SE0100567D0 - Compounds - Google Patents
CompoundsInfo
- Publication number
- SE0100567D0 SE0100567D0 SE0100567A SE0100567A SE0100567D0 SE 0100567 D0 SE0100567 D0 SE 0100567D0 SE 0100567 A SE0100567 A SE 0100567A SE 0100567 A SE0100567 A SE 0100567A SE 0100567 D0 SE0100567 D0 SE 0100567D0
- Authority
- SE
- Sweden
- Prior art keywords
- compounds
- compound
- relates
- present
- gnrh
- Prior art date
Links
- 150000001875 compounds Chemical class 0.000 title abstract 5
- 239000000579 Gonadotropin-Releasing Hormone Substances 0.000 abstract 2
- 101000857870 Squalus acanthias Gonadoliberin Proteins 0.000 abstract 2
- XLXSAKCOAKORKW-AQJXLSMYSA-N gonadorelin Chemical compound C([C@@H](C(=O)NCC(=O)N[C@@H](CC(C)C)C(=O)N[C@@H](CCCNC(N)=N)C(=O)N1[C@@H](CCC1)C(=O)NCC(N)=O)NC(=O)[C@H](CO)NC(=O)[C@H](CC=1C2=CC=CC=C2NC=1)NC(=O)[C@H](CC=1N=CNC=1)NC(=O)[C@H]1NC(=O)CC1)C1=CC=C(O)C=C1 XLXSAKCOAKORKW-AQJXLSMYSA-N 0.000 abstract 2
- 229940035638 gonadotropin-releasing hormone Drugs 0.000 abstract 2
- 238000000034 method Methods 0.000 abstract 2
- 239000005557 antagonist Substances 0.000 abstract 1
- 239000003814 drug Substances 0.000 abstract 1
- 230000000694 effects Effects 0.000 abstract 1
- 238000004519 manufacturing process Methods 0.000 abstract 1
- 239000008194 pharmaceutical composition Substances 0.000 abstract 1
- 230000001225 therapeutic effect Effects 0.000 abstract 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
- A61P5/00—Drugs for disorders of the endocrine system
Landscapes
- Organic Chemistry (AREA)
- Chemical & Material Sciences (AREA)
- Health & Medical Sciences (AREA)
- Engineering & Computer Science (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Diabetes (AREA)
- Chemical Kinetics & Catalysis (AREA)
- General Chemical & Material Sciences (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Medicinal Chemistry (AREA)
- Life Sciences & Earth Sciences (AREA)
- Pharmacology & Pharmacy (AREA)
- Endocrinology (AREA)
- Animal Behavior & Ethology (AREA)
- General Health & Medical Sciences (AREA)
- Public Health (AREA)
- Veterinary Medicine (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Medicines That Contain Protein Lipid Enzymes And Other Medicines (AREA)
- Nitrogen Condensed Heterocyclic Rings (AREA)
Priority Applications (3)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| SE0100567A SE0100567D0 (sv) | 2001-02-20 | 2001-02-20 | Compounds |
| PCT/GB2002/000634 WO2002066477A2 (fr) | 2001-02-20 | 2002-02-15 | Composes |
| AU2002229976A AU2002229976A1 (en) | 2001-02-20 | 2002-02-15 | Imidazopyridines |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| SE0100567A SE0100567D0 (sv) | 2001-02-20 | 2001-02-20 | Compounds |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| SE0100567D0 true SE0100567D0 (sv) | 2001-02-20 |
Family
ID=20283057
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| SE0100567A SE0100567D0 (sv) | 2001-02-20 | 2001-02-20 | Compounds |
Country Status (3)
| Country | Link |
|---|---|
| AU (1) | AU2002229976A1 (fr) |
| SE (1) | SE0100567D0 (fr) |
| WO (1) | WO2002066477A2 (fr) |
Families Citing this family (53)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| DE10246890A1 (de) * | 2002-10-08 | 2004-04-22 | Grünenthal GmbH | Substituierte C-Imidazo[1,2-alpyridin-3-yl-methylamine |
| DE10247271A1 (de) * | 2002-10-10 | 2004-08-26 | Grünenthal GmbH | Substituierte C-Imidazo[1,2-a]pyridin-3-yle |
| GB0320806D0 (en) | 2003-09-05 | 2003-10-08 | Astrazeneca Ab | Therapeutic treatment |
| WO2005044818A2 (fr) | 2003-10-28 | 2005-05-19 | Sepracor, Inc. | Anxiolytiques d'imidazo[1,2-a]pyridine |
