CY1110392T1 - Υποκατεστημενα παραγωγα μορφολινης και θειομορφολινης - Google Patents
Υποκατεστημενα παραγωγα μορφολινης και θειομορφολινηςInfo
- Publication number
- CY1110392T1 CY1110392T1 CY20081100969T CY081100969T CY1110392T1 CY 1110392 T1 CY1110392 T1 CY 1110392T1 CY 20081100969 T CY20081100969 T CY 20081100969T CY 081100969 T CY081100969 T CY 081100969T CY 1110392 T1 CY1110392 T1 CY 1110392T1
- Authority
- CY
- Cyprus
- Prior art keywords
- substituted morpholine
- thiomorpholine derivatives
- thiomorpholine
- derivatives
- morpholine
- Prior art date
Links
Classifications
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D265/00—Heterocyclic compounds containing six-membered rings having one nitrogen atom and one oxygen atom as the only ring hetero atoms
- C07D265/28—1,4-Oxazines; Hydrogenated 1,4-oxazines
- C07D265/30—1,4-Oxazines; Hydrogenated 1,4-oxazines not condensed with other rings
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D265/00—Heterocyclic compounds containing six-membered rings having one nitrogen atom and one oxygen atom as the only ring hetero atoms
- C07D265/04—1,3-Oxazines; Hydrogenated 1,3-oxazines
- C07D265/06—1,3-Oxazines; Hydrogenated 1,3-oxazines not condensed with other rings
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P25/00—Drugs for disorders of the nervous system
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P25/00—Drugs for disorders of the nervous system
- A61P25/04—Centrally acting analgesics, e.g. opioids
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P25/00—Drugs for disorders of the nervous system
- A61P25/06—Antimigraine agents
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P25/00—Drugs for disorders of the nervous system
- A61P25/08—Antiepileptics; Anticonvulsants
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P25/00—Drugs for disorders of the nervous system
- A61P25/14—Drugs for disorders of the nervous system for treating abnormal movements, e.g. chorea, dyskinesia
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P25/00—Drugs for disorders of the nervous system
- A61P25/14—Drugs for disorders of the nervous system for treating abnormal movements, e.g. chorea, dyskinesia
- A61P25/16—Anti-Parkinson drugs
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P25/00—Drugs for disorders of the nervous system
- A61P25/18—Antipsychotics, i.e. neuroleptics; Drugs for mania or schizophrenia
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P25/00—Drugs for disorders of the nervous system
- A61P25/20—Hypnotics; Sedatives
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P25/00—Drugs for disorders of the nervous system
- A61P25/22—Anxiolytics
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P25/00—Drugs for disorders of the nervous system
- A61P25/24—Antidepressants
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P25/00—Drugs for disorders of the nervous system
- A61P25/28—Drugs for disorders of the nervous system for treating neurodegenerative disorders of the central nervous system, e.g. nootropic agents, cognition enhancers, drugs for treating Alzheimer's disease or other forms of dementia
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D279/00—Heterocyclic compounds containing six-membered rings having one nitrogen atom and one sulfur atom as the only ring hetero atoms
- C07D279/10—1,4-Thiazines; Hydrogenated 1,4-thiazines
- C07D279/12—1,4-Thiazines; Hydrogenated 1,4-thiazines not condensed with other rings
