JP2018527340A - アリール置換ジヒドロキノリノン、その調製及び医薬品としてのその使用 - Google Patents
アリール置換ジヒドロキノリノン、その調製及び医薬品としてのその使用 Download PDFInfo
- Publication number
- JP2018527340A JP2018527340A JP2018506998A JP2018506998A JP2018527340A JP 2018527340 A JP2018527340 A JP 2018527340A JP 2018506998 A JP2018506998 A JP 2018506998A JP 2018506998 A JP2018506998 A JP 2018506998A JP 2018527340 A JP2018527340 A JP 2018527340A
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- Prior art keywords
- alkyl
- cancer
- mmol
- compound
- disease
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Pending
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- 0 *c(c(*)c1*)c(*)c(*C2)c1N(*)C2=O Chemical compound *c(c(*)c1*)c(*)c(*C2)c1N(*)C2=O 0.000 description 6
- YWPJLDIAZYVZTB-UHFFFAOYSA-N Oc(cc(cc1CC2)Br)c1NC2=O Chemical compound Oc(cc(cc1CC2)Br)c1NC2=O YWPJLDIAZYVZTB-UHFFFAOYSA-N 0.000 description 3
- XMZBPYHAUVWSGQ-UHFFFAOYSA-N CC(CC(c(cc1)c(Cc(cc2)ccc2C#N)c(CC2)c1NC2=O)=CN1C)C1=O Chemical compound CC(CC(c(cc1)c(Cc(cc2)ccc2C#N)c(CC2)c1NC2=O)=CN1C)C1=O XMZBPYHAUVWSGQ-UHFFFAOYSA-N 0.000 description 1
- HEOVJSGWXXRDQL-UHFFFAOYSA-N CC(Cc(c(CC1)c2)cc(COC3CCCC3)c2N)C(C)C1=O Chemical compound CC(Cc(c(CC1)c2)cc(COC3CCCC3)c2N)C(C)C1=O HEOVJSGWXXRDQL-UHFFFAOYSA-N 0.000 description 1
- YKDUBDWGMORWNZ-UHFFFAOYSA-N CC(OCc1ncccc1C)=O Chemical compound CC(OCc1ncccc1C)=O YKDUBDWGMORWNZ-UHFFFAOYSA-N 0.000 description 1
- VQPMESRHIUIYFJ-UHFFFAOYSA-N CC(c1ccccn1)Nc(cc(cc1CC2)C(C=C3C)=CN(C)C3=O)c1NC2=O Chemical compound CC(c1ccccn1)Nc(cc(cc1CC2)C(C=C3C)=CN(C)C3=O)c1NC2=O VQPMESRHIUIYFJ-UHFFFAOYSA-N 0.000 description 1
- ZJTKSXUAVVEKPY-UHFFFAOYSA-N CC(c1cccnc1)Oc(cc(cc1CC2)Br)c1NC2=O Chemical compound CC(c1cccnc1)Oc(cc(cc1CC2)Br)c1NC2=O ZJTKSXUAVVEKPY-UHFFFAOYSA-N 0.000 description 1
- YLUSCNMBGNZTNO-UHFFFAOYSA-N CC1=CC(c(cc2)c(Cc3cccc(N)c3)c(CC3)c2NC3=O)=CN(C)C1=O Chemical compound CC1=CC(c(cc2)c(Cc3cccc(N)c3)c(CC3)c2NC3=O)=CN(C)C1=O YLUSCNMBGNZTNO-UHFFFAOYSA-N 0.000 description 1
- NJQXAEGADHOZSQ-UHFFFAOYSA-N CC1=CC(c(cc2)c(Cc3ccccn3)c(CC3)c2NC3=O)=CN(C)C1=O Chemical compound CC1=CC(c(cc2)c(Cc3ccccn3)c(CC3)c2NC3=O)=CN(C)C1=O NJQXAEGADHOZSQ-UHFFFAOYSA-N 0.000 description 1
- FKEZNRMWEHHVMC-UHFFFAOYSA-N CC1=CC(c(cc2)c(Cc3cccnc3)c(CC3)c2NC3=O)=CN(C)C1=O Chemical compound CC1=CC(c(cc2)c(Cc3cccnc3)c(CC3)c2NC3=O)=CN(C)C1=O FKEZNRMWEHHVMC-UHFFFAOYSA-N 0.000 description 1
- GJIWAODVOVRCIZ-UHFFFAOYSA-N CC1=CC(c(cc2CC3)cc(CNC4CCCCC4)c2NC3=O)=CN(C)C1=O Chemical compound CC1=CC(c(cc2CC3)cc(CNC4CCCCC4)c2NC3=O)=CN(C)C1=O GJIWAODVOVRCIZ-UHFFFAOYSA-N 0.000 description 1
- QMOVGPAFKWTLLR-UHFFFAOYSA-N CC1=CC(c(cc2CC3)cc(N)c2NC3=O)=CN(C)C1=O Chemical compound CC1=CC(c(cc2CC3)cc(N)c2NC3=O)=CN(C)C1=O QMOVGPAFKWTLLR-UHFFFAOYSA-N 0.000 description 1
- JEHZLHJHGHNPAX-UHFFFAOYSA-N CC1=CC(c(cc2CC3)cc(NC4CCOCC4)c2NC3=O)=CN(C)C1=O Chemical compound CC1=CC(c(cc2CC3)cc(NC4CCOCC4)c2NC3=O)=CN(C)C1=O JEHZLHJHGHNPAX-UHFFFAOYSA-N 0.000 description 1
