CL2008003848A1 - Compuestos derivados de fenilo o heteroarilo bis-sulfonilamino sustituidos, inhibidores de prostaglandina e sintasa-1 microsomal; composicion farmaceutica; procedimiento de preparacion; procedimiento de preparacion de la composicion farmaceutica; y uso en el tratamiento del dolor agudo o cronico, dolor nociceptivo o dolor neuropatico. - Google Patents

Compuestos derivados de fenilo o heteroarilo bis-sulfonilamino sustituidos, inhibidores de prostaglandina e sintasa-1 microsomal; composicion farmaceutica; procedimiento de preparacion; procedimiento de preparacion de la composicion farmaceutica; y uso en el tratamiento del dolor agudo o cronico, dolor nociceptivo o dolor neuropatico.

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Publication number
CL2008003848A1
CL2008003848A1 CL2008003848A CL2008003848A CL2008003848A1 CL 2008003848 A1 CL2008003848 A1 CL 2008003848A1 CL 2008003848 A CL2008003848 A CL 2008003848A CL 2008003848 A CL2008003848 A CL 2008003848A CL 2008003848 A1 CL2008003848 A1 CL 2008003848A1
Authority
CL
Chile
Prior art keywords
pharmaceutical composition
pain
preparation
acute
bis
Prior art date
Application number
CL2008003848A
Other languages
English (en)
Inventor
J Bylund
M Ek
Y Gravenfors
G Nordvall
A Minidis
K Vallin
J Viklund
J Holenz
Berg S Von
Original Assignee
Astrazeneca Ab
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Family has litigation
First worldwide family litigation filed litigation Critical https://patents.darts-ip.com/?family=40789387&utm_source=google_patent&utm_medium=platform_link&utm_campaign=public_patent_search&patent=CL2008003848(A1) "Global patent litigation dataset” by Darts-ip is licensed under a Creative Commons Attribution 4.0 International License.
Application filed by Astrazeneca Ab filed Critical Astrazeneca Ab
Publication of CL2008003848A1 publication Critical patent/CL2008003848A1/es

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    • C07ORGANIC CHEMISTRY
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    • C07D307/00Heterocyclic compounds containing five-membered rings having one oxygen atom as the only ring hetero atom
    • C07D307/77Heterocyclic 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
    • C07D307/78Benzo [b] furans; Hydrogenated benzo [b] furans
    • C07D307/79Benzo [b] furans; Hydrogenated benzo [b] furans with only hydrogen atoms, hydrocarbon or substituted hydrocarbon radicals, directly attached to carbon atoms of the hetero ring
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P11/00Drugs for disorders of the respiratory system
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    • A61P25/00Drugs for disorders of the nervous system
    • A61P25/04Centrally acting analgesics, e.g. opioids
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    • A61P29/00Non-central analgesic, antipyretic or antiinflammatory agents, e.g. antirheumatic agents; Non-steroidal antiinflammatory drugs [NSAID]
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    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
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    • A61P9/00Drugs for disorders of the cardiovascular system
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    • C07C311/00Amides of sulfonic acids, i.e. compounds having singly-bound oxygen atoms of sulfo groups replaced by nitrogen atoms, not being part of nitro or nitroso groups
    • C07C311/30Sulfonamides, the carbon skeleton of the acid part being further substituted by singly-bound nitrogen atoms, not being part of nitro or nitroso groups
    • C07C311/37Sulfonamides, the carbon skeleton of the acid part being further substituted by singly-bound nitrogen atoms, not being part of nitro or nitroso groups having the sulfur atom of at least one of the sulfonamide groups bound to a carbon atom of a six-membered aromatic ring
    • C07C311/38Sulfonamides, the carbon skeleton of the acid part being further substituted by singly-bound nitrogen atoms, not being part of nitro or nitroso groups having the sulfur atom of at least one of the sulfonamide groups bound to a carbon atom of a six-membered aromatic ring having sulfur atoms of sulfonamide groups and amino groups bound to carbon atoms of six-membered rings of the same carbon skeleton
    • C07C311/39Sulfonamides, the carbon skeleton of the acid part being further substituted by singly-bound nitrogen atoms, not being part of nitro or nitroso groups having the sulfur atom of at least one of the sulfonamide groups bound to a carbon atom of a six-membered aromatic ring having sulfur atoms of sulfonamide groups and amino groups bound to carbon atoms of six-membered rings of the same carbon skeleton having the nitrogen atom of at least one of the sulfonamide groups bound to hydrogen atoms or to an acyclic carbon atom
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Abstract

Compuestos derivados de fenilo o heteroarilo bis-sulfonilamino sustituidos; proceso de preparación; composición farmacéutica; y uso en el tratamiento del dolor agudo o crónico, dolor nociceptivo o dolor neuropático.
CL2008003848A 2007-12-20 2008-12-19 Compuestos derivados de fenilo o heteroarilo bis-sulfonilamino sustituidos, inhibidores de prostaglandina e sintasa-1 microsomal; composicion farmaceutica; procedimiento de preparacion; procedimiento de preparacion de la composicion farmaceutica; y uso en el tratamiento del dolor agudo o cronico, dolor nociceptivo o dolor neuropatico. CL2008003848A1 (es)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
US1528707P 2007-12-20 2007-12-20

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CL2008003848A1 true CL2008003848A1 (es) 2010-02-05

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CL2008003848A CL2008003848A1 (es) 2007-12-20 2008-12-19 Compuestos derivados de fenilo o heteroarilo bis-sulfonilamino sustituidos, inhibidores de prostaglandina e sintasa-1 microsomal; composicion farmaceutica; procedimiento de preparacion; procedimiento de preparacion de la composicion farmaceutica; y uso en el tratamiento del dolor agudo o cronico, dolor nociceptivo o dolor neuropatico.

Country Status (23)

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US (2) US20090163586A1 (es)
EP (1) EP2234993B1 (es)
JP (1) JP5555175B2 (es)
KR (1) KR20100098711A (es)
CN (1) CN101945859B (es)
AR (1) AR069919A1 (es)
AU (1) AU2008341173B2 (es)
BR (1) BRPI0821299A2 (es)
CA (1) CA2709510A1 (es)
CL (1) CL2008003848A1 (es)
CO (1) CO6270307A2 (es)
CR (1) CR11517A (es)
DO (1) DOP2010000191A (es)
EA (1) EA017940B1 (es)
EC (1) ECSP10010272A (es)
ES (1) ES2397502T3 (es)
IL (1) IL205758A0 (es)
NI (1) NI201000109A (es)
PE (1) PE20091175A1 (es)
TW (1) TW200932210A (es)
UY (1) UY31546A1 (es)
WO (1) WO2009082347A1 (es)
ZA (1) ZA201004226B (es)

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DK2035369T3 (da) 2006-07-05 2014-10-06 Fibrotech Therapeutics Pty Ltd Terapeutiske
TW200930369A (en) * 2007-11-15 2009-07-16 Astrazeneca Ab Bis-(sulfonylamino) derivatives in therapy
WO2009079692A1 (en) 2007-12-21 2009-07-02 Fibrotech Therapeutics Pty Ltd Halogenated analogues of anti-fibrotic agents
WO2010132016A1 (en) * 2009-05-14 2010-11-18 Astrazeneca Ab Bis-(sulfonylamino) derivatives for treatment of pain and inflammation
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