NO20082496L - Pyrazinderivater - Google Patents

Pyrazinderivater

Info

Publication number
NO20082496L
NO20082496L NO20082496A NO20082496A NO20082496L NO 20082496 L NO20082496 L NO 20082496L NO 20082496 A NO20082496 A NO 20082496A NO 20082496 A NO20082496 A NO 20082496A NO 20082496 L NO20082496 L NO 20082496L
Authority
NO
Norway
Prior art keywords
compounds
pyrazine derivatives
preparation
solvates
pain
Prior art date
Application number
NO20082496A
Other languages
English (en)
Inventor
Stephen Martin Denton
Mark Ian Kemp
Karl Richard Gibson
Cedric Poinsard
Melanie Susanne Glossop
Original Assignee
Pfizer Ltd
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by Pfizer Ltd filed Critical Pfizer Ltd
Publication of NO20082496L publication Critical patent/NO20082496L/no

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D403/00Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00
    • C07D403/02Heterocyclic 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
    • C07D403/12Heterocyclic 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 linked by a chain containing hetero atoms as chain links
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K31/00Medicinal preparations containing organic active ingredients
    • A61K31/33Heterocyclic compounds
    • A61K31/395Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
    • A61K31/495Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with two or more nitrogen atoms as the only ring heteroatoms, e.g. piperazine or tetrazines
    • A61K31/4965Non-condensed pyrazines
    • A61K31/497Non-condensed pyrazines containing further heterocyclic rings
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P23/00Anaesthetics
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P25/00Drugs for disorders of the nervous system
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P25/00Drugs for disorders of the nervous system
    • A61P25/02Drugs for disorders of the nervous system for peripheral neuropathies
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P25/00Drugs for disorders of the nervous system
    • A61P25/04Centrally acting analgesics, e.g. opioids
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P43/00Drugs for specific purposes, not provided for in groups A61P1/00-A61P41/00
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D413/00Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms
    • C07D413/02Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms containing two hetero rings
    • C07D413/12Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms containing two hetero rings linked by a chain containing hetero atoms as chain links

Abstract

Foreliggende oppfinnelse angår forbindelser med formel (I): og farmasøytisk akseptable salter og solvater derav, fremgangsmåter for fremstillingen av, intermediater anvendt ved fremstillingen av, og sammensetninger som inneholder slike forbindelser og anvendelsene av slike forbindelser for behandlingen av smerte.
NO20082496A 2005-11-04 2008-06-04 Pyrazinderivater NO20082496L (no)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
US73366205P 2005-11-04 2005-11-04
PCT/IB2006/003055 WO2007052123A2 (en) 2005-11-04 2006-10-23 Pyrazine derivatives as sodium channel modulators for the treatment of pain

Publications (1)

Publication Number Publication Date
NO20082496L true NO20082496L (no) 2008-07-24

Family

ID=37890558

Family Applications (1)

Application Number Title Priority Date Filing Date
NO20082496A NO20082496L (no) 2005-11-04 2008-06-04 Pyrazinderivater

Country Status (27)

Country Link
US (1) US7572797B2 (no)
EP (1) EP1945630B1 (no)
JP (1) JP2009514937A (no)
KR (1) KR20080066073A (no)
CN (1) CN101356169A (no)
AP (1) AP2008004468A0 (no)
AR (1) AR057855A1 (no)
AT (1) ATE525372T1 (no)
AU (1) AU2006310215A1 (no)
BR (1) BRPI0618129A2 (no)
CA (1) CA2624621C (no)
CR (1) CR9954A (no)
DO (1) DOP2006000243A (no)
EA (1) EA200801011A1 (no)
EC (1) ECSP088412A (no)
ES (1) ES2371932T3 (no)
GT (1) GT200600475A (no)
IL (1) IL191059A0 (no)
MA (1) MA29926B1 (no)
NL (1) NL2000284C2 (no)
NO (1) NO20082496L (no)
PE (1) PE20070715A1 (no)
TN (1) TNSN08196A1 (no)
TW (1) TW200804353A (no)
UY (1) UY29893A1 (no)
WO (1) WO2007052123A2 (no)
ZA (1) ZA200803671B (no)

