CN101945872B - 作为mch拮抗剂的(1-吖嗪酮)-取代的吡啶并吲哚 - Google Patents
作为mch拮抗剂的(1-吖嗪酮)-取代的吡啶并吲哚 Download PDFInfo
- Publication number
- CN101945872B CN101945872B CN200980105529.7A CN200980105529A CN101945872B CN 101945872 B CN101945872 B CN 101945872B CN 200980105529 A CN200980105529 A CN 200980105529A CN 101945872 B CN101945872 B CN 101945872B
- Authority
- CN
- China
- Prior art keywords
- compound
- methyl
- pyrido
- pyridin
- mmol
- 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.)
- Active
Links
- 0 O=C(C=C(C=C1)OCc2ccccc2)N1c(cc1)cc2c1C(CNCC1)=C1*2C1N2CC1C2 Chemical compound O=C(C=C(C=C1)OCc2ccccc2)N1c(cc1)cc2c1C(CNCC1)=C1*2C1N2CC1C2 0.000 description 19
- KTTBYMQDYBLZAE-UHFFFAOYSA-N C=[I]CC1Cc2cc(N(C=CC(OCc3ccccc3)=C3)C3=N)ccc2C(CN(CC2)C(OCCN3CCCC3)=[ClH])=C2C1 Chemical compound C=[I]CC1Cc2cc(N(C=CC(OCc3ccccc3)=C3)C3=N)ccc2C(CN(CC2)C(OCCN3CCCC3)=[ClH])=C2C1 KTTBYMQDYBLZAE-UHFFFAOYSA-N 0.000 description 1
- RXZDDJVNEHOXIV-UHFFFAOYSA-O C=[I]c(ccc(N[NH3+])c1)c1Br Chemical compound C=[I]c(ccc(N[NH3+])c1)c1Br RXZDDJVNEHOXIV-UHFFFAOYSA-O 0.000 description 1
- LXUYMVNEOIAXNT-UHFFFAOYSA-N CN(C1C2)C(CCNC3)=C3C1=CC=C2N(C=CC([U]Cc1ccccc1)=C1)C1=N Chemical compound CN(C1C2)C(CCNC3)=C3C1=CC=C2N(C=CC([U]Cc1ccccc1)=C1)C1=N LXUYMVNEOIAXNT-UHFFFAOYSA-N 0.000 description 1
- BEMUVFSHSKQDMN-UHFFFAOYSA-N C[N](C)(CC1)CC(C2=CC3)=C1NC2=CC3N(C=CC([ClH]Cc(nc1)ccc1Cl)=C1)C1=[ClH] Chemical compound C[N](C)(CC1)CC(C2=CC3)=C1NC2=CC3N(C=CC([ClH]Cc(nc1)ccc1Cl)=C1)C1=[ClH] BEMUVFSHSKQDMN-UHFFFAOYSA-N 0.000 description 1
- OHYGNKPCSMSVSX-UHFFFAOYSA-N C[n]1c2cc(N(C=CC(OCc3ccccc3)=C3)C3=O)ccc2c2c1CCN(CC(F)(F)F)C2 Chemical compound C[n]1c2cc(N(C=CC(OCc3ccccc3)=C3)C3=O)ccc2c2c1CCN(CC(F)(F)F)C2 OHYGNKPCSMSVSX-UHFFFAOYSA-N 0.000 description 1
- PNVMZRVMHQNONA-UHFFFAOYSA-N C[n]1c2cc(N(C=CC(OCc3ccccc3)=C3)C3=O)ccc2c2c1CCN(CCC(F)(F)F)C2 Chemical compound C[n]1c2cc(N(C=CC(OCc3ccccc3)=C3)C3=O)ccc2c2c1CCN(CCC(F)(F)F)C2 PNVMZRVMHQNONA-UHFFFAOYSA-N 0.000 description 1
- DJOUSOBWJSYKKA-UHFFFAOYSA-N C[n]1c2cc(N(C=CC([ClH]Cc3ccccc3)=C3)C3=O)ccc2c2c1CCN(CC(F)(F)[I]=C)C2 Chemical compound C[n]1c2cc(N(C=CC([ClH]Cc3ccccc3)=C3)C3=O)ccc2c2c1CCN(CC(F)(F)[I]=C)C2 DJOUSOBWJSYKKA-UHFFFAOYSA-N 0.000 description 1
- WQPYGRMNZWYNMO-UHFFFAOYSA-N C[n]1c2cc(N(C=CC(c(c(F)c3)ccc3[ClH]C=C)=C3)C3=O)ccc2c(C2)c1CCN2C=C Chemical compound C[n]1c2cc(N(C=CC(c(c(F)c3)ccc3[ClH]C=C)=C3)C3=O)ccc2c(C2)c1CCN2C=C WQPYGRMNZWYNMO-UHFFFAOYSA-N 0.000 description 1
- PBNXNYDVSJZKTP-UHFFFAOYSA-N Cc(cc1)ccc1C(C=CN1C)=CC1=[IH]1C[IH]C1 Chemical compound Cc(cc1)ccc1C(C=CN1C)=CC1=[IH]1C[IH]C1 PBNXNYDVSJZKTP-UHFFFAOYSA-N 0.000 description 1
- AXRDCUPZFSYSAC-UHFFFAOYSA-O Clc(cc1)cc(Cl)c1-c1cc[nH+]cc1 Chemical compound Clc(cc1)cc(Cl)c1-c1cc[nH+]cc1 AXRDCUPZFSYSAC-UHFFFAOYSA-O 0.000 description 1
- QIJJXTLIWXUAPB-TYYBGVCCSA-N IC[n]1c2cc(CCC(C=CC(C/C=C/Cc(cc3)c[n]4c3ncc4)=C3)C3=[U])ccc2c2c1CCNC2 Chemical compound IC[n]1c2cc(CCC(C=CC(C/C=C/Cc(cc3)c[n]4c3ncc4)=C3)C3=[U])ccc2c2c1CCNC2 QIJJXTLIWXUAPB-TYYBGVCCSA-N 0.000 description 1
- VMZAIZOVHPVQAS-UHFFFAOYSA-N O=C(C=C(C=C1)[ClH]Cc2ccccc2)N1c(cc(c(c1c2CCNC1)c1)[n]2[IH]I)c1F Chemical compound O=C(C=C(C=C1)[ClH]Cc2ccccc2)N1c(cc(c(c1c2CCNC1)c1)[n]2[IH]I)c1F VMZAIZOVHPVQAS-UHFFFAOYSA-N 0.000 description 1
- RBCJXJZHVUKVKA-UHFFFAOYSA-N [ClH]=C1NC=CC(OCc(cc2)c[n]3c2ncc3)=C1 Chemical compound [ClH]=C1NC=CC(OCc(cc2)c[n]3c2ncc3)=C1 RBCJXJZHVUKVKA-UHFFFAOYSA-N 0.000 description 1
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
- A61P1/00—Drugs for disorders of the alimentary tract or the digestive system
- A61P1/16—Drugs for disorders of the alimentary tract or the digestive system for liver or gallbladder disorders, e.g. hepatoprotective agents, cholagogues, litholytics
-
- 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
- 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
- A61P35/00—Antineoplastic agents
-
- 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
- A61P9/10—Drugs for disorders of the cardiovascular system for treating ischaemic or atherosclerotic diseases, e.g. antianginal drugs, coronary vasodilators, drugs for myocardial infarction, retinopathy, cerebrovascula insufficiency, renal arteriosclerosis
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D519/00—Heterocyclic compounds containing more than one system of two or more relevant hetero rings condensed among themselves or condensed with a common carbocyclic ring system not provided for in groups C07D453/00 or C07D455/00
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D521/00—Heterocyclic compounds containing unspecified hetero rings
Landscapes
- Health & Medical Sciences (AREA)
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Animal Behavior & Ethology (AREA)
- Veterinary Medicine (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Public Health (AREA)
- General Health & Medical Sciences (AREA)
- Engineering & Computer Science (AREA)
- Chemical Kinetics & Catalysis (AREA)
- General Chemical & Material Sciences (AREA)
- Medicinal Chemistry (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Life Sciences & Earth Sciences (AREA)
- Pharmacology & Pharmacy (AREA)
- Diabetes (AREA)
- Hematology (AREA)
- Obesity (AREA)
- Neurosurgery (AREA)
- Neurology (AREA)
- Biomedical Technology (AREA)
- Vascular Medicine (AREA)
- Heart & Thoracic Surgery (AREA)
- Emergency Medicine (AREA)
