HRP20161039T1 - Deuterirani derivati kateholamina i lijekovi koji sadrže navedene spojeve - Google Patents
Deuterirani derivati kateholamina i lijekovi koji sadrže navedene spojeve Download PDFInfo
- Publication number
- HRP20161039T1 HRP20161039T1 HRP20161039TT HRP20161039T HRP20161039T1 HR P20161039 T1 HRP20161039 T1 HR P20161039T1 HR P20161039T T HRP20161039T T HR P20161039TT HR P20161039 T HRP20161039 T HR P20161039T HR P20161039 T1 HRP20161039 T1 HR P20161039T1
- Authority
- HR
- Croatia
- Prior art keywords
- trihydroxybenzyl
- hydrazide
- acceptable salts
- physiologically acceptable
- serine
- Prior art date
Links
- 150000001875 compounds Chemical class 0.000 title claims 2
- 239000003814 drug Substances 0.000 title claims 2
- 150000003943 catecholamines Chemical class 0.000 title 1
- 150000003839 salts Chemical class 0.000 claims 5
- BNQDCRGUHNALGH-UHFFFAOYSA-N benserazide Chemical compound OCC(N)C(=O)NNCC1=CC=C(O)C(O)=C1O BNQDCRGUHNALGH-UHFFFAOYSA-N 0.000 claims 4
- TZFNLOMSOLWIDK-JTQLQIEISA-N carbidopa (anhydrous) Chemical compound NN[C@@](C(O)=O)(C)CC1=CC=C(O)C(O)=C1 TZFNLOMSOLWIDK-JTQLQIEISA-N 0.000 claims 4
- 239000002532 enzyme inhibitor Substances 0.000 claims 4
- WTDRDQBEARUVNC-QMUVANLASA-N (2s)-2-amino-2,3-dideuterio-3-(3,4-dihydroxyphenyl)propanoic acid Chemical compound OC(=O)[C@@]([2H])(N)C([2H])C1=CC=C(O)C(O)=C1 WTDRDQBEARUVNC-QMUVANLASA-N 0.000 claims 3
- 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 3
- IGLYMJRIWWIQQE-QUOODJBBSA-N (1S,2R)-2-phenylcyclopropan-1-amine (1R,2S)-2-phenylcyclopropan-1-amine Chemical compound N[C@H]1C[C@@H]1C1=CC=CC=C1.N[C@@H]1C[C@H]1C1=CC=CC=C1 IGLYMJRIWWIQQE-QUOODJBBSA-N 0.000 claims 2
- BUZLUQORXILCMY-LBPRGKRZSA-N (2s)-2-amino-3-(4-hydroxyphenyl)-n'-[(2,3,4-trihydroxyphenyl)methyl]propanehydrazide Chemical compound C([C@H](N)C(=O)NNCC=1C(=C(O)C(O)=CC=1)O)C1=CC=C(O)C=C1 BUZLUQORXILCMY-LBPRGKRZSA-N 0.000 claims 2
- BNQDCRGUHNALGH-LURJTMIESA-N (2s)-2-amino-3-hydroxy-n'-[(2,3,4-trihydroxyphenyl)methyl]propanehydrazide Chemical compound OC[C@H](N)C(=O)NNCC1=CC=C(O)C(O)=C1O BNQDCRGUHNALGH-LURJTMIESA-N 0.000 claims 2
- VEWUMDXDCNJDHA-UHFFFAOYSA-N 2-amino-n'-[(2,3,4-trihydroxyphenyl)methyl]acetohydrazide Chemical compound NCC(=O)NNCC1=CC=C(O)C(O)=C1O VEWUMDXDCNJDHA-UHFFFAOYSA-N 0.000 claims 2
- KORNTPPJEAJQIU-KJXAQDMKSA-N Cabaser Chemical compound C1=CC([C@H]2C[C@H](CN(CC=C)[C@@H]2C2)C(=O)N(CCCN(C)C)C(=O)NCC)=C3C2=CNC3=C1 KORNTPPJEAJQIU-KJXAQDMKSA-N 0.000 claims 2
- 229960000911 benserazide Drugs 0.000 claims 2
- 229960004596 cabergoline Drugs 0.000 claims 2
- XMRLUNALKLDUPT-UHFFFAOYSA-L calcium;5-butylpyridine-2-carboxylate Chemical compound [Ca+2].CCCCC1=CC=C(C([O-])=O)N=C1.CCCCC1=CC=C(C([O-])=O)N=C1 XMRLUNALKLDUPT-UHFFFAOYSA-L 0.000 claims 2
- VIKKBVWEWMBLAT-UHFFFAOYSA-N calcium;pentyl pyridine-2-carboxylate Chemical compound [Ca].CCCCCOC(=O)C1=CC=CC=N1 VIKKBVWEWMBLAT-UHFFFAOYSA-N 0.000 claims 2
- 229960004205 carbidopa Drugs 0.000 claims 2
