CN103221404B - 可用作pde10抑制剂的不饱和氮杂环化合物 - Google Patents
可用作pde10抑制剂的不饱和氮杂环化合物 Download PDFInfo
- Publication number
- CN103221404B CN103221404B CN201180034741.6A CN201180034741A CN103221404B CN 103221404 B CN103221404 B CN 103221404B CN 201180034741 A CN201180034741 A CN 201180034741A CN 103221404 B CN103221404 B CN 103221404B
- Authority
- CN
- China
- Prior art keywords
- pyrazin
- azetidin
- quinoline
- quinolin
- benzimidazol
- 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.)
- Expired - Fee Related
Links
- 0 C*c1nc2ccccc2cc1 Chemical compound C*c1nc2ccccc2cc1 0.000 description 13
- VRVUOIHXJJWKIY-UHFFFAOYSA-N CC(C)(C)OC(N(CC1)CCC1C(N(C)C)=O)=O Chemical compound CC(C)(C)OC(N(CC1)CCC1C(N(C)C)=O)=O VRVUOIHXJJWKIY-UHFFFAOYSA-N 0.000 description 2
- QQFDVJXNIXQJGW-UHFFFAOYSA-N CC(C)(C)OC(N(CC1)CCN1C(C)=O)=O Chemical compound CC(C)(C)OC(N(CC1)CCN1C(C)=O)=O QQFDVJXNIXQJGW-UHFFFAOYSA-N 0.000 description 2
- ZQLSMWMTXZPLME-UHFFFAOYSA-N CC(CC1)CN1c1nccnc1C1CNC1 Chemical compound CC(CC1)CN1c1nccnc1C1CNC1 ZQLSMWMTXZPLME-UHFFFAOYSA-N 0.000 description 2
- HEGNGLPBQBDBMW-UHFFFAOYSA-N C(CNCC1)C1c1ncccc1-c1ccccc1 Chemical compound C(CNCC1)C1c1ncccc1-c1ccccc1 HEGNGLPBQBDBMW-UHFFFAOYSA-N 0.000 description 1
- HRLQZWRDEUWSGA-UHFFFAOYSA-N CC(C)(C)OC(N(C1)CC1c1ncccc1-c1ccccc1)=O Chemical compound CC(C)(C)OC(N(C1)CC1c1ncccc1-c1ccccc1)=O HRLQZWRDEUWSGA-UHFFFAOYSA-N 0.000 description 1
- OBOPLRSFRBGBJA-UHFFFAOYSA-N CC(C)(C)OC(N(CC1)CC=C1c1nccnc1C1CNC1)=O Chemical compound CC(C)(C)OC(N(CC1)CC=C1c1nccnc1C1CNC1)=O OBOPLRSFRBGBJA-UHFFFAOYSA-N 0.000 description 1
- KVOUHLVOTMOJBS-UHFFFAOYSA-N CC(C)(C)OC(N1CC2(CNC2)C1)=O Chemical compound CC(C)(C)OC(N1CC2(CNC2)C1)=O KVOUHLVOTMOJBS-UHFFFAOYSA-N 0.000 description 1
- STCQTYCEUVUIQM-ALDSOSFCSA-N CC(C)/C(/C1=NCCN=C1[C@H](C)CNc1nc(C(C)=CCC2)c2cc1)=C\C(OC)=C Chemical compound CC(C)/C(/C1=NCCN=C1[C@H](C)CNc1nc(C(C)=CCC2)c2cc1)=C\C(OC)=C STCQTYCEUVUIQM-ALDSOSFCSA-N 0.000 description 1
- RYRCJKCDYLPAIM-UHFFFAOYSA-N CC(CC1)CN1c1nccnc1C(C1)CN1C(OC(C)(C)C)=O Chemical compound CC(CC1)CN1c1nccnc1C(C1)CN1C(OC(C)(C)C)=O RYRCJKCDYLPAIM-UHFFFAOYSA-N 0.000 description 1
- QOUYZLCEJIVBDE-BPQKFIKYSA-N CC(CCC1)CN1C(/C(/C(C1)CN1/C(/C=C)=C/C=C1\[C@H](C)CCCC1)=N\CCN)=C Chemical compound CC(CCC1)CN1C(/C(/C(C1)CN1/C(/C=C)=C/C=C1\[C@H](C)CCCC1)=N\CCN)=C QOUYZLCEJIVBDE-BPQKFIKYSA-N 0.000 description 1
- PKDPUENCROCRCH-UHFFFAOYSA-N CC(N1CCNCC1)=O Chemical compound CC(N1CCNCC1)=O PKDPUENCROCRCH-UHFFFAOYSA-N 0.000 description 1
- AVBGIJNNMIBMQG-MQWKRIRWSA-N CC1CC(C)(C)[C@@H](C)C1 Chemical compound CC1CC(C)(C)[C@@H](C)C1 AVBGIJNNMIBMQG-MQWKRIRWSA-N 0.000 description 1
- UZOFELREXGAFOI-UHFFFAOYSA-N CC1CCNCC1 Chemical compound CC1CCNCC1 UZOFELREXGAFOI-UHFFFAOYSA-N 0.000 description 1
- NKVHPQHTLUBZHH-UHFFFAOYSA-N CCCNC(CC)CCC=N Chemical compound CCCNC(CC)CCC=N NKVHPQHTLUBZHH-UHFFFAOYSA-N 0.000 description 1
- VPFSBLPQTSHASP-UHFFFAOYSA-N CC[I]1C(C(C2)CN2C(OC(C)(C)C)=O)=C(C)N=CC1 Chemical compound CC[I]1C(C(C2)CN2C(OC(C)(C)C)=O)=C(C)N=CC1 VPFSBLPQTSHASP-UHFFFAOYSA-N 0.000 description 1
- KYINPWAJIVTFBW-YFKPBYRVSA-N C[C@@H]1CNCC1 Chemical compound C[C@@H]1CNCC1 KYINPWAJIVTFBW-YFKPBYRVSA-N 0.000 description 1
- MQOZLILWSRAAII-UHFFFAOYSA-N Cl[N-][NH+](C1)CC1C1=NC2C=CC=CC2C=C1C1=CCCC=C1 Chemical compound Cl[N-][NH+](C1)CC1C1=NC2C=CC=CC2C=C1C1=CCCC=C1 MQOZLILWSRAAII-UHFFFAOYSA-N 0.000 description 1
- QQWXLVQYDYXYAS-UHFFFAOYSA-N Fc1cnc(C2CNC2)c(-c2ccccc2)c1 Chemical compound Fc1cnc(C2CNC2)c(-c2ccccc2)c1 QQWXLVQYDYXYAS-UHFFFAOYSA-N 0.000 description 1
Classifications
-
- 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
- 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
- A61P25/24—Antidepressants
-
- 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
