AR054393A1 - Derivados de benzo(b)furano y benzo(b)tiofeno, composiciones farmaceuticas que los contienen y su uso en la fabricacion de un medicamento para el tratamiento de enfermedades mediadas por la inhibicion de la reabsorcion de neurotransmisores de amina biogenicos. - Google Patents
Derivados de benzo(b)furano y benzo(b)tiofeno, composiciones farmaceuticas que los contienen y su uso en la fabricacion de un medicamento para el tratamiento de enfermedades mediadas por la inhibicion de la reabsorcion de neurotransmisores de amina biogenicos.Info
- Publication number
- AR054393A1 AR054393A1 ARP060102490A ARP060102490A AR054393A1 AR 054393 A1 AR054393 A1 AR 054393A1 AR P060102490 A ARP060102490 A AR P060102490A AR P060102490 A ARP060102490 A AR P060102490A AR 054393 A1 AR054393 A1 AR 054393A1
- Authority
- AR
- Argentina
- Prior art keywords
- cycloalkyl
- alkyl
- group
- benzo
- amino
- Prior art date
Links
- 201000010099 disease Diseases 0.000 title abstract 2
- 208000037265 diseases, disorders, signs and symptoms Diseases 0.000 title abstract 2
- 230000005764 inhibitory process Effects 0.000 title abstract 2
- 230000001404 mediated effect Effects 0.000 title abstract 2
- 239000008194 pharmaceutical composition Substances 0.000 title abstract 2
- FCEHBMOGCRZNNI-UHFFFAOYSA-N 1-benzothiophene Chemical compound C1=CC=C2SC=CC2=C1 FCEHBMOGCRZNNI-UHFFFAOYSA-N 0.000 title 1
- 238000004519 manufacturing process Methods 0.000 title 1
- 229940126601 medicinal product Drugs 0.000 title 1
- 230000002787 reinforcement Effects 0.000 title 1
- 125000000753 cycloalkyl group Chemical group 0.000 abstract 14
- 125000000217 alkyl group Chemical group 0.000 abstract 8
- VYFYYTLLBUKUHU-UHFFFAOYSA-N dopamine Chemical compound NCCC1=CC=C(O)C(O)=C1 VYFYYTLLBUKUHU-UHFFFAOYSA-N 0.000 abstract 4
- 125000005347 halocycloalkyl group Chemical group 0.000 abstract 4
- QZAYGJVTTNCVMB-UHFFFAOYSA-N serotonin Chemical compound C1=C(O)C=C2C(CCN)=CNC2=C1 QZAYGJVTTNCVMB-UHFFFAOYSA-N 0.000 abstract 4
- SFLSHLFXELFNJZ-QMMMGPOBSA-N (-)-norepinephrine Chemical compound NC[C@H](O)C1=CC=C(O)C(O)=C1 SFLSHLFXELFNJZ-QMMMGPOBSA-N 0.000 abstract 2
- 125000006552 (C3-C8) cycloalkyl group Chemical group 0.000 abstract 2
- 125000004093 cyano group Chemical group *C#N 0.000 abstract 2
- 229960003638 dopamine Drugs 0.000 abstract 2
- 229910052736 halogen Inorganic materials 0.000 abstract 2
- 150000002367 halogens Chemical class 0.000 abstract 2
- 229910052760 oxygen Inorganic materials 0.000 abstract 2
- 229910052717 sulfur Inorganic materials 0.000 abstract 2
- 125000006273 (C1-C3) alkyl group Chemical group 0.000 abstract 1
- 101100495912 Arabidopsis thaliana CHR12 gene Chemical group 0.000 abstract 1
- 150000001875 compounds Chemical class 0.000 abstract 1
- 229940079593 drug Drugs 0.000 abstract 1
- 239000003814 drug Substances 0.000 abstract 1
- 239000012458 free base Substances 0.000 abstract 1
- 125000005842 heteroatom Chemical group 0.000 abstract 1
- 125000002887 hydroxy group Chemical group [H]O* 0.000 abstract 1
- -1 nitro, amino Chemical group 0.000 abstract 1
- 229960002748 norepinephrine Drugs 0.000 abstract 1
- SFLSHLFXELFNJZ-UHFFFAOYSA-N norepinephrine Natural products NCC(O)C1=CC=C(O)C(O)=C1 SFLSHLFXELFNJZ-UHFFFAOYSA-N 0.000 abstract 1
- 230000009103 reabsorption Effects 0.000 abstract 1
