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)
- Organic Chemistry (AREA)
- Chemical & Material Sciences (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Engineering & Computer Science (AREA)
- Life Sciences & Earth Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Medicinal Chemistry (AREA)
- Pharmacology & Pharmacy (AREA)
- General Chemical & Material Sciences (AREA)
- Animal Behavior & Ethology (AREA)
- General Health & Medical Sciences (AREA)
- Public Health (AREA)
- Veterinary Medicine (AREA)
- Neurology (AREA)
- Biomedical Technology (AREA)
- Neurosurgery (AREA)
- Psychology (AREA)
- Ophthalmology & Optometry (AREA)
- Psychiatry (AREA)
- Virology (AREA)
- Molecular Biology (AREA)
- Tropical Medicine & Parasitology (AREA)
- AIDS & HIV (AREA)
- Communicable Diseases (AREA)
- Oncology (AREA)
- Anesthesiology (AREA)
- Hospice & Palliative Care (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 |
|---|---|---|---|---|
| AU2011305568B2 (en) | 2010-09-20 | 2015-12-10 | Ironwood Pharmaceuticals, Inc. | Imidazotriazinone compounds |
| CN106905324B (zh) * | 2011-10-10 | 2018-09-25 | H.隆德贝克有限公司 | 具有咪唑并吡嗪酮骨架的pde9抑制剂 |
| CN104093720B (zh) * | 2012-01-26 | 2017-04-12 | H.隆德贝克有限公司 | 具有咪唑并三嗪酮骨架的pde9抑制剂 |
| HK1206726A1 (en) | 2012-03-19 | 2016-01-15 | Ironwood Pharmaceuticals, Inc. | Imidazotriazinone compounds |
| WO2014024125A1 (en) | 2012-08-08 | 2014-02-13 | Celon Pharma S.A. | Pyrazolo[4,3-d]pyrimidin-7(6h)-one derivatives as pde9 inhibitors |
| 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 |
| 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 |
| BR112018000254A2 (pt) | 2015-07-07 | 2018-09-04 | H Lundbeck As | inibidores de pde9 com cadeia principal de imidazotriazinona e cadeia principal de imidazopirazinona para o tratamento de doenças periféricas |
| 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 |
| AU2017292650A1 (en) | 2016-07-06 | 2018-12-13 | H. Lundbeck A/S | PDE9 inhibitors for treatment of peripheral diseases |
| EP3529250B1 (en) | 2016-10-18 | 2023-12-06 | H. Lundbeck A/S | Imidazopyrazinones, pyrazolopyrimidinones and pyrazolopyridinones as pde1 inhibitors |
| SG11201903770UA (en) | 2016-10-28 | 2019-05-30 | H Lundbeck As | Combination treatments comprising imidazopyrazinones for the treatment of psychiatric and/or cognitive disorders |
| BR112018013084A2 (pt) | 2016-10-28 | 2018-12-11 | H Lundbeck As | tratamentos de combinação compreendendo a administração de imidazopirazinonas |
| SI3630772T1 (sl) | 2017-05-26 | 2024-05-31 | Cardurion Pharmaceuticals, Inc., | Postopki izdelave in uporabe zaviralcev pde9 |
| EP3801526B1 (en) | 2018-05-25 | 2023-12-27 | Imara Inc. | Monohydrate and crystalline forms of 6-[(3s,4s)-4-methyl-1- (pyrimidin-2-ylmethyl)pyrrolidin-3-yl]-3-tetrahydropyran-4-yl- 7h-imid azo [1,5- a] pyrazin-8-one |
| CN112996512B (zh) | 2018-08-31 | 2025-01-03 | 卡都瑞恩医药公司 | 用于治疗镰状细胞病的pde9抑制剂 |
| US20220041667A1 (en) * | 2018-11-14 | 2022-02-10 | 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 |
| EP4049661A4 (en) * | 2019-10-21 | 2023-11-08 | SK Biopharmaceuticals Co., Ltd. | USE OF AN IMIDAZOPYRIMIDINE OR IMIDAZOTRIAZINE COMPOUND TO PREVENT, RELIEF OR TREAT DEVELOPMENTAL DISABILITIES |
| 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 |
Citations (5)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| WO2002098873A1 (en) * | 2001-06-01 | 2002-12-12 | Bayer Healthcare Ag | 2-heteroaryl-imidazotriazinones and their use in the treatment of inflammatory or immune diseases |
| WO2003037432A1 (en) * | 2001-11-02 | 2003-05-08 | Pfizer Products Inc. | Treatment of insulin resistance syndrome and type 2 diabetes with pde9 inhibitors |