Families Citing this family (20)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
SI0934061T1 (en) 1996-07-24 2003-10-31 Warner-Lambert Company Llc Isobutylgaba and its derivatives for the treatment of pain
EP1741708A1 (en) * 2005-06-28 2007-01-10 Sanofi-Aventis Deutschland GmbH Heteroaryl-substituted amides comprising an unsaturated or cyclic linker group, and their use as pharmaceuticals
US7977359B2 (en) 2005-11-04 2011-07-12 Amira Pharmaceuticals, Inc. 5-lipdxygenase-activating protein (FLAP) inhibitors
US8399666B2 (en) 2005-11-04 2013-03-19 Panmira Pharmaceuticals, Llc 5-lipoxygenase-activating protein (FLAP) inhibitors
GB2431927B (en) 2005-11-04 2010-03-17 Amira Pharmaceuticals Inc 5-Lipoxygenase-activating protein (FLAP) inhibitors
WO2008135826A2 (en) 2007-05-03 2008-11-13 Pfizer Limited 2 -pyridine carboxamide derivatives as sodium channel modulators
CA2685952C (en) * 2007-05-03 2012-03-13 Pfizer Limited N- [6-amino-5- (phenyl) pyrazin-2-yl] -isoxazole-4-carboxamide derivatives and related compounds as nav1.8 channel modulators for the treatment of pain
US8614255B2 (en) * 2007-08-21 2013-12-24 Civitas Therapeutics, Inc. Pulmonary pharmaceutical formulations
PE20091096A1 (es) 2007-12-10 2009-08-25 Novartis Ag Compuestos organicos
US8252810B2 (en) 2008-02-13 2012-08-28 Eisai R&D Management Co., Ltd. Bicycloamine derivatives
WO2010068311A1 (en) 2008-05-23 2010-06-17 Amira Pharmaceuticals, Inc. 5-lipoxygenase-activating protein inhibitor
US8546431B2 (en) 2008-10-01 2013-10-01 Panmira Pharmaceuticals, Llc 5-lipoxygenase-activating protein (FLAP) inhibitors
US10703722B2 (en) 2010-04-27 2020-07-07 Calcimedica, Inc. Compounds that modulate intracellular calcium
US9856240B2 (en) * 2011-10-19 2018-01-02 Calcimedica, Inc. Compounds that modulate intracellular calcium
US9187475B2 (en) * 2012-04-25 2015-11-17 Raqualia Pharma Inc. Pyrrolopyridinone derivatives as TTX-S blockers
TWI644899B (zh) * 2013-02-04 2018-12-21 健生藥品公司 Flap調節劑
US9745328B2 (en) 2013-02-04 2017-08-29 Janssen Pharmaceutica Nv Flap modulators
AU2015315167A1 (en) * 2014-09-10 2017-03-16 Epizyme, Inc. Isoxazole carboxamide compounds
AR103807A1 (es) 2015-02-27 2017-06-07 Calcimedica Inc Tratamiento de la pancreatitis
WO2017027400A1 (en) * 2015-08-07 2017-02-16 Calcimedica, Inc. Use of crac channel inhibitors for the treatment of stroke and traumatic brain injury

Family Cites Families (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
MA26473A1 (fr) * 1997-03-01 2004-12-20 Glaxo Group Ltd Composes pharmacologiquement actifs.
BR0214309A (pt) * 2001-11-21 2004-10-13 Upjohn Co Derivados aril-1,4-pirazina substituìdos
US20030187026A1 (en) 2001-12-13 2003-10-02 Qun Li Kinase inhibitors
BRPI0415863A (pt) * 2003-10-27 2007-01-09 Astellas Pharma Inc derivados pirazina e seus usos farmacêuticos
JP5008569B2 (ja) * 2004-10-22 2012-08-22 ジヤンセン・フアーマシユーチカ・ナームローゼ・フエンノートシヤツプ C−fmsキナーゼのインヒビターとしての芳香族アミド

Also Published As

Publication number Publication date
CR9954A (es) 2008-05-28
CN101356169A (zh) 2009-01-28
TNSN08196A1 (fr) 2009-10-30
JP2009514937A (ja) 2009-04-09
ZA200803671B (en) 2009-03-25
DOP2006000243A (es) 2007-05-31
PE20070715A1 (es) 2007-08-11
TW200804353A (en) 2008-01-16
AU2006310215A1 (en) 2007-05-10
IL191059A0 (en) 2008-12-29
CA2624621A1 (en) 2007-05-10
ECSP088412A (es) 2008-05-30
CA2624621C (en) 2010-11-30
MA29926B1 (fr) 2008-11-03
ES2371932T3 (es) 2012-01-11
EA200801011A1 (ru) 2009-02-27
NL2000284A1 (nl) 2007-05-07
AR057855A1 (es) 2007-12-19
ATE525372T1 (de) 2011-10-15
BRPI0618129A2 (pt) 2011-08-16
WO2007052123A2 (en) 2007-05-10
NL2000284C2 (nl) 2007-09-28
AP2008004468A0 (en) 2008-06-30
WO2007052123A3 (en) 2007-07-12
US20070105872A1 (en) 2007-05-10
EP1945630B1 (en) 2011-09-21
EP1945630A2 (en) 2008-07-23
GT200600475A (es) 2007-07-06
US7572797B2 (en) 2009-08-11
UY29893A1 (es) 2007-06-29
KR20080066073A (ko) 2008-07-15

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Legal Events

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FC2A Withdrawal, rejection or dismissal of laid open patent application