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D295/00—Heterocyclic compounds containing polymethylene-imine rings with at least five ring members, 3-azabicyclo [3.2.2] nonane, piperazine, morpholine or thiomorpholine rings, having only hydrogen atoms directly attached to the ring carbon atoms
- C07D295/04—Heterocyclic compounds containing polymethylene-imine rings with at least five ring members, 3-azabicyclo [3.2.2] nonane, piperazine, morpholine or thiomorpholine rings, having only hydrogen atoms directly attached to the ring carbon atoms with substituted hydrocarbon radicals attached to ring nitrogen atoms
- C07D295/12—Heterocyclic compounds containing polymethylene-imine rings with at least five ring members, 3-azabicyclo [3.2.2] nonane, piperazine, morpholine or thiomorpholine rings, having only hydrogen atoms directly attached to the ring carbon atoms with substituted hydrocarbon radicals attached to ring nitrogen atoms substituted by singly or doubly bound nitrogen atoms
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D295/00—Heterocyclic compounds containing polymethylene-imine rings with at least five ring members, 3-azabicyclo [3.2.2] nonane, piperazine, morpholine or thiomorpholine rings, having only hydrogen atoms directly attached to the ring carbon atoms
- C07D295/04—Heterocyclic compounds containing polymethylene-imine rings with at least five ring members, 3-azabicyclo [3.2.2] nonane, piperazine, morpholine or thiomorpholine rings, having only hydrogen atoms directly attached to the ring carbon atoms with substituted hydrocarbon radicals attached to ring nitrogen atoms
- C07D295/12—Heterocyclic compounds containing polymethylene-imine rings with at least five ring members, 3-azabicyclo [3.2.2] nonane, piperazine, morpholine or thiomorpholine rings, having only hydrogen atoms directly attached to the ring carbon atoms with substituted hydrocarbon radicals attached to ring nitrogen atoms substituted by singly or doubly bound nitrogen atoms
- C07D295/135—Heterocyclic compounds containing polymethylene-imine rings with at least five ring members, 3-azabicyclo [3.2.2] nonane, piperazine, morpholine or thiomorpholine rings, having only hydrogen atoms directly attached to the ring carbon atoms with substituted hydrocarbon radicals attached to ring nitrogen atoms substituted by singly or doubly bound nitrogen atoms with the ring nitrogen atoms and the substituent nitrogen atoms separated by carbocyclic rings or by carbon chains interrupted by carbocyclic rings
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D307/00—Heterocyclic compounds containing five-membered rings having one oxygen atom as the only ring hetero atom
- C07D307/77—Heterocyclic compounds containing five-membered rings having one oxygen atom as the only ring hetero atom ortho- or peri-condensed with carbocyclic rings or ring systems
- C07D307/78—Benzo [b] furans; Hydrogenated benzo [b] furans
- C07D307/82—Benzo [b] furans; Hydrogenated benzo [b] furans 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 hetero ring
- C07D307/84—Carbon atoms having three bonds to hetero atoms with at the most one bond to halogen
- C07D307/85—Carbon atoms having three bonds to hetero atoms with at the most one bond to halogen attached in position 2
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D413/00—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms
- C07D413/02—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms containing two hetero rings
- C07D413/04—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms containing two hetero rings directly linked by a ring-member-to-ring-member bond
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D417/00—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by group C07D415/00
- C07D417/02—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by group C07D415/00 containing two hetero rings
- C07D417/04—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by group C07D415/00 containing two hetero rings directly linked by a ring-member-to-ring-member bond
Landscapes
- Organic Chemistry (AREA)
- Chemical & Material Sciences (AREA)
- Health & Medical Sciences (AREA)
- Engineering & Computer Science (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Biomedical Technology (AREA)
- Neurology (AREA)
- Neurosurgery (AREA)
- Pharmacology & Pharmacy (AREA)
- Veterinary Medicine (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- General Chemical & Material Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Life Sciences & Earth Sciences (AREA)
- Animal Behavior & Ethology (AREA)
- General Health & Medical Sciences (AREA)
- Public Health (AREA)
- Medicinal Chemistry (AREA)
- Pain & Pain Management (AREA)
- Psychiatry (AREA)
- Psychology (AREA)
- Anesthesiology (AREA)
- Hospice & Palliative Care (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Heterocyclic Carbon Compounds Containing A Hetero Ring Having Nitrogen And Oxygen As The Only Ring Hetero Atoms (AREA)
- Plural Heterocyclic Compounds (AREA)
- Pyridine Compounds (AREA)
Applications Claiming Priority (3)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US55257404P | 2004-03-12 | 2004-03-12 | |
DKPA200400412 | 2004-03-12 | ||
EP05706819A EP1727809B8 (en) | 2004-03-12 | 2005-03-09 | Substituted morpholine and thiomorpholine derivatives |
Publications (1)
Publication Number | Publication Date |
---|---|
CY1110392T1 true CY1110392T1 (el) | 2015-04-29 |
Family
ID=37730781
Family Applications (2)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
CY20081100969T CY1110392T1 (el) | 2004-03-12 | 2008-09-10 | Υποκατεστημενα παραγωγα μορφολινης και θειομορφολινης |
CY20091101325T CY1109656T1 (el) | 2004-03-12 | 2009-12-21 | Υποκατεστημενα παραγωγα μορφολινης και θειομορφολινης |
Family Applications After (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
CY20091101325T CY1109656T1 (el) | 2004-03-12 | 2009-12-21 | Υποκατεστημενα παραγωγα μορφολινης και θειομορφολινης |
Country Status (32)
Families Citing this family (30)
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US7799832B2 (en) | 2003-10-23 | 2010-09-21 | Valeant Pharmaceuticals North America | Combinations of retigabine and sodium channel inhibitors or sodium channel-influencing active compounds for treating pains |
TWI357901B (en) | 2004-03-12 | 2012-02-11 | Lundbeck & Co As H | Substituted morpholine and thiomorpholine derivati |
UA89503C2 (uk) * | 2004-09-13 | 2010-02-10 | Х. Луннбек А/С | Заміщені похідні аніліну |
UA92340C2 (en) * | 2005-03-03 | 2010-10-25 | Х. Луннбек А/С | Substituted pyridine derivatives |
MX2007010547A (es) * | 2005-03-03 | 2007-10-03 | Lundbeck & Co As H | Derivados de piridina sustituidos. |
KR20080096659A (ko) * | 2006-02-07 | 2008-10-31 | 하. 룬트벡 아크티에 셀스카브 | 정신분열증 증상의 치료 또는 감소를 위한 kcnq개방제의 용도 |
