PE20081386A1 - 4-imidazolinas como ligandos de taar - Google Patents
4-imidazolinas como ligandos de taarInfo
- Publication number
- PE20081386A1 PE20081386A1 PE2007001804A PE2007001804A PE20081386A1 PE 20081386 A1 PE20081386 A1 PE 20081386A1 PE 2007001804 A PE2007001804 A PE 2007001804A PE 2007001804 A PE2007001804 A PE 2007001804A PE 20081386 A1 PE20081386 A1 PE 20081386A1
- Authority
- PE
- Peru
- Prior art keywords
- phenyl
- lower alkyl
- taar
- imidazolines
- compounds
- Prior art date
Links
- 239000011230 binding agent Substances 0.000 title 1
- -1 AMINO Chemical class 0.000 abstract 3
- 150000001875 compounds Chemical class 0.000 abstract 3
- 102000011829 Trace amine associated receptor Human genes 0.000 abstract 2
- 108050002178 Trace amine associated receptor Proteins 0.000 abstract 2
- FCEAPTWKOZFSHD-UHFFFAOYSA-N 5-[(2,3-dichlorophenyl)sulfanylmethyl]-1h-imidazole Chemical compound ClC1=CC=CC(SCC=2NC=NC=2)=C1Cl FCEAPTWKOZFSHD-UHFFFAOYSA-N 0.000 abstract 1
- ZRLKJHCVZXLPNC-UHFFFAOYSA-N 5-[2-(2-chlorophenyl)ethyl]-1h-imidazole Chemical compound ClC1=CC=CC=C1CCC1=CNC=N1 ZRLKJHCVZXLPNC-UHFFFAOYSA-N 0.000 abstract 1
- 208000019901 Anxiety disease Diseases 0.000 abstract 1
- 208000020401 Depressive disease Diseases 0.000 abstract 1
- 208000018737 Parkinson disease Diseases 0.000 abstract 1
- CIUQDSCDWFSTQR-UHFFFAOYSA-N [C]1=CC=CC=C1 Chemical group [C]1=CC=CC=C1 CIUQDSCDWFSTQR-UHFFFAOYSA-N 0.000 abstract 1
- 229910052736 halogen Inorganic materials 0.000 abstract 1
- 150000002367 halogens Chemical class 0.000 abstract 1
- 238000000034 method Methods 0.000 abstract 1
- 239000008194 pharmaceutical composition Substances 0.000 abstract 1
- 201000000980 schizophrenia Diseases 0.000 abstract 1
Classifications
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D233/00—Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, not condensed with other rings
- C07D233/54—Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, not condensed with other rings having two double bonds between ring members or between ring members and non-ring members
- C07D233/64—Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, not condensed with other rings having two double bonds between ring members or between ring members and non-ring members with substituted hydrocarbon radicals attached to ring carbon atoms, e.g. histidine
-
- 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
- A61K31/41—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having five-membered rings with two or more ring hetero atoms, at least one of which being nitrogen, e.g. tetrazole
- A61K31/415—1,2-Diazoles
-
- 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
- A61P25/06—Antimigraine agents
-
- 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
-
- 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
- A61P25/00—Drugs for disorders of the nervous system
- A61P25/30—Drugs for disorders of the nervous system for treating abuse or dependence
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P3/00—Drugs for disorders of the metabolism
- A61P3/04—Anorexiants; Antiobesity agents