- 150000003839 salts Chemical class 0.000 abstract 1
- 229940076279 serotonin Drugs 0.000 abstract 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D307/00—Heterocyclic compounds containing five-membered rings having one oxygen atom as the only ring hetero atom
- C07D307/77—Heterocyclic 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
- C07D307/78—Benzo [b] furans; Hydrogenated benzo [b] furans
- C07D307/82—Benzo [b] furans; Hydrogenated benzo [b] furans 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 hetero ring
-
- 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
- A61K31/335—Heterocyclic compounds having oxygen as the only ring hetero atom, e.g. fungichromin
- A61K31/34—Heterocyclic compounds having oxygen as the only ring hetero atom, e.g. fungichromin having five-membered rings with one oxygen as the only ring hetero atom, e.g. isosorbide
- A61K31/343—Heterocyclic compounds having oxygen as the only ring hetero atom, e.g. fungichromin having five-membered rings with one oxygen as the only ring hetero atom, e.g. isosorbide condensed with a carbocyclic ring, e.g. coumaran, bufuralol, befunolol, clobenfurol, amiodarone
-
- 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
- A61K31/38—Heterocyclic compounds having sulfur as a ring hetero atom
- A61K31/381—Heterocyclic compounds having sulfur as a ring hetero atom having five-membered rings
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P13/00—Drugs for disorders of the urinary system
- A61P13/02—Drugs for disorders of the urinary system of urine or of the urinary tract, e.g. urine acidifiers
-
- 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
- A61P25/00—Drugs for disorders of the nervous system
- A61P25/14—Drugs for disorders of the nervous system for treating abnormal movements, e.g. chorea, dyskinesia
- A61P25/16—Anti-Parkinson drugs
-
- 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
- A61P25/18—Antipsychotics, i.e. neuroleptics; Drugs for mania or schizophrenia
-
- 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
- C07D333/00—Heterocyclic compounds containing five-membered rings having one sulfur atom as the only ring hetero atom
- C07D333/50—Heterocyclic compounds containing five-membered rings having one sulfur atom as the only ring hetero atom condensed with carbocyclic rings or ring systems
- C07D333/52—Benzo[b]thiophenes; Hydrogenated benzo[b]thiophenes
- C07D333/62—Benzo[b]thiophenes; Hydrogenated benzo[b]thiophenes 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 hetero ring
Landscapes
- Health & Medical Sciences (AREA)
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Engineering & Computer Science (AREA)
- General Health & Medical Sciences (AREA)
- Public Health (AREA)
- Medicinal Chemistry (AREA)
- Veterinary Medicine (AREA)
- Pharmacology & Pharmacy (AREA)
- Life Sciences & Earth Sciences (AREA)
- Animal Behavior & Ethology (AREA)
- Neurology (AREA)
- General Chemical & Material Sciences (AREA)
- Biomedical Technology (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Neurosurgery (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Psychiatry (AREA)
- Pain & Pain Management (AREA)
- Epidemiology (AREA)
- Hospice & Palliative Care (AREA)
- Urology & Nephrology (AREA)
