AR058388A1 - DERIVADOS DE COMPUESTOS AROMATICOS SUSTITUIDOS uTILES PARA TRASTORNOS RESPIRATORIOS , COMPOSICIONES FARMACÉUTICAS Y PROCESOS PARA SU PREPARACIoN - Google Patents
DERIVADOS DE COMPUESTOS AROMATICOS SUSTITUIDOS uTILES PARA TRASTORNOS RESPIRATORIOS , COMPOSICIONES FARMACÉUTICAS Y PROCESOS PARA SU PREPARACIoNInfo
- Publication number
- AR058388A1 AR058388A1 ARP060105551A ARP060105551A AR058388A1 AR 058388 A1 AR058388 A1 AR 058388A1 AR P060105551 A ARP060105551 A AR P060105551A AR P060105551 A ARP060105551 A AR P060105551A AR 058388 A1 AR058388 A1 AR 058388A1
- Authority
- AR
- Argentina
- Prior art keywords
- cycloalkyl
- alkyl
- optionally substituted
- halogen
- hydrogen
- Prior art date
Links
- 150000001491 aromatic compounds Chemical class 0.000 title abstract 2
- 238000000034 method Methods 0.000 title abstract 2
- 239000008194 pharmaceutical composition Substances 0.000 title abstract 2
- 208000023504 respiratory system disease Diseases 0.000 title abstract 2
- 125000006552 (C3-C8) cycloalkyl group Chemical group 0.000 abstract 20
- 125000005843 halogen group Chemical group 0.000 abstract 18
- 125000004169 (C1-C6) alkyl group Chemical group 0.000 abstract 16
- 229910052736 halogen Inorganic materials 0.000 abstract 16
- 229910052739 hydrogen Inorganic materials 0.000 abstract 14
- 239000001257 hydrogen Substances 0.000 abstract 14
- 125000004435 hydrogen atom Chemical class [H]* 0.000 abstract 14
- 229910052717 sulfur Inorganic materials 0.000 abstract 12
- 150000002367 halogens Chemical class 0.000 abstract 10
- 229910052757 nitrogen Inorganic materials 0.000 abstract 10
- 229910052760 oxygen Inorganic materials 0.000 abstract 10
- 125000003118 aryl group Chemical group 0.000 abstract 6
- 125000001072 heteroaryl group Chemical group 0.000 abstract 6
- 125000001424 substituent group Chemical group 0.000 abstract 6
- 125000006273 (C1-C3) alkyl group Chemical group 0.000 abstract 4
- 125000004429 atom Chemical group 0.000 abstract 4
- 125000004433 nitrogen atom Chemical group N* 0.000 abstract 4
- -1 OR3 and NR7R8 Chemical group 0.000 abstract 3
- 125000006272 (C3-C7) cycloalkyl group Chemical group 0.000 abstract 2
- 125000002915 carbonyl group Chemical group [*:2]C([*:1])=O 0.000 abstract 2
- 150000001875 compounds Chemical class 0.000 abstract 2
- 125000005842 heteroatom Chemical group 0.000 abstract 2
- 125000002887 hydroxy group Chemical group [H]O* 0.000 abstract 2
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 abstract 2
- 229920006395 saturated elastomer Polymers 0.000 abstract 2
- 238000011282 treatment Methods 0.000 abstract 2
- 125000004178 (C1-C4) alkyl group Chemical group 0.000 abstract 1
- 125000004209 (C1-C8) alkyl group Chemical group 0.000 abstract 1
- 101100295741 Gallus gallus COR4 gene Proteins 0.000 abstract 1
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 abstract 1
- 125000006615 aromatic heterocyclic group Chemical group 0.000 abstract 1
- 201000010099 disease Diseases 0.000 abstract 1
- 208000037265 diseases, disorders, signs and symptoms Diseases 0.000 abstract 1
- 239000003814 drug Substances 0.000 abstract 1
- 238000004519 manufacturing process Methods 0.000 abstract 1
- 230000001404 mediated effect Effects 0.000 abstract 1
- 125000000449 nitro group Chemical group [O-][N+](*)=O 0.000 abstract 1
- 238000011321 prophylaxis Methods 0.000 abstract 1
- BHMBVRSPMRCCGG-OUTUXVNYSA-N prostaglandin D2 Chemical compound CCCCC[C@H](O)\C=C\[C@@H]1[C@@H](C\C=C/CCCC(O)=O)[C@@H](O)CC1=O BHMBVRSPMRCCGG-OUTUXVNYSA-N 0.000 abstract 1
- BHMBVRSPMRCCGG-UHFFFAOYSA-N prostaglandine D2 Natural products CCCCCC(O)C=CC1C(CC=CCCCC(O)=O)C(O)CC1=O BHMBVRSPMRCCGG-UHFFFAOYSA-N 0.000 abstract 1
