JP2012523425A - 脂肪酸アミドヒドロラーゼの阻害薬 - Google Patents
脂肪酸アミドヒドロラーゼの阻害薬 Download PDFInfo
- Publication number
- JP2012523425A JP2012523425A JP2012504832A JP2012504832A JP2012523425A JP 2012523425 A JP2012523425 A JP 2012523425A JP 2012504832 A JP2012504832 A JP 2012504832A JP 2012504832 A JP2012504832 A JP 2012504832A JP 2012523425 A JP2012523425 A JP 2012523425A
- Authority
- JP
- Japan
- Prior art keywords
- compound
- alkyl
- pain
- aryl
- disorder
- Prior art date
- Legal status (The legal status 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 status listed.)
- Pending
Links
- 0 *B(*)C(C(*)(*)C(*)(*)C(*)(*)N1*)C1(*)I Chemical compound *B(*)C(C(*)(*)C(*)(*)C(*)(*)N1*)C1(*)I 0.000 description 1
- RKHLWLKAYLBVNI-QENXGIAESA-N C/C(/COC(N1CCC(B(O)O)CC1)O)=C\C=C/C#C Chemical compound C/C(/COC(N1CCC(B(O)O)CC1)O)=C\C=C/C#C RKHLWLKAYLBVNI-QENXGIAESA-N 0.000 description 1
- WHYUAGZAHLUISP-UHFFFAOYSA-N CC(C)(C)OC(N1CC=C(B(O)O)CC1)=O Chemical compound CC(C)(C)OC(N1CC=C(B(O)O)CC1)=O WHYUAGZAHLUISP-UHFFFAOYSA-N 0.000 description 1
- KMECCEOFWNIQFT-UHFFFAOYSA-N CC(C)(C)OC(N1CCC(B(O)O)CC1)=O Chemical compound CC(C)(C)OC(N1CCC(B(O)O)CC1)=O KMECCEOFWNIQFT-UHFFFAOYSA-N 0.000 description 1
- UZTQRIAEVDHZBR-UHFFFAOYSA-N CC(N1CC=C(B(O)O)CC1)=O Chemical compound CC(N1CC=C(B(O)O)CC1)=O UZTQRIAEVDHZBR-UHFFFAOYSA-N 0.000 description 1
- KSPHGFYHABNECV-UHFFFAOYSA-N Cc1c(C(N2CC=C(B(O)O)CC2)=O)[s]c2c1CCC=C2 Chemical compound Cc1c(C(N2CC=C(B(O)O)CC2)=O)[s]c2c1CCC=C2 KSPHGFYHABNECV-UHFFFAOYSA-N 0.000 description 1
- OYKCFNQUJRNAPE-UHFFFAOYSA-N Cc1c(CC(N2CC=C(B(O)O)CC2)O)[s]c(C=CC2)c1CC2=C Chemical compound Cc1c(CC(N2CC=C(B(O)O)CC2)O)[s]c(C=CC2)c1CC2=C OYKCFNQUJRNAPE-UHFFFAOYSA-N 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07F—ACYCLIC, CARBOCYCLIC OR HETEROCYCLIC COMPOUNDS CONTAINING ELEMENTS OTHER THAN CARBON, HYDROGEN, HALOGEN, OXYGEN, NITROGEN, SULFUR, SELENIUM OR TELLURIUM
- C07F5/00—Compounds containing elements of Groups 3 or 13 of the Periodic Table
- C07F5/02—Boron compounds
- C07F5/025—Boronic and borinic acid compounds
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P1/00—Drugs for disorders of the alimentary tract or the digestive system
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P19/00—Drugs for skeletal disorders
- A61P19/02—Drugs for skeletal disorders for joint disorders, e.g. arthritis, arthrosis
-
- 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
- A61P25/04—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
- A61P25/06—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
- A61P25/18—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
- A61P25/20—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
- A61P27/00—Drugs for disorders of the senses
- A61P27/02—Ophthalmic agents
- A61P27/06—Antiglaucoma agents or miotics
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P29/00—Non-central analgesic, antipyretic or antiinflammatory agents, e.g. antirheumatic agents; Non-steroidal antiinflammatory drugs [NSAID]
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P37/00—Drugs for immunological or allergic disorders
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P37/00—Drugs for immunological or allergic disorders
- A61P37/02—Immunomodulators
-
- 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
-
- 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)
- Veterinary Medicine (AREA)
- Chemical Kinetics & Catalysis (AREA)
- General Chemical & Material Sciences (AREA)
- Medicinal Chemistry (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Pharmacology & Pharmacy (AREA)
- Life Sciences & Earth Sciences (AREA)
- Animal Behavior & Ethology (AREA)
- General Health & Medical Sciences (AREA)
- Public Health (AREA)
- Engineering & Computer Science (AREA)
