MA52092A - Composés et leurs utilisations - Google Patents
Composés et leurs utilisationsInfo
- Publication number
- MA52092A MA52092A MA052092A MA52092A MA52092A MA 52092 A MA52092 A MA 52092A MA 052092 A MA052092 A MA 052092A MA 52092 A MA52092 A MA 52092A MA 52092 A MA52092 A MA 52092A
- Authority
- MA
- Morocco
- Prior art keywords
- compounds
- Prior art date
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Classifications
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K45/00—Medicinal preparations containing active ingredients not provided for in groups A61K31/00 - A61K41/00
- A61K45/06—Mixtures of active ingredients without chemical characterisation, e.g. antiphlogistics and cardiaca
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D491/00—Heterocyclic compounds containing in the condensed ring system both one or more rings having oxygen atoms as the only ring hetero atoms and one or more rings having nitrogen atoms as the only ring hetero atoms, not provided for by groups C07D451/00 - C07D459/00, C07D463/00, C07D477/00 or C07D489/00
- C07D491/02—Heterocyclic compounds containing in the condensed ring system both one or more rings having oxygen atoms as the only ring hetero atoms and one or more rings having nitrogen atoms as the only ring hetero atoms, not provided for by groups C07D451/00 - C07D459/00, C07D463/00, C07D477/00 or C07D489/00 in which the condensed system contains two hetero rings
- C07D491/10—Spiro-condensed systems
- C07D491/107—Spiro-condensed systems with only one oxygen atom as ring hetero atom in the oxygen-containing ring
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- 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
- A61K31/435—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with one nitrogen as the only ring hetero atom
- A61K31/44—Non condensed pyridines; Hydrogenated derivatives thereof
- A61K31/4427—Non condensed pyridines; Hydrogenated derivatives thereof containing further heterocyclic ring systems
- A61K31/4439—Non condensed pyridines; Hydrogenated derivatives thereof containing further heterocyclic ring systems containing a five-membered ring with nitrogen as a ring hetero atom, e.g. omeprazole
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
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- A61K31/33—Heterocyclic compounds
- A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
- A61K31/495—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with two or more nitrogen atoms as the only ring heteroatoms, e.g. piperazine or tetrazines
- A61K31/50—Pyridazines; Hydrogenated pyridazines
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
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- A61K31/33—Heterocyclic compounds
- A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
- A61K31/495—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with two or more nitrogen atoms as the only ring heteroatoms, e.g. piperazine or tetrazines
- A61K31/50—Pyridazines; Hydrogenated pyridazines
- A61K31/501—Pyridazines; Hydrogenated pyridazines not condensed and containing further heterocyclic rings
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
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- A61K31/33—Heterocyclic compounds
- A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
- A61K31/495—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with two or more nitrogen atoms as the only ring heteroatoms, e.g. piperazine or tetrazines
- A61K31/505—Pyrimidines; Hydrogenated pyrimidines, e.g. trimethoprim
- A61K31/506—Pyrimidines; Hydrogenated pyrimidines, e.g. trimethoprim not condensed and containing further heterocyclic rings
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- A—HUMAN NECESSITIES
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D213/00—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members
- C07D213/02—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members
- C07D213/04—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen or carbon atoms directly attached to the ring nitrogen atom
- C07D213/60—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen or carbon atoms directly attached to the ring nitrogen atom with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, directly attached to ring carbon atoms
- C07D213/62—Oxygen or sulfur atoms
- C07D213/63—One oxygen atom
- C07D213/64—One oxygen atom attached in position 2 or 6
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- C07D213/00—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members
- C07D213/02—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members
- C07D213/04—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen or carbon atoms directly attached to the ring nitrogen atom
- C07D213/60—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen or carbon atoms directly attached to the ring nitrogen atom with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, directly attached to ring carbon atoms
- C07D213/72—Nitrogen atoms
- C07D213/75—Amino or imino radicals, acylated by carboxylic or carbonic acids, or by sulfur or nitrogen analogues thereof, e.g. carbamates
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- C07D213/02—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members
- C07D213/04—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen or carbon atoms directly attached to the ring nitrogen atom
- C07D213/60—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen or carbon atoms directly attached to the ring nitrogen atom with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, directly attached to ring carbon atoms
- C07D213/78—Carbon atoms having three bonds to hetero atoms, with at the most one bond to halogen, e.g. ester or nitrile radicals
- C07D213/81—Amides; Imides
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- C07D213/00—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members
- C07D213/02—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members
- C07D213/04—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen or carbon atoms directly attached to the ring nitrogen atom
- C07D213/60—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen or carbon atoms directly attached to the ring nitrogen atom with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, directly attached to ring carbon atoms
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- C07D213/81—Amides; Imides