| WO2004096811A1 (en) * | 2003-04-30 | 2004-11-11 | Pfizer Products Inc. | Pde9 inhibitors for treating type 2 diabetes, metabokic syndrome, and cardiovascular disease |
| RU2260593C2 (ru) * | 1997-11-12 | 2005-09-20 | Байер ХельсКер АГ | 2-фенилзамещенные имидазотриазиноны, способ их получения и фармацевтическая композиция на их основе, обладающая свойствами ингибитора фосфодиэстеразы i,ii и v |
| WO2008139293A1 (en) * | 2007-05-11 | 2008-11-20 | Pfizer Inc. | Amino-heterocyclic compounds |
Family Cites Families (11)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| PT72878B (en) | 1980-04-24 | 1983-03-29 | Merck & Co Inc | Process for preparing mannich-base hydroxamic acid pro-drugs for the improved delivery of non-steroidal anti-inflammatory agents |
| TR200001338T2 (tr) | 1997-11-12 | 2000-08-21 | Bayer Aktiengesellschaft | 2-Fenil-ikameli imidazotriazinonlar |
| US7087605B2 (en) | 2001-06-01 | 2006-08-08 | Bayer Aktiengesellschaft | 5-Ethyl-imidazotriazinones |
| DE10229778A1 (de) * | 2002-07-03 | 2004-01-29 | Bayer Ag | Neue Verwendung von Imidazotriazinonen |
| CA2514733A1 (en) | 2003-02-28 | 2004-09-16 | Transform Pharmaceuticals, Inc. | Pharmaceutical co-crystal compositions of drugs such as carbamazepine, celecoxib, olanzapine, itraconazole, topiramate, modafinil, 5-fluorouracil, hydrochlorothiazide, acetaminophen, aspirin, flurbiprofen, phenytoin and ibuprofen |
| WO2006127368A2 (en) | 2005-05-20 | 2006-11-30 | Lexicon Genetics Incorporated | Methods for synthesizing imidazotriazinones |
| EP1896476A2 (en) | 2005-06-28 | 2008-03-12 | Orchid Research Laboratories Limited | Novel pyrazolopyrimidinone derivatives |
| BRPI0914772A2 (pt) | 2008-06-25 | 2015-10-20 | Envivo Pharmaceuticals Inc | compostos heterocíclicos 1,2-dissubstituídos |
| AU2011305568B2 (en) | 2010-09-20 | 2015-12-10 | Ironwood Pharmaceuticals, Inc. | Imidazotriazinone compounds |
| CN104093720B (zh) | 2012-01-26 | 2017-04-12 | H.隆德贝克有限公司 | 具有咪唑并三嗪酮骨架的pde9抑制剂 |
| HK1206726A1 (en) | 2012-03-19 | 2016-01-15 | Ironwood Pharmaceuticals, Inc. | Imidazotriazinone compounds |
-
2011
- 2011-09-20 AU AU2011305568A patent/AU2011305568B2/en not_active Ceased
- 2011-09-20 ES ES11761793.6T patent/ES2610360T3/es active Active
- 2011-09-20 EP EP16197573.5A patent/EP3181566A1/en not_active Withdrawn
- 2011-09-20 EP EP11761793.6A patent/EP2619208B1/en not_active Not-in-force
- 2011-09-20 AR ARP110103426A patent/AR083058A1/es unknown
- 2011-09-20 CN CN201180055157.9A patent/CN103313988B/zh not_active Expired - Fee Related
- 2011-09-20 PL PL11761793T patent/PL2619208T3/pl unknown
- 2011-09-20 RU RU2013118362/04A patent/RU2603140C2/ru not_active IP Right Cessation
- 2011-09-20 MX MX2013003093A patent/MX2013003093A/es active IP Right Grant
- 2011-09-20 WO PCT/US2011/052399 patent/WO2012040230A1/en not_active Ceased
- 2011-09-20 US US13/237,795 patent/US20120157458A1/en not_active Abandoned
- 2011-09-20 DK DK11761793.6T patent/DK2619208T3/en active
- 2011-09-20 CA CA2811714A patent/CA2811714C/en not_active Expired - Fee Related
- 2011-09-20 JP JP2013530234A patent/JP5855109B2/ja not_active Expired - Fee Related
- 2011-09-20 TW TW100133825A patent/TWI541244B/zh not_active IP Right Cessation
- 2011-09-20 BR BR112013008140A patent/BR112013008140A8/pt not_active IP Right Cessation
- 2011-09-20 UY UY0001033616A patent/UY33616A/es unknown
-
2014
- 2014-07-17 US US14/334,073 patent/US9540380B2/en not_active Expired - Fee Related
-
2015
- 2015-12-08 JP JP2015239514A patent/JP2016104747A/ja active Pending
-
2016