- A61P25/00—Drugs for disorders of the nervous system
- A61P25/30—Drugs for disorders of the nervous system for treating abuse or dependence
-
- 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
- A61P25/30—Drugs for disorders of the nervous system for treating abuse or dependence
- A61P25/36—Opioid-abuse
-
- 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
- A61P3/00—Drugs for disorders of the metabolism
- A61P3/08—Drugs for disorders of the metabolism for glucose homeostasis
- A61P3/10—Drugs for disorders of the metabolism for glucose homeostasis for hyperglycaemia, e.g. antidiabetics
-
- 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
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P7/00—Drugs for disorders of the blood or the extracellular fluid
- A61P7/12—Antidiuretics, e.g. drugs for diabetes insipidus
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C53/00—Saturated compounds having only one carboxyl group bound to an acyclic carbon atom or hydrogen
- C07C53/15—Saturated compounds having only one carboxyl group bound to an acyclic carbon atom or hydrogen containing halogen
- C07C53/16—Halogenated acetic acids
- C07C53/18—Halogenated acetic acids containing fluorine
-
- 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
- C07D403/14—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 three or more hetero rings
-
- 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
- C07D409/00—Heterocyclic compounds containing two or more hetero rings, at least one ring having sulfur atoms as the only ring hetero atoms
- C07D409/14—Heterocyclic compounds containing two or more hetero rings, at least one ring having sulfur atoms as the only ring hetero atoms 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
-
- 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
-
- 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
- C07D471/08—Bridged systems
-
- 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
-
- 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
- C07D487/08—Bridged systems
-
- 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
- C07D487/10—Spiro-condensed systems
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D491/00—Heterocyclic compounds containing in the condensed ring system both one or more rings having oxygen atoms as the only ring hetero atoms and one or more rings having nitrogen atoms as the only ring hetero atoms, not provided for by groups C07D451/00 - C07D459/00, C07D463/00, C07D477/00 or C07D489/00
- C07D491/02—Heterocyclic compounds containing in the condensed ring system both one or more rings having oxygen atoms as the only ring hetero atoms and one or more rings having nitrogen atoms as the only ring hetero atoms, not provided for by groups C07D451/00 - C07D459/00, C07D463/00, C07D477/00 or C07D489/00 in which the condensed system contains two hetero rings
- C07D491/04—Ortho-condensed systems
- C07D491/056—Ortho-condensed systems with two or more oxygen atoms as ring hetero atoms in the oxygen-containing ring
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D491/00—Heterocyclic compounds containing in the condensed ring system both one or more rings having oxygen atoms as the only ring hetero atoms and one or more rings having nitrogen atoms as the only ring hetero atoms, not provided for by groups C07D451/00 - C07D459/00, C07D463/00, C07D477/00 or C07D489/00
- C07D491/02—Heterocyclic compounds containing in the condensed ring system both one or more rings having oxygen atoms as the only ring hetero atoms and one or more rings having nitrogen atoms as the only ring hetero atoms, not provided for by groups C07D451/00 - C07D459/00, C07D463/00, C07D477/00 or C07D489/00 in which the condensed system contains two hetero rings