- 150000003839 salts Chemical class 0.000 abstract 1
Classifications
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C317/00—Sulfones; Sulfoxides
- C07C317/16—Sulfones; Sulfoxides having sulfone or sulfoxide groups and singly-bound oxygen atoms bound to the same carbon skeleton
- C07C317/22—Sulfones; Sulfoxides having sulfone or sulfoxide groups and singly-bound oxygen atoms bound to the same carbon skeleton with sulfone or sulfoxide groups bound to carbon atoms of six-membered aromatic rings of the carbon skeleton
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P11/00—Drugs for disorders of the respiratory system
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P11/00—Drugs for disorders of the respiratory system
- A61P11/02—Nasal agents, e.g. decongestants
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P11/00—Drugs for disorders of the respiratory system
- A61P11/06—Antiasthmatics
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P11/00—Drugs for disorders of the respiratory system
- A61P11/08—Bronchodilators
-
- 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
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C317/00—Sulfones; Sulfoxides
- C07C317/44—Sulfones; Sulfoxides having sulfone or sulfoxide groups and carboxyl groups bound to the same carbon skeleton
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C323/00—Thiols, sulfides, hydropolysulfides or polysulfides substituted by halogen, oxygen or nitrogen atoms, or by sulfur atoms not being part of thio groups
- C07C323/64—Thiols, sulfides, hydropolysulfides or polysulfides substituted by halogen, oxygen or nitrogen atoms, or by sulfur atoms not being part of thio groups containing thio groups and sulfur atoms, not being part of thio groups, bound to the same carbon skeleton
- C07C323/65—Thiols, sulfides, hydropolysulfides or polysulfides substituted by halogen, oxygen or nitrogen atoms, or by sulfur atoms not being part of thio groups containing thio groups and sulfur atoms, not being part of thio groups, bound to the same carbon skeleton containing sulfur atoms of sulfone or sulfoxide groups bound to the carbon skeleton
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D205/00—Heterocyclic compounds containing four-membered rings with one nitrogen atom as the only ring hetero atom
- C07D205/02—Heterocyclic compounds containing four-membered rings with one nitrogen atom as the only ring hetero atom not condensed with other rings
- C07D205/04—Heterocyclic compounds containing four-membered rings with one nitrogen atom as the only ring hetero atom not condensed with other rings having no double bonds between ring members or between ring members and non-ring members
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D231/00—Heterocyclic compounds containing 1,2-diazole or hydrogenated 1,2-diazole rings
- C07D231/02—Heterocyclic compounds containing 1,2-diazole or hydrogenated 1,2-diazole rings not condensed with other rings
- C07D231/10—Heterocyclic compounds containing 1,2-diazole or hydrogenated 1,2-diazole rings not condensed with other rings having two or three double bonds between ring members or between ring members and non-ring members
- C07D231/14—Heterocyclic compounds containing 1,2-diazole or hydrogenated 1,2-diazole rings not condensed with other rings having two or three double bonds between ring members or between ring members and non-ring members 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 ring carbon atoms
- C07D231/18—One oxygen or sulfur atom
- C07D231/20—One oxygen atom attached in position 3 or 5
