HUP0002030A2 - GluR5 receptorantagonisták alkalmazása fájdalom kezelésére - Google Patents
GluR5 receptorantagonisták alkalmazása fájdalom kezeléséreInfo
- Publication number
- HUP0002030A2 HUP0002030A2 HU0002030A HUP0002030A HUP0002030A2 HU P0002030 A2 HUP0002030 A2 HU P0002030A2 HU 0002030 A HU0002030 A HU 0002030A HU P0002030 A HUP0002030 A HU P0002030A HU P0002030 A2 HUP0002030 A2 HU P0002030A2
- Authority
- HU
- Hungary
- Prior art keywords
- treatment
- pain
- methyl
- decahydroisoquinoline
- receptorantagonists
- Prior art date
Links
- 239000002464 receptor antagonist Substances 0.000 title abstract 4
- 229940044551 receptor antagonist Drugs 0.000 title abstract 4
- 108010009117 Gluk1 kainate receptor Proteins 0.000 abstract 3
- NENLYAQPNATJSU-UHFFFAOYSA-N 1,2,3,4,4a,5,6,7,8,8a-decahydroisoquinoline Chemical class C1NCCC2CCCCC21 NENLYAQPNATJSU-UHFFFAOYSA-N 0.000 abstract 1
- -1 1H-tetrazol-5-yl Chemical group 0.000 abstract 1
- 241000124008 Mammalia Species 0.000 abstract 1
- 238000000034 method Methods 0.000 abstract 1
- 150000003839 salts Chemical class 0.000 abstract 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D217/00—Heterocyclic compounds containing isoquinoline or hydrogenated isoquinoline ring systems
- C07D217/22—Heterocyclic compounds containing isoquinoline or hydrogenated isoquinoline ring systems 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 carbon atoms of the nitrogen-containing ring
- C07D217/26—Carbon atoms having three bonds to hetero atoms with at the most one bond to halogen
-
- 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
- A61K31/47—Quinolines; Isoquinolines
- A61K31/472—Non-condensed isoquinolines, e.g. papaverine
-
- 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
-
- 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
- A61K31/47—Quinolines; Isoquinolines
-
- 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
- A61K31/47—Quinolines; Isoquinolines
- A61K31/472—Non-condensed isoquinolines, e.g. papaverine
- A61K31/4725—Non-condensed isoquinolines, e.g. papaverine containing further heterocyclic rings
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P25/00—Drugs for disorders of the nervous system
- A61P25/04—Centrally acting analgesics, e.g. opioids
-
- 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
- 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
Landscapes
- Health & Medical Sciences (AREA)
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- General Health & Medical Sciences (AREA)
- Veterinary Medicine (AREA)
- Public Health (AREA)
- Medicinal Chemistry (AREA)
- Animal Behavior & Ethology (AREA)
- Life Sciences & Earth Sciences (AREA)
- Pharmacology & Pharmacy (AREA)
- Epidemiology (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Engineering & Computer Science (AREA)
- General Chemical & Material Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Pain & Pain Management (AREA)
- Biomedical Technology (AREA)
- Neurology (AREA)
- Neurosurgery (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Medicines That Contain Protein Lipid Enzymes And Other Medicines (AREA)
- Nitrogen Condensed Heterocyclic Rings (AREA)
- Other In-Based Heterocyclic Compounds (AREA)
- Plural Heterocyclic Compounds (AREA)
Abstract