- 2016-02-16 AU AU2016200970A patent/AU2016200970A1/en not_active Abandoned
- 2016-12-07 US US15/371,935 patent/US20170152265A1/en not_active Abandoned
Patent Citations (5)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| RU2260593C2 (ru) * | 1997-11-12 | 2005-09-20 | Байер ХельсКер АГ | 2-фенилзамещенные имидазотриазиноны, способ их получения и фармацевтическая композиция на их основе, обладающая свойствами ингибитора фосфодиэстеразы i,ii и v |
| WO2002098873A1 (en) * | 2001-06-01 | 2002-12-12 | Bayer Healthcare Ag | 2-heteroaryl-imidazotriazinones and their use in the treatment of inflammatory or immune diseases |
| WO2003037432A1 (en) * | 2001-11-02 | 2003-05-08 | Pfizer Products Inc. | Treatment of insulin resistance syndrome and type 2 diabetes with pde9 inhibitors |
| WO2004096811A1 (en) * | 2003-04-30 | 2004-11-11 | Pfizer Products Inc. | Pde9 inhibitors for treating type 2 diabetes, metabokic syndrome, and cardiovascular disease |
| WO2008139293A1 (en) * | 2007-05-11 | 2008-11-20 | Pfizer Inc. | Amino-heterocyclic compounds |
Also Published As
| Publication number | Publication date |
|---|---|
| DK2619208T3 (en) | 2017-01-30 |
| BR112013008140A2 (pt) | 2017-12-05 |
| AR083058A1 (es) | 2013-01-30 |
| EP3181566A1 (en) | 2017-06-21 |
| JP5855109B2 (ja) | 2016-02-09 |
| UY33616A (es) | 2012-04-30 |
| CN103313988A (zh) | 2013-09-18 |
| US20140330014A1 (en) | 2014-11-06 |
| EP2619208B1 (en) | 2016-11-09 |
| CN103313988B (zh) | 2016-06-08 |
| AU2011305568A1 (en) | 2013-04-04 |
| US20120157458A1 (en) | 2012-06-21 |
| TW201217381A (en) | 2012-05-01 |
| CA2811714A1 (en) | 2012-03-29 |
| BR112013008140A8 (pt) | 2018-04-03 |
| PL2619208T3 (pl) | 2017-03-31 |
| TWI541244B (zh) | 2016-07-11 |
| EP2619208A1 (en) | 2013-07-31 |
| RU2013118362A (ru) | 2014-10-27 |
| CA2811714C (en) | 2017-11-21 |
| AU2016200970A1 (en) | 2016-03-03 |
| US20170152265A1 (en) | 2017-06-01 |
| WO2012040230A1 (en) | 2012-03-29 |
| JP2016104747A (ja) | 2016-06-09 |
| JP2013540755A (ja) | 2013-11-07 |
| US9540380B2 (en) | 2017-01-10 |
| HK1187908A1 (en) | 2014-04-17 |
| ES2610360T3 (es) | 2017-04-27 |
| AU2011305568B2 (en) | 2015-12-10 |
| MX2013003093A (es) | 2013-10-28 |
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| EP2619208B1 (en) | Imidazotriazinone compounds | |
| US9969742B2 (en) | Imidazotriazinone compounds | |
| TWI829676B (zh) | 噁二唑暫時受體電位通道抑制劑 | |
| EP3204387B1 (en) | Triazolopyrazinones as pde1 inhibitors | |
| JP2016537369A (ja) | カゼインキナーゼ１ｄ／ｅ阻害剤としての置換された４，５，６，７−テトラヒドロピラゾロ［１，５−ａ］ピラジン誘導体 | |
| KR20150027267A (ko) | LRRK2 억제제로서의 4-(치환된-아미노)-7H-피롤로[2,3-d]피리미딘 | |
| JP2019532985A (ja) | ＰＤＥ２阻害剤としての［１，２，４］トリアゾロ［１，５−ａ］ピリミジン誘導体 | |
| JP2018513184A (ja) | Ｐｄｅ１阻害剤としてのイミダゾトリアジノン | |
| JP2024545591A (ja) | ミエロイド細胞に発現するトリガー受容体２アゴニストとしての複素環化合物及び使用方法 | |
| JP2019532990A (ja) | ＰＤＥ２阻害剤としての［１，２，４］トリアゾロ［１，５−ａ］ピリミジン化合物 | |
| JP2019532983A (ja) | ＰＤＥ２阻害剤としての［１，２，４］トリアゾロ［１，５−ａ］ピリミジン化合物 | |
| KR20260057425A (ko) | 화합물, 조성물, 및 방법 | |
| HK1187908B (en) | Imidazotriazinone compounds | |
| HK1234039A1 (en) | Imidazotriazinone compounds | |
| EP4640274A1 (en) | Lpar1 inhibitors | |
| CN117659023A (zh) | 吡啶乙酰胺类衍生物、包含其的药物组合物及其医药用途 | |
| HK40031697B (en) | Tetrahydro-imidazo quinoline compositions as cbp/p300 inhibitors | |
| HK40031697A (en) | Tetrahydro-imidazo quinoline compositions as cbp/p300 inhibitors |
Legal Events
| Date | Code | Title | Description |
|---|---|---|---|
| HZ9A | Changing address for correspondence with an applicant | ||
| HZ9A | Changing address for correspondence with an applicant | ||
| MM4A | The patent is invalid due to non-payment of fees |
Effective date: 20180921 |