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D233/00—Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, not condensed with other rings
- C07D233/54—Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, not condensed with other rings having two double bonds between ring members or between ring members and non-ring members
- C07D233/64—Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, not condensed with other rings having two double bonds between ring members or between ring members and non-ring members with substituted hydrocarbon radicals attached to ring carbon atoms, e.g. histidine
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D257/00—Heterocyclic compounds containing rings having four nitrogen atoms as the only ring hetero atoms
- C07D257/02—Heterocyclic compounds containing rings having four nitrogen atoms as the only ring hetero atoms not condensed with other rings
- C07D257/04—Five-membered rings
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D271/00—Heterocyclic compounds containing five-membered rings having two nitrogen atoms and one oxygen atom as the only ring hetero atoms
- C07D271/02—Heterocyclic compounds containing five-membered rings having two nitrogen atoms and one oxygen atom as the only ring hetero atoms not condensed with other rings
- C07D271/06—1,2,4-Oxadiazoles; Hydrogenated 1,2,4-oxadiazoles
- C07D271/07—1,2,4-Oxadiazoles; Hydrogenated 1,2,4-oxadiazoles with oxygen, sulfur or nitrogen atoms, directly attached to ring carbon atoms, the nitrogen atoms not forming part of a nitro radical
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D401/00—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom
- C07D401/02—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing two hetero rings
- C07D401/12—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing two hetero rings linked by a chain containing hetero atoms as chain links
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D403/00—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00
- C07D403/02—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00 containing two hetero rings
- C07D403/04—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00 containing two hetero rings directly linked by a ring-member-to-ring-member bond
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Health & Medical Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- General Health & Medical Sciences (AREA)
- General Chemical & Material Sciences (AREA)
- Medicinal Chemistry (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Pharmacology & Pharmacy (AREA)
- Engineering & Computer Science (AREA)
- Animal Behavior & Ethology (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Public Health (AREA)
- Veterinary Medicine (AREA)
- Pulmonology (AREA)
- Otolaryngology (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Acyclic And Carbocyclic Compounds In Medicinal Compositions (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
- Plural Heterocyclic Compounds (AREA)
- Heterocyclic Carbon Compounds Containing A Hetero Ring Having Nitrogen And Oxygen As The Only Ring Hetero Atoms (AREA)
Abstract
Compuestos aromáticos sustituidos , como compuestos farmacéuticos utiles para el tratamiento de trastornos respiratorios, composiciones farmacéuticas que los incluyen, procesos para su preparacion. Reivindicacion 1: El uso de un compuesto de formula (1) o una sal aceptable para uso farmacéutico del mismo caracterizado porque es en la fabricacion de un medicamento para el tratamiento o profilaxis de una enfermedad mediada por prostaglandina D2, en el cual: Y se selecciona (i) entre O, N, S(O)n, O-CR1R2, CR1R2-O, N-CR1R2, CR1R2-N, S(O)n-CR1R2, CR1R2-S(O)n, CR1R2, CC, CR1CR2, CR1R2CR1R2, donde