CN105517547A - 吡咯并吡咯氨基甲酸酯和相关的有机化合物、药物组合物及其医学用途 - Google Patents
吡咯并吡咯氨基甲酸酯和相关的有机化合物、药物组合物及其医学用途 Download PDFInfo
- Publication number
- CN105517547A CN105517547A CN201480048531.6A CN201480048531A CN105517547A CN 105517547 A CN105517547 A CN 105517547A CN 201480048531 A CN201480048531 A CN 201480048531A CN 105517547 A CN105517547 A CN 105517547A
- Authority
- CN
- China
- Prior art keywords
- pyrrole
- methyl
- carboxylate
- octahydropyrrolo
- hexafluoropropan
- 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
Links
- 0 *N(C1)Cc2c1cccn2 Chemical compound *N(C1)Cc2c1cccn2 0.000 description 16
- NIACSPCNAXLBFY-FWNKGETMSA-N CC(C)[n]1nc(/C(/C=C\C=C)=C/C(Cl)=C)c(CN(C2)CC3C2CN(COC(C(F)(F)F)C(F)(F)F)C3)c1 Chemical compound CC(C)[n]1nc(/C(/C=C\C=C)=C/C(Cl)=C)c(CN(C2)CC3C2CN(COC(C(F)(F)F)C(F)(F)F)C3)c1 NIACSPCNAXLBFY-FWNKGETMSA-N 0.000 description 1
- NMZNVNVEUDQUHS-UHFFFAOYSA-N CC(C)[n]1nc(C(CC2)CCN2C(C)=O)c(CN(C2)CC(C3)C2CN3C(ON(C(CC2)=O)C2=O)=O)c1 Chemical compound CC(C)[n]1nc(C(CC2)CCN2C(C)=O)c(CN(C2)CC(C3)C2CN3C(ON(C(CC2)=O)C2=O)=O)c1 NMZNVNVEUDQUHS-UHFFFAOYSA-N 0.000 description 1
- GROSUVLLDKTZMY-UHFFFAOYSA-N CC(C)[n]1nc(C)cc1CN(C1)CC(C2)C1CN2C(OC(C(F)(F)F)C(F)(F)F)=O Chemical compound CC(C)[n]1nc(C)cc1CN(C1)CC(C2)C1CN2C(OC(C(F)(F)F)C(F)(F)F)=O GROSUVLLDKTZMY-UHFFFAOYSA-N 0.000 description 1
- JIOJVBJJJBSYHI-UHFFFAOYSA-N CC(C1)C(CNCc2ccccc2)CN1C(OC(C)(C)C)=O Chemical compound CC(C1)C(CNCc2ccccc2)CN1C(OC(C)(C)C)=O JIOJVBJJJBSYHI-UHFFFAOYSA-N 0.000 description 1
- YYXQBHNHXSHRGC-UHFFFAOYSA-N CCCON(C(CC(C)(C)CC1C)=O)C1=O Chemical compound CCCON(C(CC(C)(C)CC1C)=O)C1=O YYXQBHNHXSHRGC-UHFFFAOYSA-N 0.000 description 1
- UPCOFZNLELZYCO-STWBTFQISA-N CCN/C(/C(NCc1ccccc1)=O)=C(/CN(C1)CC(C2)C1CN2C(OC(C(F)(F)F)C(F)(F)F)=O)\C=N Chemical compound CCN/C(/C(NCc1ccccc1)=O)=C(/CN(C1)CC(C2)C1CN2C(OC(C(F)(F)F)C(F)(F)F)=O)\C=N UPCOFZNLELZYCO-STWBTFQISA-N 0.000 description 1
- RSFZFEUKACJJAF-UHFFFAOYSA-N CCN1Cc2ncc[n]2CC1 Chemical compound CCN1Cc2ncc[n]2CC1 RSFZFEUKACJJAF-UHFFFAOYSA-N 0.000 description 1
- RTPZFBRQWOMQPX-UHFFFAOYSA-N Cc(cccc1CN(C2)CC(C3)C2CN3C(ON(C(CC2)=O)C2=O)=O)c1N1CCN(C)CC1 Chemical compound Cc(cccc1CN(C2)CC(C3)C2CN3C(ON(C(CC2)=O)C2=O)=O)c1N1CCN(C)CC1 RTPZFBRQWOMQPX-UHFFFAOYSA-N 0.000 description 1
- RBLUADGCZMXOAX-UHFFFAOYSA-N O=C(N1CC(CN(Cc(c(N2CCCC2)c2)ccc2Cl)C2)C2C1)ON(C(CC1)=O)C1=O Chemical compound O=C(N1CC(CN(Cc(c(N2CCCC2)c2)ccc2Cl)C2)C2C1)ON(C(CC1)=O)C1=O RBLUADGCZMXOAX-UHFFFAOYSA-N 0.000 description 1
- WGCTUGFXQLBHFW-UHFFFAOYSA-N O=C(N1CC(CN(Cc(c(N2CCOCC2)c2)ccc2F)C2)C2C1)ON(C(CC1)=O)C1=O Chemical compound O=C(N1CC(CN(Cc(c(N2CCOCC2)c2)ccc2F)C2)C2C1)ON(C(CC1)=O)C1=O WGCTUGFXQLBHFW-UHFFFAOYSA-N 0.000 description 1