- Psychology (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Furan Compounds (AREA)
Abstract
Composiciones farmacéuticas que los contienen y su uso en medicamentos para el tratamiento de enfermedades mediadas por la inhibicion de la reabsorcion de serotonina 5-HT noradrenalina (NA) y dopamina (DA). Reivindicacion 1: La presente se refiere a un compuesto representado por la formula general (1) en la cual U es O o S; R1-R2 son seleccionados independientemente del grupo que consiste en H, alqu(en/in)ilo C1-6, cicloalqu(en)ilo C3-8, y cicloalqu(en)il C3-8-alqu(en/in)ilo C1-6, o R1 y R2 forman conjuntamente con el N al que están unidos un anillo de 4-7 miembros que no contiene ninguno o contiene un doble enlace, comprendiendo opcionalmente dicho anillo además de dicho N otro heteroátomo seleccionado de O y S; R3-R6 se seleccionan independientemente del grupo que consiste en H, halogeno, ciano, alqu(en/in)ilo C1-6, cicloalqu(en)ilo C3-8, y cicloalqu(en)il C3-8-alqu(en/in)ilo C1-6, haloalqu(en/in)ilo C1-6, halocicloalqu(en)ilo C3-8 y halocicloalqu(en)il C3-8-alqu(en/in)ilo 1- 6; R7 se selecciona del grupo que consiste en , alqu(en/in)ilo C1-6, cicloalqu(en)ilo C3-8 y cicloalqu(en)il C3-8-alqu(en/in)ilo C1-6; R8 -R11 se seleccionan independientemente del grupo que consiste en H, halogeno, ciano, alqu(en/in)ilo C1-6, cicloalqu(en)ilo C3-8, cicloalqu(en)il C3-8-alqu(en/in)ilo C1-6, haloalqu(en/in)ilo C1-6, halocicloalqu(en)ilo C3-8, halocicloalqu(en)il C3-8-alqu(en/in)ilo C1-6, nitro, amino, alqu(en/in)il C1-6-amino, di-(alqu(en/in)il C1-6)-amino, cicloalqu(en)il C3-8-amino, cicloalqu(en)il C3-8-alqu(en/in)il C1-6-amino, hidroxilo, alqu(en/in)iloxilo C1-6, cicloalqu(en)iloxilo C3-8, cicloalqu(en)il C3-8-alqu(en/in)iloxilo C1-6, alqu(en/in)il C1-6-sulfanilo, cicloalqu(en)il C3-8-sulfanilo y cicloalqu(en)il C3- 8-alqu(en/in)il C1-6-sulfanilo; m, n, o y p son independientemente 0 o 1; X se selecciona del grupo que consiste en CH2, CHR12 y CR13R14; Y se selecciona del grupo que consiste en CH2, CHR15 y CR16R17; Z se selecciona del grupo que consiste en CH2, CHR18 y CR19R20; y Q se selecciona del grupo que consiste en CH2, CHR21 y CR22R23; en donde R12-R23 se seleccionan independientemente del grupo que consiste en alqu(en/in)ilo C1-6, cicloalqu(en)ilo C3-8 y cicloalqu(en)il C3-8-alqu(en/in)ilo C1-6; como la base libre o una sal del mismo.
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| DKPA200500895 | 2005-06-17 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| AR054393A1 true AR054393A1 (es) | 2007-06-20 |
Family
ID=37574258
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| ARP060102490A AR054393A1 (es) | 2005-06-17 | 2006-06-13 | Derivados de benzo(b)furano y benzo(b)tiofeno, composiciones farmaceuticas que los contienen y su uso en la fabricacion de un medicamento para el tratamiento de enfermedades mediadas por la inhibicion de la reabsorcion de neurotransmisores de amina biogenicos. |
Country Status (15)
| Country | Link |
|---|---|
| US (2) | US7534791B2 (es) |
| EP (1) | EP1893596A2 (es) |
| JP (1) | JP2008546680A (es) |
| KR (1) | KR20080016655A (es) |
| CN (1) | CN101208324A (es) |
| AR (1) | AR054393A1 (es) |
| AU (1) | AU2006283224A1 (es) |
| BR (1) | BRPI0612236A2 (es) |
| CA (1) | CA2611736A1 (es) |
| EA (1) | EA200800073A1 (es) |