- JRURYQJSLYLRLN-BJMVGYQFSA-N entacapone Chemical compound CCN(CC)C(=O)C(\C#N)=C\C1=CC(O)=C(O)C([N+]([O-])=O)=C1 JRURYQJSLYLRLN-BJMVGYQFSA-N 0.000 claims 2
- 229960003337 entacapone Drugs 0.000 claims 2
- 229940125532 enzyme inhibitor Drugs 0.000 claims 2
- YHXISWVBGDMDLQ-UHFFFAOYSA-N moclobemide Chemical compound C1=CC(Cl)=CC=C1C(=O)NCCN1CCOCC1 YHXISWVBGDMDLQ-UHFFFAOYSA-N 0.000 claims 2
- 229960004644 moclobemide Drugs 0.000 claims 2
- 239000000825 pharmaceutical preparation Substances 0.000 claims 2
- MEZLKOACVSPNER-GFCCVEGCSA-N selegiline Chemical compound C#CCN(C)[C@H](C)CC1=CC=CC=C1 MEZLKOACVSPNER-GFCCVEGCSA-N 0.000 claims 2
- 229960003946 selegiline Drugs 0.000 claims 2
- 229960003741 tranylcypromine Drugs 0.000 claims 2
- 208000014094 Dystonic disease Diseases 0.000 claims 1
- 108010051696 Growth Hormone Proteins 0.000 claims 1
- 208000005903 Manganese Poisoning Diseases 0.000 claims 1
- 208000001089 Multiple system atrophy Diseases 0.000 claims 1
- 206010060860 Neurological symptom Diseases 0.000 claims 1
- 208000018737 Parkinson disease Diseases 0.000 claims 1
- 102100024819 Prolactin Human genes 0.000 claims 1
- 108010057464 Prolactin Proteins 0.000 claims 1
- 208000005793 Restless legs syndrome Diseases 0.000 claims 1
- 102100038803 Somatotropin Human genes 0.000 claims 1
- 239000000654 additive Substances 0.000 claims 1
- 206010002026 amyotrophic lateral sclerosis Diseases 0.000 claims 1
- 230000001684 chronic effect Effects 0.000 claims 1
- 208000010118 dystonia Diseases 0.000 claims 1
- 239000000122 growth hormone Substances 0.000 claims 1
- 239000000546 pharmaceutical excipient Substances 0.000 claims 1
- 229940097325 prolactin Drugs 0.000 claims 1
- 230000028327 secretion Effects 0.000 claims 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07B—GENERAL METHODS OF ORGANIC CHEMISTRY; APPARATUS THEREFOR
- C07B59/00—Introduction of isotopes of elements into organic compounds ; Labelled organic compounds per se
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C229/00—Compounds containing amino and carboxyl groups bound to the same carbon skeleton
- C07C229/02—Compounds containing amino and carboxyl groups bound to the same carbon skeleton having amino and carboxyl groups bound to acyclic carbon atoms of the same carbon skeleton
- C07C229/34—Compounds containing amino and carboxyl groups bound to the same carbon skeleton having amino and carboxyl groups bound to acyclic carbon atoms of the same carbon skeleton the carbon skeleton containing six-membered aromatic rings
- C07C229/36—Compounds containing amino and carboxyl groups bound to the same carbon skeleton having amino and carboxyl groups bound to acyclic carbon atoms of the same carbon skeleton the carbon skeleton containing six-membered aromatic rings with at least one amino group and one carboxyl group bound to the same carbon atom of the carbon skeleton
-
- 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
- A61P25/14—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
- A61P43/00—Drugs for specific purposes, not provided for in groups A61P1/00-A61P41/00