- C07D491/08—Bridged systems
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D491/00—Heterocyclic compounds containing in the condensed ring system both one or more rings having oxygen atoms as the only ring hetero atoms and one or more rings having nitrogen atoms as the only ring hetero atoms, not provided for by groups C07D451/00 - C07D459/00, C07D463/00, C07D477/00 or C07D489/00
- C07D491/02—Heterocyclic compounds containing in the condensed ring system both one or more rings having oxygen atoms as the only ring hetero atoms and one or more rings having nitrogen atoms as the only ring hetero atoms, not provided for by groups C07D451/00 - C07D459/00, C07D463/00, C07D477/00 or C07D489/00 in which the condensed system contains two hetero rings
- C07D491/10—Spiro-condensed systems
- C07D491/107—Spiro-condensed systems with only one oxygen atom as ring hetero atom in the oxygen-containing ring
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D513/00—Heterocyclic compounds containing in the condensed system at least one hetero ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for in groups C07D463/00, C07D477/00 or C07D499/00 - C07D507/00
- C07D513/02—Heterocyclic compounds containing in the condensed system at least one hetero ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for in groups C07D463/00, C07D477/00 or C07D499/00 - C07D507/00 in which the condensed system contains two hetero rings
- C07D513/04—Ortho-condensed systems
Landscapes
- Organic Chemistry (AREA)
- Chemical & Material Sciences (AREA)
- Health & Medical Sciences (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Engineering & Computer Science (AREA)
- Animal Behavior & Ethology (AREA)
- Public Health (AREA)
- Veterinary Medicine (AREA)
- General Health & Medical Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- General Chemical & Material Sciences (AREA)
- Medicinal Chemistry (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Life Sciences & Earth Sciences (AREA)
- Pharmacology & Pharmacy (AREA)
- Neurology (AREA)
- Neurosurgery (AREA)
- Biomedical Technology (AREA)
- Diabetes (AREA)
- Psychiatry (AREA)
- Addiction (AREA)
- Hematology (AREA)
- Obesity (AREA)
- Psychology (AREA)
- Emergency Medicine (AREA)
- Pain & Pain Management (AREA)
- Endocrinology (AREA)
- Hospice & Palliative Care (AREA)
- Child & Adolescent Psychology (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Plural Heterocyclic Compounds (AREA)
- Nitrogen Condensed Heterocyclic Rings (AREA)
Applications Claiming Priority (4)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US33452510P | 2010-05-13 | 2010-05-13 | |
| US61/334,525 | 2010-05-13 | ||
| US61/334525 | 2010-05-13 | ||
| PCT/US2011/036148 WO2011143365A1 (en) | 2010-05-13 | 2011-05-11 | Nitrogen heterocyclic compounds useful as pde10 inhibitors |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| CN103221404A CN103221404A (zh) | 2013-07-24 |
| CN103221404B true CN103221404B (zh) | 2015-12-16 |
Family
ID=44278966
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| CN201180034741.6A Expired - Fee Related CN103221404B (zh) | 2010-05-13 | 2011-05-11 | 可用作pde10抑制剂的不饱和氮杂环化合物 |
Country Status (26)
| Country | Link |
|---|---|
| US (3) | US8957073B2 (OSRAM) |
| EP (1) | EP2569300A1 (OSRAM) |
| JP (1) | JP5702855B2 (OSRAM) |
| KR (1) | KR101564806B1 (OSRAM) |
| CN (1) | CN103221404B (OSRAM) |
| AR (1) | AR081627A1 (OSRAM) |
| AU (1) | AU2011253057B2 (OSRAM) |
| BR (1) | BR112012029026A2 (OSRAM) |
| CA (1) | CA2798490A1 (OSRAM) |
| CL (1) | CL2012003178A1 (OSRAM) |
| CO (1) | CO6630189A2 (OSRAM) |
| CR (1) | CR20120635A (OSRAM) |