| IL (1) | IL188063A0 (es) |
| MX (1) | MX2007015401A (es) |
| NO (1) | NO20080268L (es) |
| WO (1) | WO2007023395A2 (es) |
| ZA (1) | ZA200710884B (es) |
Families Citing this family (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US7629473B2 (en) * | 2005-06-17 | 2009-12-08 | H. Lundbeck A/S | 2-(1H-indolylsulfanyl)-aryl amine derivatives |
| JP2012512172A (ja) * | 2008-12-15 | 2012-05-31 | タイゲン バイオテクノロジー カンパニー,リミテッド | ピペリジン誘導体の立体選択的合成 |
Family Cites Families (89)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US3803143A (en) | 1969-09-08 | 1974-04-09 | Eisai Co Ltd | 6-amino alkylene 6,7-dihydro-5h-dibenzo (b,g),(1,5)thiazocines |
| US4018830A (en) | 1969-09-22 | 1977-04-19 | Merck & Co., Inc. | Phenylthioaralkylamines |
| US4055665A (en) | 1974-11-25 | 1977-10-25 | Merck & Co., Inc. | Treating arrythmia with phenylthioaralkylamines |
| US4056632A (en) * | 1975-07-21 | 1977-11-01 | Burroughs Wellcome Co. | 2-Hydroxymethyl-2'-aminomethyl-diphenylsulfides and method of use |
| US4241071A (en) | 1977-01-27 | 1980-12-23 | American Hoechst Corporation | Antidepressant (α-phenyl-2-tolyl)azacycloalkanes |
| US4198417A (en) | 1979-01-10 | 1980-04-15 | American Hoechst Corporation | Phenoxyphenylpiperidines |
| DE3640475A1 (de) | 1986-11-27 | 1988-06-09 | Hoechst Sa Lab | Arzneimittel auf basis von derivaten des 3,4-diphenylpiperidins, die verwendung der derivate als arzneimittel sowie neue 3,4-diphenylpiperidinderivate und verfahren zu ihrer herstellung |
| EP0396827A1 (en) * | 1989-05-09 | 1990-11-14 | SPOFA Spojené Podniky Pro Zdravotnickou Vyrobu | 2-Phenylthiobenzylamine dervivatives and acid addition salts thereof |
| GB8912971D0 (en) * | 1989-06-06 | 1989-07-26 | Wellcome Found | Halogen substituted diphenylsulfides |
| US6645969B1 (en) | 1991-05-10 | 2003-11-11 | Aventis Pharmaceuticals Inc. | Aryl and heteroaryl quinazoline compounds which inhibit CSF-1R receptor tyrosine kinase |
| ATE190608T1 (de) | 1991-11-25 | 2000-04-15 | Pfizer | 5-(hetero- oder carbocyclylamino)-indol derivate, deren herstellung und deren verwendung als 5-ht1 agonisten |
| GB9126311D0 (en) | 1991-12-11 | 1992-02-12 | Wellcome Found | Substituted diphenylsulfides |
| GB9226532D0 (en) | 1992-12-21 | 1993-02-17 | Smithkline Beecham Plc | Compounds |
| US5945425A (en) | 1994-04-29 | 1999-08-31 | G.D. Searle & Co. | Method of using (H+ /K+)ATPase inhibitors as antiviral agents |
| KR100533431B1 (ko) | 1995-01-23 | 2006-05-03 | 다이이치 아스비오파마 가부시키가이샤 | 허혈성질환에기인하는증상의완화또는치료용약제및이에유용한화합물 |
| ATE195125T1 (de) | 1995-11-06 | 2000-08-15 | Dsm Nv | Verfahren zur de-esterifikation |
| CZ293595A3 (cs) | 1995-11-09 | 1999-12-15 | Farmak A. S. | Deriváty N,N-dimethyl-2-(arylthio)benzylaminu, jejich soli, způsoby jejich přípravy a jejich použití v léčivých přípravcích |
| US5912256A (en) | 1996-06-20 | 1999-06-15 | Eli Lilly And Company | Compounds having effects on serotonin-related systems |
| AU4091697A (en) | 1996-08-27 | 1998-03-19 | American Home Products Corporation | 4-aminoethoxy indoles as dopamin d2 agonists and as 5ht1a ligands |
| GB9725953D0 (en) * | 1997-12-08 | 1998-02-04 | Pfizer Ltd | Compounds useful in therapy |
| DE19756036A1 (de) | 1997-12-17 | 1999-06-24 | Merck Patent Gmbh | Amid- und Harnstoffderivate |