A szelektív GluR5 receptor-antagonisták alkalmasak a fájdalomkezelésére. A találmány tárgya eljárás a fájdalom kezelésére, melyabból áll, hogy a kezelésre szoruló emlős szervezetébe hatásosmennyiségű szelektív GluR5 receptor-antagonistát juttatnak. Atalálmány további tárgyát képezik azok az új dekahidroizokinolin-származékok, melyek szelektív GluR5 receptor-antagonista aktivitássalrendelkeznek, nevezetesen a 3S,4aR,6S,8aR-6-{[(1H-tetrazol-5-il)-metil]-oxi-metil}-1,2,3,4,4a,5,6,7,8,8a-dekahidroizokinolin-3-karbonsav és a 3S,4aR,6S,8aR-6-{[(4-karboxi)-fenil]-metil}-1,2,3,4,4a,5,6,7,8,8a- dekahidroizokinolin-3-karbonsav és gyógyászatiszempontból alkalmazható sóik. Ó
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US4279597P | 1997-04-07 | 1997-04-07 | |
PCT/US1998/006905 WO1998045270A1 (en) | 1997-04-07 | 1998-04-06 | Pharmacological agents |
Publications (2)
Publication Number | Publication Date |
---|---|
HUP0002030A2 true HUP0002030A2 (hu) | 2001-04-28 |
HUP0002030A3 HUP0002030A3 (en) | 2002-01-28 |
Family
ID=21923795
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
HU0002030A HUP0002030A3 (en) | 1997-04-07 | 1998-04-06 | Use of glur5 receptorantagonists for the treatment of pain |
Country Status (17)
Country | Link |
---|---|
US (1) | US6242462B1 (hu) |
EP (1) | EP0980358A4 (hu) |
JP (1) | JP2001521505A (hu) |
KR (1) | KR20010006075A (hu) |
CN (1) | CN1259126A (hu) |
AU (1) | AU734657B2 (hu) |
BR (1) | BR9809071A (hu) |
CA (1) | CA2285192A1 (hu) |
EA (1) | EA199900912A1 (hu) |
HU (1) | HUP0002030A3 (hu) |
ID (1) | ID23013A (hu) |
IL (1) | IL132086A0 (hu) |
NO (1) | NO994850L (hu) |
NZ (1) | NZ337827A (hu) |
PL (1) | PL336068A1 (hu) |
TR (1) | TR199902449T2 (hu) |
WO (1) | WO1998045270A1 (hu) |
Families Citing this family (22)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
IL146697A0 (en) | 1999-07-06 | 2002-07-25 | Lilly Co Eli | SELECTIVE iGluR5 RECEPTOR FOR THE TREATMENT OF MIGRAINE |
AU5591900A (en) * | 1999-07-06 | 2001-01-22 | Eli Lilly And Company | Diester prodrugs of a decahydroisoquinoline-3-carboxylic acid |
AU2574801A (en) | 1999-12-22 | 2001-07-03 | Eli Lilly And Company | Selective iGLUR5 receptor antagonists |
US7205313B2 (en) | 2001-01-05 | 2007-04-17 | Eli Lilly And Company | Excitatory amino acid receptor antagonists |
ES2306690T3 (es) * | 2001-01-05 | 2008-11-16 | Eli Lilly And Company | Antagonistas de receptores de aminoacidos excitatorios. |
US6924294B2 (en) | 2001-01-05 | 2005-08-02 | Eli Lilly And Company | Excitatory amino acid receptor antagonists |
WO2002053555A2 (en) | 2001-01-05 | 2002-07-11 | Eli Lilly And Company | Pyrrolidinylmethyl- and piperidinyl substituted decahydroisoquinolines as excitatory amino acid receptor antagonists |
AU2002241565A1 (en) * | 2001-01-05 | 2002-07-16 | Eli Lilly And Company | Excitatory amino acid receptor antagonist and 5-ht1f agonist combination: a method for the treatment of neurological disorders |
AU2002228736A1 (en) | 2001-01-05 | 2002-07-16 | Eli Lilly And Company | Pyrrolidinylmethyl substituted decahydroisoquinolines as excitatory amino acid receptor antagonists |
WO2002058691A1 (en) * | 2001-01-23 | 2002-08-01 | Neurosearch A/S | Use of non-competitive and selective glur5 antagonists as glutamate receptor modulating compounds |
JP2005529892A (ja) | 2002-04-26 | 2005-10-06 | イーライ・リリー・アンド・カンパニー | 鎮痛剤としてのデカヒドロイソキノリン−3−カルボン酸のエステルプロドラッグ |