- FZFPMYOMIZBFKT-UHFFFAOYSA-N O=C(N1CC(CN(Cc(c(N2Cc3ncn[n]3CC2)c2)ccc2Cl)C2)C2C1)OC(C(F)(F)F)C(F)(F)F Chemical compound O=C(N1CC(CN(Cc(c(N2Cc3ncn[n]3CC2)c2)ccc2Cl)C2)C2C1)OC(C(F)(F)F)C(F)(F)F FZFPMYOMIZBFKT-UHFFFAOYSA-N 0.000 description 1
- QKKJXUOPLBNLKW-UHFFFAOYSA-N O=C(N1CC(CN(Cc(cc2)ccc2-c2ccccc2)C2)C2C1)ON(C(CC1)=O)C1=O Chemical compound O=C(N1CC(CN(Cc(cc2)ccc2-c2ccccc2)C2)C2C1)ON(C(CC1)=O)C1=O QKKJXUOPLBNLKW-UHFFFAOYSA-N 0.000 description 1
- CQQXADPTIFZTKE-UHFFFAOYSA-N O=C(N1CC(CN(Cc2cccc(Cl)c2N(CC2)CCC2F)C2)C2C1)OC(C(F)(F)F)C(F)(F)F Chemical compound O=C(N1CC(CN(Cc2cccc(Cl)c2N(CC2)CCC2F)C2)C2C1)OC(C(F)(F)F)C(F)(F)F CQQXADPTIFZTKE-UHFFFAOYSA-N 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D487/00—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, not provided for by groups C07D451/00 - C07D477/00
- 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
- C07D487/04—Ortho-condensed systems
-
- 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
- A61P25/00—Drugs for disorders of the nervous system
- A61P25/20—Hypnotics; Sedatives
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P25/00—Drugs for disorders of the nervous system
- A61P25/28—Drugs for disorders of the nervous system for treating neurodegenerative disorders of the central nervous system, e.g. nootropic agents, cognition enhancers, drugs for treating Alzheimer's disease or other forms of dementia
-
- 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]
- A61P29/02—Non-central analgesic, antipyretic or antiinflammatory agents, e.g. antirheumatic agents; Non-steroidal antiinflammatory drugs [NSAID] without antiinflammatory effect
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P3/00—Drugs for disorders of the metabolism
- A61P3/04—Anorexiants; Antiobesity agents
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P31/00—Antiinfectives, i.e. antibiotics, antiseptics, chemotherapeutics
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P31/00—Antiinfectives, i.e. antibiotics, antiseptics, chemotherapeutics
- A61P31/04—Antibacterial agents
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P31/00—Antiinfectives, i.e. antibiotics, antiseptics, chemotherapeutics
- A61P31/10—Antimycotics
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P31/00—Antiinfectives, i.e. antibiotics, antiseptics, chemotherapeutics
- A61P31/12—Antivirals
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P33/00—Antiparasitic agents
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P35/00—Antineoplastic agents
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P43/00—Drugs for specific purposes, not provided for in groups A61P1/00-A61P41/00