- Urology & Nephrology (AREA)
- Psychiatry (AREA)
- Pain & Pain Management (AREA)
- Cardiology (AREA)
- Endocrinology (AREA)
- Child & Adolescent Psychology (AREA)
- Gastroenterology & Hepatology (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Nitrogen Condensed Heterocyclic Rings (AREA)
- Nitrogen And Oxygen Or Sulfur-Condensed Heterocyclic Ring Systems (AREA)
Applications Claiming Priority (5)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US2053008P | 2008-01-11 | 2008-01-11 | |
| US61/020,530 | 2008-01-11 | ||
| US4867708P | 2008-04-29 | 2008-04-29 | |
| US61/048,677 | 2008-04-29 | ||
| PCT/US2009/030646 WO2009089482A1 (en) | 2008-01-11 | 2009-01-09 | (1-azinone) -substituted pyridoindoles as mch antagonists |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| CN101945872A CN101945872A (zh) | 2011-01-12 |
| CN101945872B true CN101945872B (zh) | 2014-07-23 |
Family
ID=40429805
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| CN200980105529.7A Active CN101945872B (zh) | 2008-01-11 | 2009-01-09 | 作为mch拮抗剂的(1-吖嗪酮)-取代的吡啶并吲哚 |
Country Status (13)
| Country | Link |
|---|---|
| US (4) | US8716308B2 (enExample) |
| EP (2) | EP2476680B1 (enExample) |
| JP (2) | JP5501251B2 (enExample) |
| KR (1) | KR101614723B1 (enExample) |
| CN (1) | CN101945872B (enExample) |
| AU (1) | AU2009204048B2 (enExample) |
| BR (1) | BRPI0907122B8 (enExample) |
| CA (1) | CA2727055C (enExample) |
| ES (1) | ES2523580T3 (enExample) |
| IL (1) | IL206594A (enExample) |
| MX (1) | MX2010007430A (enExample) |
| NZ (1) | NZ586120A (enExample) |
| WO (1) | WO2009089482A1 (enExample) |
Families Citing this family (17)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| KR101614723B1 (ko) * | 2008-01-11 | 2016-04-22 | 알바니 몰레큘라 리써치, 인크. | Mch 길항물질로서 (1-아지논)-치환된 피리도인돌 |
| US9187455B2 (en) * | 2009-02-23 | 2015-11-17 | Hoffmann-La Roche Inc. | Substituted pyridazines as PDE10A inhibitors |
| US8618299B2 (en) | 2009-07-01 | 2013-12-31 | Albany Molecular Research, Inc. | Azinone-substituted azapolycycle MCH-1 antagonists, methods of making, and use thereof |
| US8629158B2 (en) | 2009-07-01 | 2014-01-14 | Albany Molecular Research, Inc. | Azabicycloalkane-indole and azabicycloalkane-pyrrolo-pyridine MCH-1 antagonists, methods of making, and use thereof |
| WO2011003021A1 (en) | 2009-07-01 | 2011-01-06 | Albany Molecular Research, Inc. | Azinone-substituted azabicycloalkane-indole and azabicycloalkane-pyrrolo-pyridine mch-1 antagonists, methods of making, and use thereof |
| JP2012532144A (ja) | 2009-07-01 | 2012-12-13 | アルバニー モレキュラー リサーチ, インコーポレイテッド | アジノン置換アゼピノ[b]インドールおよびピリド−ピロロ−アゼピンmch−1拮抗薬、ならびにその作製方法および使用 |
| US8993765B2 (en) | 2010-12-21 | 2015-03-31 | Albany Molecular Research, Inc. | Tetrahydro-azacarboline MCH-1 antagonists, methods of making, and uses thereof |
| US8697700B2 (en) | 2010-12-21 | 2014-04-15 | Albany Molecular Research, Inc. | Piperazinone-substituted tetrahydro-carboline MCH-1 antagonists, methods of making, and uses thereof |
| EP2802571A1 (en) * | 2012-01-12 | 2014-11-19 | Takeda Pharmaceutical Company Limited | Benzimidazole derivatives as mch receptor antagonists |
| HU230880B1 (hu) * | 2015-04-15 | 2018-11-29 | Richter Gedeon Nyrt | Indol származékok |
| CN112739689B (zh) | 2018-12-07 | 2022-06-03 | 优迈特株式会社 | 含氟嘧啶化合物及其制造方法 |
| EP3937932B1 (en) * | 2019-03-13 | 2025-01-08 | The Rockefeller University | Inhibitors of cgas for treating autoinflammatory diseases and cancer metastasis |
| EP4151210A3 (en) * | 2020-01-10 | 2023-06-14 | Harmony Biosciences, LLC | Pyridine-carboline derivatives as mchr1 antagonists for use in therapy |
| JP7471407B2 (ja) | 2020-05-19 | 2024-04-19 | ユニマテック株式会社 | 含フッ素ピリミジン化合物および含フッ素ピリミジノン化合物 |
| US12378229B2 (en) * | 2021-02-02 | 2025-08-05 | Liminal Biosciences Limited | GPR84 antagonists and uses thereof |
| WO2023085142A1 (ja) | 2021-11-12 | 2023-05-19 | ユニマテック株式会社 | 含フッ素ピリミジン化合物、有害菌類防除剤および含フッ素ピリミジン化合物の製造方法 |
| HUP2200222A1 (hu) | 2022-06-17 | 2023-12-28 | Richter Gedeon Nyrt | MCHR1 antagonisták a Prader-Willi szindróma kezelésére |
Family Cites Families (206)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US3514462A (en) | 1966-10-21 | 1970-05-26 | Upjohn Co | 1 and 2 ethoxy 3,4,5,10 - tetrahydroazepino(3,4-b) and (2,3-b)indoles and corresponding amino derivatives thereof |
| CH649553A5 (de) | 1982-05-06 | 1985-05-31 | Sandoz Ag | Azepinoindole und verfahren zu deren herstellung. |
| DE3784594T2 (de) | 1986-08-11 | 1994-01-05 | Innovata Biomed Ltd | Mikrokapseln enthaltende pharmazeutische Zusammensetzungen. |
| US5179079A (en) | 1986-12-16 | 1993-01-12 | Novo Nordisk A/S | Nasal formulation and intranasal administration therewith |
| GB8723846D0 (en) | 1987-10-10 | 1987-11-11 | Danbiosyst Ltd | Bioadhesive microsphere drug delivery system |
| IT1223343B (it) | 1987-11-03 | 1990-09-19 | Also Lab Sas | Formulazioni farmaceutiche per somministrazione transdermica |
| JPH0256485A (ja) | 1988-04-27 | 1990-02-26 | Glaxo Group Ltd | ラクタム誘導体 |
| HU207078B (en) | 1988-08-02 | 1993-03-01 | Glaxo Group Ltd | Process for producing lactam derivatives and pharmaceutical compositions comprising such compounds |
| US5223625A (en) | 1988-12-22 | 1993-06-29 | Duphar International Research B.V. | Annelated indolo [3,2,-C]lactams |
