SG10201401169QA - Dihydroorotate dehydrogenase inhibitors - Google Patents
Dihydroorotate dehydrogenase inhibitorsInfo
- Publication number
- SG10201401169QA SG10201401169QA SG10201401169QA SG10201401169QA SG10201401169QA SG 10201401169Q A SG10201401169Q A SG 10201401169QA SG 10201401169Q A SG10201401169Q A SG 10201401169QA SG 10201401169Q A SG10201401169Q A SG 10201401169QA SG 10201401169Q A SG10201401169Q A SG 10201401169QA
- Authority
- SG
- Singapore
- Prior art keywords
- dehydrogenase inhibitors
- dihydroorotate dehydrogenase
- dihydroorotate
- inhibitors
- dehydrogenase
- Prior art date
Links
Classifications
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D209/00—Heterocyclic compounds containing five-membered rings, condensed with other rings, with one nitrogen atom as the only ring hetero atom
- C07D209/02—Heterocyclic compounds containing five-membered rings, condensed with other rings, with one nitrogen atom as the only ring hetero atom condensed with one carbocyclic ring
- C07D209/04—Indoles; Hydrogenated indoles
- C07D209/08—Indoles; Hydrogenated indoles with only hydrogen atoms or radicals containing only hydrogen and carbon atoms, directly attached to carbon atoms of the hetero ring
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P1/00—Drugs for disorders of the alimentary tract or the digestive system
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P1/00—Drugs for disorders of the alimentary tract or the digestive system
- A61P1/04—Drugs for disorders of the alimentary tract or the digestive system for ulcers, gastritis or reflux esophagitis, e.g. antacids, inhibitors of acid secretion, mucosal protectants
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P19/00—Drugs for skeletal disorders
- A61P19/02—Drugs for skeletal disorders for joint disorders, e.g. arthritis, arthrosis
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P25/00—Drugs for disorders of the nervous system
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P29/00—Non-central analgesic, antipyretic or antiinflammatory agents, e.g. antirheumatic agents; Non-steroidal antiinflammatory drugs [NSAID]
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P35/00—Antineoplastic agents
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P37/00—Drugs for immunological or allergic disorders
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P37/00—Drugs for immunological or allergic disorders
- A61P37/02—Immunomodulators
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P37/00—Drugs for immunological or allergic disorders
- A61P37/02—Immunomodulators
- A61P37/06—Immunosuppressants, e.g. drugs for graft rejection
-
- 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
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D235/00—Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, condensed with other rings
- C07D235/02—Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, condensed with other rings condensed with carbocyclic rings or ring systems
- C07D235/04—Benzimidazoles; Hydrogenated benzimidazoles
- C07D235/18—Benzimidazoles; Hydrogenated benzimidazoles with aryl radicals directly attached in position 2
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D401/00—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom
- C07D401/02—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing two hetero rings
- C07D401/04—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing two hetero rings directly linked by a ring-member-to-ring-member bond
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D401/00—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom
- C07D401/02—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing two hetero rings
- C07D401/10—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing two hetero rings linked by a carbon chain containing aromatic rings
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D401/00—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom
- C07D401/02—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing two hetero rings
- C07D401/12—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing two hetero rings linked by a chain containing hetero atoms as chain links
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D403/00—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00
- C07D403/02—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00 containing two hetero rings
- C07D403/04—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00 containing two hetero rings directly linked by a ring-member-to-ring-member bond
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D403/00—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00
- C07D403/02—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00 containing two hetero rings
- C07D403/10—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00 containing two hetero rings linked by a carbon chain containing aromatic rings
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D403/00—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00
- C07D403/02—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00 containing two hetero rings
- C07D403/12—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00 containing two hetero rings linked by a chain containing hetero atoms as chain links
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D409/00—Heterocyclic compounds containing two or more hetero rings, at least one ring having sulfur atoms as the only ring hetero atoms
- C07D409/02—Heterocyclic compounds containing two or more hetero rings, at least one ring having sulfur atoms as the only ring hetero atoms containing two hetero rings
- C07D409/10—Heterocyclic compounds containing two or more hetero rings, at least one ring having sulfur atoms as the only ring hetero atoms containing two hetero rings linked by a carbon chain containing aromatic rings
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D413/00—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms
- C07D413/02—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms containing two hetero rings
- C07D413/10—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms containing two hetero rings linked by a carbon chain containing aromatic rings
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D417/00—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
- C07D417/02—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
- C07D417/10—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 carbon chain containing aromatic rings
-
- 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
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Health & Medical Sciences (AREA)
- Pharmacology & Pharmacy (AREA)
- Life Sciences & Earth Sciences (AREA)
- Public Health (AREA)
- General Health & Medical Sciences (AREA)
- Animal Behavior & Ethology (AREA)
- Chemical Kinetics & Catalysis (AREA)
- General Chemical & Material Sciences (AREA)
- Medicinal Chemistry (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Veterinary Medicine (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Engineering & Computer Science (AREA)
- Immunology (AREA)
- Rheumatology (AREA)
- Neurosurgery (AREA)
- Neurology (AREA)
- Pain & Pain Management (AREA)
- Biomedical Technology (AREA)
- Orthopedic Medicine & Surgery (AREA)
- Physical Education & Sports Medicine (AREA)