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D519/00—Heterocyclic compounds containing more than one system of two or more relevant hetero rings condensed among themselves or condensed with a common carbocyclic ring system not provided for in groups C07D453/00 or C07D455/00
Landscapes
- Health & Medical Sciences (AREA)
- Organic Chemistry (AREA)
- Chemical & Material Sciences (AREA)
- Veterinary Medicine (AREA)
- Life Sciences & Earth Sciences (AREA)
- General Health & Medical Sciences (AREA)
- General Chemical & Material Sciences (AREA)
- Pharmacology & Pharmacy (AREA)
- Medicinal Chemistry (AREA)
- Animal Behavior & Ethology (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Public Health (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Engineering & Computer Science (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Neurosurgery (AREA)
- Biomedical Technology (AREA)
- Communicable Diseases (AREA)
- Oncology (AREA)
- Neurology (AREA)
- Virology (AREA)
- Anesthesiology (AREA)
- Tropical Medicine & Parasitology (AREA)
- Pain & Pain Management (AREA)
- Rheumatology (AREA)
- Child & Adolescent Psychology (AREA)
- Diabetes (AREA)
- Hematology (AREA)
- Obesity (AREA)
- Hospice & Palliative Care (AREA)
- Psychiatry (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Nitrogen Condensed Heterocyclic Rings (AREA)
- Nitrogen And Oxygen Or Sulfur-Condensed Heterocyclic Ring Systems (AREA)
Applications Claiming Priority (3)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US201361842543P | 2013-07-03 | 2013-07-03 | |
| US61/842,543 | 2013-07-03 | ||
| PCT/US2014/045145 WO2015003002A1 (en) | 2013-07-03 | 2014-07-01 | Pyrrolo-pyrrole carbamate and related organic compounds, pharmaceutical compositions, and medical uses thereof |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| CN105517547A true CN105517547A (zh) | 2016-04-20 |
Family
ID=52144176
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| CN201480048531.6A Pending CN105517547A (zh) | 2013-07-03 | 2014-07-01 | 吡咯并吡咯氨基甲酸酯和相关的有机化合物、药物组合物及其医学用途 |
Country Status (7)
| Country | Link |
|---|---|
| US (1) | US9828379B2 (https=) |
| EP (1) | EP3016653A4 (https=) |
| JP (1) | JP6647592B2 (https=) |
| CN (1) | CN105517547A (https=) |
| CA (1) | CA2917050A1 (https=) |
| MX (1) | MX2015017961A (https=) |
| WO (1) | WO2015003002A1 (https=) |
Cited By (6)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CN109996790A (zh) * | 2016-09-19 | 2019-07-09 | 阿比德治疗公司 | 哌嗪氨基甲酸酯及其制备和使用方法 |
| CN110267962A (zh) * | 2016-11-16 | 2019-09-20 | 灵北拉荷亚研究中心公司 | Magl抑制剂 |
| CN110290791A (zh) * | 2016-11-16 | 2019-09-27 | 灵北拉荷亚研究中心公司 | 药物制剂 |
| CN110382479A (zh) * | 2017-01-20 | 2019-10-25 | 辉瑞大药厂 | 作为magl抑制剂的氨基甲酸1,1,1-三氟-3-羟基丙-2-基酯衍生物 |