| US4994439A (en) | 1989-01-19 | 1991-02-19 | California Biotechnology Inc. | Transmembrane formulations for drug administration |
| FI913899A7 (fi) | 1989-02-23 | 1991-08-19 | Rorer Int Holdings Inc | Terapeuttiset aerosoliseokset |
| GB8904551D0 (en) | 1989-02-28 | 1989-04-12 | Glaxo Group Ltd | Chemical compounds |
| US4978669A (en) | 1989-06-08 | 1990-12-18 | Neurex Corporation | Method of suppressing appetite by administration of tetrahydro-beta-carboline derivatives |
| US5169852A (en) | 1989-06-08 | 1992-12-08 | Neurex Corporation | Method of suppressing appetite by administration of tetrahydro-beta-carboline derivatives |
| GB8921222D0 (en) | 1989-09-20 | 1989-11-08 | Riker Laboratories Inc | Medicinal aerosol formulations |
| CA2036337C (fr) | 1990-02-15 | 2003-04-15 | Francois Clemence | Derives de la 20,21-dinoreburnamenine, leur procede de preparation et les nouveaux intermediaires ainsi obtenus, leur application comme medicaments et les compositions les renfermant |
| US5225407A (en) | 1990-02-22 | 1993-07-06 | Glaxo Group Limited | 5-HT3 receptor antagonists for the treatment of autism |
| US5162336A (en) | 1990-06-21 | 1992-11-10 | Rhone-Poulenc Rorer Pharmaceuticals Inc. | Tetrahydro-pyrido-indoles as cholecystokinin and gastrin antagonists |
| US5187180A (en) | 1990-07-26 | 1993-02-16 | Merck Frosst Canada, Inc. | (quinolin-2-ylmethoxy)heterotetrahydrocarbazoles as inhibitors of the biosynthesis of leukotrienes |
| US5230884A (en) | 1990-09-11 | 1993-07-27 | University Of Wales College Of Cardiff | Aerosol formulations including proteins and peptides solubilized in reverse micelles and process for making the aerosol formulations |
| US5292499A (en) | 1990-09-11 | 1994-03-08 | University Of Wales College Of Cardiff | Method of preparing medical aerosol formulations including drug dissolved in reverse micelles |
| JP2951434B2 (ja) | 1991-04-18 | 1999-09-20 | 三菱製紙株式会社 | 電子写真感光体 |
| DE4130933A1 (de) | 1991-09-13 | 1993-03-18 | Schering Ag | Neue (beta)-carbolinderivate, deren herstellung und verwendung in arzneimitteln |
| DE4240672A1 (de) | 1992-11-24 | 1994-05-26 | Schering Ag | Neues Verfahren zur Herstellung von beta-Carbolinen |
| US5767131A (en) | 1993-04-05 | 1998-06-16 | Synaptic Pharmaceutical Corporation | Dihydropyridines and new uses thereof |
| IL109220A0 (en) | 1993-04-05 | 1994-07-31 | Synaptic Pharma Corp | Dihydropyridines and new uses thereof |
| US6632456B1 (en) | 1993-06-24 | 2003-10-14 | Astrazeneca Ab | Compositions for inhalation |
| GB9418326D0 (en) | 1994-09-12 | 1994-11-02 | Lilly Industries Ltd | Pharmaceutical compounds |
| JP3155008B2 (ja) | 1994-07-26 | 2001-04-09 | ファイザー・インコーポレーテッド | セロトニンアゴニストおよびアンタゴニストとしての4−インドール誘導体 |
| DE4436190A1 (de) | 1994-10-10 | 1996-04-11 | Gerhard Prof Dr Bringmann | Halogenierte ß-Carbolin-Derivate, Verfahren zu ihrer Herstellung und Verwendung dieser Substanzen zur Hemmung der Atmungskette |
| US5707641A (en) | 1994-10-13 | 1998-01-13 | Pharmaderm Research & Development Ltd. | Formulations comprising therapeutically-active proteins or polypeptides |
| AU3831495A (en) | 1994-10-20 | 1996-05-15 | American Home Products Corporation | Indole derivatives useful as serotonergic agents |
| US5466688A (en) | 1994-10-20 | 1995-11-14 | American Home Products Corporation | Pyrido[3,4-B]indole derivatives as serotonergic agents |
| US6524557B1 (en) | 1994-12-22 | 2003-02-25 | Astrazeneca Ab | Aerosol formulations of peptides and proteins |
| CH689139A5 (de) | 1995-04-03 | 1998-10-30 | Cerbios Pharma Sa | Verfahren zur Herstellung einer liposomalen, in Wasser dispergierbaren, oral zu verabreichenden, festen, trockenen therapeutischen Formulierung. |
| US6309671B1 (en) | 1995-04-14 | 2001-10-30 | Inhale Therapeutic Systems | Stable glassy state powder formulations |
| GB9508195D0 (en) | 1995-04-20 | 1995-06-07 | Univ British Columbia | Novel biologically active compounds and compositions,their use and derivation |
| US5635161A (en) | 1995-06-07 | 1997-06-03 | Abbott Laboratories | Aerosol drug formulations containing vegetable oils |
| US6120794A (en) | 1995-09-26 | 2000-09-19 | University Of Pittsburgh | Emulsion and micellar formulations for the delivery of biologically active substances to cells |
| AU6966696A (en) | 1995-10-05 | 1997-04-28 | Warner-Lambert Company | Method for treating and preventing inflammation and atherosclerosis |
| US6001866A (en) | 1995-10-05 | 1999-12-14 | Warner-Lambert Company | Method for treating and preventing inflammation and atherosclerosis |
| US5972980A (en) | 1995-10-05 | 1999-10-26 | Warner-Lambert Company | Method for treating and preventing inflammation and atherosclerosis |
| HUP9801834A3 (en) | 1995-10-12 | 2000-06-28 | Supergen Inc Emeryville | Liposome formulations of 5beta steroids |
| ZA9610738B (en) | 1995-12-22 | 1997-06-24 | Warner Lambert Co | Subtype selective nmda receptor ligands and the use thereof |
| AU712082B2 (en) | 1996-02-28 | 1999-10-28 | Merck & Co., Inc. | Fibrinogen receptor antagonists |
| EP0912175A4 (en) | 1996-06-28 | 1999-09-08 | Merck & Co Inc | FIBRINOGENIC RECEPTOR ANTAGONISTS |
| US5932582A (en) | 1996-06-28 | 1999-08-03 | Merck & Co., Inc. | Fibrinogen receptor antagonist prodrugs |
| JP2000513375A (ja) | 1996-06-28 | 2000-10-10 | メルク エンド カンパニー インコーポレーテッド | フィブリノーゲンレセプター拮抗薬プロドラッグ |
| US5854245A (en) | 1996-06-28 | 1998-12-29 | Merck & Co., Inc. | Fibrinogen receptor antagonists |
