isoquinolin-1(2H)-one Chemical class C1=CC=C2C(=O)NC=CC2=C1 VDBNYAPERZTOOF-UHFFFAOYSA-N 0.000 title abstract description 23
- 150000001875 compounds Chemical class 0.000 claims abstract description 154
- -1 6-substituted isoquinoline Chemical class 0.000 claims abstract description 43
- 102000000568 rho-Associated Kinases Human genes 0.000 claims abstract description 17
- 108010041788 rho-Associated Kinases Proteins 0.000 claims abstract description 17
- 238000011282 treatment Methods 0.000 claims abstract description 16
- 230000026731 phosphorylation Effects 0.000 claims abstract description 7
- 238000006366 phosphorylation reaction Methods 0.000 claims abstract description 7
- 230000001404 mediated effect Effects 0.000 claims abstract description 6
- 102000011131 Myosin-Light-Chain Phosphatase Human genes 0.000 claims abstract description 5
- 108010037801 Myosin-Light-Chain Phosphatase Proteins 0.000 claims abstract description 5
- 125000004169 (C1-C6) alkyl group Chemical group 0.000 claims description 190
- 125000000217 alkyl group Chemical group 0.000 claims description 154
- 125000000623 heterocyclic group Chemical group 0.000 claims description 110
- 125000003118 aryl group Chemical group 0.000 claims description 97
- 229910052736 halogen Inorganic materials 0.000 claims description 86
- 150000002367 halogens Chemical class 0.000 claims description 85
- 238000000034 method Methods 0.000 claims description 61
- 150000003839 salts Chemical class 0.000 claims description 39
- 125000004178 (C1-C4) alkyl group Chemical group 0.000 claims description 32
- 125000000753 cycloalkyl group Chemical group 0.000 claims description 26
- 125000006552 (C3-C8) cycloalkyl group Chemical group 0.000 claims description 23
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 claims description 20
- 229910052739 hydrogen Inorganic materials 0.000 claims description 19
- 125000004433 nitrogen atom Chemical group N* 0.000 claims description 18
- 125000000882 C2-C6 alkenyl group Chemical group 0.000 claims description 17
- 125000000041 C6-C10 aryl group Chemical group 0.000 claims description 17
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 claims description 17
- 125000002947 alkylene group Chemical group 0.000 claims description 16
- 125000006297 carbonyl amino group Chemical group [H]N([*:2])C([*:1])=O 0.000 claims description 15
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims description 14
- 229910052757 nitrogen Inorganic materials 0.000 claims description 14
- 125000003342 alkenyl group Chemical group 0.000 claims description 13
- 206010020772 Hypertension Diseases 0.000 claims description 12
- 125000004432 carbon atom Chemical group C* 0.000 claims description 12
- 239000003814 drug Substances 0.000 claims description 12
- 201000010260 leiomyoma Diseases 0.000 claims description 12
- 208000030831 Peripheral arterial occlusive disease Diseases 0.000 claims description 10
- 206010012601 diabetes mellitus Diseases 0.000 claims description 10
- 125000001072 heteroaryl group Chemical group 0.000 claims description 10
- 239000001257 hydrogen Substances 0.000 claims description 10
- 206010028980 Neoplasm Diseases 0.000 claims description 9