- C07D213/82—Amides; Imides in position 3
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- C07D213/00—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members
- C07D213/02—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members
- C07D213/04—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen or carbon atoms directly attached to the ring nitrogen atom
- C07D213/60—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen or carbon atoms directly attached to the ring nitrogen atom with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, directly attached to ring carbon atoms
- C07D213/78—Carbon atoms having three bonds to hetero atoms, with at the most one bond to halogen, e.g. ester or nitrile radicals
- C07D213/84—Nitriles
- C07D213/85—Nitriles in position 3
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- C07D237/00—Heterocyclic compounds containing 1,2-diazine or hydrogenated 1,2-diazine rings
- C07D237/02—Heterocyclic compounds containing 1,2-diazine or hydrogenated 1,2-diazine rings not condensed with other rings
- C07D237/04—Heterocyclic compounds containing 1,2-diazine or hydrogenated 1,2-diazine rings not condensed with other rings having less than three double bonds between ring members or between ring members and non-ring members
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- C07D237/00—Heterocyclic compounds containing 1,2-diazine or hydrogenated 1,2-diazine rings
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- C07D237/14—Oxygen atoms
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- C07D417/12—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by group C07D415/00 containing two hetero rings linked by a chain containing hetero atoms as chain links
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- 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
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- C07D487/02—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, not provided for by groups C07D451/00 - C07D477/00 in which the condensed system contains two hetero rings
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| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
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| CA3049010A1 (fr) | 2017-01-06 | 2018-07-12 | Yumanity Therapeutics, Inc. | Methodes de traitement de troubles neurologiques |
| CA3083000A1 (fr) | 2017-10-24 | 2019-05-02 | Yumanity Therapeutics, Inc. | Composes et utilisations de ces composes |
| CA3094527A1 (fr) | 2018-03-23 | 2019-09-26 | Yumanity Therapeutics, Inc. | Composes et leurs utilisations |
| US12098146B2 (en) * | 2019-01-24 | 2024-09-24 | Janssen Pharmaceutica Nv | Compounds and uses thereof |
| CN114174273A (zh) * | 2019-03-22 | 2022-03-11 | 优曼尼蒂治疗公司 | 化合物和其用途 |
| EA202192047A1 (ru) | 2019-11-13 | 2021-12-08 | Юманити Терапьютикс, Инк. | Соединения и их применение |
| WO2021197276A1 (fr) | 2020-03-30 | 2021-10-07 | Hutchison Medipharma Limited | Composés amides et leurs utilisations |
| EP4253383A4 (fr) * | 2020-12-31 | 2024-07-17 | Tsinghua University | Dérivé de pyridine-2-amine, composition pharmaceutique et utilisation associée |
| EP4337202A4 (fr) | 2021-06-18 | 2025-04-02 | Aligos Therapeutics, Inc. | Méthodes et compositions pour le ciblage de pd-l1 |
| CA3240346A1 (fr) | 2021-12-16 | 2023-06-22 | Aligos Therapeutics, Inc. | Methodes et compositions pour le ciblage de pd-l1 |
| WO2023111996A1 (fr) | 2021-12-17 | 2023-06-22 | Reglagene Holding, Inc. | Compositions et procédés de fabrication et d'utilisation de petites molécules dans le traitement du cancer |
| US12215102B2 (en) | 2023-02-28 | 2025-02-04 | Reglagene, Inc. | Compositions and methods for making and using small molecules for tubulin-targeted therapy in the treatment of cancers and related conditions |
Family Cites Families (277)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US4782071A (en) | 1986-11-03 | 1988-11-01 | Warner-Lambert Company | Tetrasubstituted urea cholinergic agents |
| CA2184919C (fr) | 1995-01-11 | 2000-03-14 | Eui-Hwan Cho | Nouveaux derives piperazines, leurs procedes de preparation, et compositions les contenant |
| TW360653B (en) | 1995-03-01 | 1999-06-11 | Janssen Pharmaceutica Nv | A oxadiazole compound having colon motility stimulating properties, its preparation process and its pharmaceutical composition |
| AU4414999A (en) | 1998-06-08 | 1999-12-30 | Sambasiva R. Chavali | Inhibition of delta-9-desaturase activity by saponins |
| US6107313A (en) | 1998-10-02 | 2000-08-22 | Combichem, Inc. | Dopamine receptor antagonists |
| US20070087363A1 (en) | 1998-12-22 | 2007-04-19 | Myriad Genetics, Incorporated | Therapeutic methods, compounds and compositions |
| MXPA02000253A (es) * | 1999-07-01 | 2002-06-21 | Ajinomoto Kk | Compuestos heterociclicos y uso medico de los mismos. |
| JP2003528806A (ja) | 1999-07-20 | 2003-09-30 | ダウ・アグロサイエンス・エル・エル・シー | 殺菌・殺カビ性複素環式芳香族アミドおよびそれらの組成物、使用および製造方法 |
| BR0013469B1 (pt) | 1999-08-20 | 2011-01-25 | amidas aromáticas heterocìclicas fungicidas, composição fungicida compreendendo as mesmas, bem como método para o controle ou a prevenção de infestação fúngica. | |
| PT1315831E (pt) | 2000-02-24 | 2010-11-04 | Xenon Pharmaceuticals Inc | Estearoil-coa dessaturase para identificar agentes terapêuticos que reduzem triglicéridos |
| PT1300396E (pt) | 2000-06-12 | 2009-04-20 | Eisai R&D Man Co Ltd | Compostos de 1,2-di-hidropiridina, processos para a sua preparação e sua utilização |
| WO2001095856A2 (fr) | 2000-06-15 | 2001-12-20 | Chaconne Nsi Co., Ltd. | Derive d'uree en tant qu'agent anticancereux et son procede de preparation |
| EP1346042A2 (fr) | 2000-11-17 | 2003-09-24 | Xenon Genetics, Inc. | Genes a regulation lipidique, utilisations de ces genes et composes permettant leur modulation |
| US6995162B2 (en) * | 2001-01-12 | 2006-02-07 | Amgen Inc. | Substituted alkylamine derivatives and methods of use |
| US20050256068A1 (en) | 2001-05-18 | 2005-11-17 | Sirna Therapeutics, Inc. | RNA interference mediated inhibition of stearoyl-CoA desaturase (SCD) gene expression using short interfering nucleic acid (siNA) |
| US20050043256A1 (en) | 2001-07-30 | 2005-02-24 | Isis Pharmaceuticals, Inc. | Antisense modulation of stearoyl-CoA desaturase expression |
| US6727247B2 (en) | 2001-12-10 | 2004-04-27 | Hoffman-La Roche Inc. | Substituted benzothiazole amide derivatives |
| AU2003215203A1 (en) | 2002-02-20 | 2003-09-09 | Sirna Therapeutics, Inc. | Short interfering nucleic acid inhibition of stearoyl-coa desaturase (scd) gene |