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07B—GENERAL METHODS OF ORGANIC CHEMISTRY; APPARATUS THEREFOR
- C07B59/00—Introduction of isotopes of elements into organic compounds ; Labelled organic compounds per se
- C07B59/001—Acyclic or carbocyclic compounds
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C229/00—Compounds containing amino and carboxyl groups bound to the same carbon skeleton
- C07C229/02—Compounds containing amino and carboxyl groups bound to the same carbon skeleton having amino and carboxyl groups bound to acyclic carbon atoms of the same carbon skeleton
- C07C229/04—Compounds containing amino and carboxyl groups bound to the same carbon skeleton having amino and carboxyl groups bound to acyclic carbon atoms of the same carbon skeleton the carbon skeleton being acyclic and saturated
- C07C229/26—Compounds containing amino and carboxyl groups bound to the same carbon skeleton having amino and carboxyl groups bound to acyclic carbon atoms of the same carbon skeleton the carbon skeleton being acyclic and saturated having more than one amino group bound to the carbon skeleton, e.g. lysine
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07B—GENERAL METHODS OF ORGANIC CHEMISTRY; APPARATUS THEREFOR
- C07B2200/00—Indexing scheme relating to specific properties of organic compounds
- C07B2200/07—Optical isomers
Landscapes
- Organic Chemistry (AREA)
- Chemical & Material Sciences (AREA)
- Health & Medical Sciences (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Engineering & Computer Science (AREA)
- General Health & Medical Sciences (AREA)
- Veterinary Medicine (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- General Chemical & Material Sciences (AREA)
- Pharmacology & Pharmacy (AREA)
- Life Sciences & Earth Sciences (AREA)
- Animal Behavior & Ethology (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Public Health (AREA)
- Medicinal Chemistry (AREA)
- Neurosurgery (AREA)
- Biomedical Technology (AREA)
- Neurology (AREA)
- Psychology (AREA)
- Psychiatry (AREA)
- Acyclic And Carbocyclic Compounds In Medicinal Compositions (AREA)
- Low-Molecular Organic Synthesis Reactions Using Catalysts (AREA)
- Medicines That Contain Protein Lipid Enzymes And Other Medicines (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Claims (5)
1. L-2-Amino-2,3-dideutero-3-(3,4-dihidroksifenil) propionska kiselina i stereoizomeri, enantiomeri ili diastereomeri u optički čistom obliku kao i njihove fiziološki prihvatljive soli naznačeni time da su za uporabu kao lijek.
2. L-2-Amino-2,3-dideutero-3-(3,4-dihidroksifenil) propionska kiselina i stereoizomeri, enantiomeri ili diastereomeri u optički čistom obliku kao i njihove fiziološki prihvatljive soli naznačeni time da su za liječenje Parkinsonove bolesti, sindroma nemirnih nogu, distonije, za inhibiranje izlučivanja prolaktina, za stimuliranje oslobađanja hormona rasta, za liječenje neuroloških simptoma kroničnih intoksikacija manganom, amiotrofične lateralne skleroze i multiple sistemske atrofije.