- Neurosurgery (AREA)
- Biomedical Technology (AREA)
- Neurology (AREA)
- Immunology (AREA)
- Pain & Pain Management (AREA)
- Ophthalmology & Optometry (AREA)
- Psychiatry (AREA)
- Rheumatology (AREA)
- Cardiology (AREA)
- Anesthesiology (AREA)
- Heart & Thoracic Surgery (AREA)
- Orthopedic Medicine & Surgery (AREA)
- Physical Education & Sports Medicine (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
Applications Claiming Priority (3)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US16746409P | 2009-04-07 | 2009-04-07 | |
| US61/167,464 | 2009-04-07 | ||
| PCT/US2010/030276 WO2010118159A1 (en) | 2009-04-07 | 2010-04-07 | Inhibitors of fatty acid amide hydrolase |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| JP2012523425A true JP2012523425A (ja) | 2012-10-04 |
| JP2012523425A5 JP2012523425A5 (enExample) | 2013-05-30 |
Family
ID=42936566
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP2012504832A Pending JP2012523425A (ja) | 2009-04-07 | 2010-04-07 | 脂肪酸アミドヒドロラーゼの阻害薬 |
Country Status (6)
| Country | Link |
|---|---|
| US (2) | US8541581B2 (enExample) |
| EP (1) | EP2417115A4 (enExample) |
| JP (1) | JP2012523425A (enExample) |
| AU (1) | AU2010234449A1 (enExample) |
| CA (1) | CA2757622A1 (enExample) |
| WO (1) | WO2010118159A1 (enExample) |
Families Citing this family (7)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JO3598B1 (ar) | 2006-10-10 | 2020-07-05 | Infinity Discovery Inc | الاحماض والاسترات البورونية كمثبطات اميد هيدروليز الحامض الدهني |
| WO2011085216A2 (en) | 2010-01-08 | 2011-07-14 | Ironwood Pharmaceuticals, Inc. | Use of faah inhibitors for treating parkinson's disease and restless legs syndrome |
| CA2788587C (en) | 2010-02-03 | 2020-03-10 | Infinity Pharmaceuticals, Inc. | Fatty acid amide hydrolase inhibitors |
| WO2011123719A2 (en) | 2010-03-31 | 2011-10-06 | Ironwood Pharmaceuticals, Inc. | Use of faah inhibitors for treating abdominal, visceral and pelvic pain |
| CN105566368B (zh) * | 2016-01-11 | 2017-09-15 | 沧州普瑞东方科技有限公司 | 一种合成n‑取代哌啶‑4‑硼酸酯的方法 |
| EP3762034B1 (en) | 2018-03-05 | 2025-08-27 | Wylder Nation Foundation | A fatty acid amide hydrolase (faahi) inhibitor for use in inhibiting the cellular accumulation of a sphingolipid in a subject that has lysosomal storage disease or disorder |
| CN111171063B (zh) * | 2020-01-08 | 2022-06-14 | 大连双硼医药化工有限公司 | 一种合成n-取代哌啶-4-硼酸的工艺方法 |
Family Cites Families (166)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US4270537A (en) | 1979-11-19 | 1981-06-02 | Romaine Richard A | Automatic hypodermic syringe |
| US4596556A (en) | 1985-03-25 | 1986-06-24 | Bioject, Inc. | Hypodermic injection apparatus |
| CA1268808A (en) | 1985-07-23 | 1990-05-08 | Alan G. Macdiarmid | High capacity polyaniline electrodes |
| CH671400A5 (enExample) | 1986-12-17 | 1989-08-31 | Nii Prikladnych | |
| CA1283827C (en) | 1986-12-18 | 1991-05-07 | Giorgio Cirelli | Appliance for injection of liquid formulations |
| GB8704027D0 (en) | 1987-02-20 | 1987-03-25 | Owen Mumford Ltd | Syringe needle combination |
| US4940460A (en) | 1987-06-19 | 1990-07-10 | Bioject, Inc. | Patient-fillable and non-invasive hypodermic injection device assembly |
| US4941880A (en) | 1987-06-19 | 1990-07-17 | Bioject, Inc. | Pre-filled ampule and non-invasive hypodermic injection device assembly |
| US4790824A (en) | 1987-06-19 | 1988-12-13 | Bioject, Inc. | Non-invasive hypodermic injection device |
| DE3807862A1 (de) | 1988-03-10 | 1989-09-21 | Merck Patent Gmbh | Smektische fluessigkristallphase |
| US5273680A (en) | 1988-03-10 | 1993-12-28 | Merck Patent Gesellschaft Mit Beschrankter Haftung | Fluorinated oligophenyls and their use in liquid crystal materials |