- KGKLJQQYYZQCDH-UHFFFAOYSA-N CC1=CC(c(cc2CC3)cc(OCc4cnccc4)c2NC3=O)=CN(C)C1=O Chemical compound CC1=CC(c(cc2CC3)cc(OCc4cnccc4)c2NC3=O)=CN(C)C1=O KGKLJQQYYZQCDH-UHFFFAOYSA-N 0.000 description 1
- NYLYMDOWRDKLGR-UHFFFAOYSA-N CC1=CC(c(cc2CC3)cc(Oc4ccccc4)c2NC3=O)=CN(C)C1=O Chemical compound CC1=CC(c(cc2CC3)cc(Oc4ccccc4)c2NC3=O)=CN(C)C1=O NYLYMDOWRDKLGR-UHFFFAOYSA-N 0.000 description 1
- GUCAWRLLFMDZMS-UHFFFAOYSA-N CC1=CC(c2c(Cc3ccccn3)cc(CCC(N3)=O)c3c2)=CN(C)C1=O Chemical compound CC1=CC(c2c(Cc3ccccn3)cc(CCC(N3)=O)c3c2)=CN(C)C1=O GUCAWRLLFMDZMS-UHFFFAOYSA-N 0.000 description 1
- MYHTUECTQKXLQP-ZETCQYMHSA-N CCO[C@@H]1COCCC1 Chemical compound CCO[C@@H]1COCCC1 MYHTUECTQKXLQP-ZETCQYMHSA-N 0.000 description 1
- MYHTUECTQKXLQP-SSDOTTSWSA-N CCO[C@H]1COCCC1 Chemical compound CCO[C@H]1COCCC1 MYHTUECTQKXLQP-SSDOTTSWSA-N 0.000 description 1
- HACIXUFIWAKFLS-ZETCQYMHSA-N COC[C@H]1OCCCC1 Chemical compound COC[C@H]1OCCCC1 HACIXUFIWAKFLS-ZETCQYMHSA-N 0.000 description 1
- KOBPCNIZLKUGLA-UHFFFAOYSA-N COCc(cc1)ncc1F Chemical compound COCc(cc1)ncc1F KOBPCNIZLKUGLA-UHFFFAOYSA-N 0.000 description 1
- MJXPDBFDHSMVNS-ZETCQYMHSA-N C[C@@H](c1ncccc1)NC Chemical compound C[C@@H](c1ncccc1)NC MJXPDBFDHSMVNS-ZETCQYMHSA-N 0.000 description 1
- DFYCSUKTANLTHI-UHFFFAOYSA-N Cc1c(COc(cc(cc2CC3)C(C=C4C)=CN(C)C4=O)c2NC3=O)nccc1 Chemical compound Cc1c(COc(cc(cc2CC3)C(C=C4C)=CN(C)C4=O)c2NC3=O)nccc1 DFYCSUKTANLTHI-UHFFFAOYSA-N 0.000 description 1
- ACDAPUOXXWLLSC-UHFFFAOYSA-N Cc1cccnc1CO Chemical compound Cc1cccnc1CO ACDAPUOXXWLLSC-UHFFFAOYSA-N 0.000 description 1
- ZSAONVGPMHUZDW-UHFFFAOYSA-N Cc1cccnc1COC Chemical compound Cc1cccnc1COC ZSAONVGPMHUZDW-UHFFFAOYSA-N 0.000 description 1
- GIPAMQFKKFURER-GLGOKHISSA-N Cc1cnc(CO[IH]C2CO[C@@H](COI)CC2)cc1 Chemical compound Cc1cnc(CO[IH]C2CO[C@@H](COI)CC2)cc1 GIPAMQFKKFURER-GLGOKHISSA-N 0.000 description 1
- FOJOQBLFRRLVTF-UHFFFAOYSA-N O=C(CC1)Nc(c(Oc2ccccc2)c2)c1cc2Br Chemical compound O=C(CC1)Nc(c(Oc2ccccc2)c2)c1cc2Br FOJOQBLFRRLVTF-UHFFFAOYSA-N 0.000 description 1
- IKOHIWNOKVSKLN-UHFFFAOYSA-N O=C(CC1)Nc(cc2)c1c(Cc1ccccn1)c2Cl Chemical compound O=C(CC1)Nc(cc2)c1c(Cc1ccccn1)c2Cl IKOHIWNOKVSKLN-UHFFFAOYSA-N 0.000 description 1
- FAVFLDZYCFEKRU-UHFFFAOYSA-N O=C(CCc1cc(Br)c2)Nc1c2OC1CCCCC1 Chemical compound O=C(CCc1cc(Br)c2)Nc1c2OC1CCCCC1 FAVFLDZYCFEKRU-UHFFFAOYSA-N 0.000 description 1
- ZFVGIFUMELHDOX-UHFFFAOYSA-N OC(CCc1cc(Br)c2)Nc1c2OCc1cncnc1 Chemical compound OC(CCc1cc(Br)c2)Nc1c2OCc1cncnc1 ZFVGIFUMELHDOX-UHFFFAOYSA-N 0.000 description 1
Classifications
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- 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
- C07D401/14—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 three or more hetero rings
-
- 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
- A61K31/47—Quinolines; Isoquinolines
- A61K31/472—Non-condensed isoquinolines, e.g. papaverine
- A61K31/4725—Non-condensed isoquinolines, e.g. papaverine containing further heterocyclic rings