US7960436B2 (en) | 2006-06-05 | 2011-06-14 | Valeant Pharmaceuticals International | Substituted arylamino-1,2,3,4-tetrahydro naphthalenes and-2,3-dihydro-1H-indenes as potassium channel modulators |
ES2420960T3 (es) | 2006-08-23 | 2013-08-28 | Valeant Pharmaceuticals International | Derivados de 4-(N-azacicloalquil)anilidas como moduladores de los canales de potasio |
US8993593B2 (en) | 2006-08-23 | 2015-03-31 | Valeant Pharmaceuticals International | N-(4-(6-fluoro-3,4-dihydroisoquinolin-2(1H)-yl)-2,6-dimethylphenyl)-3,3-dimethylbutanamide as potassium channel modulators |
EP2086925B1 (en) | 2006-11-28 | 2011-12-21 | Valeant Pharmaceuticals International | 1,4 diamino bicyclic retigabine analogues as potassium channel modulators |
US20100197564A1 (en) * | 2007-04-19 | 2010-08-05 | Schering Corporation | Diaryl morpholines as cb1 modulators |
US8367684B2 (en) | 2007-06-13 | 2013-02-05 | Valeant Pharmaceuticals International | Derivatives of 4-(N-azacycloalkyl) anilides as potassium channel modulators |
EP2185149A1 (en) * | 2007-08-01 | 2010-05-19 | H. Lundbeck A/S | Use of kncq potassium channel openers for reducing symptoms of or treating disorders or conditions wherein the dopaminergic system is disrupted |
US7786146B2 (en) | 2007-08-13 | 2010-08-31 | Valeant Pharmaceuticals International | Derivatives of 5-amino-4,6-disubstituted indole and 5-amino-4,6-disubstituted indoline as potassium channel modulators |
EP2116618A1 (en) | 2008-05-09 | 2009-11-11 | Agency for Science, Technology And Research | Diagnosis and treatment of Kawasaki disease |
WO2010094644A1 (en) * | 2009-02-17 | 2010-08-26 | Neurosearch A/S | Substituted pyridine derivatives and their medical use |
WO2010094645A1 (en) * | 2009-02-17 | 2010-08-26 | Neurosearch A/S | Substituted pyridine derivatives and their medical use |
TW201041857A (en) * | 2009-05-11 | 2010-12-01 | Lundbeck & Co As H | Stable forms of N-(2,6-dimethyl-4-morpholin-4-yl-phenyl)-3,3-dimethyl-butyramide |
US20100286138A1 (en) * | 2009-05-11 | 2010-11-11 | H. Lundbeck A/S | Stable forms of N-(2,6-Dimethyl-4-morpholin-4-yl-phenyl)-3,3-dimethyl-butyramide |
US20120232058A1 (en) * | 2009-09-07 | 2012-09-13 | Neurosearch A/S | Substituted pyridine derivatives and their medical use |
JP5763758B2 (ja) | 2010-07-08 | 2015-08-12 | ファイザー・インク | Kv7カリウムチャネル開口薬としてのピペリジニルピリミジンアミド |
CN103073455B (zh) | 2011-10-25 | 2015-08-19 | 中国科学院上海药物研究所 | 一类新型的kcnq钾通道激动剂、其制备方法和用途 |
EP2844247A4 (en) * | 2012-04-20 | 2015-11-25 | Anderson Gaweco | ROR MODULATORS AND ITS USES |
CN103044431A (zh) * | 2012-10-22 | 2013-04-17 | 中国药科大学 | 制备五氟磺草胺的新方法 |
US8652527B1 (en) | 2013-03-13 | 2014-02-18 | Upsher-Smith Laboratories, Inc | Extended-release topiramate capsules |
US9101545B2 (en) | 2013-03-15 | 2015-08-11 | Upsher-Smith Laboratories, Inc. | Extended-release topiramate capsules |
WO2016090317A1 (en) * | 2014-12-05 | 2016-06-09 | Aquinnah Pharmaceuticals, Inc. | Sulfonamide derivatives, compositions and methods of use in the treatment of neurodegenerative diseases |
EP3366683A1 (en) * | 2017-02-28 | 2018-08-29 | Acousia Therapeutics GmbH | Cyclic amides, acteamides and ureas useful as potassium channel openers |
WO2020157126A1 (en) | 2019-01-29 | 2020-08-06 | Università degli Studi di Salerno | Modulators of potassium ion channels and uses thereof |
IL282188A (en) * | 2021-04-08 | 2022-11-01 | Yeda Res & Dev | Combined use of ketamine and bretigabine for the treatment of psychiatric disorders |
