JP2007523155A5 - - Google Patents
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- JP2007523155A5 JP2007523155A5 JP2006553706A JP2006553706A JP2007523155A5 JP 2007523155 A5 JP2007523155 A5 JP 2007523155A5 JP 2006553706 A JP2006553706 A JP 2006553706A JP 2006553706 A JP2006553706 A JP 2006553706A JP 2007523155 A5 JP2007523155 A5 JP 2007523155A5
- Authority
- JP
- Japan
- Prior art keywords
- pyridin
- benzamide
- amino
- pyrrolo
- carboxylic acid
- 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.)
- Pending
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- -1 nitro, hydroxyl Chemical group 0.000 claims 25
- 150000001875 compounds Chemical class 0.000 claims 19
- 229910052739 hydrogen Inorganic materials 0.000 claims 9
- 239000001257 hydrogen Substances 0.000 claims 9
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims 8
- 125000003118 aryl group Chemical group 0.000 claims 8
- KKWUYHFACPLBGF-UHFFFAOYSA-N 1-amino-n-pyridin-4-yl-2,3-dihydro-1h-indene-5-carboxamide Chemical compound C=1C=C2C(N)CCC2=CC=1C(=O)NC1=CC=NC=C1 KKWUYHFACPLBGF-UHFFFAOYSA-N 0.000 claims 6
- 125000001424 substituent group Chemical group 0.000 claims 6
- 238000006467 substitution reaction Methods 0.000 claims 6
- OTGLOKZMFREKRJ-UHFFFAOYSA-N 4-(4,5-dihydro-1h-imidazol-2-yl)-n-pyridin-4-ylbenzamide Chemical compound C=1C=C(C=2NCCN=2)C=CC=1C(=O)NC1=CC=NC=C1 OTGLOKZMFREKRJ-UHFFFAOYSA-N 0.000 claims 5
- IQNKRAWRKBNOKR-UHFFFAOYSA-N 4-piperidin-2-yl-n-(1h-pyrrolo[2,3-b]pyridin-4-yl)benzamide Chemical compound C=1C=NC=2NC=CC=2C=1NC(=O)C(C=C1)=CC=C1C1CCCCN1 IQNKRAWRKBNOKR-UHFFFAOYSA-N 0.000 claims 5
- SQQWULIZIPGEIA-UHFFFAOYSA-N 5-amino-n-(1h-pyrrolo[2,3-b]pyridin-4-yl)-5,6,7,8-tetrahydronaphthalene-2-carboxamide Chemical compound C=1C=C2C(N)CCCC2=CC=1C(=O)NC1=CC=NC2=C1C=CN2 SQQWULIZIPGEIA-UHFFFAOYSA-N 0.000 claims 5
- NHUPJCHRWRHUKF-UHFFFAOYSA-N n-pyridin-4-yl-4-pyrrolidin-2-ylbenzamide Chemical compound C=1C=C(C2NCCC2)C=CC=1C(=O)NC1=CC=NC=C1 NHUPJCHRWRHUKF-UHFFFAOYSA-N 0.000 claims 5
- QEMYLDYQDFRTRT-UHFFFAOYSA-N 1,2,3,4-tetrahydroisoquinolin-2-ium-6-carboxylate Chemical compound C1NCCC2=CC(C(=O)O)=CC=C21 QEMYLDYQDFRTRT-UHFFFAOYSA-N 0.000 claims 4
- ZCYGCPVXXJYQDY-UHFFFAOYSA-N 4-piperidin-2-yl-n-pyridin-4-ylbenzamide Chemical compound C=1C=C(C2NCCCC2)C=CC=1C(=O)NC1=CC=NC=C1 ZCYGCPVXXJYQDY-UHFFFAOYSA-N 0.000 claims 4
- 125000003277 amino group Chemical group 0.000 claims 4