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P3/00—Drugs for disorders of the metabolism
- A61P3/06—Antihyperlipidemics
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P3/00—Drugs for disorders of the metabolism
- A61P3/08—Drugs for disorders of the metabolism for glucose homeostasis
- A61P3/10—Drugs for disorders of the metabolism for glucose homeostasis for hyperglycaemia, e.g. antidiabetics
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P9/00—Drugs for disorders of the cardiovascular system
Landscapes
- Health & Medical Sciences (AREA)
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Engineering & Computer Science (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Pharmacology & Pharmacy (AREA)
- Veterinary Medicine (AREA)
- Public Health (AREA)
- General Health & Medical Sciences (AREA)
- Animal Behavior & Ethology (AREA)
- Medicinal Chemistry (AREA)
- Life Sciences & Earth Sciences (AREA)
- General Chemical & Material Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Neurology (AREA)
- Biomedical Technology (AREA)
- Neurosurgery (AREA)
- Diabetes (AREA)
- Psychiatry (AREA)
- Obesity (AREA)
- Hematology (AREA)
- Pain & Pain Management (AREA)
- Psychology (AREA)
- Emergency Medicine (AREA)
- Hospice & Palliative Care (AREA)
- Heart & Thoracic Surgery (AREA)
- Addiction (AREA)
- Cardiology (AREA)
- Endocrinology (AREA)
- Child & Adolescent Psychology (AREA)
- Epidemiology (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Plural Heterocyclic Compounds (AREA)
Abstract
SE REFIERE A COMPUESTOS DERIVADOS DE 4-IMIDAZOLINAS DE FORMULA (I) DONDE R ES H, ALQUILO INFERIOR O AMINO; X-R1 ES -CH2-, -CH(ALCOXI INFERIOR)-, -CH(OH)- O -NH-; Y-R2 ES -CH2, -CH(ALQUILO INFERIOR)-, -S(O)2-, -CH(FENIL)-, ENTRE OTROS; Ar ES FENILO, NAFTILO O BENZOFURANILO OPCIONALMENTE SUSTITUIDO CON ALQUILO INFERIOR, HALOGENO, HIDROXI, AMINO, FENILO, ENTRE OTROS SUSTITUYENTES. SON COMPUESTOS PREFERIDOS: 4-[2-(2-CLORO-FENIL)-ETIL]-1H-IMIDAZOL, 4-(2,3-DICLORO-FENOXIMETIL)-1H-IMIDAZOL, 5-(2,3-DICLORO-FENILSULFANILMETIL)-1H-IMIDAZOL, ENTRE OTROS. SE REFIERE TAMBIEN A UN PROCEDIMIENTO DE PREPARACION Y A UNA COMPOSICION FARMACEUTICA. DICHOS COMPUESTOS TIENEN BUENA AFINIDAD CON LOS RECEPTORES DE LAS AMINAS TRAZAS (TAAR) SIENDO UTILES EN EL TRATAMIENTO DE DEPRESION, TRASTORNOS DE ANSIEDAD, ESQUIZOFRENIA, ENFERMEDAD DE PARKINSON
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
EP06126307 | 2006-12-18 |
Publications (1)
Publication Number | Publication Date |
---|---|
PE20081386A1 true PE20081386A1 (es) | 2008-09-18 |
Family
ID=39153757
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
PE2007001804A PE20081386A1 (es) | 2006-12-18 | 2007-12-14 | 4-imidazolinas como ligandos de taar |
Country Status (18)
Country | Link |
---|---|
US (3) | US20080146523A1 (es) |
EP (1) | EP2094668A2 (es) |
JP (1) | JP5175297B2 (es) |
KR (1) | KR101188992B1 (es) |
CN (1) | CN101578271B (es) |
AR (1) | AR064376A1 (es) |
AU (1) | AU2007336351A1 (es) |
BR (1) | BRPI0721291A2 (es) |
CA (1) | CA2671838A1 (es) |
CL (1) | CL2007003653A1 (es) |
IL (1) | IL198878A0 (es) |