| US5339163A (en) | 1988-03-16 | 1994-08-16 | Canon Kabushiki Kaisha | Automatic exposure control device using plural image plane detection areas |
| FR2638359A1 (fr) | 1988-11-03 | 1990-05-04 | Tino Dalto | Guide de seringue avec reglage de la profondeur de penetration de l'aiguille dans la peau |
| GB8829296D0 (en) | 1988-12-15 | 1989-01-25 | Ici Plc | Anti-tumour compounds |
| US5064413A (en) | 1989-11-09 | 1991-11-12 | Bioject, Inc. | Needleless hypodermic injection device |
| US5312335A (en) | 1989-11-09 | 1994-05-17 | Bioject Inc. | Needleless hypodermic injection device |
| EP0440082B1 (de) | 1990-02-01 | 1998-04-15 | MERCK PATENT GmbH | Verfahren zur Umsetzung von fluorierten Aromaten mit Elektrophilen |
| DE4014488A1 (de) | 1990-05-07 | 1991-11-14 | Merck Patent Gmbh | Dioxaborinane und fluessigkristallines medium |
| US5190521A (en) | 1990-08-22 | 1993-03-02 | Tecnol Medical Products, Inc. | Apparatus and method for raising a skin wheal and anesthetizing skin |
| US5527288A (en) | 1990-12-13 | 1996-06-18 | Elan Medical Technologies Limited | Intradermal drug delivery device and method for intradermal delivery of drugs |
| EP0501268B1 (de) | 1991-02-25 | 1996-06-12 | F. Hoffmann-La Roche Ag | Flüssigkristalline Verbindungen mit endständigem 1-Alkinylrest |
| GB2258232B (en) | 1991-07-31 | 1995-03-15 | Merck Patent Gmbh | Alkoxymethylene fluoroterphenyls and liquid crystalline medium |
| GB9118204D0 (en) | 1991-08-23 | 1991-10-09 | Weston Terence E | Needle-less injector |
| SE9102652D0 (sv) | 1991-09-13 | 1991-09-13 | Kabi Pharmacia Ab | Injection needle arrangement |
| AU661533B2 (en) | 1992-01-20 | 1995-07-27 | Astrazeneca Ab | Quinazoline derivatives |
| US5328483A (en) | 1992-02-27 | 1994-07-12 | Jacoby Richard M | Intradermal injection device with medication and needle guard |
| CH683522A5 (de) | 1992-03-13 | 1994-03-31 | Hoffmann La Roche | Verfahren zur Herstellung von Diarylen. |
| FR2688790B1 (fr) | 1992-03-23 | 1994-05-13 | Rhone Poulenc Chimie | Compositions a base de polyorganosiloxanes a groupements fonctionnels reticulables et leur utilisation pour la realisation de revetements anti-adhesifs. |
| US5541061A (en) | 1992-04-29 | 1996-07-30 | Affymax Technologies N.V. | Methods for screening factorial chemical libraries |
| PL167141B1 (pl) | 1992-05-12 | 1995-07-31 | Wojskowa Akad Tech | Sposób otrzymywania związków ciekłokrystalicznych zawierających pierścień 1,3-dioksa- -2-boranu |
| DE4220065A1 (de) | 1992-06-19 | 1993-12-23 | Merck Patent Gmbh | Verfahren zur Herstellung von Pyrimidin-Derivaten |
| US5383851A (en) | 1992-07-24 | 1995-01-24 | Bioject Inc. | Needleless hypodermic injection device |
| GB9220189D0 (en) | 1992-09-24 | 1992-11-04 | Central Research Lab Ltd | Dioxane derivatives |
| US5569189A (en) | 1992-09-28 | 1996-10-29 | Equidyne Systems, Inc. | hypodermic jet injector |
| GB9220750D0 (en) | 1992-10-02 | 1992-11-18 | Merck Patent Gmbh | Liquid crystalline material forming ananisotropic |
| DE4236103A1 (de) | 1992-10-26 | 1994-04-28 | Hoechst Ag | Verfahren zur Kreuzkupplung von aromatischen Boronsäuren mit aromatischen Halogenverbindungen oder Perfluoralkylsulfonaten |
| US5334144A (en) | 1992-10-30 | 1994-08-02 | Becton, Dickinson And Company | Single use disposable needleless injector |
| US5576220A (en) | 1993-02-19 | 1996-11-19 | Arris Pharmaceutical Corporation | Thin film HPMP matrix systems and methods for constructing and displaying ligands |
| US5417885A (en) | 1993-08-03 | 1995-05-23 | Showa Shell Sekiyu Kabushiki Kaisha | Antiferroelectric liquid crystal compound |
| DE19502178A1 (de) | 1994-01-27 | 1995-08-03 | Hoechst Ag | Thiadiazolderivate, Verfahren zu ihrer Herstellung und ihre Verwendung als Vorprodukte zur Herstellung von Flüssigkristallen |