-
- 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
- A61P17/00—Drugs for dermatological disorders
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P17/00—Drugs for dermatological disorders
- A61P17/06—Antipsoriatics
-
- 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
-
- 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
- C07D405/00—Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom
- C07D405/14—Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom containing three or more hetero 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
- C07D413/14—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms containing three or more hetero 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
- C07D417/14—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 three or more hetero rings
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Health & Medical Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- Veterinary Medicine (AREA)
- Public Health (AREA)
- General Health & Medical Sciences (AREA)
- Medicinal Chemistry (AREA)
- Animal Behavior & Ethology (AREA)
- Pharmacology & Pharmacy (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- General Chemical & Material Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Engineering & Computer Science (AREA)
- Immunology (AREA)
- Rheumatology (AREA)
- Pain & Pain Management (AREA)
- Dermatology (AREA)
- Epidemiology (AREA)
- Transplantation (AREA)
- Biomedical Technology (AREA)
- Neurology (AREA)
- Neurosurgery (AREA)
- Orthopedic Medicine & Surgery (AREA)
- Physical Education & Sports Medicine (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Plural Heterocyclic Compounds (AREA)
Applications Claiming Priority (5)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US201562203623P | 2015-08-11 | 2015-08-11 | |
| US62/203,623 | 2015-08-11 | ||
| US201662356579P | 2016-06-30 | 2016-06-30 | |
| US62/356,579 | 2016-06-30 | ||
| PCT/CA2016/050943 WO2017024408A1 (en) | 2015-08-11 | 2016-08-11 | Aryl-substituted dihydroquinolinones, their preparation and their use as pharmaceuticals |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| JP2018527340A true JP2018527340A (ja) | 2018-09-20 |
| JP2018527340A5 JP2018527340A5 (enExample) | 2019-09-26 |
Family
ID=57982883
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP2018506998A Pending JP2018527340A (ja) | 2015-08-11 | 2016-08-11 | アリール置換ジヒドロキノリノン、その調製及び医薬品としてのその使用 |
Country Status (11)
| Country | Link |
|---|---|
| US (2) | US10501438B2 (enExample) |
| EP (1) | EP3334717B1 (enExample) |
| JP (1) | JP2018527340A (enExample) |
| KR (1) | KR20180039117A (enExample) |
| CN (1) | CN108290856A (enExample) |
| AU (1) | AU2016305513A1 (enExample) |
| CA (1) | CA2994472A1 (enExample) |
| HK (1) | HK1256753A1 (enExample) |
| IL (1) | IL257347A (enExample) |
| MX (1) | MX2018001751A (enExample) |