MX (1) | MX2009006215A (es) |
NO (1) | NO20091936L (es) |
PE (1) | PE20081386A1 (es) |
RU (1) | RU2465269C2 (es) |
TW (1) | TWI345467B (es) |
WO (1) | WO2008074679A2 (es) |
ZA (1) | ZA200903841B (es) |
Families Citing this family (8)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JP5130305B2 (ja) | 2007-02-15 | 2013-01-30 | エフ.ホフマン−ラ ロシュ アーゲー | Taar1リガンドとしての2−アミノオキサゾリン |
WO2009097995A1 (de) * | 2008-02-07 | 2009-08-13 | Sanofi-Aventis | Neue phenyl-substituierte imidazolidine, verfahren zu deren herstellung, diese verbindungen enthaltende arzneimittel und deren verwendung |
AU2011338339A1 (en) | 2010-12-08 | 2013-06-27 | Vanderbilt University | Bicyclic pyrazole compounds as allosteric modulators of mGluR5 receptors |
US8865725B2 (en) | 2011-03-15 | 2014-10-21 | Vanderbilt University | Substituted imidazopyrimidin-5(6H)-ones as allosteric modulators of MGLUR5 receptors |
AU2012229983A1 (en) * | 2011-03-15 | 2013-10-03 | Vanderbilt University | Substituted imadazapyrinidin-5(6H)-ones as allosteric modulators of mGluR5 receptors |
EP2567959B1 (en) | 2011-09-12 | 2014-04-16 | Sanofi | 6-(4-hydroxy-phenyl)-3-styryl-1h-pyrazolo[3,4-b]pyridine-4-carboxylic acid amide derivatives as kinase inhibitors |
CN103910658B (zh) * | 2013-12-23 | 2016-08-17 | 宁夏大学 | 一种硫醚氧化成砜的方法 |
WO2015165085A1 (en) * | 2014-04-30 | 2015-11-05 | F.Hoffmann-La Roche Ag | Morpholin-pyridine derivatives |
Family Cites Families (68)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US2731471A (en) * | 1956-01-17 | Nxg hi | ||
US2161938A (en) * | 1934-07-31 | 1939-06-13 | Soc Of Chemical Ind | Imidazolines |
US2457047A (en) * | 1946-02-13 | 1948-12-21 | Monsanto Chemicals | 2-(2'-thenyl)-4, 5-dihydroimidazoles and process for making the same |
GB725514A (en) | 1952-08-28 | 1955-03-02 | Abbott Lab | Improvements in or relating to 4(5)-aryloxymethylimidazoles and their preparation |
US2778836A (en) * | 1954-04-02 | 1957-01-22 | Union Chimique Belge Sa | Substituted 2-methyl-delta2 imidazolines |
US2744910A (en) * | 1955-06-27 | 1956-05-08 | Bristol Lab Inc | 2-(ortho-benzylbenzyl)-imidazoline and acid addition salts |
US2744909A (en) * | 1955-06-27 | 1956-05-08 | Bristol Lab Inc | 2-(ortho-phenylbenzyl) imidazoline and acid addition salts |
US2919274A (en) * | 1957-09-17 | 1959-12-29 | Sahyun Melville | Amidines |
GB877306A (en) | 1958-04-21 | 1961-09-13 | Pfizer & Co C | Halogenated derivatives of tetrahydro-1-naphthyl cyclic amidines |
DE1121054B (de) * | 1960-11-23 | 1962-01-04 | Merck Ag E | Verfahren zur Herstellung eines neuen Imidazolinderivates und dessen Saeureadditionssalzen |
US3202660A (en) | 1961-10-09 | 1965-08-24 | Boehringer Sohn Ingelheim | Process for the preparation of 3-arylamino-1, 3-diazacycloalkenes |
DE1150180B (de) * | 1962-04-12 | 1963-06-12 | Merck Ag E | Mittel zur Vorbehandlung der Haut fuer die Rasur |
ES323985A1 (es) | 1966-02-26 | 1966-12-16 | Blade Pique Juan | Procedimiento para la obtenciën de derivados del imidazol |
US3377247A (en) * | 1967-04-28 | 1968-04-09 | Dow Chemical Co | Antidepressant method |