- 125000003178 carboxy group Chemical group [H]OC(*)=O 0.000 claims description 9
- 125000001544 thienyl group Chemical group 0.000 claims description 9
- 229910052799 carbon Inorganic materials 0.000 claims description 8
- 125000001559 cyclopropyl group Chemical group [H]C1([H])C([H])([H])C1([H])* 0.000 claims description 8
- 125000001153 fluoro group Chemical group F* 0.000 claims description 8
- 125000004076 pyridyl group Chemical group 0.000 claims description 8
- 206010019280 Heart failures Diseases 0.000 claims description 7
- 208000037265 diseases, disorders, signs and symptoms Diseases 0.000 claims description 7
- 208000015181 infectious disease Diseases 0.000 claims description 7
- 125000000391 vinyl group Chemical group [H]C([*])=C([H])[H] 0.000 claims description 7
- 229920002554 vinyl polymer Polymers 0.000 claims description 7
- 125000004209 (C1-C8) alkyl group Chemical group 0.000 claims description 6
- 208000006545 Chronic Obstructive Pulmonary Disease Diseases 0.000 claims description 6
- 208000006011 Stroke Diseases 0.000 claims description 6
- 201000011510 cancer Diseases 0.000 claims description 6
- PAFZNILMFXTMIY-UHFFFAOYSA-N cyclohexylamine Chemical group NC1CCCCC1 PAFZNILMFXTMIY-UHFFFAOYSA-N 0.000 claims description 6
- 238000011161 development Methods 0.000 claims description 6
- 230000005764 inhibitory process Effects 0.000 claims description 6
- 210000004072 lung Anatomy 0.000 claims description 6
- 125000004430 oxygen atom Chemical group O* 0.000 claims description 6
- 230000002265 prevention Effects 0.000 claims description 6
- 125000003161 (C1-C6) alkylene group Chemical group 0.000 claims description 5
- 208000030507 AIDS Diseases 0.000 claims description 5
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- 206010002383 Angina Pectoris Diseases 0.000 claims description 5
- 201000001320 Atherosclerosis Diseases 0.000 claims description 5
- 241000894006 Bacteria Species 0.000 claims description 5
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- 208000006029 Cardiomegaly Diseases 0.000 claims description 5
- 206010008120 Cerebral ischaemia Diseases 0.000 claims description 5
- 208000010228 Erectile Dysfunction Diseases 0.000 claims description 5
- 206010061218 Inflammation Diseases 0.000 claims description 5
- 208000001145 Metabolic Syndrome Diseases 0.000 claims description 5
- 206010030043 Ocular hypertension Diseases 0.000 claims description 5
- 208000002193 Pain Diseases 0.000 claims description 5
- 208000001647 Renal Insufficiency Diseases 0.000 claims description 5
- 208000017442 Retinal disease Diseases 0.000 claims description 5
- 206010038923 Retinopathy Diseases 0.000 claims description 5
- 208000007536 Thrombosis Diseases 0.000 claims description 5
- 201000000690 abdominal obesity-metabolic syndrome Diseases 0.000 claims description 5
- 239000004480 active ingredient Substances 0.000 claims description 5
- 208000006673 asthma Diseases 0.000 claims description 5
- 206010008118 cerebral infarction Diseases 0.000 claims description 5
- 208000029078 coronary artery disease Diseases 0.000 claims description 5
- 230000004064 dysfunction Effects 0.000 claims description 5
