RU2603140C2 - Соединения имидазотриазинона - Google Patents
Соединения имидазотриазинона Download PDFInfo
- Publication number
- RU2603140C2 RU2603140C2 RU2013118362/04A RU2013118362A RU2603140C2 RU 2603140 C2 RU2603140 C2 RU 2603140C2 RU 2013118362/04 A RU2013118362/04 A RU 2013118362/04A RU 2013118362 A RU2013118362 A RU 2013118362A RU 2603140 C2 RU2603140 C2 RU 2603140C2
- Authority
- RU
- Russia
- Prior art keywords
- imidazo
- trans
- alkyl
- triazin
- pyran
- Prior art date
Links
- 0 *C(*)N(CC1*)CC1C(NC1=O)=N[n]2c1cnc2* Chemical compound *C(*)N(CC1*)CC1C(NC1=O)=N[n]2c1cnc2* 0.000 description 4
- VMMIDYYLWGCUFX-UHFFFAOYSA-N CC(CNC1)C1C(NC1=O)=N[n]2c1cnc2C1CCOCC1 Chemical compound CC(CNC1)C1C(NC1=O)=N[n]2c1cnc2C1CCOCC1 VMMIDYYLWGCUFX-UHFFFAOYSA-N 0.000 description 4
- BGBNHMFVGJJHAQ-UHFFFAOYSA-N CC(CN(Cc1ccccc1)C1)C1C(N1)=NN=C(CN)C1=O Chemical compound CC(CN(Cc1ccccc1)C1)C1C(N1)=NN=C(CN)C1=O BGBNHMFVGJJHAQ-UHFFFAOYSA-N 0.000 description 3
- JXILLBAMGVRSCN-UHFFFAOYSA-N CCS(N(CC1)CCC1c1ncc2[n]1N=C(C1C(C)CN(Cc3ccccc3)C1)NC2=O)(=O)=O Chemical compound CCS(N(CC1)CCC1c1ncc2[n]1N=C(C1C(C)CN(Cc3ccccc3)C1)NC2=O)(=O)=O JXILLBAMGVRSCN-UHFFFAOYSA-N 0.000 description 2
- RPZAAFUKDPKTKP-UHFFFAOYSA-N COCN(Cc1ccccc1)C[Si](C)(C)C Chemical compound COCN(Cc1ccccc1)C[Si](C)(C)C RPZAAFUKDPKTKP-UHFFFAOYSA-N 0.000 description 2
- MSFVEEFXECBJPG-UHFFFAOYSA-N ClCc1ncccn1 Chemical compound ClCc1ncccn1 MSFVEEFXECBJPG-UHFFFAOYSA-N 0.000 description 2
- JPSJBVNIHGQGNR-UHFFFAOYSA-N O=C(C1COCCC1)ON(C(CC1)=O)C1=O Chemical compound O=C(C1COCCC1)ON(C(CC1)=O)C1=O JPSJBVNIHGQGNR-UHFFFAOYSA-N 0.000 description 2
- DCVIMWRFFDRWJM-GSQGTZRGSA-N C/C=C/C(N([C@@H](CO1)c2ccccc2)C1=O)=O Chemical compound C/C=C/C(N([C@@H](CO1)c2ccccc2)C1=O)=O DCVIMWRFFDRWJM-GSQGTZRGSA-N 0.000 description 1
- JBBPETZJSIMBKB-UHFFFAOYSA-N CC(C)(C(ON(C(CC1)=O)C1=O)=O)OCc1ccccc1 Chemical compound CC(C)(C(ON(C(CC1)=O)C1=O)=O)OCc1ccccc1 JBBPETZJSIMBKB-UHFFFAOYSA-N 0.000 description 1
- YVYICMXHUOSHCD-UHFFFAOYSA-N CC(CN(Cc1c[n]2ncccc2n1)C1)C1C(NC1=O)=N[n]2c1cnc2C1CCOCC1 Chemical compound CC(CN(Cc1c[n]2ncccc2n1)C1)C1C(NC1=O)=N[n]2c1cnc2C1CCOCC1 YVYICMXHUOSHCD-UHFFFAOYSA-N 0.000 description 1
- PABAEZJKJVXISR-UHFFFAOYSA-N CC(CN(Cc1cccc(OC)n1)C1)C1C(NC1=O)=N[n]2c1cnc2C1CCOCC1 Chemical compound CC(CN(Cc1cccc(OC)n1)C1)C1C(NC1=O)=N[n]2c1cnc2C1CCOCC1 PABAEZJKJVXISR-UHFFFAOYSA-N 0.000 description 1