US3586695A (en) * | 1968-01-26 | 1971-06-22 | Dow Chemical Co | Substituted imidazolinyl indoles |
BE754935A (fr) * | 1969-08-13 | 1971-02-17 | Hoechst Ag | 2-(thienyl-3'-amino)-1,3-diazacycloalcenes et leur preparation |
US3818094A (en) * | 1969-08-28 | 1974-06-18 | Boehringer Sohn Ingelheim | Hypotensive pharmaceutical compositions containing certain 2-anilino-1,3-diazacyclopentenes-(2) |
US3622579A (en) * | 1969-08-28 | 1971-11-23 | Boehringer Sohn Ingelheim | Derivatives of 2-anilino-1,3-diazacyclopentene-(2) |
US3660423A (en) * | 1970-02-13 | 1972-05-02 | Dow Chemical Co | 2-(substituted benzyl)methyl-2-imidazolines |
GB1333471A (en) * | 1971-01-27 | 1973-10-10 | Labaz | Imidazoline derivatives and process for preparing the same |
JPS49134834A (es) * | 1973-05-07 | 1974-12-25 | ||
US4125620A (en) * | 1974-10-01 | 1978-11-14 | Boehringer Ingelheim Gmbh | 2-[(2',6'-Disubstituted-phenyl)-imino]-imidazolidines and salts thereof |
US3992403A (en) * | 1975-05-30 | 1976-11-16 | Schering Corporation | 2-Imidazolines and their use as hypoglycemic agents |
GB1538097A (en) * | 1976-01-26 | 1979-01-10 | Lafon Labor | Substituted phenyl-amidines |
US4323570A (en) * | 1978-11-15 | 1982-04-06 | Beiersdorf Aktiengesellschaft | Substituted aminopyrimidines |
AU518569B2 (en) | 1979-08-07 | 1981-10-08 | Farmos-Yhtyma Oy | 4-benzyl- and 4-benzoyl imidazole derivatives |
GB2069481B (en) * | 1980-02-13 | 1983-07-27 | Farmos Oy | Substituted imidazole derivatives |
GB2092569B (en) * | 1981-02-05 | 1984-09-19 | Farmos Oy | Substituted imidazole derivatives and their preparation and use |
GB2101114B (en) * | 1981-07-10 | 1985-05-22 | Farmos Group Ltd | Substituted imidazole derivatives and their preparation and use |
US4540705A (en) | 1983-03-14 | 1985-09-10 | Sterling Drug Inc. | Antidepressant imidazolines and related compounds |
EP0166937B1 (en) | 1984-06-06 | 1991-08-28 | Abbott Laboratories | Adrenergic compounds |
US4605661A (en) * | 1984-06-18 | 1986-08-12 | Eli Lilly And Company | Aromastase inhibiting α,α-diarylimidazole-4(5)-propionitriles, α,α-diarylimidazole-4(5)-propionamides, and 4(5)-(2,2-diarylethyl)imidazoles |
LU85747A1 (fr) * | 1985-01-28 | 1986-08-04 | Continental Pharma | Derives d'imidazole leur preparation et utilisation ainsi que les compositions pharmaceutiques contenant des derives |
US4665095A (en) * | 1985-12-11 | 1987-05-12 | Abbott Laboratories | Use of 2-[(3,5-dihalo-4-aminobenzyl)]imidazolines to stimulate alpha-1 adrenergic receptors and to treat nasal congestion |
JPS62265270A (ja) * | 1986-05-13 | 1987-11-18 | Zeria Shinyaku Kogyo Kk | 新規イミダゾ−ル誘導体およびそれらを有効成分とする抗潰瘍剤 |
JPH0774205B2 (ja) * | 1986-12-04 | 1995-08-09 | 三井石油化学工業株式会社 | 新規イミダゾ−ル誘導体 |
GB2215206B (en) | 1988-02-29 | 1991-07-03 | Farmos Oy | 4-substituted imidazole derivatives useful in perioperative care |
GB2229719B (en) * | 1989-03-30 | 1992-04-29 | Farmos Oy | Novel aromatase inhibiting 4(5)-imidazoles |
FI894911A0 (fi) | 1989-10-17 | 1989-10-17 | Farmos Oy | En terapeutiskt vaerdefull foerening. |
FR2669030B1 (fr) * | 1990-11-14 | 1992-12-31 | Adir | Nouveaux derives d'imidazole, leur procede de preparation et les compositions pharmaceutiques qui les contiennent. |