- 230000002124 endocrine Effects 0.000 claims description 5
- 210000001035 gastrointestinal tract Anatomy 0.000 claims description 5
- 201000001881 impotence Diseases 0.000 claims description 5
- 230000004054 inflammatory process Effects 0.000 claims description 5
- 208000001286 intracranial vasospasm Diseases 0.000 claims description 5
- 208000017169 kidney disease Diseases 0.000 claims description 5
- 201000006370 kidney failure Diseases 0.000 claims description 5
- 230000004770 neurodegeneration Effects 0.000 claims description 5
- 208000002815 pulmonary hypertension Diseases 0.000 claims description 5
- 208000037803 restenosis Diseases 0.000 claims description 5
- 208000020431 spinal cord injury Diseases 0.000 claims description 5
- 125000006570 (C5-C6) heteroaryl group Chemical group 0.000 claims description 4
- 206010001052 Acute respiratory distress syndrome Diseases 0.000 claims description 4
- 206010003210 Arteriosclerosis Diseases 0.000 claims description 4
- 208000023275 Autoimmune disease Diseases 0.000 claims description 4
- 206010004446 Benign prostatic hyperplasia Diseases 0.000 claims description 4
- 208000020084 Bone disease Diseases 0.000 claims description 4
- 208000010412 Glaucoma Diseases 0.000 claims description 4
- 206010019663 Hepatic failure Diseases 0.000 claims description 4
- 206010020880 Hypertrophy Diseases 0.000 claims description 4
- 206010053159 Organ failure Diseases 0.000 claims description 4
- 208000005107 Premature Birth Diseases 0.000 claims description 4
- 206010036590 Premature baby Diseases 0.000 claims description 4
- 208000004403 Prostatic Hyperplasia Diseases 0.000 claims description 4
- 208000013616 Respiratory Distress Syndrome Diseases 0.000 claims description 4
- 206010040047 Sepsis Diseases 0.000 claims description 4
- 239000000654 additive Substances 0.000 claims description 4
- 208000011341 adult acute respiratory distress syndrome Diseases 0.000 claims description 4
- 201000000028 adult respiratory distress syndrome Diseases 0.000 claims description 4
- 208000011775 arteriosclerosis disease Diseases 0.000 claims description 4
- 210000004204 blood vessel Anatomy 0.000 claims description 4
- 208000035475 disorder Diseases 0.000 claims description 4
- 206010061989 glomerulosclerosis Diseases 0.000 claims description 4
- 208000023589 ischemic disease Diseases 0.000 claims description 4
- 230000000302 ischemic effect Effects 0.000 claims description 4
- 210000003734 kidney Anatomy 0.000 claims description 4
- 210000004185 liver Anatomy 0.000 claims description 4
- 208000007903 liver failure Diseases 0.000 claims description 4
- 231100000835 liver failure Toxicity 0.000 claims description 4
- 210000000056 organ Anatomy 0.000 claims description 4
- 230000008816 organ damage Effects 0.000 claims description 4
- 230000002093 peripheral effect Effects 0.000 claims description 4
- 201000004240 prostatic hypertrophy Diseases 0.000 claims description 4
- 229910052717 sulfur Inorganic materials 0.000 claims description 4
- 125000006526 (C1-C2) alkyl group Chemical group 0.000 claims description 3
- 201000010099 disease Diseases 0.000 claims description 3