| US6995144B2 (en) | 2002-03-14 | 2006-02-07 | Eisai Co., Ltd. | Nitrogen containing heterocyclic compounds and medicines containing the same |
| US7105505B2 (en) | 2002-04-18 | 2006-09-12 | Schering Corporation | Benzimidazole derivatives useful as histamine H3 antagonists |
| WO2004014902A2 (fr) | 2002-08-09 | 2004-02-19 | Astrazeneca Ab | Nouveaux composes |
| WO2004014892A1 (fr) | 2002-08-13 | 2004-02-19 | Warner-Lambert Company Llc | Derives monocycliques en tant qu'inhibiteurs de metalloproteinases matricielles |
| AU2003303373B8 (en) | 2002-12-18 | 2010-06-10 | Cytovia, Inc. | 3,5-disubstituted-[1,2,4]-oxadiazoles and analogs as activators of caspases and inducers of apoptosis and the use thereof |
| EP1635800A2 (fr) * | 2003-06-10 | 2006-03-22 | Kalypsys, Inc. | Composes carbonyle utilises comme inhibiteurs de l'histone desacetylase a des fins therapeutiques |
| ES2386354T3 (es) | 2003-07-29 | 2012-08-17 | Xenon Pharmaceuticals Inc. | Derivados de piridilo y su uso como agentes terapéuticos |
| US7754711B2 (en) | 2003-07-30 | 2010-07-13 | Xenon Pharmaceuticals Inc. | Pyridazine derivatives and their use as therapeutic agents |
| US7759348B2 (en) | 2003-07-30 | 2010-07-20 | Xenon Pharmaceuticals Inc. | Pyridazine derivatives and their use as therapeutic agents |
| JP4782008B2 (ja) | 2003-07-30 | 2011-09-28 | ゼノン・ファーマシューティカルズ・インコーポレイテッド | ピリジル誘導体および治療剤としてのその用途 |
| US7456180B2 (en) | 2003-07-30 | 2008-11-25 | Xenon Pharmaceuticals Inc. | Piperazine derivatives and their use as therapeutic agents |
| EP3042895A1 (fr) | 2003-07-30 | 2016-07-13 | Xenon Pharmaceuticals Inc. | Dérivés de la pipérazine et leur utilisation en tant qu'agents thérapeutiques |
| AU2004261249B2 (en) | 2003-07-30 | 2008-09-04 | Xenon Pharmaceuticals Inc. | Pyridazine derivatives and their use as therapeutic agents |
| CA2534529A1 (fr) * | 2003-08-06 | 2005-02-24 | Pfizer Products Inc. | Composes d'oxazole destines au traitement de troubles neurodegenerescents |
| US7504401B2 (en) | 2003-08-29 | 2009-03-17 | Locus Pharmaceuticals, Inc. | Anti-cancer agents and uses thereof |
| DE602004008658T2 (de) | 2003-09-05 | 2008-06-12 | Cellzome Ag | Behandlung neurodegenerativer krankheiten |
| MXPA06002567A (es) * | 2003-09-06 | 2006-09-04 | Vertex Pharma | Moduladores de transportadores con casete de union de atp. |
| US8188064B2 (en) | 2003-11-25 | 2012-05-29 | Wisconsin Alumni Research Foundation | Vitamin D analogs for obesity prevention and treatment |
| BRPI0418149A (pt) | 2003-12-24 | 2007-04-17 | Prosidion Ltd | derivados heterocìclicos como agonistas do receptor de gprc |
| JP2005213233A (ja) | 2004-02-02 | 2005-08-11 | Fuji Oil Co Ltd | 肝臓ステアロイル‐CoA不飽和化酵素1合成抑制剤 |
| US7459562B2 (en) | 2004-04-23 | 2008-12-02 | Bristol-Myers Squibb Company | Monocyclic heterocycles as kinase inhibitors |
| WO2006012325A1 (fr) | 2004-06-25 | 2006-02-02 | E.I. Dupont De Nemours And Company | Desaturase delta-8 et son utilisation dans la fabrication d'acides gras polyinsatures |
| BRPI0418939A (pt) | 2004-07-06 | 2008-04-08 | Xenon Pharmaceuticals Inc | derivados de nicotinamida e sua utilização como agentes terapêuticos |
| ES2325836T3 (es) | 2004-07-26 | 2009-09-21 | Merck Serono Sa | Derivados de la n.hidroxiamida y uso de los mismos. |
| CA2575300A1 (fr) | 2004-08-09 | 2006-02-16 | Cellzome Ag | Traitement des maladies neurodegeneratives au moyen d'inhibiteur de degs |
| WO2006022442A1 (fr) * | 2004-08-24 | 2006-03-02 | Santen Pharmaceutical Co., Ltd. | Nouveaux derives d’amides heterocycliques ayant une activite d’inhibition de la dihydroorotate deshydrogenase |
| MX2007003332A (es) | 2004-09-20 | 2007-06-05 | Xenon Pharmaceuticals Inc | Derivados heterociclicos y su uso como inhibidores de estearoil-coa-desaturasa. |
| EP1799667B1 (fr) | 2004-09-20 | 2013-03-20 | Xenon Pharmaceuticals Inc. | Derives heterocycliques et leur utilisation comme agents therapeutiques |
| EP2289510A1 (fr) | 2004-09-20 | 2011-03-02 | Xenon Pharmaceuticals Inc. | Dérivés hétérocycliques pour le traitement des maladies induites par des enzymes stearoyl-coa desaturase |
| US7547698B2 (en) | 2004-09-20 | 2009-06-16 | Xenon Pharmaceuticals Inc. | Bicyclic heterocyclic derivatives and their use as inhibitors of stearoyl-coadesaturase (SCD) |
| MX2007003327A (es) | 2004-09-20 | 2007-06-05 | Xenon Pharmaceuticals Inc | Derivados heterociclicos, y su uso como mediadores de estearoil-coa desaturasa. |
| JP4958786B2 (ja) | 2004-09-20 | 2012-06-20 | ゼノン・ファーマシューティカルズ・インコーポレイテッド | 複素環誘導体および治療薬としてのそれらの使用 |
| US20080167321A1 (en) | 2004-09-20 | 2008-07-10 | Xenon Pharmaceuticals Inc. | Pyridine Derivatives For Inhibiting Human Stearoyl-Coa-Desaturase |
| MX2007003319A (es) | 2004-09-20 | 2007-06-05 | Xenon Pharmaceuticals Inc | Derivados heterociclicos y su uso como agentes terapeuticos. |
| KR101368228B1 (ko) | 2004-11-10 | 2014-02-27 | 인사이트 코포레이션 | 락탐 화합물 및 약제로서의 이의 용도 |
| US8399438B2 (en) | 2004-11-22 | 2013-03-19 | Wisconsin Alumni Research Foundation | 2α-methyl-19-nor-1α-hydroxy-homopregnacalciferol and its uses |
| US20060167044A1 (en) | 2004-12-20 | 2006-07-27 | Arnaiz Damian O | Piperidine derivatives and their use as anti-inflammatory agents |
| WO2006067531A1 (fr) | 2004-12-24 | 2006-06-29 | Prosidion Ltd | Agonistes du récepteur couplé aux protéines g (gpr116) et leur emploi dans le traitement de l'obésité et du diabète |
| CN101128435A (zh) | 2004-12-27 | 2008-02-20 | 阿斯利康(瑞典)有限公司 | 作为代谢型谷氨酸受体激动剂用于治疗神经病学及精神病学病症的吡唑酮化合物 |
| EP1836179B1 (fr) | 2004-12-30 | 2015-05-06 | Janssen Pharmaceutica NV | Dérivés amides de l'acide pipéridine- et pipérazine-1-carboxylique et composés similaires en tant que modulateurs d'hydrolase d'amide d'acide gras (faah) pour le traitement de l'anxiété, de la douleur et des outres états |
| AU2005324024B2 (en) | 2005-01-07 | 2011-02-17 | F. Hoffmann-La Roche Ag | [4-(Heteroaryl) piperazin-1-yl]-(2,5-substituted -phenyl)methanone derivatives as glycine transporter 1 (GlyT-1) inhibitors for the treatment of neurological and neuropsychiatric disorders |
| GT200600046A (es) | 2005-02-09 | 2006-09-25 | Terapia de combinacion | |
| JO2787B1 (en) | 2005-04-27 | 2014-03-15 | امجين إنك, | Alternative amide derivatives and methods of use |
| WO2006125181A2 (fr) | 2005-05-19 | 2006-11-23 | Xenon Pharmaceuticals Inc. | Derives piperidiniques: utilisation comme agents therapeutiques |