| WO (1) | WO2017024408A1 (enExample) |
Cited By (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JP2022523860A (ja) * | 2019-03-11 | 2022-04-26 | コラボレイティブ メディシナル デベロップメント， エルエルシー | フェロトーシス関連障害の処置のための複素芳香族およびヘテロ二環式芳香族誘導体 |
Families Citing this family (4)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| WO2020093162A1 (en) * | 2018-11-07 | 2020-05-14 | Neomed Institute | Treatment of bet inhibitor-resistant cancers and other diseases responsive to dual bet and cbp/ep300 inhibition therapy |
| CN112239456B (zh) * | 2020-06-09 | 2021-09-07 | 浙江理工大学 | 一种取代2，3-二氢喹诺酮化合物的制备方法 |
| CN114276333B (zh) * | 2020-09-28 | 2023-05-09 | 中国科学院上海药物研究所 | 二氢喹喔啉类溴结构域二价抑制剂 |
| CN118005653B (zh) * | 2023-04-23 | 2024-12-10 | 信义核新(北京)生物科技有限公司 | 喹诺酮类似物及其用途 |
Citations (4)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US4785005A (en) * | 1986-06-25 | 1988-11-15 | Rorer Pharmaceutical Corporation | 6-(6-alkylpyridone)-carbostyril compounds and their cardiotonic uses |
| WO2014095774A1 (de) * | 2012-12-20 | 2014-06-26 | Bayer Pharma Aktiengesellschaft | Bet-proteininhibitorische dihydropyridopyrazinone |
| WO2014096965A2 (en) * | 2012-12-21 | 2014-06-26 | Rvx Therapeutics Inc. | Novel heterocyclic compounds as bromodomain inhibitors |
| WO2015004075A1 (de) * | 2013-07-09 | 2015-01-15 | Bayer Pharma Aktiengesellschaft | Modifizierte bet-proteininhibitorische dihydrochinoxalinone und dihydropyridopyrazinone |
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| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US4550166A (en) | 1984-05-21 | 1985-10-29 | American Cyanamid Company | (Pyridinyl)-1,2,4-triazolo[4,3-a]pyridines |
| US5093330A (en) | 1987-06-15 | 1992-03-03 | Ciba-Geigy Corporation | Staurosporine derivatives substituted at methylamino nitrogen |
| DE4237656A1 (de) | 1992-06-13 | 1993-12-16 | Merck Patent Gmbh | Benzimidazolderivate |
| US6162804A (en) | 1997-09-26 | 2000-12-19 | Merck & Co., Inc. | Tyrosine kinase inhibitors |
| US6465484B1 (en) | 1997-09-26 | 2002-10-15 | Merck & Co., Inc. | Angiogenesis inhibitors |
| CA2341409A1 (en) | 1998-08-31 | 2000-03-09 | Merck And Co., Inc. | Novel angiogenesis inhibitors |
| MY139563A (en) | 2002-09-04 | 2009-10-30 | Bristol Myers Squibb Co | Heterocyclic aromatic compounds useful as growth hormone secretagogues |
| AU2004305318A1 (en) | 2003-12-18 | 2005-07-07 | Pfizer Products Inc. | Methods of treating acute inflammation in animals with p38 MAP kinase inhibitors |
| JP2007529496A (ja) | 2004-03-19 | 2007-10-25 | ワーナー−ランバート カンパニー リミテッド ライアビリティー カンパニー | 抗菌剤としてのイミダゾピリジン及びイミダゾピリミジン誘導体 |
| PE20121506A1 (es) | 2006-07-14 | 2012-11-26 | Amgen Inc | Compuestos triazolopiridinas como inhibidores de c-met |
| 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 |
| US8119658B2 (en) | 2007-10-01 | 2012-02-21 | Bristol-Myers Squibb Company | Triazolopyridine 11-beta hydroxysteroid dehydrogenase type I inhibitors |
