BRPI0822405A8 - METHOD FOR TREATMENT OF AN OPHTHALMIC CONDITION OR DISEASE, PHARMACEUTICAL COMPOSITION, DEVICE FOR INTRABODY USE, METHOD FOR INHIBITING CELL PROLIFERATION, COMPOUND, AND METHOD FOR MANUFACTURING A COMPOUND - Google Patents
METHOD FOR TREATMENT OF AN OPHTHALMIC CONDITION OR DISEASE, PHARMACEUTICAL COMPOSITION, DEVICE FOR INTRABODY USE, METHOD FOR INHIBITING CELL PROLIFERATION, COMPOUND, AND METHOD FOR MANUFACTURING A COMPOUNDInfo
- Publication number
- BRPI0822405A8 BRPI0822405A8 BRPI0822405A BRPI0822405A BRPI0822405A8 BR PI0822405 A8 BRPI0822405 A8 BR PI0822405A8 BR PI0822405 A BRPI0822405 A BR PI0822405A BR PI0822405 A BRPI0822405 A BR PI0822405A BR PI0822405 A8 BRPI0822405 A8 BR PI0822405A8
- Authority
- BR
- Brazil
- Prior art keywords
- compound
- group
- pharmaceutical composition
- disease
- treatment
- Prior art date
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Classifications
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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
- A61K31/70—Carbohydrates; Sugars; Derivatives thereof
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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
- A61K31/4353—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
- A61K31/436—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 containing a six-membered ring having oxygen as a ring hetero atom, e.g. rapamycin
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- 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
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- 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
- A61P27/06—Antiglaucoma agents or miotics
-
- 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
- A61P27/10—Ophthalmic agents for accommodation disorders, e.g. myopia
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P29/00—Non-central analgesic, antipyretic or antiinflammatory agents, e.g. antirheumatic agents; Non-steroidal antiinflammatory drugs [NSAID]
-
- 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
- A61P37/00—Drugs for immunological or allergic disorders
- A61P37/02—Immunomodulators
- A61P37/06—Immunosuppressants, e.g. drugs for graft rejection
-
- 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
Landscapes
- Health & Medical Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- Animal Behavior & Ethology (AREA)
- Chemical & Material Sciences (AREA)
- Veterinary Medicine (AREA)
- Medicinal Chemistry (AREA)
- Public Health (AREA)
- General Health & Medical Sciences (AREA)
- Pharmacology & Pharmacy (AREA)
- General Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Engineering & Computer Science (AREA)
- Ophthalmology & Optometry (AREA)
- Immunology (AREA)
- Epidemiology (AREA)
- Molecular Biology (AREA)
- Heart & Thoracic Surgery (AREA)
- Cardiology (AREA)
- Transplantation (AREA)
- Pain & Pain Management (AREA)
- Rheumatology (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
- Medicinal Preparation (AREA)
- Medicines That Contain Protein Lipid Enzymes And Other Medicines (AREA)
- Nitrogen And Oxygen Or Sulfur-Condensed Heterocyclic Ring Systems (AREA)
Abstract