DE69534283T2 (de) | 1993-10-13 | 2006-03-16 | Horacek, H. Joseph | Clonidinhaltiges arzneimittel mit verzögerter wirkstoffabgabe |
EP0729459B1 (en) * | 1993-11-15 | 2003-03-12 | Schering Corporation | Phenyl-alkyl imidazoles as h3-receptor antagonists |
GB9425211D0 (en) * | 1994-12-14 | 1995-02-15 | Ucb Sa | Substituted 1H-imidazoles |
US5610174A (en) * | 1995-06-02 | 1997-03-11 | Synaptic Pharmaceutical Corporation | Use of α1A -selective adrenoceptor agonists for the treatment of urinary incontinence |
GB9520150D0 (en) | 1995-10-03 | 1995-12-06 | Orion Yhtymae Oy | New imidazole derivatives |
US5969137A (en) | 1996-09-19 | 1999-10-19 | Virginia Commonwealth University | Benzylamidine derivatives with serotonin receptor binding activity |
CA2229123A1 (en) | 1997-02-11 | 1998-08-11 | Mitchell Irvin Steinberg | Pharmaceutical agents |
US5866579A (en) * | 1997-04-11 | 1999-02-02 | Synaptic Pharmaceutical Corporation | Imidazole and imidazoline derivatives and uses thereof |
US6841684B2 (en) | 1997-12-04 | 2005-01-11 | Allergan, Inc. | Imidiazoles having reduced side effects |
SK8542000A3 (en) | 1997-12-04 | 2001-03-12 | Allergan Sales Inc | Substituted imidazole derivatives having agonist-like activity at alpha 2b or 2b/2c adrenergic receptors |
EP0924209B1 (en) | 1997-12-19 | 2003-05-02 | Eli Lilly And Company | Hypoglycemic imidazoline compounds |
DE69924717T2 (de) * | 1998-04-23 | 2006-03-09 | Takeda Pharmaceutical Co. Ltd. | Naphthalene derivate ,ihre herstellung und verwendung |
CA2246027A1 (en) | 1998-08-27 | 2000-02-27 | Virginia Commonwealth University | Benzylamidine derivatives with serotonin receptor binding activity |
EP1013244A1 (en) | 1998-12-21 | 2000-06-28 | Benoist Girard Et Cie | Prosthetic femoral component |
PE20010781A1 (es) | 1999-10-22 | 2001-08-08 | Takeda Chemical Industries Ltd | Compuestos 1-(1h-imidazol-4-il)-1-(naftil-2-sustituido)etanol, su produccion y utilizacion |
FI20000073A0 (fi) | 2000-01-14 | 2000-01-14 | Orion Yhtymae Oy | Uusia imidatsolijohdannaisia |
JP2001302643A (ja) | 2000-04-21 | 2001-10-31 | Suntory Ltd | 環状アミジン化合物 |
US6495464B1 (en) | 2000-06-30 | 2002-12-17 | Lam Research Corporation | Method and apparatus for fixed abrasive substrate preparation and use in a cluster CMP tool |
CA2422288A1 (en) | 2000-09-12 | 2002-03-21 | Oregon Health & Science University | Novel mammalian receptor genes and uses |
PL362549A1 (en) | 2000-11-14 | 2004-11-02 | F.Hoffmann-La Roche Ag | Substituted 2-phenylaminoimidazoline phenyl ketone derivatives as ip antagonists |
IL147921A0 (en) * | 2002-01-31 | 2002-08-14 | Abdulrazik Mohammad | A method for treating central nervous system disorders by ocular dosing |
TW200306783A (en) | 2002-04-29 | 2003-12-01 | Fmc Corp | Pesticidal heterocycles |
KR100492252B1 (ko) | 2002-08-09 | 2005-05-30 | 한국화학연구원 | 이미다졸을 포함하는 이차아민으로 치환된 벤조피란유도체 및 그의 제조방법 |
JP2008540441A (ja) | 2005-05-03 | 2008-11-20 | バイエル・クロツプサイエンス・アクチエンゲゼルシヤフト | 殺虫性の置換されたアミノアルキル複素環式及びヘテロアリール誘導体 |
JP2009506047A (ja) | 2005-08-25 | 2009-02-12 | シェーリング コーポレイション | 機能的に選択的なα2Cアドレナリン受容体アゴニストとしてのイミダゾール誘導体 |