| US5811551A (en) | 1996-08-13 | 1998-09-22 | Merck & Co., Inc. | Palladium catalyzed indolization |
| US6177440B1 (en) | 1996-10-30 | 2001-01-23 | Eli Lilly And Company | Substituted tricyclics |
| US6713645B1 (en) | 1996-10-30 | 2004-03-30 | Eli Lilly And Company | Substituted tricyclics |
| CN1115342C (zh) | 1998-03-17 | 2003-07-23 | 玛西夫公司 | 催眠性b一咔啉衍生物,它们的制备方法和作为医药产品的用途 |
| ID23219A (id) | 1998-04-17 | 2000-03-30 | Lilly Co Eli | Trisiklik tersubstitusi |
| JP2002535242A (ja) | 1998-05-20 | 2002-10-22 | ザ リポソーム カンパニー、インコーポレーテッド | 新規な粒子状剤型 |
| AU778735B2 (en) | 1998-06-16 | 2004-12-16 | Centre National De La Recherche Scientifique | Fused azepinone cyclin dependent kinase inhibitors |
| GB9814172D0 (en) | 1998-06-30 | 1998-08-26 | Andaris Ltd | Formulation for inhalation |
| US6451349B1 (en) | 1998-08-19 | 2002-09-17 | Quadrant Healthcare (Uk) Limited | Spray-drying process for the preparation of microparticles |
| AUPP494798A0 (en) | 1998-07-29 | 1998-08-20 | Pacific Biolink Pty Limited | Protective protein formulation |
| US6290987B1 (en) | 1998-09-27 | 2001-09-18 | Generex Pharmaceuticals, Inc. | Mixed liposome pharmaceutical formulation with amphiphiles and phospholipids |
| CN1226290C (zh) | 1998-12-14 | 2005-11-09 | 阿里根公司 | 新颖的核受体配体 |
| US6294153B1 (en) | 1998-12-21 | 2001-09-25 | Generex Pharmaceuticals, Inc. | Aerosol pharmaceutical formulation for pulmonary and nasal delivery |
| EP1338272A1 (en) | 1998-12-21 | 2003-08-27 | Generex Pharmaceuticals Inc. | Aerosol formulations for buccal and pulmonary application comprising chenodeoxycholate or deoxycholate |
| US6436367B1 (en) | 1998-12-21 | 2002-08-20 | Generex Pharmaceuticals Inc. | Aerosol formulations for buccal and pulmonary application |
| KR100845769B1 (ko) | 1999-02-03 | 2008-07-11 | 파우더젝트 리서치 리미티드 | 하이드로겔 입자 제제 |
| AU2879100A (en) | 1999-02-12 | 2000-08-29 | Miles A. Libbey Iii | Formulation and system for intra-oral delivery of pharmaceutical agents |
| JP2002538195A (ja) | 1999-03-08 | 2002-11-12 | パウダージェクト リサーチ リミテッド | 生物活性化合物の持続放出用の無針注射器を使用する微粒子製剤の送達 |
| WO2000062759A1 (en) | 1999-04-16 | 2000-10-26 | Novo Nordisk A/S | Dry, mouldable drug formulation |
| US6407092B1 (en) | 1999-04-23 | 2002-06-18 | Pharmacia & Upjohn Company | Tetracyclic azepinoindole compounds |
| AR023574A1 (es) | 1999-04-23 | 2002-09-04 | Pharmacia & Upjohn Co Llc | Compuestos de azepinindol tetraciclico,composiciones farmaceuticas y el uso de dichos compuestos para preparar un medicamento, e intermediarios |
| US6485706B1 (en) | 1999-06-04 | 2002-11-26 | Delrx Pharmaceutical Corp. | Formulations comprising dehydrated particles of pharma-ceutical agents and process for preparing the same |
| US6713471B1 (en) | 1999-06-15 | 2004-03-30 | Bristol-Myers Squibb Pharma Company | Substituted heterocycle fused gamma-carbolines |
| HK1043112A1 (zh) | 1999-06-15 | 2002-09-06 | Bristol-Myers Squibb Pharma Company | 取代的稠杂环γ-咔啉 |
| MY122278A (en) | 1999-07-19 | 2006-04-29 | Upjohn Co | 1,2,3,4,5,6-hexahydroazepino[4,5-b]indoles containing arylsulfones at the 9-position |
| US20010036481A1 (en) | 1999-08-25 | 2001-11-01 | Advanced Inhalation Research, Inc. | Modulation of release from dry powder formulations |
| WO2001013891A2 (en) | 1999-08-25 | 2001-03-01 | Advanced Inhalation Research, Inc. | Modulation of release from dry powder formulations |
| ATE267582T1 (de) | 2000-01-20 | 2004-06-15 | Basilea Pharmaceutica Ag | Nasal verabreichbare cyclische antimykotische peptidzusammensetzungen |
| EP1254115A2 (en) | 2000-02-11 | 2002-11-06 | Bristol-Myers Squibb Company | Cannabinoid receptor modulators, their processes of preparation, and use of cannabinoid receptor modulators for treating respiratory and non-respiratory diseases |
| EP1129705A1 (en) | 2000-02-17 | 2001-09-05 | Rijksuniversiteit te Groningen | Powder formulation for inhalation |
| US6890933B1 (en) | 2000-02-24 | 2005-05-10 | President And Fellows Of Harvard College | Kinesin inhibitors |
| CO5300399A1 (es) | 2000-02-25 | 2003-07-31 | Astrazeneca Ab | Heterocicliocs que contienen nitrogeno, proceso para su preparacion y composiciones farmaceuticas que los contienen |
| CO5261594A1 (es) | 2000-03-02 | 2003-03-31 | Smithkline Beecham Corp | Inhibidores de myt1 cinasa |
| CA2402549A1 (en) | 2000-03-15 | 2001-09-20 | Aventis Pharma Deutschland Gmbh | Substituted beta-carbolines |
| EP1268477B1 (en) | 2000-03-15 | 2010-04-21 | Sanofi-Aventis Deutschland GmbH | Substituted beta-carbolines with ikb-kinase inhibiting activity |
| PE20011227A1 (es) | 2000-04-17 | 2002-01-07 | Chiesi Farma Spa | Formulaciones farmaceuticas para inhaladores de polvo seco en la forma de aglomerados duros |
| GB0009468D0 (en) | 2000-04-17 | 2000-06-07 | Vectura Ltd | Improvements in or relating to formulations for use in inhaler devices |
| CA2406206C (en) | 2000-04-17 | 2012-03-20 | Vectura Limited | Improvements in or relating to formulations for use in inhaler devices |
| EP1286994A1 (en) | 2000-05-15 | 2003-03-05 | Darwin Discovery Limited | Hydroxamic and carboxylic acid derivatives having mmp and tnf inhibitory activity |
| UA74826C2 (en) | 2000-05-17 | 2006-02-15 | Ortho Mcneil Pharm Inc | ?-carboline derivatives as phosphodiesterase inhibitors |
