NZ602948A - Inhibitors of protein tyrosine kinase activity and use thereof to treat ophthalmic disorders - Google Patents
Inhibitors of protein tyrosine kinase activity and use thereof to treat ophthalmic disordersInfo
- Publication number
- NZ602948A NZ602948A NZ602948A NZ60294811A NZ602948A NZ 602948 A NZ602948 A NZ 602948A NZ 602948 A NZ602948 A NZ 602948A NZ 60294811 A NZ60294811 A NZ 60294811A NZ 602948 A NZ602948 A NZ 602948A
- Authority
- NZ
- New Zealand
- Prior art keywords
- pyridin
- thieno
- methyl
- urea
- cyclopropylureido
- Prior art date
Links
- 102000004022 Protein-Tyrosine Kinases Human genes 0.000 title 1
- 108090000412 Protein-Tyrosine Kinases Proteins 0.000 title 1
- 239000003112 inhibitor Substances 0.000 title 1
- 208000037265 diseases, disorders, signs and symptoms Diseases 0.000 abstract 6
- 201000010099 disease Diseases 0.000 abstract 3
- 208000035475 disorder Diseases 0.000 abstract 3
- FHMXGMUZEKYIOC-UHFFFAOYSA-N 1-[[2-[7-[2-fluoro-4-(propan-2-ylcarbamoylamino)phenoxy]thieno[3,2-b]pyridin-2-yl]-3-methylimidazol-4-yl]methyl]-1-(2-methoxyethyl)-3-propan-2-ylurea Chemical compound CN1C(CN(CCOC)C(=O)NC(C)C)=CN=C1C1=CC2=NC=CC(OC=3C(=CC(NC(=O)NC(C)C)=CC=3)F)=C2S1 FHMXGMUZEKYIOC-UHFFFAOYSA-N 0.000 abstract 1
- FPJHCRUFSLQUPR-UHFFFAOYSA-N 1-[[6-[7-[4-(cyclopropylcarbamoylamino)-2-fluorophenoxy]thieno[3,2-b]pyridin-2-yl]pyridin-3-yl]methyl]-3-ethyl-1-(2-methoxyethyl)urea Chemical compound N1=CC(CN(CCOC)C(=O)NCC)=CC=C1C1=CC2=NC=CC(OC=3C(=CC(NC(=O)NC4CC4)=CC=3)F)=C2S1 FPJHCRUFSLQUPR-UHFFFAOYSA-N 0.000 abstract 1
- VYDLYKCORPUVSS-UHFFFAOYSA-N 1-cyclopropyl-3-[3-fluoro-4-[2-[1-(2-morpholin-4-ylethyl)imidazol-4-yl]thieno[3,2-b]pyridin-7-yl]oxyphenyl]urea Chemical compound C=1C=C(OC=2C=3SC(=CC=3N=CC=2)C=2N=CN(CCN3CCOCC3)C=2)C(F)=CC=1NC(=O)NC1CC1 VYDLYKCORPUVSS-UHFFFAOYSA-N 0.000 abstract 1
- VKLZEGBMRPRXHF-UHFFFAOYSA-N 1-cyclopropyl-3-[3-fluoro-4-[2-[1-[2-[2-hydroxyethyl(methyl)amino]ethyl]pyrazol-4-yl]thieno[3,2-b]pyridin-7-yl]oxyphenyl]urea Chemical compound C1=NN(CCN(CCO)C)C=C1C1=CC2=NC=CC(OC=3C(=CC(NC(=O)NC4CC4)=CC=3)F)=C2S1 VKLZEGBMRPRXHF-UHFFFAOYSA-N 0.000 abstract 1
- SQSKLMYYPRSMPJ-UHFFFAOYSA-N 1-cyclopropyl-3-[3-fluoro-4-[2-[5-[(2-methylsulfonylethylamino)methyl]pyridin-2-yl]thieno[3,2-b]pyridin-7-yl]oxyphenyl]urea Chemical compound N1=CC(CNCCS(=O)(=O)C)=CC=C1C1=CC2=NC=CC(OC=3C(=CC(NC(=O)NC4CC4)=CC=3)F)=C2S1 SQSKLMYYPRSMPJ-UHFFFAOYSA-N 0.000 abstract 1
- BBBWXOIQCLHMQG-UHFFFAOYSA-N 1-cyclopropyl-3-[3-fluoro-4-[2-[5-[4-(4-methylpiperazin-1-yl)piperidine-1-carbonyl]pyridin-2-yl]thieno[3,2-b]pyridin-7-yl]oxyphenyl]urea Chemical compound C1CN(C)CCN1C1CCN(C(=O)C=2C=NC(=CC=2)C=2SC3=C(OC=4C(=CC(NC(=O)NC5CC5)=CC=4)F)C=CN=C3C=2)CC1 BBBWXOIQCLHMQG-UHFFFAOYSA-N 0.000 abstract 1
- 206010012689 Diabetic retinopathy Diseases 0.000 abstract 1
- 201000010183 Papilledema Diseases 0.000 abstract 1
- 206010038886 Retinal oedema Diseases 0.000 abstract 1
- XSQUKJJJFZCRTK-UHFFFAOYSA-N Urea Chemical compound NC(N)=O XSQUKJJJFZCRTK-UHFFFAOYSA-N 0.000 abstract 1
- IZMVYXCZWXIDDF-HKBQPEDESA-N [2-[4-[[6-[7-[4-(cyclopropylcarbamoylamino)-2-fluorophenoxy]thieno[3,2-b]pyridin-2-yl]pyridin-3-yl]methyl]piperazin-1-yl]-2-oxoethyl] (2s)-2-amino-3-methylbutanoate Chemical compound C1CN(C(=O)COC(=O)[C@@H](N)C(C)C)CCN1CC1=CC=C(C=2SC3=C(OC=4C(=CC(NC(=O)NC5CC5)=CC=4)F)C=CN=C3C=2)N=C1 IZMVYXCZWXIDDF-HKBQPEDESA-N 0.000 abstract 1