| WO1995024176A1 (en) | 1994-03-07 | 1995-09-14 | Bioject, Inc. | Ampule filling device |
| US5466220A (en) | 1994-03-08 | 1995-11-14 | Bioject, Inc. | Drug vial mixing and transfer device |
| US5643893A (en) | 1994-06-22 | 1997-07-01 | Macronex, Inc. | N-substituted-(Dihydroxyboryl)alkyl purine, indole and pyrimidine derivatives, useful as inhibitors of inflammatory cytokines |
| FR2724660B1 (fr) | 1994-09-16 | 1997-01-31 | Rhone Poulenc Chimie | Amorceurs de reticulation, par voie cationique, de polymeres a groupements organofonctionnels, compositions a base de polyorganosiloxanes reticulables et contenant ces amorceurs et application desdites compositions en antiadherence |
| FR2727416A1 (fr) | 1994-11-24 | 1996-05-31 | Rhone Poulenc Chimie | Nouveaux amorceurs cationiques thermoactivables, de polymerisation et/ou de reticulation et compositions monomeres et/ou polymeres fonctionnels les mettant en oeuvre |
| DE4445224B4 (de) | 1994-12-17 | 2014-03-27 | Merck Patent Gmbh | Benzolderivate |
| US5599302A (en) | 1995-01-09 | 1997-02-04 | Medi-Ject Corporation | Medical injection system and method, gas spring thereof and launching device using gas spring |
| US6271015B1 (en) | 1995-06-12 | 2001-08-07 | The Scripps Research Institute | Fatty-acid amide hydrolase |
| EP0755918B1 (de) | 1995-07-28 | 2000-09-06 | Rolic AG | Photovernetzbare flüssigkristalline 1,2-Phenylen-Derivate |
| US5893397A (en) | 1996-01-12 | 1999-04-13 | Bioject Inc. | Medication vial/syringe liquid-transfer apparatus |
| JP3555325B2 (ja) | 1996-04-12 | 2004-08-18 | チッソ株式会社 | ビアリール誘導体の製造方法 |
| US5892131A (en) | 1997-05-29 | 1999-04-06 | American Cyanamid Company | Process for the preparation of pesticidal fluoroolefin compounds |
| US5998673A (en) | 1996-06-03 | 1999-12-07 | American Cyanamid Company | 1, 4-diaryl-2-fluoro-2-butene insecticidal and acaricidal agents |
| US5849958A (en) | 1997-03-17 | 1998-12-15 | American Cyanamid Company | 1,4,diaryl-2-fluoro-2-butene insecticidal and acaricidal agents |
| CA2206192A1 (en) | 1996-06-13 | 1997-12-13 | F. Hoffmann-La Roche Ag | Modulation of lc132 (opioid-like) receptor function |
| US5856537A (en) | 1996-06-26 | 1999-01-05 | The Scripps Research Institute | Inhibitors of oleamide hydrolase |
| AU729320B2 (en) | 1996-07-31 | 2001-02-01 | Shionogi & Co., Ltd. | Novel para-terphenyl compounds |
| FR2752582B1 (fr) | 1996-08-21 | 2003-06-13 | Rhone Poulenc Chimie | Compositions a base de polyorganosiloxanes a groupements fonctionnels reticulables et leur utilisation pour la realisation de revetements anti-adherents |
| JP4526605B2 (ja) | 1996-08-28 | 2010-08-18 | チッソ株式会社 | ラテラルハロゲン置換基を有する4環化合物および液晶組成物 |
| US6177440B1 (en) | 1996-10-30 | 2001-01-23 | Eli Lilly And Company | Substituted tricyclics |
| FR2757870B1 (fr) | 1996-12-30 | 1999-03-26 | Rhodia Chimie Sa | Utilisation de compositions silicones reticulables par voie cationique sous uv et d'un photoamorceur du type borate d'onium, pour le revetements de joints plats, notamment de joints de culasse |
| FR2758329B1 (fr) | 1997-01-16 | 1999-02-12 | Synthelabo | Derives d'imidazole-4-butane boronique, leur preparation et leur utilisation en therapeutique |
| FR2758723B1 (fr) | 1997-01-28 | 1999-04-23 | Sanofi Sa | Utilisation des antagonistes des recepteurs aux cannabinoides centraux pour la preparation de medicaments |
| WO1998035924A1 (en) | 1997-02-13 | 1998-08-20 | Chisso Corporation | Liquid-crystalline compounds having bicyclo[1.1.1]pentane structure, liquid-crystal composition, and liquid-crystal display element |
| DE19710614A1 (de) | 1997-03-14 | 1998-09-17 | Hoechst Ag | (1,2,4)-Thiadiazolderivate, Verfahren zu ihrer Herstellung und ihre Verwendung |
| US5993412A (en) | 1997-05-19 | 1999-11-30 | Bioject, Inc. | Injection apparatus |