WO2005007106A2 (en) * | 2003-07-10 | 2005-01-27 | Pharmacia Corporation | Compositions of a cyclooxygenase-2 selective inhibitor and a non-nmda glutamate modulator for the treatment of central nervous system damage |
WO2005030148A2 (en) * | 2003-09-25 | 2005-04-07 | Cenomed, Inc. | Tetrahydroindolone derivatives for treatment of neurological conditions |
US20050107439A1 (en) * | 2003-11-10 | 2005-05-19 | Helton David R. | Composition and method for treating emesis |
PT2083811T (pt) | 2006-11-22 | 2017-01-23 | Clinical Res Ass Llc | Métodos de tratamento da síndrome de down, síndrome do x frágil e autismo |
US8603980B2 (en) | 2007-01-16 | 2013-12-10 | The Johns Hopkins University | Glutamate receptor antagonists and methods of use |
EP2219648A4 (en) * | 2007-11-09 | 2010-11-03 | Cenomed Biosciences Llc | TREATMENT OF POSTRAUMATIC STRESS WITH TETRAHYDROINDOLONE ARYLPIPERAZINE COMPOUNDS |
US20090264443A1 (en) * | 2008-04-18 | 2009-10-22 | David Helton | Treatment of organophosphate exposure with tetrahydroindolone arylpiperazine compounds |
WO2011109398A2 (en) | 2010-03-02 | 2011-09-09 | President And Fellows Of Harvard College | Methods and compositions for treatment of angelman syndrome and autism spectrum disorders |
WO2011150380A1 (en) | 2010-05-28 | 2011-12-01 | Xenoport, Inc. | Methods of treatment of fragile x syndrome, down's syndrome, autism and related disorders |
WO2012009646A1 (en) | 2010-07-15 | 2012-01-19 | Xenoport, Inc. | Methods of treating fragile x syndrome, down's syndrome, autism and related disorders |
KR101746944B1 (ko) * | 2015-09-23 | 2017-06-14 | 주식회사 포스코 | 도장 선영성이 우수한 도금강판의 제조방법 및 이에 의해 제조된 도금강판 |
Family Cites Families (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US5284957A (en) | 1992-09-03 | 1994-02-08 | Eli Lilly And Company | Excitatory amino acid receptor antagonists |
US5446051A (en) * | 1994-05-31 | 1995-08-29 | Eli Lilly And Company | Aryl-spaced decahydroisoquinoline-3-carboxylic acids as excitatory amino acid receptor antagonists |
CA2216648A1 (en) * | 1995-02-15 | 1996-08-22 | Bearsden Bio, Inc. | Alkylcarboxy amino acids-modulators of the kainate receptor |
-
1998
- 1998-04-06 CA CA002285192A patent/CA2285192A1/en not_active Abandoned
- 1998-04-06 ID IDW991132A patent/ID23013A/id unknown
- 1998-04-06 TR TR1999/02449T patent/TR199902449T2/xx unknown
- 1998-04-06 WO PCT/US1998/006905 patent/WO1998045270A1/en not_active Application Discontinuation
- 1998-04-06 CN CN98805687A patent/CN1259126A/zh active Pending
- 1998-04-06 BR BR9809071-2A patent/BR9809071A/pt not_active IP Right Cessation
- 1998-04-06 EA EA199900912A patent/EA199900912A1/ru unknown
- 1998-04-06 IL IL13208698A patent/IL132086A0/xx unknown
- 1998-04-06 KR KR1019997009153A patent/KR20010006075A/ko not_active Application Discontinuation
- 1998-04-06 EP EP98915346A patent/EP0980358A4/en not_active Withdrawn
- 1998-04-06 HU HU0002030A patent/HUP0002030A3/hu unknown
- 1998-04-06 NZ NZ337827A patent/NZ337827A/xx unknown
- 1998-04-06 US US09/402,174 patent/US6242462B1/en not_active Expired - Fee Related
- 1998-04-06 PL PL98336068A patent/PL336068A1/xx unknown
- 1998-04-06 AU AU69555/98A patent/AU734657B2/en not_active Ceased
- 1998-04-06 JP JP54212798A patent/JP2001521505A/ja active Pending
-
1999
- 1999-10-05 NO NO994850A patent/NO994850L/no not_active Application Discontinuation
Also Published As
Publication number | Publication date |
