UY26874A1 - Compuestos heterocíclicos como ligandos de los receptores gaba - Google Patents
Compuestos heterocíclicos como ligandos de los receptores gabaInfo
- Publication number
- UY26874A1 UY26874A1 UY26874A UY26874A UY26874A1 UY 26874 A1 UY26874 A1 UY 26874A1 UY 26874 A UY26874 A UY 26874A UY 26874 A UY26874 A UY 26874A UY 26874 A1 UY26874 A1 UY 26874A1
- Authority
- UY
- Uruguay
- Prior art keywords
- gaba
- heterocyclic compounds
- agonists
- receivers
- links
- Prior art date
Links
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D471/00—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, at least one ring being a six-membered ring with one nitrogen atom, not provided for by groups C07D451/00 - C07D463/00
- C07D471/02—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, at least one ring being a six-membered ring with one nitrogen atom, not provided for by groups C07D451/00 - C07D463/00 in which the condensed system contains two hetero rings
- C07D471/04—Ortho-condensed systems
-
- 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
-
- 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
- A61P25/20—Hypnotics; Sedatives
-
- 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
- A61P25/22—Anxiolytics
-
- 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
- A61P25/24—Antidepressants
-
- 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
- A61P25/28—Drugs for disorders of the nervous system for treating neurodegenerative disorders of the central nervous system, e.g. nootropic agents, cognition enhancers, drugs for treating Alzheimer's disease or other forms of dementia
-
- 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
- C07D471/00—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, at least one ring being a six-membered ring with one nitrogen atom, not provided for by groups C07D451/00 - C07D463/00
- C07D471/12—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, at least one ring being a six-membered ring with one nitrogen atom, not provided for by groups C07D451/00 - C07D463/00 in which the condensed system contains three hetero rings
- C07D471/14—Ortho-condensed systems
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D487/00—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, not provided for by groups C07D451/00 - C07D477/00
- C07D487/02—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, not provided for by groups C07D451/00 - C07D477/00 in which the condensed system contains two hetero rings
- C07D487/04—Ortho-condensed systems
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D487/00—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, not provided for by groups C07D451/00 - C07D477/00
- C07D487/12—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, not provided for by groups C07D451/00 - C07D477/00 in which the condensed system contains three hetero rings
- C07D487/14—Ortho-condensed systems
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D513/00—Heterocyclic compounds containing in the condensed system at least one hetero ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for in groups C07D463/00, C07D477/00 or C07D499/00 - C07D507/00
- C07D513/02—Heterocyclic compounds containing in the condensed system at least one hetero ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for in groups C07D463/00, C07D477/00 or C07D499/00 - C07D507/00 in which the condensed system contains two hetero rings
- C07D513/04—Ortho-condensed systems
Abstract
Lo que se divulga en el presente son compuestos heterocíclicos de la fórmula y sales farmacéuticamente aceptables de la misma cuya característica es que las variables A, V, Y, J, E, X, T, G, Q, W, Z, b, n y m se definen en el presente. Estos compuestos son agonistas, antagonistas o agonistas invertidos altamente selectivos para los receptores cerebrales GABA o profármacos de agonistas, antagonistas o agonistas invertidos para los receptores cerebrales GABA.