- 206010064930 age-related macular degeneration Diseases 0.000 abstract 1
- 230000033115 angiogenesis Effects 0.000 abstract 1
- 239000004202 carbamide Substances 0.000 abstract 1
- 150000001875 compounds Chemical class 0.000 abstract 1
- 239000003937 drug carrier Substances 0.000 abstract 1
- 208000002780 macular degeneration Diseases 0.000 abstract 1
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 abstract 1
- FNKYANORZXLDDE-UHFFFAOYSA-N n-[[2-[7-[4-(cyclopropylcarbamoylamino)-2-fluorophenoxy]thieno[3,2-b]pyridin-2-yl]-3-methylimidazol-4-yl]methyl]-2-hydroxy-n-(2-methoxyethyl)acetamide Chemical compound CN1C(CN(CCOC)C(=O)CO)=CN=C1C1=CC2=NC=CC(OC=3C(=CC(NC(=O)NC4CC4)=CC=3)F)=C2S1 FNKYANORZXLDDE-UHFFFAOYSA-N 0.000 abstract 1
- TVCGHDKFWBDODT-UHFFFAOYSA-N n-[[6-[7-[4-(cyclopropylcarbamoylamino)-2,3-difluorophenoxy]thieno[3,2-b]pyridin-2-yl]pyridin-3-yl]methyl]-n-(2-methoxyethyl)acetamide Chemical compound N1=CC(CN(CCOC)C(C)=O)=CC=C1C1=CC2=NC=CC(OC=3C(=C(F)C(NC(=O)NC4CC4)=CC=3)F)=C2S1 TVCGHDKFWBDODT-UHFFFAOYSA-N 0.000 abstract 1
- 201000011195 retinal edema Diseases 0.000 abstract 1
- DBDCNCCRPKTRSD-UHFFFAOYSA-N thieno[3,2-b]pyridine Chemical class C1=CC=C2SC=CC2=N1 DBDCNCCRPKTRSD-UHFFFAOYSA-N 0.000 abstract 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D495/00—Heterocyclic compounds containing in the condensed system at least one hetero ring having sulfur atoms as the only ring hetero atoms
- C07D495/02—Heterocyclic compounds containing in the condensed system at least one hetero ring having sulfur atoms as the only ring hetero atoms in which the condensed system contains two hetero rings
- C07D495/04—Ortho-condensed systems
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K31/00—Medicinal preparations containing organic active ingredients
- A61K31/33—Heterocyclic compounds
- A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
- A61K31/435—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with one nitrogen as the only ring hetero atom
- A61K31/4353—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with one nitrogen as the only ring hetero atom ortho- or peri-condensed with heterocyclic ring systems
- A61K31/4365—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with one nitrogen as the only ring hetero atom ortho- or peri-condensed with heterocyclic ring systems the heterocyclic ring system having sulfur as a ring hetero atom, e.g. ticlopidine
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K38/00—Medicinal preparations containing peptides
- A61K38/005—Enzyme inhibitors
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P27/00—Drugs for disorders of the senses
- A61P27/02—Ophthalmic agents
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P35/00—Antineoplastic agents
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P43/00—Drugs for specific purposes, not provided for in groups A61P1/00-A61P41/00
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P9/00—Drugs for disorders of the cardiovascular system
- A61P9/10—Drugs for disorders of the cardiovascular system for treating ischaemic or atherosclerotic diseases, e.g. antianginal drugs, coronary vasodilators, drugs for myocardial infarction, retinopathy, cerebrovascula insufficiency, renal arteriosclerosis