n = 0, 1 o 2; y A y D se seleccionan en forma independiente entre hidrogeno, halogeno, CN, OR3, S(O)nR3 (donde n es 0, 1 o 2), nitro, cicloalquilo C3-8 o alquilo C1-4, donde este ultimo se sustituye opcionalmente con átomos de halogeno, A y D también pueden representar en forma independiente un anillo aromático de cinco o seis miembros con entre 0 y 3 heteroátomos seleccionados en forma independiente entre N, S y O; E es O, S, NR3 o CH2; V es CN, hidrogeno, halogeno, cicloalquilo C3-8 o alquilo C1-6 ,opcionalmente sustituido con uno o más tomos de halogeno; W es hidrogeno, halogeno, CN, SO2NR4R5, CONR4R5, SO2R6, COR4, cicloalquilo C3-8 o alquilo C1-6 opcionalmente sustituido con uno o más átomos de halogeno; X es CN, hidrogeno, halogeno, cicloalquilo C3-8 o alquilo C1-6 opcionalmente sustituido con uno o más átomos de halogeno; Z se selecciona de entre el grupo de formulas (2), donde G representa un anillo aromático heterocíclico de cinco miembros que contiene uno o más heteroátomos seleccionados en forma independiente entre N, S, O; R1 y R2 representan en forma independiente un átomo de hidrogeno, halogeno, cicloalquilo C3-8 o un grupo alquilo C1-6 , donde estos ultimos dos grupos se sustituyen opcionalmente con uno o más átomos de halogeno; o R1 y R2 juntos pueden formar un anillo de 3 a 8 miembros que contiene opcionalmente uno o más átomos seleccionados entre O, S, NR3 y el mismo se sustituye opcionalmente con uno o más halogeno, cicloalquilo C3-8 o alquilo C1-3, donde estos ultimos dos grupos se sustituyen opcionalmente con uno o más átomos de halogeno; R3 representa hidrogeno, cicloalquilo C3-8 o alquilo C1-6 , donde estos ultimos dos grupos se sustituyen opcionalmente con halogeno o NR4R5; R3' representa hidrogeno, cicloalquilo C3-8 o alquilo C1-6 , donde estos ultimos dos grupos se sustituyen opcionalmente con átomos de halogeno; R4 y R5 representan en forma independiente hidrogeno, cicloalquilo C3-8 o alquilo C1-6 , donde estos ultimos dos grupos se sustituyen opcionalmente con uno o más sustituyentes seleccionados en forma independiente entre halogeno, CN, cicloalquilo C3-7, alquilo C1-6 , OR3 y NR7R8, arilo, heteroarilo, S(O)nR9 (donde n = 0, 1 o 2), CONR7R8, NR3COR10, SO2NR4R5 y NR3SO2R9; o R4 y R5 junto con el átomo de nitrogeno al cual se encuentran unidos pueden formar un anillo saturado de 3 a 8 miembros que contiene opcionalmente uno o más átomos seleccionados entre O, N, S(O)n (donde n = 0, 1 o 2), NR3, y el mismo se sustituye opcionalmente con uno o más halogeno, OR3, cicloalquilo C3-8 o alquilo C1-6 , donde estos ultimos dos grupos se sustituyen opcionalmente con uno o más halogenos; R6 representa arilo, heteroarilo, cicloalquilo C3-8 o alquilo C1-6 todos los cuales se sustituyen opcionalmente con uno o más sustituyentes seleccionados en forma independiente entre halogeno, cicloalquilo C3-7, alquilo C1-6 , OR3, CN, NR7R8, arilo, heteroarilo, S(O)nR9 (donde n = 0, 1 o 2), CONR7R8, NR3COR10, SO2NR4R5 y NR3SO2R9; R7 y R8 representan en forma independiente hidrogeno, cicloalquilo C3-8 o alquilo C1-6, donde estos ultimos dos grupos se sustituyen opcionalmente con uno o más átomos de halogeno; o R7 y R8 junto con el átomo de nitrogeno al cual se encuentran unidos pueden formar un anillo saturado de 3 a 8 miembros, opcionalmente sustituido con halogeno, cicloalquilo C3-8 o alquilo C1-3; R9 representa cicloalquilo C3-8 o alquilo C1-6 (opcionalmente sustituido con átomos de halogeno); R10 representa hidrogeno, arilo, heteroarilo, OR3, cicloalquilo C3-8 o alquilo C1-6 , donde los ultimos tres grupos se sustituyen opcionalmente con átomos de halogeno; R11 y R12 representan