- 239000003814 drug Substances 0.000 claims 4
- 229910052736 halogen Inorganic materials 0.000 claims 4
- 150000002367 halogens Chemical class 0.000 claims 4
- 208000030159 metabolic disease Diseases 0.000 claims 4
- 238000000034 method Methods 0.000 claims 4
- IIVCSIFQZZMOBI-UHFFFAOYSA-N n-pyridin-4-yl-1,2,3,4-tetrahydroisoquinoline-6-carboxamide Chemical compound C=1C=C2CNCCC2=CC=1C(=O)NC1=CC=NC=C1 IIVCSIFQZZMOBI-UHFFFAOYSA-N 0.000 claims 4
- 208000008589 Obesity Diseases 0.000 claims 3
- 125000004432 carbon atom Chemical group C* 0.000 claims 3
- 125000004093 cyano group Chemical group *C#N 0.000 claims 3
- 125000005842 heteroatom Chemical group 0.000 claims 3
- 235000020824 obesity Nutrition 0.000 claims 3
- 229920006395 saturated elastomer Polymers 0.000 claims 3
- 208000024891 symptom Diseases 0.000 claims 3
- 208000001072 type 2 diabetes mellitus Diseases 0.000 claims 3
- ZFBHHXHSPRMSQS-UHFFFAOYSA-N 1-amino-2,3-dihydro-1h-indene-5-carboxylic acid Chemical compound OC(=O)C1=CC=C2C(N)CCC2=C1 ZFBHHXHSPRMSQS-UHFFFAOYSA-N 0.000 claims 2
- ZMRMIGRTPQOGOL-UHFFFAOYSA-N 1-amino-n-(1h-pyrrolo[2,3-b]pyridin-4-yl)-2,3-dihydro-1h-indene-5-carboxamide Chemical compound C=1C=C2C(N)CCC2=CC=1C(=O)NC1=CC=NC2=C1C=CN2 ZMRMIGRTPQOGOL-UHFFFAOYSA-N 0.000 claims 2
- KRAYOARFOGSKJI-UHFFFAOYSA-N 4-(1-amino-2,2-dimethylpropyl)-n-pyridin-4-ylbenzamide Chemical compound C1=CC(C(N)C(C)(C)C)=CC=C1C(=O)NC1=CC=NC=C1 KRAYOARFOGSKJI-UHFFFAOYSA-N 0.000 claims 2
- JTVBXQAYBIJXRP-UHFFFAOYSA-N 4-(1-aminoethyl)-n-(1h-pyrrolo[2,3-b]pyridin-4-yl)benzamide Chemical compound C1=CC(C(N)C)=CC=C1C(=O)NC1=CC=NC2=C1C=CN2 JTVBXQAYBIJXRP-UHFFFAOYSA-N 0.000 claims 2
- LLSFXOUAPAZFIV-UHFFFAOYSA-N 4-(1-aminoethyl)-n-pyridin-4-ylbenzamide Chemical compound C1=CC(C(N)C)=CC=C1C(=O)NC1=CC=NC=C1 LLSFXOUAPAZFIV-UHFFFAOYSA-N 0.000 claims 2
- GMDVSDXMBONTNR-UHFFFAOYSA-N 4-(aminomethyl)-2,5-dimethyl-n-pyridin-4-ylbenzamide Chemical compound C1=C(CN)C(C)=CC(C(=O)NC=2C=CN=CC=2)=C1C GMDVSDXMBONTNR-UHFFFAOYSA-N 0.000 claims 2
- RZZGLZFZZYYVCO-UHFFFAOYSA-N 4-[2-(1-aminocyclobutyl)ethyl]-n-(1h-pyrrolo[2,3-b]pyridin-4-yl)benzamide Chemical compound C=1C=C(C(=O)NC=2C=3C=CNC=3N=CC=2)C=CC=1CCC1(N)CCC1 RZZGLZFZZYYVCO-UHFFFAOYSA-N 0.000 claims 2
- BREHCBBQUGUALM-UHFFFAOYSA-N 4-[2-(1-aminocyclopentyl)ethyl]-n-(1h-pyrrolo[2,3-b]pyridin-4-yl)benzamide Chemical compound C=1C=C(C(=O)NC=2C=3C=CNC=3N=CC=2)C=CC=1CCC1(N)CCCC1 BREHCBBQUGUALM-UHFFFAOYSA-N 0.000 claims 2