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D519/00—Heterocyclic compounds containing more than one system of two or more relevant hetero rings condensed among themselves or condensed with a common carbocyclic ring system not provided for in groups C07D453/00 or C07D455/00
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07F—ACYCLIC, CARBOCYCLIC OR HETEROCYCLIC COMPOUNDS CONTAINING ELEMENTS OTHER THAN CARBON, HYDROGEN, HALOGEN, OXYGEN, NITROGEN, SULFUR, SELENIUM OR TELLURIUM
- C07F9/00—Compounds containing elements of Groups 5 or 15 of the Periodic Table
- C07F9/02—Phosphorus compounds
- C07F9/547—Heterocyclic compounds, e.g. containing phosphorus as a ring hetero atom
- C07F9/6561—Heterocyclic compounds, e.g. containing phosphorus as a ring hetero atom containing systems of two or more relevant hetero rings condensed among themselves or condensed with a common carbocyclic ring or ring system, with or without other non-condensed hetero rings
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07K—PEPTIDES
- C07K5/00—Peptides containing up to four amino acids in a fully defined sequence; Derivatives thereof
- C07K5/04—Peptides containing up to four amino acids in a fully defined sequence; Derivatives thereof containing only normal peptide links
- C07K5/06—Dipeptides
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Health & Medical Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- General Health & Medical Sciences (AREA)
- Medicinal Chemistry (AREA)
- Veterinary Medicine (AREA)
- Public Health (AREA)
- Pharmacology & Pharmacy (AREA)
- Animal Behavior & Ethology (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Engineering & Computer Science (AREA)
- General Chemical & Material Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Biochemistry (AREA)
- Proteomics, Peptides & Aminoacids (AREA)
- Molecular Biology (AREA)
- Epidemiology (AREA)
- Immunology (AREA)
- Biophysics (AREA)
- Genetics & Genomics (AREA)
- Ophthalmology & Optometry (AREA)
- Heart & Thoracic Surgery (AREA)
- Cardiology (AREA)
- Vascular Medicine (AREA)
- Urology & Nephrology (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Heterocyclic Carbon Compounds Containing A Hetero Ring Having Oxygen Or Sulfur (AREA)
- Nitrogen And Oxygen Or Sulfur-Condensed Heterocyclic Ring Systems (AREA)
- Nitrogen Condensed Heterocyclic Rings (AREA)
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US32480310P | 2010-04-16 | 2010-04-16 | |
| PCT/CA2011/000390 WO2011127565A1 (en) | 2010-04-16 | 2011-04-08 | Inhibitors of protein tyrosine kinase activity and use thereof to treat ophthalmic disorders |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| NZ602948A true NZ602948A (en) | 2014-09-26 |
Family
ID=44788641
Family Applications (2)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| NZ602948A NZ602948A (en) | 2010-04-16 | 2011-04-08 | Inhibitors of protein tyrosine kinase activity and use thereof to treat ophthalmic disorders |
| NZ602954A NZ602954A (en) | 2010-04-16 | 2011-04-08 | Inhibitors of protein tyrosine kinase activity |