| WO2006125179A1 (fr) | 2005-05-19 | 2006-11-23 | Xenon Pharmaceuticals Inc. | Composes tricycliques: utilisation comme agents therapeutiques |
| WO2007046868A2 (fr) | 2005-05-19 | 2007-04-26 | Xenon Pharmaceuticals Inc. | Derives de thiazolidine et leurs utilisations en tant qu’agents therapeutiques |
| WO2007044085A2 (fr) | 2005-05-19 | 2007-04-19 | Xenon Pharmaceuticals Inc. | Composes heteroaryle et leurs utilisations en tant qu'agents therapeutiques |
| WO2006125194A2 (fr) | 2005-05-19 | 2006-11-23 | Xenon Pharmaceuticals Inc. | Derives de piperazine et leurs utilisations en tant qu'agents therapeutiques |
| BRPI0611187A2 (pt) | 2005-06-03 | 2010-08-24 | Xenon Pharmaceuticals Inc | derivados aminotiazàis como inibidores da estearoil-coa desaturase humana |
| CA2610196A1 (fr) | 2005-06-09 | 2006-12-14 | Merck Frosst Canada Ltd. | Derives d'azacyclohexane comme inhibiteurs de la stearoyl-coenzyme a delta-9 desaturase |
| US20090118296A1 (en) | 2005-07-20 | 2009-05-07 | Merck Frosst Canada Ltd. | Heteroaromatic Compounds As Inhibitors Of Stearoyl-Coenzyme A Delta-9 Desaturase |
| EP1951731A4 (fr) | 2005-11-15 | 2010-07-07 | Merck Frosst Canada Ltd | Dérivés d'azacyclohexane en tant qu'inhibiteurs de la stéaroyl-coenzyme a delta-9 désaturase |
| WO2007076055A2 (fr) | 2005-12-22 | 2007-07-05 | Entremed, Inc. | Compositions et methodes comprenant l'utilisation d'antagonistes du recepteur active par des proteases |
| MX2008008529A (es) | 2005-12-29 | 2008-09-26 | Organon Nv | Inhibidores de amida hidrolasa de acido graso. |
| PE20071221A1 (es) | 2006-04-11 | 2007-12-14 | Arena Pharm Inc | Agonistas del receptor gpr119 en metodos para aumentar la masa osea y para tratar la osteoporosis y otras afecciones caracterizadas por masa osea baja, y la terapia combinada relacionada a estos agonistas |
| WO2007136746A2 (fr) | 2006-05-19 | 2007-11-29 | Xenon Pharmaceuticals Inc. | Composés macrocycliques et leurs utilisations en tant qu'agents thérapeutiques |
| WO2007134457A1 (fr) | 2006-05-22 | 2007-11-29 | Merck Frosst Canada Ltd. | Dérivés d'amines cycliques en tant qu'inhibiteurs de la stéaroyl-coenzyme a delta-9-désaturase |
| CL2007001597A1 (es) | 2006-06-05 | 2008-05-16 | Novartis Ag Xenon Pharmaceutic | Compuestos derivados de 2-oxo-piridin-1(2h)-il-tiazol, imidazol o tiofen-carboxamida; composicion farmaceutica; y uso para el tratamiento de una enfermedad mediada por la estearoil-coa-desaturasa, tal como sindrome metabolico, hipertension y diabetes |
| CA2654792A1 (fr) | 2006-06-12 | 2007-12-21 | Merck Frosst Canada Ltd. | Derives d'azetidine comme inhibiteurs de la stearoyl-coenzyme a delta-9 desaturase |
| JP2009539885A (ja) | 2006-06-13 | 2009-11-19 | メルク フロスト カナダ リミテツド | ステアロイルコエンザイムaデルタ−9デサチュラーゼの阻害剤としてのアザシクロペンタン誘導体 |
| US20080280891A1 (en) | 2006-06-27 | 2008-11-13 | Locus Pharmaceuticals, Inc. | Anti-cancer agents and uses thereof |
| WO2008003753A1 (fr) | 2006-07-07 | 2008-01-10 | Biovitrum Ab (Publ) | Analogues de pyrazolo [1,5-a] pyrimidine utilisables comme inhibiteurs de l'activité stéaroyl-coa désaturase (scd) |
| JP2009543802A (ja) | 2006-07-11 | 2009-12-10 | エモリー・ユニバーシテイ | 医学的疾患の治療のためのジアジン及びトリアジン構造を含むcxcr4アンタゴニスト |
| WO2008008852A2 (fr) | 2006-07-11 | 2008-01-17 | Emory University | Antagonistes de cxcr4 comprenant des hétéroatomes pour le traitement de troubles médicaux |
| WO2008008059A1 (fr) | 2006-07-12 | 2008-01-17 | Locus Pharmaceuticals, Inc. | Agents anti-cancer et leurs utilisations |
| WO2008017161A1 (fr) | 2006-08-09 | 2008-02-14 | Merck Frosst Canada Ltd. | Dérivés d'azacycloalcane en tant qu'inhibiteurs de la stéaroyl-coenzyme a delta-9 désaturase |
| WO2008127349A2 (fr) | 2006-08-15 | 2008-10-23 | Novartis Ag | Composés organiques |
| WO2008024139A2 (fr) | 2006-08-18 | 2008-02-28 | N.V. Organon | Inhibiteurs d'hydrolase des amides d'acides gras |
| WO2008023720A1 (fr) | 2006-08-23 | 2008-02-28 | Astellas Pharma Inc. | COMPOSÉ D'URÉE OU SEL DUDIT COMPOSé |
| RU2009110254A (ru) | 2006-08-24 | 2010-09-27 | Новартис АГ (CH) | Производные 2-(пиразин-2-ил)тиазола и 2-(1н-пиразол-3-ил)тиразола и связанные с ним соединения в качестве ингибиторов стеароил-соа десатуразы для лечения метаболических, сердечно-сосудистых и других нарушений |
| WO2008029266A1 (fr) | 2006-09-08 | 2008-03-13 | Glenmark Pharmaceuticals S.A. | Inhibiteurs de la stéaroyl coa désaturase |
| CN101516877B (zh) | 2006-09-22 | 2013-09-11 | 诺瓦提斯公司 | 杂环有机化合物 |
| CN101522676A (zh) | 2006-10-05 | 2009-09-02 | Cv医药有限公司 | 用作硬脂酰-CoA脱氢酶抑制剂的双环含氮杂环化合物 |
| US7893066B2 (en) | 2006-10-05 | 2011-02-22 | Gilead Palo Alto, Inc. | Pyridol[2,3-B]pyrazinones for use as stearoyl CoA desaturase inhibitors |
| WO2008044767A1 (fr) * | 2006-10-13 | 2008-04-17 | Takeda Pharmaceutical Company Limited | Dérivé d'amine aromatique et utilisation de celui-ci |
| AU2007312866A1 (en) | 2006-10-20 | 2008-04-24 | Merck Frosst Canada Ltd. | Azacycloalkane derivatives as inhibitors of stearoyl-coenzyme A delta-9 desaturase |
| WO2008057280A1 (fr) | 2006-10-27 | 2008-05-15 | Amgen Inc. | Composés à cycles multiples et procédés d'utilisation |
| WO2008056687A1 (fr) | 2006-11-09 | 2008-05-15 | Daiichi Sankyo Company, Limited | Nouveau dérivé de spiropipéridine |
| JP2010510201A (ja) | 2006-11-20 | 2010-04-02 | グレンマーク・ファーマシューティカルズ・エスエー | ステアリン酸CoA脱飽和酵素阻害剤としてのアセチレン誘導体 |
| BRPI0719379A2 (pt) * | 2006-11-24 | 2014-02-11 | Ac Immune Sa | Composto, composição farmacêutica, uso de composto, mistura, métodos para coletar dados para o diagnóstico de uma doença ou condição associada com amilóide em uma amostra ou um paciente, para determinar a extensão da carga de placa amiloidogênica em um tecido e/ou um fluido corporal, para coletar dados para determinar a predisposição a uma doença ou condição associada com amilóide em um paciente, para coletar dados para monitorar a doença residual mínima em um paciente seguindo o tratamento com um anticorpo ou uma composição de vacina e para coletar dados para predizer a responsividade de um paciente sendo tratado com um anticorpo ou uma composição de vacina, e, kit de teste |
| CN101589039B (zh) | 2006-12-01 | 2012-09-05 | 默克弗罗斯特加拿大有限公司 | 作为硬脂酰辅酶a △-9去饱和酶抑制剂的氮杂环烷衍生物 |
| TW200826936A (en) | 2006-12-01 | 2008-07-01 | Merck Frosst Canada Ltd | Azacycloalkane derivatives as inhibitors of stearoyl-coenzyme a delta-9 desaturase |
| CN101562977A (zh) | 2006-12-15 | 2009-10-21 | 艾博特公司 | 新的二唑化合物 |
| EP2121671A1 (fr) | 2006-12-20 | 2009-11-25 | Novartis AG | Hétérocycles à 5 chaînons substitués en position 2 comme inhibiteurs de scd |