3. Spoj za uporabu prema zahtjevu 2, naznačen time da je u kombinaciji s inhibitorom enzima ili nekoliko inhibitora enzima, koji se biraju iz skupine koju čine D,L-serin 2-(2,3,4-trihidroksibenzil) hidrazid (benzerazid), (-)-L-α-hydrazino-3,4 dihidroksi-α- metilhidrocimetna kiselina (karbidopa), L-serin 2-(2,3,4-trihidroksibenzil) hidrazid, glicin 2-(2,3,4-trihidroksibenzil) hidrazid i L-tirozin 2-(2,3,4-trihidroksibenzil) hidrazid, entakapon, kabergolin, selegilin, moklobemid, tranilcipromin, kalcijev 5-butil pikolinat i kalcijev 5-pentil pikolinat kao i njihove fiziološki prihvatljive soli.
4. Farmaceutski pripravak, naznačen time da pored farmaceutski prihvatljivih pomoćnih tvari i dodataka sadrži L-2-Amino-2,3-dideutero-3-(3,4-dihidroksifenil) propionsku kiselinu i stereoizomere, enantiomere ili diastereomere u optički čistom obliku kao i njihove fiziološki prihvatljive soli.
5. Farmaceutski pripravak prema zahtjevu 4, naznačen time da dodatno sadrži inhibitor enzima ili nekoliko inhibitora enzima, koji se biraju iz skupine koju čine D,L-serin 2-(2,3,4-trihidroksibenzil) hidrazid (benzerazid), (-)-L-α-hydrazino-3,4 dihidroksi-α-metilhidrocimetna kiselina (karbidopa), L-serin 2-(2,3,4-trihidroksibenzil) hidrazid, glicin 2-(2,3,4-trihidroksibenzil) hidrazid i L-tirozin 2-(2,3,4-trihidroksibenzil) hidrazid, entakapon, kabergolin, selegilin, moklobemid, tranilcipromin, kalcijev 5-butil pikolinat i kalcijev 5-pentil pikolinat kao i njihove fiziološki prihvatljive soli.
Applications Claiming Priority (3)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| DE102006008316 | 2006-02-17 | ||
| PCT/EP2007/001555 WO2007093450A2 (en) | 2006-02-17 | 2007-02-16 | Deuterated catecholamine derivatives and medicaments comprising said compounds |
| EP07703542.6A EP1991522B1 (en) | 2006-02-17 | 2007-02-16 | Deuterated catecholamine derivatives and medicaments comprising said compounds |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| HRP20161039T1 true HRP20161039T1 (hr) | 2016-11-04 |
Family
ID=38236462
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| HRP20161039TT HRP20161039T1 (hr) | 2006-02-17 | 2016-08-17 | Deuterirani derivati kateholamina i lijekovi koji sadrže navedene spojeve |
Country Status (24)
| Country | Link |
|---|---|
| US (2) | US8247603B2 (hr) |
| EP (2) | EP1991522B1 (hr) |
| JP (1) | JP5248331B2 (hr) |
| KR (1) | KR101411422B1 (hr) |
| CN (1) | CN101384545B (hr) |
| AU (1) | AU2007214622B2 (hr) |
| BR (1) | BRPI0708071A8 (hr) |
| CA (1) | CA2642593C (hr) |
| CY (1) | CY1117995T1 (hr) |
| DK (1) | DK1991522T3 (hr) |
| EA (1) | EA017983B1 (hr) |
| ES (1) | ES2587368T3 (hr) |
| HR (1) | HRP20161039T1 (hr) |
| HU (1) | HUE028777T2 (hr) |
| IL (1) | IL193102A (hr) |
| LT (1) | LT1991522T (hr) |
| ME (1) | ME02508B (hr) |
| PL (1) | PL1991522T3 (hr) |
| PT (1) | PT1991522T (hr) |
| RS (1) | RS55142B1 (hr) |
| SI (1) | SI1991522T1 (hr) |
| UA (1) | UA97795C2 (hr) |
| WO (1) | WO2007093450A2 (hr) |
| ZA (1) | ZA200806568B (hr) |
Families Citing this family (22)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US7776314B2 (en) | 2002-06-17 | 2010-08-17 | Grunenthal Gmbh | Abuse-proofed dosage system |