- 125000002887 hydroxy group Chemical group [H]O* 0.000 claims description 3
- 125000000956 methoxy group Chemical group [H]C([H])([H])O* 0.000 claims description 3
- 150000002825 nitriles Chemical class 0.000 claims description 3
- 125000004399 C1-C4 alkenyl group Chemical group 0.000 claims description 2
- 125000003601 C2-C6 alkynyl group Chemical group 0.000 claims description 2
- 239000000546 pharmaceutical excipient Substances 0.000 claims description 2
- 125000005913 (C3-C6) cycloalkyl group Chemical group 0.000 claims 3
- QFWUBFCBZKNUDS-HAQNSBGRSA-N N[C@H]1CC[C@@H](CC1)Sc1ccc2c(N)nccc2c1 Chemical compound N[C@H]1CC[C@@H](CC1)Sc1ccc2c(N)nccc2c1 QFWUBFCBZKNUDS-HAQNSBGRSA-N 0.000 claims 1
- 239000000969 carrier Substances 0.000 claims 1
- 125000004435 hydrogen atom Chemical class [H]* 0.000 claims 1
- OSILBMSORKFRTB-UHFFFAOYSA-N isoquinolin-1-amine Chemical compound C1=CC=C2C(N)=NC=CC2=C1 OSILBMSORKFRTB-UHFFFAOYSA-N 0.000 claims 1
- 239000000203 mixture Substances 0.000 abstract description 11
- 230000006806 disease prevention Effects 0.000 abstract description 3
- YMWUJEATGCHHMB-UHFFFAOYSA-N Dichloromethane Chemical compound ClCCl YMWUJEATGCHHMB-UHFFFAOYSA-N 0.000 description 39
- XEKOWRVHYACXOJ-UHFFFAOYSA-N Ethyl acetate Chemical compound CCOC(C)=O XEKOWRVHYACXOJ-UHFFFAOYSA-N 0.000 description 31
- 239000000243 solution Substances 0.000 description 31
- 238000006243 chemical reaction Methods 0.000 description 22
- 125000001424 substituent group Chemical group 0.000 description 19
- 239000002904 solvent Substances 0.000 description 16
- YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 description 15
- 239000000047 product Substances 0.000 description 15
- QNNTUJSIGVWFAS-UHFFFAOYSA-N 6-bromo-2-oxidoisoquinolin-2-ium Chemical compound C1=C(Br)C=CC2=C[N+]([O-])=CC=C21 QNNTUJSIGVWFAS-UHFFFAOYSA-N 0.000 description 14
- HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 description 14
- QTBSBXVTEAMEQO-UHFFFAOYSA-N Acetic acid Chemical compound CC(O)=O QTBSBXVTEAMEQO-UHFFFAOYSA-N 0.000 description 12
- OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 12
- ZMANZCXQSJIPKH-UHFFFAOYSA-N Triethylamine Chemical compound CCN(CC)CC ZMANZCXQSJIPKH-UHFFFAOYSA-N 0.000 description 12
- 239000002585 base Substances 0.000 description 12
- 125000002183 isoquinolinyl group Chemical group C1(=NC=CC2=CC=CC=C12)* 0.000 description 12
- VOAHGGQULSSGQW-UHFFFAOYSA-N 6-bromo-1-chloroisoquinoline Chemical compound BrC1=CC=C2C(Cl)=NC=CC2=C1 VOAHGGQULSSGQW-UHFFFAOYSA-N 0.000 description 11
- IMNFDUFMRHMDMM-UHFFFAOYSA-N N-Heptane Chemical compound CCCCCCC IMNFDUFMRHMDMM-UHFFFAOYSA-N 0.000 description 10
- DTQVDTLACAAQTR-UHFFFAOYSA-N Trifluoroacetic acid Chemical compound OC(=O)C(F)(F)F DTQVDTLACAAQTR-UHFFFAOYSA-N 0.000 description 10
- 229940093499 ethyl acetate Drugs 0.000 description 10
- 235000019439 ethyl acetate Nutrition 0.000 description 10
- 239000000651 prodrug Substances 0.000 description 10
- 229940002612 prodrug Drugs 0.000 description 10
- 239000000126 substance Substances 0.000 description 10
- 239000012044 organic layer Substances 0.000 description 9
- ZDYXSEQHOVSTPA-UHFFFAOYSA-N 6-bromo-2h-isoquinolin-1-one Chemical compound C1=CNC(=O)C=2C1=CC(Br)=CC=2 ZDYXSEQHOVSTPA-UHFFFAOYSA-N 0.000 description 8