- Transplantation (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Plural Heterocyclic Compounds (AREA)
- Heterocyclic Carbon Compounds Containing A Hetero Ring Having Nitrogen And Oxygen As The Only Ring Hetero Atoms (AREA)
- Nitrogen Condensed Heterocyclic Rings (AREA)
Applications Claiming Priority (3)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
IN696DE2009 | 2009-04-02 | ||
US17815609P | 2009-05-14 | 2009-05-14 | |
EP09160526 | 2009-05-18 |
Publications (1)
Publication Number | Publication Date |
---|---|
SG10201401169QA true SG10201401169QA (en) | 2014-05-29 |
Family
ID=54256941
Family Applications (2)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
SG10201401169QA SG10201401169QA (en) | 2009-04-02 | 2010-03-26 | Dihydroorotate dehydrogenase inhibitors |
SG2011055167A SG174125A1 (en) | 2009-04-02 | 2010-03-26 | Dihydroorotate dehydrogenase inhibitors |
Family Applications After (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
SG2011055167A SG174125A1 (en) | 2009-04-02 | 2010-03-26 | Dihydroorotate dehydrogenase inhibitors |
Country Status (11)
Country | Link |
---|---|
US (1) | US9006454B2 (en) |
EP (1) | EP2414328B1 (en) |
JP (1) | JP5680054B2 (en) |
CN (2) | CN104030987B (en) |
AR (1) | AR076183A1 (en) |
AU (1) | AU2010233917B2 (en) |
ES (1) | ES2882797T3 (en) |
MY (1) | MY159575A (en) |
NZ (1) | NZ595819A (en) |
SG (2) | SG10201401169QA (en) |
WO (1) | WO2010115736A2 (en) |
Families Citing this family (51)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
WO2013130370A2 (en) * | 2012-03-01 | 2013-09-06 | Merck Sharp & Dohme Corp. | Compounds as dgat-1 inhibitors |
MX2015000830A (en) * | 2012-07-18 | 2015-10-26 | Sunshine Lake Pharma Co Ltd | Nitrogenous heterocyclic derivatives and their application in drugs. |
KR101916443B1 (en) * | 2012-07-26 | 2018-11-08 | 글락소 그룹 리미티드 | 2-(azaindol-2-yl) benzimidazoles as pad4 inhibitors |
CN103087045B (en) * | 2013-01-11 | 2015-08-12 | 上海交通大学 | A kind of benzimidazole-like heterocyclic compound, medical composition and its use |
TWI644899B (en) | 2013-02-04 | 2018-12-21 | 健生藥品公司 | Flap modulators |
JP6424173B2 (en) * | 2013-02-04 | 2018-11-14 | ヤンセン ファーマシューティカ エヌ.ベー. | FLAP regulator |
RS57962B1 (en) * | 2013-02-25 | 2019-01-31 | Aurigene Discovery Tech Ltd | Trisubstituted benzotriazole derivatives as dihydroorotate oxygenase inhibitors |
TWI607995B (en) * | 2013-08-13 | 2017-12-11 | 廣東東陽光藥業有限公司 | Nitrogenous heterocyclic derivatives and their application in drugs |
CN103483237B (en) * | 2013-10-15 | 2015-04-08 | 安徽工业大学 | Method for preparing pyrrole derivatives by catalyzing double-sulfonate ionic liquid |
JP6703553B2 (en) * | 2015-05-21 | 2020-06-03 | グラクソスミスクライン、インテレクチュアル、プロパティー、ディベロップメント、リミテッドGlaxosmithkline Intellectual Property Development Limited | Benzimidazole derivatives as PAD4 inhibitors |
CN106397408B (en) * | 2015-07-30 | 2019-04-02 | 四川大学 | 5- methyl -2 (1H) Pyridione derivatives and its preparation method and application |
EP3365340B1 (en) | 2015-10-19 | 2022-08-10 | Incyte Corporation | Heterocyclic compounds as immunomodulators |
HRP20221035T1 (en) | 2015-11-19 | 2022-11-11 | Incyte Corporation | Heterocyclic compounds as immunomodulators |
WO2017102091A1 (en) | 2015-12-18 | 2017-06-22 | Bayer Pharma Aktiengesellschaft | Heteroarylbenzimidazole compounds |
PE20230731A1 (en) | 2015-12-22 | 2023-05-03 | Incyte Corp | HETEROCYCLIC COMPOUNDS AS IMMUNOMODULATORS |
AR108396A1 (en) | 2016-05-06 | 2018-08-15 | Incyte Corp | HETEROCYCLIC COMPOUNDS AS IMMUNOMODULATORS |
CN107375279B (en) * | 2016-05-17 | 2022-11-01 | 华东理工大学 | Use of novel thiazole derivatives for the treatment of inflammatory bowel disease |