| US6927223B1 (en) | 2000-05-26 | 2005-08-09 | Washington State University Research Foundation | Use of serotonin agents for adjunct therapy in the treatment of cancer |
| US20020155084A1 (en) | 2000-06-02 | 2002-10-24 | The Regents Of The University Of The Michigan | Nanoemulsion formulations |
| AU2001268064A1 (en) | 2000-06-07 | 2001-12-17 | Lilly Icos Llc | Derivatives of 2,3,6,7,12,12a-hexahydropyrazino(1',2':1,6)pyrido(3,4-b)indole-1,4-dione |
| CA2412215A1 (en) | 2000-06-16 | 2001-12-27 | Curis, Inc. | Angiogenesis-modulating compositions and uses |
| WO2002004456A1 (en) | 2000-07-06 | 2002-01-17 | Pharmacia & Upjohn Company | SUBSTITUTED 2,3,7,8,9,10,11,12-OCTAHYDROAZEPINO[4,5-b]PYRANO[3,2-e]INDOLES |
| AR035493A1 (es) | 2000-09-20 | 2004-06-02 | Upjohn Co | Derivados de azepino (4,5b) indolina sustituidos, composicion farmaceutica y el uso de dichos derivados para preparar un medicamento |
| ATE302776T1 (de) | 2000-10-02 | 2005-09-15 | Lilly Icos Llc | Kondensierte pyridoindolderivate |
| ATE332903T1 (de) | 2000-10-03 | 2006-08-15 | Lilly Icos Llc | Kondensierte pyridoindolderivate |
| FI20002768L (fi) | 2000-12-18 | 2002-06-19 | Licentia Oy | Enteropäällysteisiä lääkekoostumuksia ja niiden valmistus |
| EP1345898A2 (en) | 2000-12-18 | 2003-09-24 | Eli Lilly And Company | Teracyclic carbazole derivates and their use as spla2 inhibitors |
| HUP0303432A3 (en) | 2000-12-20 | 2012-09-28 | Bristol Myers Squibb Co | Substituted pyridoindoles as serotonin agonists and antagonists and pharmaceutical compositions containing the compounds and their use |
| US6849619B2 (en) | 2000-12-20 | 2005-02-01 | Bristol-Myers Squibb Company | Substituted pyridoindoles as serotonin agonists and antagonists |
| WO2002059082A2 (en) | 2000-12-20 | 2002-08-01 | Bristol-Myers Squibb Pharma Company | Aryl and aminoaryl substituted serotonin receptor agonist and antagonist ligands |
| ES2272695T3 (es) | 2001-02-12 | 2007-05-01 | Lilly Icos Llc | Derivados de carbolina. |
| WO2002064590A2 (en) | 2001-02-12 | 2002-08-22 | Lilly Icos Llc | Carboline derivatives |
| GB0107106D0 (en) | 2001-03-21 | 2001-05-09 | Boehringer Ingelheim Pharma | Powder inhaler formulations |
| CA2441792C (en) | 2001-04-25 | 2010-08-03 | Lilly Icos Llc | Carboline derivatives as inhibitors of phosphodiesterase 5 (pdes) for the treatment of cardiovascular diseases and erectile dysfunction |
| AU2002256418A1 (en) | 2001-04-27 | 2002-11-11 | Vertex Pharmaceuticals Incorporated | Inhibitors of bace |
| MXPA03011081A (es) | 2001-06-05 | 2004-07-08 | Lilly Icos Llc | Derivados de carbolina como inhibidores de pde5. |
| US6727264B1 (en) | 2001-07-05 | 2004-04-27 | Synaptic Pharmaceutical Corporation | Substituted anilinic piperidines as MCH selective antagonists |
| US20030019437A1 (en) | 2001-07-26 | 2003-01-30 | John Fore | Ungulate game animal feed system and method |
| GB0119243D0 (en) | 2001-08-07 | 2001-10-03 | Pharma Mar Sa | Antitumoral analogs of ET-743 |
| WO2003014118A1 (en) | 2001-08-08 | 2003-02-20 | Pharmacia & Upjohn Company | THERAPEUTIC 1H-PYRIDO[4,3-b]INDOLES |
| WO2003015750A1 (en) | 2001-08-16 | 2003-02-27 | Baxter International, Inc. | Propellant-based microparticle formulations |
| JP2005507876A (ja) | 2001-09-05 | 2005-03-24 | ミナーバ バイオテクノロジーズ コーポレイション | 癌を治療する組成物および方法 |
| WO2003072080A1 (en) | 2002-02-22 | 2003-09-04 | Advanced Inhalation Research, Inc. | Inhalable formulations for sustained release |
| AU2003230689B2 (en) | 2002-03-20 | 2006-06-29 | Alkermes, Inc. | Inhalable sustained therapeutic formulations |
| AU2003233118B8 (en) | 2002-05-07 | 2009-07-30 | Ferring Bv | Desmopressin in an orodispersible dosage form |
| US6906095B2 (en) | 2002-05-10 | 2005-06-14 | Wyeth | Indolylalkylidenehydrazine-carboximidamide derivatives as 5-hydroxytryptamine-6 ligands |
| US6951881B2 (en) | 2002-05-10 | 2005-10-04 | Wyeth | (1-substituted-indol-3-yl) alkylidenehydrazinecarboximidamide derivatives as 5-hydroxytryptamine-6 ligands |
| TWI329111B (en) | 2002-05-24 | 2010-08-21 | X Ceptor Therapeutics Inc | Azepinoindole and pyridoindole derivatives as pharmaceutical agents |
| US7595311B2 (en) | 2002-05-24 | 2009-09-29 | Exelixis, Inc. | Azepinoindole derivatives as pharmaceutical agents |
| AU2003277215A1 (en) | 2002-10-01 | 2004-04-23 | Predix Pharmaceuticals Holdings, Inc. | Novel neurokinin antagonists and methods of use thereof |
| US7250514B1 (en) | 2002-10-21 | 2007-07-31 | Takeda San Diego, Inc. | Histone deacetylase inhibitors |
| GB0305553D0 (en) | 2003-03-11 | 2003-04-16 | Glaxo Group Ltd | Compounds |
| EP1462103A1 (en) | 2003-03-25 | 2004-09-29 | Faust Pharmaceuticals | NO donors, combination products and uses as modulators of neurotransmitter release |
| WO2004103958A2 (en) | 2003-05-19 | 2004-12-02 | Michigan State University | Preparation of hymenialdisine derivatives and use thereof |
| EP1479677A1 (en) | 2003-05-19 | 2004-11-24 | Aventis Pharma Deutschland GmbH | New indole derivatives as factor xa inhibitors |
| CN1798556A (zh) | 2003-06-06 | 2006-07-05 | 麦克公司 | 作为治疗或者预防糖尿病的二肽基肽酶抑制剂的稠合吲哚 |
| US20060235012A1 (en) | 2003-06-16 | 2006-10-19 | Chroma Therapeutics Limited | Carboline and betacarboline derivatives for use as hdac enzyme inhibitors |
| WO2005012293A1 (ja) | 2003-08-01 | 2005-02-10 | Nippon Soda Co., Ltd. | フェニルアゾール化合物、製造法および抗酸化薬 |
| NL1026826C2 (nl) | 2003-08-13 | 2007-01-04 | Pharmacia Corp | Gesubstitueerde pyridinonen. |