| US20070048228A1 (en) | 2003-08-06 | 2007-03-01 | Elisabeth Arkenau-Maric | Abuse-proofed dosage form |
| ES2659394T5 (es) | 2008-06-06 | 2021-12-13 | Pharma Two B Ltd | Composiciones farmacéuticas para el tratamiento de la enfermedad de Parkinson |
| BRPI0916769A2 (pt) | 2008-07-15 | 2017-09-26 | Theracos Inc | derivados de benzilbenzeno deuterados e métodos de uso |
| BR112014019988A8 (pt) | 2012-02-28 | 2017-07-11 | Gruenenthal Gmbh | Forma de dosagem resistente a socamento compreendendo um composto farmacologicamente ativo e um polímero aniônico |
| EP2897615A4 (en) | 2012-09-18 | 2016-04-27 | Auspex Pharmaceuticals Inc | PHARMACOKINETIC FORMULATIONS OF DEUTERATED BENZOCHINOL INHIBITORS OF THE VESICLE MONOAMINE TRANSPORTER 2 |
| US9550780B2 (en) | 2012-09-18 | 2017-01-24 | Auspex Pharmaceuticals, Inc. | Formulations pharmacokinetics of deuterated benzoquinoline inhibitors of vesicular monoamine transporter 2 |
| US9763904B2 (en) | 2013-02-05 | 2017-09-19 | Teva Pharmaceuticals International Gmbh | Position-specific asymmetric deuterium enriched catecholamine derivatives and medicaments comprising said compounds |
| AU2014214055A1 (en) * | 2013-02-05 | 2015-07-16 | Teva Pharmaceuticals International Gmbh | Position-specific asymmetric deuterium enriched catecholamine derivatives and medicaments comprising said compounds |
| WO2014174425A2 (en) * | 2013-04-24 | 2014-10-30 | Mahesh Kandula | Compositions and methods for the treatment of orthostasis and neurological diseases |
| MX2016000219A (es) * | 2013-07-08 | 2016-05-31 | Auspex Pharmaceuticals Inc | Compuestos neurotransmisores de dihidroxifenilo, composiciones y metodos. |
| WO2015077520A1 (en) * | 2013-11-22 | 2015-05-28 | Auspex Pharmaceuticals, Inc. | Methods of treating abnormal muscular activity |
| EA032920B1 (ru) | 2013-12-03 | 2019-08-30 | Оспекс Фармасьютикалз, Инк. | Способы получения соединений бензохинолина |
| KR20160117596A (ko) | 2014-02-07 | 2016-10-10 | 오스펙스 파마슈티칼스, 인코포레이티드 | 신규 제약 제제 |
| EP2918266A1 (en) | 2014-03-11 | 2015-09-16 | CDRD Berolina AB | Composition comprising a dopamine agonist and an L-DOPA derivative for treating Parkinson's disease |
| GB201420341D0 (en) * | 2014-11-17 | 2014-12-31 | Evolution Valves Ltd | Valve arrangement |
| SG11201706959TA (en) | 2015-03-06 | 2017-09-28 | Auspex Pharmaceuticals Inc | Methods for the treatment of abnormal involuntary movement disorders |
| CN106343013A (zh) * | 2015-07-19 | 2017-01-25 | 中国科学院上海有机化学研究所 | 一种粮食储存方法 |
| AR106313A1 (es) | 2015-10-09 | 2018-01-03 | Teva Pharmaceuticals Int Gmbh | Combinación de levodopa deuterada con carbidopa y opicapona para el tratamiento de enfermedad de parkinson |
| CN105360267B (zh) * | 2015-10-09 | 2017-11-10 | 青岛振坤食品机械有限公司 | 一种全自动穿串机 |
| CN105862897B (zh) * | 2016-04-11 | 2018-01-16 | 江苏省华建建设股份有限公司 | 砂质泥岩地基浅基础原槽浇筑施工工法 |
| AU2019395020A1 (en) * | 2018-12-06 | 2021-06-17 | Senda Biosciences, Inc. | Decarboxylase inhibitors for treating Parkinson's disease |