- HFIGSUCJPBFTMU-UHFFFAOYSA-N CC(CN(Cc1ccccc1)C1)C1C(N1)=NN=C(CNC(C(C)(C)OCc2ccccc2)=O)C1=O Chemical compound CC(CN(Cc1ccccc1)C1)C1C(N1)=NN=C(CNC(C(C)(C)OCc2ccccc2)=O)C1=O HFIGSUCJPBFTMU-UHFFFAOYSA-N 0.000 description 1
- RTSFLNQFAPBKOZ-UHFFFAOYSA-N CC(CN(Cc1ccccc1)C1)C1C(N1)=NN=C(CNC(C2COCCC2)=O)C1=O Chemical compound CC(CN(Cc1ccccc1)C1)C1C(N1)=NN=C(CNC(C2COCCC2)=O)C1=O RTSFLNQFAPBKOZ-UHFFFAOYSA-N 0.000 description 1
- GXQCWOAJLHKWTA-UHFFFAOYSA-N CC(CN(Cc1ccccc1)C1)C1C(N1)=NN=C(CNC(c(c(C)c2)ccc2F)=O)C1=O Chemical compound CC(CN(Cc1ccccc1)C1)C1C(N1)=NN=C(CNC(c(c(C)c2)ccc2F)=O)C1=O GXQCWOAJLHKWTA-UHFFFAOYSA-N 0.000 description 1
- AZDIEPCCONVLKL-UHFFFAOYSA-N CC(CN(Cc1ccccc1)C1)C1C(NC1=O)=N[n]2c1cnc2C(C)(C)O Chemical compound CC(CN(Cc1ccccc1)C1)C1C(NC1=O)=N[n]2c1cnc2C(C)(C)O AZDIEPCCONVLKL-UHFFFAOYSA-N 0.000 description 1
- MVCWZQVACBTJHE-UHFFFAOYSA-N CC(CN(Cc1ccccc1)C1)C1C(NC1=O)=N[n]2c1cnc2C1CCNCC1 Chemical compound CC(CN(Cc1ccccc1)C1)C1C(NC1=O)=N[n]2c1cnc2C1CCNCC1 MVCWZQVACBTJHE-UHFFFAOYSA-N 0.000 description 1
- UECRIHHANVMNHP-UHFFFAOYSA-N CC(CN(Cc1ccccc1)C1)C1C(NC1=O)=N[n]2c1cnc2C1CCOCC1 Chemical compound CC(CN(Cc1ccccc1)C1)C1C(NC1=O)=N[n]2c1cnc2C1CCOCC1 UECRIHHANVMNHP-UHFFFAOYSA-N 0.000 description 1
- KLQYKJMMAPSQCP-UHFFFAOYSA-N CC(CN(Cc1ccccc1)C1)C1C(OC)=O Chemical compound CC(CN(Cc1ccccc1)C1)C1C(OC)=O KLQYKJMMAPSQCP-UHFFFAOYSA-N 0.000 description 1
- PFBMCRPVEXEABN-UHFFFAOYSA-N CC(CN(Cc1nc2ccccc2cc1)C1)C1C(NC1=O)=N[n]2c1cnc2C1CCOCC1 Chemical compound CC(CN(Cc1nc2ccccc2cc1)C1)C1C(NC1=O)=N[n]2c1cnc2C1CCOCC1 PFBMCRPVEXEABN-UHFFFAOYSA-N 0.000 description 1
- HKDOZTIOPAGQIS-UHFFFAOYSA-N CC(CN(Cc1ncccn1)C1)C1C(NC1=O)=N[n]2c1cnc2C1CCOCC1 Chemical compound CC(CN(Cc1ncccn1)C1)C1C(NC1=O)=N[n]2c1cnc2C1CCOCC1 HKDOZTIOPAGQIS-UHFFFAOYSA-N 0.000 description 1
- OSPAFZLTSDSZGL-UHFFFAOYSA-N CCS(N(CC1)CCC1c1ncc2[n]1N=C(C1C(C)CN(Cc3ncccn3)C1)NC2=O)(=O)=O Chemical compound CCS(N(CC1)CCC1c1ncc2[n]1N=C(C1C(C)CN(Cc3ncccn3)C1)NC2=O)(=O)=O OSPAFZLTSDSZGL-UHFFFAOYSA-N 0.000 description 1
- WOWZRTFXRWWAPS-UHFFFAOYSA-N CCS(N(CC1)CCC1c1ncc2[n]1N=C(C1C(C)CNC1)NC2=O)(=O)=O Chemical compound CCS(N(CC1)CCC1c1ncc2[n]1N=C(C1C(C)CNC1)NC2=O)(=O)=O WOWZRTFXRWWAPS-UHFFFAOYSA-N 0.000 description 1
- OIWHGYGUHGWJOI-UHFFFAOYSA-N CCc1n[n](cccc2)c2n1 Chemical compound CCc1n[n](cccc2)c2n1 OIWHGYGUHGWJOI-UHFFFAOYSA-N 0.000 description 1
- HVGPUQMGDVWEGP-UHFFFAOYSA-N COc1cccc(CCl)n1 Chemical compound COc1cccc(CCl)n1 HVGPUQMGDVWEGP-UHFFFAOYSA-N 0.000 description 1