| US6333146B1 (en) | 1999-03-10 | 2001-12-25 | Fuji Photo Film Co., Ltd. | Methine compound and silver halide photographic material containing the same |
| EA200101017A1 (ru) | 1999-04-02 | 2002-04-25 | Айкос Корпорейшен | Ингибиторы связывания lfa-1 с icam и их использование |
| AU780725B2 (en) | 1999-04-30 | 2005-04-14 | Trustees Of The University Of Pennsylvania, The | Spect imaging agents for serotonin transporters |
| MXPA02001160A (es) | 1999-08-04 | 2002-07-02 | Millennium Pharm Inc | Compuestos que se unen a los receptores para melanocortina-4, y metodo de uso de estos. |
| PL355289A1 (en) | 1999-10-13 | 2004-04-05 | Pfizer Products Inc. | Biaryl ether derivatives useful as monoamine reuptake inhibitors |
| US6410736B1 (en) | 1999-11-29 | 2002-06-25 | Pfizer Inc. | Biaryl ether derivatives useful as monoamine reuptake inhibitors |
| DE60011817T2 (de) | 1999-12-30 | 2005-07-14 | H. Lundbeck A/S | 4-phenyl-1-piperazinyl, -piperidinyl und -tetrahydropyridyl-derivate |
| NZ519647A (en) | 1999-12-30 | 2004-02-27 | H | Substituted phenyl-piperazine derivatives, their preparation and use |
| FR2803592A1 (fr) | 2000-01-06 | 2001-07-13 | Aventis Cropscience Sa | Nouveaux derives de l'acide 3-hydroxypicolinique, leur procede de preparation et compositions fongicides les contenant. |
| WO2001064206A2 (en) | 2000-02-29 | 2001-09-07 | Integriderm, Inc. | Inhibitors of melanocyte tyrosinase as topical skin lighteners |
| CN1251671C (zh) | 2000-05-19 | 2006-04-19 | 武田药品工业株式会社 | β分泌酶抑制剂 |
| US6455738B1 (en) | 2000-07-13 | 2002-09-24 | Rhodia Chimie | Process for the sulfonation of an aromatic compound |
| US20030187023A1 (en) | 2000-07-17 | 2003-10-02 | Keiji Kubo | Sulfone derivatives, process for their production and use thereof |
| WO2002015910A1 (en) | 2000-08-18 | 2002-02-28 | Sterix Limited | 2-substituted estradiol derivative for inhibiting superoxid dismutase |
| BR0113445A (pt) | 2000-09-01 | 2005-04-12 | Fmc Corp | Composto, composição, e, método para o controle de insetos |
| WO2002020463A2 (en) | 2000-09-05 | 2002-03-14 | Tularik Inc. | Fxr modulators |
| EP1193268A1 (en) | 2000-09-27 | 2002-04-03 | Applied Research Systems ARS Holding N.V. | Pharmaceutically active sulfonamide derivatives bearing both lipophilic and ionisable moieties as inhibitors of protein Junkinases |
| DE60129148T2 (de) | 2000-10-06 | 2008-02-28 | Biocompatibles Uk Ltd., Farnham | Zwitterionische polymere |
| EP1578341A4 (en) | 2000-10-11 | 2005-09-28 | Tularik Inc | MODULATION OF THE CCR4 FUNCTION |
| DE60131675T2 (de) | 2000-11-14 | 2008-11-20 | Merck Patent Gmbh | Neue verwendung von substanzen mit kombinierten 5-ht1a agonistischen und serotonin reuptake inhibitor-aktivitäten |
| US6436938B1 (en) | 2001-01-22 | 2002-08-20 | Pfizer Inc. | Combination treatment for depression |
| WO2002062766A2 (en) | 2001-02-07 | 2002-08-15 | Millennium Pharmaceuticals, Inc. | Melanocortin-4 receptor binding compounds and methods of use thereof |
| DE60218037T2 (de) | 2001-06-07 | 2007-08-23 | F. Hoffmann-La Roche Ag | Neue indolderivate mit affinität zum 5-ht6-rezeptor |
| US7199147B2 (en) | 2001-06-12 | 2007-04-03 | Dainippon Sumitomo Pharma Co., Ltd. | Rho kinase inhibitors |
| UA81749C2 (uk) | 2001-10-04 | 2008-02-11 | Х. Луннбек А/С | Фенілпіперазинові похідні як інгібітори зворотного захоплення серотоніну |