Family Cites Families (11)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US3699158A (en) | 1969-08-25 | 1972-10-17 | Merck & Co Inc | Selective deuteration of tyrosine, aspartic and glutamic acids |
| DE2049807A1 (en) | 1970-10-10 | 1972-04-13 | Hartmeyer H | Conversion of closed cell plastics foam to - open cell structure |
| DE2049115C3 (de) | 1970-10-06 | 1981-07-30 | Zaidan Hojin Biseibutsu Kagaku Kenkyu Kai, Tokyo | Verwendung von Calcium-5-butylpicolinat und/oder Calcium-5-pentylpicolinat bei der Bekämpfung des Parkinsonismus mit 3-(3,4-Dihydroxyphenyl)-L-alanin (L-Dopa) |
| ES2042520T3 (es) * | 1986-06-10 | 1993-12-16 | Chiesi Farma Spa | Composiciones farmaceuticas que contienen el ester metilico de levodopa, preparacion y aplicaciones terapeuticas del mismo. |
| IT1226902B (it) | 1988-07-12 | 1991-02-21 | Mini Ricerca Scient Tecnolog | Processo per la sintesi del levodopa |
| US5354885A (en) * | 1992-12-24 | 1994-10-11 | Yissum Research Development Company Of The Hebrew University Of Jerusalem | Process for preparing ethyl ester of L-DOPA |
| US6221335B1 (en) * | 1994-03-25 | 2001-04-24 | Isotechnika, Inc. | Method of using deuterated calcium channel blockers |
| US6440710B1 (en) * | 1998-12-10 | 2002-08-27 | The Scripps Research Institute | Antibody-catalyzed deuteration, tritiation, dedeuteration or detritiation of carbonyl compounds |
| EP1104760B1 (en) * | 1999-12-03 | 2003-03-12 | Pfizer Products Inc. | Sulfamoylheteroaryl pyrazole compounds as anti-inflammatory/analgesic agents |
| DE10261808A1 (de) * | 2002-12-19 | 2004-07-08 | Turicum Drug Development Ag | Verwendung von L-DOPA, seiner Derivate und diese Verbindungen enthaltender Arzneimittel zur Prophylaxe psychotischer Erkrankungen |
| DE10261807A1 (de) * | 2002-12-19 | 2004-07-01 | Turicum Drug Development Ag | Deuterierte Catecholaminderivate sowie diese Verbindungen enthaltende Arzneimittel |
-
2007
- 2007-02-16 UA UAA200811184A patent/UA97795C2/uk unknown
- 2007-02-16 ES ES07703542.6T patent/ES2587368T3/es active Active
- 2007-02-16 HU HUE07703542A patent/HUE028777T2/en unknown
- 2007-02-16 DK DK07703542.6T patent/DK1991522T3/en active
- 2007-02-16 PT PT77035426T patent/PT1991522T/pt unknown
- 2007-02-16 RS RS20160674A patent/RS55142B1/sr unknown
- 2007-02-16 JP JP2008554702A patent/JP5248331B2/ja not_active Expired - Fee Related
- 2007-02-16 WO PCT/EP2007/001555 patent/WO2007093450A2/en active Application Filing
- 2007-02-16 EP EP07703542.6A patent/EP1991522B1/en active Active
- 2007-02-16 CN CN200780005912.6A patent/CN101384545B/zh not_active Expired - Fee Related
- 2007-02-16 CA CA2642593A patent/CA2642593C/en active Active
- 2007-02-16 LT LTEP07703542.6T patent/LT1991522T/lt unknown
- 2007-02-16 EP EP16170031.5A patent/EP3101001B1/en active Active
- 2007-02-16 SI SI200731819A patent/SI1991522T1/sl unknown
- 2007-02-16 EA EA200801826A patent/EA017983B1/ru not_active IP Right Cessation
- 2007-02-16 PL PL07703542T patent/PL1991522T3/pl unknown
- 2007-02-16 BR BRPI0708071A patent/BRPI0708071A8/pt not_active Application Discontinuation
- 2007-02-16 US US12/224,120 patent/US8247603B2/en not_active Ceased