- HEDRZPFGACZZDS-UHFFFAOYSA-N Chloroform Chemical compound ClC(Cl)Cl HEDRZPFGACZZDS-UHFFFAOYSA-N 0.000 description 8
- 150000001412 amines Chemical class 0.000 description 8
- IEMKXFLENZAFAZ-UHFFFAOYSA-N n-[(4-bromophenyl)methyl]-2,2-dimethoxyethanamine Chemical compound COC(OC)CNCC1=CC=C(Br)C=C1 IEMKXFLENZAFAZ-UHFFFAOYSA-N 0.000 description 8
- 239000000825 pharmaceutical preparation Substances 0.000 description 8
- 238000000746 purification Methods 0.000 description 8
- 229920006395 saturated elastomer Polymers 0.000 description 8
- ZTEATMVVGQUULZ-UHFFFAOYSA-N 6-bromoisoquinoline Chemical class C1=NC=CC2=CC(Br)=CC=C21 ZTEATMVVGQUULZ-UHFFFAOYSA-N 0.000 description 7
- VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 description 7
- 239000000872 buffer Substances 0.000 description 7
- 230000000694 effects Effects 0.000 description 7
- 150000003840 hydrochlorides Chemical class 0.000 description 7
- AWJUIBRHMBBTKR-UHFFFAOYSA-N iso-quinoline Natural products C1=NC=CC2=CC=CC=C21 AWJUIBRHMBBTKR-UHFFFAOYSA-N 0.000 description 7
- MNLWRVRXGBORJM-UHFFFAOYSA-N n-[(4-bromophenyl)methyl]-n-(2,2-dimethoxyethyl)-4-methylbenzenesulfonamide Chemical compound C=1C=C(C)C=CC=1S(=O)(=O)N(CC(OC)OC)CC1=CC=C(Br)C=C1 MNLWRVRXGBORJM-UHFFFAOYSA-N 0.000 description 7
- 238000002360 preparation method Methods 0.000 description 7
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- 125000000896 monocarboxylic acid group Chemical group 0.000 description 6
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- BCZPUVXMWIBIRE-UHFFFAOYSA-N 7-chloro-6-fluoroisoquinoline Chemical compound C1=NC=C2C=C(Cl)C(F)=CC2=C1 BCZPUVXMWIBIRE-UHFFFAOYSA-N 0.000 description 5
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- XJDNKRIXUMDJCW-UHFFFAOYSA-J titanium tetrachloride Chemical compound Cl[Ti](Cl)(Cl)Cl XJDNKRIXUMDJCW-UHFFFAOYSA-J 0.000 description 1
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Classifications
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- C07D—HETEROCYCLIC COMPOUNDS
- C07D217/00—Heterocyclic compounds containing isoquinoline or hydrogenated isoquinoline ring systems
- C07D217/12—Heterocyclic compounds containing isoquinoline or hydrogenated isoquinoline ring systems with radicals, substituted by hetero atoms, attached to carbon atoms of the nitrogen-containing ring
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D217/00—Heterocyclic compounds containing isoquinoline or hydrogenated isoquinoline ring systems
- C07D217/22—Heterocyclic compounds containing isoquinoline or hydrogenated isoquinoline ring systems with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, directly attached to carbon atoms of the nitrogen-containing ring
- C07D217/24—Oxygen atoms
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D401/00—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom
- C07D401/02—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing two hetero rings
- C07D401/12—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing two hetero rings linked by a chain containing hetero atoms as chain links