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US22366900P | 2000-08-07 | 2000-08-07 |
Publications (1)
Publication Number | Publication Date |
---|---|
UY26874A1 true UY26874A1 (es) | 2002-03-22 |
Family
ID=22837525
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
UY26874A UY26874A1 (es) | 2000-08-07 | 2001-08-07 | Compuestos heterocíclicos como ligandos de los receptores gaba |
Country Status (18)
Country | Link |
---|---|
US (2) | US6653471B2 (es) |
EP (1) | EP1325006A2 (es) |
JP (1) | JP2004505942A (es) |
KR (1) | KR20030036678A (es) |
CN (1) | CN1468241A (es) |
AU (1) | AU2001285401A1 (es) |
BR (1) | BR0113120A (es) |
CA (1) | CA2420967A1 (es) |
CO (1) | CO5310576A1 (es) |
EC (1) | ECSP014130A (es) |
HN (1) | HN2002000193A (es) |
IL (1) | IL154310A0 (es) |
MX (1) | MXPA03001186A (es) |
PA (1) | PA8524601A1 (es) |
PE (1) | PE20020275A1 (es) |
TN (1) | TNSN01122A1 (es) |
UY (1) | UY26874A1 (es) |
WO (1) | WO2002012442A2 (es) |
Families Citing this family (52)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JP2005500253A (ja) * | 2001-02-23 | 2005-01-06 | オーソ−マクニール・フアーマシユーチカル・インコーポレーテツド | トロンビン受容体アンタゴニストとしてのアミノメチルピロロキナゾリン化合物 |
JP2005525333A (ja) | 2002-02-07 | 2005-08-25 | ニューロジェン コーポレイション | 置換縮合ピラゾールカルボン酸アリールアミド及び関連化合物 |
FR2857363B1 (fr) * | 2003-07-10 | 2007-09-07 | Aventis Pharma Sa | 4,5,6,7-tetrahydro-1h-pyrazolo[3,4-c] pyridines substituees compositions les contenant et utilisation |
AR045037A1 (es) | 2003-07-10 | 2005-10-12 | Aventis Pharma Sa | Tetrahidro-1h-pirazolo [3,4-c] piridinas sustituidas, composiciones que las contienen y su utilizacion. |
DK1848430T3 (da) * | 2004-12-31 | 2017-11-06 | Dr Reddys Laboratories Ltd | Nye benzylamin-derivativer som cetp-inhibitors |
US7737279B2 (en) | 2005-05-10 | 2010-06-15 | Bristol-Myers Squibb Company | 1,6-dihydro-1,3,5,6-tetraaza-as-indacene based tricyclic compounds and pharmaceutical compositions comprising same |
US8583926B1 (en) | 2005-09-19 | 2013-11-12 | Jpmorgan Chase Bank, N.A. | System and method for anti-phishing authentication |
WO2007053352A2 (en) * | 2005-10-28 | 2007-05-10 | Wyeth | Pyrroloquinolinone derivatives as 5-hydroxytryptamine-6 ligands |
US20070099911A1 (en) * | 2005-10-28 | 2007-05-03 | Wyeth | Pyrroloquinolinone derivatives as 5-hydroxytryptamine-6 ligands |
EP1968941A1 (en) * | 2005-12-29 | 2008-09-17 | Novartis AG | Pyridinyl amine derivatives as inhibitors of cholesteryl ester transfer protein (cetp) |
CA2650954C (en) | 2006-05-10 | 2014-02-11 | Novartis Ag | Bicyclic derivatives as cetp inhibitors |
US20090181929A1 (en) * | 2006-05-11 | 2009-07-16 | Kazuhide Konishi | Organic compounds |
KR20090080523A (ko) * | 2006-11-15 | 2009-07-24 | 노파르티스 아게 | Cετρ 억제제로서의 헤테로시클릭 유도체 |
EP2190850A4 (en) * | 2007-07-03 | 2011-03-09 | Univ British Columbia | DELTAF508 CFTR DELTAF508 DELTAFLECTIVE TRANSPORTATION MOLECULES |
ME02340B (me) | 2008-06-10 | 2017-02-20 | Abbvie Inc | Triciklična jedinjenja |
CN102414203B (zh) * | 2009-05-07 | 2014-11-26 | 弗·哈夫曼-拉罗切有限公司 | 用作gaba调节剂的异*唑-吡啶衍生物 |
AU2010326030A1 (en) | 2009-12-01 | 2012-06-07 | Abbvie Inc. | Novel tricyclic compounds |
UY33071A (es) | 2009-12-01 | 2011-05-31 | Abbott Lab | Nuevos compuestos tricíclicos |
US8461328B2 (en) * | 2010-01-12 | 2013-06-11 | Genentech, Inc. | Tricyclic heterocyclic compounds, compositions and methods of use thereof |
WO2012088266A2 (en) | 2010-12-22 | 2012-06-28 | Incyte Corporation | Substituted imidazopyridazines and benzimidazoles as inhibitors of fgfr3 |