| US7064139B2 (en) | 2001-10-29 | 2006-06-20 | Uniroyal Chemical Company, Inc. | Method for treating retroviral infections |
| HUP0401924A3 (en) | 2001-11-14 | 2009-07-28 | Schering Corp | Cannabinoid receptor ligands, their use and pharmaceutical compositions containing them |
| MXPA04006119A (es) | 2001-12-21 | 2004-11-01 | Lundbeck & Co As H | Derivados aminoindano como inhibidores de la absorcion de la serotonina y de la norepinefrina. |
| EP1465933B1 (en) | 2002-01-16 | 2007-08-29 | Biocompatibles UK Limited | Polymer conjugates |
| US20050261298A1 (en) | 2002-01-18 | 2005-11-24 | David Solow-Cordero | Methods of treating conditions associated with an Edg-7 receptor |
| JP4151842B2 (ja) | 2002-03-04 | 2008-09-17 | 独立行政法人科学技術振興機構 | 新規なホスホン酸アミド化合物、その製造方法及び用途 |
| EP2557139B1 (en) | 2002-03-29 | 2021-05-05 | Massachusetts Institute Of Technology | Light emitting device including semiconductor nanocrystals |
| DE10217006A1 (de) | 2002-04-16 | 2003-11-06 | Merck Patent Gmbh | Substituierte Indole |
| US7217732B2 (en) | 2002-06-19 | 2007-05-15 | Schering Corporation | Cannabinoid receptor agonists |
| TW200401641A (en) | 2002-07-18 | 2004-02-01 | Wyeth Corp | 1-Heterocyclylalkyl-3-sulfonylindole or-indazole derivatives as 5-hydroxytryptamine-6 ligands |
| CA2498946A1 (en) | 2002-09-17 | 2004-04-01 | F. Hoffmann-La Roche Ag | 2,4-substituted indoles and their use as 5-ht6 modulators |
| ATE362469T1 (de) | 2002-09-17 | 2007-06-15 | Hoffmann La Roche | 2,7-disubstituierteindole und ihre verwendung als 5-ht6 modulatoren |
| EP1402888A1 (en) | 2002-09-18 | 2004-03-31 | Jerini AG | The use of substituted carbocyclic compounds as rotamases inhibitors |
| US20040266732A1 (en) | 2002-09-20 | 2004-12-30 | Jorge Galvez | Therapeutic agents, methods, and treatments |
| US20040137389A1 (en) | 2002-12-19 | 2004-07-15 | Kouta Fukui | Heat-developable light-sensitive material |
| NZ541234A (en) | 2002-12-20 | 2008-06-30 | Amgen Inc | Asthma and allergic inflammation modulators |
| US7189501B2 (en) | 2002-12-27 | 2007-03-13 | Fuji Photo Film Co., Ltd. | Silver halide color photographic photosensitive material |
| DE10300098A1 (de) | 2003-01-07 | 2004-07-15 | Bayer Ag | Kupfer-Carben-Komplexe und ihre Verwendung |
| US7820753B2 (en) | 2003-02-05 | 2010-10-26 | Biocompatibles Uk Limited | Block copolymers |
| AR043633A1 (es) | 2003-03-20 | 2005-08-03 | Schering Corp | Ligandos de receptores de canabinoides |
| EP1608369B1 (en) | 2003-03-28 | 2013-06-26 | Novartis Vaccines and Diagnostics, Inc. | Use of organic compounds for immunopotentiation |
| US7244763B2 (en) | 2003-04-17 | 2007-07-17 | Warner Lambert Company Llc | Compounds that modulate PPAR activity and methods of preparation |
| JPWO2005035516A1 (ja) | 2003-10-10 | 2006-12-21 | 小野薬品工業株式会社 | 新規縮合複素環化合物およびその用途 |
| US7229751B2 (en) | 2003-11-20 | 2007-06-12 | Konica Minolta Medical & Graphic, Inc. | Silver salt photothermographic dry imaging material and image forming method using the same |
| WO2005060711A2 (en) | 2003-12-19 | 2005-07-07 | Elixir Pharmaceuticals, Inc. | Methods of treating a disorder |
| DK1701940T3 (da) | 2003-12-23 | 2008-09-08 | Lundbeck & Co As H | 2-(1H-indolylsulfanyl)-bensylaminderivater som SSRI |