| GB0403781D0 (en) * | 2004-02-20 | 2004-03-24 | Astrazeneca Ab | Chemical compounds |
| US7772271B2 (en) | 2004-07-14 | 2010-08-10 | Ptc Therapeutics, Inc. | Methods for treating hepatitis C |
| US7781478B2 (en) | 2004-07-14 | 2010-08-24 | Ptc Therapeutics, Inc. | Methods for treating hepatitis C |
| EA200700243A1 (ru) | 2004-07-14 | 2007-08-31 | ПиТиСи ТЕРАПЬЮТИКС, ИНК. | Способы лечения гепатита с |
| US7868037B2 (en) | 2004-07-14 | 2011-01-11 | Ptc Therapeutics, Inc. | Methods for treating hepatitis C |
| CA2578636A1 (fr) | 2004-07-22 | 2006-02-23 | Ptc Therapeutics, Inc. | Thienopyridines utilisees pour traiter l'hepatite c |
| WO2007069565A1 (fr) | 2005-12-12 | 2007-06-21 | Ono Pharmaceutical Co., Ltd. | Compose heterocyclique bicyclique |
| WO2007113226A1 (fr) * | 2006-03-31 | 2007-10-11 | Novartis Ag | Composés organiques |
| US7563797B2 (en) | 2006-08-28 | 2009-07-21 | Forest Laboratories Holding Limited | Substituted imidazo(1,2-A)pyrimidines and imidazo(1,2-A) pyridines as cannabinoid receptor ligands |
| JP5159630B2 (ja) | 2006-09-13 | 2013-03-06 | 協和発酵キリン株式会社 | 縮環複素環誘導体 |
| CN101679408B (zh) | 2006-12-22 | 2016-04-27 | Astex治疗学有限公司 | 作为fgfr抑制剂的双环杂环化合物 |
| HRP20151398T1 (hr) | 2006-12-22 | 2016-02-12 | Astex Therapeutics Limited | Tricikliäśni derivati amina kao inhibitori protein tirozin kinaze |
| EP1964840A1 (fr) | 2007-02-28 | 2008-09-03 | sanofi-aventis | Imidazo[1,2-a]pyridines et leur utilisation en tant que produits pharmaceutiques |
| UA101611C2 (ru) | 2007-04-03 | 2013-04-25 | Аррей Байофарма Инк. | СОЕДИНЕНИЯ ИМИДАЗО[1,2-а]ПИРИДИНА КАК ИНГИБИТОРЫ ТИРОЗИНКИНАЗЫ РЕЦЕПТОРОВ |
| GB0720038D0 (en) | 2007-10-12 | 2007-11-21 | Astex Therapeutics Ltd | New compounds |
| GB0720041D0 (en) | 2007-10-12 | 2007-11-21 | Astex Therapeutics Ltd | New Compounds |
| EP2213672A4 (fr) * | 2007-10-24 | 2012-05-02 | Nihon Mediphysics Co Ltd | Nouveau composé possédant une affinité vis-à-vis d'une substance amyloïde |
| WO2009143156A2 (fr) * | 2008-05-19 | 2009-11-26 | Sepracor Inc. | Composés imidazo[1,2-a]pyridines |
| GB0810902D0 (en) | 2008-06-13 | 2008-07-23 | Astex Therapeutics Ltd | New compounds |
| GB0906470D0 (en) | 2009-04-15 | 2009-05-20 | Astex Therapeutics Ltd | New compounds |
| GB0906472D0 (en) | 2009-04-15 | 2009-05-20 | Astex Therapeutics Ltd | New compounds |
| TW201242965A (en) | 2011-02-01 | 2012-11-01 | Kyowa Hakko Kirin Co Ltd | Ring-fused heterocyclic derivative |
| US8975276B2 (en) | 2011-06-29 | 2015-03-10 | Bristol-Myers Squibb Company | Inhibitors of PDE10 |
| UY34305A (es) | 2011-09-01 | 2013-04-30 | Novartis Ag | Derivados de heterociclos bicíclicos para el tratamiento de la hipertensión arterial pulmonar |
| US9540366B2 (en) | 2012-07-31 | 2017-01-10 | Kyowa Hakko Kirin Co., Ltd. | Ring-fused heterocyclic compound |
| US9073921B2 (en) | 2013-03-01 | 2015-07-07 | Novartis Ag | Salt forms of bicyclic heterocyclic derivatives |
| EP3365340B1 (fr) | 2015-10-19 | 2022-08-10 | Incyte Corporation | Composés hétérocycliques utilisés comme immunomodulateurs |
| HUE060680T2 (hu) | 2015-11-19 | 2023-04-28 | Incyte Corp | Heterociklusos vegyületek mint immunmodulátorok |
| EP3394033B1 (fr) | 2015-12-22 | 2020-11-25 | Incyte Corporation | Composés hétérocycliques utilisés comme immunomodulateurs |
| US9926316B2 (en) * | 2016-03-03 | 2018-03-27 | The Cleveland Clinic Foundation | Antitumor derivatives for differentiation therapy |
| WO2017192961A1 (fr) | 2016-05-06 | 2017-11-09 | Incyte Corporation | Composés hétérocycliques utilisés comme immunomodulateurs |
| TW201808902A (zh) | 2016-05-26 | 2018-03-16 | 美商英塞特公司 | 作為免疫調節劑之雜環化合物 |