| AU2006249350B2 (en) | 2003-11-19 | 2012-02-16 | Metabasis Therapeutics, Inc. | Thyromimetics for the treatment of fatty liver diseases |
| DE10360792A1 (de) | 2003-12-23 | 2005-07-28 | Grünenthal GmbH | Spirocyclische Cyclohexan-Derivate |
| JP2007518822A (ja) | 2004-01-23 | 2007-07-12 | カイロン コーポレイション | 抗癌剤としてのテトラヒドロカルボリン化合物 |
| CA2553670A1 (en) | 2004-01-29 | 2005-08-11 | Elixir Pharmaceuticals, Inc. | Anti-viral therapeutics |
| US7994196B2 (en) | 2004-02-12 | 2011-08-09 | Mitsubishi Tanabe Pharma Corporation | Indazole compound and pharmaceutical use thereof |
| US20070049593A1 (en) | 2004-02-24 | 2007-03-01 | Japan Tobacco Inc. | Tetracyclic fused heterocyclic compound and use thereof as HCV polymerase inhibitor |
| US20050187387A1 (en) * | 2004-02-25 | 2005-08-25 | Lynch John K. | Antagonists of melanin concentrating hormone effects on the melanin concentrating hormone receptor |
| US7705017B2 (en) | 2004-05-03 | 2010-04-27 | En Vivo Pharmaceuticals, Inc. | Compounds for treatment of neurodegenerative diseases |
| ATE485715T1 (de) | 2004-05-12 | 2010-11-15 | Bayer Cropscience Ag | Regulation des pflanzenwachstums |
| JP2008501628A (ja) | 2004-06-02 | 2008-01-24 | 武田薬品工業株式会社 | インドール誘導体およびがんの治療用途 |
| WO2006015035A1 (en) | 2004-08-02 | 2006-02-09 | Smithkline Beecham Corporation | Useful compounds for hpv infection |
| DE102004039382A1 (de) | 2004-08-13 | 2006-02-23 | Grünenthal GmbH | Spirocyclische Cyclohexan-Derivate |
| EP2371811B1 (en) | 2004-12-13 | 2014-10-08 | Ono Pharmaceutical Co., Ltd. | Azetidinecarboxylic acid derivative and medicinal use thereof |
| EP1831227B1 (en) | 2004-12-17 | 2013-06-19 | Glenmark Pharmaceuticals S.A. | Novel heterocyclic compounds useful for the treatment of inflammatory and allergic disorders |
| US20060167259A1 (en) | 2005-01-21 | 2006-07-27 | Cephalon, Inc. | Direct racemization of indole derivatives |
| WO2006081072A1 (en) | 2005-01-24 | 2006-08-03 | Abbott Laboratories | Antagonists of the mglu receptor and uses thereof |
| WO2006089874A1 (en) | 2005-02-22 | 2006-08-31 | Gpc Biotech Ag | Benzo[2,3]azepino[4,5-b]indol-6-ones |
| DE102005016460A1 (de) | 2005-04-11 | 2006-10-19 | Grünenthal GmbH | Spriocyclische Cyclohexanderivate zur Behandlung von Substanzabhängigkeit |
| WO2006117212A2 (en) | 2005-05-04 | 2006-11-09 | Develogen Aktiengesellschaft | Use of gsk-3 inhibitors for preventing and treating pancreatic autoimmune disorders |
| ATE542535T1 (de) | 2005-05-04 | 2012-02-15 | Develogen Ag | Verwendung von azapaullonen zur vorbeugung und behandlung pankreatischer autoimmunkrankheiten |
| GB0509225D0 (en) | 2005-05-05 | 2005-06-15 | Chroma Therapeutics Ltd | Inhibitors of enzymatic activity |
| WO2006122931A1 (en) | 2005-05-20 | 2006-11-23 | Biovitrum Ab (Publ) | Beta-carboline derivatives and theri use as ghsr modulators |
| WO2006138418A2 (en) | 2005-06-14 | 2006-12-28 | President And Fellows Of Harvard College | Improvement of cognitive performance with sirtuin activators |
| WO2007002051A1 (en) | 2005-06-22 | 2007-01-04 | Smithkline Beecham Corporation | Carboline derivatives and their use as inhibitors of flaviviridae infections |
| WO2009032123A2 (en) | 2007-08-29 | 2009-03-12 | Schering Corporation | Tetracyclic indole derivatives and their use for treating or preventing viral infections |
| PL1910338T3 (pl) | 2005-07-14 | 2011-02-28 | Irm Llc | Związki heterotetracykliczne jako mimetyki TPO |
| US20070027178A1 (en) | 2005-07-28 | 2007-02-01 | Bristol-Myers Squibb Company | Substituted tetrahydro-1H-pyrido[4,3-b]indoles as serotonin receptors agonists and antagonists |
| CA2619276A1 (en) | 2005-08-12 | 2007-02-22 | Genentech, Inc. | Pentacyclic kinase inhibitors |
| EP1757607A1 (en) | 2005-08-24 | 2007-02-28 | Molisa GmbH | N5-substituted benzo¬2,3|azepino¬4,5-b|indol-6-ones for treating tropical diseases |
| CA2619770A1 (en) | 2005-08-24 | 2007-03-01 | Banyu Pharmaceutical Co., Ltd. | Phenylpyridone derivative |
| US20090264426A1 (en) | 2005-09-07 | 2009-10-22 | Shunji Sakuraba | Bicyclic aromatic substituted pyridone derivative |
| AU2006292429A1 (en) | 2005-09-16 | 2007-03-29 | Serenex, Inc. | Carbazole derivatives |
| CA2623026A1 (en) | 2005-09-23 | 2007-04-05 | Schering Corporation | Fused tetracyclic mglur1 antagonists as therapeutic agents |
| US20070149557A1 (en) | 2005-11-21 | 2007-06-28 | Amgen Inc. | CXCR3 antagonists |
| AU2006325815B2 (en) | 2005-12-15 | 2012-07-05 | Exelixis, Inc. | Azepinoindole derivatives as pharmaceutical agents |
| AU2006342024A1 (en) | 2005-12-16 | 2007-10-25 | Genentech, Inc. | Tetracyclic kinase inhibitors |
| EP1966164B1 (en) | 2005-12-21 | 2013-03-06 | Janssen Pharmaceutica N.V. | Novel substituted pyrazinone derivatives for use in mch-1 mediated diseases |
| WO2007124288A1 (en) | 2006-04-19 | 2007-11-01 | Novartis Ag | Indazole compounds and methods for inhibition of cdc7 |
| DE102006019597A1 (de) | 2006-04-27 | 2007-10-31 | Grünenthal GmbH | Spirocyclische Cyclohexan-Derivate |
| US20080124319A1 (en) | 2006-05-16 | 2008-05-29 | Charalabos Pothoulakis | Methods for treating inflammation by disrupting MCH-mediated signaling |
| HRP20110917T1 (hr) | 2006-05-19 | 2012-03-31 | Abbott Laboratories | Derivati azabicikličkih alkana supstituirani fuzioniranim bicikloheterociklima aktivni u središnjem živčanom sustavu |