AU2012229952A1 (en) * | 2011-03-15 | 2013-04-18 | Abbvie Inc. | Nuclear hormone receptor modulators |
EP3718547A1 (en) | 2011-10-03 | 2020-10-07 | The University of Utah Research Foundation | Application of 5-ht6 receptor antagonists for the alleviation of cognitive deficits of down syndrome |
US20150374705A1 (en) | 2012-02-14 | 2015-12-31 | Shanghai Institues for Biological Sciences | Substances for treatment or relief of pain |
BR112014030812B1 (pt) | 2012-06-13 | 2022-11-08 | Incyte Holdings Corporation | Compostos tricíclicos substituídos como inibidores de fgfr, seus usos, composição farmacêutica e método para inibir uma enzima fgfr |
US9388185B2 (en) | 2012-08-10 | 2016-07-12 | Incyte Holdings Corporation | Substituted pyrrolo[2,3-b]pyrazines as FGFR inhibitors |
TW201422590A (zh) | 2012-09-07 | 2014-06-16 | Abbvie Inc | 雜環核激素受體調節劑 |
US9266892B2 (en) | 2012-12-19 | 2016-02-23 | Incyte Holdings Corporation | Fused pyrazoles as FGFR inhibitors |
WO2014094357A1 (en) | 2012-12-21 | 2014-06-26 | Abbvie Inc. | Heterocyclic nuclear hormone receptor modulators |
KR101663864B1 (ko) * | 2013-04-19 | 2016-10-07 | 영남대학교 산학협력단 | 아미도피리딘올 유도체 또는 이의 약제학적 허용가능한 염을 유효성분으로 함유하는 염증성 장질환의 예방 또는 치료용 약학조성물 |
SG10201708520YA (en) | 2013-04-19 | 2017-12-28 | Incyte Corp | Bicyclic heterocycles as fgfr inhibitors |
WO2015125858A1 (ja) * | 2014-02-24 | 2015-08-27 | 日本曹達株式会社 | ヘテロアリール化合物およびその用途 |
US10851105B2 (en) | 2014-10-22 | 2020-12-01 | Incyte Corporation | Bicyclic heterocycles as FGFR4 inhibitors |
MA41551A (fr) | 2015-02-20 | 2017-12-26 | Incyte Corp | Hétérocycles bicycliques utilisés en tant qu'inhibiteurs de fgfr4 |
AU2016219822B2 (en) | 2015-02-20 | 2020-07-09 | Incyte Holdings Corporation | Bicyclic heterocycles as FGFR inhibitors |
WO2016134294A1 (en) | 2015-02-20 | 2016-08-25 | Incyte Corporation | Bicyclic heterocycles as fgfr4 inhibitors |
US11512092B2 (en) | 2015-10-16 | 2022-11-29 | Abbvie Inc. | Processes for the preparation of (3S,4R)-3-ethyl-4-(3H-imidazo[1,2-a]pyrrolo[2,3-e]-pyrazin-8-yl)-n-(2,2,2-trifluoroethyl)pyrrolidine-1-carboxamide and solid state forms thereof |
US11773106B2 (en) | 2015-10-16 | 2023-10-03 | Abbvie Inc. | Processes for the preparation of (3S,4R)-3-ethyl-4-(3H-imidazo[1,2-a]pyrrolo[2,3-e]-pyrazin-8-yl)-N-(2,2,2-trifluoroethyl)pyrrolidine-1-carboxamide and solid state forms thereof |
US11524964B2 (en) | 2015-10-16 | 2022-12-13 | Abbvie Inc. | Processes for the preparation of (3S,4R)-3-ethyl-4-(3H-imidazo[1,2-a]pyrrolo[2,3-e]-pyrazin-8-yl)-n-(2,2,2-trifluoroethyl)pyrrolidine-1-carboxamide and solid state forms thereof |
US11365198B2 (en) | 2015-10-16 | 2022-06-21 | Abbvie Inc. | Processes for the preparation of (3S,4R)-3-ethyl-4-(3H-imidazo[1,2-a]pyrrolo[2,3-e]-pyrazin-8-yl)-N-(2,2,2-trifluoroethyl)pyrrolidine-1-carboxamide and solid state forms thereof |
US10550126B2 (en) | 2015-10-16 | 2020-02-04 | Abbvie Inc. | Processes for the preparation of (3S,4R)-3-ethyl-4-(3H-imidazo[1,2-A]pyrrolo[2,3-e]-pyrazin-8-yl)-N-(2,2,2-trifluoroethyl)pyrrolidine-1-carboxamide and solid state forms thereof |
MX2018004605A (es) | 2015-10-16 | 2018-11-29 | Abbvie Inc | Procesos para la preparacion de (3s,4r)-3-etil-4-(3h-imidazo-[1,2- a]-pirrolo-[2,3-e]-pirazin-8-il)-n-(2,2,2-trifluoroetil)-pirrolid in-1-carboxamida y formas en estado solido de la misma. |
AR111960A1 (es) | 2017-05-26 | 2019-09-04 | Incyte Corp | Formas cristalinas de un inhibidor de fgfr y procesos para su preparación |
KR20210018265A (ko) | 2018-05-04 | 2021-02-17 | 인사이트 코포레이션 | Fgfr 억제제의 고체 형태 및 이의 제조 방법 |