Family Applications After (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| NZ602954A NZ602954A (en) | 2010-04-16 | 2011-04-08 | Inhibitors of protein tyrosine kinase activity |
Country Status (19)
| Country | Link |
|---|---|
| US (3) | US8455484B2 (enExample) |
| EP (2) | EP2563794A4 (enExample) |
| JP (2) | JP2013523846A (enExample) |
| KR (2) | KR20130100234A (enExample) |
| CN (2) | CN103025740B (enExample) |
| AR (2) | AR080871A1 (enExample) |
| AU (2) | AU2011241420B2 (enExample) |
| CA (2) | CA2796008A1 (enExample) |
| CO (2) | CO6630193A2 (enExample) |
| EA (2) | EA201291055A1 (enExample) |
| MX (2) | MX2012012032A (enExample) |
| MY (1) | MY157319A (enExample) |
| NZ (2) | NZ602948A (enExample) |
| PH (2) | PH12012502073A1 (enExample) |
| SG (2) | SG184882A1 (enExample) |
| TW (2) | TW201204735A (enExample) |
| UA (1) | UA108878C2 (enExample) |
| WO (2) | WO2011127567A1 (enExample) |
| ZA (2) | ZA201207482B (enExample) |
Families Citing this family (11)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| ES2635131T3 (es) * | 2007-08-29 | 2017-10-02 | Methylgene Inc. | Inhibidores de la actividad de la proteína tirosina cinasa |
| BRPI0923670A2 (pt) * | 2008-03-05 | 2013-07-30 | Methylgene Inc | inibidores da atividade de proteÍna tirosina quinase e seu uso, bem como composiÇço compreendendo os mesmos |
| MY157319A (en) * | 2010-04-16 | 2016-05-31 | Methylgene Inc | Inhibitors of protein tyrosine kinase activity |
| US20130090327A1 (en) * | 2011-09-30 | 2013-04-11 | Methylgene Inc. | Inhibitors of Protein Tyrosine Kinase Activity |
| US20130096135A1 (en) * | 2011-09-30 | 2013-04-18 | Methylgene Inc. | Selected Inhibitors of Protein Tyrosine Kinase Activity |
| WO2013044361A1 (en) * | 2011-09-30 | 2013-04-04 | Methylgene Inc. | Inhibitors of protein tyrosine kinase activity |
| EP2791108B1 (en) | 2011-12-15 | 2016-07-27 | Pfizer Limited | Sulfonamide derivatives |
| WO2016040554A1 (en) | 2014-09-10 | 2016-03-17 | Temple University-Of The Commonwealth System Of Higher Education | Novel 5-hydroxytryptamine receptor 7 activity modulators and their method of use |
| US20180221365A1 (en) * | 2015-05-12 | 2018-08-09 | Temple University-Of The Commonwealth System Of Higher Education | Novel sigma-2 receptor binders and their method of use |
| JP6664170B2 (ja) * | 2015-08-31 | 2020-03-13 | 広栄化学工業株式会社 | アミノヒドロキシピリジン化合物の製造方法 |
| CN108530464B (zh) * | 2017-03-02 | 2020-10-27 | 深圳海王医药科技研究院有限公司 | 一种多靶点激酶抑制剂 |
Family Cites Families (11)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US20050020619A1 (en) * | 2003-07-24 | 2005-01-27 | Patrick Betschmann | Thienopyridine kinase inhibitors |
| WO2006010264A1 (en) * | 2004-07-30 | 2006-02-02 | Methylgene, Inc. | Inhibitors of vegf receptor and hgf receptor signaling |
| AU2006229343A1 (en) * | 2005-03-28 | 2006-10-05 | Kirin Pharma Kabushiki Kaisha | Thienopyridine derivative, or quinoline derivative, or quinazoline derivative, having c-Met autophosphorylation inhibiting potency |
| JO2787B1 (en) * | 2005-04-27 | 2014-03-15 | امجين إنك, | Alternative amide derivatives and methods of use |
| EP1904504B1 (en) * | 2005-05-20 | 2014-03-19 | MethylGene Inc. | Inhibitors of vegf receptor and hgf receptor signaling |
| BRPI0610322B8 (pt) * | 2005-05-20 | 2021-05-25 | Methylgene Inc | inibidores de sinalização de receptor de vegf e de receptor de hgf e composição farmacêutica |