| PE20080150A1 (es) * | 2006-06-02 | 2008-04-11 | Janssen Pharmaceutica Nv | Derivados de piridinona n-aril y n-heteroaril sustituidos como antagonistas del receptor de la hormona concentradora de melanina (mch) |
| WO2007142217A1 (ja) * | 2006-06-07 | 2007-12-13 | Banyu Pharmaceutical Co., Ltd. | 1-フェニルピリドン誘導体 |
| CN101074207B (zh) | 2006-06-08 | 2014-03-26 | 中国科学院成都有机化学有限公司 | 一类水溶性的手性二胺衍生物及其应用和制备 |
| CN101108859A (zh) | 2006-07-17 | 2008-01-23 | 上海恒瑞医药有限公司 | 长春碱类化合物、其制备方法及其在医药上的用途 |
| RU2317989C1 (ru) | 2006-08-24 | 2008-02-27 | Андрей Александрович Иващенко | ЗАМЕЩЕННЫЕ АЗЕПИНО[4,3-b]ИНДОЛЫ, ФАРМАЦЕВТИЧЕСКАЯ КОМПОЗИЦИЯ, СПОСОБ ИХ ПОЛУЧЕНИЯ И ПРИМЕНЕНИЯ |
| CA2657183A1 (en) | 2006-08-25 | 2008-02-28 | Boehringer Ingelheim International Gmbh | New pyridone derivatives with mch antagonistic activity and medicaments comprising these compounds |
| DE102006046745A1 (de) | 2006-09-29 | 2008-04-03 | Grünenthal GmbH | Gemischte ORL1/µ-Agonisten zur Behandlung von Schmerz |
| WO2008046155A1 (en) | 2006-10-20 | 2008-04-24 | Dia-B Tech Limited | Methods for regulating glucose homeostasis and agents therefor |
| RU2329044C1 (ru) | 2006-11-16 | 2008-07-20 | Андрей Александрович Иващенко | Лиганды 5-ht6 рецепторов, фармацевтическая композиция, способ ее получения и лекарственное средство |
| ES2483866T3 (es) | 2006-12-05 | 2014-08-08 | Janssen Pharmaceutica Nv | Derivados de diaza-espiro-piridinona sustituidos novedosos para uso en enfermedades mediadas por MCH-1 |
| WO2008081282A2 (en) | 2006-12-20 | 2008-07-10 | Glenmark Pharmaceuticals S.A. | Process for the synthesis of n9-(3,5-dichloro-4-pyridyl)-6- difluoromethoxybenzo(4,5)furo(3,2-c)pyridine-9-carboxamide and salts thereof |
| JP2010515745A (ja) | 2007-01-10 | 2010-05-13 | アルバニー モレキュラー リサーチ, インコーポレイテッド | 5−フロピリジノン置換インダゾール |
| KR20090101370A (ko) | 2007-01-10 | 2009-09-25 | 알바니 몰레큘라 리써치, 인크. | 5-피리디논 치환된 인다졸 |
| WO2008103470A2 (en) | 2007-02-21 | 2008-08-28 | Trustees Of Columbia University In The City Of New York | Oncogenic-ras-signal dependent lethal compounds |
| DE102007009319A1 (de) | 2007-02-22 | 2008-08-28 | Grünenthal GmbH | Spirocyclische Cyclohexan-Derivate |
| DE102007009235A1 (de) | 2007-02-22 | 2008-09-18 | Grünenthal GmbH | Spirocyclische Cyclohexan-Derivate |
| US8063089B2 (en) | 2007-02-28 | 2011-11-22 | Arizona Board Of Regents On Behalf Of The University Of Arizona | Inhibitors of nucleophosmin (NPM) and methods for inducing apoptosis |
| KR101805914B1 (ko) | 2007-03-12 | 2017-12-06 | 인트라-셀룰라 써래피스, 인코퍼레이티드. | 치환된 헤테로환 융합 감마-카르볼린 합성 |
| US20090214529A9 (en) | 2007-05-22 | 2009-08-27 | Taigen Biotechnology Co., Ltd. | Kinesin inhibitors |
| EP2003129B1 (en) | 2007-06-11 | 2017-08-09 | Nerviano Medical Sciences S.r.l. | 1H-Pyrido[3,4-B]indol-1-one and 2,3,4,9-Tetrahydro-1H-Beta-Carbolin-1-one Derivatives |
| US20110002855A1 (en) | 2007-06-25 | 2011-01-06 | Neurogen Corporation | Piperazinyl oxoalkyl tetrahydro-beta-carbolines and related analogues |
| CA2689945A1 (en) | 2007-06-26 | 2008-12-31 | Astrazeneca Ab | 1-cyanocyclopropyl-derivatives as cathepsin k inhibitors |
| ES2382982T3 (es) | 2007-07-21 | 2012-06-15 | Albany Molecular Research, Inc. | Indazoles sustituidos con 5-piridinona y composiciones farmacéuticas de los mismos |
| WO2009022104A1 (en) | 2007-08-13 | 2009-02-19 | De Montfort University | Fascaplysin derivatives and their use in the treatment of cancer |
| CA2597193A1 (en) | 2007-08-13 | 2009-02-13 | De Montfort University | Compounds and uses |
| US11202775B2 (en) | 2007-09-25 | 2021-12-21 | Minerva Biotechnologies Corporation | Methods for treatment of cancer |
| KR101614723B1 (ko) * | 2008-01-11 | 2016-04-22 | 알바니 몰레큘라 리써치, 인크. | Mch 길항물질로서 (1-아지논)-치환된 피리도인돌 |
| US9625475B2 (en) | 2008-09-29 | 2017-04-18 | Abbvie Inc. | Indole and indoline derivatives and methods of use thereof |
| JP2012532144A (ja) | 2009-07-01 | 2012-12-13 | アルバニー モレキュラー リサーチ, インコーポレイテッド | アジノン置換アゼピノ[b]インドールおよびピリド−ピロロ−アゼピンmch−1拮抗薬、ならびにその作製方法および使用 |
| US8618299B2 (en) | 2009-07-01 | 2013-12-31 | Albany Molecular Research, Inc. | Azinone-substituted azapolycycle MCH-1 antagonists, methods of making, and use thereof |
| WO2011003021A1 (en) | 2009-07-01 | 2011-01-06 | Albany Molecular Research, Inc. | Azinone-substituted azabicycloalkane-indole and azabicycloalkane-pyrrolo-pyridine mch-1 antagonists, methods of making, and use thereof |
| US8629158B2 (en) | 2009-07-01 | 2014-01-14 | Albany Molecular Research, Inc. | Azabicycloalkane-indole and azabicycloalkane-pyrrolo-pyridine MCH-1 antagonists, methods of making, and use thereof |
| US8697700B2 (en) | 2010-12-21 | 2014-04-15 | Albany Molecular Research, Inc. | Piperazinone-substituted tetrahydro-carboline MCH-1 antagonists, methods of making, and uses thereof |
| US8993765B2 (en) | 2010-12-21 | 2015-03-31 | Albany Molecular Research, Inc. | Tetrahydro-azacarboline MCH-1 antagonists, methods of making, and uses thereof |
-
2009
- 2009-01-09 KR KR1020107017685A patent/KR101614723B1/ko active Active
- 2009-01-09 WO PCT/US2009/030646 patent/WO2009089482A1/en not_active Ceased
- 2009-01-09 EP EP12163813.4A patent/EP2476680B1/en active Active
- 2009-01-09 ES ES12163813.4T patent/ES2523580T3/es active Active
- 2009-01-09 US US12/351,561 patent/US8716308B2/en active Active
- 2009-01-09 BR BRPI0907122A patent/BRPI0907122B8/pt active IP Right Grant