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JPH03175086A (ja) * | 1989-09-14 | 1991-07-30 | Fuji Photo Film Co Ltd | ジアゾ感熱記録材料 |
DE4200259A1 (de) | 1992-01-08 | 1993-07-15 | Asta Medica Ag | Neue 1,2,4-triaminobenzol-derivate und verfahren zu deren herstellung |
US5688792A (en) * | 1994-08-16 | 1997-11-18 | Pharmacia & Upjohn Company | Substituted oxazine and thiazine oxazolidinone antimicrobials |
DE19539861A1 (de) | 1995-10-26 | 1997-04-30 | Asta Medica Ag | Verwendung von 4-Amino-4-(4-fluorbenzylamino)-1-ethoxy-carbonylaminobenzen zur Prophylaxe und Behandlung der Folgen der akuten und chronischen zerebralen Minderdurchblutung sowie neurodegenerativer Erkrankungen |
NZ329200A (en) * | 1996-12-16 | 1999-05-28 | Hoechst Ag | Sulphonamide substituted quinazoline, isoquinoline, quinoline or benzo[1,3-]oxazine derivatives and medicaments |
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JP2001506271A (ja) * | 1996-12-23 | 2001-05-15 | デュポン ファーマシューティカルズ カンパニー | Xa因子阻害剤としての酸素またはイオウを含む複素環式芳香族化合物 |
JP2001526268A (ja) * | 1997-12-22 | 2001-12-18 | デュポン ファーマシューティカルズ カンパニー | Xa因子阻害剤としての、オルト−置換P1を有する、窒素含有複素環式芳香族化合物 |
WO1999050255A2 (en) | 1998-03-27 | 1999-10-07 | Du Pont Pharmaceuticals Company | Disubstituted pyrazolines and triazolines as factor xa inhibitors |
BR0012934A (pt) * | 1999-08-04 | 2003-07-29 | Icagen Inc | Processos para a redução de dor e de ansiedade |
US6495550B2 (en) * | 1999-08-04 | 2002-12-17 | Icagen, Inc. | Pyridine-substituted benzanilides as potassium ion channel openers |
US6117900A (en) | 1999-09-27 | 2000-09-12 | Asta Medica Aktiengesellschaft | Use of retigabine for the treatment of neuropathic pain |
CA2410489A1 (en) | 2000-05-26 | 2001-12-06 | Bristol-Myers Squibb Company | Human kcnq5 potassium channel, methods and compositions thereof |
WO2001096540A2 (en) | 2000-06-11 | 2001-12-20 | Dupont Pharmaceuticals Company | Hepatitis c protease exosite for inhibitor design |
PE20020044A1 (es) * | 2000-06-16 | 2002-01-30 | Upjohn Co | Tiazina oxazolidinona |
US6589986B2 (en) | 2000-12-20 | 2003-07-08 | Wyeth | Methods of treating anxiety disorders |
NZ526699A (en) * | 2001-01-16 | 2005-03-24 | Astrazeneca Ab | 8-amino derivatives and their use in treating migraine |
KR20030070916A (ko) * | 2001-01-16 | 2003-09-02 | 아스트라제네카 아베 | 치료용 크로몬 화합물 |
CN1250519C (zh) * | 2001-01-19 | 2006-04-12 | 中国人民解放军军事医学科学院毒物药物研究所 | 具有调节钾通道功能的胺衍生物及其制备方法和应用 |
CA2438231A1 (en) * | 2001-02-20 | 2002-08-29 | Gene G. Kinney | 2,4-disubstituted pyrimidine-5-carboxamide derivatives as kcnq potassium channel modulators |
SE0103648D0 (sv) * | 2001-11-01 | 2001-11-01 | Astrazeneca Ab | Therapeutic quinolone compounds |
SE0103649D0 (sv) * | 2001-11-01 | 2001-11-01 | Astrazeneca Ab | Therapeutic quinoline compounds |
TWI357901B (en) * | 2004-03-12 | 2012-02-11 | Lundbeck & Co As H | Substituted morpholine and thiomorpholine derivati |
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2005
- 2005-03-03 TW TW096141845A patent/TWI357901B/zh not_active IP Right Cessation
- 2005-03-03 TW TW094106488A patent/TWI349666B/zh not_active IP Right Cessation
- 2005-03-08 AR ARP050100893A patent/AR049784A1/es active IP Right Grant
- 2005-03-09 WO PCT/DK2005/000159 patent/WO2005087754A1/en active Application Filing
- 2005-03-09 RS RSP-2009/0558A patent/RS51066B/sr unknown
- 2005-03-09 JP JP2007502191A patent/JP5006184B2/ja active Active
- 2005-03-09 RS RSP-2008/0412A patent/RS50606B/sr unknown