- 230000003345 hyperglycaemic effect Effects 0.000 claims 2
- NOESYZHRGYRDHS-UHFFFAOYSA-N insulin Chemical compound N1C(=O)C(NC(=O)C(CCC(N)=O)NC(=O)C(CCC(O)=O)NC(=O)C(C(C)C)NC(=O)C(NC(=O)CN)C(C)CC)CSSCC(C(NC(CO)C(=O)NC(CC(C)C)C(=O)NC(CC=2C=CC(O)=CC=2)C(=O)NC(CCC(N)=O)C(=O)NC(CC(C)C)C(=O)NC(CCC(O)=O)C(=O)NC(CC(N)=O)C(=O)NC(CC=2C=CC(O)=CC=2)C(=O)NC(CSSCC(NC(=O)C(C(C)C)NC(=O)C(CC(C)C)NC(=O)C(CC=2C=CC(O)=CC=2)NC(=O)C(CC(C)C)NC(=O)C(C)NC(=O)C(CCC(O)=O)NC(=O)C(C(C)C)NC(=O)C(CC(C)C)NC(=O)C(CC=2NC=NC=2)NC(=O)C(CO)NC(=O)CNC2=O)C(=O)NCC(=O)NC(CCC(O)=O)C(=O)NC(CCCNC(N)=N)C(=O)NCC(=O)NC(CC=3C=CC=CC=3)C(=O)NC(CC=3C=CC=CC=3)C(=O)NC(CC=3C=CC(O)=CC=3)C(=O)NC(C(C)O)C(=O)N3C(CCC3)C(=O)NC(CCCCN)C(=O)NC(C)C(O)=O)C(=O)NC(CC(N)=O)C(O)=O)=O)NC(=O)C(C(C)CC)NC(=O)C(CO)NC(=O)C(C(C)O)NC(=O)C1CSSCC2NC(=O)C(CC(C)C)NC(=O)C(NC(=O)C(CCC(N)=O)NC(=O)C(CC(N)=O)NC(=O)C(NC(=O)C(N)CC=1C=CC=CC=1)C(C)C)CC1=CN=CN1 NOESYZHRGYRDHS-UHFFFAOYSA-N 0.000 claims 2
- RCWISWVYKNLXHC-UHFFFAOYSA-N 1h-pyrrolo[2,3-b]pyridin-4-amine Chemical compound NC1=CC=NC2=C1C=CN2 RCWISWVYKNLXHC-UHFFFAOYSA-N 0.000 claims 1
- HVFBLNMGJWVBOH-UHFFFAOYSA-N 4-(1-amino-2,2-dimethylbutyl)-n-(1h-pyrrolo[2,3-b]pyridin-4-yl)benzamide Chemical compound C1=CC(C(N)C(C)(C)CC)=CC=C1C(=O)NC1=CC=NC2=C1C=CN2 HVFBLNMGJWVBOH-UHFFFAOYSA-N 0.000 claims 1
- IZTDNPWBQHCWAF-UHFFFAOYSA-N 4-(1-amino-2,2-dimethylbutyl)-n-pyridin-4-ylbenzamide Chemical compound C1=CC(C(N)C(C)(C)CC)=CC=C1C(=O)NC1=CC=NC=C1 IZTDNPWBQHCWAF-UHFFFAOYSA-N 0.000 claims 1
- QRIIJGVRMJWJMC-UHFFFAOYSA-N 4-(1-amino-2,2-dimethylpropyl)-n-(1h-pyrrolo[2,3-b]pyridin-4-yl)benzamide Chemical compound C1=CC(C(N)C(C)(C)C)=CC=C1C(=O)NC1=CC=NC2=C1C=CN2 QRIIJGVRMJWJMC-UHFFFAOYSA-N 0.000 claims 1
- MFYXHARIDVVKQE-UHFFFAOYSA-N 4-(1-amino-2-methylpropyl)-n-pyridin-4-ylbenzamide Chemical compound C1=CC(C(N)C(C)C)=CC=C1C(=O)NC1=CC=NC=C1 MFYXHARIDVVKQE-UHFFFAOYSA-N 0.000 claims 1
- GUVVJWIZMJTOHB-UHFFFAOYSA-N 4-(1-amino-3,3-dimethylbutyl)-n-pyridin-4-ylbenzamide Chemical compound C1=CC(C(N)CC(C)(C)C)=CC=C1C(=O)NC1=CC=NC=C1 GUVVJWIZMJTOHB-UHFFFAOYSA-N 0.000 claims 1
- DMIYJAIUCNVDNZ-UHFFFAOYSA-N 4-(1-aminobutyl)-n-(1h-pyrrolo[2,3-b]pyridin-4-yl)benzamide Chemical compound C1=CC(C(N)CCC)=CC=C1C(=O)NC1=CC=NC2=C1C=CN2 DMIYJAIUCNVDNZ-UHFFFAOYSA-N 0.000 claims 1
- OXBJQHBEBMMYCJ-UHFFFAOYSA-N 4-(1-aminoethyl)-n-pyridin-4-ylnaphthalene-1-carboxamide Chemical compound C12=CC=CC=C2C(C(N)C)=CC=C1C(=O)NC1=CC=NC=C1 OXBJQHBEBMMYCJ-UHFFFAOYSA-N 0.000 claims 1
