GT200200257A - Combinacion de una forma de farmaco cristalina y una sal de tiotropio - Google Patents
Combinacion de una forma de farmaco cristalina y una sal de tiotropioInfo
- Publication number
- GT200200257A GT200200257A GT200200257A GT200200257A GT200200257A GT 200200257 A GT200200257 A GT 200200257A GT 200200257 A GT200200257 A GT 200200257A GT 200200257 A GT200200257 A GT 200200257A GT 200200257 A GT200200257 A GT 200200257A
- Authority
- GT
- Guatemala
- Prior art keywords
- tiotropio
- salt
- crystal
- combination
- farmaco
- Prior art date
Links
Classifications
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- B—PERFORMING OPERATIONS; TRANSPORTING
- B82—NANOTECHNOLOGY
- B82Y—SPECIFIC USES OR APPLICATIONS OF NANOSTRUCTURES; MEASUREMENT OR ANALYSIS OF NANOSTRUCTURES; MANUFACTURE OR TREATMENT OF NANOSTRUCTURES
- B82Y5/00—Nanobiotechnology or nanomedicine, e.g. protein engineering or drug delivery
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- 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
- A61K31/439—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 the ring forming part of a bridged ring system, e.g. quinuclidine
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- 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
- A61K31/46—8-Azabicyclo [3.2.1] octane; Derivatives thereof, e.g. atropine, cocaine
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- 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
- A61K31/47—Quinolines; Isoquinolines
- A61K31/4738—Quinolines; Isoquinolines ortho- or peri-condensed with heterocyclic ring systems
- A61K31/4745—Quinolines; Isoquinolines ortho- or peri-condensed with heterocyclic ring systems condensed with ring systems having nitrogen as a ring hetero atom, e.g. phenantrolines
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- A61K31/7042—Compounds having saccharide radicals and heterocyclic rings
- A61K31/7052—Compounds having saccharide radicals and heterocyclic rings having nitrogen as a ring hetero atom, e.g. nucleosides, nucleotides
- A61K31/706—Compounds having saccharide radicals and heterocyclic rings having nitrogen as a ring hetero atom, e.g. nucleosides, nucleotides containing six-membered rings with nitrogen as a ring hetero atom
- A61K31/7064—Compounds having saccharide radicals and heterocyclic rings having nitrogen as a ring hetero atom, e.g. nucleosides, nucleotides containing six-membered rings with nitrogen as a ring hetero atom containing condensed or non-condensed pyrimidines
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- A61K31/7042—Compounds having saccharide radicals and heterocyclic rings
- A61K31/7052—Compounds having saccharide radicals and heterocyclic rings having nitrogen as a ring hetero atom, e.g. nucleosides, nucleotides
- A61K31/706—Compounds having saccharide radicals and heterocyclic rings having nitrogen as a ring hetero atom, e.g. nucleosides, nucleotides containing six-membered rings with nitrogen as a ring hetero atom
- A61K31/7064—Compounds having saccharide radicals and heterocyclic rings having nitrogen as a ring hetero atom, e.g. nucleosides, nucleotides containing six-membered rings with nitrogen as a ring hetero atom containing condensed or non-condensed pyrimidines
- A61K31/7076—Compounds having saccharide radicals and heterocyclic rings having nitrogen as a ring hetero atom, e.g. nucleosides, nucleotides containing six-membered rings with nitrogen as a ring hetero atom containing condensed or non-condensed pyrimidines containing purines, e.g. adenosine, adenylic acid
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- A61K47/50—Medicinal preparations characterised by the non-active ingredients used, e.g. carriers or inert additives; Targeting or modifying agents chemically bound to the active ingredient the non-active ingredient being chemically bound to the active ingredient, e.g. polymer-drug conjugates
- A61K47/69—Medicinal preparations characterised by the non-active ingredients used, e.g. carriers or inert additives; Targeting or modifying agents chemically bound to the active ingredient the non-active ingredient being chemically bound to the active ingredient, e.g. polymer-drug conjugates the conjugate being characterised by physical or galenical forms, e.g. emulsion, particle, inclusion complex, stent or kit