- 2007-02-16 US US14/464,568 patent/USRE46555E1/en active Active
- 2007-02-16 AU AU2007214622A patent/AU2007214622B2/en not_active Ceased
- 2007-02-16 ME MEP-2016-167A patent/ME02508B/me unknown
- 2007-02-16 KR KR1020087022011A patent/KR101411422B1/ko active IP Right Grant
-
2008
- 2008-07-28 ZA ZA200806568A patent/ZA200806568B/xx unknown
- 2008-07-29 IL IL193102A patent/IL193102A/en active IP Right Grant
-
2016
- 2016-08-17 HR HRP20161039TT patent/HRP20161039T1/hr unknown
- 2016-08-17 CY CY20161100808T patent/CY1117995T1/el unknown
Also Published As
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| HRP20161039T1 (hr) | Deuterirani derivati kateholamina i lijekovi koji sadrže navedene spojeve | |
| WO2009067703A3 (en) | Tapentadol compositions | |
| EA201290865A1 (ru) | Применение леводопы, карбидопы и энтакапона для лечения болезни паркинсона | |
| EA200800147A1 (ru) | Способ получения олмесартан медоксомила | |
| NZ591326A (en) | An extended release pharmaceutical composition of entacapone or salts thereof | |
| WO2013003629A3 (en) | Methods and compositions for inhibition of bone resorption | |
| EA200800161A1 (ru) | Новые фармацевтические композиции с модифицированным высвобождением и способ получения таких композиций | |
| TW200630354A (en) | Substituted amino carboxylic acids | |
| EA200800783A1 (ru) | Композиция тразодона для введения один раз в день | |
| EA201170018A1 (ru) | Разагилин для изменения течения болезни паркинсона | |
| RU2012142811A (ru) | Фармацевтические композиции и пероральные дозированные формы пролекарства леводопы и способы применения | |
| BRPI1008727B8 (pt) | derivado de azol substituído, inibidor de monoamina-oxidase b (maob) e composição farmacêutica contendo os derivadospara o tratamento de doença de parkinson | |
| ATE507827T1 (de) | Behandlung pervasiver entwicklungsstörungen | |
| CO2020006789A2 (es) | Procedimiento para la preparación de (3s)-3-(4-cloro-3-{[(2s,3r)-2-(4-clorofenil)-4,4,4-trifluor-3-metilbutanoil]amino}fenil)-3-ácido ciclopropilpropanoico y su forma cristalina para uso como principio activo farmacéutico | |
| EA200901237A1 (ru) | Применение димирацетама при лечении хронической боли | |
| WO2006037061A3 (en) | Compositions and methods of using d-dopa to treat parkinson's disease | |
| JOP20210019A1 (ar) | شكل جرعة صيدلانية تعطى عن طريق الفم ذات اطلاق مُعدّل | |
| EA202190334A1 (ru) | Фармацевтическая лекарственная форма для перорального введения с модифицированным высвобождением | |
| JP2019515881A5 (hr) | ||
| CA2513088A1 (en) | Deuterated catecholamine derivatives and medicaments comprising said compounds | |
| WO2006133231A3 (en) | Treatment for neurodegenerative diseases | |
| EA201691818A1 (ru) | Фармацевтическая композиция для лечения болезни паркинсона | |
| WO2012161622A3 (ru) | Стимуляторы секреции инкретиновых гормонов, способ их получения и применения | |
| EP3119403B1 (fr) | Composition à base d'acides carboxyliques et son application pour le traitement des hyperkératoses | |
| PH12020551900A1 (en) | Novel compound exhibiting enteropeptidase inhibitory activity |