BRPI0718054A2 (pt) | 2006-11-02 | 2013-11-05 | Hoffmann La Roche | 2-imidazóis substituídos como moduladores de receptores associados à traços de aminas |
CA2669112A1 (en) | 2006-11-16 | 2008-05-22 | F. Hoffmann-La Roche Ag | Substituted 4-imidazoles |
JP2010513238A (ja) | 2006-12-13 | 2010-04-30 | エフ.ホフマン−ラ ロシュ アーゲー | 微量アミン関連受容体(taar)に対するリガンドとしての新規2−イミダゾール |
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2007
- 2007-12-05 US US11/950,449 patent/US20080146523A1/en not_active Abandoned
- 2007-12-10 RU RU2009122665/04A patent/RU2465269C2/ru not_active IP Right Cessation
- 2007-12-10 CN CN2007800469972A patent/CN101578271B/zh not_active Expired - Fee Related
- 2007-12-10 BR BRPI0721291-7A patent/BRPI0721291A2/pt not_active IP Right Cessation
- 2007-12-10 WO PCT/EP2007/063585 patent/WO2008074679A2/en active Application Filing
- 2007-12-10 MX MX2009006215A patent/MX2009006215A/es active IP Right Grant
- 2007-12-10 KR KR1020097012493A patent/KR101188992B1/ko not_active Expired - Fee Related
- 2007-12-10 EP EP07857315A patent/EP2094668A2/en not_active Withdrawn
- 2007-12-10 AU AU2007336351A patent/AU2007336351A1/en not_active Abandoned
- 2007-12-10 CA CA002671838A patent/CA2671838A1/en not_active Abandoned
- 2007-12-10 JP JP2009541972A patent/JP5175297B2/ja not_active Expired - Fee Related
- 2007-12-14 PE PE2007001804A patent/PE20081386A1/es not_active Application Discontinuation
- 2007-12-17 CL CL200703653A patent/CL2007003653A1/es unknown
- 2007-12-17 TW TW096148251A patent/TWI345467B/zh not_active IP Right Cessation
- 2007-12-17 AR ARP070105650A patent/AR064376A1/es unknown
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2009
- 2009-05-19 NO NO20091936A patent/NO20091936L/no not_active Application Discontinuation
- 2009-05-21 IL IL198878A patent/IL198878A0/en unknown
- 2009-06-02 ZA ZA200903841A patent/ZA200903841B/xx unknown
-
2010
- 2010-04-23 US US12/765,898 patent/US20100204233A1/en not_active Abandoned
-
2011
- 2011-09-19 US US13/235,542 patent/US8399463B2/en not_active Expired - Fee Related
Also Published As
Publication number | Publication date |
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US20120004230A1 (en) | 2012-01-05 |
IL198878A0 (en) | 2010-02-17 |
CA2671838A1 (en) | 2008-06-26 |
MX2009006215A (es) | 2009-06-22 |
KR101188992B1 (ko) | 2012-10-08 |
CN101578271A (zh) | 2009-11-11 |
WO2008074679A3 (en) | 2008-10-09 |
TWI345467B (en) | 2011-07-21 |
WO2008074679A2 (en) | 2008-06-26 |
US20080146523A1 (en) | 2008-06-19 |
JP2010513373A (ja) | 2010-04-30 |
EP2094668A2 (en) | 2009-09-02 |
RU2465269C2 (ru) | 2012-10-27 |
CL2007003653A1 (es) | 2008-07-11 |
JP5175297B2 (ja) | 2013-04-03 |
TW200833327A (en) | 2008-08-16 |
US8399463B2 (en) | 2013-03-19 |
CN101578271B (zh) | 2013-06-19 |
AU2007336351A1 (en) | 2008-06-26 |
RU2009122665A (ru) | 2011-01-27 |
KR20090081431A (ko) | 2009-07-28 |
BRPI0721291A2 (pt) | 2014-03-25 |
NO20091936L (no) | 2009-07-14 |
ZA200903841B (en) | 2010-03-31 |
US20100204233A1 (en) | 2010-08-12 |
AR064376A1 (es) | 2009-04-01 |
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