- AFPVZEOZNLCEFO-UHFFFAOYSA-N 4-(1-aminopentyl)-n-pyridin-4-ylbenzamide Chemical compound C1=CC(C(N)CCCC)=CC=C1C(=O)NC1=CC=NC=C1 AFPVZEOZNLCEFO-UHFFFAOYSA-N 0.000 claims 1
- ZZGFVFADCZZOTR-UHFFFAOYSA-N 4-(1-aminopropyl)-n-(1h-pyrrolo[2,3-b]pyridin-4-yl)benzamide Chemical compound C1=CC(C(N)CC)=CC=C1C(=O)NC1=CC=NC2=C1C=CN2 ZZGFVFADCZZOTR-UHFFFAOYSA-N 0.000 claims 1
- GQRHXVADWRNQSJ-UHFFFAOYSA-N 4-(1-aminopropyl)-n-pyridin-4-ylbenzamide Chemical compound C1=CC(C(N)CC)=CC=C1C(=O)NC1=CC=NC=C1 GQRHXVADWRNQSJ-UHFFFAOYSA-N 0.000 claims 1
- BEIPZGFAWMRBKW-UHFFFAOYSA-N 4-(aminomethyl)-n-pyridin-4-ylbenzamide Chemical compound C1=CC(CN)=CC=C1C(=O)NC1=CC=NC=C1 BEIPZGFAWMRBKW-UHFFFAOYSA-N 0.000 claims 1
- XQKMBMGZZKVNKI-UHFFFAOYSA-N 4-[(1-aminocyclohexa-2,4-dien-1-yl)methyl]-n-pyridin-4-ylbenzamide Chemical compound C=1C=C(C(=O)NC=2C=CN=CC=2)C=CC=1CC1(N)CC=CC=C1 XQKMBMGZZKVNKI-UHFFFAOYSA-N 0.000 claims 1
- RXVVCDYBIKNPMY-UHFFFAOYSA-N 4-[(1-aminocyclohexyl)methyl]-n-pyridin-4-ylbenzamide Chemical compound C=1C=C(C(=O)NC=2C=CN=CC=2)C=CC=1CC1(N)CCCCC1 RXVVCDYBIKNPMY-UHFFFAOYSA-N 0.000 claims 1
- UTWIBGAVMAMFLG-UHFFFAOYSA-N 4-[(1-aminocyclopentyl)methyl]-n-pyridin-4-ylbenzamide Chemical compound C=1C=C(C(=O)NC=2C=CN=CC=2)C=CC=1CC1(N)CCCC1 UTWIBGAVMAMFLG-UHFFFAOYSA-N 0.000 claims 1
- KVEPLQYOHUJLRM-UHFFFAOYSA-N 4-[2-(1-aminocyclobutyl)ethyl]-n-pyridin-4-ylbenzamide Chemical compound C=1C=C(C(=O)NC=2C=CN=CC=2)C=CC=1CCC1(N)CCC1 KVEPLQYOHUJLRM-UHFFFAOYSA-N 0.000 claims 1
- DYNBQBMJMRSQIS-UHFFFAOYSA-N 4-[2-(1-aminocyclopropyl)ethyl]-n-(1h-pyrrolo[2,3-b]pyridin-4-yl)benzamide Chemical compound C=1C=C(C(=O)NC=2C=3C=CNC=3N=CC=2)C=CC=1CCC1(N)CC1 DYNBQBMJMRSQIS-UHFFFAOYSA-N 0.000 claims 1
- OAGHQOGYIPJBMH-UHFFFAOYSA-N 4-[2-(1-aminocyclopropyl)ethyl]-n-pyridin-4-ylbenzamide Chemical compound C=1C=C(C(=O)NC=2C=CN=CC=2)C=CC=1CCC1(N)CC1 OAGHQOGYIPJBMH-UHFFFAOYSA-N 0.000 claims 1
- HBQICHDVACJWLN-UHFFFAOYSA-N 4-[amino-(4-methoxyphenyl)methyl]-n-pyridin-4-ylbenzamide Chemical compound C1=CC(OC)=CC=C1C(N)C1=CC=C(C(=O)NC=2C=CN=CC=2)C=C1 HBQICHDVACJWLN-UHFFFAOYSA-N 0.000 claims 1
- NUKYPUAOHBNCPY-UHFFFAOYSA-N 4-aminopyridine Chemical compound NC1=CC=NC=C1 NUKYPUAOHBNCPY-UHFFFAOYSA-N 0.000 claims 1
- 125000000339 4-pyridyl group Chemical group N1=C([H])C([H])=C([*])C([H])=C1[H] 0.000 claims 1