| AU8140898A (en) | 1997-06-13 | 1998-12-30 | Northwestern University | Inhibitors of beta-lactamases and uses therefor |
| DE19909761A1 (de) | 1998-04-17 | 1999-10-21 | Merck Patent Gmbh | Benzofuran- und Benzodifuran-Derivate |
| DZ2769A1 (fr) | 1998-04-17 | 2003-12-01 | Lilly Co Eli | Composés tricycliques substitués. |
| JP2000001463A (ja) | 1998-06-12 | 2000-01-07 | Dainippon Ink & Chem Inc | 4−シアノベンゼン誘導体の製造方法 |
| GB9814450D0 (en) | 1998-07-04 | 1998-09-02 | Sharp Kk | Novel compounds |
| DE19857765A1 (de) | 1998-12-15 | 2000-06-21 | Clariant Gmbh | Verfahren zur Herstellung von para-Oxadiazolyl-phenyl-boronsäuren |
| DE19858594A1 (de) | 1998-12-18 | 2000-06-21 | Merck Patent Gmbh | Verfahren zur Herstellung von Cyanbenzolboronsäuren |
| DE59904576D1 (de) | 1998-12-19 | 2003-04-17 | Basell Polyolefine Gmbh | Verfahren zur herstellung von mono- oder di-organo-boranen |
| JP4507294B2 (ja) | 1999-05-27 | 2010-07-21 | チッソ株式会社 | ビアリール誘導体の製造方法 |
| US6309406B1 (en) | 1999-11-24 | 2001-10-30 | Hamit-Darwin-Fresh, Inc. | Apparatus and method for inducing epileptic seizures in test animals for anticonvulsant drug screening |
| HUP0300641A2 (hu) | 1999-12-03 | 2003-06-28 | Ono Pharmaceutical Co., Ltd. | Triazaspiro[5.5]undekán-származékok és hatóanyagként ezeket tartalmazó gyógyszerkészítmények |
| US20030096854A1 (en) | 2002-06-12 | 2003-05-22 | Ho-Shen Lin | Substituted tricyclics |
| FR2805273B1 (fr) | 2000-02-18 | 2006-08-11 | Rhodia Chimie Sa | Traitement de surface de materiau plastique avec une composition a fonctions reactives polymerisable et/ou reticulable |
| DE10009714A1 (de) | 2000-03-01 | 2001-09-06 | Targor Gmbh | Verfahren zur Herstellung von Mono- oder Di-organo-boranen |
| US20020164769A1 (en) | 2000-10-05 | 2002-11-07 | Curtis Rory A.J. | 32144, a novel human fatty acid amide hydrolase family member and uses thereof |
| GB2362882A (en) | 2000-06-02 | 2001-12-05 | Sharp Kk | Liquid crystalline optionally laterally fluorinated terphenyl with chiral 3,4-di[(un)saturated-alkoxy]butoxy or 1,4-di[(un)saturated-alkoxy]but-2-oxy terminus |
| WO2002018355A1 (en) | 2000-08-23 | 2002-03-07 | Eli Lilly And Company | Oxazolyl-aryloxyacetic acid derivatives and their use as ppar agonists |
| US6927216B2 (en) | 2000-10-03 | 2005-08-09 | Bristol-Myers Squibb Pharma Company | Cyclic sulfonyl compounds as inhibitors of metalloproteases |
| JP4721027B2 (ja) | 2001-03-29 | 2011-07-13 | Dic株式会社 | フェニルピリミジン誘導体の製造方法 |
| US6617125B2 (en) | 2001-06-29 | 2003-09-09 | Perkinelmer Life Sciences, Inc. | Compositions for enhanced catalyzed reporter deposition |
| US6858592B2 (en) | 2001-06-29 | 2005-02-22 | Genzyme Corporation | Aryl boronic acids for treating obesity |
| ATE303389T1 (de) | 2001-07-09 | 2005-09-15 | Merck Patent Gmbh | Thienothiophen-derivate |
| US7217701B2 (en) | 2001-10-11 | 2007-05-15 | Katsuhiko Mikoshiba | Intracellular calcium concentration increase inhibitors |
| US20050090383A1 (en) | 2001-10-12 | 2005-04-28 | Thiele Sven K. | Metal complex compositions and their use as catalysts to produce polydienes |
| DE60219569T2 (de) | 2001-11-07 | 2007-12-27 | Merck Patent Gmbh | Flüssigkristalline Verbindung, flüssigkristallines Medium und Flüssigkristallanzeige |
| GB0126844D0 (en) | 2001-11-08 | 2002-01-02 | Qinetiq Ltd | Novel compounds |
| DE10211597A1 (de) | 2002-03-15 | 2003-10-02 | Merck Patent Gmbh | Verfahren zur Herstellung von Ringverbindungen |
| WO2003105860A1 (en) | 2002-06-14 | 2003-12-24 | Novo Nordisk A/S | Pharmaceutical use of boronic acids and esters thereof |
| BR0311788A (pt) | 2002-06-27 | 2005-03-15 | Fujisawa Pharmaceutical Co | Composto derivado aminoalcoólico, processo para sua preparação, composição farmacêutica, compreendendo o mesmo, seu uso e método de tratamento |