| ES2635131T3 (es) * | 2007-08-29 | 2017-10-02 | Methylgene Inc. | Inhibidores de la actividad de la proteína tirosina cinasa |
| WO2009026720A1 (en) * | 2007-08-29 | 2009-03-05 | Methylgene Inc. | Processes and intermediates for preparing fused heterocyclic kinase inhibitors |
| BRPI0923670A2 (pt) * | 2008-03-05 | 2013-07-30 | Methylgene Inc | inibidores da atividade de proteÍna tirosina quinase e seu uso, bem como composiÇço compreendendo os mesmos |
| MY157319A (en) * | 2010-04-16 | 2016-05-31 | Methylgene Inc | Inhibitors of protein tyrosine kinase activity |
| WO2013044361A1 (en) * | 2011-09-30 | 2013-04-04 | Methylgene Inc. | Inhibitors of protein tyrosine kinase activity |
-
2011
- 2011-04-08 MY MYPI2012004621A patent/MY157319A/en unknown
- 2011-04-08 SG SG2012076725A patent/SG184882A1/en unknown
- 2011-04-08 AU AU2011241420A patent/AU2011241420B2/en not_active Ceased
- 2011-04-08 EA EA201291055A patent/EA201291055A1/ru unknown
- 2011-04-08 TW TW100112308A patent/TW201204735A/zh unknown
- 2011-04-08 PH PH1/2012/502073A patent/PH12012502073A1/en unknown
- 2011-04-08 NZ NZ602948A patent/NZ602948A/en not_active IP Right Cessation
- 2011-04-08 JP JP2013504075A patent/JP2013523846A/ja not_active Ceased
- 2011-04-08 NZ NZ602954A patent/NZ602954A/en not_active IP Right Cessation
- 2011-04-08 PH PH1/2012/502070A patent/PH12012502070A1/en unknown
- 2011-04-08 EA EA201291052A patent/EA201291052A1/ru unknown
- 2011-04-08 AR ARP110101191A patent/AR080871A1/es unknown
- 2011-04-08 US US13/082,944 patent/US8455484B2/en not_active Expired - Fee Related
- 2011-04-08 EP EP20110768305 patent/EP2563794A4/en not_active Withdrawn
- 2011-04-08 JP JP2013504076A patent/JP2013525286A/ja not_active Ceased
- 2011-04-08 US US13/082,923 patent/US8906852B2/en not_active Expired - Fee Related
- 2011-04-08 CN CN201180029735.1A patent/CN103025740B/zh not_active Expired - Fee Related
- 2011-04-08 UA UAA201211687A patent/UA108878C2/ru unknown
- 2011-04-08 AR ARP110101195A patent/AR080875A1/es unknown
- 2011-04-08 CA CA2796008A patent/CA2796008A1/en not_active Abandoned
- 2011-04-08 SG SG2012076733A patent/SG184883A1/en unknown
- 2011-04-08 CA CA2796054A patent/CA2796054A1/en not_active Abandoned
- 2011-04-08 CN CN2011800297313A patent/CN102947315A/zh active Pending
- 2011-04-08 TW TW100112307A patent/TW201204734A/zh unknown
- 2011-04-08 MX MX2012012032A patent/MX2012012032A/es not_active Application Discontinuation
- 2011-04-08 MX MX2012012031A patent/MX2012012031A/es active IP Right Grant
- 2011-04-08 AU AU2011241422A patent/AU2011241422B2/en not_active Ceased
- 2011-04-08 WO PCT/CA2011/000394 patent/WO2011127567A1/en not_active Ceased
- 2011-04-08 KR KR1020127029841A patent/KR20130100234A/ko not_active Withdrawn
- 2011-04-08 WO PCT/CA2011/000390 patent/WO2011127565A1/en not_active Ceased
- 2011-04-08 KR KR1020127030161A patent/KR20130058006A/ko not_active Withdrawn
- 2011-04-08 EP EP11768307.8A patent/EP2563795A4/en not_active Withdrawn
-
2012
- 2012-10-05 ZA ZA2012/07482A patent/ZA201207482B/en unknown
- 2012-10-09 ZA ZA2012/07557A patent/ZA201207557B/en unknown
- 2012-11-15 CO CO12207310A patent/CO6630193A2/es active IP Right Grant
- 2012-11-15 CO CO12207317A patent/CO6640224A2/es active IP Right Grant