---|---|
NZ337827A (en) | 2000-12-22 |
US6242462B1 (en) | 2001-06-05 |
PL336068A1 (en) | 2000-06-05 |
ID23013A (id) | 1999-12-30 |
EP0980358A4 (en) | 2001-02-07 |
EA199900912A1 (ru) | 2000-04-24 |
HUP0002030A3 (en) | 2002-01-28 |
EP0980358A1 (en) | 2000-02-23 |
CA2285192A1 (en) | 1998-10-15 |
BR9809071A (pt) | 2000-08-01 |
WO1998045270A1 (en) | 1998-10-15 |
AU734657B2 (en) | 2001-06-21 |
NO994850D0 (no) | 1999-10-05 |
CN1259126A (zh) | 2000-07-05 |
NO994850L (no) | 1999-10-05 |
JP2001521505A (ja) | 2001-11-06 |
AU6955598A (en) | 1998-10-30 |
TR199902449T2 (xx) | 2000-07-21 |
KR20010006075A (ko) | 2001-01-15 |
IL132086A0 (en) | 2001-03-19 |
Similar Documents
Publication | Publication Date | Title |
---|---|---|
HUP0002030A2 (hu) | GluR5 receptorantagonisták alkalmazása fájdalom kezelésére | |
ES2096312T3 (es) | Derivado de quinuclidina como antagonista de la sustancia p. | |
WO1999017755A3 (en) | Medicaments | |
DK0975602T3 (da) | Imidazol- og imidazolinderivater samt anvendelse heraf | |
NO20001754L (no) | Prostaglandinagonister og anvendelse derav for behandling av benforstyrrelser | |
HUP0003852A3 (en) | Use of highly selective butyrylcholinesterase inhibitors for the treatment and diagnosis of alzheimer's disease and dementias | |
NO963064L (no) | Behandling av normotensive glaukoma med angiotensin-II-antagonister | |
HUP0202253A2 (hu) | Szelektív iGluR5-receptorantagonisták a migrén kezelésére | |
WO1997010824A8 (en) | Use of 5ht1b receptor antagonist for the treatment of vascular disease | |
FR2845000B1 (fr) | Utilisation d'un compose heterocyclique ou de l'un de ses sels pour stimuler ou induire la pousse des cheveux et/ou freiner leur chute | |
BG104797A (en) | Use of dexmedetomi dine for sedative effect in patients in an intensive care unit | |
ATE266420T1 (de) | Kombinationspräparat, das selektive nmda nr2b- antagonisten und cox-2 inhibitoren enthält | |
EA200200562A1 (ru) | Антагонисты аденозиновых рецепторов и способы их получения и использования | |
IT1277904B1 (it) | Metodo per determinare l'attivita' terapeutica di composti inibitori di metalloproteinasi, nuovi composti inibitori, e loro impiego | |
NO932391D0 (no) | Angiotensin-ii reseptorantagonister for behandling av hjerterytmeforstyrrelser | |
BR0007686A (pt) | Uso de antagonistas receptores da angiotensina ii para tratar enfartação miocárdia aguda | |
EA200601592A1 (ru) | Фармацевтическая композиция, содержащая ингибитор pde4 или pde3/4 и антагонист гистаминового рецептора | |
AU9139791A (en) | Use of quisqualate-receptor antagonists for treating Parkinson's disease | |
HU9700661D0 (en) | Use of alpha-1-adrenoreceptor antagonists for profilacting and treating cancer | |
WO2000076500A3 (en) | Compound for use as a medicament for treatment of disorders involving bronchocontraction | |
CA2416879A1 (en) | Methods of treating cancer and the pain associated therewith using endothelin antagonists | |
GEP20043286B (en) | Dual Inhibitors of Cholesteryl Ester and Wax Ester Synthesis for Sebaceous Gland Disorders | |
HUP0103712A2 (hu) | Paroxetin sók, eljárás az előállításukra és gyógyászati alkalmazásuk | |
WO2004014307A3 (en) | Gal3 antagonists for the treatment of neuropathic pain | |
EP2140864A3 (en) | Use of GAL3 receptor antagonists for the treatment of depression and / or anxiety and compounds useful in such methods |