| EA (1) | EA201291236A1 (OSRAM) |
| IL (1) | IL222898A (OSRAM) |
| MA (1) | MA34300B1 (OSRAM) |
| MX (1) | MX2012013130A (OSRAM) |
| NZ (1) | NZ603876A (OSRAM) |
| PE (1) | PE20130576A1 (OSRAM) |
| PH (1) | PH12012502212A1 (OSRAM) |
| SG (1) | SG185515A1 (OSRAM) |
| TN (1) | TN2012000530A1 (OSRAM) |
| TW (1) | TW201206902A (OSRAM) |
| UA (1) | UA109438C2 (OSRAM) |
| UY (1) | UY33382A (OSRAM) |
| WO (1) | WO2011143365A1 (OSRAM) |
| ZA (1) | ZA201208510B (OSRAM) |
Families Citing this family (84)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US8952037B2 (en) | 2010-05-13 | 2015-02-10 | Amgen Inc. | Heteroaryloxycarbocyclyl compounds as PDE10 inhibitors |
| CA2800578A1 (en) | 2010-05-13 | 2011-11-17 | Amgen Inc. | Nitrogen-heterocyclic compounds as phosphodiesterase 10 inhibitors |
| WO2011143495A1 (en) | 2010-05-13 | 2011-11-17 | Amgen Inc. | Heteroaryloxyheterocyclyl compounds as pde10 inhibitors |
| CN103221404B (zh) * | 2010-05-13 | 2015-12-16 | 安姆根有限公司 | 可用作pde10抑制剂的不饱和氮杂环化合物 |
| MX2013009575A (es) | 2011-02-18 | 2014-10-14 | Exonhit Therapeutics Sa | Derivados de 6, 7-dialcoxi-3-isoquinolinol sustituidos como inhibidores de fosfodiesterasa 10 (pdei0a). |
| LT2718270T (lt) | 2011-06-10 | 2022-08-10 | Merck Patent Gmbh | Pirimidino ir piridino junginių, turinčių btk inhibitorinį aktyvumą, kompozicijos ir gamybos būdai |
| US8623860B2 (en) * | 2011-12-30 | 2014-01-07 | Boehringer Ingelheim International Gmbh | Azetidine derivatives, pharmaceutical compositions and uses thereof |
| TW201348231A (zh) | 2012-02-29 | 2013-12-01 | Amgen Inc | 雜雙環化合物 |
| JP6049866B2 (ja) * | 2012-05-09 | 2016-12-21 | ゾエティス・サービシーズ・エルエルシー | 駆虫剤としてのアゼチジン誘導体 |
| UY34858A (es) | 2012-06-14 | 2013-11-29 | Amgen Inc | Compuestos de azetidina y piperidina útiles como inhibidores de pde10 |
| WO2014071044A1 (en) | 2012-11-01 | 2014-05-08 | Allergan, Inc. | Substituted 6,7-dialkoxy-3-isoquinoline derivatives as inhibitors of phosphodiesterase 10 (pde10a) |
| MX2015007205A (es) | 2012-12-06 | 2016-03-31 | Quanticel Pharmaceuticals Inc | Inhibidores de la desmetilasa de histona. |
| WO2014121885A1 (en) * | 2013-02-07 | 2014-08-14 | Merck Patent Gmbh | Substituted quinoxaline derivatives and their use as positive allosteric modulators of mglur4 |
| US9200016B2 (en) | 2013-12-05 | 2015-12-01 | Allergan, Inc. | Substituted 6, 7-dialkoxy-3-isoquinoline derivatives as inhibitors of phosphodiesterase 10 (PDE 10A) |
| WO2015123408A1 (en) | 2014-02-13 | 2015-08-20 | Incyte Corporation | Cyclopropylamines as lsd1 inhibitors |
| TWI720451B (zh) | 2014-02-13 | 2021-03-01 | 美商英塞特控股公司 | 作為lsd1抑制劑之環丙胺 |
| WO2015123437A1 (en) | 2014-02-13 | 2015-08-20 | Incyte Corporation | Cyclopropylamines as lsd1 inhibitors |
| US9670210B2 (en) | 2014-02-13 | 2017-06-06 | Incyte Corporation | Cyclopropylamines as LSD1 inhibitors |
| CA2939382A1 (en) * | 2014-02-14 | 2015-08-20 | Takeda Pharmaceutical Company Limited | Pyrazines modulators of gpr6 |
| CN104016909B (zh) * | 2014-04-03 | 2016-04-20 | 定陶县友帮化工有限公司 | 一种2-氨基-3-溴-5-氯吡啶的合成方法 |
| CN104016911A (zh) * | 2014-04-03 | 2014-09-03 | 定陶县友帮化工有限公司 | 一种2-氨基-3,5-二溴吡啶的合成方法 |
| AR100530A1 (es) | 2014-05-19 | 2016-10-12 | Merial Inc | Compuestos antihelmínticos |
| TWI687419B (zh) | 2014-07-10 | 2020-03-11 | 美商英塞特公司 | 作為lsd1抑制劑之咪唑并吡啶及咪唑并吡嗪 |
| WO2016007736A1 (en) | 2014-07-10 | 2016-01-14 | Incyte Corporation | Imidazopyrazines as lsd1 inhibitors |
| WO2016007722A1 (en) | 2014-07-10 | 2016-01-14 | Incyte Corporation | Triazolopyridines and triazolopyrazines as lsd1 inhibitors |
| WO2016007727A1 (en) | 2014-07-10 | 2016-01-14 | Incyte Corporation | Triazolopyridines and triazolopyrazines as lsd1 inhibitors |