| MD3472167T2 (ro) | 2016-06-20 | 2023-02-28 | Incyte Corp | Compuși heterociclici ca imunomodulatori |
| WO2018013789A1 (fr) | 2016-07-14 | 2018-01-18 | Incyte Corporation | Composés hétérocycliques utilisés comme immunomodulateurs |
| US20180057486A1 (en) | 2016-08-29 | 2018-03-01 | Incyte Corporation | Heterocyclic compounds as immunomodulators |
| EP3558973B1 (fr) | 2016-12-22 | 2021-09-15 | Incyte Corporation | Dérivés pyridine utilisés en tant qu'immunomodulateurs |
| PE20200005A1 (es) | 2016-12-22 | 2020-01-06 | Incyte Corp | Derivados de tetrahidro imidazo[4,5-c]piridina como inductores de internalizacion pd-l1 |
| EP3558989B1 (fr) | 2016-12-22 | 2021-04-14 | Incyte Corporation | Dérivés de triazolo[1,5-a]pyridine en tant qu'immunomodulateurs |
| MA47123A (fr) | 2016-12-22 | 2021-03-17 | Incyte Corp | Dérivés de benzooxazole en tant qu'mmunomodulateurs |
| EP3558963B1 (fr) | 2016-12-22 | 2022-03-23 | Incyte Corporation | Composés hétéroaromatiques bicycliques utilisés en tant qu'immunomodulateurs |
| PL4212529T3 (pl) | 2018-03-30 | 2025-07-07 | Incyte Corporation | Związki heterocykliczne jako immunomodulatory |
| HRP20230306T1 (hr) | 2018-05-11 | 2023-05-12 | Incyte Corporation | Derivati tetrahidro-imidazo[4,5-c]piridina kao pd-l1 imunomodulatori |
| WO2021030162A1 (fr) | 2019-08-09 | 2021-02-18 | Incyte Corporation | Sels d'un inhibiteur de pd-1/pd-l1 |
| IL291471B2 (en) | 2019-09-30 | 2025-04-01 | Incyte Corp | Pyrimido[3,2–D]pyrimidine compounds as immunomodulators |
| CR20220237A (es) | 2019-11-11 | 2022-08-05 | Incyte Corp | Sales y formas cristalinas de un inhibidor de pd-1/pd-l1 |
| AR124001A1 (es) | 2020-11-06 | 2023-02-01 | Incyte Corp | Proceso para fabricar un inhibidor pd-1 / pd-l1 y sales y formas cristalinas del mismo |
| WO2022099075A1 (fr) | 2020-11-06 | 2022-05-12 | Incyte Corporation | Forme cristalline d'un inhibiteur pd-1/pd-l1 |
| US11780836B2 (en) | 2020-11-06 | 2023-10-10 | Incyte Corporation | Process of preparing a PD-1/PD-L1 inhibitor |
| CN113666926A (zh) * | 2021-09-08 | 2021-11-19 | 桂林理工大学 | 一种便捷的2-苯基咪唑[1,2-a]吡啶与查尔酮的Michal加成反应 |
Family Cites Families (7)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| DE19544212A1 (de) * | 1995-11-28 | 1997-06-05 | Asta Medica Ag | Neue LH-RH-Antagonisten mit verbesserter Wirkung |
| ATE338754T1 (de) * | 1996-07-19 | 2006-09-15 | Takeda Pharmaceutical | Heterocyclische verbindungen, ihre herstellung und verwendung |
| EP1028690A2 (fr) * | 1997-10-20 | 2000-08-23 | Novo Nordisk A/S | Antagonistes de l'hormone luteinisante utiles pour le traitement de carences oestrogeniques ou utilises en tant que contraceptif |
| EP1068195A1 (fr) * | 1998-02-11 | 2001-01-17 | Merck & Co., Inc. | Antagonistes de l'hormone de liberation de la gonadotrophine |
| AU2597899A (en) * | 1998-02-11 | 1999-08-30 | Merck & Co., Inc. | Antagonists of gonadotropin releasing hormone |
| DK1255738T3 (da) * | 2000-01-25 | 2012-06-25 | Neurocrine Biosciences Inc | Gonadotropin-frigivende hormonreceptor-antagonister og fremgangsmåder relateret dertil |
| ES2244613T3 (es) * | 2000-04-27 | 2005-12-16 | Astellas Pharma Inc. | Derivados de imidazopiridina. |
-
2001
- 2001-02-20 SE SE0100567A patent/SE0100567D0/xx unknown
-
2002
- 2002-02-15 WO PCT/GB2002/000634 patent/WO2002066477A2/fr not_active Ceased
- 2002-02-15 AU AU2002229976A patent/AU2002229976A1/en not_active Abandoned
Also Published As
| Publication number | Publication date |
|---|---|
| AU2002229976A1 (en) | 2002-09-04 |
| WO2002066477A2 (fr) | 2002-08-29 |
| WO2002066477A3 (fr) | 2002-10-17 |
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