- BGBNHMFVGJJHAQ-JTDNENJMSA-N C[C@H](CN(Cc1ccccc1)C1)C1C(N1)=NN=C(CN)C1=O Chemical compound C[C@H](CN(Cc1ccccc1)C1)C1C(N1)=NN=C(CN)C1=O BGBNHMFVGJJHAQ-JTDNENJMSA-N 0.000 description 1
- QWFKQOUZRAUJKO-HZULEVJDSA-N C[C@H](CN(Cc1ccccc1)C1)[C@@H]1C(N(C1O[C@H]1OC1)[C@@H]1c1ccccc1)=O Chemical compound C[C@H](CN(Cc1ccccc1)C1)[C@@H]1C(N(C1O[C@H]1OC1)[C@@H]1c1ccccc1)=O QWFKQOUZRAUJKO-HZULEVJDSA-N 0.000 description 1
- FNNHZCNVDAHYQW-DNVCBOLYSA-N C[C@H](CN(Cc1ccccc1)C1)[C@@H]1C(N1)=NN=C(CN(C(c2c3cccc2)=O)C3=O)C1=O Chemical compound C[C@H](CN(Cc1ccccc1)C1)[C@@H]1C(N1)=NN=C(CN(C(c2c3cccc2)=O)C3=O)C1=O FNNHZCNVDAHYQW-DNVCBOLYSA-N 0.000 description 1
- KZUXJRQQHJREGH-UHFFFAOYSA-N Cc1cc(F)ccc1C(Cl)=O Chemical compound Cc1cc(F)ccc1C(Cl)=O KZUXJRQQHJREGH-UHFFFAOYSA-N 0.000 description 1
- SRKDRUWQKBCCJU-UHFFFAOYSA-N ClCc1c[n]2ncccc2n1 Chemical compound ClCc1c[n]2ncccc2n1 SRKDRUWQKBCCJU-UHFFFAOYSA-N 0.000 description 1
- DDEAEWMDOSXKBX-UHFFFAOYSA-N ClCc1nc2ccccc2cc1 Chemical compound ClCc1nc2ccccc2cc1 DDEAEWMDOSXKBX-UHFFFAOYSA-N 0.000 description 1
- OPIZSFSIIDDGFE-BVSSSWPKSA-N N=C/C=C\c1nc(CCl)c[nH]1 Chemical compound N=C/C=C\c1nc(CCl)c[nH]1 OPIZSFSIIDDGFE-BVSSSWPKSA-N 0.000 description 1
- TWCRMRZDNRRWDC-UHFFFAOYSA-N O=C(c1c[o]cc1)ON(C(CC1)=O)C1=O Chemical compound O=C(c1c[o]cc1)ON(C(CC1)=O)C1=O TWCRMRZDNRRWDC-UHFFFAOYSA-N 0.000 description 1
- MIBCYYGVLHFYSD-UHFFFAOYSA-N OC(C1=COCCC1)=O Chemical compound OC(C1=COCCC1)=O MIBCYYGVLHFYSD-UHFFFAOYSA-N 0.000 description 1
- YEWPVCUHKJABMV-UHFFFAOYSA-N OC(C1COCCC1)=O Chemical compound OC(C1COCCC1)=O YEWPVCUHKJABMV-UHFFFAOYSA-N 0.000 description 1
- IHCCAYCGZOLTEU-UHFFFAOYSA-N OC(c1c[o]cc1)=O Chemical compound OC(c1c[o]cc1)=O IHCCAYCGZOLTEU-UHFFFAOYSA-N 0.000 description 1
- LFCWHDGQCWJKCG-UHFFFAOYSA-N OCc1nccnc1 Chemical compound OCc1nccnc1 LFCWHDGQCWJKCG-UHFFFAOYSA-N 0.000 description 1
- NQTADLQHYWFPDB-UHFFFAOYSA-N ON(C(CC1)=O)C1=O Chemical compound ON(C(CC1)=O)C1=O NQTADLQHYWFPDB-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
- A61P21/00—Drugs for disorders of the muscular or neuromuscular 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
-
- 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
- A61P25/14—Drugs for disorders of the nervous system for treating abnormal movements, e.g. chorea, dyskinesia
-
- 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
- A61P25/14—Drugs for disorders of the nervous system for treating abnormal movements, e.g. chorea, dyskinesia
- A61P25/16—Anti-Parkinson drugs