en forma independiente hidrogeno, arilo, heteroarilo, cicloalquilo C3-8 o alquilo C1-8, donde este ultimo se sustituye opcionalmente con uno o más átomos de halogeno, OR3, =O o NR13R14; o R11 y R12 junto con el átomo de nitrogeno al cual se encuentran unidos pueden formar un anillo de 3 a 8 miembros que contiene opcionalmente uno o más átomos seleccionados entre O, S, NR3. Este mismo anillo se sustituye opcionalmente con uno o más cicloalquilo C3-8, alquilo C1-3, halogeno, OR3 o NR13R14; R13 y R14 representan en forma independiente hidrogeno, cicloalquilo C3-8 o alquilo C1-6, donde estos ultimos dos grupos se sustituyen opcionalmente con uno o más sustituyentes seleccionados en forma independiente entre halogeno, OR3, CN, S(O)nR9 (donde n = 0, 1 o 2), CONR7R8, NR3COR10, SO2NR4R5 y NR3SO2R9; o R13 y R14 junto con el átomo de nitrogeno al cual se encuentran unidos pueden formar' un anillo heteroarilo insaturado de 5 a 10 miembros que contiene. opcionalmente uno o más átomos seleccionados entre O, N, S(O)n (donde n = 0, 1 o 2), NR3, y el mismo se sustituye opcionalmente con halogeno, CN, S(O)nR9 (donde n = 0, 1 o 2), OR3, cicloalquilo C3-8 o alquilo C1-3; R15 representa uno o más sustituyentes seleccionados en forma independiente entre hidrogeno, halogeno, CN, OR3, S(O)nR9 (donde n = 0, 1 o 2), cicloalquilo C3-8 o alquilo C1-6, donde estos ultimos dos grupos se sustituyen opcionalmente con átomos de halogeno; con la salvedad de que: A y D no pueden ser los dos hidrogeno; uno de V, W y X debe ser un sustituyente distinto de hidrogeno, o Y es (ii) una union, y A, D, V y X tienen los valores que se definen precedentemente; E es O o S; W es SO2R6; Z se representa con el elemento (a) del grupo de formulas (2) donde G y R15 tienen los valores que se definen precedentemente. con la salvedad de que: al menos uno de los sustituyentes para R15 debe ser hidroxi o el sustituyente carbonilo tautomérico respectivo; y al menos uno de los sustituyentes hidroxi o carbonilo tautomérico mencionados debe estar sustituido en la posicion orto- respectiva a la union Y que une Z al anillo fenilo. E se conecta al grupo fenilo en la posicion meta- con respecto a Y.
Applications Claiming Priority (3)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| GB0525477A GB0525477D0 (en) | 2005-12-15 | 2005-12-15 | Novel compounds |
| GB0607409A GB0607409D0 (en) | 2006-04-13 | 2006-04-13 | Npvel compounds |
| GB0614787A GB0614787D0 (en) | 2006-07-26 | 2006-07-26 | Novel compounds |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| AR058388A1 true AR058388A1 (es) | 2008-01-30 |
Family
ID=38038557
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| ARP060105551A AR058388A1 (es) | 2005-12-15 | 2006-12-15 | DERIVADOS DE COMPUESTOS AROMATICOS SUSTITUIDOS uTILES PARA TRASTORNOS RESPIRATORIOS , COMPOSICIONES FARMACÉUTICAS Y PROCESOS PARA SU PREPARACIoN |
Country Status (8)
| Country | Link |
|---|---|
| US (1) | US20080293775A1 (es) |
| EP (2) | EP2305640A3 (es) |
| JP (1) | JP2009519308A (es) |
| AR (1) | AR058388A1 (es) |
| AT (1) | ATE545637T1 (es) |
| ES (1) | ES2380683T3 (es) |
| TW (1) | TW200732296A (es) |
| WO (1) | WO2007068894A2 (es) |
Families Citing this family (28)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| SE0301010D0 (sv) | 2003-04-07 | 2003-04-07 | Astrazeneca Ab | Novel compounds |
| SE0301009D0 (sv) * | 2003-04-07 | 2003-04-07 | Astrazeneca Ab | Novel compounds |
| SA04250253B1 (ar) | 2003-08-21 | 2009-11-10 | استرازينيكا ايه بي | احماض فينوكسي اسيتيك مستبدلة باعتبارها مركبات صيدلانية لعلاج الامراض التنفسية مثل الربو ومرض الانسداد الرئوي المزمن |
| GB0415320D0 (en) | 2004-07-08 | 2004-08-11 | Astrazeneca Ab | Novel compounds |