MÉTODO PARA TRATAR UMA CONDIÇÃO OU DOENÇA OFTÁLMICA, COMPOSIÇÃO FARMACÊUTICA, DISPOSITIVO PARA O USO INTRACORPORAL, E, MÉTODO PARA INIBIR A PROLIFERAÇÃO CELULAR. A presente invenção fornece uma composição farmacêutica que compreende um excipiente farmaceuticamente aceitável e um composto da fórmula (I) em que R1, R2, R3, R5, R6, R8, M1, M2, M3, M4, M5, M6 e M7 são cada um independentemente um membro selecionado do grupo que consiste de H, alquila C1-6, OH e hidroxialquila C1-6; R4, R7 e R9 são cada um independentemente selecionados do grupo que consiste de alcóxi C1-6 e OH; R10 é um membro selecionado do grupo que consiste de H, -OH, -OP(O)Me2, -O-(CH2)n-OH e -O-(CH2)m,-O-(CH2)0-CH3, em que os subscritos n e m são cada um independentemente de 2 a 8 e o subscrito o é de 1 a 6; cada um de L1 e L4 é independentemente selecionado do grupo que consiste de em que cada M8 é independentemente um membro selecionado do grupo que consiste de alquila C1-6, OH e hidroxialquila C1-6; cada um de L2 e L3 é independentemente selecionado do grupo que consiste de; e sais, hidratos, isômeros, metabolitos, N-óxidos e pré-drogas do mesmo.METHOD FOR TREATMENT OF AN OPHTHALMIC CONDITION OR DISEASE, PHARMACEUTICAL COMPOSITION, DEVICE FOR INTRABODY USE, AND, METHOD FOR INHIBITING CELL PROLIFERATION. The present invention provides a pharmaceutical composition comprising a pharmaceutically acceptable excipient and a compound of formula (I) wherein R1, R2, R3, R5, R6, R8, M1, M2, M3, M4, M5, M6 and M7 are each one is independently a member selected from the group consisting of H, C1-6 alkyl, OH and hydroxyC1-6 alkyl; R4, R7 and R9 are each independently selected from the group consisting of C1-6 alkoxy and OH; R10 is a member selected from the group consisting of H, -OH, -OP(O)Me2, -O-(CH2)n-OH and -O-(CH2)m,-O-(CH2)O-CH3, wherein the subscripts n and m are each independently from 2 to 8 and the subscript o is from 1 to 6; each of L1 and L4 is independently selected from the group consisting of wherein each M8 is independently a member selected from the group consisting of C1-6 alkyl, OH and C1-6 hydroxyalkyl; each of L2 and L3 is independently selected from the group it consists of; and salts, hydrates, isomers, metabolites, N-oxides and pre-drugs thereof.
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
PCT/US2008/056501 WO2009114010A1 (en) | 2008-03-11 | 2008-03-11 | Macrocyclic lactone compounds and methods for their use |
Publications (2)
Publication Number | Publication Date |
---|---|
BRPI0822405A2 BRPI0822405A2 (en) | 2018-05-15 |
BRPI0822405A8 true BRPI0822405A8 (en) | 2018-06-05 |
Family
ID=41065507
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
BRPI0822405A BRPI0822405A8 (en) | 2008-03-11 | 2008-03-11 | METHOD FOR TREATMENT OF AN OPHTHALMIC CONDITION OR DISEASE, PHARMACEUTICAL COMPOSITION, DEVICE FOR INTRABODY USE, METHOD FOR INHIBITING CELL PROLIFERATION, COMPOUND, AND METHOD FOR MANUFACTURING A COMPOUND |
Country Status (6)
Country | Link |
---|---|
EP (1) | EP2254412A4 (en) |
JP (1) | JP2011525890A (en) |
CN (1) | CN102215682A (en) |
BR (1) | BRPI0822405A8 (en) |
IL (1) | IL208026A0 (en) |
WO (1) | WO2009114010A1 (en) |
Families Citing this family (7)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US10695327B2 (en) | 2006-09-13 | 2020-06-30 | Elixir Medical Corporation | Macrocyclic lactone compounds and methods for their use |
US8088789B2 (en) | 2006-09-13 | 2012-01-03 | Elixir Medical Corporation | Macrocyclic lactone compounds and methods for their use |
WO2013011511A1 (en) | 2011-07-18 | 2013-01-24 | Mor Research Applications Ltd. | A device for adjusting the intraocular pressure |