SG11202010882XA (en) | 2018-05-04 | 2020-11-27 | Incyte Corp | Salts of an fgfr inhibitor |
US11628162B2 (en) | 2019-03-08 | 2023-04-18 | Incyte Corporation | Methods of treating cancer with an FGFR inhibitor |
US11591329B2 (en) | 2019-07-09 | 2023-02-28 | Incyte Corporation | Bicyclic heterocycles as FGFR inhibitors |
JP2022552324A (ja) | 2019-10-14 | 2022-12-15 | インサイト・コーポレイション | Fgfr阻害剤としての二環式複素環 |
WO2021076728A1 (en) | 2019-10-16 | 2021-04-22 | Incyte Corporation | Bicyclic heterocycles as fgfr inhibitors |
EP4069695A1 (en) | 2019-12-04 | 2022-10-12 | Incyte Corporation | Derivatives of an fgfr inhibitor |
CA3163875A1 (en) | 2019-12-04 | 2021-06-10 | Incyte Corporation | Tricyclic heterocycles as fgfr inhibitors |
AR126102A1 (es) | 2021-06-09 | 2023-09-13 | Incyte Corp | Heterociclos tricíclicos como inhibidores de fgfr |
US11891377B1 (en) | 2023-09-06 | 2024-02-06 | King Faisal University | Pyrrolo[3,2-c][2,7]naphthyridine-2-carboxylic acid compounds as CK2 inhibitors |
Family Cites Families (9)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US5206415A (en) | 1991-12-20 | 1993-04-27 | Washington University | Tricyclic steroid analogs |
US5344626A (en) * | 1992-06-26 | 1994-09-06 | Minnesota Mining And Manufacturing Company | Dual impregnated activated carbon |
US5723462A (en) | 1996-04-26 | 1998-03-03 | Neurogen Corporation | Certain fused pyrrolecarboxamides a new class of GABA brain receptor ligands |
GB9708945D0 (en) * | 1997-05-01 | 1997-06-25 | Merck Sharp & Dohme | Therapeutic agents |
DE69807074T2 (de) * | 1997-05-08 | 2003-04-03 | Merck Sharp & Dohme | Substituierte 1,2,4-triazolo[3,4,-a]phthalazin-derivate als gaba-alpha 5-liganden |
GB9713707D0 (en) | 1997-06-27 | 1997-09-03 | Merck Sharp & Dohme | Therapeutic agents |
WO1999029319A2 (en) | 1997-12-09 | 1999-06-17 | Neurosearch A/S | Chemical compounds for use as anxiolytic agents and a method for the identification of anxiolytic compounds |
AU2879799A (en) * | 1998-02-26 | 1999-09-15 | Neurogen Corporation | 4-(4-piperidylmethylamino) substituted heteroaryl fused pyridines: gaba brain receptor ligands |
WO1999043682A1 (en) * | 1998-02-26 | 1999-09-02 | Neurogen Corporation | 2-(het-)aryl-4-(cyclic amino substituted) heteroaryl fused pyridine derivatives, their preparation and their use as (ant-)agonists for gaba (a) brain receptors |
-
2001
- 2001-08-06 AU AU2001285401A patent/AU2001285401A1/en not_active Abandoned
- 2001-08-06 BR BR0113120-6A patent/BR0113120A/pt not_active IP Right Cessation
- 2001-08-06 US US09/924,174 patent/US6653471B2/en not_active Expired - Fee Related
- 2001-08-06 CN CNA018169902A patent/CN1468241A/zh active Pending
- 2001-08-06 EP EP01964561A patent/EP1325006A2/en not_active Withdrawn
- 2001-08-06 WO PCT/US2001/041572 patent/WO2002012442A2/en active Application Filing
- 2001-08-06 KR KR10-2003-7001844A patent/KR20030036678A/ko not_active Application Discontinuation
- 2001-08-06 MX MXPA03001186A patent/MXPA03001186A/es active IP Right Grant
- 2001-08-06 JP JP2002517733A patent/JP2004505942A/ja active Pending
- 2001-08-06 IL IL15431001A patent/IL154310A0/xx unknown
- 2001-08-06 CA CA002420967A patent/CA2420967A1/en not_active Abandoned
- 2001-08-07 PE PE2001000785A patent/PE20020275A1/es not_active Application Discontinuation
- 2001-08-07 PA PA20018524601A patent/PA8524601A1/es unknown
- 2001-08-07 UY UY26874A patent/UY26874A1/es not_active Application Discontinuation
- 2001-08-07 EC EC2001004130A patent/ECSP014130A/es unknown