EP3464279B1 (en) | 2016-05-26 | 2021-11-24 | Incyte Corporation | Heterocyclic compounds as immunomodulators |
WO2017207534A1 (en) | 2016-06-03 | 2017-12-07 | Bayer Pharma Aktiengesellschaft | Substituted heteroarylbenzimidazole compounds |
CN105878243B (en) * | 2016-06-14 | 2019-05-21 | 四川大学 | Application of the pirfenidone derivative in pharmacy |
TWI771305B (en) | 2016-06-20 | 2022-07-21 | 美商英塞特公司 | Heterocyclic compounds as immunomodulators |
WO2018013789A1 (en) | 2016-07-14 | 2018-01-18 | Incyte Corporation | Heterocyclic compounds as immunomodulators |
CN106220611A (en) * | 2016-08-08 | 2016-12-14 | 青岛科技大学 | The new preparation process of 2 (1H indole 3 base) 1H benzimidizole derivatives |
US20180057486A1 (en) | 2016-08-29 | 2018-03-01 | Incyte Corporation | Heterocyclic compounds as immunomodulators |
JP2019535689A (en) | 2016-10-27 | 2019-12-12 | バイエル アクチェンゲゼルシャフトBayer Aktiengesellschaft | 4,5-fused 1,2,4-triazolone |
PL3555064T3 (en) | 2016-12-16 | 2023-03-06 | Pfizer Inc. | Glp-1 receptor agonists and uses thereof |
WO2018119266A1 (en) | 2016-12-22 | 2018-06-28 | Incyte Corporation | Benzooxazole derivatives as immunomodulators |
PE20200005A1 (en) | 2016-12-22 | 2020-01-06 | Incyte Corp | DERIVATIVES OF TETRAHYDRO IMIDAZO [4,5-C] PYRIDINE AS INDUCTORS OF INTERNALIZATION PD-L1 |
ES2874756T3 (en) | 2016-12-22 | 2021-11-05 | Incyte Corp | Triazolo [1,5-A] pyridine derivatives as immunomodulators |
WO2018119221A1 (en) | 2016-12-22 | 2018-06-28 | Incyte Corporation | Pyridine derivatives as immunomodulators |
AU2018223982B2 (en) | 2017-02-24 | 2022-02-03 | Merck Patent Gmbh | 1, 4, 6-trisubstituted-2-alkyl-1H-benzo[d]imidazole derivatives as dihydroorotate oxygenase inhibitors |
US20180369206A1 (en) | 2017-04-24 | 2018-12-27 | Aurigene Discovery Technologies Limited | Methods of Use for Trisubstituted Benzotriazole Derivatives as Dihydroorotate Oxygenase Inhibitors |
MA48459B1 (en) | 2017-04-24 | 2021-09-30 | Aurigene Discovery Tech Ltd | Methods of using trisubstituted benzotriazole derivatives as dihydroorotate oxygenase inhibitors |
WO2019018562A1 (en) | 2017-07-19 | 2019-01-24 | Ideaya Biosciences, Inc. | AMIDO COMPOUNDS AS AhR MODULATORS |
CN107384882B (en) * | 2017-08-22 | 2021-06-29 | 西南大学 | Molecular cloning and identification method of silkworm gene |
JP7434185B2 (en) | 2018-02-20 | 2024-02-20 | レ ラボラトワール セルヴィエ | How to use trisubstituted benzotriazole derivatives |
FI3774791T3 (en) | 2018-03-30 | 2023-03-21 | Incyte Corp | Heterocyclic compounds as immunomodulators |
BR112020022936A2 (en) | 2018-05-11 | 2021-02-02 | Incyte Corporation | tetrahydro-imidazo [4,5-c] pyridine derivatives as pd-l1 immunomodulators |
EP3858361A4 (en) * | 2018-09-28 | 2021-12-01 | FUJIFILM Corporation | Antitumor agent containing cytarabine, antitumor effect enhancer used in combination with cytarabine, antitumor kit, and antitumor agent used in combination with cytarabine |
JP7413346B2 (en) | 2019-03-06 | 2024-01-15 | 第一三共株式会社 | Pyrrolopyrazole derivative |
WO2021030162A1 (en) | 2019-08-09 | 2021-02-18 | Incyte Corporation | Salts of a pd-1/pd-l1 inhibitor |
JP7559059B2 (en) | 2019-09-30 | 2024-10-01 | インサイト・コーポレイション | Pyrido[3,2-D]pyrimidine compounds as immunomodulators - Patents.com |
MX2022005651A (en) | 2019-11-11 | 2022-07-27 | Incyte Corp | Salts and crystalline forms of a pd-1/pd-l1 inhibitor. |
TW202128675A (en) | 2019-12-06 | 2021-08-01 | 美商維泰克斯製藥公司 | Substituted tetrahydrofurans as modulators of sodium channels |
KR20230117573A (en) | 2020-11-06 | 2023-08-08 | 인사이트 코포레이션 | Methods for preparing PD-1 and PD-L1 inhibitors and salts and crystalline forms thereof |