| GB0625604D0 (en) | 2006-12-21 | 2007-01-31 | Smithkline Beecham Corp | Compounds |
| GB0625594D0 (en) | 2006-12-21 | 2007-01-31 | Smithkline Beecham Corp | Compounds |
| GB0625654D0 (en) | 2006-12-21 | 2007-01-31 | Smithkline Beecham Corp | Compounds |
| AU2007336781C1 (en) | 2006-12-21 | 2014-10-09 | Sloan-Kettering Institute For Cancer Research | Pyridazinones and furan-containing compounds |
| GB0625605D0 (en) | 2006-12-21 | 2007-01-31 | Smithkline Beecham Corp | Compounds |
| AR064965A1 (es) | 2007-01-26 | 2009-05-06 | Merck Frosst Canada Inc | Derivados de azacicloalcanos como inhibidores de estearoil - coenzima a delta -9 desaturasa |
| US8575167B2 (en) | 2007-02-06 | 2013-11-05 | Takeda Pharmaceutical Company Limited | Spiro compounds having stearoyl-CoA desaturase action |
| US20100120669A1 (en) | 2007-02-28 | 2010-05-13 | Anne Marie Jeanne Bouillot | Thiadiazole derivatives, inhibitors of stearoyl-coa desaturase |
| EP2137187A1 (fr) | 2007-03-28 | 2009-12-30 | Inovacia AB | Pyrazolo [1,5-a]pyrimidines utilisés comme inhibiteurs de la stéaroyl-coa désaturase |
| WO2008123469A1 (fr) * | 2007-03-30 | 2008-10-16 | Japan Tobacco Inc. | Composé amide à six chaînons et son utilisation |
| WO2008120759A1 (fr) | 2007-03-30 | 2008-10-09 | Japan Tobacco Inc. | Composé d'urée et son utilisation |
| WO2008120744A1 (fr) | 2007-03-30 | 2008-10-09 | Japan Tobacco Inc. | Composé d'amide cyclique à cinq chaînons et son utilisation |
| JP2010523653A (ja) | 2007-04-09 | 2010-07-15 | ギリアード・パロ・アルト・インコーポレイテッド | ステアロイルCoAデサチュラーゼのインヒビターとして使用するためのプテリジノン誘導体 |
| US20080255161A1 (en) | 2007-04-11 | 2008-10-16 | Dmitry Koltun | 3-HYDROQUINAZOLIN-4-ONE DERIVATIVES FOR USE AS STEAROYL CoA DESATURASE INHIBITORS |
| CA2683948A1 (fr) | 2007-04-20 | 2008-10-30 | Merck Frosst Canada Ltd. | Nouveaux composes heteroaromatiques comme inhibiteurs de la stearoyl-coenzyme a delta-9 desaturase |
| WO2008139845A1 (fr) | 2007-04-24 | 2008-11-20 | Daiichi Sankyo Company, Limited | Nouveau dérivé amide |
| US20100152208A1 (en) | 2007-05-23 | 2010-06-17 | Merck Frosst Canada Ltd. | Bicyclic heteroaromatic compounds as inhibitors of stearoyl-coenzyme a delta-9 desaturase |
| US7842696B2 (en) | 2007-06-21 | 2010-11-30 | Forest Laboratories Holdings Limited | Piperazine derivatives as inhibitors of stearoyl-CoA desaturase |
| JP2009019013A (ja) | 2007-07-12 | 2009-01-29 | Daiichi Sankyo Co Ltd | 新規ヘテロアリールピペリジン誘導体 |
| GB0714129D0 (en) | 2007-07-19 | 2007-08-29 | Smithkline Beecham Corp | compounds |
| JP2010533658A (ja) | 2007-07-20 | 2010-10-28 | メルク フロスト カナダ リミテツド | ステアロイル補酵素aデルタ−9デサチュラーゼ阻害剤としての二環性へテロ芳香族化合物 |
| GB0715055D0 (en) | 2007-08-02 | 2007-09-12 | Smithkline Beecham Corp | Compounds |
| ES2352098T3 (es) | 2007-08-08 | 2011-02-15 | Graceway Pharmaceuticals, Llc | Derivado de fenoxi-pirrolidina y su uso y composiciones. |
| DE602008005894D1 (de) | 2007-08-14 | 2011-05-12 | Bayer Schering Pharma Ag | Kondensierte imidazole zur krebsbehandlung |
| WO2009037542A2 (fr) | 2007-09-20 | 2009-03-26 | Glenmark Pharmaceuticals, S.A. | Composés spirocycliques en tant qu'inhibiteurs de stéaroyle coa désaturase |
| CA2697551C (fr) | 2007-09-20 | 2013-03-12 | Irm Llc | Composes et compositions en tant que modulateurs de l'activite de gpr119 |
| GB0721419D0 (en) * | 2007-10-31 | 2007-12-12 | Smithkline Beecham Corp | Compounds |
| GB0722077D0 (en) | 2007-11-09 | 2007-12-19 | Smithkline Beecham Corp | Compounds |
| GB0722075D0 (en) | 2007-11-09 | 2007-12-19 | Smithkline Beecham Corp | Compounds |
| WO2009070533A1 (fr) | 2007-11-29 | 2009-06-04 | Complegen, Inc. | Procédés d'inhibition de stéaroyle-coa désaturase |
| AU2008334705B2 (en) | 2007-12-11 | 2011-06-16 | F. Hoffmann-La Roche Ag | Inhibitors of stearoyl-CoA desaturase |
| WO2009073973A1 (fr) | 2007-12-11 | 2009-06-18 | Merck Frosst Canada Ltd. | Nouveaux composés hétéroaromatiques en tant qu'inhibiteurs de la coenzyme stéaroyle a delta-9 désaturase |
| US8642660B2 (en) | 2007-12-21 | 2014-02-04 | The University Of Rochester | Method for altering the lifespan of eukaryotic organisms |
| ES2387714T3 (es) | 2007-12-28 | 2012-09-28 | Wisconsin Alumni Research Foundation | Análogos de 2-metilen-20-metil-19,24,25,26,27-pentanor-vitamina D |
| KR101584826B1 (ko) | 2008-02-20 | 2016-01-18 | 노파르티스 아게 | 스테아로일-CoA 데새투라제의 헤테로시클릭 억제제 |
| JP5523352B2 (ja) * | 2008-02-28 | 2014-06-18 | バーテックス ファーマシューティカルズ インコーポレイテッド | Cftr修飾因子としてのへテロアリール誘導体 |
| NZ588634A (en) | 2008-03-20 | 2012-03-30 | Forest Lab Holdings Ltd | Novel piperazine derivatives as inhibitors of stearoyl-coa desaturase |
| KR20100134680A (ko) | 2008-03-20 | 2010-12-23 | 포레스트 래보러토리즈 홀딩스 리미티드 | 스테아로일-coa 불포화효소의 저해물질로서 신규한 피페리딘 유도체 |
| DK2615085T3 (en) * | 2008-03-31 | 2015-10-05 | Vertex Pharma | Pyridyl derivatives as CFTR modulators |
| JP2011516498A (ja) | 2008-04-04 | 2011-05-26 | ギリアード サイエンシーズ, インコーポレイテッド | ステアロイル−CoAデサチュラーゼの阻害剤として使用するためのトリアゾロピリジノン誘導体 |
| CA2719362A1 (fr) | 2008-04-04 | 2009-10-08 | Gilead Sciences, Inc. | Derives de pyrrolotriazinone pouvant etre utilises a titre d'inhibiteurs de stearoyl-coa desaturase |
| JP2011516494A (ja) | 2008-04-07 | 2011-05-26 | ギリアード サイエンシーズ, インコーポレイテッド | ステアロイル−CoAデサチュラーゼの阻害剤として使用するための2H−ベンゾ[b][1,4]オキサジン−3(4H)−オン誘導体 |
| EP2279177A1 (fr) | 2008-04-22 | 2011-02-02 | Merck Frosst Canada Ltd. | Nouveaux composés hétéroaromatiques substitués en tant qu inhibiteurs de la stéaroyl-coenzyme a delta-9 désaturase |
| GB0810913D0 (en) | 2008-06-13 | 2008-07-23 | Smithkline Beecham Corp | Comppounds |
| US8822513B2 (en) | 2010-03-01 | 2014-09-02 | Gtx, Inc. | Compounds for treatment of cancer |
| US9447049B2 (en) | 2010-03-01 | 2016-09-20 | University Of Tennessee Research Foundation | Compounds for treatment of cancer |
| MX2010014572A (es) | 2008-06-27 | 2011-03-24 | Novartis Ag | Compuestos organicos. |
| TWI434842B (zh) | 2008-07-14 | 2014-04-21 | Astellas Pharma Inc | Azole compounds |
| FR2933979B1 (fr) | 2008-07-15 | 2012-08-24 | Pf Medicament | Derives de triazines et uraciles, leur preparation et leur application en therapeutique humaine |
| WO2010007482A2 (fr) | 2008-07-16 | 2010-01-21 | Glenmark Pharmaceuticals S.A. | Dérivés de thiazole en tant qu’inhibiteurs de stéaroyl-coa désaturase |
| GB0813740D0 (en) | 2008-07-28 | 2008-09-03 | Angeletti P Ist Richerche Biologica | Therapeutic compounds |
| JP2010043052A (ja) | 2008-08-18 | 2010-02-25 | Mitsubishi Chemicals Corp | カロテノイド類の分離方法 |