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Applications Claiming Priority (3)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| EP06026895.0 | 2006-12-27 | ||
| EP06026895 | 2006-12-27 | ||
| PCT/EP2007/011166 WO2008077553A1 (en) | 2006-12-27 | 2007-12-19 | Cycloalkylamine substituted isoquinolone and isoquinolinone derivatives |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| AU2007338409A1 AU2007338409A1 (en) | 2008-07-03 |
| AU2007338409B2 true AU2007338409B2 (en) | 2012-12-13 |
Family
ID=38069270
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| AU2007338409A Ceased AU2007338409B2 (en) | 2006-12-27 | 2007-12-19 | Cycloalkylamine substituted isoquinolone and isoquinolinone derivatives |
Country Status (22)
| Country | Link |
|---|---|
| US (1) | US20100056568A1 (https=) |
| EP (1) | EP2125744B1 (https=) |
| JP (1) | JP5318778B2 (https=) |
| KR (1) | KR20090103903A (https=) |
| CN (1) | CN101573338B (https=) |
| AT (1) | ATE505458T1 (https=) |
| AU (1) | AU2007338409B2 (https=) |
| BR (1) | BRPI0720710A2 (https=) |
| CA (1) | CA2673919C (https=) |
| CO (1) | CO6210725A2 (https=) |
| DE (1) | DE602007013950D1 (https=) |
| DK (1) | DK2125744T3 (https=) |
| ES (1) | ES2364511T3 (https=) |
| IL (1) | IL199536A (https=) |
| MA (1) | MA31023B1 (https=) |
| MX (1) | MX2009005828A (https=) |
| MY (1) | MY148514A (https=) |
| NO (1) | NO20092431L (https=) |
| PT (1) | PT2125744E (https=) |
| RU (1) | RU2009128688A (https=) |
| WO (1) | WO2008077553A1 (https=) |
| ZA (1) | ZA200903553B (https=) |
Families Citing this family (25)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| WO2007008926A1 (en) | 2005-07-11 | 2007-01-18 | Aerie Pharmaceuticals, Inc. | Isoquinoline compounds |
| WO2008036540A2 (en) | 2006-09-20 | 2008-03-27 | Boehringer Ingelheim International Gmbh | Rho kinase inhibitors |
| US8455513B2 (en) | 2007-01-10 | 2013-06-04 | Aerie Pharmaceuticals, Inc. | 6-aminoisoquinoline compounds |
| US8455514B2 (en) | 2008-01-17 | 2013-06-04 | Aerie Pharmaceuticals, Inc. | 6-and 7-amino isoquinoline compounds and methods for making and using the same |
| CN102131784B (zh) * | 2008-06-24 | 2014-08-27 | 赛诺菲-安万特 | 作为rho激酶抑制剂的取代的异喹啉和异喹啉酮 |
| PT2313374E (pt) * | 2008-06-24 | 2013-11-29 | Sanofi Sa | Isoquinolinas e isoquinolinonas 6-substituídas |
| HRP20131040T1 (hr) * | 2008-06-24 | 2013-12-06 | Sanofi | Bi- i policikliäśki supstituirani izokinolin i derivati izokinolina kao inhibitori rho-kinaze |
| US8450344B2 (en) | 2008-07-25 | 2013-05-28 | Aerie Pharmaceuticals, Inc. | Beta- and gamma-amino-isoquinoline amide compounds and substituted benzamide compounds |
| EP3053913B1 (en) | 2009-05-01 | 2018-03-07 | Aerie Pharmaceuticals, Inc. | Dual mechanism inhibitors for the treatment of disease |
| AU2010261206B2 (en) | 2009-06-19 | 2015-10-08 | D. Western Therapeutics Institute, Inc. | Substituted isoquinoline derivative |
| US20150202220A1 (en) * | 2011-10-26 | 2015-07-23 | Northwind Medical, Inc. | Agents, methods, and devices for affecting nerve function |
| DK3811943T3 (da) | 2013-03-15 | 2023-04-03 | Aerie Pharmaceuticals Inc | Forbindelse til anvendelse til behandling af øjenlidelser |
| FR3017868A1 (fr) | 2014-02-21 | 2015-08-28 | Servier Lab | Derives d'isoquinoleine, leur procede de preparation et les compositions pharmaceutiques qui les contiennent |