- NWUKZQQHKGVGHB-UHFFFAOYSA-N 5-amino-5,6,7,8-tetrahydronaphthalene-2-carboxylic acid Chemical compound OC(=O)C1=CC=C2C(N)CCCC2=C1 NWUKZQQHKGVGHB-UHFFFAOYSA-N 0.000 claims 1
- SLRGZZIYYHTKSM-XYPYZODXSA-N C1C[C@@H](CN)CC[C@@H]1C(=O)NC1=CC=NC=C1 Chemical compound C1C[C@@H](CN)CC[C@@H]1C(=O)NC1=CC=NC=C1 SLRGZZIYYHTKSM-XYPYZODXSA-N 0.000 claims 1
- 201000005948 Donohue syndrome Diseases 0.000 claims 1
- 206010060378 Hyperinsulinaemia Diseases 0.000 claims 1
- 208000031226 Hyperlipidaemia Diseases 0.000 claims 1
- 206010020772 Hypertension Diseases 0.000 claims 1
- 102000004877 Insulin Human genes 0.000 claims 1
- 108090001061 Insulin Proteins 0.000 claims 1
- 206010022489 Insulin Resistance Diseases 0.000 claims 1
- 206010022491 Insulin resistant diabetes Diseases 0.000 claims 1
- 206010024604 Lipoatrophy Diseases 0.000 claims 1
- 208000001145 Metabolic Syndrome Diseases 0.000 claims 1
- 208000001132 Osteoporosis Diseases 0.000 claims 1
- 206010067584 Type 1 diabetes mellitus Diseases 0.000 claims 1
- 201000011032 Werner Syndrome Diseases 0.000 claims 1
- IYOZTVGMEWJPKR-IJLUTSLNSA-N Y-27632 Chemical compound C1C[C@@H]([C@H](N)C)CC[C@@H]1C(=O)NC1=CC=NC=C1 IYOZTVGMEWJPKR-IJLUTSLNSA-N 0.000 claims 1
- 201000000690 abdominal obesity-metabolic syndrome Diseases 0.000 claims 1
- 206010012601 diabetes mellitus Diseases 0.000 claims 1
- 239000003085 diluting agent Substances 0.000 claims 1
- 201000010099 disease Diseases 0.000 claims 1
- 208000016097 disease of metabolism Diseases 0.000 claims 1
- 208000037265 diseases, disorders, signs and symptoms Diseases 0.000 claims 1
- 125000004435 hydrogen atom Chemical group [H]* 0.000 claims 1
- 230000003451 hyperinsulinaemic effect Effects 0.000 claims 1
- 201000008980 hyperinsulinism Diseases 0.000 claims 1
- 208000015978 inherited metabolic disease Diseases 0.000 claims 1
- 229940125396 insulin Drugs 0.000 claims 1
- 230000003212 lipotrophic effect Effects 0.000 claims 1
- 239000000546 pharmaceutical excipient Substances 0.000 claims 1
- 150000003839 salts Chemical class 0.000 claims 1
- 230000007863 steatosis Effects 0.000 claims 1
- 231100000240 steatosis hepatitis Toxicity 0.000 claims 1
- 0 CC1(*)C=NC=CC(C)=C1 Chemical compound CC1(*)C=NC=CC(C)=C1 0.000 description 5
- GPCQIJHZALEOMP-UHFFFAOYSA-N Cc1cc(CCC2N)c2cc1 Chemical compound Cc1cc(CCC2N)c2cc1 GPCQIJHZALEOMP-UHFFFAOYSA-N 0.000 description 1
- RVYMOWKHMXUHRS-UHFFFAOYSA-N Cc1ccc(C(CCC2)N)c2c1 Chemical compound Cc1ccc(C(CCC2)N)c2c1 RVYMOWKHMXUHRS-UHFFFAOYSA-N 0.000 description 1