| WO2010022055A2 (fr) | 2008-08-20 | 2010-02-25 | Amgen Inc. | Inhibiteurs de canaux sodiques sensibles au potentiel |
| JP2012501975A (ja) | 2008-09-08 | 2012-01-26 | メルク カナダ インコーポレイテッド | ステアロイルコエンザイムAδ−9デサチュラーゼの阻害剤としての芳香族複素環化合物 |
| WO2010028761A1 (fr) | 2008-09-09 | 2010-03-18 | Sanofi-Aventis | Dérivés de 2-hétéro-aryl-pyrrolo[3, 4-c]pyrrol et leur utilisation en tant qu'inhibiteurs de scd |
| WO2010039186A2 (fr) | 2008-09-23 | 2010-04-08 | Renovis, Inc. | Composés utiles en tant que modulateurs de la faah et leurs utilisations |
| US20110184027A1 (en) | 2008-09-25 | 2011-07-28 | Glenmark Pharmaceuticals S.A. | Tissue selective stearoyl-coa desaturase 1 inhibitors and cell based screening assay for their identification |
| WO2010037225A1 (fr) | 2008-10-02 | 2010-04-08 | Merck Frosst Canada Ltd. | Composés hétéroaromatiques en tant qu'inhibiteurs de la stéaroyl-coenzyme a delta-9 désaturase |
| CA2740389A1 (fr) | 2008-10-15 | 2010-05-20 | Gilead Sciences, Inc. | Derives de 3-hydroquinazoline-4-one utilises comme inhibiteurs de stearyl-acp desaturase |
| US20100267752A1 (en) | 2008-10-15 | 2010-10-21 | Gilead Palo Alto, Inc. | 3-HYDROQUINAZOLIN-4-ONE DERIVATIVES FOR USE AS STEAROYL CoA DESATURASE INHIBITORS |
| US20100267748A1 (en) | 2008-10-15 | 2010-10-21 | Gilead Palo Alto, Inc. | HETEROCYCLIC COMPOUNDS USEFUL AS STEAROYL CoA DESATURASE INHIBITORS |
| EP2350054A4 (fr) | 2008-10-17 | 2012-03-28 | Merck Canada Inc | Dérivés d'azétidine comme inhibiteurs de la stéaroyl-coenzyme a delta-9 désaturase |
| WO2010048149A2 (fr) | 2008-10-20 | 2010-04-29 | Kalypsys, Inc. | Modulateurs hétérocycliques de gpr119 pour le traitement d'une maladie |
| GB0821307D0 (en) | 2008-11-21 | 2008-12-31 | Summit Corp Plc | Compounds for treatment of duchenne muscular dystrophy |
| EP2192196A1 (fr) | 2008-11-27 | 2010-06-02 | Helmholtz Zentrum München Deutsches Forschungszentrum für Gesundheit und Umwelt (GmbH) | Prédiction de susceptibilités physiologiques associées au métabotype de lipide |
| US20100160323A1 (en) | 2008-12-23 | 2010-06-24 | Alexander Bischoff | NOVEL PIPERAZINE DERIVATIVES AS INHIBITORS OF STEAROYL-CoA DESATURASE |
| WO2010094120A1 (fr) | 2009-02-17 | 2010-08-26 | Merck Frosst Canada Ltd. | Nouveaux composés spiro utiles comme inhibiteurs de la stéaroyl-coenzyme a delta-9 désaturase |
| JP2012518603A (ja) | 2009-02-23 | 2012-08-16 | メルク カナダ インコーポレイテッド | ステアロイル−コエンザイムaデルタ−9デサチュラーゼの阻害剤としての複素環誘導体 |
| US8901306B2 (en) | 2009-03-02 | 2014-12-02 | Stemsynergy Therapeutics, Inc. | Methods and compositions useful in treating cancer and reducing Wnt mediated effects in a cell |
| US20120010186A1 (en) | 2009-03-23 | 2012-01-12 | Merck Frosst Canada Ltd. | Heterocyclic compounds as inhibitors of stearoyl-coenzyme a delta-9 desaturase |
| EP2414366A1 (fr) | 2009-04-01 | 2012-02-08 | Novartis AG | Dérivés spiro pour la modulation de la stéaroyl-coa désaturase |
| US20120220567A1 (en) | 2009-07-23 | 2012-08-30 | Shipps Jr Gerald W | Benzo-fused oxazepine compounds as stearoyl-coenzyme a delta-9 desaturase inhibitors |
| WO2011011506A1 (fr) | 2009-07-23 | 2011-01-27 | Schering Corporation | Composés oxazépine spirocyclique en tant qu'inhibiteurs de la stéaroyl-coenzyme a delta-9 désaturase |
| WO2011011872A1 (fr) | 2009-07-28 | 2011-02-03 | Merck Frosst Canada Ltd. | Nouveaux composés spiro utiles en tant qu'inhibiteurs de la stéaroyl-coenzyme a delta-9 désaturase |
| FR2948939B1 (fr) | 2009-08-05 | 2013-03-22 | Pf Medicament | Derives de 2h pyridazin-3-ones, leur preparation et leur application en therapeutique humaine |
| US8354403B2 (en) | 2009-08-27 | 2013-01-15 | Merck Sharp & Dohme Corp. | Pyrrolidine derived beta 3 adrenergic receptor agonists |
| RU2569063C2 (ru) | 2009-09-01 | 2015-11-20 | Катабэйсис Фармасьютикалз, Инк. | Конъюгаты жирных кислот и ниацина и их применение |
| EP2475367A1 (fr) | 2009-09-10 | 2012-07-18 | Centre National De La Recherche Scientifique | Nouveaux inhibiteurs de stearoyl-coa-desaturase-1 et leurs utilisations |
| EP2483264A1 (fr) | 2009-10-01 | 2012-08-08 | Novartis AG | Dérivés de pyrazole qui modulent la stéaroyl-coa désaturase |
| WO2011047481A1 (fr) | 2009-10-23 | 2011-04-28 | Merck Frosst Canada Ltd. | Nouveaux composés spiro utiles en tant qu'inhibiteurs de stéaroyl-coenzyme a delta-9 désaturase |
| BR112012015248B1 (pt) | 2009-12-23 | 2022-01-04 | Jasco Pharmaceuticals, LLC | Composto |
| KR101939704B1 (ko) | 2010-03-01 | 2019-01-17 | 지티엑스, 인코포레이티드 | 암 치료용 화합물 |
| WO2011123681A1 (fr) | 2010-03-31 | 2011-10-06 | Rigel Pharmaceuticals, Inc. | Procédés d'utilisation de composés de carboxamides, sulfonamides et amines |
| WO2012046681A1 (fr) | 2010-10-04 | 2012-04-12 | 興和株式会社 | Agent capable d'inhiber l'expression d'un arnm lié au métabolisme lipidique |
| FR2958935B1 (fr) | 2010-04-19 | 2012-06-22 | Pf Medicament | Derives d'heterocycles azotes, leur preparation et leur application en therapeutique humaine |
| EP2582681A1 (fr) | 2010-06-17 | 2013-04-24 | Novartis AG | Dérivés de 1,3 dihydro-benzoimidazol-2-ylidène-amine à substitution pipéridinyle |
| US20130259830A1 (en) | 2010-07-12 | 2013-10-03 | Ironwood Pharmaceuticals, Inc. | Crth2 modulators |
| WO2012016133A2 (fr) | 2010-07-29 | 2012-02-02 | President And Fellows Of Harvard College | Inhibiteurs de la ros1 kinase pour le traitement de glioblastome et d'autres cancers déficients en p53 |
| KR101764952B1 (ko) | 2010-07-29 | 2017-08-03 | 리겔 파마슈티칼스, 인크. | Ampk-활성화 헤테로시클릭 화합물 및 그의 사용 방법 |
| CA2812081A1 (fr) | 2010-09-13 | 2012-03-22 | Novartis Ag | Triazine-oxadiazoles |
| WO2012066077A1 (fr) | 2010-11-18 | 2012-05-24 | Prosidion Limited | Dérivés 1,4 di substitués pyrolidine-3-yl-amine et leur utilisation pour le traitement de troubles métaboliques |
| GB201114389D0 (en) | 2011-08-22 | 2011-10-05 | Prosidion Ltd | Novel compounds |
| EP2455081A1 (fr) | 2010-11-23 | 2012-05-23 | Almirall, S.A. | Agonistes de récepteur S1P1 à utiliser dans le traitement de la maladie de Crohn |
| EP2455080A1 (fr) | 2010-11-23 | 2012-05-23 | Almirall, S.A. | Agonistes de récepteur S1P1 à utiliser dans le traitement de la sclérose en plaques |
| GB201021103D0 (en) | 2010-12-13 | 2011-01-26 | Univ Leuven Kath | New compounds for the treatment of neurodegenerative diseases |
| US20140031547A1 (en) | 2010-12-14 | 2014-01-30 | Electrophoretics Limited | CASEIN KINASE 1delta (CK 1delta) INHIBITORS AND THEIR USE IN THE TREATMENT OF NEURODE-GENERATIVE DISEASES SUCH AS TAUOPATHIES |