US11780836B2 (en) | 2020-11-06 | 2023-10-10 | Incyte Corporation | Process of preparing a PD-1/PD-L1 inhibitor |
TW202233615A (en) | 2020-11-06 | 2022-09-01 | 美商英塞特公司 | Crystalline form of a pd-1/pd-l1 inhibitor |
WO2022200615A1 (en) | 2021-03-26 | 2022-09-29 | Georg-August-Universität Göttingen Stiftung Öffentlichen Rechts, Universitätsmedizin | Pyrimidine biosynthesis inhibitor combination for use in treating viral infections |
PE20241335A1 (en) | 2021-06-04 | 2024-07-03 | Vertex Pharma | N-(HYDROXYALKYL (HETERO)ARYL) TETRAHYDROFURAN CARBOXAMIDES AS SODIUM CHANNEL MODULATORS |
CN118401519A (en) | 2021-10-25 | 2024-07-26 | 拓臻制药公司 | Compounds as GLP-1R agonists |
CN114105800B (en) * | 2021-11-25 | 2023-09-01 | 杭州国瑞生物科技有限公司 | Preparation method of 2, 3-diaminomethyl benzoate |
Family Cites Families (40)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS625966A (en) * | 1985-07-03 | 1987-01-12 | Nippon Shinyaku Co Ltd | Benzimidazole derivative |
US5494911A (en) | 1990-05-18 | 1996-02-27 | Hoechst Aktiengesellschaft | Isoxazole-4-carboxamides and hydroxyalkylidenecyanoacetamides, pharmaceuticals containing these compounds and their use |
JP3119713B2 (en) * | 1992-03-03 | 2000-12-25 | サントリー株式会社 | New benzoxazole compounds |
US5814651A (en) * | 1992-12-02 | 1998-09-29 | Pfizer Inc. | Catechol diethers as selective PDEIV inhibitors |
JP3477238B2 (en) * | 1994-04-27 | 2003-12-10 | 株式会社大塚製薬工場 | Imidazo [1,2-a] pyridine derivative |
HUP9902645A3 (en) * | 1996-03-18 | 1999-12-28 | Eisai Co Ltd | Fused-ring carboxylic acid derivatives |
US5904937A (en) | 1997-10-03 | 1999-05-18 | Fmc Corporation | Taste masked pharmaceutical compositions |
US6251686B1 (en) | 1998-02-26 | 2001-06-26 | Edward J. Studer | Liquid transfer apparatus |
US6251689B1 (en) | 1998-05-14 | 2001-06-26 | Telik, Inc. | Methods for the solid phase synthesis of combinatorial libraries of benzimidazoles benzoxazoles benzothiazoles and derivatives thereof |
BR9915013A (en) * | 1998-11-03 | 2001-08-07 | Basf Ag | Compound, use of the same, process to prepare them, drug, and, method for in vitro detection for parp inhibitors |
PE20010306A1 (en) * | 1999-07-02 | 2001-03-29 | Agouron Pharma | INDAZOLE COMPOUNDS AND PHARMACEUTICAL COMPOSITIONS CONTAINING THEM USEFUL FOR THE INHIBITION OF PROTEIN KINASE |
AU7314200A (en) * | 1999-09-17 | 2001-04-24 | Yamanouchi Pharmaceutical Co., Ltd. | Benzimidazole derivatives |
US6841561B1 (en) | 1999-10-01 | 2005-01-11 | Institute Of Molecular And Cell Biology | Dihydroorotate dehydrogenase inhibitors for the treatment of viral-mediated diseases |
DE10021468A1 (en) * | 2000-05-04 | 2001-11-08 | Basf Ag | Use of PARP inhibitors in cosmetic preparations |
WO2003030905A1 (en) * | 2001-10-01 | 2003-04-17 | Shionogi & Co., Ltd. | Dihydroorotate dehydrogenase inhibitor |
JP2006505570A (en) * | 2002-10-17 | 2006-02-16 | アムジエン・インコーポレーテツド | Benzimidazole derivatives and their use as vanilloid receptor ligands |
HU0301154D0 (en) * | 2003-04-28 | 2003-07-28 | Hideg Kalman Dr | Pharmaceutical composition |
AU2004238508B2 (en) * | 2003-05-13 | 2009-11-19 | F. Hoffmann-La Roche Ag | Imidazo-benzothiazoles |
EP1644320B1 (en) | 2003-07-03 | 2008-01-16 | Eli Lilly And Company | Indane derivates as muscarinic receptor agonists |
US7378409B2 (en) | 2003-08-21 | 2008-05-27 | Bristol-Myers Squibb Company | Substituted cycloalkylamine derivatives as modulators of chemokine receptor activity |
SE0400234D0 (en) * | 2004-02-06 | 2004-02-06 | Active Biotech Ab | New compounds, methods for their preparation and use thereof |
WO2006009734A1 (en) | 2004-06-17 | 2006-01-26 | Wyeth | Gonadotropin releasing hormone receptor antagonists |