- JQOUGGPGOWRLPX-UHFFFAOYSA-N Cc1ccc(CNCC2)c2c1 Chemical compound Cc1ccc(CNCC2)c2c1 JQOUGGPGOWRLPX-UHFFFAOYSA-N 0.000 description 1
Applications Claiming Priority (3)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US54554504P | 2004-02-18 | 2004-02-18 | |
| GBGB0403635.6A GB0403635D0 (en) | 2004-02-18 | 2004-02-18 | Pyridinocarboxamides with improved activity as kinase inhibitors |
| PCT/IB2005/000600 WO2005082367A1 (en) | 2004-02-18 | 2005-02-18 | Kinase inhibitors |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| JP2007523155A JP2007523155A (ja) | 2007-08-16 |
| JP2007523155A5 true JP2007523155A5 (enExample) | 2008-03-13 |
Family
ID=32039983
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP2006553706A Pending JP2007523155A (ja) | 2004-02-18 | 2005-02-18 | キナーゼ阻害剤 |
Country Status (5)
| Country | Link |
|---|---|
| US (1) | US20070191420A1 (enExample) |
| EP (1) | EP1715862A1 (enExample) |
| JP (1) | JP2007523155A (enExample) |
| GB (1) | GB0403635D0 (enExample) |
| WO (1) | WO2005082367A1 (enExample) |
Families Citing this family (45)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| PT1696920E (pt) | 2003-12-19 | 2015-01-14 | Plexxikon Inc | Compostos e métodos para o desenvolvimento de moduladores de ret |
| US7498342B2 (en) | 2004-06-17 | 2009-03-03 | Plexxikon, Inc. | Compounds modulating c-kit activity |
| WO2007060028A1 (en) * | 2004-12-31 | 2007-05-31 | Gpc Biotech Ag | Napthyridine compounds as rock inhibitors |
| US7737279B2 (en) | 2005-05-10 | 2010-06-15 | Bristol-Myers Squibb Company | 1,6-dihydro-1,3,5,6-tetraaza-as-indacene based tricyclic compounds and pharmaceutical compositions comprising same |
| KR20080027775A (ko) | 2005-05-17 | 2008-03-28 | 플렉시콘, 인코퍼레이티드 | 피롤(２,３-ｂ)피리딘 유도체 단백질 키나제 억제제 |
| PL1893612T3 (pl) | 2005-06-22 | 2012-01-31 | Plexxikon Inc | Pochodne pirolo-[2,3-b]pirydyny jako inhibitory kinazy białkowej |
| BRPI0615524A2 (pt) * | 2005-07-11 | 2010-04-06 | Devgen Nv | derivados da amida como inibidores da quinase |
| EP1922306A2 (en) | 2005-09-02 | 2008-05-21 | Astellas Pharma Inc. | Amide derivatives as rock inhibitors |
| WO2007143119A2 (en) * | 2006-06-01 | 2007-12-13 | The Board Of Trustees Of The Leland Stanford Junior University | Method of preventing progression of hypertension-induced heart failure with pkc peptides |