| EP2651930B1 (fr) * | 2010-12-16 | 2015-10-28 | Boehringer Ingelheim International GmbH | Inhibiteurs biarylamide de production de leukotriènes |
| US8853213B2 (en) | 2011-01-03 | 2014-10-07 | Hanmi Pharm. Co., Ltd | Bicyclic compound for modulating G protein-coupled receptors |
| US8822471B2 (en) | 2011-03-14 | 2014-09-02 | Boehringer Ingelheim International Gmbh | Compounds, pharmaceutical compositions and uses thereof |
| EP2694482A1 (fr) | 2011-04-04 | 2014-02-12 | Siena Biotech S.p.A. | Antagonistes de la voie wnt |
| CA2833507A1 (fr) | 2011-06-07 | 2012-12-13 | Dainippon Sumitomo Pharma Co., Ltd. | Derive d'indazole et pyrrolopyridine et utilisation pharmaceutique de celui-ci |
| US20120316182A1 (en) * | 2011-06-10 | 2012-12-13 | Calcimedica, Inc. | Compounds that modulate intracellular calcium |
| ES2540956T3 (es) | 2011-07-01 | 2015-07-15 | Remynd Nv | Derivados de 1,2,4-tiadiazol-5-ilpiperazina útiles en el tratamiento de enfermedades neurodegenerativas |
| BR112014003963A2 (pt) | 2011-09-01 | 2017-03-21 | Irm Llc | compostos e composições como inibidores de quinase c-kit |
| AU2012313888B2 (en) | 2011-09-27 | 2016-03-31 | Novartis Ag | 3-pyrimidin-4-yl-oxazolidin-2-ones as inhibitors of mutant IDH |
| MX2014004426A (es) | 2011-10-15 | 2014-07-09 | Genentech Inc | Metodos de uso de antagonistas de scd1. |
| WO2013070660A1 (fr) | 2011-11-07 | 2013-05-16 | Emory University | Composés contenant des acides aminés tricycliques pour le traitement ou la prévention de symptômes associés à un dysfonctionnement endocrinien |
| WO2013085957A1 (fr) | 2011-12-06 | 2013-06-13 | Janssen Pharmaceutica Nv | Dérivés de pipéridinyl-pyridazinyle substitué utiles comme inhibiteurs de scd 1 |
| US9238658B2 (en) | 2011-12-06 | 2016-01-19 | Janssen Pharmaceutica Nv | Substituted piperidinyl-carboxamide derivatives useful as SCD 1 inhibitors |
| US8530461B2 (en) | 2011-12-29 | 2013-09-10 | Boehringer Ingelheim International Gmbh | Azetidine derivatives |
| US20130225529A1 (en) | 2012-02-27 | 2013-08-29 | Basil Rigas | Phospho-ester derivatives and uses thereof |
| US9233102B2 (en) | 2012-03-07 | 2016-01-12 | Mayo Foundation For Medical Education And Research | Methods and materials for treating cancer |
| US20150290265A1 (en) | 2012-04-23 | 2015-10-15 | Piramal Enterprises Limited | Composition for treating metabolic disorders |
| WO2013170072A2 (fr) | 2012-05-09 | 2013-11-14 | Neurop, Inc. | Composés pour le traitement de troubles neurologiques |
| WO2013175474A2 (fr) | 2012-05-22 | 2013-11-28 | Yissum Research Development Company Of The Hebrew University Of Jerusalem Ltd. | Inhibiteurs sélectifs de cellules indifférenciées |
| WO2014003153A1 (fr) | 2012-06-28 | 2014-01-03 | 協和発酵キリン株式会社 | Composé amide substitué |
| US20140073634A1 (en) | 2012-08-24 | 2014-03-13 | Institute For Applied Cancer Science/The University of Texas MD Anderson Cancer Center | Heterocyclic modulators of hif activity for treatment of disease |
| AU2013328301A1 (en) | 2012-10-10 | 2015-05-28 | Actelion Pharmaceuticals Ltd | Orexin receptor antagonists which are [ortho bi (hetero-)aryl]-[2-(meta bi (hetero-)aryl)-pyrrolidin-1-yl]-methanone derivatives |
| WO2014065860A1 (fr) * | 2012-10-24 | 2014-05-01 | The General Hospital Corporation | Composés 1,2,4,5-tétrazines fonctionnalisés destinés à être utilisés dans des réactions de couplage bioorthogonaux |
| WO2014086704A1 (fr) | 2012-12-03 | 2014-06-12 | F. Hoffmann-La Roche Ag | Composés d'amide d'isoxazole substitués en tant qu'inhibiteurs de stéaroyl-coa désaturase 1 (scd1) |
| CN104822420A (zh) | 2012-12-03 | 2015-08-05 | 霍夫曼-拉罗奇有限公司 | 作为scd1的抑制剂的取代的异噁唑胺类化合物 |
| JP2016028016A (ja) | 2012-12-12 | 2016-02-25 | 大日本住友製薬株式会社 | オキサジアゾール誘導体とその医薬用途 |
| US9416102B2 (en) | 2013-01-23 | 2016-08-16 | Wisconsin Alumni Research Foundation | (22E)-2-methylene-22-dehydro-1α,24,25-trihydroxy-19-nor-vitamin D3 analogs |
| TWI594975B (zh) * | 2013-04-24 | 2017-08-11 | 第一三共股份有限公司 | 二羧酸化合物 |
| KR101524650B1 (ko) | 2013-07-30 | 2015-06-03 | 경상대학교산학협력단 | 테트라하이드로이소퀴놀린 알칼로이드계 화합물 ys-51s를 포함하는 대사성 질환의 예방 및 치료용 조성물 |
| KR20150015305A (ko) | 2013-07-31 | 2015-02-10 | 안동대학교 산학협력단 | 주박 추출물을 유효성분으로 함유하는 비만의 예방 또는 치료용 약학적 조성물 및 건강 기능 식품 |
| US20150087673A1 (en) | 2013-09-26 | 2015-03-26 | Rigel Pharmaceuticals, Inc. | Methods for using and biomarkers for ampk-activating compounds |
| US9840493B2 (en) * | 2013-10-11 | 2017-12-12 | Sutro Biopharma, Inc. | Modified amino acids comprising tetrazine functional groups, methods of preparation, and methods of their use |
| CN104163794A (zh) | 2013-10-17 | 2014-11-26 | 中国药科大学 | 2-氨基芳环类血管内皮生长因子受体(vegfr)抑制剂及其制备方法和用途 |
| CA2935103C (fr) | 2013-12-31 | 2018-08-28 | Xuanzhu Pharma Co., Ltd. | Inhibiteur kinase et son utilisation |
| CA2937989A1 (fr) | 2014-01-29 | 2015-08-06 | Bayer Pharma Aktiengesellschaft | Isothiazoles amino-substitues |
| GB201403969D0 (en) | 2014-03-06 | 2014-04-23 | Isis Innovation | Compounds for use in controlling body fat |
| US20170015654A1 (en) | 2014-03-12 | 2017-01-19 | Takeda Pharmaceutical Company Limited | Pyridazine compound |
| EP3119774A1 (fr) | 2014-03-17 | 2017-01-25 | reMynd NV | Composés d'oxadiazole |
| WO2016022626A1 (fr) | 2014-08-06 | 2016-02-11 | Merck Sharp & Dohme Corp. | Antagonistes hétérocycliques des récepteurs cgrp |
| EP4180041A1 (fr) | 2014-08-07 | 2023-05-17 | Mayo Foundation for Medical Education and Research | Composés et procédés pour le traitement du cancer |
| KR101715449B1 (ko) | 2014-08-13 | 2017-03-30 | 주식회사 큐리언트 | 염증성 질환 치료용 화합물 |
| EP3842514A1 (fr) | 2014-09-12 | 2021-06-30 | Whitehead Institute for Biomedical Research | Cellules exprimant l'apolipoprotéine e et leurs utilisations |
| US10662164B2 (en) | 2014-09-25 | 2020-05-26 | University Of Notre Dame Du Lac | Non-beta lactam antibiotics |
| EP3034500A1 (fr) | 2014-12-17 | 2016-06-22 | Genkyotex Sa | Dérivés d'amido-thiazole en tant qu'inhibiteurs d'oxydase NADPH |
| CN105753814A (zh) | 2015-01-01 | 2016-07-13 | 成都贝斯凯瑞生物科技有限公司 | 取代氮杂环衍生物及其应用 |
| US20160223559A1 (en) * | 2015-02-02 | 2016-08-04 | The Regents Of The University Of California | Tetrazine-containing compounds and synthetic methods thereof |
| EP3257510B1 (fr) | 2015-02-09 | 2021-10-20 | National University Corporation Okayama University | Inhibiteur de la lactate déshydrogénase et médicament antiépileptique le contenant |
| CN106146391A (zh) | 2015-04-15 | 2016-11-23 | 中国科学院上海药物研究所 | 5-芳香炔基取代的苯甲酰胺类化合物及其制备方法、药物组合物和用途 |