-
- 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
- A61P25/18—Antipsychotics, i.e. neuroleptics; Drugs for mania or schizophrenia
-
- 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
- A61P25/22—Anxiolytics
-
- 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
- A61P27/00—Drugs for disorders of the senses
- A61P27/02—Ophthalmic agents
- A61P27/06—Antiglaucoma agents or miotics
-
- 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
- A61P31/14—Antivirals for RNA viruses
- A61P31/18—Antivirals for RNA viruses for HIV
-
- 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)
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Engineering & Computer Science (AREA)
- Life Sciences & Earth Sciences (AREA)
- General Health & Medical Sciences (AREA)
- Veterinary Medicine (AREA)
- Chemical Kinetics & Catalysis (AREA)
- General Chemical & Material Sciences (AREA)
- Medicinal Chemistry (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Pharmacology & Pharmacy (AREA)
- Animal Behavior & Ethology (AREA)
- Public Health (AREA)
- Neurology (AREA)
- Biomedical Technology (AREA)
- Neurosurgery (AREA)
- Virology (AREA)
- Psychology (AREA)
- Psychiatry (AREA)
- Ophthalmology & Optometry (AREA)
- Tropical Medicine & Parasitology (AREA)
- AIDS & HIV (AREA)
- Oncology (AREA)
- Hospice & Palliative Care (AREA)
- Molecular Biology (AREA)
- Communicable Diseases (AREA)
- Anesthesiology (AREA)
- Orthopedic Medicine & Surgery (AREA)
- Physical Education & Sports Medicine (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 |
|---|---|---|---|
| US38469410P | 2010-09-20 | 2010-09-20 | |
| US61/384,694 | 2010-09-20 | ||
| PCT/US2011/052399 WO2012040230A1 (en) | 2010-09-20 | 2011-09-20 | Imidazotriazinone compounds |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| RU2013118362A RU2013118362A (ru) | 2014-10-27 |
| RU2603140C2 true RU2603140C2 (ru) | 2016-11-20 |
Family
ID=44720178
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| RU2013118362/04A RU2603140C2 (ru) | 2010-09-20 | 2011-09-20 | Соединения имидазотриазинона |
Country Status (16)
| Country | Link |
|---|---|
| US (3) | US20120157458A1 (enExample) |
| EP (2) | EP3181566A1 (enExample) |
| JP (2) | JP5855109B2 (enExample) |
| CN (1) | CN103313988B (enExample) |
| AR (1) | AR083058A1 (enExample) |
| AU (2) | AU2011305568B2 (enExample) |
| BR (1) | BR112013008140A8 (enExample) |
| CA (1) | CA2811714C (enExample) |