| EP1388538B1 (en) | 2002-07-09 | 2010-09-01 | Merck Patent GmbH | Polymerisation Initiator |
| US20040115475A1 (en) | 2002-08-14 | 2004-06-17 | Matsushita Electric Industrial Co., Ltd. | Aromatic methylidene compound, methylstyrul compound for producing the same, production electroluminescent element |
| WO2004044169A2 (en) | 2002-11-14 | 2004-05-27 | The Scripps Research Institute | Crystalline form of fatty acid amine hydrolase (faah) |
| US7638641B2 (en) | 2002-11-27 | 2009-12-29 | Merck Patent Gmbh | Tetrahydropyran derivatives |
| US6924269B2 (en) | 2002-12-04 | 2005-08-02 | Vdf Futureceuticals, Inc. | Enzyme inhibitors and methods therefor |
| US7390806B2 (en) | 2002-12-18 | 2008-06-24 | Anacor Pharmaceuticals, Inc. | Antibiotics containing borinic acid complexes and methods of use |
| JP4787150B2 (ja) | 2003-03-06 | 2011-10-05 | エーザイ・アール・アンド・ディー・マネジメント株式会社 | Jnk阻害剤 |
| WO2004080989A1 (ja) | 2003-03-10 | 2004-09-23 | Sumitomo Chemical Company Limited | フラン化合物の製造方法 |
| JP2006520397A (ja) | 2003-03-14 | 2006-09-07 | アストラゼネカ アクチボラグ | 新規融合トリアゾロン類及びその使用 |
| DE10325438A1 (de) | 2003-05-21 | 2004-12-09 | Bayer Cropscience Ag | Difluormethylbenzanilide |
| PT1656370E (pt) | 2003-06-03 | 2012-11-29 | Rib X Pharmaceuticals Inc | Compostos biaril-heterocíclicos e métodos de os produzir e de os utilizar |
| CA2528587A1 (en) | 2003-06-10 | 2005-01-20 | Fulcrum Pharmaceuticals, Inc. | .beta.-lactamase inhibitors and methods of use thereof |
| CN1829521B (zh) | 2003-06-16 | 2011-01-26 | 安纳考尔医药公司 | 耐水解的含硼治疗剂和使用方法 |
| DE10337497A1 (de) | 2003-08-14 | 2005-03-10 | Bayer Cropscience Ag | 4-Biphenylsubstituierte-Pyrazolidin-3,5-dion-Derivate |
| WO2005037227A2 (en) | 2003-10-16 | 2005-04-28 | Microbia, Inc. | Selective cox-2 inhibitors |
| KR20070050861A (ko) | 2003-11-10 | 2007-05-16 | 마이크로비아 인코포레이티드 | 4-비아릴일-1-페닐아제티딘-2-온 |
| US20070010559A1 (en) | 2003-11-25 | 2007-01-11 | Novo Nordisk A/S | Indole derivatives for use as chemical uncoupler |
| JP4491666B2 (ja) | 2003-12-02 | 2010-06-30 | 東ソー株式会社 | フルオレン骨格を有するアリールアミン誘導体の製造方法とその合成中間体 |
| GB2410745B (en) | 2004-02-06 | 2007-07-25 | Merck Patent Gmbh | Cholestanyl derivatives |
| AU2005212092B2 (en) | 2004-02-13 | 2011-01-20 | Msd K.K. | Fused-ring 4-oxopyrimidine derivative |
| GB0403744D0 (en) | 2004-02-20 | 2004-03-24 | Astrazeneca Ab | Chemical process |
| JP2007530516A (ja) * | 2004-03-26 | 2007-11-01 | スミスクライン・ビーチャム・コーポレイション | 抗ウイルス剤として有用な4−カルボキシピラゾール誘導体 |
| DE102004041532A1 (de) | 2004-08-27 | 2006-03-02 | Bayer Cropscience Ag | Biphenylthiazolcarboxamide |
| DE102004041530A1 (de) | 2004-08-27 | 2006-03-02 | Bayer Cropscience Ag | Biphenylthiazolcarboxamide |
| WO2006050054A2 (en) | 2004-11-01 | 2006-05-11 | Nuada, Llc | Compounds and methods of use thereof |
| EP1812451A4 (en) | 2004-11-01 | 2009-10-21 | Nuada Llc | COMPOUNDS AND METHODS OF USE THEREOF |
| WO2006050236A2 (en) | 2004-11-01 | 2006-05-11 | Nuada, Llc | Compounds and methods of use thereof |
| CA2586479A1 (en) | 2004-11-12 | 2006-05-18 | Trustees Of Tufts College | Lipase inhibitors |
| DE102005023834A1 (de) | 2004-11-20 | 2006-05-24 | Bayer Healthcare Ag | Substituierte[(Phenylethanoyl)amino]benzamide |
| WO2006060625A2 (en) | 2004-12-02 | 2006-06-08 | Displaytech, Inc. | Liquid crystal compositions comprising an organogermanium compound and methods for using the same |
| US7553496B2 (en) | 2004-12-21 | 2009-06-30 | University Of Kentucky Research Foundation | VEGF-A as an inhibitor of angiogenesis and methods of using same |
| AU2006204917A1 (en) | 2005-01-14 | 2006-07-20 | Smithkline Beecham Corporation | Indole derivatives for treating viral infections |
| US20090005321A1 (en) | 2005-02-09 | 2009-01-01 | Microbia, Inc. | Phenylazetidinone Derivatives |