CN103387572B (en) * | 2013-07-17 | 2015-09-30 | 成都雅途生物技术有限公司 | Everolimus defects inspecting reference marker and preparation method thereof |
CN107759616B (en) * | 2016-08-23 | 2020-11-17 | 上海微创医疗器械(集团)有限公司 | Compound and preparation method and application thereof |
US11654036B2 (en) | 2020-05-26 | 2023-05-23 | Elixir Medical Corporation | Anticoagulant compounds and methods and devices for their use |
CN113801104B (en) * | 2020-06-15 | 2023-12-08 | 鲁南制药集团股份有限公司 | Preparation method of hydrolysis impurity of ivermectin Mo Sida cyclic lactone |
Family Cites Families (8)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
ZA935112B (en) * | 1992-07-17 | 1994-02-08 | Smithkline Beecham Corp | Rapamycin derivatives |
GB9221220D0 (en) * | 1992-10-09 | 1992-11-25 | Sandoz Ag | Organic componds |
WO1994012655A1 (en) * | 1992-11-20 | 1994-06-09 | Smithkline Beecham Corporation | Process for producing rapamycin derivatives |
US20070059336A1 (en) * | 2004-04-30 | 2007-03-15 | Allergan, Inc. | Anti-angiogenic sustained release intraocular implants and related methods |
WO2006108065A2 (en) * | 2005-04-05 | 2006-10-12 | Elixir Medical Corporation | Degradable implantable medical devices |
US20070014760A1 (en) * | 2005-07-18 | 2007-01-18 | Peyman Gholam A | Enhanced recovery following ocular surgery |
WO2007011880A2 (en) * | 2005-07-18 | 2007-01-25 | Minu, L.L.C. | Enhanced ocular neuroprotection/neurostimulation |
CN104906087A (en) * | 2006-09-13 | 2015-09-16 | 万能医药公司 | Macrocyclic lactone compounds and methods for their use |
-
2008
- 2008-03-11 BR BRPI0822405A patent/BRPI0822405A8/en not_active IP Right Cessation
- 2008-03-11 EP EP08731883A patent/EP2254412A4/en not_active Withdrawn
- 2008-03-11 WO PCT/US2008/056501 patent/WO2009114010A1/en active Application Filing
- 2008-03-11 JP JP2010550655A patent/JP2011525890A/en active Pending
- 2008-03-11 CN CN200880128027.1A patent/CN102215682A/en active Pending
-
2010
- 2010-09-06 IL IL208026A patent/IL208026A0/en unknown
Also Published As
Publication number | Publication date |
---|---|
BRPI0822405A2 (en) | 2018-05-15 |
WO2009114010A1 (en) | 2009-09-17 |
EP2254412A1 (en) | 2010-12-01 |
EP2254412A4 (en) | 2012-05-09 |
CN102215682A (en) | 2011-10-12 |
IL208026A0 (en) | 2010-12-30 |
JP2011525890A (en) | 2011-09-29 |
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Legal Events
Date | Code | Title | Description |
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B15K | Others concerning applications: alteration of classification |
Ipc: A61K 31/70 (2006.01), A61K 31/436 (2006.01) |
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B07D | Technical examination (opinion) related to article 229 of industrial property law [chapter 7.4 patent gazette] |
Free format text: DE ACORDO COM O ARTIGO 229-C DA LEI NO 10196/2001 |
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B08F | Application dismissed because of non-payment of annual fees [chapter 8.6 patent gazette] |
Free format text: REFERENTE A 11A ANUIDADE. |
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B08K | Patent lapsed as no evidence of payment of the annual fee has been furnished to inpi [chapter 8.11 patent gazette] |
Free format text: EM VIRTUDE DO ARQUIVAMENTO PUBLICADO NA RPI 2505 DE 08-01-2019 E CONSIDERANDO AUSENCIA DE MANIFESTACAO DENTRO DOS PRAZOS LEGAIS, INFORMO QUE CABE SER MANTIDO O ARQUIVAMENTO DO PEDIDO DE PATENTE, CONFORME O DISPOSTO NO ARTIGO 12, DA RESOLUCAO 113/2013. |