| SE528250C2 (sv) | 2004-02-27 | 2006-10-03 | Calignum Technologies Ab | Komposition innefattande en initiator och ett förfarande för att behandla trä med kompositionen |
| JP4569142B2 (ja) | 2004-03-22 | 2010-10-27 | コニカミノルタホールディングス株式会社 | 表示素子 |
| JP4448730B2 (ja) | 2004-04-20 | 2010-04-14 | 富士フイルム株式会社 | 感光性組成物、該感光性組成物に用いられる化合物及び該感光性組成物を用いたパターン形成方法 |
| US20090156471A1 (en) | 2004-07-15 | 2009-06-18 | Ramot At Tel Aviv University Ltd. | Use of anti-amyloid agents for treating and typing pathogen infections |
| AR052308A1 (es) | 2004-07-16 | 2007-03-14 | Lundbeck & Co As H | Derivados de 2-(1h-indolilsulfanil)-arilamina y una composicion farmaceutica que contiene al compuesto |
| ATE539745T1 (de) | 2004-08-19 | 2012-01-15 | Univ Tel Aviv Future Tech Dev | Zusammensetzungen zur behandlung von amyloid- assoziierten erkrankungen |
| EP1793272A4 (en) | 2004-08-24 | 2008-01-23 | Fujifilm Corp | PHOTOGRAPHIC PHOTOSENSITIVE COLOR MATERIAL BASED ON SILVER HALIDE AND METHOD OF FORMING IMAGES |
| CA2582658A1 (en) | 2004-10-08 | 2006-04-13 | Banyu Pharmaceutical Co., Ltd. | Method for producing thioether compound |
| US20060135540A1 (en) | 2004-11-30 | 2006-06-22 | Jack Lin | PPAR active compounds |
| WO2006063606A1 (en) | 2004-12-16 | 2006-06-22 | Pirelli & C. S.P.A. | Process for manufacturing a thermoplastic elastomeric material |
| JP4989881B2 (ja) | 2004-12-28 | 2012-08-01 | 富士フイルム株式会社 | 有機電界発光素子 |
| US7456289B2 (en) | 2004-12-31 | 2008-11-25 | National Health Research Institutes | Anti-tumor compounds |
| US20060276440A1 (en) | 2005-01-03 | 2006-12-07 | An Wenqian F | Treatment of inflammatory disorders |
| EP1867704B1 (en) | 2005-03-15 | 2010-09-15 | FUJIFILM Corporation | Surface treatment method using disc-like compound, (lubricating) composition for surface treatment, and surface-treated article |
| US20060216546A1 (en) | 2005-03-28 | 2006-09-28 | Fuji Photo Film Co., Ltd. | Organic electroluminescent element |
| US7629473B2 (en) | 2005-06-17 | 2009-12-08 | H. Lundbeck A/S | 2-(1H-indolylsulfanyl)-aryl amine derivatives |
| DE102005037336A1 (de) * | 2005-08-04 | 2007-02-08 | Degussa Ag | Kohlenstoffmaterial |
-
2006
- 2006-06-13 AR ARP060102490A patent/AR054393A1/es not_active Application Discontinuation
- 2006-06-14 CA CA002611736A patent/CA2611736A1/en not_active Abandoned
- 2006-06-14 WO PCT/IB2006/003395 patent/WO2007023395A2/en not_active Ceased
- 2006-06-14 AU AU2006283224A patent/AU2006283224A1/en not_active Abandoned
- 2006-06-14 US US11/452,823 patent/US7534791B2/en not_active Expired - Fee Related
- 2006-06-14 BR BRPI0612236A patent/BRPI0612236A2/pt not_active IP Right Cessation
- 2006-06-14 JP JP2008516453A patent/JP2008546680A/ja not_active Withdrawn
- 2006-06-14 EA EA200800073A patent/EA200800073A1/ru unknown
- 2006-06-14 KR KR1020077029522A patent/KR20080016655A/ko not_active Withdrawn
- 2006-06-14 MX MX2007015401A patent/MX2007015401A/es not_active Application Discontinuation
- 2006-06-14 ZA ZA200710884A patent/ZA200710884B/xx unknown
- 2006-06-14 EP EP06809255A patent/EP1893596A2/en not_active Withdrawn
- 2006-06-14 CN CNA2006800205293A patent/CN101208324A/zh active Pending
-
2007
- 2007-12-11 IL IL188063A patent/IL188063A0/en unknown
-
2008
- 2008-01-15 NO NO20080268A patent/NO20080268L/no not_active Application Discontinuation
-
2009
- 2009-02-20 US US12/389,735 patent/US20090192213A1/en not_active Abandoned