- 2001-08-07 TN TNTNSN01122A patent/TNSN01122A1/fr unknown
- 2001-08-08 CO CO01063854A patent/CO5310576A1/es not_active Application Discontinuation
-
2002
- 2002-07-24 HN HN2002000193A patent/HN2002000193A/es unknown
-
2003
- 2003-09-23 US US10/670,077 patent/US6949562B2/en not_active Expired - Fee Related
Also Published As
Publication number | Publication date |
---|---|
US6949562B2 (en) | 2005-09-27 |
MXPA03001186A (es) | 2004-04-20 |
JP2004505942A (ja) | 2004-02-26 |
PA8524601A1 (es) | 2003-09-05 |
US6653471B2 (en) | 2003-11-25 |
CN1468241A (zh) | 2004-01-14 |
PE20020275A1 (es) | 2002-04-09 |
TNSN01122A1 (fr) | 2005-11-10 |
ECSP014130A (es) | 2002-03-25 |
WO2002012442A3 (en) | 2003-05-01 |
BR0113120A (pt) | 2004-06-22 |
US20040110778A1 (en) | 2004-06-10 |
HN2002000193A (es) | 2002-11-05 |
US20030105081A1 (en) | 2003-06-05 |
CO5310576A1 (es) | 2003-08-29 |
CA2420967A1 (en) | 2002-02-14 |
WO2002012442A2 (en) | 2002-02-14 |
KR20030036678A (ko) | 2003-05-09 |
AU2001285401A1 (en) | 2002-02-18 |
IL154310A0 (en) | 2003-09-17 |
EP1325006A2 (en) | 2003-07-09 |
Similar Documents
Publication | Publication Date | Title |
---|---|---|
UY26874A1 (es) | Compuestos heterocíclicos como ligandos de los receptores gaba | |
UY26872A1 (es) | Derivados de la 4- fenil piridina | |
UY27918A1 (es) | Derivados de benzodioxol | |
HN1999000149A (es) | Derivados de 4,4-biarilpiperidina | |
UY26276A1 (es) | 1,2,4,5- tetrahidro-benzo (d) azepinas ley 17164 | |
HN2004000544A (es) | Nuevos derivados de quinolinas | |
PA8600501A1 (es) | Ligandos de receptor cannabinoide y usos de los mismos | |
DOP2001000170A (es) | Derivados de tiofeno utiles como agentes anticancesoros | |
CR7932A (es) | Pirazolo (1,5-a) (1,3,5) derivados de triazina como ligandos de receptor de cannabinoides | |
ECSP055684A (es) | Antagonistas del receptor opiode | |
UY28135A1 (es) | Derivados de pirimidina para el tratamiento de crecimiento celular anormal | |
NO20041504L (no) | Lactamderivater som antagonister for humane 11CBY reseptorer. | |
CR8333A (es) | Derivados biciclicos [3.1.0 ] como inhibidores del transportador de glicina | |
UY27551A1 (es) | Derivados de benzotiazol | |
CL2003002770A1 (es) | Compuestos derivados de pirrol e imiddazol; composiciones farmaceuticas que los contienen; procedimiento de preparacion; y su uso en el tratamiento y/o prevencion de enfermedades que estan asociadas con la modulacion de los receptores a canabinoides | |
UY26729A1 (es) | Alquilaminas heterocíclicas como antagonistas de los receptores muscarínicos | |
ECSP034917A (es) | Nuevos derivados de acido sulfonico | |
PA8561501A1 (es) | Lactamas como antagonistas de taquiquininas | |
PA8589801A1 (es) | Aminoalcoxiindoles | |
CU24550B1 (es) | Compuestos de aza-indazol útiles en lesiones de tendones y/o ligamentos | |
EA200700364A1 (ru) | Производные амида кинуреновой кислоты как антагонисты nr2b подтипа рецептора nmda | |
CR9436A (es) | Derivados de aril 1,4-pirazina sustituidos | |
PA8486701A1 (es) | Antagonistas de 5ht1 para terapia antidepresiva | |
AR028743A1 (es) | DERIVADOS DE N-TRIAZOLILMETIL-PIPERAZINA CON ACCIoN ANTAGONISTA DE RECEPTORES DE NEUROQUININA | |
ES2107505T3 (es) | Derivados de bencimidazol, un metodo para producirlo, fungicidas agricolas y horticolas que lo contienen como ingrediente activo y compuestos intermedios en su preparacion. |
Legal Events
Date | Code | Title | Description |
---|---|---|---|
109 | Application deemed to be withdrawn |
Effective date: 20140807 |