- 2005-03-09 KR KR1020127029156A patent/KR20120136422A/ko not_active Application Discontinuation
- 2005-03-09 DE DE602005007474T patent/DE602005007474D1/de active Active
- 2005-03-09 EA EA200601686A patent/EA015120B1/ru unknown
- 2005-03-09 AU AU2005221762A patent/AU2005221762B2/en not_active Ceased
- 2005-03-09 DK DK08007169.9T patent/DK1947093T3/da active
- 2005-03-09 CN CN201110328836.0A patent/CN102516204B/zh active Active
- 2005-03-09 AT AT08007169T patent/ATE443702T1/de active
- 2005-03-09 PL PL08007169T patent/PL1947093T3/pl unknown
- 2005-03-09 EP EP09170831A patent/EP2138487A1/en not_active Withdrawn
- 2005-03-09 EP EP05706819A patent/EP1727809B8/en active Active
- 2005-03-09 KR KR1020067018688A patent/KR101411204B1/ko active IP Right Grant
- 2005-03-09 SG SG200901657-7A patent/SG151254A1/en unknown
- 2005-03-09 SI SI200530344T patent/SI1727809T1/sl unknown
- 2005-03-09 ES ES08007169T patent/ES2334076T3/es active Active
- 2005-03-09 NZ NZ549133A patent/NZ549133A/en not_active IP Right Cessation
- 2005-03-09 SI SI200530872T patent/SI1947093T1/sl unknown
- 2005-03-09 PL PL05706819T patent/PL1727809T3/pl unknown
- 2005-03-09 UA UAA200911734A patent/UA102517C2/ru unknown
- 2005-03-09 BR BRPI0508570A patent/BRPI0508570B8/pt not_active IP Right Cessation
- 2005-03-09 DE DE602005016849T patent/DE602005016849D1/de active Active
- 2005-03-09 DK DK05706819T patent/DK1727809T3/da active
- 2005-03-09 CN CNA2005800078857A patent/CN1930138A/zh active Pending
- 2005-03-09 CA CA2559397A patent/CA2559397C/en active Active
- 2005-03-09 EP EP08007169A patent/EP1947093B9/en active Active
- 2005-03-09 PT PT05706819T patent/PT1727809E/pt unknown
- 2005-03-09 ES ES05706819T patent/ES2306087T3/es active Active
- 2005-03-09 AT AT05706819T patent/ATE398112T1/de active
- 2005-03-09 PT PT08007169T patent/PT1947093E/pt unknown
- 2005-03-11 MY MYPI20051046A patent/MY143698A/en unknown
- 2005-03-11 MY MYPI20094719A patent/MY147786A/en unknown
- 2005-09-03 UA UAA200610517A patent/UA90670C2/uk unknown
- 2005-12-21 US US11/314,802 patent/US7501414B2/en active Active
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2006
- 2006-08-31 ZA ZA2006/07286A patent/ZA200607286B/en unknown
- 2006-09-03 IL IL177859A patent/IL177859A/en active IP Right Grant
- 2006-09-12 EG EGNA2006000856 patent/EG25344A/xx active
- 2006-09-12 CO CO06091597A patent/CO5721001A2/es active IP Right Grant
- 2006-10-10 NO NO20064599A patent/NO337161B1/no not_active IP Right Cessation
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2007
- 2007-11-12 ZA ZA200709718A patent/ZA200709718B/xx unknown
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2008
- 2008-09-10 CY CY20081100969T patent/CY1110392T1/el unknown
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2009
- 2009-01-28 US US12/361,404 patent/US20090143369A1/en not_active Abandoned
- 2009-01-28 US US12/361,509 patent/US7632835B2/en not_active Expired - Fee Related
- 2009-11-03 US US12/611,249 patent/US8012962B2/en not_active Expired - Fee Related
- 2009-11-05 US US12/612,727 patent/US7812023B2/en active Active
- 2009-12-21 CY CY20091101325T patent/CY1109656T1/el unknown
- 2009-12-23 HR HR20090685T patent/HRP20090685T1/hr unknown
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2011
- 2011-07-28 US US13/192,833 patent/US8299075B2/en active Active
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2012
- 2012-12-27 HK HK12113443.2A patent/HK1172618A1/zh unknown
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