JP2006089485A (en) * | 2004-08-24 | 2006-04-06 | Santen Pharmaceut Co Ltd | New heterocyclic amide derivative having dihydroorotate dehydrogenase inhibitory activity |
US20070054916A1 (en) * | 2004-10-01 | 2007-03-08 | Amgen Inc. | Aryl nitrogen-containing bicyclic compounds and methods of use |
EP1815206B1 (en) * | 2004-10-13 | 2016-04-06 | PTC Therapeutics, Inc. | Compounds for nonsense suppression, and methods for their use |
AU2006209117B2 (en) * | 2005-01-28 | 2009-12-10 | Daewoong Pharmaceutical Co., Ltd. | Novel benzoimidazole derivatives and pharmaceutical composition comprising the same |
KR20060087386A (en) * | 2005-01-28 | 2006-08-02 | 주식회사 대웅제약 | Novel benzoimidazole derivatives and a pharmaceutical composition comprising the same |
WO2006130673A1 (en) * | 2005-05-31 | 2006-12-07 | Janssen Pharmaceutica, N.V. | 3-benzoimidazolyl-pyrazolopyridines useful in treating kinase disorders |
JP2007015952A (en) * | 2005-07-06 | 2007-01-25 | Shionogi & Co Ltd | Naphthalene derivative |
EP1957477B1 (en) * | 2005-09-29 | 2011-12-07 | Abbott Laboratories | 1h-benzimidazole-4-carboxamides substituted with phenyl at the 2-position are potent parp inhibitors |
WO2007056155A1 (en) * | 2005-11-03 | 2007-05-18 | Chembridge Research Laboratories, Inc. | Heterocyclic compounds as tyrosine kinase modulators |
TW200736229A (en) * | 2005-11-15 | 2007-10-01 | Abbott Lab | Substituted 1H-benzimidazole-4-carboxamides are potent PARP inhibitors |
US7507737B2 (en) * | 2006-03-31 | 2009-03-24 | Janssen Pharmaceutica, N.V. | Benzoimidazol-2-yl pyrimidines and pyrazines as modulators of the histamine H4receptor |
EP2001480A4 (en) * | 2006-03-31 | 2011-06-15 | Abbott Lab | Indazole compounds |
ATE553104T1 (en) * | 2006-05-02 | 2012-04-15 | Abbott Lab | SUBSTITUTED 1H-BENZIMIDAZOLE-4-CARBOXAMIDE AS POTENT PARP INHIBITORS |
PE20080707A1 (en) * | 2006-06-01 | 2008-05-22 | Wyeth Corp | BENZOXAZOLE AND BENZOTHIAZOLE DERIVATIVES AS 5-HYDROXITRIPTAMINE-6 BINDERS |
WO2008073451A2 (en) * | 2006-12-11 | 2008-06-19 | Sirtris Pharmaceuticals, Inc. | Benzoimidazole derivatives as sirtuin (sir) modulating compounds |
US8067613B2 (en) * | 2007-07-16 | 2011-11-29 | Abbott Laboratories | Benzimidazole poly(ADP ribose)polymerase inhibitors |
UY31272A1 (en) * | 2007-08-10 | 2009-01-30 | Almirall Lab | NEW DERIVATIVES OF AZABIFENILAMINOBENZOIC ACID |
DE102009033208A1 (en) * | 2009-07-15 | 2011-01-20 | Merck Patent Gmbh | aminopyridine derivatives |
-
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- 2010-03-26 US US13/262,640 patent/US9006454B2/en active Active
- 2010-03-26 JP JP2012502605A patent/JP5680054B2/en active Active
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- 2010-03-26 CN CN201410197910.3A patent/CN104030987B/en active Active
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- 2010-03-26 CN CN2010800147415A patent/CN102574786A/en active Pending
- 2010-03-26 WO PCT/EP2010/054034 patent/WO2010115736A2/en active Application Filing
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US9006454B2 (en) | 2015-04-14 |
CN104030987A (en) | 2014-09-10 |
US20120028959A1 (en) | 2012-02-02 |
EP2414328A2 (en) | 2012-02-08 |
WO2010115736A9 (en) | 2015-11-19 |
SG174125A1 (en) | 2011-10-28 |
AR076183A1 (en) | 2011-05-26 |
WO2010115736A2 (en) | 2010-10-14 |
NZ595819A (en) | 2013-02-22 |
AU2010233917A1 (en) | 2011-08-25 |
JP2012524715A (en) | 2012-10-18 |
CN104030987B (en) | 2017-04-12 |
ES2882797T3 (en) | 2021-12-02 |
JP5680054B2 (en) | 2015-03-04 |
MY159575A (en) | 2017-01-13 |
EP2414328B1 (en) | 2021-05-26 |
AU2010233917B2 (en) | 2015-07-02 |
WO2010115736A3 (en) | 2015-10-01 |
CN102574786A (en) | 2012-07-11 |
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