- A61K47/6949—Medicinal preparations characterised by the non-active ingredients used, e.g. carriers or inert additives; Targeting or modifying agents chemically bound to the active ingredient the non-active ingredient being chemically bound to the active ingredient, e.g. polymer-drug conjugates the conjugate being characterised by physical or galenical forms, e.g. emulsion, particle, inclusion complex, stent or kit inclusion complexes, e.g. clathrates, cavitates or fullerenes
- A61K47/6951—Medicinal preparations characterised by the non-active ingredients used, e.g. carriers or inert additives; Targeting or modifying agents chemically bound to the active ingredient the non-active ingredient being chemically bound to the active ingredient, e.g. polymer-drug conjugates the conjugate being characterised by physical or galenical forms, e.g. emulsion, particle, inclusion complex, stent or kit inclusion complexes, e.g. clathrates, cavitates or fullerenes using cyclodextrin
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07H—SUGARS; DERIVATIVES THEREOF; NUCLEOSIDES; NUCLEOTIDES; NUCLEIC ACIDS
- C07H19/00—Compounds containing a hetero ring sharing one ring hetero atom with a saccharide radical; Nucleosides; Mononucleotides; Anhydro-derivatives thereof
- C07H19/02—Compounds containing a hetero ring sharing one ring hetero atom with a saccharide radical; Nucleosides; Mononucleotides; Anhydro-derivatives thereof sharing nitrogen
- C07H19/04—Heterocyclic radicals containing only nitrogen atoms as ring hetero atom
- C07H19/16—Purine radicals
Landscapes
- Health & Medical Sciences (AREA)
- Chemical & Material Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- General Health & Medical Sciences (AREA)
- Pharmacology & Pharmacy (AREA)
- Medicinal Chemistry (AREA)
- Engineering & Computer Science (AREA)
- Public Health (AREA)
- Veterinary Medicine (AREA)
- Animal Behavior & Ethology (AREA)
- Organic Chemistry (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Chemical Kinetics & Catalysis (AREA)
- General Chemical & Material Sciences (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Epidemiology (AREA)
- Molecular Biology (AREA)
- Pulmonology (AREA)
- Biotechnology (AREA)
- Dermatology (AREA)
- Diabetes (AREA)
- Cardiology (AREA)
- Heart & Thoracic Surgery (AREA)
- Nanotechnology (AREA)
- Genetics & Genomics (AREA)
- Biochemistry (AREA)
- Endocrinology (AREA)
- Emergency Medicine (AREA)
- Reproductive Health (AREA)
- Pain & Pain Management (AREA)
- Neurosurgery (AREA)
- Hematology (AREA)
- Immunology (AREA)
- Biomedical Technology (AREA)
- Neurology (AREA)
- Crystallography & Structural Chemistry (AREA)
- Biophysics (AREA)
- Rheumatology (AREA)
- General Engineering & Computer Science (AREA)
- Medical Informatics (AREA)
Abstract
LA PRESENTE INVENCION SE REFIERE A UNA COMBINACION DE UNA FORMA DE FARMACO CRISTALINA Y UNA SAL DE TIOTROPIO QUE ES UN AGONISTA FUNCIONAL SELECTIVO DEL RECEPTOR A2A DE ADENOSINA HUMANO POR LO QUE PUEDE UTILIZARSE COMO AGENTE ANTIINFLAMATORIO EN CASOS TALES COMO SINDROME DE INSUFICIENCIA RESPIRATORIA, ASMA, FIBROSIS QUISTICA, RINITIS, ENTRE OTROS DESCRITOS EN LA SOLICITUD.
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
GBGB0129273.9A GB0129273D0 (en) | 2001-12-06 | 2001-12-06 | Crystalline drug form |
Publications (1)
Publication Number | Publication Date |
---|---|
GT200200257A true GT200200257A (es) | 2003-07-11 |
Family
ID=9927165
Family Applications (2)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
GT200200256A GT200200256A (es) | 2001-12-06 | 2002-12-05 | Forma de farmaco cristalina |
GT200200257A GT200200257A (es) | 2001-12-06 | 2002-12-05 | Combinacion de una forma de farmaco cristalina y una sal de tiotropio |
Family Applications Before (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
GT200200256A GT200200256A (es) | 2001-12-06 | 2002-12-05 | Forma de farmaco cristalina |
Country Status (41)
Families Citing this family (6)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US20030225089A1 (en) * | 2002-04-10 | 2003-12-04 | Boehringer Ingelheim Pharma Gmbh & Co. Kg | Pharmaceutical compositions based on anticholinergics and p38 kinase inhibitors |