| GB0418830D0 (en) * | 2004-08-24 | 2004-09-22 | Astrazeneca Ab | Novel compounds |
| GB0422057D0 (en) * | 2004-10-05 | 2004-11-03 | Astrazeneca Ab | Novel compounds |
| UY29223A1 (es) | 2004-11-23 | 2006-06-30 | Astrazeneca Ab | Ácidos fenoxiacéticos sustituidos, composiciones farmacéuticas que los contienen y procesos para su preparación |
| US8148572B2 (en) | 2005-10-06 | 2012-04-03 | Astrazeneca Ab | Compounds |
| TW200745003A (en) | 2005-10-06 | 2007-12-16 | Astrazeneca Ab | Novel compounds |
| US20080255150A1 (en) * | 2005-11-05 | 2008-10-16 | Astrazeneca Ab | Novel Compounds |
| UA100983C2 (ru) * | 2007-07-05 | 2013-02-25 | Астразенека Аб | Бифенилоксипропановая кислота как модулятор crth2 и интермедиаты |
| US8067445B2 (en) | 2008-02-01 | 2011-11-29 | Panmira Pharmaceuticals, Llc | N,N-disubstituted aminoalkylbiphenyl antagonists of prostaglandin D2 receptors |
| US8242145B2 (en) | 2008-02-14 | 2012-08-14 | Panmira Pharmaceuticals, Llc | Cyclic diaryl ether compounds as antagonists of prostaglandin D2 receptors |
| JP2011513242A (ja) | 2008-02-25 | 2011-04-28 | アミラ ファーマシューティカルズ,インク. | プロスタグランジンd2受容体アンタゴニスト |
| JP2011518130A (ja) | 2008-04-02 | 2011-06-23 | アミラ ファーマシューティカルズ,インク. | プロスタグランジンd2受容体のアミノアルキルフェニルアンタゴニスト |
| MX2010014172A (es) * | 2008-07-03 | 2011-02-22 | Amira Pharmaceuticals Inc | Antagonistas de receptores de prostaglandina d2. |
| GB2463788B (en) | 2008-09-29 | 2010-12-15 | Amira Pharmaceuticals Inc | Heteroaryl antagonists of prostaglandin D2 receptors |
| US8378107B2 (en) | 2008-10-01 | 2013-02-19 | Panmira Pharmaceuticals, Llc | Heteroaryl antagonists of prostaglandin D2 receptors |
| WO2010042652A2 (en) | 2008-10-08 | 2010-04-15 | Amira Pharmaceuticals, Inc. | Heteroalkyl biphenyl antagonists of prostaglandin d2 receptors |
| WO2010057118A2 (en) | 2008-11-17 | 2010-05-20 | Amira Pharmaceuticals, Inc. | Heterocyclic antagonists of prostaglandin d2 receptors |
| WO2011014587A2 (en) | 2009-07-31 | 2011-02-03 | Amira Pharmaceuticals, Inc. | Ophthalmic pharmaceutical compositions of dp2 receptor antagonists |
| KR20120047273A (ko) | 2009-08-05 | 2012-05-11 | 판미라 파마슈티칼스, 엘엘씨 | Dp2 길항제 및 이의 용도 |
| AU2011203649A1 (en) * | 2010-01-06 | 2012-06-14 | Brickell Biotech, Inc. | DP2 antagonist and uses thereof |
| EP2590951B1 (en) | 2010-07-09 | 2015-01-07 | Pfizer Limited | Benzenesulfonamides useful as sodium channel inhibitors |
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-
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- 2006-12-12 JP JP2008545074A patent/JP2009519308A/ja active Pending
- 2006-12-12 US US12/096,557 patent/US20080293775A1/en not_active Abandoned
- 2006-12-12 ES ES06820474T patent/ES2380683T3/es active Active
- 2006-12-12 AT AT06820474T patent/ATE545637T1/de active
- 2006-12-12 TW TW095146480A patent/TW200732296A/zh unknown
- 2006-12-12 EP EP10173760A patent/EP2305640A3/en not_active Withdrawn
- 2006-12-12 EP EP06820474A patent/EP1963259B1/en not_active Not-in-force
- 2006-12-12 WO PCT/GB2006/004607 patent/WO2007068894A2/en not_active Ceased
- 2006-12-15 AR ARP060105551A patent/AR058388A1/es not_active Application Discontinuation
Also Published As
| Publication number | Publication date |
|---|---|
| US20080293775A1 (en) | 2008-11-27 |
| TW200732296A (en) | 2007-09-01 |
| ATE545637T1 (de) | 2012-03-15 |
| WO2007068894A3 (en) | 2007-12-06 |
| WO2007068894A2 (en) | 2007-06-21 |
| EP1963259A2 (en) | 2008-09-03 |
| EP2305640A3 (en) | 2011-07-20 |
| EP2305640A2 (en) | 2011-04-06 |
| ES2380683T3 (es) | 2012-05-17 |
| JP2009519308A (ja) | 2009-05-14 |
| EP1963259B1 (en) | 2012-02-15 |
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