| CN111148746A (zh) * | 2017-09-29 | 2020-05-12 | 武田药品工业株式会社 | 杂环化合物 |
| US11993588B2 (en) | 2016-11-16 | 2024-05-28 | H. Lundbeck A/S | Crystalline forms of a MAGL inhibitor |
Families Citing this family (19)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| PE20141702A1 (es) | 2012-01-06 | 2014-11-19 | Abide Therapeutics Inc | Compuestos de carbamato y preparacion y uso de los mismos |
| JP6647592B2 (ja) | 2013-07-03 | 2020-02-14 | ルンドベック ラ ホーヤ リサーチ センター,インク. | ピロロピロールカルバメート、および関連する有機化合物、医薬組成物、ならびにその医学的使用 |
| TN2017000544A1 (en) * | 2015-07-31 | 2019-04-12 | Pfizer | 1,1,1-trifluoro-3-hydroxypropan-2-yl carbamate derivatives and 1,1,1-trifluoro-4-hydroxybutan-2-yl carbamate derivatives as magl inhibitors |
| US10463753B2 (en) | 2016-02-19 | 2019-11-05 | Lundbeck La Jolla Research Center, Inc. | Radiolabeled monoacylglycerol lipase occupancy probe |
| US10781211B2 (en) | 2016-05-12 | 2020-09-22 | Lundbeck La Jolla Research Center, Inc. | Spirocycle compounds and methods of making and using same |
| JOP20190106A1 (ar) | 2016-11-16 | 2019-05-09 | Lundbeck La Jolla Research Center Inc | مثبطات أحادي أسيل جليسرول ليباز (magl) |
| JOP20190105A1 (ar) | 2016-11-16 | 2019-05-09 | Lundbeck La Jolla Research Center Inc | مثبطات أحادي أسيل جليسرول ليباز (magl) |
| NZ797702A (en) * | 2017-03-13 | 2026-03-27 | Lundbeck La Jolla Research Center Inc | Dual magl and faah inhibitors |
| JP7257387B2 (ja) | 2017-08-29 | 2023-04-13 | ハー・ルンドベック・アクチエゼルスカベット | スピロ環化合物並びにその作製及び使用方法 |
| CN111032034B (zh) * | 2017-08-29 | 2023-05-02 | H.隆德贝克有限公司 | 螺环化合物及其制造和使用方法 |
| GEP20227443B (en) | 2018-05-15 | 2022-11-25 | H Lundbeck As | Magl inhibitors |
| MX2021000549A (es) * | 2018-07-19 | 2021-03-25 | Pfizer | Compuestos espiro heterociclicos como inhibidores de magl. |
| WO2021062232A1 (en) * | 2019-09-26 | 2021-04-01 | The Board Of Trustees Of The Leland Stanford Junior University | Methods for reducing rewarding effects of morphine without affecting its analgesic effects |
| WO2021214550A1 (en) | 2020-04-21 | 2021-10-28 | H. Lundbeck A/S | Synthesis of a monoacylglycerol lipase inhibitor |
| TWI904281B (zh) | 2020-11-13 | 2025-11-11 | 丹麥商H 朗德貝克公司 | Magl抑制劑 |
| EP4317153A4 (en) * | 2021-04-01 | 2024-02-21 | ONO Pharmaceutical Co., Ltd. | Abhd6 antagonist |
| CA3242372A1 (en) | 2021-12-29 | 2023-07-06 | Psy Therapeutics, Inc. | Inhibiting monoacylglycerol lipase (magl) |
| KR20250005229A (ko) | 2022-05-04 | 2025-01-09 | 하. 룬드벡 아크티에셀스카브 | 모노아실글리세롤 리파제 억제제로서 1,1,1,3,3,3-헥사플루오로프로판-2-일 (s)-1-(피리다진-3-일카르바모일)-6 아자스피로[2.5]옥탄-6-카르복실레이트의 결정질 형태 |
| EP4665718A1 (en) | 2023-02-13 | 2025-12-24 | Apogee Pharmaceuticals, Inc. | Small molecules as monoacylglycerol lipase (magl) inhibitors, compositions and use thereof |