| JP6769963B2 (ja) | 2014-08-29 | 2020-10-14 | ティエエッセ ファルマ ソチエタ レスポンサビリタ リミタータ | α−アミノ−β−カルボキシムコン酸セミアルデヒド脱炭酸酵素の阻害剤 |
| US9855249B2 (en) | 2014-10-02 | 2018-01-02 | Flatley Discovery Lab, Llc | Isoxazole compounds and methods for the treatment of cystic fibrosis |
| MX373154B (es) | 2015-04-03 | 2020-04-22 | Incyte Holdings Corp | Compuestos heterocíclicos como inhibidores de demetilasa 1 específica de lisina (lsd1). |
| WO2017009751A1 (en) | 2015-07-15 | 2017-01-19 | Pfizer Inc. | Pyrimidine derivatives |
| LT3334709T (lt) | 2015-08-12 | 2025-03-10 | Incyte Holdings Corporation | Lsd1 inhibitoriaus druskos |
| UA125559C2 (uk) | 2016-04-22 | 2022-04-20 | Інсайт Корпорейшн | Композиції інгібітора lsd1 |
| US20200321533A1 (en) * | 2016-05-24 | 2020-10-08 | President And Fellows Of Harvard College | Compounds for organic light emitting diode materials |
| AU2017275657B2 (en) | 2016-06-02 | 2021-08-19 | Novartis Ag | Potassium channel modulators |
| CN110325530B (zh) | 2016-12-16 | 2022-01-11 | 辉瑞大药厂 | Glp-1受体激动剂及其用途 |
| EP3571193B1 (en) | 2017-01-23 | 2021-12-01 | Cadent Therapeutics, Inc. | Potassium channel modulators |
| CN106957300A (zh) * | 2017-04-12 | 2017-07-18 | 苏州汉德创宏生化科技有限公司 | 抗肿瘤杂环药物中间体2‑(3‑氮杂环丁基)吡啶二盐酸盐的合成方法 |
| EP3700935A4 (en) | 2017-10-25 | 2021-08-04 | University Of South Florida | DRUG-INDUCED ACTIVATION OF THE REELIN SIGNALING SYSTEM |
| MX387232B (es) | 2017-10-27 | 2025-03-18 | Boehringer Ingelheim Int | Derivados de piridincarbonilo y usos terapéuticos de los mismos como inhibidores de trpc6. |
| AU2018393409A1 (en) * | 2017-12-26 | 2020-08-13 | Mediconns (Shanghai) Biopharmaceutical Co., Ltd | Tetrahydropyrrole compound, preparation method therefor, pharmaceutical composition containing same, and use thereof |
| RS63124B1 (sr) | 2018-03-08 | 2022-05-31 | Incyte Corp | Aminopirazin diol jedinjenja kao pi3k-y inhibitori |
| US10934279B2 (en) | 2018-06-13 | 2021-03-02 | Pfizer Inc. | GLP-1 receptor agonists and uses thereof |
| PL3806855T3 (pl) * | 2018-06-15 | 2023-07-24 | Pfizer Inc. | Agoniści receptora GLP-1 oraz ich zastosowania |
| US11046658B2 (en) | 2018-07-02 | 2021-06-29 | Incyte Corporation | Aminopyrazine derivatives as PI3K-γ inhibitors |
| US10968200B2 (en) | 2018-08-31 | 2021-04-06 | Incyte Corporation | Salts of an LSD1 inhibitor and processes for preparing the same |
| BR112021006225A2 (pt) | 2018-10-02 | 2021-07-06 | Syngenta Participations Ag | compostos de benzeno- e azina-amida ativos em termos pesticidas |
| EP3870291A1 (en) | 2018-10-22 | 2021-09-01 | Cadent Therapeutics, Inc. | Crystalline forms of potassium channel modulators |
| WO2020102216A1 (en) | 2018-11-13 | 2020-05-22 | Incyte Corporation | Substituted heterocyclic derivatives as pi3k inhibitors |
| WO2020102198A1 (en) | 2018-11-13 | 2020-05-22 | Incyte Corporation | Heterocyclic derivatives as pi3k inhibitors |
| US11161838B2 (en) | 2018-11-13 | 2021-11-02 | Incyte Corporation | Heterocyclic derivatives as PI3K inhibitors |
| EP3883928A4 (en) | 2018-11-22 | 2022-06-29 | Qilu Regor Therapeutics Inc. | Glp-1r agonists and uses thereof |
| CN113165139B (zh) | 2018-11-26 | 2023-06-09 | 京瓷株式会社 | 气体喷嘴和气体喷嘴的制造方法以及等离子体处理装置 |
| CA3121202A1 (en) | 2018-11-30 | 2020-06-04 | Nuvation Bio Inc. | Pyrrole and pyrazole compounds and methods of use thereof |
| TWI853009B (zh) | 2019-03-29 | 2024-08-21 | 瑞士商先正達農作物保護公司 | 殺有害生物活性之二-醯胺化合物 |
| PE20220171A1 (es) | 2019-04-05 | 2022-01-28 | Syngenta Crop Protection Ag | Compuestos de diazina-amida activos como pesticidas |
| US20220169629A1 (en) | 2019-04-11 | 2022-06-02 | Syngenta Crop Protection Ag | Pesticidally active diazine-amide compounds |
| PH12021552557A1 (en) | 2019-04-12 | 2022-07-04 | Qilu Regor Therapeutics Inc | Glp-1r agonists and uses thereof |