| DK (1) | DK2619208T3 (enExample) |
| ES (1) | ES2610360T3 (enExample) |
| MX (1) | MX2013003093A (enExample) |
| PL (1) | PL2619208T3 (enExample) |
| RU (1) | RU2603140C2 (enExample) |
| TW (1) | TWI541244B (enExample) |
| UY (1) | UY33616A (enExample) |
| WO (1) | WO2012040230A1 (enExample) |
Families Citing this family (27)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| DK2619208T3 (en) * | 2010-09-20 | 2017-01-30 | Ironwood Pharmaceuticals Inc | IMIDAZOTRIAZINON COMPOUNDS |
| EP2906562B1 (en) * | 2011-10-10 | 2016-10-05 | H. Lundbeck A/S | Pde9i with imidazo pyrazinone backbone |
| AP2014007820A0 (en) | 2012-01-26 | 2014-07-31 | Lundbeck & Co As H | PDE9 inhibitors with imidazo triazinone backbone |
| HK1206726A1 (en) * | 2012-03-19 | 2016-01-15 | Ironwood Pharmaceuticals, Inc. | Imidazotriazinone compounds |
| CN102786525B (zh) | 2012-08-08 | 2014-12-17 | 中山大学 | N-取代吡唑并[3,4-d]嘧啶酮类化合物、其制备方法及其应用 |
| WO2014024125A1 (en) | 2012-08-08 | 2014-02-13 | Celon Pharma S.A. | Pyrazolo[4,3-d]pyrimidin-7(6h)-one derivatives as pde9 inhibitors |
| CN104884449A (zh) | 2012-10-31 | 2015-09-02 | 拜尔农作物科学股份公司 | 作为害虫防治剂的新的杂环化合物 |
| TW201629064A (zh) | 2014-10-10 | 2016-08-16 | Ｈ 朗德貝克公司 | 作爲ｐｄｅ１抑制劑之三唑並吡酮 |
| US20180044343A1 (en) * | 2015-03-16 | 2018-02-15 | Sumitomo Dainippon Pharma Co., Ltd. | Bicyclic imidazolo derivative |
| US20160311831A1 (en) * | 2015-04-22 | 2016-10-27 | H. Lundbeck A/S | Imidazotriazinones as PDE1 Inhibitors |
| JO3627B1 (ar) * | 2015-04-30 | 2020-08-27 | H Lundbeck As | إيميدازو بيرازينونات على هيئة مثبطات pde1 |
| HRP20210543T1 (hr) | 2015-07-07 | 2021-05-14 | H. Lundbeck A/S | Inhibitori pde9 s imidazo triazinonskom okosnicom i imidazo pirazinonskom okosnicom za liječenje perifernih bolesti |
| WO2017070293A1 (en) * | 2015-10-20 | 2017-04-27 | Ironwood Pharmaceuticals, Inc. | Phosphodiesterase 9 inhibitor and levodopa therapy |
| CN105669680B (zh) * | 2016-03-24 | 2018-02-23 | 南京药捷安康生物科技有限公司 | 吡咯并[2,1‑f][1,2,4]三嗪‑4(1H)‑酮衍生物类PDE9A抑制剂 |
| TWI729109B (zh) | 2016-04-12 | 2021-06-01 | 丹麥商Ｈ 朗德貝克公司 | 作爲PDE1抑制劑的1,5-二氫-4H-吡唑并[3,4-d]嘧啶-4-酮和1,5-二氫-4H-吡唑并[4,3-c]吡啶-4-酮 |
| WO2018009424A1 (en) | 2016-07-06 | 2018-01-11 | Imara, Inc. | Pde9 inhibitors for treatment of peripheral diseases |
| CN109843884B (zh) | 2016-10-18 | 2022-03-04 | H.隆德贝克有限公司 | 作为pde1抑制剂的咪唑并吡嗪酮、吡唑并嘧啶酮和吡唑并吡啶酮 |
| HRP20201326T1 (hr) | 2016-10-28 | 2020-11-27 | H. Lundbeck A/S | Kombinacijska liječenja koja sadrže imidazopirazinone za liječenje psihijatrijskih i/ili kognitivnih poremećaja |