Also Published As
| Publication number | Publication date |
|---|---|
| EP1893596A2 (en) | 2008-03-05 |
| MX2007015401A (es) | 2008-03-04 |
| NO20080268L (no) | 2008-02-07 |
| ZA200710884B (en) | 2009-04-29 |
| US20060287386A1 (en) | 2006-12-21 |
| EA200800073A1 (ru) | 2008-06-30 |
| KR20080016655A (ko) | 2008-02-21 |
| WO2007023395A2 (en) | 2007-03-01 |
| CN101208324A (zh) | 2008-06-25 |
| CA2611736A1 (en) | 2007-03-01 |
| JP2008546680A (ja) | 2008-12-25 |
| US20090192213A1 (en) | 2009-07-30 |
| IL188063A0 (en) | 2008-03-20 |
| BRPI0612236A2 (pt) | 2016-11-22 |
| US7534791B2 (en) | 2009-05-19 |
| WO2007023395A3 (en) | 2007-07-12 |
| AU2006283224A1 (en) | 2007-03-01 |
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| MX2020009928A (es) | Compuestos organicos. | |
| UY32547A (es) | Piperidinas sustituidas como antagonistas de ccr3 | |
| MX2020000261A (es) | Nuevos compuestos. | |
| PE20211333A1 (es) | Compuestos de sulfonamidaurea novedosos | |
| GT200800189A (es) | Derivados de amida y su aplicación para el tratamiento de enfermedades relacionadas con proteína-g | |
| UY31545A1 (es) | Nuevos derivados de 2-carboxamida cianoaminourea, sus sales y profarmacos farmacéuticamente aceptables, procesos de preparacion y aplicaciones | |
| AR083849A1 (es) | Antagonistas de mdm2 de espiro-oxindol | |
| PE20190705A1 (es) | COMPUESTOS DE BENZO[b] TIOFENO COMO AGONISTAS DE STING | |
| AR077267A1 (es) | Derivados nitrogenados heterociclicos inhibidores selectivos de pi3k, composiciones farmaceuticas que los contienen y uso de los mismos en el tratamiento de enfermedades inflamatorias y/o autoinmunes. | |
| MX387700B (es) | Gamma-carbolinas fusionadas con heterociclo deuterado. | |
| MX2015015893A (es) | 2-fenilimidazo[1,2-a]pirimidinas como agentes formadores de imagen. | |
| UY32391A (es) | Compuestos amino-heterocíclicos | |
| AR054560A1 (es) | Espiropiperidina como inhibidores de beta-secretasa para el tratamiento de la enfermedad de alzheimer | |
| BR112013025420A2 (pt) | medicamento, composição farmacêutica, métodos para produzir uma composição farmacêutica e para prevenir ou tratar uma doença, kit, uso de um composto, e de um medicamento, e, medicamento | |
| MX2016007056A (es) | Metodos para preparar compuestos de benzoquinolina. | |
| AR066063A1 (es) | Derivados de triazol que son antagonistas de smo | |
| CL2022003646A1 (es) | Derivados de amidopirimidona | |
| MX2017012396A (es) | Derivado de anillo fusionado de 9 elementos. | |
| AR067904A1 (es) | Derivados de piperazina-amida | |
| UY29393A1 (es) | Nuevos derivados de amidas, sales farmacéuticas aceptables, composiciones que los contienen, procedimientos de preparación y aplicaciones. | |
| CL2020000944A1 (es) | Compuestos bicíclicos y métodos de utilización de los mismos. | |
| PE20211769A1 (es) | Compuestos heteroaromaticos como inhibidores de vanina | |
| CO2018001700A2 (es) | Derivados de n-[1h-bencimidazol-2-il] metil-pirazin-2-il-carboxamida, composiciones y procedimientos de preparación de los mismos | |
| CL2020001817A1 (es) | Moduladores del receptor c5a | |
| BR112018010107A2 (pt) | composição farmacêutica para o tratamento ou prevenção de nash |
Legal Events
| Date | Code | Title | Description |
|---|---|---|---|
| FA | Abandonment or withdrawal |