| US10954221B2 (en) | 2019-04-12 | 2021-03-23 | Qilu Regor Therapeutics Inc. | GLP-1R agonists and uses thereof |
| WO2020234726A1 (en) * | 2019-05-20 | 2020-11-26 | Pfizer Inc. | Combinations comprising benzodioxol as glp-1r agonists for use in the treatment of nash/nafld and related diseases |
| CN114269732A (zh) | 2019-08-23 | 2022-04-01 | 先正达农作物保护股份公司 | 杀有害生物活性的吡嗪-酰胺化合物 |
| WO2021050913A1 (en) * | 2019-09-12 | 2021-03-18 | Disarm Therapeutics, Inc. | Inhibitors of sarm1 |
| PH12022550932A1 (en) | 2019-10-25 | 2023-06-14 | Gilead Sciences Inc | Glp-1r modulating compounds |
| PE20221422A1 (es) * | 2019-11-15 | 2022-09-20 | Ildong Pharmaceutical Co Ltd | Agonista del receptor glp-1 y uso de este |
| WO2021138391A1 (en) | 2019-12-30 | 2021-07-08 | Tyra Biosciences, Inc. | Indazole compounds |
| AU2021212669B2 (en) | 2020-01-29 | 2023-10-26 | Gilead Sciences, Inc. | GLP-1R modulating compounds |
| EP4119555A4 (en) * | 2020-03-18 | 2023-08-23 | Lg Chem, Ltd. | GLP-1 RECEPTOR AGONIST, PHARMACEUTICAL COMPOSITION THEREOF AND PROCESS FOR MANUFACTURE THEREOF |
| IL296336A (en) * | 2020-03-18 | 2022-11-01 | Lg Chemical Ltd | Glp-1 receptor agonist, pharmaceutical composition comprising same, and method for preparing same |
| US12059408B2 (en) | 2020-08-13 | 2024-08-13 | Boehringer Ingelheim International Gmbh | Treatment of cognitive impairment associated with schizophrenia |
| WO2022078927A1 (en) | 2020-10-13 | 2022-04-21 | Boehringer Ingelheim International Gmbh | Process of reworking |
| US20240016959A1 (en) * | 2020-11-19 | 2024-01-18 | Cerecin Inc. | Radiopharmaceutical ketone and dual tracer imaging in alzheimer's disease, cognitive impairment, and other conditions of altered cerebral metabolism |
| WO2022109182A1 (en) | 2020-11-20 | 2022-05-27 | Gilead Sciences, Inc. | Polyheterocyclic glp-1 r modulating compounds |
| CA3205986A1 (en) | 2020-12-30 | 2022-07-07 | Tyra Biosciences, Inc. | Indazole compounds as kinase inhibitors |
| US12180197B2 (en) | 2021-03-11 | 2024-12-31 | Gilead Sciences, Inc. | GLP-1R modulating compounds |
| CR20230530A (es) | 2021-05-13 | 2024-02-19 | Carmot Therapeutics Inc | Moduladores de los receptores acoplados a proteínas g. |
| US20240287047A1 (en) | 2021-06-09 | 2024-08-29 | Syngenta Crop Protection Ag | Pesticidally active diazine-amide compounds |
| AU2022291768A1 (en) * | 2021-06-16 | 2023-11-30 | Celgene Corporation | Azetidinyl compounds comprising a carboxylic acid group for the treatment of neurodegenerative diseases |
| BR112023026747A2 (pt) | 2021-06-18 | 2024-03-12 | Aligos Therapeutics Inc | Métodos e composições para direcionamento de pd-l1 |
| AU2022349020A1 (en) | 2021-09-27 | 2024-05-09 | Terns Pharmaceuticals, Inc. | Benzimidazole carboxylic acids as glp-1r agonists |
| AU2022375634A1 (en) | 2021-10-25 | 2024-06-06 | Terns Pharmaceuticals, Inc. | Compounds as glp-1r agonists |
| US12428427B2 (en) | 2021-12-16 | 2025-09-30 | Aligos Therapeutics, Inc. | Methods and compositions for targeting PD-L1 |
| JP2025508812A (ja) | 2022-02-23 | 2025-04-10 | ターンズ・ファーマシューティカルズ・インコーポレイテッド | Glp-1rアゴニストとしての化合物 |
| TWI866545B (zh) * | 2022-10-20 | 2024-12-11 | 南韓商東亞St股份有限公司 | 氮雜環丁烷基苯并唑化合物及其等作為mer及axl抑制劑的用途 |
| KR20250166323A (ko) | 2023-04-07 | 2025-11-27 | 테른스 파마슈티칼스, 인크. | 간 장애 또는 심장대사 질환의 치료에 사용하기 위한 thr베타 효현제 및 glp-1r 효현제를 포함하는 조합 |
| WO2025147609A1 (en) * | 2024-01-05 | 2025-07-10 | Dewpoint Therapeutics, Inc. | Amino quinoline compounds and uses thereof |
Citations (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| WO2009081197A1 (en) * | 2007-12-21 | 2009-07-02 | Astrazeneca Ab | Bicyclic derivatives for use in the treatment of androgen receptor associated conditions |