| CA2597982C (en) | 2005-02-16 | 2014-07-08 | Anacor Pharmaceuticals, Inc. | Boron-containing small molecules |
| KR101274442B1 (ko) | 2005-02-22 | 2013-06-18 | 수미토모 케미칼 컴퍼니 리미티드 | 고 밴드갭 아릴렌 중합체 |
| US7589066B2 (en) | 2005-03-11 | 2009-09-15 | The University Of North Carolina At Chapel Hill | Potent and specific immunoproteasome inhibitors |
| GB2424881B (en) | 2005-04-07 | 2010-11-24 | Merck Patent Gmbh | Halophenyl derivatives of bisalkylfluorene |
| JP4792796B2 (ja) | 2005-04-08 | 2011-10-12 | 東ソー株式会社 | 2,3−ジハロビフェニレン誘導体、その前駆化合物及び製造方法 |
| EP1879860A2 (en) | 2005-05-10 | 2008-01-23 | Microbia Inc. | 1,4-diphenyl-3-hydroxyalkyl-2-azetidinone derivatives for treating hypercholestrolemia |
| JP2008540573A (ja) | 2005-05-13 | 2008-11-20 | マイクロビア インコーポレーテッド | 4−ビアリーリル−1−フェニラゼチジン−2−オン類 |
| EP1726581A1 (en) | 2005-05-25 | 2006-11-29 | Fraunhofer-Gesellschaft zur Förderung der angewandten Forschung e.V. | Synthesis of novel monomers containing the Trifluorovinylidene-group and the Cyanato-group and polymers thereof |
| JP2008546651A (ja) | 2005-06-14 | 2008-12-25 | メルク フロスト カナダ リミテツド | モノアミンオキシダーゼa及びbの可逆的阻害剤 |
| KR100659088B1 (ko) | 2005-07-15 | 2006-12-21 | 삼성에스디아이 주식회사 | 디플루오로피리딘계 화합물 및 이를 이용한 유기 발광 소자 |
| DE102005037925A1 (de) | 2005-08-11 | 2007-02-15 | Merck Patent Gmbh | Hydro-cyclopenta[a]naphthaline |
| US7589239B2 (en) | 2005-09-02 | 2009-09-15 | Auspex Pharmaceuticals | Therapeutic agents for the treatment of cancer, metabolic diseases and skin disorders |
| WO2007031512A2 (en) | 2005-09-13 | 2007-03-22 | Bayer Cropscience Ag | Pesticide bi-phenyl-amidine derivatives |
| RU2396269C2 (ru) | 2005-12-01 | 2010-08-10 | Ф.Хоффманн-Ля Рош Аг | Производные гетероарилзамещенного пиперидина в качестве ингибиторов печеночной карнитин пальмитоилтрансферазы (l-cpt1) |
| EP1960078B1 (en) | 2005-12-02 | 2014-03-12 | Sachem, Inc. | Anion-exchange displacement chromatography process |
| KR20080110984A (ko) | 2005-12-30 | 2008-12-22 | 아나코르 파마슈티칼스 인코포레이티드 | 보론함유 소분자 |
| EP1976495A2 (en) | 2006-01-06 | 2008-10-08 | Aarhus Universitet | Compounds acting on the serotonin transporter |
| GB0602046D0 (en) | 2006-02-01 | 2006-03-15 | Smithkline Beecham Corp | Compounds |
| RS54108B1 (sr) | 2006-02-16 | 2015-12-31 | Anacor Pharmaceuticals Inc. | Mali molekuli koji sadrže boron kao agensi protiv zapaljenja |
| DE102007009944B4 (de) | 2006-03-15 | 2016-04-28 | Merck Patent Gmbh | Flüssigkristallines Medium und seine Verwendung |
| AU2007240082A1 (en) | 2006-04-13 | 2007-10-25 | Aegera Therapeutics Inc. | Use of imidazo[2,1-b)]-1,3,4-thiadiazole-2-sulfonamide compounds to treat neuropathic pain |
| JP5145753B2 (ja) | 2006-04-20 | 2013-02-20 | Jnc株式会社 | フルオロイソプロピル基を側鎖として有する化合物およびこれを用いた液晶組成物 |
| WO2007146965A2 (en) | 2006-06-12 | 2007-12-21 | Anacor Pharmaceuticals, Inc. | Compounds for the treatment of periodontal disease |
| US7838542B2 (en) | 2006-06-29 | 2010-11-23 | Kinex Pharmaceuticals, Llc | Bicyclic compositions and methods for modulating a kinase cascade |
| RU2008151762A (ru) | 2006-07-27 | 2010-06-27 | Си Ви Терапьютикс, Инк. (Us) | Adlh-2 ингибиторы для лечения аддикции |
| US8236783B2 (en) | 2006-08-15 | 2012-08-07 | Duke University | ROS-sensitive iron chelators and methods of using the same |
| ATE515553T1 (de) | 2006-08-16 | 2011-07-15 | Merck Patent Gmbh | Cyclohexen-verbindungen für flüssigkristalline mischungen |
| EP1900792B1 (de) | 2006-09-13 | 2010-08-04 | Merck Patent GmbH | Fluorphenyl-Verbindungen für flüssigkristalline Mischungen |
| WO2008039829A2 (en) | 2006-09-26 | 2008-04-03 | Ironwood Pharmaceuticals, Inc. | Diphenylheterocycle cholesterol absorption inhibitors |
| JO3598B1 (ar) * | 2006-10-10 | 2020-07-05 | Infinity Discovery Inc | الاحماض والاسترات البورونية كمثبطات اميد هيدروليز الحامض الدهني |