| AU2017350477A1 (en) | 2016-10-28 | 2019-04-18 | H. Lundbeck A/S | Combination treatments comprising administration of imidazopyrazinones |
| CA3064004A1 (en) * | 2017-05-26 | 2018-11-29 | Imara Inc. | Methods of making and using pde9 inhibitors |
| CN112469413B (zh) | 2018-05-25 | 2024-01-12 | 伊马拉公司 | 6-[(3s,4s)-4-甲基-1-(嘧啶-2-基甲基)吡咯烷-3-基]-3-四氢吡喃-4-基-7h-咪唑并[1,5-a]吡嗪-8-酮的一水合物和结晶形态 |
| EP3843737A4 (en) | 2018-08-31 | 2022-06-01 | Imara Inc. | PDE9 INHIBITORS FOR THE TREATMENT OF SICKLE CELL DISEASE |
| WO2020102374A1 (en) * | 2018-11-14 | 2020-05-22 | The Board Of Trustees Of The Leland Stanford Junior University | Targeting of makap-pde4d3 complexes in neurodegenerative disease |
| KR102712818B1 (ko) | 2018-12-06 | 2024-09-30 | 한국화학연구원 | Pde9a 저해 활성을 가지는 화합물 및 이들의 의약 용도 |
| KR20220086607A (ko) * | 2019-10-21 | 2022-06-23 | 에스케이바이오팜 주식회사 | 발달 장애의 예방, 경감 또는 치료를 위한 이미다조피리미딘 또는 이미다조트리아진 화합물의 용도 |
| CN112724079A (zh) * | 2021-02-04 | 2021-04-30 | 康化（上海）新药研发有限公司 | 一种6-甲氧基吡啶甲酸甲酯的合成方法 |
| GB2632307A (en) * | 2023-08-02 | 2025-02-05 | Duke Street Bio Ltd | PARP1 inhibitor compounds |
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- 2011-09-20 DK DK11761793.6T patent/DK2619208T3/en active
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| AR083058A1 (es) | 2013-01-30 |
| WO2012040230A1 (en) | 2012-03-29 |
| BR112013008140A8 (pt) | 2018-04-03 |
| CA2811714A1 (en) | 2012-03-29 |
| US20140330014A1 (en) | 2014-11-06 |
| CN103313988A (zh) | 2013-09-18 |
| UY33616A (es) | 2012-04-30 |
| EP2619208A1 (en) | 2013-07-31 |
| EP2619208B1 (en) | 2016-11-09 |
| US9540380B2 (en) | 2017-01-10 |
| AU2016200970A1 (en) | 2016-03-03 |
| BR112013008140A2 (pt) | 2017-12-05 |
| RU2013118362A (ru) | 2014-10-27 |
| AU2011305568A1 (en) | 2013-04-04 |
| PL2619208T3 (pl) | 2017-03-31 |
| ES2610360T3 (es) | 2017-04-27 |
| US20120157458A1 (en) | 2012-06-21 |
| JP5855109B2 (ja) | 2016-02-09 |
| TWI541244B (zh) | 2016-07-11 |
| AU2011305568B2 (en) | 2015-12-10 |
| TW201217381A (en) | 2012-05-01 |
| JP2013540755A (ja) | 2013-11-07 |
| DK2619208T3 (en) | 2017-01-30 |
| US20170152265A1 (en) | 2017-06-01 |
| MX2013003093A (es) | 2013-10-28 |
| CA2811714C (en) | 2017-11-21 |
| EP3181566A1 (en) | 2017-06-21 |
| CN103313988B (zh) | 2016-06-08 |
| JP2016104747A (ja) | 2016-06-09 |
| HK1187908A1 (en) | 2014-04-17 |
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