| EA201000615A1 (ru) | 2007-10-17 | 2010-12-30 | Новартис Аг | Производные имидазо[1,2-а]пиридина, применимые в качестве ингибиторов апк (активиноподобной киназы) |
| MY153913A (en) | 2009-05-12 | 2015-04-15 | Janssen Pharmaceuticals Inc | 7-aryl-1,2,4-triazolo[4,3-a]pyridine derivatives and their use as positive allosteric modulators of mglur2 receptors |
| GB0919423D0 (en) | 2009-11-05 | 2009-12-23 | Glaxosmithkline Llc | Novel compounds |
| US20120225885A1 (en) | 2009-11-16 | 2012-09-06 | Rao Ashwin U | Imidazole derivatives and methods of use thereof |
| UY33801A (es) | 2010-12-13 | 2013-06-28 | Array Biopharma Inc | COMPUESTOS SUSTITUIDOS DE N-(1H-INDAZOL-4IL)IMIDAZO[1,2-a]PIRIDIN-3-CARBOXAMIDA COMO INHIBIDORES DE LA TIROSINA QUINASA RECEPTORA DE TIPO III |
| GB201114103D0 (en) | 2011-08-17 | 2011-09-28 | Glaxosmithkline Llc | Novel compounds |
| PE20141371A1 (es) | 2011-08-29 | 2014-10-13 | Infinity Pharmaceuticals Inc | Compuestos heterociclicos y usos de los mismos |
| CA2874303C (en) | 2012-06-11 | 2020-10-13 | Ucb Biopharma Sprl | Tnf -alpha modulating benz imidazoles |
| HK1208681A1 (en) | 2012-06-12 | 2016-03-11 | Abbvie Inc. | Pyridinone and pyridazinone derivatives |
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-
2016
- 2016-08-11 HK HK18115833.9A patent/HK1256753A1/zh unknown
- 2016-08-11 EP EP16834368.9A patent/EP3334717B1/en active Active
- 2016-08-11 US US15/751,800 patent/US10501438B2/en active Active
- 2016-08-11 MX MX2018001751A patent/MX2018001751A/es unknown
- 2016-08-11 AU AU2016305513A patent/AU2016305513A1/en not_active Abandoned
- 2016-08-11 JP JP2018506998A patent/JP2018527340A/ja active Pending
- 2016-08-11 CA CA2994472A patent/CA2994472A1/en not_active Abandoned
- 2016-08-11 CN CN201680058648.1A patent/CN108290856A/zh active Pending
- 2016-08-11 WO PCT/CA2016/050943 patent/WO2017024408A1/en not_active Ceased
- 2016-08-11 KR KR1020187006580A patent/KR20180039117A/ko not_active Withdrawn
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2018
- 2018-02-04 IL IL257347A patent/IL257347A/en unknown
-
2019
- 2019-10-28 US US16/665,198 patent/US20200299262A1/en not_active Abandoned
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| JP2022523860A (ja) * | 2019-03-11 | 2022-04-26 | コラボレイティブ メディシナル デベロップメント， エルエルシー | フェロトーシス関連障害の処置のための複素芳香族およびヘテロ二環式芳香族誘導体 |
Also Published As
| Publication number | Publication date |
|---|---|
| WO2017024408A1 (en) | 2017-02-16 |
| CA2994472A1 (en) | 2017-02-16 |
| US10501438B2 (en) | 2019-12-10 |
| HK1256753A1 (zh) | 2019-10-04 |
| EP3334717A4 (en) | 2019-02-13 |
| KR20180039117A (ko) | 2018-04-17 |
| US20200299262A1 (en) | 2020-09-24 |
| EP3334717B1 (en) | 2020-07-01 |
| US20180230130A1 (en) | 2018-08-16 |
| AU2016305513A1 (en) | 2018-03-08 |
| EP3334717A1 (en) | 2018-06-20 |
| CN108290856A (zh) | 2018-07-17 |
| MX2018001751A (es) | 2018-08-01 |
| IL257347A (en) | 2018-03-29 |
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