| SI2076508T1 (sl) | 2006-10-18 | 2011-04-29 | Pfizer Prod Inc | Spojine biaril eter sečnine |
| KR101435236B1 (ko) | 2007-01-24 | 2014-08-28 | 제이엔씨 석유 화학 주식회사 | 액정성 화합물, 액정 조성물 및 액정 표시 소자 |
| JP5299265B2 (ja) | 2007-02-28 | 2013-09-25 | Jnc石油化学株式会社 | Cf2o結合基を有する5環液晶化合物、液晶組成物および液晶表示素子 |
| TW200900065A (en) | 2007-03-07 | 2009-01-01 | Janssen Pharmaceutica Nv | 3-cyano-4-(4-pyridinyloxy-phenyl)-pyridin-2-one derivatives |
| WO2009011904A1 (en) | 2007-07-19 | 2009-01-22 | Renovis, Inc. | Compounds useful as faah modulators and uses thereof |
| TW201000107A (en) | 2008-04-09 | 2010-01-01 | Infinity Pharmaceuticals Inc | Inhibitors of fatty acid amide hydrolase |
| EP2287141B1 (en) | 2008-05-08 | 2015-10-21 | Sumitomo Chemical Company, Limited | Method for producing unsaturated organic compound |
| DE102008023801A1 (de) | 2008-05-15 | 2009-11-19 | Bayer Schering Pharma Aktiengesellschaft | Substituierte Imidazo- und Triazolopyrimidine, Imidazo- und Pyrazolopyrazine und Imidazotriazine |
-
2010
- 2010-04-07 EP EP10762391A patent/EP2417115A4/en not_active Withdrawn
- 2010-04-07 AU AU2010234449A patent/AU2010234449A1/en not_active Abandoned
- 2010-04-07 CA CA2757622A patent/CA2757622A1/en not_active Abandoned
- 2010-04-07 JP JP2012504832A patent/JP2012523425A/ja active Pending
- 2010-04-07 WO PCT/US2010/030276 patent/WO2010118159A1/en not_active Ceased
- 2010-04-07 US US13/263,324 patent/US8541581B2/en not_active Expired - Fee Related
-
2013
- 2013-08-19 US US13/970,495 patent/US8802119B2/en not_active Expired - Fee Related
Also Published As
| Publication number | Publication date |
|---|---|
| US20130338107A1 (en) | 2013-12-19 |
| US8541581B2 (en) | 2013-09-24 |
| US8802119B2 (en) | 2014-08-12 |
| CA2757622A1 (en) | 2010-10-14 |
| US20120088738A1 (en) | 2012-04-12 |
| WO2010118159A1 (en) | 2010-10-14 |
| EP2417115A4 (en) | 2012-10-31 |
| AU2010234449A1 (en) | 2011-11-03 |
| EP2417115A1 (en) | 2012-02-15 |
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| JP5637982B2 (ja) | 脂肪酸アミド加水分解酵素の阻害剤 | |
| CA2666224C (en) | Boronic acids and esters as inhibitors of fatty acid amide hydrolase | |
| JP2012523425A (ja) | 脂肪酸アミドヒドロラーゼの阻害薬 | |
| JP2010505955A5 (enExample) | ||
| EP3774767B1 (en) | Aryl hydrocarbon receptor modulators and uses thereof | |
| CA3130349A1 (en) | Lipid prodrugs of jak inhibitors and uses thereof | |
| JP7455133B2 (ja) | インドールアミン-2,3-ジオキシゲナーゼ阻害活性を有するキノロン誘導体 | |
| JP2018531987A (ja) | Malt1阻害剤およびその使用 | |
| PT2017314E (pt) | Ácidos e ésteres borónicos como inibidores da hidrolase das amidas de ácidos gordos | |
| JP2012523424A (ja) | 脂肪酸アミドヒドロラーゼの阻害薬 |
Legal Events
| Date | Code | Title | Description |
|---|---|---|---|
| A521 | Request for written amendment filed |
Free format text: JAPANESE INTERMEDIATE CODE: A523 Effective date: 20130405 |
|
| A621 | Written request for application examination |
Free format text: JAPANESE INTERMEDIATE CODE: A621 Effective date: 20130405 |
|
| A977 | Report on retrieval |
Free format text: JAPANESE INTERMEDIATE CODE: A971007 Effective date: 20140220 |
|
| A131 | Notification of reasons for refusal |
Free format text: JAPANESE INTERMEDIATE CODE: A131 Effective date: 20140304 |
|
| A601 | Written request for extension of time |
Free format text: JAPANESE INTERMEDIATE CODE: A601 Effective date: 20140528 |
|
| A602 | Written permission of extension of time |
Free format text: JAPANESE INTERMEDIATE CODE: A602 Effective date: 20140604 |
|
| A521 | Request for written amendment filed |
Free format text: JAPANESE INTERMEDIATE CODE: A523 Effective date: 20140902 |
|
| A02 | Decision of refusal |
Free format text: JAPANESE INTERMEDIATE CODE: A02 Effective date: 20150310 |