| WO2008063888A2 (en) | 2006-11-22 | 2008-05-29 | Plexxikon, Inc. | Compounds modulating c-fms and/or c-kit activity and uses therefor |
| WO2008079909A1 (en) | 2006-12-21 | 2008-07-03 | Plexxikon, Inc. | Pyrrolo [2,3-b] pyridines as kinase modulators |
| PE20121126A1 (es) | 2006-12-21 | 2012-08-24 | Plexxikon Inc | Compuestos pirrolo [2,3-b] piridinas como moduladores de quinasa |
| JP2010514695A (ja) | 2006-12-21 | 2010-05-06 | プレキシコン，インコーポレーテッド | キナーゼ調節のための化合物および方法およびそのための適応症 |
| TWI444379B (zh) | 2007-06-29 | 2014-07-11 | Sunesis Pharmaceuticals Inc | 有用於作為Ｒａｆ激酶抑制劑之化合物 |
| BRPI0814423B1 (pt) | 2007-07-17 | 2022-04-19 | Plexxikon, Inc | Compostos que modulam quinase e composição farmacêutica compreendendo os mesmos |
| US20100292509A1 (en) * | 2008-01-21 | 2010-11-18 | Shiseido Company, Ltd | Vegfc production promoter |
| CN106243100B (zh) * | 2008-10-10 | 2019-04-09 | Vm生物医药公司 | 治疗酒精使用障碍，疼痛和其他疾病的药物组合与方法 |
| MY160737A (en) | 2009-04-03 | 2017-03-15 | Hoffmann La Roche | Propane-i-sulfonic acid {3- [5-(4-chloro-phenyl) -1h -pyrrolo [2, 3-b] pyridine-3-carbonyl] -2,4 difluoro-phenyl} - amide compositions and uses thereof |
| TW201103904A (en) * | 2009-06-11 | 2011-02-01 | Hoffmann La Roche | Janus kinase inhibitor compounds and methods |
| US8329724B2 (en) | 2009-08-03 | 2012-12-11 | Hoffmann-La Roche Inc. | Process for the manufacture of pharmaceutically active compounds |
| GB0914726D0 (en) * | 2009-08-24 | 2009-09-30 | Univ Manchester | Kinase inhibitors |
| SG10201407129SA (en) | 2009-11-06 | 2014-12-30 | Plexxikon Inc | Compounds and methods for kinase modulation, and indications therefor |
| KR20140015162A (ko) | 2010-01-12 | 2014-02-06 | 에프. 호프만-라 로슈 아게 | 트라이사이클릭 헤테로사이클릭 화합물, 조성물 및 이의 사용 방법 |
| US8785648B1 (en) | 2010-08-10 | 2014-07-22 | The Regents Of The University Of California | PKC-epsilon inhibitors |
| CN103517710B (zh) | 2011-02-07 | 2017-05-31 | 普莱希科公司 | 用于激酶调节的化合物 |
| TWI558702B (zh) | 2011-02-21 | 2016-11-21 | 普雷辛肯公司 | 醫藥活性物質的固態形式 |
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2004
- 2004-02-18 GB GBGB0403635.6A patent/GB0403635D0/en not_active Ceased
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2005
- 2005-02-18 EP EP05708700A patent/EP1715862A1/en not_active Withdrawn
- 2005-02-18 WO PCT/IB2005/000600 patent/WO2005082367A1/en not_active Ceased
- 2005-02-18 JP JP2006553706A patent/JP2007523155A/ja active Pending
- 2005-02-18 US US10/589,875 patent/US20070191420A1/en not_active Abandoned