Family Cites Families (24)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US4107288A (en) | 1974-09-18 | 1978-08-15 | Pharmaceutical Society Of Victoria | Injectable compositions, nanoparticles useful therein, and process of manufacturing same |
| 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 |
| US5145684A (en) | 1991-01-25 | 1992-09-08 | Sterling Drug Inc. | Surface modified drug nanoparticles |
| AR036608A1 (es) * | 2001-09-24 | 2004-09-22 | Bayer Corp | Derivados de imidazol, composiciones farmaceuticas y el uso de dichos derivados para la fabricacion de un medicamento para el tratamiento de la obesidad |
| PT1511710E (pt) * | 2002-05-31 | 2014-02-26 | Proteotech Inc | Compostos, composições e métodos para o tratamento de doenças da amiloide e sinucleínopatias tais como doença de alzheimer, diabetes do tipo 2, e doença de parkinson |
| JP2006505570A (ja) | 2002-10-17 | 2006-02-16 | アムジエン・インコーポレーテツド | ベンズイミダゾール誘導体およびそれのバニロイド受容体リガンドとしての使用 |
| JP2007508241A (ja) | 2003-07-31 | 2007-04-05 | バイエル・フアーマシユーチカルズ・コーポレーシヨン | Pde10a阻害剤を用いる糖尿病および関連障害の処置方法 |
| GB0325287D0 (en) * | 2003-10-29 | 2003-12-03 | Merck Sharp & Dohme | Therapeutic agents |
| WO2005116009A1 (en) * | 2004-05-18 | 2005-12-08 | Schering Corporation | Substituted 2-quinolyl-oxazoles useful as pde4 inhibitors |
| US20060019975A1 (en) | 2004-07-23 | 2006-01-26 | Pfizer Inc | Novel piperidyl derivatives of quinazoline and isoquinoline |
| US20070072908A1 (en) | 2005-06-08 | 2007-03-29 | Japan Tobacco Inc. | Heterocyclic compounds |
| US7709501B2 (en) * | 2005-12-23 | 2010-05-04 | Amgen Inc. | Vanilloid receptor ligands and their use in treatments |
| EP1981868A2 (en) * | 2006-01-27 | 2008-10-22 | Pfizer Products Inc. | Aminophthalazine derivative compounds |
| US20110294836A1 (en) | 2008-06-20 | 2011-12-01 | Metabolex, Inc. | Aryl gpr119 agonists and uses thereof |
| US20100041663A1 (en) * | 2008-07-18 | 2010-02-18 | Novartis Ag | Organic Compounds as Smo Inhibitors |
| US20100204265A1 (en) | 2009-02-09 | 2010-08-12 | Genelabs Technologies, Inc. | Certain Nitrogen Containing Bicyclic Chemical Entities for Treating Viral Infections |
| ES2440001T3 (es) | 2009-05-12 | 2014-01-27 | Janssen Pharmaceuticals, Inc. | Derivados de 1,2,4-triazolo[4,3-A]piridina y su uso para el tratamiento o prevención de trastornos neurológicos y psiquiátricos |
| MX2012002274A (es) | 2009-09-03 | 2012-09-07 | Bioenergenix | Compuestos heterociclicos para la inhibicion de pask. |
| EP2479165B1 (en) | 2009-09-16 | 2017-10-25 | Astellas Pharma Inc. | Glycine compound |
| CN103221404B (zh) * | 2010-05-13 | 2015-12-16 | 安姆根有限公司 | 可用作pde10抑制剂的不饱和氮杂环化合物 |
| CA2800578A1 (en) | 2010-05-13 | 2011-11-17 | Amgen Inc. | Nitrogen-heterocyclic compounds as phosphodiesterase 10 inhibitors |
| US8952037B2 (en) | 2010-05-13 | 2015-02-10 | Amgen Inc. | Heteroaryloxycarbocyclyl compounds as PDE10 inhibitors |
| WO2011143495A1 (en) | 2010-05-13 | 2011-11-17 | Amgen Inc. | Heteroaryloxyheterocyclyl compounds as pde10 inhibitors |
| UY34858A (es) * | 2012-06-14 | 2013-11-29 | Amgen Inc | Compuestos de azetidina y piperidina útiles como inhibidores de pde10 |
-
2011
- 2011-05-11 CN CN201180034741.6A patent/CN103221404B/zh not_active Expired - Fee Related
- 2011-05-11 PE PE2012002159A patent/PE20130576A1/es not_active Application Discontinuation
- 2011-05-11 JP JP2013510285A patent/JP5702855B2/ja not_active Expired - Fee Related
- 2011-05-11 NZ NZ603876A patent/NZ603876A/en not_active IP Right Cessation
- 2011-05-11 MX MX2012013130A patent/MX2012013130A/es unknown
- 2011-05-11 AU AU2011253057A patent/AU2011253057B2/en not_active Ceased
- 2011-05-11 CA CA2798490A patent/CA2798490A1/en not_active Abandoned