| JP6695879B2 (ja) | 2014-12-11 | 2020-05-20 | シンジェンタ パーティシペーションズ アーゲー | 硫黄含有置換基を有する殺有害生物的に活性な四環式誘導体 |
| BR112017013440A2 (pt) | 2014-12-24 | 2018-01-09 | Gilead Sciences, Inc. | compostos de isoquinolina para o tratamento de hiv |
| ES2735087T3 (es) | 2014-12-24 | 2019-12-16 | Gilead Sciences Inc | Compuestos de pirimidina fusionados para el tratamiento de VIH |
| TWI699355B (zh) | 2014-12-24 | 2020-07-21 | 美商基利科學股份有限公司 | 喹唑啉化合物 |
| US9643927B1 (en) | 2015-11-17 | 2017-05-09 | Aerie Pharmaceuticals, Inc. | Process for the preparation of kinase inhibitors and intermediates thereof |
| US10550087B2 (en) | 2015-11-17 | 2020-02-04 | Aerie Pharmaceuticals, Inc. | Process for the preparation of kinase inhibitors and intermediates thereof |
| KR102568079B1 (ko) | 2016-08-31 | 2023-08-17 | 에어리 파마슈티컬즈, 인코포레이티드 | 안과용 조성물 |
| KR20190135027A (ko) | 2017-03-31 | 2019-12-05 | 에어리 파마슈티컬즈, 인코포레이티드 | 아릴 시클로프로필-아미노-이소퀴놀리닐 아미드 화합물 |
| AU2019337703B2 (en) | 2018-09-14 | 2023-02-02 | Aerie Pharmaceuticals, Inc. | Aryl cyclopropyl-amino-isoquinolinyl amide compounds |
| CN112969694B (zh) | 2018-11-09 | 2023-06-13 | 北京泰德制药股份有限公司 | Rho相关蛋白激酶抑制剂、包含其的药物组合物及其用途 |
| CN110670090B (zh) * | 2019-11-13 | 2021-06-29 | 广西师范大学 | 一种基于电化学合成异喹啉酮类化合物的方法 |
| KR102889687B1 (ko) * | 2020-11-03 | 2025-11-21 | 주식회사 엘지화학 | 작물보호제용 신규 화합물 |
Citations (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| WO2005030791A2 (en) * | 2003-09-23 | 2005-04-07 | Merck & Co., Inc. | Isoquinolinone potassium channel inhibitors |
| WO2008020081A1 (en) * | 2006-08-18 | 2008-02-21 | N.V. Organon | 6-substituted isoquinoline derivatives as rock-1 inhibitors |
Family Cites Families (13)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US5480883A (en) * | 1991-05-10 | 1996-01-02 | Rhone-Poulenc Rorer Pharmaceuticals Inc. | Bis mono- and bicyclic aryl and heteroaryl compounds which inhibit EGF and/or PDGF receptor tyrosine kinase |
| TW575567B (en) * | 1998-10-23 | 2004-02-11 | Akzo Nobel Nv | Serine protease inhibitor |
| IL150650A0 (en) * | 2000-01-20 | 2003-02-12 | Eisai Co Ltd | Piperidine derivatives and pharmaceutical compositions containing the same |
| US7217722B2 (en) * | 2000-02-01 | 2007-05-15 | Kirin Beer Kabushiki Kaisha | Nitrogen-containing compounds having kinase inhibitory activity and drugs containing the same |
| JPWO2002100833A1 (ja) * | 2001-06-12 | 2004-09-24 | 住友製薬株式会社 | Ｒｈｏキナーゼ阻害剤 |
| SE0104340D0 (sv) | 2001-12-20 | 2001-12-20 | Astrazeneca Ab | New compounds |
| AU2003281623B8 (en) * | 2002-07-22 | 2009-06-11 | Asahi Kasei Pharma Corporation | 5-substituted isoquinoline derivative |
| JPWO2005035516A1 (ja) * | 2003-10-10 | 2006-12-21 | 小野薬品工業株式会社 | 新規縮合複素環化合物およびその用途 |
| WO2005054202A1 (en) * | 2003-11-25 | 2005-06-16 | Eli Lilly And Company | 7-phenyl-isoquinoline-5-sulfonylamino derivatives as inhibitors of akt (proteinkinase b) |
| JP2005232175A (ja) * | 2004-01-21 | 2005-09-02 | Asahi Kasei Pharma Kk | ５−置換イソキノリン医薬 |
| US7517991B2 (en) * | 2004-10-12 | 2009-04-14 | Bristol-Myers Squibb Company | N-sulfonylpiperidine cannabinoid receptor 1 antagonists |