-
2014
- 2014-06-18 US US14/308,408 patent/US20140315801A1/en not_active Abandoned
Also Published As
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| NZ602948A (en) | Inhibitors of protein tyrosine kinase activity and use thereof to treat ophthalmic disorders | |
| MY167423A (en) | Quinoline carboxamide and quinoline carbonitrile derivatives as mglur2-negative allosteric modulators,compositions,and their use | |
| RU2650895C2 (ru) | Соединения замещенных пиразолонов и способы использования | |
| ES2572527T3 (es) | Inhibidores de PDE10 de pirimidina | |
| NO20052893L (no) | Ftalazinderivater for behandling av inflammatoriske sykdommer | |
| RU2015148189A (ru) | ПРОИЗВОДНЫЕ 2-АМИДОПИРИДО[4, 3-d]ПИРИМИДИН-5-ОНА И ИХ ПРИМЕНЕНИЕ В КАЧЕСТВЕ ИНГИБИТОРОВ WEE-1 | |
| SG10201903578VA (en) | Indole carboxamides compounds useful as kinase inhibitors | |
| HRP20121069T1 (hr) | Supstituirani derivati amida kao inhibitori protein kinaze | |
| ATE482708T1 (de) | Behandlung von neovaskulären augenerkrankungen, wie z.b. maculadegeneration, angioiden streifen, uveitis und makulaödemen | |
| MX2008013836A (es) | Derivados de 2-piridona para el tratamiento de enfermedades o condiciones en las cuales es benefica la inhibicion de la actividad de elastasa de neutrofilos. | |
| NZ630719A (en) | Imidazo [1, 2 - b] pyridazine - based compounds, compositions comprising them, and uses thereof | |
| ME02409B (me) | Novi heterociklični derivati i njihova upotreba u tretmanu neuroloških poremećaja | |
| IL288508A (en) | History of n-(5-(6-ethoxypyrazin-2-yl)pyridin-2-yl)-4-(2-(methylsulfonamido)pyrimidin-4-yl)tetrahydro-h2-pyran-4-carboxamide and related compounds as human ctps1 inhibitors to treat proliferative diseases | |
| TW200833341A (en) | 6-aminoimidazo[1,2-b]pyridazine analogs as rho kinase inhibitors for the treatment of rho kinase-mediated diseases and conditions | |
| HRP20191268T1 (hr) | Derivati tieno[2,3-c]pirol-4-ona kao inhibitori erk | |
| RU2016121150A (ru) | Терапевтическое средство против заболеваний, связанных с гибелью клеток эндотелия роговицы, обусловленной состоянием эндоплазматического ретикулума | |
| NZ612000A (en) | Bicyclo[3.2.1]octyl amide derivatives and uses of same | |
| RU2006136881A (ru) | Фармацевтическая композиция, содержащая производное бензодиазепина и ингибитор белка слияния rsv | |
| NZ590954A (en) | Compounds as kinase inhibitors | |
| NZ601684A (en) | Salt of fused heterocyclic derivative and crystal thereof | |
| PE20030714A1 (es) | Derivados de amidas de acido antranilico como inhibidores del receptor de tirosina quinasa vegf | |
| RU2016106641A (ru) | Терапевтические средства, направленные на ecm эндотелия роговицы | |
| EA200601418A1 (ru) | ПРОИЗВОДНЫЕ 1Н-ТИЕНО [2,3-с] ПИРАЗОЛА, ПРЕДНАЗНАЧЕННЫЕ ДЛЯ ИСПОЛЬЗОВАНИЯ В КАЧЕСТВЕ ИНГИБИТОРОВ КИНАЗЫ | |
| HRP20030912A2 (en) | Piperazine oxime derivatives having nk-1 receptorantagonistic activity | |
| JP2013540791A5 (enExample) |
Legal Events
| Date | Code | Title | Description |
|---|---|---|---|
| PSEA | Patent sealed | ||
| RENW | Renewal (renewal fees accepted) |
Free format text: PATENT RENEWED FOR 1 YEAR UNTIL 08 APR 2016 BY BALDWINS INTELLECTUAL PROPERTY Effective date: 20150204 |
|
| LAPS | Patent lapsed |