- 2011-05-11 BR BR112012029026A patent/BR112012029026A2/pt not_active Application Discontinuation
- 2011-05-11 EA EA201291236A patent/EA201291236A1/ru unknown
- 2011-05-11 MA MA35440A patent/MA34300B1/fr unknown
- 2011-05-11 EP EP11721618A patent/EP2569300A1/en not_active Withdrawn
- 2011-05-11 PH PH1/2012/502212A patent/PH12012502212A1/en unknown
- 2011-05-11 US US13/105,860 patent/US8957073B2/en active Active
- 2011-05-11 KR KR1020127032541A patent/KR101564806B1/ko not_active Expired - Fee Related
- 2011-05-11 SG SG2012082939A patent/SG185515A1/en unknown
- 2011-05-11 WO PCT/US2011/036148 patent/WO2011143365A1/en not_active Ceased
- 2011-05-12 UY UY0001033382A patent/UY33382A/es not_active Application Discontinuation
- 2011-05-13 TW TW100116952A patent/TW201206902A/zh unknown
- 2011-05-13 AR ARP110101668A patent/AR081627A1/es unknown
- 2011-11-05 UA UAA201214182A patent/UA109438C2/uk unknown
-
2012
- 2012-11-06 IL IL222898A patent/IL222898A/en not_active IP Right Cessation
- 2012-11-07 TN TNP2012000530A patent/TN2012000530A1/en unknown
- 2012-11-12 ZA ZA2012/08510A patent/ZA201208510B/en unknown
- 2012-11-13 CL CL2012003178A patent/CL2012003178A1/es unknown
- 2012-11-15 CO CO12207172A patent/CO6630189A2/es active IP Right Grant
- 2012-12-13 CR CR20120635A patent/CR20120635A/es unknown
-
2014
- 2014-04-01 US US14/242,432 patent/US20140213572A1/en not_active Abandoned
-
2015
- 2015-12-17 US US14/973,491 patent/US9718803B2/en active Active
Patent Citations (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| WO2009081197A1 (en) * | 2007-12-21 | 2009-07-02 | Astrazeneca Ab | Bicyclic derivatives for use in the treatment of androgen receptor associated conditions |
Also Published As
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| CN103221404B (zh) | 可用作pde10抑制剂的不饱和氮杂环化合物 | |
| US11390609B2 (en) | Rho-associated protein kinase inhibitor, pharmaceutical composition comprising same, and preparation method and use thereof | |
| US8946230B2 (en) | Aryl- and heteroaryl- nitrogen-heterocyclic compounds as PDE10 inhibitors | |
| AU2011253003B2 (en) | Heteroaryloxyheterocyclyl compounds as PDE10 inhibitors | |
| CN102300860B (zh) | 作为磷酸二酯酶10抑制剂的吡嗪类化合物 | |
| TW202136266A (zh) | Sos1抑制劑 | |
| CN113166139A (zh) | 作为HPK1抑制剂的吡咯并[2,3-b]吡啶及其用途 | |
| CN118027041A (zh) | 一种btk抑制剂环衍生物及其制备方法和药学上的应用 | |
| KR101921486B1 (ko) | PARP억제제인 4H-피라졸로[1,5-a]벤즈이미다졸 화합물의 아날로그 | |
| CN116589467A (zh) | 通过缀合btk抑制剂与e3连接酶配体降解布鲁顿氏酪氨酸激酶(btk)及其使用方法 | |
| KR20160058188A (ko) | Btk의 치환된 니코틴이미드 저해제 및 그의 제조 방법 및 암, 염증 및 자가면역 질환에의 용도 | |
| AU2011253058A1 (en) | Heteroaryloxycarbocyclyl compounds as PDE10 inhibitors | |
| KR20130094710A (ko) | Jak 키나아제의 억제제로서 5,7-치환된-이미다조[1,2-c]피리미딘 | |
| CN112010858A (zh) | 一种btk抑制剂及其制备方法和药学上的应用 | |
| WO2022134641A1 (zh) | 芳香杂环类化合物、药物组合物及其应用 | |
| JP2025514758A (ja) | PI3Kα阻害剤 | |
| CA3245810A1 (en) | PYRIDO[3,2-D]PYRIMIDINS USED AS HPK1 INHIBITORS | |
| HK1261891B (en) | Rho-associated protein kinase inhibitor, pharmaceutical composition comprising the same, as well as preparation method and use thereof | |
| HK1261891A1 (en) | Rho-associated protein kinase inhibitor, pharmaceutical composition comprising the same, as well as preparation method and use thereof | |
| HK40025018B (en) | Rho-associated protein kinase inhibitor, pharmaceutical composition comprising same, and preparation method and 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 | ||
| C14 | Grant of patent or utility model | ||
| GR01 | Patent grant | ||
| CF01 | Termination of patent right due to non-payment of annual fee |
Granted publication date: 20151216 Termination date: 20170511 |
|
| CF01 | Termination of patent right due to non-payment of annual fee |