| NZ565040A (en) * | 2005-06-28 | 2010-05-28 | Sanofi Aventis | Isoquinoline derivatives as inhibitors of RHO-kinase |
| US7618985B2 (en) * | 2005-12-08 | 2009-11-17 | N.V. Organon | Isoquinoline derivatives |
-
2007
- 2007-12-19 KR KR1020097013521A patent/KR20090103903A/ko not_active Abandoned
- 2007-12-19 BR BRPI0720710-7A2A patent/BRPI0720710A2/pt not_active IP Right Cessation
- 2007-12-19 DK DK07856889.6T patent/DK2125744T3/da active
- 2007-12-19 CA CA2673919A patent/CA2673919C/en not_active Expired - Fee Related
- 2007-12-19 ES ES07856889T patent/ES2364511T3/es active Active
- 2007-12-19 PT PT07856889T patent/PT2125744E/pt unknown
- 2007-12-19 RU RU2009128688/04A patent/RU2009128688A/ru not_active Application Discontinuation
- 2007-12-19 AT AT07856889T patent/ATE505458T1/de active
- 2007-12-19 WO PCT/EP2007/011166 patent/WO2008077553A1/en not_active Ceased
- 2007-12-19 CN CN2007800485212A patent/CN101573338B/zh not_active Expired - Fee Related
- 2007-12-19 MY MYPI20092205A patent/MY148514A/en unknown
- 2007-12-19 MX MX2009005828A patent/MX2009005828A/es active IP Right Grant
- 2007-12-19 AU AU2007338409A patent/AU2007338409B2/en not_active Ceased
- 2007-12-19 EP EP07856889A patent/EP2125744B1/en active Active
- 2007-12-19 JP JP2009543374A patent/JP5318778B2/ja not_active Expired - Fee Related
- 2007-12-19 DE DE602007013950T patent/DE602007013950D1/de active Active
-
2009
- 2009-05-22 ZA ZA200903553A patent/ZA200903553B/xx unknown
- 2009-06-12 CO CO09061596A patent/CO6210725A2/es not_active Application Discontinuation
- 2009-06-18 US US12/487,525 patent/US20100056568A1/en not_active Abandoned
- 2009-06-24 MA MA32038A patent/MA31023B1/fr unknown
- 2009-06-24 IL IL199536A patent/IL199536A/en not_active IP Right Cessation
- 2009-06-26 NO NO20092431A patent/NO20092431L/no not_active Application Discontinuation
Patent Citations (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| WO2005030791A2 (en) * | 2003-09-23 | 2005-04-07 | Merck & Co., Inc. | Isoquinolinone potassium channel inhibitors |
| WO2008020081A1 (en) * | 2006-08-18 | 2008-02-21 | N.V. Organon | 6-substituted isoquinoline derivatives as rock-1 inhibitors |
Also Published As
| Publication number | Publication date |
|---|---|
| IL199536A (en) | 2014-07-31 |
| CO6210725A2 (es) | 2010-10-20 |
| EP2125744B1 (en) | 2011-04-13 |
| CA2673919C (en) | 2015-06-23 |
| ZA200903553B (en) | 2010-04-28 |
| MY148514A (en) | 2013-04-30 |
| DE602007013950D1 (de) | 2011-05-26 |
| ES2364511T3 (es) | 2011-09-05 |
| MA31023B1 (fr) | 2009-12-01 |
| CN101573338A (zh) | 2009-11-04 |
| RU2009128688A (ru) | 2011-02-10 |
| CN101573338B (zh) | 2013-03-20 |
| JP5318778B2 (ja) | 2013-10-16 |
| MX2009005828A (es) | 2009-06-16 |
| PT2125744E (pt) | 2011-07-01 |
| ATE505458T1 (de) | 2011-04-15 |
| NO20092431L (no) | 2009-09-21 |
| JP2010514718A (ja) | 2010-05-06 |
| DK2125744T3 (da) | 2011-08-01 |
| US20100056568A1 (en) | 2010-03-04 |
| CA2673919A1 (en) | 2008-07-03 |
| HK1138583A1 (en) | 2010-08-27 |
| EP2125744A1 (en) | 2009-12-02 |
| BRPI0720710A2 (pt) | 2014-12-23 |
| KR20090103903A (ko) | 2009-10-01 |
| WO2008077553A1 (en) | 2008-07-03 |
| AU2007338409A1 (en) | 2008-07-03 |
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