Citations (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| WO2012052730A1 (en) * | 2010-10-21 | 2012-04-26 | Centro Nacional De Investigaciones Oncológicas (Cnio) | Use of pi3k inibitors for the treatment of obesity, steatosis and ageing |
| US20120208812A1 (en) * | 2009-10-23 | 2012-08-16 | Janssen Pharmaceutica N.V. | DISUBSTITUTED OCTAHYDROPYRROLO[3,4-c]PYRROLES AS OREXIN RECEPTOR MODULATORS |
Family Cites Families (6)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| SE0100326D0 (sv) * | 2001-02-02 | 2001-02-02 | Astrazeneca Ab | New compounds |
| CA2440803A1 (en) * | 2001-03-07 | 2002-09-12 | Pfizer Products Inc. | Modulators of chemokine receptor activity |
| JP2011513421A (ja) | 2008-03-05 | 2011-04-28 | ターガセプト,インコーポレイテッド | サブタイプ選択的なジアザビシクロアルカンのアミド |
| WO2011109277A1 (en) * | 2010-03-04 | 2011-09-09 | Merck Sharp & Dohme Corp. | Positive allosteric modulators of mglur2 |
| KR102179599B1 (ko) | 2012-09-25 | 2020-11-19 | 에프. 호프만-라 로슈 아게 | 이환형 유도체 |
| JP6647592B2 (ja) | 2013-07-03 | 2020-02-14 | ルンドベック ラ ホーヤ リサーチ センター,インク. | ピロロピロールカルバメート、および関連する有機化合物、医薬組成物、ならびにその医学的使用 |
-
2014
- 2014-07-01 JP JP2016524330A patent/JP6647592B2/ja not_active Expired - Fee Related
- 2014-07-01 EP EP14820480.3A patent/EP3016653A4/en not_active Withdrawn
- 2014-07-01 WO PCT/US2014/045145 patent/WO2015003002A1/en not_active Ceased
- 2014-07-01 CA CA2917050A patent/CA2917050A1/en not_active Abandoned
- 2014-07-01 CN CN201480048531.6A patent/CN105517547A/zh active Pending
- 2014-07-01 US US14/902,324 patent/US9828379B2/en not_active Expired - Fee Related
- 2014-07-01 MX MX2015017961A patent/MX2015017961A/es unknown
Patent Citations (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US20120208812A1 (en) * | 2009-10-23 | 2012-08-16 | Janssen Pharmaceutica N.V. | DISUBSTITUTED OCTAHYDROPYRROLO[3,4-c]PYRROLES AS OREXIN RECEPTOR MODULATORS |
| WO2012052730A1 (en) * | 2010-10-21 | 2012-04-26 | Centro Nacional De Investigaciones Oncológicas (Cnio) | Use of pi3k inibitors for the treatment of obesity, steatosis and ageing |
Cited By (10)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CN109996790A (zh) * | 2016-09-19 | 2019-07-09 | 阿比德治疗公司 | 哌嗪氨基甲酸酯及其制备和使用方法 |
| CN109996790B (zh) * | 2016-09-19 | 2023-05-16 | H.隆德贝克有限公司 | 哌嗪氨基甲酸酯及其制备和使用方法 |
| CN110267962A (zh) * | 2016-11-16 | 2019-09-20 | 灵北拉荷亚研究中心公司 | Magl抑制剂 |
| CN110290791A (zh) * | 2016-11-16 | 2019-09-27 | 灵北拉荷亚研究中心公司 | 药物制剂 |
| CN110267962B (zh) * | 2016-11-16 | 2022-04-01 | H.隆德贝克有限公司 | Magl抑制剂 |
| US11993588B2 (en) | 2016-11-16 | 2024-05-28 | H. Lundbeck A/S | Crystalline forms of a MAGL inhibitor |
| CN110382479A (zh) * | 2017-01-20 | 2019-10-25 | 辉瑞大药厂 | 作为magl抑制剂的氨基甲酸1,1,1-三氟-3-羟基丙-2-基酯衍生物 |