DE10345065A1 (de) * | 2003-09-26 | 2005-04-14 | Boehringer Ingelheim Pharma Gmbh & Co. Kg | Aerosolformulierung für die Inhalation enthaltend ein Anticholinergikum |
PE20060272A1 (es) | 2004-05-24 | 2006-05-22 | Glaxo Group Ltd | (2r,3r,4s,5r,2'r,3'r,4's,5's)-2,2'-{trans-1,4-ciclohexanodiilbis-[imino(2-{[2-(1-metil-1h-imidazol-4-il)etil]amino}-9h-purin-6,9-diil)]}bis[5-(2-etil-2h-tetrazol-5-il)tetrahidro-3,4-furanodiol] como agonista a2a |
GB0514809D0 (en) | 2005-07-19 | 2005-08-24 | Glaxo Group Ltd | Compounds |
WO2021084791A1 (ja) * | 2019-10-28 | 2021-05-06 | 有限会社イムノ | アデノシンa2a受容体を標的とする組成物 |
CN115400140B (zh) * | 2022-01-27 | 2024-02-20 | 宁波熙健医药科技有限公司 | 呋喃核糖基吡啶衍生物用于预防或治疗癫痫或惊厥的用途 |
Family Cites Families (14)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US5376645A (en) | 1990-01-23 | 1994-12-27 | University Of Kansas | Derivatives of cyclodextrins exhibiting enhanced aqueous solubility and the use thereof |
KR0166088B1 (ko) | 1990-01-23 | 1999-01-15 | . | 수용해도가 증가된 시클로덱스트린 유도체 및 이의 용도 |
IT1254915B (it) * | 1992-04-24 | 1995-10-11 | Gloria Cristalli | Derivati di adenosina ad attivita' a2 agonista |
GB9711643D0 (en) | 1997-06-05 | 1997-07-30 | Janssen Pharmaceutica Nv | Glass thermoplastic systems |
GB9913932D0 (en) * | 1999-06-15 | 1999-08-18 | Pfizer Ltd | Purine derivatives |
WO2001020089A1 (fr) | 1999-09-10 | 2001-03-22 | Maeda Corporation | Structure de beton et procede de construction |
GB0003960D0 (en) * | 2000-02-18 | 2000-04-12 | Pfizer Ltd | Purine derivatives |
GB0009606D0 (en) * | 2000-04-18 | 2000-06-07 | Glaxo Group Ltd | Therapeutic combinations |
GB0009605D0 (en) * | 2000-04-18 | 2000-06-07 | Glaxo Group Ltd | Medicaments |
GB0009592D0 (en) * | 2000-04-18 | 2000-06-07 | Glaxo Group Ltd | Respiratory combinations |
GB0009583D0 (en) * | 2000-04-18 | 2000-06-07 | Glaxo Group Ltd | Respiratory formulations |
TWI227240B (en) * | 2000-06-06 | 2005-02-01 | Pfizer | 2-aminocarbonyl-9H-purine derivatives |
AU5800800A (en) | 2000-07-26 | 2002-02-05 | Swisscom Mobile Ag | Method for the assembly of a mobile radio network base station and connection ofthe base station to the network |
WO2002096462A1 (en) * | 2001-05-25 | 2002-12-05 | Pfizer Inc. | An adenosine a2a receptor agonist and an anticholinergic agent in combination for treating obstructive airways diseases |
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2001
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2002
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- 2002-12-03 HN HN2002000352A patent/HN2002000352A/es unknown
- 2002-12-03 US US10/308,829 patent/US20030144243A1/en not_active Abandoned
- 2002-12-03 US US10/308,805 patent/US6852746B2/en not_active Expired - Fee Related
- 2002-12-04 AR ARP020104683A patent/AR038547A1/es unknown
- 2002-12-04 AR ARP020104684A patent/AR037633A1/es not_active Application Discontinuation
- 2002-12-05 UY UY27568A patent/UY27568A1/es not_active Application Discontinuation
- 2002-12-05 GT GT200200256A patent/GT200200256A/es unknown
- 2002-12-05 TW TW091135301A patent/TW200301129A/zh unknown
- 2002-12-05 GT GT200200257A patent/GT200200257A/es unknown
- 2002-12-05 SV SV2002001425A patent/SV2004001425A/es not_active Application Discontinuation
- 2002-12-05 TW TW091135302A patent/TW200301130A/zh unknown
- 2002-12-06 PA PA20028560301A patent/PA8560301A1/es unknown
- 2002-12-06 PA PA20028560501A patent/PA8560501A1/es unknown
-
2004
- 2004-05-20 IL IL162101A patent/IL162101A/en not_active IP Right Cessation
- 2004-05-21 ZA ZA200403967A patent/ZA200403967B/en unknown
- 2004-05-21 IS IS7279A patent/IS7279A/is unknown
- 2004-06-02 MA MA27711A patent/MA27151A1/fr unknown
- 2004-06-04 TN TNP2004000103A patent/TNSN04103A1/fr unknown
- 2004-06-04 EC EC2004005141A patent/ECSP045141A/es unknown
- 2004-06-07 HR HR20040516A patent/HRP20040516A2/hr not_active Application Discontinuation
- 2004-07-05 NO NO20042837A patent/NO20042837L/no not_active Application Discontinuation
- 2004-09-03 US US10/934,903 patent/US7022727B2/en not_active Expired - Fee Related
-
2005
- 2005-05-06 HK HK05103825A patent/HK1071143A1/xx not_active IP Right Cessation
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2007
- 2007-08-27 CY CY20071101103T patent/CY1106822T1/el unknown
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