- 2009-01-09 NZ NZ586120A patent/NZ586120A/en unknown
- 2009-01-09 AU AU2009204048A patent/AU2009204048B2/en active Active
- 2009-01-09 JP JP2010542381A patent/JP5501251B2/ja active Active
- 2009-01-09 CA CA2727055A patent/CA2727055C/en active Active
- 2009-01-09 EP EP09700411A patent/EP2240481A1/en not_active Withdrawn
- 2009-01-09 MX MX2010007430A patent/MX2010007430A/es active IP Right Grant
- 2009-01-09 CN CN200980105529.7A patent/CN101945872B/zh active Active
-
2010
- 2010-06-24 IL IL206594A patent/IL206594A/en active IP Right Grant
-
2014
- 2014-03-11 JP JP2014047896A patent/JP2014129417A/ja active Pending
- 2014-03-24 US US14/223,151 patent/US9296743B2/en active Active
-
2016
- 2016-02-17 US US15/045,652 patent/US9650378B2/en active Active
-
2017
- 2017-04-03 US US15/477,984 patent/US20170204095A1/en not_active Abandoned
Also Published As
| Publication number | Publication date |
|---|---|
| ES2523580T3 (es) | 2014-11-27 |
| JP2011509937A (ja) | 2011-03-31 |
| BRPI0907122B8 (pt) | 2021-05-25 |
| IL206594A (en) | 2015-05-31 |
| US20170204095A1 (en) | 2017-07-20 |
| CA2727055A1 (en) | 2009-07-16 |
| US20160159798A1 (en) | 2016-06-09 |
| AU2009204048A1 (en) | 2009-07-16 |
| EP2476680A1 (en) | 2012-07-18 |
| MX2010007430A (es) | 2010-12-21 |
| WO2009089482A1 (en) | 2009-07-16 |
| US8716308B2 (en) | 2014-05-06 |
| KR20100124251A (ko) | 2010-11-26 |
| CA2727055C (en) | 2016-12-20 |
| US20100331339A9 (en) | 2010-12-30 |
| JP2014129417A (ja) | 2014-07-10 |
| EP2476680B1 (en) | 2014-08-27 |
| JP5501251B2 (ja) | 2014-05-21 |
| AU2009204048B2 (en) | 2013-08-01 |
| BRPI0907122B1 (pt) | 2019-04-16 |
| US9650378B2 (en) | 2017-05-16 |
| KR101614723B1 (ko) | 2016-04-22 |
| US20090275590A1 (en) | 2009-11-05 |
| US20140206696A1 (en) | 2014-07-24 |
| NZ586120A (en) | 2012-07-27 |
| US9296743B2 (en) | 2016-03-29 |
| CN101945872A (zh) | 2011-01-12 |
| BRPI0907122A2 (pt) | 2015-07-14 |
| IL206594A0 (en) | 2010-12-30 |
| EP2240481A1 (en) | 2010-10-20 |
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| CN101945872B (zh) | 作为mch拮抗剂的(1-吖嗪酮)-取代的吡啶并吲哚 | |
| US12304915B2 (en) | SOS1 inhibitors | |
| US11390609B2 (en) | Rho-associated protein kinase inhibitor, pharmaceutical composition comprising same, and preparation method and use thereof | |
| CN104619709B (zh) | 作为tnf活性调节剂的咪唑并吡啶衍生物 | |
| CN116589467A (zh) | 通过缀合btk抑制剂与e3连接酶配体降解布鲁顿氏酪氨酸激酶(btk)及其使用方法 | |
| CN113316576A (zh) | 用于治疗癌症的作为HPK1抑制剂的2,3-二氢-1H-吡咯并[3,4-c]吡啶-1-酮衍生物 | |
| CN108699038A (zh) | 作为Rock抑制剂的螺环庚烷水杨酸酰胺和相关化合物 | |
| AU2008279321B2 (en) | 5-pyridinone substituted indazoles | |
| CN107295798A (zh) | 苯并氮杂*二甲酰胺化合物 | |
| CN107873031A (zh) | 作为tnf活性调节剂的苯并噁嗪酮衍生物及其类似物 | |
| WO2022199662A1 (zh) | 一种多环化合物及其应用 | |
| CN116981675A (zh) | 通过布鲁顿氏酪氨酸激酶(btk)抑制剂与e3连接酶配体的缀合降解btk和使用方法 | |
| WO2006059164A2 (en) | Pyrrolopyridine-2-carboxylic acid amides | |
| US20240238425A1 (en) | HSD17B13 Inhibitors and/or Degraders | |
| HK1169111A (en) | (1-azinone)-substituted pyridoindoles | |
| JP2024504824A (ja) | 芳香族複素環化合物及びその製造方法と用途 | |
| HK40053093A (en) | 2,3-dihydro-1h-pyrrolo[3,4-c]pyridin-1-one derivatives as hpk1 inhibitors for the treatment of cancer |
Legal Events
| Date | Code | Title | Description |
|---|---|---|---|
| C06 | Publication | ||
| PB01 | Publication | ||
| C10 | Entry into substantive examination | ||
| SE01 | Entry into force of request for substantive examination | ||
| C53 | Correction of patent of invention or patent application | ||
| CB03 | Change of inventor or designer information |
Inventor after: Hadden Mark Inventor after: Guzzo Peter Inventor after: Henderson Alan John Inventor after: M.X.Jiang Inventor after: M. Harden Inventor after: Grabowski James Inventor after: A.YORXIYASKI Inventor before: Hadden Mark Inventor before: Guzzo Peter Inventor before: Henderson Alan John Inventor before: M.X.Jiang Inventor before: M. Harden Inventor before: Grabowski James |
|
| COR | Change of bibliographic data |
Free format text: CORRECT: INVENTOR; FROM: PETER GUZZO DAVID SURMAN MATTHEW JOHN HENDERSON ALAN XIAOWU JIANG MAY MARK HADDEN JAMES GRABOWSKI TO: PETER GUZZO DAVID SURMAN MATTHEW JOHN HENDERSON ALAN XIAOWU JIANG MAY MARK HADDEN JAMES GRABOWSKI USYATINSKY ALEXANDER |
|
| C14 | Grant of patent or utility model | ||
| GR01 | Patent grant | ||
| CP03 | Change of name, title or address | ||
| CP03 | Change of name, title or address |
Address after: New York, United States Patentee after: Kuria Global Ltd. Country or region after: U.S.A. Address before: New York, United States Patentee before: ALBANY MOLECULAR RESEARCH, Inc. Country or region before: U.S.A. |
|
| TR01 | Transfer of patent right | ||
| TR01 | Transfer of patent right |
Effective date of registration: 20250122 Address after: Pennsylvania, USA Patentee after: Harmony Biotechnology Co.,Ltd. Country or region after: U.S.A. Address before: New York, United States Patentee before: Kuria Global Ltd. Country or region before: U.S.A. |
|
| TR01 | Transfer of patent right | ||
| TR01 | Transfer of patent right |
Effective date of registration: 20250207 Address after: Pennsylvania, USA Patentee after: Harmony Biotechnology Management Co. Country or region after: U.S.A. Address before: Pennsylvania, USA Patentee before: Harmony Biotechnology Co.,Ltd. Country or region before: U.S.A. |