| CN111148746A (zh) * | 2017-09-29 | 2020-05-12 | 武田药品工业株式会社 | 杂环化合物 |
| US11274101B2 (en) | 2017-09-29 | 2022-03-15 | Takeda Pharmaceutical Company Limited | Heterocyclic compound |
| CN111148746B (zh) * | 2017-09-29 | 2022-08-05 | 武田药品工业株式会社 | 杂环化合物 |
Also Published As
| Publication number | Publication date |
|---|---|
| WO2015003002A1 (en) | 2015-01-08 |
| MX2015017961A (es) | 2016-10-14 |
| US20160137649A1 (en) | 2016-05-19 |
| JP6647592B2 (ja) | 2020-02-14 |
| EP3016653A4 (en) | 2017-02-22 |
| US9828379B2 (en) | 2017-11-28 |
| JP2016525092A (ja) | 2016-08-22 |
| EP3016653A1 (en) | 2016-05-11 |
| CA2917050A1 (en) | 2015-01-08 |
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| CN105517547A (zh) | 吡咯并吡咯氨基甲酸酯和相关的有机化合物、药物组合物及其医学用途 | |
| CN107660199B (zh) | 哌嗪氨基甲酸酯及其制备和使用方法 | |
| JP7177825B2 (ja) | スピロ環化合物並びにその作製及び使用方法 | |
| JP7162622B2 (ja) | ピラゾールmagl阻害剤 | |
| EP3377060B1 (en) | Pyrazole derivatives, processes for their preparation and uses thereof | |
| CN111050765B (zh) | 螺环化合物及其制造和使用方法 | |
| CN109996790B (zh) | 哌嗪氨基甲酸酯及其制备和使用方法 | |
| AU2018271876B2 (en) | Pyrazole MAGL inhibitors | |
| TW202413351A (zh) | 藉由irak4抑制劑與e3連接酶配體的軛合降解irak4及使用方法 | |
| EP3455226B1 (en) | Spirocycle compounds and methods of making and using same | |
| CN116981675A (zh) | 通过布鲁顿氏酪氨酸激酶(btk)抑制剂与e3连接酶配体的缀合降解btk和使用方法 | |
| IL297867B1 (en) | New macrocyclic lrrk2 kinase inhibitors | |
| EP4161656A1 (en) | Inhibitors of fibroblast growth factor receptor kinases | |
| CN116783199A (zh) | 作为btk抑制剂的吡唑并[1,5-a]吡嗪衍生物 | |
| CN115698020B (zh) | 大环rip2-激酶抑制剂 | |
| EP3400226A1 (en) | Derivatives of pyrroloimidazole or analogues thereof which are useful for the treatment of inter alia cancer | |
| TW202428267A (zh) | 用於降解egfr激酶之化合物 | |
| CN110655520A (zh) | 嘧啶并环化合物及其制备方法和应用 | |
| JP2023505485A (ja) | Atmキナーゼ阻害剤及び組成物並びにそれらの使用の方法 | |
| AU2021267691B2 (en) | New Macrocyclic LRRK2 kinase inhibitors | |
| EA048670B1 (ru) | Макроциклические ингибиторы lrrk2 киназы | |
| HK40004417A (en) | Spirocycle compounds and methods of making and using same | |
| HK1256634B (en) | Pyrazole compounds and methods of making and using same | |
| HK1234388A1 (en) | Methyl-and trifluoromethyl-substituted pyrrolopyridine modulators of rorc2 an methods of use thereof |
Legal Events
| Date | Code | Title | Description |
|---|---|---|---|
| C06 | Publication | ||
| PB01 | Publication | ||
| C10 | Entry into substantive examination | ||
| SE01 | Entry into force of request for substantive examination | ||
| WD01 | Invention patent application deemed withdrawn after publication |
Application publication date: 20160420 |
|
| WD01 | Invention patent application deemed withdrawn after publication |