| US20180305334A1 (en) | 2015-10-14 | 2018-10-25 | Aquinnah Pharmaceuticals, Inc. | Compounds, compositions and methods of use against stress granules |
| US20200262799A1 (en) * | 2015-11-30 | 2020-08-20 | Universite De Bourgogne | Process for preparing functionalized 1,2,4,5-tetrazine compounds |
| JP7114076B2 (ja) | 2015-12-22 | 2022-08-08 | シャイ・セラピューティクス・エルエルシー | がん及び炎症性疾患の処置のための化合物 |
| KR20190015748A (ko) | 2016-06-08 | 2019-02-14 | 글락소스미스클라인 인털렉츄얼 프로퍼티 디벨로프먼트 리미티드 | Atf4 경로 억제제로서의 화학적 화합물 |
| US20190185567A1 (en) | 2016-08-01 | 2019-06-20 | Ignyta, Inc. | Combinations for the treatment of cancer |
| JP2019533022A (ja) | 2016-10-24 | 2019-11-14 | ユマニティ セラピューティクス,インコーポレーテッド | 化合物及びその使用 |
| US11135207B2 (en) | 2016-12-13 | 2021-10-05 | Centaurus Therapeutics | Inhibitors of dihydroceramide desaturase for treating disease |
| CA3049010A1 (fr) | 2017-01-06 | 2018-07-12 | Yumanity Therapeutics, Inc. | Methodes de traitement de troubles neurologiques |
| EP3589659B1 (fr) | 2017-02-28 | 2025-04-09 | Mayo Foundation for Medical Education and Research | Combinaisons pour utilisation dans le traitement du cancer |
| WO2018161033A1 (fr) | 2017-03-02 | 2018-09-07 | Wright, Adrian | Inhibiteurs ire1-alpha à petites molécules |
| EP3381908A1 (fr) | 2017-03-27 | 2018-10-03 | Leadiant Biosciences SA | Dérivés de benzazole 2-(4-(4-(bromo-methoxybenzamido)benzylamino)phényl) et leur utilisation comme anti-héparanase |
| WO2018195450A1 (fr) | 2017-04-21 | 2018-10-25 | Epizyme, Inc. | Thérapies d'association avec des inhibiteurs d'ehmt2 |
| WO2019018795A1 (fr) | 2017-07-20 | 2019-01-24 | Yumanity Therapeutics | Composés et utilisations de ces composés |
| CA3083000A1 (fr) | 2017-10-24 | 2019-05-02 | Yumanity Therapeutics, Inc. | Composes et utilisations de ces composes |
| EP3728200A1 (fr) | 2017-12-21 | 2020-10-28 | Gliapharm SA | Compositions et méthodes de traitement de troubles neurologiques notamment des maladies de motoneurones |
| JP2021507945A (ja) | 2017-12-21 | 2021-02-25 | グリアファーム エスエー | 認知症を含む神経障害のための組成物および治療方法 |
| KR20250057925A (ko) | 2018-01-11 | 2025-04-29 | 켄타우루스 테라퓨틱스 | 질병 치료를 위한 디하이드로세라마이드 불포화화효소의 저해제 |
| US12023332B2 (en) | 2018-03-05 | 2024-07-02 | Wylder Nation Foundation | Compositions and methods for activating signaling through the CB1 cannabinoid receptor for treating and preventing diseases and disorders characterized by abnormal cellular accumulation of sphingolipids such as sphingomyelin |
| CA3094527A1 (fr) | 2018-03-23 | 2019-09-26 | Yumanity Therapeutics, Inc. | Composes et leurs utilisations |
| US11243207B2 (en) | 2018-03-29 | 2022-02-08 | Mayo Foundation For Medical Education And Research | Assessing and treating cancer |
| WO2019209948A1 (fr) | 2018-04-25 | 2019-10-31 | Yumanity Therapeutics, Inc. | Composés et leurs utilisations |
| WO2019209962A1 (fr) | 2018-04-25 | 2019-10-31 | Yumanity Therapeutics, Inc. | Composés et leurs utilisations |
| MX2021000881A (es) | 2018-07-24 | 2021-06-08 | Epizyme Inc | Compuestos de piridin-2-ona utiles como antagonistas de smarca2. |
| WO2020132378A2 (fr) | 2018-12-22 | 2020-06-25 | Gliapharm Sa | Compositions et méthodes de traitement de troubles neurologiques comprenant la dépression |
| US12098146B2 (en) | 2019-01-24 | 2024-09-24 | Janssen Pharmaceutica Nv | Compounds and uses thereof |
| CN114174273A (zh) | 2019-03-22 | 2022-03-11 | 优曼尼蒂治疗公司 | 化合物和其用途 |
| CA3159766A1 (fr) | 2019-11-05 | 2021-05-14 | Dermira, Inc. | Antagonistes de mrgprx2 pour le traitement de troubles inflammatoires |
| CA3159628A1 (fr) | 2019-11-05 | 2021-05-14 | Dermira, Inc. | Antagonistes de mrgprx2 et leurs utilisations |
| EA202192047A1 (ru) | 2019-11-13 | 2021-12-08 | Юманити Терапьютикс, Инк. | Соединения и их применение |
| TW202136238A (zh) | 2020-01-06 | 2021-10-01 | 大陸商廣東東陽光藥業有限公司 | RORγt抑制劑及其製備方法和用途 |
| WO2021154571A1 (fr) | 2020-01-31 | 2021-08-05 | American Sterilizer Company | Tête de lumière chirurgicale avec étalement de faisceau et équilibrage de puissance réglable |
-
2019
- 2019-03-22 CA CA3094527A patent/CA3094527A1/fr active Pending
- 2019-03-22 SG SG11202009280RA patent/SG11202009280RA/en unknown
- 2019-03-22 KR KR1020207030056A patent/KR20210005593A/ko active Pending
- 2019-03-22 BR BR112020019191-4A patent/BR112020019191A2/pt unknown
- 2019-03-22 CN CN202410169808.6A patent/CN118084800A/zh active Pending
- 2019-03-22 AU AU2019238326A patent/AU2019238326B2/en not_active Expired - Fee Related
- 2019-03-22 EA EA202092225A patent/EA202092225A1/ru unknown
- 2019-03-22 JP JP2020551273A patent/JP7517992B2/ja active Active
- 2019-03-22 WO PCT/US2019/023737 patent/WO2019183587A1/fr not_active Ceased
- 2019-03-22 CN CN202410214688.7A patent/CN118084801A/zh active Pending
- 2019-03-22 CN CN201980034106.4A patent/CN112312913B/zh active Active
- 2019-03-22 MX MX2020009942A patent/MX2020009942A/es unknown
- 2019-03-22 MA MA052092A patent/MA52092A/fr unknown
- 2019-03-22 EP EP19771620.2A patent/EP3768269B1/fr active Active
- 2019-03-22 ES ES19771620T patent/ES3043183T3/es active Active
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2020
- 2020-09-22 IL IL277502A patent/IL277502A/en unknown
- 2020-09-22 US US17/028,778 patent/US12180221B2/en active Active
- 2020-09-23 MX MX2024000349A patent/MX2024000349A/es unknown
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2023
- 2023-12-15 JP JP2023211982A patent/JP2024037913A/ja active Pending
Also Published As
| Publication number | Publication date |
|---|---|
| EP3768269B1 (fr) | 2025-08-20 |
| CN112312913B (zh) | 2024-03-08 |
| US20220298168A1 (en) | 2022-09-22 |
| EP3768269C0 (fr) | 2025-08-20 |
| IL277502A (en) | 2020-11-30 |
| BR112020019191A2 (pt) | 2021-01-05 |
| EP3768269A4 (fr) | 2022-03-23 |
| JP7517992B2 (ja) | 2024-07-17 |
| WO2019183587A1 (fr) | 2019-09-26 |
| MX2020009942A (es) | 2021-01-08 |
| JP2021519263A (ja) | 2021-08-10 |
| CA3094527A1 (fr) | 2019-09-26 |
| KR20210005593A (ko) | 2021-01-14 |
| US12180221B2 (en) | 2024-12-31 |
| CN118084801A (zh) | 2024-05-28 |
| CN118084800A (zh) | 2024-05-28 |
| EP3768269A1 (fr) | 2021-01-27 |
| CN112312913A (zh) | 2021-02-02 |
| EA202092225A1 (ru) | 2021-02-09 |
| AU2019238326A1 (en) | 2020-10-15 |
| ES3043183T3 (en) | 2025-11-25 |
| MX2024000349A (es) | 2024-01-26 |
| SG11202009280RA (en) | 2020-10-29 |
| JP2024037913A (ja) | 2024-03-19 |
| AU2019238326B2 (en) | 2025-03-06 |
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